Abstract: The present invention relates to a new method for fragmenting ions in a mass spectrometer through the use of electron transfer dissociation, and for performing sequence analysis of peptides and proteins by mass spectrometry. In the case of peptides, the invention promotes fragmentation along the peptide backbone and makes it possible to deduce the amino acid sequence of the sample, including modified amino acid residues, through the use of an RF field device.

Abstract: A method for the equilibration of enriched isotope species and natural isotope species prior to mass spectrometric analysis using solid phase and/or microwave isotope ratio equilibration and measurement.

Abstract: The invention relates to a device (10) for detection of harmful substances with a measurement unit (28) for measuring at least one harmful substance and an evaluation unit (30) for determining the concentration of the at least one harmful substance. The invention also relates to a method for detecting harmful substances in a gas mixture. It is hereby provided that the gas mixture is tested for a gaseous harmful substance or simultaneously for several gaseous harmful substances, wherein the gaseous harmful substance or the gaseous harmful substances is/are measured with different sensor means, and the gaseous harmful substances are optionally chemically modified such that a measurement is performed with the existing sensor means.

Abstract: An improved detection reaction for benzene in gas analysis with a gas detector tube formed of a carrier material impregnated with gold(III) oxide in a display layer.

Abstract: Methods for determining the amount of vitamin D compounds in a sample are provided. The methods can employ LC-MS/MS techniques and optionally the use of deuterated internal standards. Methods for diagnosing vitamin D deficiencies are also provided.

Abstract: The invention relates to the use of molecular tweezers as sensitive materials in chemical sensors intended to detect or assay organic compounds in the vapour state, and in particular nitro compounds. These molecular tweezers correspond to the general formula (I): in which: MC1 and MC2 represent macrocycles; p and q are equal to 0 or 1; X and Y are optionally substituted C1 to C10 alkylene groups; while E represents an optionally substituted cyclic or heterocyclic spacer group; and in which MC1 and MC2 are positioned facing each other. Fields of application: detection of explosives, control and monitoring of atmospheric pollution and of the quality of ambient air in relatively confined spaces, and monitoring of industrial sites.

Abstract: In at least one embodiment, the inventive technology relates to in-vessel generation of a material from a solution of interest as part of a processing and/or analysis operation. Preferred embodiments of the in-vessel material generation (e.g., in-vessel solid material generation) include precipitation; in certain embodiments, analysis and/or processing of the solution of interest may include dissolution of the material, perhaps as part of a successive dissolution protocol using solvents of increasing ability to dissolve. Applications include, but are by no means limited to estimation of a coking onset and solution (e.g., oil) fractionating.

Abstract: A method for selecting at least one catalyst from a catalyst library on the basis of the reactivity thereof in a chemical conversion process includes: (a) testing the catalytic activity of a first catalyst from said catalyst library with respect to a reaction medium containing, as the compounds to be converted, at least one reactivity probe having a labeling system and including at least one reaction unit capable of reacting in said chemical conversion; (b) analyzing the reaction medium after said catalytic test for the purpose of qualitatively and/or qualitatively characterizing the resulting compounds; (c) repeating steps (a) and (b) for at least one other catalyst in said library; and (d) comparing the analysis results for each catalyst in order to characterize at least one catalyst having the required reactivity in said chemical conversion.

Abstract: The invention provides a method and apparatus for trapping, releasing and/or separating sample components in solution passing through a channel with or without packing material present by passing ion current through the channel driven by an electric field. A portion of the ion current comprises cation and/or anion species generated from second solution flows separated from the sample solution flow path by semipermeable membranes. Cation and/or Anion ion species generated in the second solution flow regions are transferred into the sample solution flow path through ion selective semipermeable membranes. Ion current moving along the sample solution flow path is controlled by varying the composition of the second solutions and/or changing the voltage between membrane sections for a given sample solution composition. The sample composition may also be varied separately or in parallel to enhance trapping, release and/or separation efficiency and range.

