DEVICES AND METHODS INCLUDING A PRECONCENTRATOR MATERIAL FOR DETECTION OF ANALYTES
Embodiments described herein provide devices and methods for the determination of analytes. The device typically includes an absorbent material that allows for an analyte sample to be concentrated and analyzed simultaneously and within a short period of time (e.g., less than 10 seconds). Embodiments described herein can provide portable and easily operable devices for on-site, real time field monitoring with high sensitivity, selectivity, and fast response time.
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Embodiments described herein relate to devices comprising absorbent materials for the determination of analytes, and related methods.
BACKGROUNDChemical sensing technologies have focused on the detection of hydrocarbon analytes. For example, benzene, toluene, and xylenes (BTX) are important chemicals as starting and intermediate materials for a wide range of products and are produced largely from petroleum, e.g., pyrolysis gasoline and reformate. BTX are, however, known to be toxic and benzene is classified as a carcinogen. Therefore, facile methods to monitor BTX in chemical and petrochemical industries and refineries can be essential for the safety of work places and the environment as well as process and quality control of products. The permissible exposure limits (PELs) as 8-hour time-weighted average (TWA) concentrations by the Occupational Safety and Health Administration (OSHA) for benzene, toluene, and xylenes are 1 ppm (5 ppm as a short-term exposure limit (STEL)), 200 ppm (500 ppm as STEL), and 100 ppm (150 ppm as STEL), respectively.
Another important analyte in chemical sensing is the fruit hormone ethylene. Fruit emits ethylene during its ripening process and ethylene gas in its vicinity can lead to accelerated ripening. Measuring ethylene at relevant levels for the food industry therefore allows an estimate of fruit ripeness and ethylene sensors can be utilized to guide decisions that lead to a reduction in waste and spoilage of produce in agriculture, storage, transportation, and distribution.
Many of the available monitoring systems for hydrocarbons such as BTX or ethylene involve gas chromatography (GC) coupled with mass spectrometer (MS) and flame ionization detection (FID). The detection limit of GC/MS or GC/FID techniques can be as low as parts-per-billion (ppb), but there are limitations for real time, on-site analysis of hydrocarbon traces due to relatively long sampling, pre-concentrating, and transferring steps prior to detection. Furthermore, special operation and analysis expertise are required for the detection.
Optical sensors based on infrared and ultraviolet spectroscopies and optical wave guides for on-site field analyte gas detection have exhibited sub-parts-per-million (ppm) detection limits. In most cases, a preconcentration step prior to sensing is necessary to detect sub-ppm level of the gases. For example, a preconcentrator consisting of polymeric or carbon-based absorbents collects analytes, and the concentrated analytes are then delivered to a sensing unit by thermal desorption. The preconcentration step typically takes from tens of minutes to several hours, and a thermal desorption system requires high power consumption, rendering such as a system challenging for portable and on-site field sensing applications.
SUMMARYDevices, systems, and methods for determining an analyte are disclosed.
In some embodiments, the device comprises a sensor material layer comprising a conductive material; and an absorbent material layer disposed on the sensor material layer, wherein the absorbent material interacts with an analyte, if present, in a manner bringing the analyte into proximity with the sensor material to produce a determinable signal from the device.
In some embodiments, the device comprises a first electrode and a second electrode; a sensor material in electrochemical communication with the first and the second electrodes, wherein resistance to current flow between the first and second electrode is affected by the sensor material; and an absorbent material in contact with the sensor material, wherein the absorbent material interacts with the analyte, if present, in a manner bringing the analyte into sufficient proximity with the sensor material such that resistance to current flow between the first and second electrodes is affected, thereby generating a signal in the device by which the analyte is determined.
In some embodiments, methods are provided comprising exposing a sample suspected of containing an analyte to a device comprising a sensor material and an absorbent material in contact with the sensor material, the absorbent material having a first analyte concentration prior to exposure to the sample and a second analyte concentration upon exposure to the sample, wherein the sensor material produces a determinable signal affected by the analyte concentration of the absorbent material; and determining the determinable signal of the sensor material, thereby determining the analyte.
In some embodiments, methods are provided comprising exposing a sample suspected of containing an analyte to a device comprising a first electrode, a second electrode, a sensor material in electrical communication with the first and second electrodes, and an absorbent material in contact with the sensor material, wherein the analyte, if present, interacts with the sensor material to cause a change in resistance between the first and second electrodes; and determining the change in resistance between the first and second electrodes, thereby determining the analyte.
Other aspects, embodiments and features of the invention will become apparent from the following detailed description when considered in conjunction with the accompanying drawings. The accompanying figures are schematic and are not intended to be drawn to scale. For purposes of clarity, not every component is labeled in every figure, nor is every component of each embodiment of the invention shown where illustration is not necessary to allow those of ordinary skill in the art to understand the invention. All patent applications and patents incorporated herein by reference are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control.
DETAILED DESCRIPTIONEmbodiments described herein provide devices and methods for the determination of analytes. In some cases, the device includes a material capable of producing a concentrated sample of a target analyte, for example, from a vapor sample, and/or delivering an analyte sample to a sensing component of the device. In some embodiments, the analyte sample may be concentrated and analyzed simultaneously and within a short period of time (e.g., less than 10 seconds). This may be advantageous in that a separate analyte preconcentration process, involving concentrating an analyte in a preconcentration material and then removing the concentrated analyte from the preconcentration material for delivery to an external sensor, may not be necessary. Additionally, devices may be configured such that unwanted phase separation between components of the device is reduced or eliminated. Embodiments described herein can provide portable and easily operable devices for on-site, real time field monitoring with high sensitivity, selectivity, and fast response time.
In some embodiments, devices for determining analytes are provided. Typically, the device may include a first electrode, a second electrode, and a sensor material arranged in electrochemical communication with the first and the second electrodes. The sensor material may include a conductive material (e.g., a carbon-based nanostructure), such that resistance to current flow between the first and second electrode is affected by interaction of the sensor material. Upon exposure to an analyte, the analyte may interact with the sensor material to affect resistance to current flow between the first and second electrodes, thereby generating a signal in the device by which the analyte is determined. In some embodiments, the sensor material is in substantially solid form.
Some embodiments involve the use of an absorbent material in combination with (e.g., in contact with) the sensor material. In some embodiments, the absorbent material may be in substantially solid form. For example, the absorbent material may be formed as a layer, coating, powder, fiber or network of fibers, or other solid articles. In some cases, the absorbent material is a polymeric material such as a cellulose-based polymer, a fluorinated polymer, or a substantially hydrophobic polymer. In some embodiments, the absorbent material comprises an ionic liquid. The absorbent material may be capable of interacting with the analyte, such that the analyte intercalates or diffuses into the absorbent material, creating a concentrated sample of the analyte. That is, the absorbent material can be useful as “preconcentrator” for analytes. The analyte may be readily determined upon intercalation of the analyte within the absorbent material layer. In some cases, the analyte may be determined without removal of the analyte from the absorbent material layer. In some embodiments, the absorbent material may include moieties that bind or otherwise associate with analytes of interest, as described more fully below. Such materials may be useful in the detection of analytes at low concentrations (e.g., low ppm) including vapor-phase analytes. The absorbent material may also interact with an analyte in a manner bringing the analyte into proximity with the sensor material to produce a determinable signal from the device. For example, the absorbent material may “deliver” an analyte sample at or near the interface between the absorbent material and the sensor material, enhancing the sensitivity of the device.
The absorbent material may also improve device performance by, for example, enhancing sensitivity, selectivity, stability, and/or lifetime of the device. For example, the absorbent material may improve the selectivity of the device by reducing or preventing contact between the sensor material and contaminants or other undesired species (e.g., polar interferents such as water). The absorbent material may also improve sensitivity of the device by interacting with the desired analyte and thus increasing the local concentration of the analyte in the vicinity of the sensor material. In some cases, the absorbent material may serve as a moisture barrier, reducing or eliminating undesired and/or irreversible interactions between the sensor material and water. The absorbent material may also provide mechanical stability to the device, and in the case that it has a high glass transition temperature, can prevent movement of the sensor material caused, for example, by exposure to solvents or by changes in temperature.
In some embodiments, the absorbent material and sensor material may be arranged in a layered structure within the device. For example, the device may include a sensor material layer with an absorbent material layer (e.g., substituted cellulose) disposed on the sensor material layer. In some cases, the absorbent material layer may form a coating on at least a portion of the sensor material layer. In some cases, the absorbent material layer may form a coating on substantially all of the sensor material layer. For example, the absorbent material layer may form a coating that encapsulates the sensor material layer and optionally the electrodes contacting the sensor material layer.
The absorbent material may include one or more binding sites that selectively interact with one or more analytes, and/or may be responsive to a change in a set of conditions in the surrounding environment (e.g., temperature, pH, etc.). The binding site may incorporated within the absorbent material in various configurations. For example, the binding site may be a small molecule, a polymer, a biological binding site, or the like. In some embodiments, the binding site may comprise ionic binding site (e.g., a salt). In some embodiments, the binding site may comprise a neutral binding site. The binding site may be an organic, organometallic, or an inorganic binding site. In some cases, the binding site may be attached to the absorbent material via a covalent bond. In some cases, the binding site may be substantially contained within (e.g., dispersed within) the absorbent material, and may not form a covalent bond to the absorbent material. In some embodiments, the absorbent material layer may include a polymer material and a plurality of binding sites. The plurality of binding sites may be covalently or non-covalently bonded to the polymer material. In some cases, the plurality of binding sites may be dispersed throughout the polymer material.
The interaction between the analyte and the binding site may comprise formation of a bond, such as a covalent bond (e.g. carbon-carbon, carbon-oxygen, oxygen-silicon, sulfur-sulfur, phosphorus-nitrogen, carbon-nitrogen, metal-oxygen or other covalent bonds), an ionic bond, a hydrogen bond (e.g., between hydroxyl, amine, carboxyl, thiol and/or similar functional groups, for example), a dative bond (e.g. complexation or chelation between metal ions and monodentate or multidentate ligands), and the like. The interaction may also comprise Van der Waals interactions. In one embodiment, the interaction comprises forming a covalent bond with an analyte. In some cases, the interaction between the binding site and the analyte may comprise a reaction, such as a charge transfer reaction. In other embodiments, the binding site and/or another device component may undergo a chemical or physical transformation upon a change in the surrounding environment (e.g., change in temperature) to produce a determinable signal from the device.
In some cases, the binding site may comprise a biological or a chemical group capable of binding another biological or chemical molecule in a medium (e.g., solution, vapor phase, solid phase). For example, the binding site may include a functional group, such as a thiol, aldehyde, ester, carboxylic acid, hydroxyl, and the like, wherein the functional group forms a bond with the analyte. In some cases, the binding site may be an electron-rich or electron-poor moiety wherein interaction between the analyte and the binding site comprises an electrostatic interaction. In some cases, the interaction between the analyte and the binding site includes binding to a metal or metal-containing moiety. The binding site may also interact with an analyte via a binding event between pairs of biological molecules including proteins, nucleic acids, glycoproteins, carbohydrates, hormones, and the like.
In some embodiments, the binding site may contain an aromatic species, including monocyclic aromatic groups (e.g., phenyl groups) or polycyclic aromatic hydrocarbons (e.g., naphthalene, phenanthrene, pyrene, anthracene, fluoranthene, perylene, benzopyrene, etc.), any of which are optionally substituted. In some cases, the aromatic species may be substituted with one or more halo-containing groups. In one set of embodiments, the binding site is a fluorine-containing aromatic species. For example, the binding site may be an aromatic species substituted with one or more fluoro-groups, or one or more fluoroalkyl groups (e.g., —CF3). As an illustrative embodiment, the binding site may include an electron-deficient aromatic group, such as a pentafluorophenyl group, which may be useful in the determination of electron-rich aromatic analytes, such as benzene, toluene, xylene, and benzopyrene (e.g., benzo[a]pyrene).
