Abstract: This invention relates to an improved electrodialysis method for preparing an amino acid from a salt of the amino acid utilizing a three-compartment bipolar membrane electrodialysis process wherein an aqueous electrolyte comprising an exogenous acid is added to the acid compartment of a three-compartment bipolar membrane apparatus. The exogenous acid is different than the amino acid and typically has a pKa less than the pKa of the amino acid.

Abstract: Many hand-held diagnostics are limited in their functionality due to the challenging physics associated with small dimensional systems. An example of this is capillary forces in hydrophilic systems, such as the tight retention of liquid passing through a small pore filtration membrane, or capillary force driven microfluidics where, to keep liquid flowing the dimensions of the system become so small that the flow rates are too low to be useful, or the manufacturing of such devices becomes uneconomical. This disclosure details methods to ‘reset’ the capillary force condition to avoid the requirement of transient pressure spikes associated with the breakthrough pressure of small pore membranes, and avoid the necessity of extremely small microfluidic channels, which can be useful in applications such as filtration of whole blood to plasma using only suction pressure or passive capillary pressure.

Abstract: A filter element comprises a membrane layer; and a feed spacer on the membrane layer, wherein the feed spacer comprises a plurality of unit cells arranged in three dimensions, wherein each of the plurality of unit cells comprises a cavity defined by a triply periodic minimal surface, and wherein the cavities of the plurality of unit cells are interconnected to allow a fluid to pass through the cavities of the plurality of unit cells.

Abstract: The present disclosure provides a hydrophilic, integrally asymmetric, semi-permeable hollow-fiber membrane made from a hydrophobic aromatic sulfone polymer and at least one hydrophilic polymer, the membrane comprising an inner surface facing towards its lumen, an outer surface facing outwards and an intermediate wall having a wall thickness and comprising an open-pore separating layer and an supporting layer having an asymmetric, sponge-like structure without finger pores, wherein adjoining to the wall of the inner surface the hollow-fiber membrane comprises an essentially isotropic zone; after which the pore size abruptly start increasing up to a maximum, after which the pore size decrease again, then adjoining an essentially isotropic supporting layer which then is adjoined by the outer surface, wherein the separating layer has a cut-off of greater than 300 000 Daltons. The present disclosure further provides a method for producing such membranes and a use of the membranes for microfiltration purposes.

Abstract: A carbonized PVDC copolymer useful for the separation of an olefin from its corresponding paraffin may be made by heating a polyvinylidene chloride copolymer film or hollow fiber having a thickness of 1 micrometer to 20 micrometers to a pretreatment temperature of 100° C. to 180° C. to form a pretreated polyvinylidene chloride copolymer film and then heating the pretreated polyvinylidene chloride copolymer film to a maximum pyrolysis temperature from 350° C. to 750° C. A process for separating an olefin from its corresponding paraffin in a gas mixture is comprised of flowing the gas mixture through the aforementioned carbonized polyvinylidene chloride (PVDC) copolymer to produce a permeate first stream having an increased concentration of the olefin and a second retentate stream having an increased concentration of its corresponding paraffin.

Abstract: A process for separating hydrogen from a gas mixture having hydrogen and a larger gas molecule is comprised of flowing the gas mixture through a carbonized polyvinylidene chloride (PVDC) copolymer membrane having a hydrogen permeance in combination with a hydrogen/methane selectivity, wherein the combination of hydrogen permeance and hydrogen/methane selectivity is (i) at least 30 GPU hydrogen permeance and at least 200 hydrogen/methane selectivity or (ii) at least 10 GPU hydrogen permeance and at least 700 hydrogen/methane selectivity. The carbonized PVDC copolymer may be made by heating and restraining a polyvinylidene chloride copolymer film or hollow fiber having a thickness of 1 micrometer to 250 micrometers to a pretreatment temperature of 100° C. to 180° C. to form a pretreated polyvinylidene chloride copolymer film and then heating and restraining the pretreated polyvinylidene chloride copolymer film to a maximum pyrolysis temperature from 350° C. to 750° C.