Abstract: Provided are mixed ligand metal nanoparticle chemical sensors in which metal nanoparticles are encapsulated by at least two kinds of different molecule ligands having a relatively low conductivity and various composition ratios, and a chemical sensor array in which a film of the metal nanoparticle sensor is formed on the substrate. The metal nanoparticle sensor using the mixed ligand improves sensitivity and reaction speed with respect to an analyte, and selectivity with respect to various analytes, and a kind and a composition of a ligand of the mixed ligand constituting the metal nanoparticle sensor are adjusted to allow the high sensitivity nanoparticle sensor to be applied to the sensor array technology, thereby enabling a design of sensor properties as well as systematic access to a configuration of the sensor array the most efficient for the analytes.

Abstract: An apparatus and method are disclosed for measuring the kinetic parameters of a catalyst powder, which include the reaction rate constants, active site concentration and intraparticle diffusivity. The measurement of the active site concentration selectively measures just the active sites and not the entire exposed atom concentration. The apparatus and method use surface concentrations less than 50% and larger than 1% the total active site concentration and a dynamic pulsed flow to avoid including weak adsorption sites not involved in the catalysis. The measurement is more accurate because (1) it uses a reactant gas and non-steady state adsorption at temperatures near to reaction temperatures, and (2) it uses the chemical kinetics expressions to extract the measured active site concentration to perform the measurement so as to count just those sites actually active for that reactant.

Abstract: The present invention relates to a method for measuring the percentage natural of a cleaning composition using radiocarbon dating data. The percentage natural of a cleaning composition is defined as the amount of material that comes from non-petroleum based or derived products. By using radiocarbon data for the entire composition or its individual components one can determine the percentage of materials which are from non-petroleum based or derived products, and calculate the percent Renewable Carbon Index (RCI). The percent RCI can be used to calculate the percent natural of the cleaning composition as defined by the methods of the present invention.

Abstract: The invention provides a method for producing a homogenous sample of a pressurized fluid stream flowing in a pipeline, the fluid stream consisting of a majority component of hydrocarbon gas, the remainder consisting of one or more hydrocarbon liquids and water in the form of vapor, aerosols, droplets and/or liquid streams, the method includes the steps of: a. injecting one or more surface active agents into the fluid stream in an injection zone at a rate that is sufficient to form a uniform foam of the gas and the one or more hydrocarbon liquids and water components; b. mixing the one or more surface active agents with the fluid stream in a mixing zone to form a uniform foam composition flowing in the pipeline downstream of the mixing zone; c. withdrawing a portion of the foam composition from the pipeline at a sampling point; d. passing the portion of the foam composition withdrawn through a sampling loop; and e.

Abstract: A method for testing the performance of catalysts used for conversion of FCC regenerator gases comprises subjecting the catalyst simultaneously to a mixture of gases including an oxidizing gas and a reducing gas in more than one cycle in which the ratio of the oxidizing gas to the reducing gas varies over the time of the cycle. Test gases comprising O2, CO, CO2, steam, nitrogen-containing gases and sulfur-containing gases in which the ratio of O2 to CO varies over time for each cycle and in which the products of combustion formed during each cycle can be measured periodically over the cycle yields important data on the usefulness of the catalysts for treatment of regenerator flue gas.

Abstract: A method of detecting organic vapors is described. More particularly, the method involves the use of an analyte sensor that contains a polymeric material having a relatively large intrinsic porosity and that is capable of fluorescence in the visible region of the electromagnetic spectrum. The method further includes exposing the analyte sensor to an environment that may contain an organic vapor and monitoring the analyte sensor for a change in a fluorescence signal. Although the organic vapor itself typically does not fluoresce in the visible wavelength range, presence of an organic vapor can alter the fluorescence signal of the analyte sensor.

Abstract: Methods for determining the amount of vitamin D compounds in a sample are provided. The methods can employ LC-MS/MS techniques and optionally the use of deuterated internal standards. Methods for diagnosing vitamin D deficiencies are also provided.