In some embodiments, the binding site may be a metal-containing binding site. For example, the binding site may include metal salts or metal complexes (e.g., organometallic complexes. In some embodiments, the metal salt is a transition metal salt. In some cases, the binding site may include a metal complex or metal salt comprising Cu(I), Cu(II), Ag(I), Ag(II), Co(II), Co(III), Rh(I), Rh(III), Ir(I), Ir(III) or Pd(II). Some examples of metal salts or metal complexes include, but are not limited to, TiO2, TiCl4, and other titanium salts, AgCl, AgPF6, Ag(OCOCF3), Ag(SO3CF3), and other silver salts, PtCl2 and other platinum salts, Au2Cl6 and other gold salts, Al(OEt)3 and other aluminum salts, Ni(SO3CF3)2, NiCl2, and other nickel salts, and Cu(SO3CF3) and other copper salts. In some cases, the binding site may be a copper-containing binding site. In some cases, the copper-containing binding site is a salt, such as a Cu(II) salt. In some cases, the binding site may be a cobalt-containing binding site. In some cases, the cobalt-containing binding site is a salt, such as a Co(II) or Co(III) salt (e.g., a cobalt (III) porphyrin compound). In some cases, the binding site may be a palladium-containing binding site. In some cases, the palladium-containing binding site is a salt, such as a Pd(II) salt. Some examples of specific metal containing binding site include, but are not limited to,
In some embodiments, the binding site may be a metal complex capable of interacting with ethylene. An example of such a metal complex is described in Esser et al., “Selective Detection of Ethylene Gas Using Carbon Nanotube-based Devices: Utility in Determination of Fruit Ripeness,” Angew. Chem. Int. Ed. 2012, 51(23), 5752-5756, the contents of which are incorporated herein by reference in its entirety for all purposes.
In some embodiments, the binding site may be a quinone-containing binding site or an oxidized derivative of an aromatic group, including polycyclic aromatic groups. Examples of such binding site include 1,4-benzoquinones or cyclohexadienediones, 1,2-benzoquinones (ortho-quinones), 1,4-naphthoquinones and 9,10-anthraquinones. And the like. In one embodiment, the binding site is 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ).
In some cases, the binding site may include a calixarene group. The calixarene group may include a plurality of aromatic rings (e.g., phenyl rings). In some embodiments, the calixarene includes 4 to 12 aromatic rings.
In some cases, the binding site may include a iptycene group (e.g., triptycene, pentiptycene, etc.).
In some cases, the binding site may include a hydrogen-bond donor. In some cases, the binding site may include a hydrogen bond acceptor. Those of ordinary skill in the art would be able to identify hydrogen-bond donors or hydrogen-bond acceptors suitable for use in embodiments described herein. For example, a hydrogen-bond donor may comprise at least one hydrogen atom capable of interacting with a pair of electrons on a hydrogen-bond acceptor to form the hydrogen bond. In some cases, the hydrogen atom may be positioned adjacent to an electron-poor group, such as fluorine, nitro, acyl, cyano, sulfonate, or the like, to increase the acidity of the hydrogen atom and, thus, the ability of the hydrogen atom to form a hydrogen bond. Other examples of groups which may form hydrogen bonds include carbonyl groups, amines, hydroxyls, and the like. In one embodiment, the hydrogen-bond donor is a fluorinated alcohol, such as hexafluoroisopropanol. In some embodiments, the hydrogen-bond acceptor may be a carbonyl group, an amine, an imine, or other groups containing a pair of electrons that can interact with a hydrogen atom on another species via hydrogen bonding.
Some specific examples of binding sites include the following groups:
Some embodiments involve the use of an absorbent material. The absorbent material may be selected, and may be appropriately functionalized, to impart desired characteristics (e.g., surface properties) to the device. In some cases, the absorbent material may include functional groups selected to facilitate absorption of an analyte, and/or to minimize or prevent absorption of undesired species (e.g., contaminants). For example, the absorbent material may be selected to have a particular surface area or surface property (e.g., hydrophobicity, hydrophilicity, electrostatic charge, etc.). In some cases, the absorbent material may be selected to be compatible with other components of the device, such as the sensor material. For example, the absorbent material may be selected to promote adhesion and reduce or prevent separation/delamination of components (e.g., layers) within the device at various temperatures.
In some cases, the absorbent material may include a conjugated polymer (e.g., pi-conjugated, sigma-conjugated), or a non-conjugated polymer (e.g., cellulose-based polymer). In some cases, the absorbent material may include primarily non-polar groups. In some cases, the absorbent material absorbent material may include a substantially hydrophobic polymer. For example, incorporation of a substantially hydrophobic polymer within a device as described herein may minimize or prevent entry of water within at least a portion of the device. In some cases, the absorbent material absorbent material may include a substantially hydrophilic polymer. In some cases, the absorbent material may be the polymer may be a fluorinated polymer. In some embodiments, the absorbent material layer includes a polyvinyl alcohol-based material. In some embodiments, the absorbent material layer includes a polyhydroxyl ethyl methacrylate-based material. In some cases, the polymer may include one or more iptycene-based groups (e.g., triptycenes, pentiptycenes, etc.). In each of these cases, the polymer may be appropriately functionalized to be responsive to a particular analyte or set of analytes.
In some embodiments, the absorbent material layer may include a cellulose-based polymer. For example, the cellulose-based polymer can be cellulose, cellulose acetate, cellulose diacetate, or cellulose triacetate, any of which is optionally substituted. In some embodiments, the cellulose-based polymer is cellulose substituted with at least one binding site. For example, the cellulose-based polymer may include a functional group that contains an aromatic moiety (e.g., an electron deficient aromatic moiety) that is capable of binding an aromatic species. The aromatic moiety may be, for example, an optionally substituted monocyclic aromatic group (e.g., phenyl group) or an optionally substituted polycyclic aromatic hydrocarbon. In some cases, the cellulose-based polymer is functionalized with a calixarene group. In cases where the target analyte is an electron rich species (e.g., benzene, toluene, xylene, benzo[a]pyrene), the aromatic moiety may be substituted with electron deficient groups, such as fluoro groups, to enhance interaction with the target analyte.
In one set of embodiments, the cellulose-based polymer contains the structure,
wherein:
R1 is a group comprising a binding site for an aromatic species;
R2 and R3 can be the same or different and are hydrogen, alkyl, aryl, a carbonyl group, any of which is optionally substituted; and
n is greater than 1.
In some cases, R2 and R3 can be the same or different and are hydrogen, —COCH3, or —F5Ph. In some cases, R2 and R3 are the same. In some cases, R2 and R3 are different.
In another set of embodiments, the cellulose-based polymer contains the structure,
wherein R4 and R5 can be the same or different and are hydrogen, alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, heteroaryl, or carbonyl group, any of which is optionally substituted.
In another set of embodiments, the cellulose-based polymer contains the structure,
wherein R6 is alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, or heteroaryl, any of which is optionally substituted.
In some cases, the cellulose-based polymer may include one of the following groups,
In some cases, the absorbent material may include an iptycene-based polymer. For example, the iptycene-based polymer may include one or more of the following groups,
wherein each R can be the same or different and is H or a substituent (e.g., an organic substituent) and n is an integer between 0 and 4. In some cases, each R is independently selected from H, halide, or an organic group (e.g., an organic side chain). In some cases, at least one R is a group comprising a binding site as described herein. In some cases, the iptycene-based polymer may include a conjugated polymer backbone (e.g., pi-conjugated polymer backbone), such as polyarylenes, poly(arylene vinylene)s, poly(arylene ethynylene)s, and the like. In some cases, the iptycene-based polymer may include a non-conjugated polymer, such as polyethers, polysulfones, polycarbonates, polyacrylates, and the like.
Some specific examples of absorbent materials include polystyrene, poly(ethylene:vinyl acetate+vinyl chloride) (“Saran wrap”), paraffin film (“Parafilm”), silicon grease, polyethylene, poly(vinyl chloride), fluorinated polymers including CYTOP A and CYTOP S (Bellex International Corp.), poly(chlorotrifluoroethylene)s (e.g., Halocarbon oil 27, Halocarbon oil 700), and polytetrafluoroethylenes (e.g., Teflon AF2400), various polymers shown in the Figures, and the like.
In some cases, the absorbent material may include an ionic liquid. Based on the teachings of this disclosure, those of ordinary skill in the art can readily select ionic liquids suitable for use in the invention. Those ionic liquids that are suitable typically will be capable of absorbing an analyte. In certain embodiments, the ionic liquid comprises an anion and/or a cation. Non-limiting examples of suitable anions include tetrafluoroborate, hexafluorophosphate, hexafluoroarsenoate, perchlorate, trifluoromethanesulfonate, bis(trifluoromethylsulfonyl)amide, and thiosaccharin anion. Non-limiting examples of suitable cations include ammonium, imidazolium, pyridinium, piperidinium and pyrrolidinium derivatives. The ionic liquid can, in some embodiments, include a combination of any one of the above anions and any one of the above cations. For example, in some embodiments, the ionic liquid comprises an imidazolium ion (e.g., a substituted imidazolium ion). Non-limiting examples of imidazolium ions include 1-Butyl-3-methylimidazolium, 1-Ethyl-3-methylimidazolium, and 1-Hexyl-3-methylimidazolium. In some cases, the counterion of the imidazolium ion may be tetrafluoroborate, hexafluorophosphate, or bis(trifluoromethanesulfone)imide.
In some embodiments, the absorbent material includes two or more materials (e.g., a first absorbent material (e.g. an ionic liquid) and a second absorbent material (e.g., a polymer)). In certain embodiments, the first absorbent material is adjacent the second absorbent material (e.g., an ionic liquid layer adjacent a polymeric layer). In some cases, the first absorbent material may be mixed with the second absorbent material (e.g., an ionic liquid mixed with a polymer, an ionic liquid absorbed within a polymer).
Absorbent materials described herein may be synthesized using various methods known in the art. In the case of absorbent materials, the polymers may be synthesized according to known methods, including, but not limited to, cationic polymerization, anionic polymerization, radical polymerization, condensation polymerization, Wittig polymerization, ring-opening polymerization, cross-coupling polymerization, addition polymerization, chain polymerization, metathesis polymerization, or the like. Those of ordinary skill in the art would be able to select the appropriate monomers in order to obtain a desired polymeric product. For example, monomers comprising two hydroxyl groups may be polymerized with monomers comprising two carbonyl groups (e.g., acyl halide, carboxylic acid, etc.) to form a polyether via condensation polymerization. Likewise, monomers comprising a styrene moiety may be polymerized to form polystyrene via radical polymerization. In one embodiment, monomers comprising di-acetylene substituted aryl groups may be polymerized with monomers comprising di-halide substituted aryl groups to form poly(arylene ethynylene)s via cross-coupling polymerization.
In some embodiments, a plurality of devices may be arranged to form an array of devices capable distinguishing, identifying, and quantifying a variety of different analytes simultaneously. For example, in an array of devices, each individual device can include a binding site capable of interacting with an analyte. In some cases, a first device of the array may include a binding site capable of interacting with a first analyte and a second device of the array may include a binding site capable of interacting with a second analyte, wherein the first and second analytes are different.
In some embodiments, a single device may include a mixture of different binding sites capable of determining a plurality of different analytes.
The absorbent material may include additional components for improving the interaction between an analyte and the absorbent material, the interaction between the absorbent material and the sensor material, the response of the sensor material to the analyte, the stability of the absorbent material and/or sensor material, or otherwise enhancing the performance of the device. For example, the sensor material layer and/or absorbent material layer may include one or more species capable of interacting with the analyte. The species may be selected to be responsive to a particular analyte, set of analytes, and/or to a change in a set of conditions in the surrounding environment, and may be integrally connected to the absorbent material and/or sensor material. As used herein, the term “integrally connected,” when referring to two or more components, means components that do not become separated from each other during the course of normal use, e.g., separation requires at least the use of tools, or by breaking bonds, by dissolving, etc. In some cases, the species may be any of the binding sites described herein.
In some embodiments, the absorbent material may be associated with species capable of interacting with analytes (e.g., binding sites). The species may be attached to the absorbent material via, for example, covalent bonds. In some cases, the species may be associated with the absorbent material via non-covalent bonds. In some cases, the species may be substantially dispersed throughout the polymer material.
In some embodiments, the species may be capable of migrating from one component of the device to another component. For example, the species may be non-covalently dispersed throughout an absorbent material layer (e.g., “loaded” onto the absorbent material) and may migrate or diffuse to a sensor material layer in contact with the absorbent material layer. The species may then facilitate or enhance the performance of the sensor material layer in responding to the presence of an analyte. In some cases, the sensor material layer may include a particular species, and an absorbent material layer disposed on the sensor material layer may contain an amount of the same species, which can migrate to the absorbent material layer. In this arrangement, the absorbent material layer can serve as a reservoir for excess species to be delivered to the sensor material layer, if needed. For example, the species in the sensor material may be consumed, may degrade, or may otherwise become depleted during operation. In another set of embodiments, the sensor material layer may include a particular species, and an absorbent material layer disposed on the sensor material layer may contain an amount of a different species, which can migrate to the absorbent material layer. This may allow for devices which are capable of determining more than one type of analyte.