Abstract: Systems and methods described herein may produce a modified substrate. A process for producing a modified substrate may include providing a substrate that is 5 microns or less in thickness, ion tracking the substrate, and etching the tracked substrate with an etchant to produce a plurality of pores in the substrate. In some implementations, the substrate may be a polymer. In some implementations, the ion tracking may include controlling a flux of ions passing through the substrate to achieve a desired pore density. In some implementations, the track-etching of the substrate may create a 10% or more porosity in the substrate. In some implementations, the process may further include using the track-etched substrate as a support substrate for at least one of a single-layer graphene film, multi-layer graphene film, stack of graphene films, nanostructure of graphene flakes, or nanostructure of graphene platelets.

Abstract: The present disclosure relates to synthetic membranes for the removal, isolation or purification of substances from a liquid, comprising at least one hydrophobic and at least one hydrophilic polymer, wherein 5-40 wt.-% of particles having an average particles size of between 0.1 and 15 ?m are entrapped and wherein the membrane has a wall thickness of below 150 ?m. Further disclosed are methods for preparing such membranes in various geometries and their use for the adsorption, isolation and/or purification of substances from a liquid.

Abstract: Described herein is a composite comprising a graphene material and a sulfonated polymer material. The graphene/sulfonated polymer composite is coated onto a substrate to provide a selectively permeable membrane. The selectively permeable membranes of the present disclosure provide high moisture permeability and low gas permeability.

Abstract: Methods and systems for controlling proppant concentration in a hydraulic fracturing slurry include measuring volumetric flow rates of fracturing fluid input to a blender and hydraulic fracturing slurry output from the blender, using these measured values to calculate a volumetric flow rate of proppant input, a slurry density and/or a slurry volume fraction, adjusting first and second valves to control rates of fluid and proppant delivery to the blender and re-measuring the volumetric flow rates and recalculating until target values of volumetric flow rate of proppant input, slurry density and/or slurry volume fraction are achieved.

Abstract: A system, method, and apparatus for oxygenation of a source of water, to increase the dissolved oxygen content of water. Aspects of the present invention harnesses and directs the power of water flowing through the system to extract oxygen present in air, rather than relying on the injection of gas or using other mechanical means. The water oxygenator is formed as an elongate cylindrical tube having a water inlet at a first end, a water outlet at a second end, and an air inlet proximal to the first end. The elongate cylindrical tube has an outer sidewall defining a mixing chamber within an interior cavity of the water oxygenator. The mixing chamber includes a plurality of baffles that are disposed in a spaced apart relation along a longitudinal length of the interior cavity.

Abstract: A mixing device (1) for cyclically imparting a force on an external surface (A) of a bag (B) for agitating a content (C) of the bag (B), the mixing device (1) comprising a lever (2) supported so as to be able to pivot about a pivot (3), a weight (4) provided on a first side of the lever (2), a driver (5) arranged to cooperate with the lever (2), a motor (6) for moving the driver (5) to lift the first side of the lever (2) with the weight (4) against gravity and to drop the first side against the external surface (A) of the bag (B), and a holder (7) for supporting the mixing device (1) such that the first side of the lever (2) can contact the external surface (A) of the bag (B) in the drop motion.

Abstract: The present invention concerns a method of mixing aqueous solutions, an apparatus for carrying out said method and the use of dosing devices with integrated dosing monitoring and stroke length control in an installation for mixing container aqueous solutions.

Abstract: The present disclosure provides derivatives of amino acids that have surface-active properties. The amino acid can be naturally-occurring or synthetic, or they may be obtained via a ring-opening reaction of a lactam, such as caprolactam. The amino acid may be functionalized to form a compound that is surface-active and have advantageous surfactant characteristics. The compounds of the present disclosure have low critical micelle concentrations (CMC) as well as superior ability to lower the surface tension of a liquid.