Abstract: Methods for analyzing aromatic hydrocarbons dissolved in water are discussed. The methods include providing a substrate coated with a thin film layer of a material, wherein the material has a high affinity for at least one aromatic hydrocarbon, the material is substantially optically transparent, and the material has near-zero auto fluorescence, inserting the coated substrate directly into an environmental location including water, waiting for an exposure time permitting at least one aromatic hydrocarbon to absorb into the thin film layer, retrieving the coated substrate from the environmental location, removing any non-absorbed matter from the coated substrate, and performing fluorescence analysis on the coated substrate to detect aromatic hydrocarbons present in the thin film layer. Also methods for analyzing aromatic hydrocarbons dissolved in water contained in coated vessels are provided.

Abstract: The invention relates to a diagnostic method and to marker substances which enable manipulations in endogenic marking to be detected and thus prevented. According to the invention, a metabolizable substance is added to non-metabolizable marker substances, said metabolizable substance revealing a manipulation when detected in excreta.

Abstract: A method of and device for sampling polycyclic aromatic hydrocarbons (PAHs) in the ambient environment, the method including: (a) providing a polymer film for collecting the PAHs; (b) exposing the polymer film to a gas containing the PAHs, and (c) performing an analysis of the PAHs collected by the polymer film, the analysis being selected from the group consisting of fluorescence analysis and Fourier Transform Imaging Microscopy (FT-SIM).

Abstract: Charged droplet spray is formed from a solution with all or a portion of the charged droplet spray current generated from reduction or oxidation (redox) reactions occurring on surfaces removed from the first or sample solution flow path. In one embodiment of the invention, two solution flow channels are separated by a semipermeable membrane. A first or sample solution flowing through the first solution flow channel exchanges cation or anion charged species through the semipermeable membrane with a second solution or gas flowing through the second flow channel. Charge exchange is driven by the electric field applied at the charged droplet sprayer sample solution outlet. Redox reactions occur at an electrode surface in contact with the second solution. The second solution or gas phase composition can be changed as a step function or as a gradient to run pH or conductivity scans in the first solution to optimize or modify Electrospray performance in Electrospray mass spectrometry applications.

Abstract: An installation for the automatic preparation of specimens by liquid/solid extraction on a column is characterized in that the extraction device comprises, on either side of the columns (3), a valve (4) controllable to switch one column (3) to the other to actuate one column (3) adapted to ensure the extraction function when another column (3) is in a non-operating condition, each switching valve (4) being connected to a controllable common direction reversing valve (5) arranged to impose one direction of circulation on the fluid in anyone of the columns (3) of the extraction device and to ensure its return to the valve (5) to distribute the treated fluid toward a circuit selectively either for its rejection or for its analysis.

Abstract: Synthetic receptor cores are provided that comprise a compound represented by the following formula: wherein R1, R2, and R3 independently comprise at least one moiety chosen from a hydroxyl group, an amine group, and derivatives thereof. Synthetic receptor cores are provided that comprise a compound represented by the following formula: wherein R comprises at least one moiety chosen from a hydroxyl group, an amine group, and derivatives thereof. Synthetic receptors are provided that comprise a synthetic receptor core; and an analyte binding moiety, wherein the analyte binding moiety is capable of complexion with an analyte. Systems, methods, and kits are also provided that use a synthetic receptor.

Abstract: Carbon nanotube devices are manipulated in a manner that is useful for a variety of implementations. According to an example embodiment of the present invention, light (632) is used to photodesorb molecules from a carbon nanotube (620).

Abstract: A process for measuring the mercury concentration within a hydrocarbon is provided that enables the mercury concentration to be measured simply and quickly, and with good reliability and good reproducibility. A process for measuring the mercury concentration within a hydrocarbon includes the steps of placing and weighing the hydrocarbon in a sample boat 12 containing an adsorbent that contains a metal capable of forming an amalgam with mercury, and heating the hydrocarbon inside the sample boat 12 in a combustion furnace 13, together with the adsorbent, and measuring the quantity of mercury within the thus generated gas.