In some cases, the sensor material (e.g., sensor material layer) may include carbon-based nanostructures as the conductive material. For example, the conductive material may include nanotubes, nanoparticles, graphene, or graphite. In some embodiments, the conductive material includes nanotubes. In some embodiments, the conductive material includes single-wall carbon nanotubes. In some embodiments, the conductive material includes multi-wall carbon nanotubes. In some embodiments, the conductive material includes graphite. In some embodiments, the conductive material includes graphene.
In one set of embodiments, the conductive material may be single-wall carbon nanotubes (SWCNTs) and functionalized cellulose acetate (CA) may be employed as a the absorbent material (e.g., “preconcentrator”) that selectively absorbs the analyte of interest.
In some cases, arranging an absorbent material layer in contact with the sensor material may improve the physical, chemical, and mechanical stability of the sensor material, or other components of the sensor material. For example, undesired phase separation between the absorbent material and the conductive material may be reduced or avoided.
Polymers may be substituted with various binding sites using methods known in the art. In some cases, a polymer containing one or more hydroxyl functional groups may be utilized as starting material. In some cases, the hydroxyl functional group may be an alcohol (e.g., a primary alcohol, secondary alcohol, tertiary alcohol). The hydroxyl group may then be functionalized using various chemical reactions known in the art, including esterification. Cellulose-based polymers contain a plurality of hydroxyl functional groups that may be functionalized with binding sites.
In one set of embodiments, a polymer containing hydroxyl groups may be functionalized using an esterification reaction. For example, the polymer may be reacted with a binding site precursor containing a functional group that can react with the hydroxyl group of the polymer via an esterification reaction. In some cases, the functional group may be an acid chloride. The esterification reaction may be catalyzed by an acid (e.g., acetic acid) or a base (e.g., triethylamine). In other embodiments, a polymer may include a hydroxyl group which may be treated with a binding site precursor, a phosphine (e.g., triphenylphosphine, TPP), and diethylazodicarboxylate (DEAD) or diisopropyl azodicarboxylate (DIAD) under Mitsunobu reaction conditions to form an ester. Those of ordinary skill in the art would be capable of selecting the appropriate combination of polymer, binding site precursor, and esterification reaction conditions suitable for a particular desired product.
In one set of embodiments, a polymer containing hydroxyl groups may be reacted to form a moiety capable of reacting via a 1,3-dipolar cycloaddition reaction, i.e., via “click chemistry.” For example, a primary alcohol may be converted to an azide group by treatment with sodium azide, and the azide group may be reacted with a binding site precursor containing a dipolarophile group (e.g., an alkyne) via a cycloaddition reaction. In some embodiments, the cycloaddition reaction may be catalyzed by a metal such as copper.
In some embodiments, a cellulose-based polymer may be functionalized with various binding sites using methods described herein.
An analyte, or a change in the environment surrounding the device, may be determined by monitoring, for example, a change in a signal of a species or material present within the device. The change in signal may be associated with an interaction (e.g., covalent bonding, non-covalent bonding) between the device (e.g., species) and the analyte. The signal may comprise an electrical, optical, or other property of the device. For example, the device may have a resistance that is affected by the presence of an analyte. As used herein, the term “determining” generally refers to the analysis of a species or signal, for example, quantitatively or qualitatively (whether the analyte is present and/or in what amount or concentration), and/or the detection of the presence or absence of the species or signals. “Determining” may also refer to the analysis of an interaction between two or more species or signals, for example, quantitatively or qualitatively, and/or by detecting the presence or absence of the interaction. For example, the method may include the use of a device capable of producing a first, determinable signal (e.g., a reference signal), such as an electrical signal, an optical signal, or the like, in the absence of an analyte. The device may then be exposed to a sample suspected of containing an analyte, wherein the analyte, if present, may interact with one or more components of the device to cause a change in the signal produced by the device. Determination of the change in the signal may then determine the analyte. In some cases, devices described herein may be useful as sensors for analytes such as explosives, chemical warfare agents, and/or toxins. In some cases, the analyte may be an aromatic species such as benzene, toluene, xylene, or benzo[a]pyrene.
In some embodiments, interaction between the device and an analyte produces a change in an electrical or electrochemical property of the device. For example, the conductive material (e.g., carbon nanotube) may be arranged in electrical communication with two electrodes and may have a particular current, voltage, conductivity, and/or resistance (e.g., signal). Upon interaction with an analyte, the current, voltage, conductivity, and/or resistance of the device may be affected (e.g., may increase or decrease) such that a change in signal is produced. In some cases, the change in signal may be associated with a charge transfer reaction and/or binding interaction between the conductive material and the analyte. In some cases, the change in the signal may be associated with a change in the orientation and/or arrangement of the conductive material. In some cases, the change in signal may be attributed to a physical or chemical disruption in the conductive pathways between conductive species (e.g., carbon nanotubes) of the device. In some cases, the conductive species and the absorbent material may have an interaction (e.g., pi-pi interaction) and the change in signal may be attributed to a physical or chemical disruption of the interaction.
In an illustrative embodiment, the device may be exposed to an analyte, which may interact with the absorbent material (e.g., absorbent material) such that the analyte intercalates within (or is absorbed by) the absorbent material to produce a concentrated amount of analyte within the absorbent material. The analyte may diffuse through the absorbent material to a location that is sufficiently proximate the sensor material so as to cause a change in signal produced by the sensor material. That is, the analyte may be present in sufficient physical proximity to the sensor material, and/or in a sufficient concentration, to cause a change in signal produced by the sensor material.
In some cases, resistance to current flow between the first and second electrode is increased in the presence of the analyte. In some cases, resistance to current flow between the first and second electrode is decreased in the presence of the analyte.
Incorporation of an absorbent material within devices described herein may improve device performance, relative to an essentially identical device lacking the absorbent material, under essentially identical conditions. In some cases, the device containing an absorbent material may, in response to an analyte, produce a signal that is 2, 5, 10, 50, 100, 500, or 1000 times greater than a signal produced by an essentially identical device lacking the absorbent material, under essentially identical conditions.
In some cases, the device may comprise additional components or species that may facilitate interaction between the device and analyte, or otherwise enhance performance of the device. In some cases, the additional component may improve the ability of the device to produce a signal or to respond to an analyte. The additional component may associate with the device such that it enhances an electrical, optical, or other property of the device. In some cases, the additional component may act as a dopant for a conductive species (e.g., carbon nanotube) present within the device. For example, the device may comprise a species capable of associating with carbon nanotubes present within the device. In some embodiments, the device includes a species that may interact with the carbon nanotubes via pi-stacking interactions.
The device may comprise additional components, such as a detector component positioned to detect the signal. In one set of embodiments, the device may be a chemiresistor device, wherein the device exhibits changes in electrical resistance upon exposure to an analyte. Chemiresistors may be advantageous in that the resistance changes can be read-out by a simple, low power and low current circuit. In other embodiments, a device of the present invention may exhibit signals, or changes in signals, that may be determined using Raman spectroscopy, adsorption and/or emission photophysics, ellipsometry, atomic force microscopy, scanning electron microscopy, electrode passivation, and the like.
In some embodiments, simple screening tests may be conducted to select appropriate absorbent materials, conductive materials (e.g., carbon nanotubes), binding sites, device configuration, set of conditions, etc., to suit a particular application. In some cases, a material or device may be screened to determine the sensitivity and/or stability of the material or device. In some cases, a material (and/or device) may be selected based on an ability to detect one or more analytes. For example, the ability of a device to detect an analyte may be determined by comparing the signal (e.g., resistance) of the device prior to and following exposure to an analyte. In another example, a device may be exposed to varying concentrations of an analyte to determine the sensitivity of the device.
Devices described herein may be useful in various applications including environmental monitoring and leak detection in chemical and petrochemical industries. In some embodiments, the device may be configured as a surface acoustic wave (SAW) sensor including an absorbent material as described herein. Such devices may include additional components in order to facilitate the transduction mechanism of a SAW device. For example, the SAW sensor may further include a piezoelectric material. In some cases, the absorbent material may be incorporated into a surface plasmon device. In some embodiments, the device may lack a piezoelectric material.
Methods for determining analytes are also provided. Typically, the method involves exposure of a sample suspected of containing an analyte to a device as described herein. In some cases, the sample is a vapor sample. The absorbent material may serve as a preconcentrator for the analyte sample. That is, the absorbent may have a first analyte concentration prior to exposure to the sample and a second, increased analyte concentration upon exposure to the sample. In some cases, a determinable signal (e.g., resistance) produced by the sensor material may be affected by the presence of the analyte. In some cases, the absorbent material may also interact with the analyte in a manner bringing the analyte into proximity with the sensor material to affect the determinable signal of the device.
In some cases, methods for fabricating the devices described herein are also provided. The method may involve, for example, forming a sensor material on a substrate, followed by forming an absorbent material on the sensor material to form a layered structure. The substrate may include additional components, including electrodes formed on the surface of the substrate such that the sensor material may be in physical contact with, or at least electrical communication with, the electrode. The materials may be formed using a variety of known methods, including drop-casting, spin-coating, spray-coating, inkjet or screen printing, and the like. For example, a solution containing the sensor material and/or absorbent material and a fluid carrier may be spun-cast or drop-cast on the surface of a substrate, and the fluid carrier (e.g., solvent) may be removed to form a substantially solid film or layer. In some cases, the sensor material and absorbent material may be formed as separate layers, i.e., using a first solution containing the sensor material to form a first layer and a second solution containing the absorbent material to form a second layer. In some cases, the sensor material and absorbent material may be formed as a single layer, e.g., using a solution containing the sensor material and the absorbent material.
The fluid carrier may be an organic solvent, including acetone, toluene, benzene, tetrahydrofuran, dimethylformamide, hexanes, dimethylsulfoxide, ethyl acetate, acetonitrile, dichloromethane, chloroform, carbon tetrachloride, and fluorinated solvents including perfluorocarbons (e.g., perfluorohexane, perfluoromethylcyclohexane, perfluorodecalin) and hydrofluoroethers. Some specific examples of fluorinated solvents include perfluorohexane, hexafluorobenzene), and CT-SOLV 180 (Bellex International Corp.). In some cases, the absorbent material (e.g., polymer absorbent material) may be combined with a fluid carrier at a concentration in the range of about 0.1 mg/mL to about 100 mg/mL. The resulting solution may then be spin-cast, drop-cast, or otherwise processed, to form a layer comprising the absorbent material.
In an illustrative embodiment, a metal electrode (e.g., gold) may be patterned, evaporated, or otherwise formed on the surface of a substrate (e.g., a glass substrate). A first layer containing the sensor material may be formed on the substrate, followed by a second layer formed on the first layer and containing the absorbent material. The conductive material may be any material capable of conducting charge, including inorganic materials (e.g., metals, alloys, semiconductors), organic materials, organometallic materials, and/or combinations thereof. For example, the conductive material may include nanostructures (e.g., nanotubes, nanoparticles, graphene, etc.), polymers (e.g., conductive polymers), metal-containing species (e.g., metals, metal salts, etc.), biological species (e.g., proteins, DNA, RNA, etc.), and/or small molecules. In some cases, the conductive material comprises a carbon-based material such as a carbon-based nanostructure (e.g., carbon nanotubes, graphite, or graphene). In some embodiments, the conductive material comprises carbon nanotubes, including single-walled carbon nanotubes and/or multi-walled carbon nanotubes. In some cases, the conductive material may be a conjugated polymer (e.g., pi-conjugated, sigma-conjugated), including iptycene-based conjugated polymers (e.g., triptycene-based conjugated polymers, pentiptycene-based conjugated polymers).
“Electrochemical communication,” as used herein, refers to materials that are in sufficient communication with each other, such that the transfer of electrons, polarons, excitons, and/or protons can occur between the two materials. For example, the first and second electrodes may not physically contact one another but may be in electrochemical communication with one another via the conductive material, such that upon application of a voltage or potential, a current flows from the one electrode through the conductive material to the other electrode.
As used herein, the term “nanostructure” refers to any chemical structure having at least one dimension on the order of nanometers. In some cases, the nanostructure has an elongated chemical structure having a diameter on the order of nanometers and a length on the order of microns to millimeters, resulting in an aspect ratio greater than 10, 100, 1000, 10,000, or greater. In some cases, the nanostructure may have a diameter less than 1 μm, less than 100 nm, 50 nm, less than 25 nm, less than 10 nm, or, in some cases, less than 1 nm. The nanostructure may have a cylindrical or pseudo-cylindrical shape. In some cases, the nanostructure may be a nanotube, such as a carbon nanotube. In some cases, the nanostructure is a nanorod, nanowire, or nanoribbon. In some cases, the nanostructure is a nanoparticle.