Abstract: The present application provides systems and methods for upgrading an oil stream. The system includes a reactor, a phase separator, an expansion device, a cooling unit, and two separation units. The reactor receives the oil stream, ammonia, and supercritical water. The supercritical water upgrades the oil stream, and the ammonia reacts with sulfur initially present in the oil stream to produce ammonia-sulfur compounds. The phase separator receives a mixture stream comprising the upgraded oil stream, supercritical water, and the ammonia-sulfur compounds, and separates out non-dissolved components. The expansion device reduces the pressure of the mixture stream below a water critical pressure. The cooling unit reduces the temperature of the mixture stream. A first separation unit separates the mixture stream it into a hydrocarbon-rich gaseous phase, a water stream containing ammonia-sulfur compounds, and a treated oil stream. A second separation unit separates the ammonia-sulfur compounds from the water stream.

Abstract: A load-following reactor system and associated facilities for improved control of a reactor under varying loads. The load-following reactor may be a tube-cooled reactor for methanol synthesis. A reactant may be controlled by at least one valve element such that a portion of the reactant is fed to the reactor through the reactor tubes, and a portion of the reactant is fed to the reactor after being heated in a heat exchanger. The heated portion of the reactant may be fed to the reactor after the tubes. The valve element may be controlled based on a temperature of the reactor and/or a flowrate of reactant feed to adapt the temperature of the reactor to the changing reactant flowrate.

Abstract: A process chamber comprising can include a curved upper wall extending longitudinally from a first end portion of the reaction chamber to a second end portion of the reaction chamber. The process chamber can include a curved lower wall cooperating with the curved upper wall to at least partially define an internal cavity, the curved lower wall connected to the curved upper wall from the first end portion to the second end portion at a first side of the reaction chamber and at a second side of the reaction chamber. A rail can extend along an exterior surface of the process chamber from the first end portion to the second end portion, the rail disposed at or near a connection between the curved upper wall and the curved lower wall.

Abstract: The invention relates to a method for treating a nanofibrillar cellulose hydrogel, wherein the method comprises the steps of: providing a nanofibrillar cellulose hydrogel, wherein the nanofibrillar cellulose is oxidized nanofibrillar cellulose, wherein the oxidation has been carried out through N-oxyl mediated catalytic oxidation of cellulose-based raw material, and has at most 50 ?mol of aldehyde groups per gram of dry nanofibrillar cellulose; and subjecting the nanofibrillar cellulose hydrogel to a heat treatment.

Abstract: Aspects of the present invention provide a modular reactor device having an outer housing, and a plurality of components contained within the outer housing, the components including: a reaction chamber; a fluid pathway connected to the reaction chamber; and a valve arranged to control flow of fluid within the device, wherein the outer housing has a plurality of connection ports providing connections from the exterior of the device to the interior, the connection ports including: a fluid input and a fluid output; an electrical input; and a pneumatic input; wherein either the electrical input or the pneumatic input is connected to the valve to provide for control of the valve, and either the fluid input or the fluid output is connected to the reaction chamber or the fluid pathway. Other aspects provide a base station for receiving and controlling a modular reactor device and methods for manufacturing the modular reactor device and for performing reactions using a modular reactor device.

Abstract: A method of synthesis of a nucleotide chain, the nucleotide chain including an ordered plurality of nucleotides, the method including: identifying a first nucleotide of the ordered plurality of nucleotides; controlling a polymerase enzyme to assemble the first nucleotide onto the nucleotide chain by electrically modulating an electrode; identifying a subsequent nucleotide in the ordered plurality of nucleotides as a current nucleotide; and controlling the polymerase enzyme to assemble the current nucleotide onto an end of the nucleotide chain by electrically modulating the electrode.

Abstract: An apparatus for manufacturing a quantum dot is provided, the apparatus including a first supplying part that provides a cationic precursor, a second supplying part that provides an anionic precursor, a mixing part connected to the first supplying part and the second supplying part, and a reaction part including a reaction tube configured to receive a liquid mixture of the cationic precursor and the anionic precursor from the mixing part and a first microwave generator configured to provide a microwave that is transmitted through the reaction tube. Therefore, the apparatus may produce a quantum dot of multi-element compounds.