Abstract: The present invention provides a method and apparatus or system for determining an amount of coal tar that can enter, and subsequently be displaced from, a given type of soil for a range of depths of the soil. The method and apparatus also provide verification of the pressure at which coal tar can be displaced from a given type of soil. In particular, the method and apparatus simulate the hydrostatic pressure that a soil sample encounters in the subsurface of the ground. Accordingly, the method and apparatus provide a relationship between the concentration of coal tar in the soil and the pressure required to displace the coal tar from the soil, which allows for an estimation of the amount of coal tar that may be displaced at a particular location or site. Further, the method and apparatus are adaptable for use in the laboratory or the field.

Abstract: A process and apparatus for testing material libraries, in particular catalysts, by means of coupled use of at least two analytical methods, preferably IR thermography and mass spectrometry. Owing to the selected arrangement, the disadvantages of the two previously known individual methods are compensated for: the subsequent selectivity determination for selected sections by means of mass spectrometry invalidates the argument against IR thermography, of only being able to determine activities; the rapid integrated determination of potentially “good” materials via IR thermography prevents an excessive loss of time by needing to test all materials of a library successively with the mass spectrometer.

Abstract: A reader is provided that, itself, addresses the issue of damage or degradation to arrays within the reader by virtue of air exposure. In doing so, experimental variability is reduced, and read/scan signal strength degradation is minimized for arrays/slides scanned or otherwise read toward the end of a run. The subject scanners employ a filter that reduces the amount of chemicals in the air inside the device that are harmful to the array, or the dye on the array. The implementation of adding a chemical filter to the reader device may be such that air is either drawn into or, alternatively, pushed through the filter into the same. It is possible that the entirety of the device may be provided with filtered air, or just the region holding slides to be scanned. Array readers so-constructed as well as associated methodology involving filtering incoming air while reading arrays are covered.

Abstract: Charged droplet spray is formed from a solution with all or a portion of the charged droplet spray current generated from reduction or oxidation (redox) reactions occurring on surfaces removed from the first or sample solution flow path. In one embodiment of the invention, two solution flow channels are separated by a semipermeable membrane. A first or sample solution flowing through the first solution flow channel exchanges cation or anion charged species through the semipermeable membrane with a second solution or gas flowing through the second flow channel. Charge exchange is driven by the electric field applied at the charged droplet sprayer sample solution outlet. Redox reactions occur at an electrode surface in contact with the second solution. The invention increases the control and range of the Electrospray ionization process during ES/MS operation.

Abstract: A multi-pin chemiresistor for use in microchemical sensors. A pair of free-standing, bare wires is supported by an electrically insulating support, and are oriented parallel to each other and spaced closely together. A free-standing film of a chemically sensitive polymer that swells when exposed to vapors of a volatile chemical is formed in-between the pair of closely-spaced wires by capillary action. Similar in construction to a thermocouple, this “chemicouple” is relatively inexpensive and easy to fabricate by dipping the pair of bare wires into a bath of well-mixed chemiresistor ink. Also, a chemiresistor “stick” is formed by dipping an electrically insulating rod with two or more linear or spiral-wrapped electrical traces into the bath of well-mixed chemiresistor ink, which deposits a uniform coating of the chemically sensitive polymer on the rod and the electrical traces. These “sticks” can be easily removed and replaced from a multi-chemiresistor plug.

Abstract: Oil aging and particulate building in a lubricant other than one exposed to combustion products is monitored by detecting light transmitted through the lubricant at least one, and preferably, two or more preselected wavelengths over a pathlength greater than about 0.5 cm wherein one wavelength is in the near infra-red spectrum and/or one wavelength is in the visible or near infra-red spectrum. The detected light when compared to predetermined values provides an indication of the condition of the lubricant.

Abstract: A method for quantitative determination of hydrocarbon species in a hydrocarbon sample is disclosed. The method uses Townsend Discharge Nitric Oxide Chemical Ionization Gas Chromatography/Mass Spectrometry.

Abstract: The invention relates to an automated method for carrying out reactions with high spatial resolution on libraries of different materials and for analysis of the products obtained using a simple robot system and an analyzer, for example a mass spectrometer.