As used herein, the term “carbon nanotube” is given its ordinary meaning in the art and refers to a substantially cylindrical molecule, in some cases, comprising a fused network of six-membered aromatic rings. In some cases, carbon nanotubes may resemble a sheet of graphite rolled up into a seamless cylindrical structure. It should be understood that the carbon nanotube may also comprise rings other than six-membered rings. Typically, at least one end of the carbon nanotube may be capped, i.e., with a curved or nonplanar aromatic group. Carbon nanotubes may have a diameter of the order of nanometers and a length on the order of millimeters, resulting in an aspect ratio greater than about 100, greater than about 1000, greater than about 10,000, or greater. The term “carbon nanotube” includes single-walled nanotubes (SWCNTs), multi-walled nanotubes (MWCNTs) (e.g., concentric carbon nanotubes), inorganic derivatives thereof, and the like. In some embodiments, the carbon nanotube is a single-walled carbon nanotube. In some cases, the carbon nanotube is a multi-walled carbon nanotube (e.g., a double-walled carbon nanotube).
The carbon nanotubes may be functionalized or substituted with a wide range of functional groups. Examples of functional groups that carbon nanotubes may be substituted with include peptides, proteins, DNA, RNA, peptide nucleic acids (PNA), metal complexes, ligands for metals, ligands for proteins, antibodies, polarizable aromatics, crown ethers, hydroxyl amines, polymers, initiators for polymerizations, liquid crystals, fluorocarbons, synthetic receptors, and the like. The properties of the nanotubes may also be tailored based on the substitution of the fused, aromatic network. Those skilled in the art would recognize what types of functional groups would afford a particular, desired property, such as increased solubility, or the ability to determine an analyte.
Substituted carbon nanotubes may be synthesized using various methods, including those described in Zhang et al., J. Am. Chem. Soc. 2007, 129(25), 7714; International Publication No. WO2008/133779, which are incorporated herein by reference in their entirety for all purposes.
In some cases, the conductive material may comprise nanoparticles. As used herein, the term “nanoparticle” generally refers to a particle having a maximum cross-sectional dimension of no more than 1 μm. Nanoparticles may comprise inorganic or organic, polymeric, ceramic, semiconductor, metallic, non-metallic, magnetic, crystalline (e.g., “nanocrystals”), or amorphous material, or a combination of two or more of these. The nanoparticles may be also selected to be positively or negatively charged. Typically, nanoparticles may have a particle size less than 250 nm in any dimension, less than 100 nm in any dimension, or less than 50 nm in any dimension. In some embodiments, the nanoparticles may have a diameter of about 2 to about 50 nm. In some embodiments, the nanoparticles may have a diameter of about 2 to about 20 nm. The particle size may be measured by methods known in the art, such as electron microscopy.
Polymers or polymeric materials, as used herein, refer to extended molecular structures comprising a backbone (e.g., non-conjugated backbone, conjugated backbone) which optionally contain pendant side groups, where “backbone” refers to the longest continuous bond pathway of the polymer. In some embodiments, the polymer is substantially non-conjugated or has a non-conjugated backbone. In some embodiments, at least a portion of the polymer is conjugated, i.e. the polymer has at least one portion along which electron density or electronic charge can be conducted, where the electronic charge is referred to as being “delocalized.” A polymer may be “pi-conjugated,” where atoms of the backbone include p-orbitals participating in conjugation and have sufficient overlap with adjacent conjugated p-orbitals. It should be understood that other types of conjugated polymers may be used, such as sigma-conjugated polymers.
The polymer can be a homo-polymer or a co-polymer such as a random co-polymer or a block co-polymer. In one embodiment, the polymer is a block co-polymer. An advantageous feature of block co-polymers is that they may mimic a multi-layer structure, wherein each block may be designed to have different band gap components and, by nature of the chemical structure of a block co-polymer, each band gap component is segregated. The band gap and/or selectivity for particular analytes can be achieved by modification or incorporation of different polymer types, as would be understood by those of ordinary skill in the art. The polymer compositions can vary continuously to give a tapered block structure and the polymers can be synthesized by either step growth or chain growth methods.
The number average molecular weight of the polymer may be selected to suit a particular application. As used herein, the term “number average molecular weight (Mn)” is given its ordinary meaning in the art and refers to the total weight of the polymer molecules in a sample, divided by the total number of polymer molecules in a sample. Those of ordinary skill in the art will be able to select methods for determining the number average molecular weight of a polymer, for example, gel permeation chromatography (GPC). In some cases, the GPC may be calibrated vs. polystyrene standards. In some cases, the number average molecular weight of the polymer is at least about 10,000, at least about 20,000, at least about 25,000, at least about 35,000, at least about 50,000, at least about 70,000, at least about 75,000, at least about 100,000, at least about 110,000, at least about 125,000, or greater. The device may also comprise an insulating material. The insulating material may be arranged between the conductive material and one or more electrodes and/or the substrate. Examples of suitable insulating materials include, but are not limited to, polysilicate glass, silicon dioxide, silicon nitride, and the like.
As used herein, the term “electrode” or “electrode material” refers to a composition, which, when connected to an electronic device, is able to sense a current or charge and convert it to a signal. An electrode may be comprised of a conductive material or combination of materials such as, for example, metals. Non-limiting examples of suitable metals include gold, copper, silver, platinum, nickel, cadmium, tin, and the like. The electrodes may also be any other metals and/or non-metals known to those of ordinary skill in the art as conductive (e.g. ceramics). The electrodes may be deposited on a surface via vacuum deposition processes (e.g., sputtering and evaporation), solution deposition (e.g., electroplating or electroless processes), or screen printing. In a specific example, gold electrodes are deposited by thermal evaporation. In another embodiment, gold electrodes are screen printed on a surface.
In some embodiments, the conductive material may comprise a conductive, semiconductive, semimetallic species, or other species capable of transporting charge to create a conductive pathway. The conductive, semiconductive, or semimetallic species may include inorganic materials (e.g., metals, alloys, semiconductors), organic materials (e.g., polymer materials), organometallic materials, and/or combinations thereof. In some cases, the conductive material may include a plurality of nanostructures (e.g., nanotubes, nanowires, nanoribbons, nanoparticles, etc.). The nanostructures may be selected to exhibit, for example, high charge mobilities and/or resistance to damage from ionizing radiation. In some cases, mixtures or assemblies of nanostructures may be utilized. Some embodiments may involve the use of carbon nanotubes, such as single-walled carbon nanotubes (SWCNTs) and/or multi-walled carbon nanotubes (MWCNTs), which can display relatively high charge mobilities (e.g., 100,000 cm2/Vs for SWCNTs). In some cases, nanowires, such as gold, silver, copper, bismuth, gadolinium nanowires, may be used as the conductive species. In some cases, the conductive, semiconductive, or semimetallic species may comprise nanoparticles (e.g., gold nanoparticles).
As used herein, an “analyte” can be any chemical, biochemical, or biological entity (e.g. a molecule) to be analyzed. The analyte may be in vapor phase, liquid phase, or solid phase. In some embodiments, the analyte is a vapor phase analyte. In some cases, the analyte may be a form of electromagnetic radiation. In some cases, the device may be selected to have high specificity for the analyte, and may be a chemical, biological, or explosives sensor, for example. In some embodiments, the analyte comprises a functional group that is capable of interacting with at least a portion of the device (e.g., a species). In some cases, the device may determine changes in pH, moisture, temperature, and the like, of a surrounding medium. The analyte may be a chemical species, such as an explosive (e.g., TNT), toxin, or chemical warfare agent. In a specific example, the analytes are chemical warfare agents (e.g., sarin gas) or analogs of chemical warfare agents (e.g., dimethyl methylphosphonate, DMMP).
In some embodiments, the analyte may be an aromatic species, including optionally substituted aryl species and/or optionally substituted heteroaryl species, such as benzene, toluene, xylene, or polycyclic aromatic hydrocarbons such as benzo[a]pyrene. In some embodiments, the analyte may be an amine-containing species such as ammonia. In some embodiments, the analyte may be a nitrile-containing species such as acetonitrile. In some embodiments, the analyte may be an oxygen-containing species, such as a species comprising an alcohol, a ketone, an ester, a carboxylate, an aldehyde, other carbonyl groups, an ether, or the like. In some embodiments, the analyte may be a species comprising a ketone, an ester, an ether, or an aldehyde, such as cyclohexanone, ethyl acetate, THF, or hexanal. In some embodiments, the analyte is a phosphorus-containing analyte such as DMMP. In some embodiments, the analyte may be a nitro-containing species such as nitromethane or TNT. Other examples of analytes include alcohols, olefins, nitric oxide, thiols, thioesters, and the like.
Specific examples of analytes include nitromethane, benzene, toluene, o-xylene, m-xylene, p-xylene, mesitylene, nitrobenzene, cyano-benzene, benzo[a]pyrene, hexane, hexene, hexenal, ethylene, 1-methylcyclopropene, propene, butenes, isoprene, cyclohexanone, acetone, tetrahydrofuran (THF), methanol, ethanol, isopropanol, hexanal, DMMP, acetonitrile, nitromethane, ethyl acetate, methyl acetate, water, dimethyformamide (DMF), formaldehyde, dimethylsulfide, ethylene, or ammonia.
In some cases, the device may determine changes in a condition, or set of conditions, of a surrounding medium. As used herein, a change in a “condition” or “set of conditions” may comprise, for example, change to a particular temperature, pH, solvent, chemical reagent, type of atmosphere (e.g., nitrogen, argon, oxygen, etc.), electromagnetic radiation, or the like. In some cases, the set of conditions may include a change in the temperature of the environment in which the device is placed. For example, the device may include a component (e.g., binding site) that undergoes a chemical or physical change upon a change in temperature, producing a determinable signal from the device.
As used herein, an “aromatic species” includes unsubstituted or substituted, monocyclic or polycyclic aromatic ring or ring radical, including unsubstituted or substituted monocyclic or polycyclic heteroaromatic rings or ring radicals (e.g., aromatic species including one or more heteroatom ring atoms). Examples of aromatic species include phenyl, naphthyl, anthracenyl, chrysenyl, fluoranthenyl, fluorenyl, phenanthrenyl, pyrenyl, perylenyl, and the like.
As used herein, “aryl” means a monocyclic or polycyclic-aromatic ring or ring radical comprising carbon and hydrogen atoms. Examples of suitable aryl groups include, but are not limited to, phenyl, tolyl, anthracenyl, fluorenyl, indenyl, azulenyl, and naphthyl, as well as benzo-fused carbocyclic moieties such as 5,6,7,8-tetrahydronaphthyl. An aryl group can be unsubstituted or substituted with one or more substituents (including without limitation alkyl (preferably, lower alkyl or alkyl substituted with one or more halo), hydroxy, alkoxy (preferably, lower alkoxy), alkylthio, cyano, halo, amino, and nitro.
As used herein, “heteroaryl” means a monocyclic or polycyclic heteroaromatic ring (or radical thereof) comprising carbon atom ring members and one or more heteroatom ring members (such as, for example, oxygen, sulfur or nitrogen). Typically, the heteroaromatic ring has from 5 to about 14 ring members in which at least 1 ring member is a heteroatom selected from oxygen, sulfur, and nitrogen. In another embodiment, the heteroaromatic ring is a 5 or 6 membered ring and may contain from 1 to about 4 heteroatoms. In another embodiment, the heteroaromatic ring system has a 7 to 14 ring members and may contain from 1 to about 7 heteroatoms. Representative heteroaryls include pyridyl, furyl, thienyl, pyrrolyl, oxazolyl, imidazolyl, indolizinyl, thiazolyl, isoxazolyl, pyrazolyl, isothiazolyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, triazolyl, pyridinyl, thiadiazolyl, pyrazinyl, quinolyl, isoquniolyl, indazolyl, benzoxazolyl, benzofuryl, benzothiazolyl, indolizinyl, imidazopyridinyl, isothiazolyl, tetrazolyl, benzimidazolyl, benzoxazolyl, benzothiazolyl, benzothiadiazolyl, benzoxadiazolyl, indolyl, tetrahydroindolyl, azaindolyl, imidazopyridyl, qunizaolinyl, purinyl, pyrrolo[2,3]pyrimidyl, pyrazolo[3,4]pyrimidyl, benzo(b)thienyl, and the like. These heteroaryl groups may be optionally substituted with one or more substituents.