Abstract: Disclosed apparatuses, systems, and materials relate to the disassociation of feedstock species (such as those in gaseous form) into constituent components, and may include an energy generator configured to provide a microwave energy. A first chamber defines a first volume and is configured to guide the microwave energy along the first chamber as a sinusoidal wave having an energy maxima at a point along the first chamber. A second chamber contains a plasma plume and is positioned substantially proximal to the first chamber, and is configured to enable propagation of the microwave energy through the first chamber and the second chamber such that the microwave energy demonstrates, at a radial center of the second chamber, a coaxial energy maxima configured to ignite the plasma plume contained in the second chamber. Carbon-containing materials may be formed by controlling flow parameters of the feedstock species into the first or second chamber.

Abstract: An apparatus for enhancing a yield and a transfer rate of a packed bed includes a packed bed, a vessel having a reaction chamber, a support frame and acoustic attenuator for holding the packed bed in the reaction chamber, at least one acoustic transducer adapted to transmit acoustic energy into the packed bed and an acoustic generator. The acoustic generator has impedance matching functionality.

Abstract: The present invention provides an improved photochemical rector assembly device, particularly a light emitting diode (LED) based small photochemical reactor and methods for performing the photochemical transformations using the instantly presented device. Accordingly, the present invention relates to an improved photochemical transformation reaction by exposing the reaction mixture to a photochemical rector device as shown in fig. A-G, comprising of (i) light emitting diode (LED) panel (1), (ii) Aluminium based heat sink, and (iii) cooling fan.

Abstract: A graphene oxide adsorbent material for filtering contaminants from water is formed of graphene oxide plates cross-linked by branched polymer nanoparticles.

Abstract: Processes for removing arsenic compounds from a feed stream using an adsorbent in disclosed. The process includes contacting a feed stream comprising at least arsenic and sulfur compounds with an adsorbent comprising an low-crystallinity manganese oxide, at least one halide and a binder, to provide a treated effluent substantially free of the arsenic and sulfur compounds.

Abstract: A composition for purifying a liquid, such as used cooking oil, unrefined edible oils, or biodiesel fuel, that comprises at least one purifying material, such as magnesium silicate, and at least one binder material that is a solid or a semi-solid at room temperature, or is water or a glycol. When the composition is placed in a liquid, and the liquid is heated, the solid composition disintegrates and the at least one purifying material is released in the liquid. Such composition minimizes or eliminates contact with the dust associated with solid adsorbent materials, and provides for a controlled release of the at least one purifying material into the liquid to be purified.

Abstract: The invention discloses a preparation method of high-absorptivity silica as lutein carrier. The method includes adding sodium silicate into a synthesis kettle, introducing steam for heating while stirring, adding water, stirring for reaction to obtain a reaction substrate A, and adding sulfuric acid to the reaction substrate A to obtain reaction solution B; simultaneously adding sulfuric acid and sodium silicate into the reaction solution B, performing synthesis reaction for a given period of time, stopping feeding of sodium silicate, adding sulfuric acid only for post-acidification, and aging to obtain dilute slurry D; and filtering the dilute slurry D, washing, slurrying, drying and packaging to obtain silica microspheres as lutein carrier. The invention accurately controls each process so that the prepared high-absorptivity silica as lutein carrier has high adsorption and good dispersibility and flowability after adsorbing lutein.

Abstract: This invention relates to a dispersion comprising porous particles dispersed in a liquid phase, wherein the porous particles comprise a zeolite and the liquid phase is a size-excluded liquid. The invention also relates to a method of adsorbing a gas into a liquid, comprising at least the step of bringing the gas into contact with the dispersion. In addition, the invention relates to an assemblage of the dispersion, the zeolite comprising a cavity and a gas contained within the cavity.

Abstract: A biochar-derived adsorbent preferably from Sargassum boveanum, macroalgae can be used for removing phenolic compounds, such as 2,4,6-trichlorophenol and 2,4-dimethylphenol, from aqueous solutions. The carbonization can improve the removal capability of the macroalgae adsorbent for such phenolic compounds with removal efficiencies of 60% or more from high salinity seawater and 100% from distilled water. The adsorption may occur through a mixed mechanism dominated by physisorption following pseudo second-order kinetics. The adsorption of the phenolic molecules may be spontaneous, endothermic and thermodynamically favorable.