Abstract: An inverse analysis method for characterizing diffusion of vapor from an underground source of volatile contaminant using data taken by an in-situ sensor. The method uses one-dimensional solutions to the diffusion equation in Cartesian, cylindrical, or spherical coordinates for isotropic and homogenous media. If the effective vapor diffusion coefficient is known, then the distance from the source to the in-situ sensor can be estimated by comparing the shape of the predicted time-dependent vapor concentration response curve to the measured response curve. Alternatively, if the source distance is known, then the effective vapor diffusion coefficient can be estimated using the same inverse analysis method. A triangulation technique can be used with multiple sensors to locate the source in two or three dimensions. The in-situ sensor can contain one or more chemiresistor elements housed in a waterproof enclosure with a gas permeable membrane.

Abstract: It is discovered that a composition comprising at least one amine and at least one stabilizer may be useful in detecting the presence of an adulterant in a urine sample. Such adulterant includes an oxidizing agent.

Abstract: The present invention provides a method for testing the accessibility of porous materials with regard to large, often high-molecular weight compounds and correlating said accessibility to the porous material's accessibility under conditions of use, i.e. the application conditions.

Abstract: Indicia of stability or thresholds of instability may be used to assess the proximity of hydrocarbon materials such as petroleum residua to deposition of carbon rich materials. The invention may be used to evaluate suitability of such hydrocarbon materials to various types of processing methodologies, or to determine processing parameters, either prior to processing or during processing. Prediction of proximity to deposition of carbon rich materials may result in continuous process parameters or increased output, decreased energy use or decreased amount of emissions per unit of such hydrocarbon materials compared to conventional processing technology. Products produced or products processed with this technology may also have a higher level of purity.

Abstract: An automatic mass spectrometry analytical system was developed for the quantitative detection of organic toxicant exposure in the human body. A cartridge (such as C18 cartridge) is integrated into the automatic mass spectrometry analytical system. The sample undergoes sample pretreatment by the cartridge before entering the mass spectrometry for analysis. This increases the accuracy and sensitivity of analysis, while also avoiding tedious manual sample pretreatment procedures. The whole analytical process is fully automatic and therefore useful for high throughput sample analysis.

Abstract: A method for determining the quantity of phenol extracted into an aqueous solution of an alkali metal hydroxide uses a measurement of the pH of the solution, from which the equivalents of phenol relative to alkali metal hydroxide in solution is determined. A method for optimizing the use of an aqueous solution of an alkali metal hydroxide in a phenol recovery process uses pH measured to regulate the feed rate of the aqueous solution.

Abstract: A process is described for determining the stability of asphaltenes in oil fields, which comprises the following steps: a) titrations of stock tank oil are carried out; the values measured are then used, together with physico-chemical analyses of the stock tank oil, to thermodynamically characterize the asphaltenes and the heavy oil fraction; b) using the physico-chemical analyses of live oil, the experimental data relating to its phase behavior are interpolated in order to provide a better representation by means of an equation of state; c) using the equation of state thus calibrated and the characterization of the asphaltenes, the stability of the latter is verified in relation to the temperature and pressure of live oil, using the equation describing the behavior of a sterically stabilized colloid.

Abstract: A test for determining the bioavailable fraction of an organic pollutant present in soil comprises determining the fraction of the organic pollutant present in the soil which may be extracted by a cyclodextrin or derivative thereof.

Abstract: A method for determining whether a fluid in an air-conditioning or refrigeration system has been altered is revealed. The method comprises preparing a non-radioactive label for a fluid used in the system, where the fluid is selected from a lubricant, a fluorescent dye and combinations thereof; adding a known quantity of the label to the fluid to form a labeled mixture of the fluid; performing an analysis of the labeled mixture to obtain a base-line profile of the labeled mixture; adding the labeled mixture to the system; providing the system to a user or customer; thereafter, performing an analysis of the fluid in the system to obtain a test profile; and determining whether the fluid in the system has been altered by comparing the base-line profile with the test profile of the fluid in the system.