The term “substituted” is contemplated to include all permissible substituents of organic compounds, “permissible” being in the context of the chemical rules of valence known to those of ordinary skill in the art. In some cases, “substituted” may generally refer to replacement of a hydrogen with a substituent as described herein. However, “substituted,” as used herein, does not encompass replacement and/or alteration of a key functional group by which a molecule is identified, e.g., such that the “substituted” functional group becomes, through substitution, a different functional group. For example, a “substituted phenyl” must still comprise the phenyl moiety and cannot be modified by substitution, in this definition, to become, e.g., a heteroaryl group such as pyridine. In a broad aspect, the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and nonaromatic substituents of organic compounds. Illustrative substituents include, for example, those described herein. The permissible substituents can be one or more and the same or different for appropriate organic compounds. For purposes of this invention, the heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valencies of the heteroatoms. This invention is not intended to be limited in any manner by the permissible substituents of organic compounds.
Examples of substituents include, but are not limited to, alkyl, aryl, aralkyl, cyclic alkyl, heterocycloalkyl, hydroxy, alkoxy, aryloxy, perhaloalkoxy, aralkoxy, heteroaryl, heteroaryloxy, heteroarylalkyl, heteroaralkoxy, azido, amino, halogen, alkylthio, oxo, acylalkyl, carboxy esters, carboxyl, carboxamido, nitro, acyloxy, aminoalkyl, alkylaminoaryl, alkylaryl, alkylaminoalkyl, alkoxyaryl, arylamino, aralkylamino, alkylsulfonyl, carboxamidoalkylaryl, carboxamidoaryl, hydroxyalkyl, haloalkyl, alkylaminoalkylcarboxy, aminocarboxamidoalkyl, alkoxyalkyl, perhaloalkyl, arylalkyloxyalkyl, and the like.
Other embodiments suitable for use in the context of the embodiments described herein are described in International Pat. Apl. Serial No.: PCT/US2009/001396, filed Mar. 4, 2009, entitled, “Devices and Methods for Determination of Species Including Chemical Warfare Agents”; International Pat. Apl. Serial No.: PCT/US2009/006512, filed Dec. 11, 2009, entitled, “High Charge Density Structures, Including Carbon-Based Nanostructures and Applications Thereof”; U.S. patent application Ser. No. 12/474,415, filed May 29, 2009, entitled, “Field Emission Devices Including Nanotubes or Other Nanoscale Articles”; International Pat. Apl. Serial No.: PCT/US2011/051610, filed Oct. 6, 2010, entitled, “Method and Apparatus for Determining Radiation”; International Pat. Apl. Serial No.: PCT/US2010/055395, filed Nov. 4, 2010, entitled, “Nanostructured Devices including Analyte Detectors, and Related Methods”; International Pat. Apl. Serial No.: PCT/US2011/053899, filed Sep. 29, 2011, entitled, “COMPOSITIONS, METHODS, AND SYSTEMS COMPRISING POLY(THIOPHENES); and International Pat. Apl. Serial No.: PCT/US2011/025863, filed Feb. 23, 2011, entitled, “Charged Polymers and Their Uses in Electronic Devices”, which applications are incorporated herein in their entireties for all purposes.
EXAMPLES AND EMBODIMENTSMaterials and Measurements. Chemicals were purchased from Sigma-Aldrich, Alfa Aesar, and Macron Chemicals and used as received except that THF was dried by distillation. Deuterated solvents for NMR were obtained from Cambridge Isotope Laboratories, Inc. Cellulose acetate (CA-320S NF/EP) with the acetyl content of 31.9 wt % was kindly provided from Eastman. The analytes including benzene, toluene, ortho-, meta-, and para-xylenes, ethanol, and n-heptane were reagent grade and used as received.
1H, 13C, and 19F NMR spectra were recorded on Varian Mercury (300 MHz) and Inova (500 MHz) NMR spectrometers. The 13C NMR spectra for functionalized cellulose acetates were recorded at 60° C. Chemical shifts are reported in parts per million (ppm) and referenced to the residual solvent resonance. FT-IR spectra were obtained on a NICOLET 6700 FT-IR (Thermo Scientific) in attenuated total reflectance (ATR) mode using a Ge crystal plate. Thermal stabilities of functionalized cellulose acetates were studied using a thermogravimetric analysis (TGA, Discovery TGA from TA Instruments). Weight loss was monitored by heating a sample from 30° C. to 600° C. at a heating rate of 20° C./min under air atmosphere. The number average molecular weight (Mn), weight average molecular weight (Mw), and polydispersity index (PDI) were obtained from a gel permeation chromatography (GPC, Agilent 1100 Series). THF was used as a solvent and a refractive index detector was used to obtain the molecular weights of functionalized cellulose acetates.
Example 1Propargyl pyrenebutyl ether was synthesized according to the following procedure. The reaction was conducted by the procedure described in J. M. Lobez, T. M. Swager, Angew. Chem. Int. Ed. 2010, 49, 95-98. Sodium hydride (NaH, 60 wt % in oil, 0.633 g, 26.39 mmol) was added to a solution of 1-pyrenebutanol (4 g, 14.58 mmol) in dry THF (45 ml) at 0° C. under argon atmosphere. The mixture was stirred at 0° C. for 30 min, and propargyl bromide (80 wt % in toluene, 3.469 g, 29.16 mmol) was added. The solution was stirred at 0° C. in the dark for 30 min and allowed to warm up to room temperature. After stirring for 15 h at room temperature, the reaction was heated to reflux for 8 h. Ethyl acetate (20 ml) and distilled water (20 ml) were added to the solution, and the aqueous phase was extracted twice with 20 ml of ethyl acetate. The combined organic phase was washed with 20 ml of brine and dried over MgSO4. The solvent was removed under vacuum, and the crude product was purified by column chromatography using toluene as an eluent to get the product (4.268 g, 93%). δH (CDCl3) 1.82 (2H, m), 1.96 (2H, m), 2.46 (1H, t, J=2.4 Hz), 3.38 (2H, t, J=7.7 Hz), 3.60 (2H, t, J=6.4 Hz), 4.17 (2H, d, J=2.4 Hz), 7.87-8.32 (9H, m); δC (CDCl3) 28.46, 29.66, 33.33, 58.19, 70.05, 74.31, 80.12, 123.55, 124.75, 124.87, 124.91, 125.12, 125.16, 125.86, 126.64, 127.27, 127.61, 136.81; HRMS (DART) m/z: [M+H]+ calcd for C23H20O, 313.1587. found, 313.1571.
Example 2As shown in
Pyrene-functionalized cellulose acetate (Py-CA) was synthesized, as shown in
Benzoate-functionalized CA (Benz-CA) was synthesized according to the method described in Example 3, except that the following reagents were utilized: CuSO4—H2O (6 mol %), sodium ascorbate (14 mol %), and propargyl benzoate (3 equiv). The degree of substitution of benzoate selector (DSBenz) was 0.42 from elemental analysis, and Benz-CA was soluble in DMSO and THF. Mn: 58 KDa, Mw: 166 KDa, PDI: 2.85; Elemental analysis: C, 50.37; H, 4.72; N, 5.69; Cu, 1.35.
Example 5As shown in
Phenylacetyl chloride (Ph-Cl) was prepared using the procedure described in Example 5.
Example 7The following example describes the synthesis of 2,3,4,5,6-pentafluorophenyl-acetyl-Functionalized Cellulose Acetate (F5Ph-CA). (
Phenylacetyl-functionalized cellulose acetate (Ph-CA) was prepared by the same procedure for F5Ph-CA as described in Example 7. The degree of substitution (DSPh) was calculated to be 0.59 from elemental analysis. Ph-CA was soluble in acetone, THF, DMSO, and DMF. Mn: 58 KDa, Mw: 102 KDa, PDI: 1.76; Elemental analysis: C, 55.97; H, 5.17; N, 0.26.
Example 9Quartz crystal microbalance (QCM) experiments were performed using Q-sense E1 to test the ability of functionalized cellulose acetates to absorb target analytes by monitoring the frequency change when they were exposed to analyte vapors. The functionalized cellulose acetates were dropcast onto a gold coated AT-cut quartz crystal sensor with 5 MHz fundamental resonance frequency. 20 μg of each material from the solution of 2 mg/ml was deposited on a QCM sensor. Acetone was used as a solvent for F5Ph-CA and Ph-CA, and THF was used for Py-CA and Benz-CA. The films on QCM sensors were tested towards 500 ppm of benzene (0.47% of the saturated vapor) and toluene (1.3% of the saturated vapor) vapors which were generated from a gas generator (FlexStream™ FlexBase Module, KIN-TEK Laboratories, Inc., TX, United States) with dry nitrogen carrier gas. The concentration of vapor was calibrated by measuring mass change of an analyte after purging nitrogen gas through the analyte as a function of time at a fixed flow rate and temperature. The frequency change (the 3rd overtone, f3) of a film on a QCM sensor was measured by three cycles of exposure of a film to an analyte vapor for 1 min. The mass change (Δm) was converted from the frequency change (Δf) using the Sauerbrey equation:
where n is the overtone and C is the mass sensitivity (C=17.7 ngcm−2s−1).
Example 10The following example describes the fabrication and use of sensors including two layers: an absorbent material layer (or “preconcentrator” layer) of functionalized cellulose acetates on top of a SWCNT sensing layer. The SWCNT dispersion was prepared by sonicating the solution of SWCNT in THF with 20 μg/ml for 1 h. The SWCNT layer was then prepared by dropcoating 2 μl of the SWCNT solution three times (total 120 ng of SWCNT deposited) onto the screen printed interdigitated array (IDA) microelectrodes (CC1.W1, batch #12C12, BVT technologies, Brno, CZ). The interdigitated array microelectrodes consist of 3 pairs of gold electrodes with 150 μm spacing between electrodes, 150 μm electrode width, and 2000 μm electrode length. The film of functionalized cellulose acetate was then prepared by dropcoating 2 μl of the solution of 1 mg/ml on top of SWCNT layer three times (total 6 μg deposited). The films on the electrodes were dried 12 h at ambient condition before use.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to analytes. The sensors deposited on IDAs were mounted on 2×30 pin edge connector and encased within a custom-built Teflon chamber with an inlet, an outlet, and an internal channel with volume of 7.38 cm3 for gas flow. The analyte vapors of varying concentrations were generated using FlexStream™ FlexBase Module (KIN-TEK Laboratories, Inc., TX, United States) with precise temperature and gas flow rate control. The vapor of varying concentrations was generated by mixing the saturated vapor with dry nitrogen gas and was delivered to the sensor chamber. The concentration of vapor was calibrated by measuring mass change of an analyte after purging nitrogen gas through the analyte as a function of time at a fixed flow rate and temperature. The conductivity measurement was carried out by measuring the current at 0.05V bias voltage using a PalmSense EmStat-MUX equipped with a 16 channel multiplexer (Palm Instruments BV, The Netherlands), and the baseline resistances of sensors were in the range of 5Ω to 15Ω. The sensors were tested by measuring the changes in conductance after several cycles of exposure to the analyte vapor.
The detection limit of a sensor was calculated by extrapolating the linear calibration curve (−ΔG/Go vs concentration) when the signal equals three times the noise (J. Li, Y. Lu, Q. Ye, M. Cinke, J. Han, M. Meyyappan, Nano Lett. 2003, 3, 929-933) The noise level of a sensor can be calculated from the root-mean square deviation of the data at the baseline. After a fifth-order polynominal fitting of the curve of the normalized conductance change as a function of concentration using Origin 8.0, the variance (Vχ2) was calculated from the residual (χ) between 10 data points at the baseline and curve fitting results by the following equation:
Vχ
where yi is the measured data point and y is the corresponding value calculated from the curve-fitting equation. The average noise level (rmsnoise) was calculated as follows:
The detection limit (LOD at signal-to-noise=3) was calculated as follows:
The detection limits of the sensors towards benzene, toluene, m-xylene vapors were 55 ppm, 19 ppm, and 14 ppm, respectively. The simultaneous preconcentrating and sensing steps took only a few seconds, and the response was fully recovered and reproducible. Since the target analyte are aromatic hydrocarbons, CA was functionalized with binding sites having aromatic rings for π-π stacking or electrophilic character for electrostatic interaction. A series of binding sites or receptors, as shown in
Quartz crystal microbalance (QCM) experiments were performed to test the ability of the functionalized cellulose acetate as a preconcentrator to absorb the target vapor. Mass uptake of the functionalized cellulose acetate film upon exposure to the target vapor was measured by monitoring the frequency change of the film dropcast onto a gold-coated 5 MHz QCM sensor. The films were tested towards 500 ppm of benzene (0.47% of the saturated vapor) and toluene (1.3% of the saturated vapor) generated from a gas generator with dry nitrogen carrier gas. The frequencies (the 3rd overtone, f3) of the four functionalized cellulose acetate films including F5Ph-CA, Ph-CA, Py-CA, and Benz-CA decreased upon exposure to both benzene and toluene vapors due to the absorbed vapor molecules on the films. (
The measured frequency change (Δf) was converted to the mass density change (Δm) using Sauerbrey's equation. The absorbed amount (mmol) of an analyte per 1 mole of functional groups was then calculated from Δm and degrees of substitution of functional groups and was summarized in
The integrated preconcentrator/sensor system was fabricated by depositing (dropcoating) SWCNT onto interdigitated array microelectrodes followed by dropcoating functionalized cellulose acetate on top of the SWCNT sensing layer. The F5Ph-CA with DSF5Ph of 0.80 was chosen as a preconcentrator from the QCM results shown in
The CA/SWCNT (with DSAc˜2.44) and (2,3,4,5,6-pentafluorophenylacetic acid)/SWCNT were also tested toward 529 ppm of benzene vapor to demonstrate the high efficiency of the F5Ph-CA preconcentrator.