Abstract: The present disclosure relates to a preparation method of a super absorbent polymer capable of improving absorption performance of the super absorbent polymer by adding a simple additive later. The preparation method includes the steps of: forming a hydrogel polymer by cross-linking and polymerizing a water-soluble ethylene-based unsaturated monomer having at least partially neutralized acidic groups in the presence of an internal cross-linking agent; drying, pulverizing and classifying the hydrogel polymer to form a base resin powder; forming a surface cross-linked layer by further cross-linking a surface of the base resin powder in the presence of a surface cross-linking agent, adding a monovalent to trivalent metal cation on the surface cross-linked base resin powder at a temperature of 25° C. to 80° C., and maintaining and aging the resulting metal cation-added product at a temperature of 40° C. to 60° C. for 10 to 30 minutes.

Abstract: An object of the present invention is to provide a separation medium and a separation method, ensuring high selectivity and good separation efficiency for specific steviol glycosides. The present invention is related to a separation medium in which polyethyleneimine is immobilized to porous particles of a (meth)acrylic polymer having a crosslinked structure and a hydroxyl group.

Abstract: Modified red mud catalyst compositions, methods for production, and methods of use in dry reforming, the composition comprising: red mud material produced from an alumina extraction process from bauxite ore; and nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition.

Abstract: Modified red mud catalyst compositions, methods for production, and methods of use in bi-reforming, the composition comprising: red mud material produced from an alumina extraction process from bauxite ore; and nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition.

Abstract: Modified red mud catalyst compositions, methods for production, and methods for use, a composition including red mud material produced from an alumina extraction process from bauxite ore; nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition; and a Periodic Table Group VIB metal oxide, the Group VIB metal oxide present at between about 1 wt. % and about 30 wt. % of the modified red mud catalyst composition.

Abstract: Methods for autothermal reforming over a modified red mud catalyst composition, one method including providing a methane feed with oxygen and carbon dioxide to react over the modified red mud catalyst composition at increased temperature and increased pressure to produce synthesis gas comprising H2 and CO, the composition comprising red mud material produced from an alumina extraction process from bauxite ore; nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition; and a Periodic Table Group VIB metal oxide, the Group VIB metal oxide present at between about 1 wt. % and about 30 wt. % of the modified red mud catalyst composition.

Abstract: Methods for bi-reforming over a modified red mud catalyst composition, one method including providing a methane feed in the presence of carbon dioxide and steam to react over the modified red mud catalyst composition at increased temperature and increased pressure to produce synthesis gas comprising H2 and CO, the composition comprising red mud material produced from an alumina extraction process from bauxite ore; nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition; and a Periodic Table Group VIB metal oxide, the Group VIB metal oxide present at between about 1 wt. % and about 30 wt. % of the modified red mud catalyst composition.

Abstract: An oxide catalyst to be used for gas-phase catalytic ammoxidation reaction of propane or isobutane, the oxide catalyst comprising a composite oxide, wherein the composite oxide comprises a catalytically active species to be isolated from the composite oxide using a hydrogen peroxide solution, and the catalytically active species has an average composition represented by the following formula (1) in STEM-EDX measurements; Formula: Mo1VaSbbNbcWdXeOn ??(1) wherein X represents at least one selected from the group consisting of Te, Ce, Ti, and Ta; a, b, c, and d satisfy relations represented by a formulae of 0.050?a?0.200, 0.050?b?0.200, 0.100?c?0.300, 0?d?0.100, 0?e?0.100, and a?c; and n represents a number determined by valences of the other elements.