Abstract: An apparatus provides for the detection, the determination of the location or the spatial distribution, and/or the quantification of an amount of a chemical species by allowing the chemical species to come into contact with a fluid medium contained in a permeable capillary, transferring the content of the capillary after the contact to a detector, and detecting the chemical species as the content of the capillary is transferred to a detector. The fluid medium can contain a selected reagent that selectively interacts with the chemical species to produce an optically detectable interaction product. The location and amount of the chemical species are determined from a characteristic of the chemical species or its interaction product measured on the content of the capillary and the time at which the characteristic is detected.

Abstract: The invention includes systems and methods which allow reactivation of supported noble metal catalysts. The method involves heating the catalyst in the presence of a gaseous hydrocarbon in the absence of oxidizing agents. Systems of the invention provide for in situ reactivation of catalytic material.

Abstract: A biomimetic reagent system is provided containing an oxygen donor and a catalyst based on porphyrin, which are applied to a carrier. A device that contains the system is also provided for determining components of gas or vapor samples, especially aromatics, such as benzene. A process for hydroxylating aromatics, such as benzene, using the biomimetic reagent system is also provided.

Abstract: The method of analyzing polyphenols and bisphenols in accordance with the present invention comprises a step of reacting a bisphenol and/or a polyphenol with a labeling reagent having a pyrene group, so as to generate a fluorescent derivative; a step of irradiating the fluorescent derivative with excitation light and detecting fluorescence emitted from the fluorescent derivative; and a step of calculating an amount of the bisphenol and/or polyphenol in a test sample according to an intensity of thus detected fluorescence and a relationship between a known concentration of a bisphenol and/or a polyphenol contained in a standard sample and fluorescence intensity.

Abstract: The present invention provides a method of estimating ingredients of liquefaction products of coal or its analogues from a resonance spectrum thereof obtained using their solid state 13C nuclear magnetic resonance spectrometer. The method comprises the first step of obtaining a resonance spectrum of coal or its analogues using a solid state 13C nuclear magnetic resonance spectrometer, the second step of determining distribution of various types of carbon having different linkage types which constitute the molecular structure of the coal or its analogues, and the third step of estimating ingredients of liquefaction products of the coal or its analogues on the basis of the determined carbon distribution.

Abstract: The present invention provides methods for detecting the presence of an analyte indicative of various medical conditions, including halitosis, periodontal disease and other diseases are also disclosed.

Abstract: A method for investigating a target environment to determine whether or in what amount a chemical species may be present therein, which comprises: (a) exposing to said environment an article of manufacture comprising a multiplicity of particles in close-packed orientation, said particles having a core of conductive metal or conductive metal alloy and deposited thereon a ligand which is capable of interacting with said species such that a property of said multiplicity of particles is altered; (b) subjecting said multiplicity of particles to conditions sufficient for said property to be exhibited; and (c) monitoring said property to determine whether there is, or the amount of, any change as an indication of whether, or in what amount, said species is present; a multiplicity of particles suitable for use in such method; and equipment suitable for implementing the method.

Abstract: A method and apparatus are disclosed for analyzing the aggregate content of asphalt-aggregate compositions. The method includes placing a preheated, preweighed container carrying a sample of an asphalt-aggregate composition into a preheated furnace with the preheated furnace being warmer than the preheated sample, continuing to heat the furnace while drawing air through the furnace at a rate that avoids impeding the heating of the furnace or the sample until the sample in the container reaches its combustion temperature and the combustion of the sample becomes exothermic, initiating a second draw of air around rather than through the furnace to moderate the exterior temperature of the furnace, accelerating the draw through the furnace to increase the rate of combustion of the exothermic reaction, and reweighing the container and sample after combustion is complete.

Abstract: A method and apparatus are disclosed for analyzing asphalt-aggregate compositions. The method includes directing sufficient microwave radiation from a microwave source to a sample of an asphalt-aggregate composition to ignite the asphalt in the composition and to thereafter entirely combust the asphalt in the sample. The apparatus includes a source of microwave radiation, a cavity in communication with the microwave source, a sample holder in the cavity for holding a sample of an asphalt-aggregate composition during exposure to microwaves from the source, thermal insulation between the sample holder and the remainder of the cavity, and means for minimizing or eliminating any undesired combustion products generated by the burning asphalt.