The selectivity of the F5Ph-CA/SWCNT sensor was studied by testing the system in response to benzene, toluene, o-xylene, m-xylene, p-xylene, n-heptane, and ethanol of 0.5% of the saturated vapors. N-heptane and ethanol commonly found in petrochemicals were tested as interferents.
In summary, a new design for a BTX sensor was demonstrated based on the integrated preconcentrator/SWCNT sensing system where a functionalized cellulose preconcentrating layer was deposited directly on top of the SWCNT sensing layer, allowing preconcentrating and sensing simultaneously within a few seconds. The cellulose acetates functionalized with selectors for target analytes were successfully demonstrated as a preconcentrator. The functionalized cellulose acetate preconcentrating layer selectively absorbed the target analyte and delivered the concentrated analyte to the SWCNT sensing layer, which allowed the system to detect low ppm of BTX vapors. The detection limits towards toluene and xylenes are significantly lower than the OSHA permissible exposure limit Interdigitated array microelectrodes with smaller gaps represent an approach to produce lower detection limits for BTX gases. The high sensitivity, selectivity, and fast response are significant benefits of the integrated preconcentrator/sensing system, which makes it promising approach for on-site field monitoring applications.
Example 11The following example describes the fabrication and use of sensors including two layers: a polymer layer of pentiptycene polyparaphenlene ethynylene (P2, where R═OC14H29) or Poly(p-phenylene butadiynylene) (P1, where R═OC14H29), as shown in
The substrate was prepared by patterning a gold electrode onto a glass slide using thermal evaporation (electrode gap size of 1 mm, gold deposited to a thickness of 100 nm). The SWCNT layer was prepared by sonicating 0.25 mg/ml SWCNT and Cu scorpionate in o-dichlorobenzene/toluene (13:3) for 3 minutes, followed by repeatedly dropcoating 0.5 μl of the solution onto the substrate until a resistance of 1-20 kΩ was achieved. The device was vacuum dried until solvent was completely removed between the addition of each aliquot of solution. Polymer solution (1 μl) was then dropcoated from a solution of 2 mg/ml polymer in THF over each electrode gap that contained SWCNT material.
The sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to analyte. The sensors deposited on the electrodes were mounted on a 2×30 pin edge connector and encased within a custom-built Teflon chamber with an inlet, an outlet, and an internal gas flow channel. 1% Ethylene gas in nitrogen was used as the analyte (AirGas 1.0001%+/−2%). Dry nitrogen gas was used as the carrier gas. Gas mixtures of varying concentrations were generated by mixing the 1% ethylene gas with dry nitrogen gas and were delivered to the sensor chamber using a Sierra Instruments gas mixing system.
The conductivity measurement was carried out by measuring the current at 0.1 V bias voltage using a PalmSense EmStat-MUX equipped with a 16 channel multiplexer (Palm Instruments BV, The Netherlands), and the baseline resistances of sensors were in the range of 1 kΩ to 20 kΩ. The sensors were tested by measuring the changes in conductance after several cycles of exposure to analyte gas.
The sensing response of P2-coated sensors to 20 ppm ethylene was determined to be 2.1% on average. The sensing response of P1-coated sensors to 20 ppm of ethylene was determined to be 2.4% on average. The sensing response of uncoated sensors to 20 ppm of ethylene was 0.35% on average. Measurements were also taken upon exposure to 10 ppm ethylene and 5 ppm ethylene, with the average responses shown in
The following example describes the fabrication and use of sensors including two layers: a polymer layer of polymer P3 (as shown in
The substrate was prepared by patterning a gold electrode onto a glass slide using thermal evaporation (electrode gap size of 1 mm, gold deposited to a thickness of 100 nm). The SWCNT layer was prepared by sonicating 0.25 mg/ml SWCNT and Cu scorpionate in o-dichlorobenzene/toluene (13:3) for 3 minutes, followed by repeatedly dropcoating 0.5 μl of the solution onto the substrate until a resistance of 1-20 kΩ was achieved. The device was vacuum dried until solvent was completely removed between the addition of each aliquot of solution. Polymer solution (1 μl) was then drop-coated from a solution of 4 mg/ml polymer in THF over each electrode gap that contained SWCNT material.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to analyte, using the methods described in Example 11. The sensing response of P3-coated sensors to 1000 ppm ethylene was determined to be 0.44% on average. The sensing response of uncoated sensors to 1000 ppm ethylene was 0.29% on average. Thus, the sensors including the polymer coating exhibited a 1.5% improvement in response to the analyte, relative to uncoated sensors. (
The following example describes the fabrication and use of sensors including two layers: a polymer layer of fluorinated CYTOP polymer (Bellex International Corporation, Japan; structure shown below) on top of a SWCNT sensing layer containing a copper(I) scorpionate selector (1,
The substrate was prepared by patterning a gold electrode onto a glass slide using thermal evaporation (electrode gap size of 1 mm, gold deposited to a thickness of 100 nm). The SWCNT layer was prepared by sonicating 0.25 mg/ml SWCNT and Cu scorpionate in o-dichlorobenzene/toluene (13:3) for 3 minutes, followed by repeatedly drop-coating 0.5 μl of the solution onto the substrate until a resistance of 1-20 kΩ was achieved. The device was vacuum dried until solvent was completely removed between the addition of each aliquot of solution. A polymer solution (0.2 ml) containing 1:2 CYTOP polymer:CYTOP solvent (Bellex International Corporation, Japan) solution was then spin-coated onto the entire device using a Model WS-400 Spin Processor (Laurell Technologies corporation, USA) at 2000 rpm for 60 seconds. The polymer coating was then dried in a vacuum chamber for 2 minutes.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to analyte, using the methods described in Example 11. The sensing response to 20 ppm ethylene of CYTOP polymer-coated sensors was determined to be 3.1%. The entire device was covered during the application of the polymer using the spin-coating technique so that limited, or substantially no, uncoated reference sensors were available. (
The following example describes the fabrication and use of sensors including two components: a polymeric material (Halocarbon Oil 27) and a SWCNT sensing layer containing copper(I) scorpionate selector (1).
A SWCNT dispersion was prepared by sonicating 0.5 mg SWCNT in 2 ml of a 13:3 mixture of dichlorobenzene:toluene containing copper(I) scorpionate selector 1 for 8 min Halocarbon oil 27 (5 mg) was mixed with 100 μl of the SWCNT solution by sonication for 30 sec.
Glass slides (VWR Microscope Slides) were cleaned by ultrasonication in acetone for 10 min, rinsing with isopropanol. After drying the glass slides were subjected to UV radiation in a UVO cleaner (Jelight Company Inc.) for 3 min Using an aluminum mask, layers of chromium (10 nm) and gold (100 nm) were deposited using a custom metal evaporator purchased from Angstrom Engineering leaving a 1 mm gap. The SWCNT sensing layer was then prepared by drop-casting 0.35 μl of the 1/SWCNT/polymer solution between the gold electrodes followed by drying in vacuum until resistances of 5-20 kΩ were achieved.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to ethylene, using the methods described in Example 11. However, ethylene/nitrogen gas mixtures with ethylene concentrations of 20 and 5 ppm were generated using a KIN-TEK gas generating system (KIN-TEK Laboratories, Inc., TX, United States) with precise temperature and gas flow rate control. The varied ethylene concentrations were generated by varying the total flow of 1% ethylene and dry nitrogen gas.
The sensors were tested by measuring the changes in conductance after several cycles of exposure to ethylene. The sensing response of the polymer-coated sensors to 20 ppm ethylene and 5 ppm ethylene was determined to be 4.9 and 1.6% on average, respectively, and the sensing response of uncoated sensors was 12.0 and 2.6% on average, respectively. (
The following example describes the fabrication and use of sensors including two layers: a polymeric material layer of different concentrations on top of a SWCNT sensing layer.
A SWCNT dispersion was prepared by sonicating a solution of 0.5 mg SWCNT in 2 ml of a 13:3 mixture of o-dichlorobenzene:toluene containing copper(I) scorpionate selector (1) for 8 min Glass slides containing layers of chromium (10 nm) and gold (100 nm) were prepared using the method described in Example 14. The SWCNT sensing layer was then prepared by drop-casting 0.35 μl of the SWCNT/polymer suspension between the gold electrodes followed by drying in vacuum until resistances of 5-20 kΩ were achieved. A film of polymer was then prepared by drop-casting 1 μl of a solution of 4 mg Halocarbon oil 27 mixed with 1 ml of THF on top of SWCNT layer once, or in another case, twice (i.e., 2 μl total). The films on the electrodes were dried in vacuum for 30 s before use.
Sensing properties of the devices were measured by monitoring the conductivity change of the sensors upon exposure to ethylene, using the methods described in Example 11. However, ethylene gases of concentrations of 40 ppm, 20 ppm, and 10 ppm were generated using the methods disclosed in Example 14.
The sensors were tested by measuring the changes in conductance after several cycles of exposure to ethylene. The sensing response of the sensors with and without polymer coating can be seen in
The following example describes the fabrication and use of sensors including two layers: a polymeric material layer of different concentrations on top of a SWCNT sensing layer.
A SWCNT dispersion was prepared by sonicating 0.5 mg SWCNT in 2 ml of a 13:3 solution of dichlorobenzene: toluene containing copper(I) scorpionate selector (1) for 8 min Glass slides containing layers of chromium (10 nm) and gold (100 nm) were prepared using the method described in Example 14. The SWCNT sensing layer was then prepared by drop-casting 0.35 μl of the SWCNT suspension between the gold electrodes followed by drying in vacuum until resistances of 5-20 kΩ were achieved. A film of polymer was then prepared by drop-casting 1 μl of a solution of 0.5 mg, 4 mg, or 32 mg of Halocarbon oil 27, mixed with 1 ml of THF, on top of SWCNT layer two times. The films on the electrodes were dried in vacuum for 30 s before use.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to ethylene, using the methods described in Example 11. However, ethylene gases of concentrations of 20 ppm, 10 ppm, and 5 ppm were generated the methods disclosed in Example 14.
The sensors were tested by measuring the changes in conductance after several cycles of exposure to ethylene. The sensing response of the sensors with and without polymer coating can be seen in
The following example describes the fabrication and use of sensors including two layers: a polymeric material layer of different concentrations on top of a SWCNT sensing layer.
A SWCNT dispersion was prepared by sonicating a solution of 0.5 mg SWCNT in 2 ml of a 13:3 mixture of o-dichlorobenzene:toluene containing copper(I) scorpionate selector (1) for 8 min Glass slides containing layers of chromium (10 nm) and gold (100 nm) were prepared using the method described in Example 14. The SWCNT sensing layer was then prepared by drop-casting 0.35 μl of the SWCNT solution in between the gold electrodes followed by drying in vacuum until resistances of 5-20 kΩ were achieved. A film of polymer was then prepared by drop-casting two times 1 μl of a solution of 32 mg, 50 mg, or 100 mg Halocarbon oil 27, mixed in 1 ml THF, on top of SWCNT layer. The films on the electrodes were dried in vacuum for 30 s before use.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to ethylene, using the methods described in Example 11. However, ethylene gases of concentrations of 20 ppm, 10 ppm, and 5 ppm were generated using the methods disclosed in Example 14.
The sensors were tested by measuring the changes in conductance after several cycles of exposure to ethylene. The sensing response of the sensors with and without polymer coating can be seen in
The following example describes the fabrication and use of sensors including two layers: a polymeric material layer of different concentrations on top of a SWCNT sensing layer.
A SWCNT dispersion was prepared by sonicating a solution of 0.5 mg SWCNT in 2 ml of a 13:3 mixture of o-dichlorobenzene:toluene containing copper(I) scorpionate selector (1) for 8 min. Glass slides containing layers of chromium (10 nm) and gold (100 nm) were prepared using the method described in Example 14. The SWCNT sensing layer was then prepared by drop-casting 0.35 μl of the SWCNT solution in between the gold electrodes followed by drying in vacuum until resistances of 5-20 kΩ were achieved. A film of polymer was then prepared by drop-casting, either once or twice (i.e., 2 μl total), 1 μl of a solution of 4 mg Halocarbon oil 700 mixed with 1 ml THF on top of SWCNT layer. The films on the electrodes were dried in vacuum for 30 s before use.
Sensing properties of the devices were measured by monitoring the conductivity change of sensors upon exposure to ethylene, using the methods described in Example 11. However, ethylene gases of concentrations of 40 ppm, 20 ppm, and 10 ppm were generated using the methods disclosed in Example 14.
The sensors were tested by measuring the changes in conductance after several cycles of exposure to ethylene. The sensing response of the sensors with and without polymer coating can be seen in
Claims
1. A device for determining an analyte, comprising:
- a sensor material layer comprising a conductive material; and
- an absorbent material layer disposed on the sensor material layer,
- wherein the absorbent material interacts with an analyte, if present, in a manner bringing the analyte into proximity with the sensor material to produce a determinable signal from the device.
2. A device as in any preceding claim, wherein the device lacks a piezoelectric material.
3. A device as in any preceding claim, wherein the absorbent material layer comprises a polymer material and a plurality of binding sites.
4. A device as in claim 3, wherein at least some of the plurality of binding sites are covalently bonded to the polymer material.
5. A device as in claim 3, wherein at least some of the plurality of binding sites are non-covalently bonded to the polymer material.
6. A device as in claim 3, wherein the plurality of binding sites are dispersed throughout the polymer material.
7. A device as in any preceding claim, wherein the plurality of binding sites comprises a mixture of different binding sites capable of determining a plurality of different analytes.
8. A device as in any preceding claim, wherein the absorbent material layer comprises polyvinyl alcohol or polyhydroxyl ethyl methacrylate, either of which is optionally substituted.
9. A device as in any preceding claim, wherein the absorbent material layer comprises a substantially hydrophobic polymer.
10. A device as in any preceding claim, wherein the absorbent material layer comprises a fluorinated polymer.
11. A device as in any preceding claim, wherein the absorbent material layer comprises an iptycene-based polymer.
12. A device as in any preceding claim, wherein the absorbent material layer comprises an ionic liquid.
13. A device as in any preceding claim, wherein the ionic liquid comprises an imidazolium ion.
14. A device as in any preceding claim, wherein the imidazolium ion is selected from a group consisting of 1-Butyl-3-methylimidazolium, 1-Ethyl-3-methylimidazolium, and 1-Hexyl-3-methylimidazolium.
15. A device as in any preceding claim, wherein the ionic liquid comprises a cation selected from a group consisting of tetrafluoroborate, hexafluorophosphate, and bis(trifluoromethanesulfone)imide.
16. A device as in any preceding claim, wherein the absorbent material layer comprises a cellulose-based polymer.
17. A device as in any preceding claim, wherein the cellulose-based polymer is cellulose acetate, cellulose diacetate, or cellulose triacetate, any of which is optionally substituted.
18. A device as in any preceding claim, wherein the cellulose-based polymer is cellulose substituted with at least one functional group comprising an aromatic moiety.
19. A device as in any preceding claim, wherein the cellulose-based polymer comprises the structure,
- wherein:
- R1 is a group comprising a binding site for an aromatic species;
- R2 and R3 can be the same or different and are hydrogen, alkyl, aryl, a carbonyl group, any of which is optionally substituted; and
- n is greater than 1.
20. A device as in claim 19, wherein the binding site comprises an aromatic moiety, a calixarene, a hydrogen bond donor, or a hydrogen bond acceptor.
21. A device as in claim 19, herein the aromatic moiety is a phenyl group, optionally substituted.
22. A device as in claim 19, wherein the aromatic moiety is a polycyclic aromatic hydrocarbon, optionally substituted.
23. A device as in claim 19, wherein the cellulose-based polymer comprises the structure,
- wherein R4 and R5 can be the same or different and are hydrogen, alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, heteroaryl, or carbonyl group, any of which is optionally substituted.
24. A device as in claim 19, wherein the cellulose-based polymer comprises the structure,
- wherein R6 is alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, or heteroaryl, any of which is optionally substituted.
25. A device as in claim 19, wherein R1 has the structure,
26. A device as in any one of claims 19-25, wherein R2 and R3 can be the same or different and are hydrogen, —COCH3, or —F5Ph.
27. A device as in claim 26, wherein R2 and R3 are the same.
28. A device as in claim 26, wherein R2 and R3 are different.
29. A device as in any preceding claim, wherein the conductive material comprises a carbon-based nanostructure.
30. A device as in any preceding claim, wherein the carbon-based nanostructure is a nanotube, nanoparticle, graphene, or graphite.
31. A device as in any preceding claim, wherein the carbon nanotubes are single-wall carbon nanotubes.
32. A device as in any preceding claim, wherein the carbon nanotubes are multi-wall carbon nanotubes.
33. A device as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a species capable of interacting with the analyte.
34. A device as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a metal-containing species.
35. A device as in claim 34, wherein the metal-containing species comprises copper, cobalt, or palladium.
36. A device as in claim 35, wherein the metal-containing species is a complex or salt comprising Cu(I), Cu(II), Ag(I), Ag(II), Co(II), Co(III), Rh(I), Rh(III), Ir(I), Ir(III) or Pd(II).
37. A device as in claim 35, wherein the metal-containing species is copper(I) scorpionate.
38. A device as in claim 35, wherein the metal-containing species is cobalt (III) porphyrin compound.
39. A device as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a fluorinated alcohol group.
40. A device as in any preceding claim, wherein the analyte is a vapor phase analyte.
41. A device as in any preceding claim, wherein the analyte is an aromatic species.
42. A device as in any preceding claim, wherein the analyte is benzene, toluene, xylene, or benzo[a]pyrene.
43. A device as in any preceding claim, wherein the analyte is a polycyclic aromatic hydrocarbon.
44. A device as in any preceding claim, wherein the determinable signal comprises resistance.
45. A device for determining an analyte, comprising:
- a first electrode and a second electrode;
- a sensor material in electrochemical communication with the first and the second electrodes, wherein resistance to current flow between the first and second electrode is affected by the sensor material; and
- an absorbent material in contact with the sensor material,
- wherein the absorbent material interacts with the analyte, if present, in a manner bringing the analyte into sufficient proximity with the sensor material such that resistance to current flow between the first and second electrodes is affected, thereby generating a signal in the device by which the analyte is determined.
46. A device as in any preceding claim, wherein the device lacks a piezoelectric material.
47. A device as in any preceding claim, wherein the absorbent material comprises a polymer material and a plurality of binding sites.
48. A device as in claim 47, wherein at least some of the plurality of binding sites are covalently bonded to the polymer material.
49. A device as in claim 47, wherein at least some of the plurality of binding sites are non-covalently bonded to the polymer material.
50. A device as in claim 47, wherein the plurality of binding sites are dispersed throughout the polymer material.
51. A device as in any preceding claim, wherein the plurality of binding sites comprises a mixture of different binding sites capable of determining a plurality of different analytes.
52. A device as in any preceding claim, wherein the absorbent material comprises polyvinyl alcohol or polyhydroxyl ethyl methacrylate, either of which is optionally substituted.
53. A device as in any preceding claim, wherein the absorbent material comprises a substantially hydrophobic polymer.
54. A device as in any preceding claim, wherein the absorbent material comprises a fluorinated polymer.
55. A device as in any preceding claim, wherein the absorbent material comprises an iptycene-based polymer.
56. A device as in any preceding claim, wherein the absorbent material comprises an ionic liquid.
57. A device as in any preceding claim, wherein the ionic liquid comprises an imidazolium ion.
58. A device as in any preceding claim, wherein the imidazolium ion is selected from a group consisting of 1-Butyl-3-methylimidazolium, 1-Ethyl-3-methylimidazolium, and 1-Hexyl-3-methylimidazolium.
59. A device as in any preceding claim, wherein the ionic liquid comprises a cation selected from a group consisting of tetrafluoroborate, hexafluorophosphate, and bis(trifluoromethanesulfone)imide.
60. A device as in any preceding claim, wherein the absorbent material layer comprises a cellulose-based polymer.
61. A device as in any preceding claim, wherein the cellulose-based polymer is cellulose acetate, cellulose diacetate, or cellulose triacetate, any of which is optionally substituted.
62. A device as in any preceding claim, wherein the cellulose-based polymer is cellulose substituted with at least one functional group comprising an aromatic moiety.
63. A device as in any preceding claim, wherein the cellulose-based polymer comprises the structure,
- wherein:
- R1 is a group comprising a binding site for an aromatic species;
- R2 and R3 can be the same or different and are hydrogen, alkyl, aryl, a carbonyl group, any of which is optionally substituted; and
- n is greater than 1.
64. A device as in claim 63, wherein the binding site comprises an aromatic moiety, a calixarene, a hydrogen bond donor, or a hydrogen bond acceptor.
65. A device as in claim 63, herein the aromatic moiety is a phenyl group, optionally substituted.
66. A device as in claim 63, wherein the aromatic moiety is a polycyclic aromatic hydrocarbon, optionally substituted.
67. A device as in claim 63, wherein the cellulose-based polymer comprises the structure,
- wherein R4 and R5 can be the same or different and are hydrogen, alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, heteroaryl, or carbonyl group, any of which is optionally substituted.
68. A device as in claim 63, wherein the cellulose-based polymer comprises the structure,
- wherein R6 is alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, or heteroaryl, any of which is optionally substituted.
69. A device as in claim 63, wherein R1 has the structure,
70. A device as in any one of claims 54-63, wherein R2 and R3 can be the same or different and are hydrogen, —COCH3, or —F5Ph.
71. A device as in claim 70, wherein R2 and R3 are the same.
72. A device as in claim 70, wherein R2 and R3 are different.
73. A device as in any preceding claim, wherein the conductive material comprises a carbon-based nanostructure.
74. A device as in any preceding claim, wherein the carbon-based nanostructure is a nanotube, nanoparticle, graphene, or graphite.
75. A device as in any preceding claim, wherein the carbon nanotubes are single-wall carbon nanotubes.
76. A device as in any preceding claim, wherein the carbon nanotubes are multi-wall carbon nanotubes.
77. A device as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a metal-containing species.
78. A device as in claim 77, wherein the metal-containing species comprises copper, cobalt, or palladium.
79. A device as in claim 78, wherein the metal-containing species is a complex or salt comprising Cu(I), Cu(II), Ag(I), Ag(II), Co(II), Co(III), Rh(I), Rh(III), Ir(I), Ir(III) or Pd(II).
80. A device as in claim 79, wherein the metal-containing species is a copper(I) scorpionate.
81. A device as in claim 79, wherein the metal-containing species is a cobalt (III) porphyrin.
82. A device as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a fluorinated alcohol group.
83. A device as in any preceding claim, wherein the analyte is a vapor phase analyte.
84. A device as in any preceding claim, wherein the analyte is an aromatic species.
85. A device as in any preceding claim, wherein the analyte is benzene, toluene, xylene, or benzo[a]pyrene.
86. A device as in any preceding claim, wherein the analyte is a polycyclic aromatic hydrocarbon.
87. A device as in any preceding claim, wherein resistance to current flow between the first and second electrode is increased in the presence of the analyte.
88. A device as in any preceding claim, wherein resistance to current flow between the first and second electrode is decreased in the presence of the analyte.
89. A system, comprising:
- a plurality of devices as in any preceding claim arranged to form an array of devices.
90. A system as in claim 89, wherein each individual device includes a binding site capable of interacting with an analyte.
91. A system as in claim 89 or 90, wherein a first device includes a binding site capable of interacting with a first analyte and a second device includes a binding site capable of interacting with a second analyte, wherein the first and second analytes are different.
92. A method for determining an analyte, comprising:
- exposing a sample suspected of containing an analyte to a device comprising a sensor material and an absorbent material in contact with the sensor material, the absorbent material having a first analyte concentration prior to exposure to the sample and a second analyte concentration upon exposure to the sample, wherein the sensor material produces a determinable signal affected by the analyte concentration of the absorbent material; and
- determining the determinable signal of the sensor material, thereby determining the analyte.
93. A method as in claim 92, wherein the device lacks a piezoelectric material.
94. A method as in any preceding claim, wherein the absorbent material interacts with the analyte, if present, in a manner bringing the analyte into proximity with the sensor material to affect the determinable signal of the device.
95. A method as in any preceding claim, wherein, if the analyte is present, the second analyte concentration is greater than the first analyte concentration.
96. A method as in any preceding claim, wherein the analyte is determined without removing the analyte from the absorbent material.
97. A method as in any preceding claim, wherein the sensor material is in electrochemical communication with a first electrode and a second electrode such that, in the presence of an analyte, the analyte concentration of the absorbent material increases, thereby affecting resistance to current flow between the first and second electrode.
98. A method as in claim 97, wherein resistance to current flow between the first and second electrode is increased in the presence of the analyte.
99. A method as in claim 97, wherein resistance to current flow between the first and second electrode is decreased in the presence of the analyte.
100. A method as in any preceding claim, wherein the absorbent material comprises a polymer material and a plurality of binding sites.
101. A method as in claim 100, wherein at least some of the plurality of binding sites are covalently bonded to the polymer material.
102. A method as in claim 100, wherein at least some of the plurality of binding sites are non-covalently bonded to the polymer material.
103. A method as in claim 100, wherein the plurality of binding sites are dispersed throughout the polymer material.
104. A method as in any one of claims 100-103, wherein the plurality of binding sites comprises a mixture of different binding sites capable of determining a plurality of different analytes.
105. A method as in any preceding claim, wherein the absorbent material comprises polyvinyl alcohol or polyhydroxyl ethyl methacrylate, either of which is optionally substituted.
106. A method as in any preceding claim, wherein the absorbent material comprises a substantially hydrophobic polymer.
107. A method as in any preceding claim, wherein the absorbent material comprises a fluorinated polymer.
108. A method as in any preceding claim, wherein the absorbent material comprises an iptycene-based polymer.
109. A method as in any preceding claim, wherein the absorbent material comprises an ionic liquid.
110. A method as in any preceding claim, wherein the ionic liquid comprises an imidazolium ion.
111. A method as in any preceding claim, wherein the imidazolium ion is selected from a group consisting of 1-Butyl-3-methylimidazolium, 1-Ethyl-3-methylimidazolium, and 1-Hexyl-3-methylimidazolium.
112. A method as in any preceding claim, wherein the ionic liquid comprises a cation selected from a group consisting of tetrafluoroborate, hexafluorophosphate, and bis(trifluoromethanesulfone)imide.
113. A method as in any preceding claim, wherein the absorbent material comprises a cellulose-based polymer.
114. A method as in claim 113, wherein the cellulose-based polymer is cellulose acetate, cellulose diacetate, or cellulose triacetate, any of which is optionally substituted.
115. A method as in claim 113 or 114, wherein the cellulose-based polymer is cellulose substituted with at least one functional group comprising an aromatic moiety.
116. A method as in any one of claims 113-115, wherein the cellulose-based polymer comprises the structure,
- wherein:
- R1 is a group comprising a binding site for an aromatic species;
- R2 and R3 can be the same or different and are hydrogen, alkyl, aryl, a carbonyl group, any of which is optionally substituted; and
- n is greater than 1.
117. A method as in claim 116, wherein the binding site comprises an aromatic moiety, a calixarene, a hydrogen bond donor, or a hydrogen bond acceptor.
118. A method as in claim 116, herein the aromatic moiety is a phenyl group, optionally substituted.
119. A method as in claim 116, wherein the aromatic moiety is a polycyclic aromatic hydrocarbon, optionally substituted.
120. A method as in claim 116, wherein the cellulose-based polymer comprises the structure,
- wherein R4 and R5 can be the same or different and are hydrogen, alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, heteroaryl, or carbonyl group, any of which is optionally substituted.
121. A method as in claim 116, wherein the cellulose-based polymer comprises the structure,
- wherein R6 is alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, or heteroaryl, any of which is optionally substituted.
122. A method as in claim 116, wherein R1 has the structure,
123. A method as in any one of claims 116-122, wherein R2 and R3 can be the same or different and are hydrogen, —COCH3, or —F5Ph.
124. A method as in claim 123, wherein R2 and R3 are the same.
125. A method as in claim 123, wherein R2 and R3 are different.
126. A method as in any preceding claim, wherein the conductive material comprises a carbon-based nanostructure.
127. A method as in any preceding claim, wherein the carbon-based nanostructure is a nanotube, nanoparticle, graphene, or graphite.
128. A method as in any preceding claim, wherein the carbon nanotubes are single-wall carbon nanotubes.
129. A method as in any preceding claim, wherein the carbon nanotubes are multi-wall carbon nanotubes.
130. A method as in any preceding claim, wherein the sensor material and/or absorbent material further comprises a species capable of interacting with the analyte.
131. A method as in claim 130, wherein the absorbent material comprises the species capable of interacting with the analyte, the method comprising allowing the species to migrate from the absorbent material to the sensor material.
132. A method as in any preceding claim, wherein the sensor material and/or absorbent material further comprises a metal-containing species.
133. A method as in claim 132, wherein the metal-containing species comprises copper, cobalt, or palladium.
134. A method as in claim 133, wherein the metal-containing species is a complex or salt comprising Cu(I), Cu(II), Ag(I), Ag(II), Co(II), Co(III), Rh(I), Rh(III), Ir(I), Ir(III) or Pd(II).
135. A method as in claim 134, wherein the metal-containing species is a copper(I) scorpionate.
136. A method as in claim 134, wherein the metal-containing species is a cobalt (III) porphyrin.
137. A method as in any preceding claim, wherein the sensor material and/or absorbent material further comprises a fluorinated alcohol group.
138. A method as in any preceding claim, wherein the analyte is a vapor phase analyte.
139. A method as in any preceding claim, wherein the analyte is an aromatic species.
140. A method as in any preceding claim, wherein the analyte is benzene, toluene, xylene, or benzo[a]pyrene.
141. A method as in any preceding claim, wherein the analyte is a polycyclic aromatic hydrocarbon.
142. A method for determining an analyte, comprising:
- exposing a sample suspected of containing an analyte to a device comprising a first electrode, a second electrode, a sensor material in electrical communication with the first and second electrodes, and an absorbent material in contact with the sensor material, wherein the analyte, if present, interacts with the sensor material to cause a change in resistance between the first and second electrodes; and
- determining the change in resistance between the first and second electrodes, thereby determining the analyte.
143. A method as in claim 142, wherein the device lacks a piezoelectric material.
144. A method as in any preceding claim, wherein the absorbent material interacts with the analyte, if present, in a manner bringing the analyte into proximity with the sensor material to affect the determinable signal of the device.
145. A method as in any preceding claim, wherein, if the analyte is present, the second analyte concentration is greater than the first analyte concentration.
146. A method as in any preceding claim, wherein the analyte is determined without removing the analyte from the absorbent material.
147. A method as in any preceding claim, wherein, in the presence of an analyte, the analyte concentration of the absorbent material increases, thereby affecting resistance to current flow between the first and second electrode.
148. A method as in claim 147, wherein resistance to current flow between the first and second electrode is increased in the presence of the analyte.
149. A method as in claim 147, wherein resistance to current flow between the first and second electrode is decreased in the presence of the analyte.
150. A method as in any preceding claim, wherein the absorbent material comprises a polymer material and a plurality of binding sites.
151. A method as in claim 150, wherein at least some of the plurality of binding sites are covalently bonded to the polymer material.
152. A method as in claim 150, wherein at least some of the plurality of binding sites are non-covalently bonded to the polymer material.
153. A method as in claim 150, wherein the plurality of binding sites are dispersed throughout the polymer material.
154. A method as in any one of claims 150-153, wherein the plurality of binding sites comprises a mixture of different binding sites capable of determining a plurality of different analytes.
155. A method as in any preceding claim, wherein the absorbent material comprises polyvinyl alcohol or polyhydroxyl ethyl methacrylate, either of which is optionally substituted.
156. A method as in any preceding claim, wherein the absorbent material layer comprises a substantially hydrophobic polymer.
157. A method as in any preceding claim, wherein the absorbent material layer comprises a fluorinated polymer.
158. A method as in any preceding claim, wherein the absorbent material comprises an iptycene-based polymer.
159. A method as in any preceding claim, wherein the absorbent material comprises an ionic liquid.
160. A method as in any preceding claim, wherein the ionic liquid comprises an imidazolium ion.
161. A method as in any preceding claim, wherein the imidazolium ion is selected from a group consisting of 1-Butyl-3-methylimidazolium, 1-Ethyl-3-methylimidazolium, and 1-Hexyl-3-methylimidazolium.
162. A method as in any preceding claim, wherein the ionic liquid comprises a cation selected from a group consisting of tetrafluoroborate, hexafluorophosphate, and bis(trifluoromethanesulfone)imide.
163. A method as in any preceding claim, wherein the absorbent material comprises a cellulose-based polymer.
164. A method as in claim 163, wherein the cellulose-based polymer is cellulose acetate, cellulose diacetate, or cellulose triacetate, any of which is optionally substituted.
165. A method as in claim 163 or 164, wherein the cellulose-based polymer is cellulose substituted with at least one functional group comprising an aromatic moiety.
166. A method as in any one of claims 163-164, wherein the cellulose-based polymer comprises the structure,
- wherein:
- R1 is a group comprising a binding site for an aromatic species;
- R2 and R3 can be the same or different and are hydrogen, alkyl, aryl, a carbonyl group, any of which is optionally substituted; and
- n is greater than 1.
167. A method as in claim 166, wherein the binding site comprises an aromatic moiety, a calixarene, a hydrogen bond donor, or a hydrogen bond acceptor.
168. A method as in claim 166, herein the aromatic moiety is a phenyl group, optionally substituted.
169. A method as in claim 166, wherein the aromatic moiety is a polycyclic aromatic hydrocarbon, optionally substituted.
170. A method as in claim 166, wherein the cellulose-based polymer comprises the structure,
- wherein R4 and R5 can be the same or different and are hydrogen, alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, heteroaryl, or carbonyl group, any of which is optionally substituted.
171. A method as in claim 166, wherein the cellulose-based polymer comprises the structure,
- wherein R6 is alkyl, alkenyl, aryl, heteroalkyl, heteroalkenyl, or heteroaryl, any of which is optionally substituted.
172. A method as in 166, wherein R1 has the structure,
173. A method as in any one of claims 166-172, wherein R2 and R3 can be the same or different and are hydrogen, —COCH3, or —F5Ph.
174. A method as in claim 173, wherein R2 and R3 are the same.
175. A method as in claim 173, wherein R2 and R3 are different.
176. A method as in any preceding claim, wherein the conductive material comprises a carbon-based nanostructure.
177. A method as in any preceding claim, wherein the carbon-based nanostructure is a nanotube, nanoparticle, graphene, or graphite.
178. A method as in any preceding claim, wherein the carbon nanotubes are single-wall carbon nanotubes.
179. A method as in any preceding claim, wherein the carbon nanotubes are multi-wall carbon nanotubes.
180. A method as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a species capable of interacting with the analyte.
181. A method as in claim 164, wherein the absorbent material layer comprises the species capable of interacting with the analyte, the method comprising allowing the species to migrate from the absorbent material layer to the sensor layer.
182. A method as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a metal-containing species.
183. A method as in claim 182, wherein the metal-containing species comprises copper, cobalt, or palladium.
184. A method as in claim 182, wherein the metal-containing species is a complex or salt comprising Cu(I), Cu(II), Ag(I), Ag(II), Co(II), Co(III), Rh(I), Rh(III), Ir(I), Ir(III) or Pd(II).
185. A method as in claim 182, wherein the metal-containing species is copper(I) scorpionate.
186. A method as in claim 182, wherein the metal-containing species is cobalt (III) porphyrin compound.
187. A method as in any preceding claim, wherein the sensor material layer and/or absorbent material layer further comprises a fluorinated alcohol group.
188. A method as in any preceding claim, wherein the analyte is a vapor phase analyte.
189. A method as in any preceding claim, wherein the analyte is an aromatic species.
190. A method as in any preceding claim, wherein the analyte is benzene, toluene, xylene, or benzo[a]pyrene.
191. A method as in any preceding claim, wherein the analyte is a polycyclic aromatic hydrocarbon.
Type: Application
Filed: Sep 5, 2014
Publication Date: Aug 11, 2016
Applicant: Massachusetts Institute of Technology (Cambridge, MA)
Inventors: Timothy M. Swager (Newton, MA), Jisun Im (Busan), Alexander R. Petty (Boston, MA), Jan Schnorr (Cambridge, MA), Cindy Schmädicke (Dresden)
Application Number: 14/916,839