Abstract: Sulfur-resistant synergized platinum group metals (SPGM) catalysts with significant oxidation capabilities are disclosed. Catalytic layers of SPGM catalyst samples are prepared using conventional synthesis techniques to build a washcoat layer completely or substantially free of PGM material. The SPGM catalyst includes a washcoat layer comprising YMn2O5 (pseudobrookite) and an overcoat layer including a Pt/Pd composition with total PGM loading of at or below 5.0 g/ft3. Resistance to sulfur poisoning and catalytic stability is observed under 5.2 gS/L condition to assess significant improvements in NO oxidation, and HC and CO conversions.

Abstract: The present disclosure relates to copper-containing molecular sieve catalysts that are highly suitable for the treatment of exhaust containing NOx pollutants. The copper-containing molecular sieve catalysts contain ion-exchanged copper as Cu+2 and Cu(OH)+1, and DRIFT spectroscopy of the catalyst exhibits perturbed T-O-T vibrational peaks corresponding to the Cu+2 and Cu(OH)+1. In spectra taken of the catalytic materials, a ratio of the Cu+2 to the Cu(OH)+1 peak integration areas preferably can be ?1. The copper-containing molecular sieve catalysts are aging stable such that the peak integration area percentage of the Cu+2 peak (area Cu+2/(area Cu+2+area Cu(OH)+1)) increases by ?20% upon aging at 800° C. for 16 hours in the presence of 10% H2O/air, compared to the fresh state.

Abstract: A composite media for non-oxidative C2H6 dehydrogenation comprises an aluminosilicate zeolite matrix, and an EDH catalyst on one or more of an external surface of the aluminosilicate zeolite matrix and internal surfaces within pores of the aluminosilicate zeolite matrix. The EDH catalyst comprises one or more of Fe, Zn, Pt, Ga, alloys thereof, and oxides thereof. A C2H6 activation system, and a method of processing a C2H6-containing stream are also described.

Abstract: Isobutanol may be converted into predominantly C12+ olefin oligomers under specified conditions. Such methods may comprise: contacting a feed comprising isobutanol with a zeolite solid acid catalyst having a MWW framework under conditions effective to convert the isobutanol into a product comprising Can olefin oligomers, wherein n is an integer having a value of two or greater and about 80 wt. % or greater of the Can olefin oligomers are larger than C8.

Abstract: The invention relates to a catalyst comprising a support based on alumina or silica or silica-alumina, at least one group VIII element, at least one group VIB element and at least one organic compound of formula (I) in which R1 is a hydrocarbon-based radical comprising from 1 to 12 carbon atoms, R2 and R3 are chosen from a hydrogen atom and a hydrocarbon-based radical comprising from 1 to 12 carbon atoms, X is chosen from an oxygen atom or a sulfur atom except when R2 and R3 represent a hydrogen atom, in which case X is an oxygen atom, Y is chosen from a hydrogen atom, a hydrocarbon-based radical comprising from 1 to 12 carbon atoms or a unit —C(O)R4, R4 being chosen from a hydrogen atom and a hydrocarbon-based radical comprising from 1 to 12 carbon atoms.

Abstract: A catalyst composition capable of forming a conjugated diene-based polymer having a narrow molecular weight distribution by being used in polymerization of a conjugated diene-based monomer, a method of preparing the same, a method of preparing a conjugated diene-based polymer using the catalyst composition, and a conjugated diene-based polymer prepared by the method of preparing the polymer are provided. Since the catalyst composition according to the present invention includes a polymer having a number-average molecular weight of 3,000 g/mol to 10,000 g/mol and including a conjugated diene-based monomer-derived unit, the catalyst composition may be used in the polymerization of a conjugated diene-based monomer to prepare a conjugated diene-based polymer having a narrower molecular weight distribution in comparison to a conventional neodymium catalyst composition.

Abstract: The present invention relates to a bisphosphine ligand compound, a chromium compound prepared using same, an ethylene oligomerization catalyst system containing the chromium compound, and an ethylene oligomer preparing method, wherein the bisphosphine ligand compound is suitable for mass production and commercial processes, allows extremely high activity to be compatible with excellent economical benefit, and increases selectivity for ethylene oligomerization reaction, thereby being able to be used to manufacture 1-hexene and/or 1-octene at high yield.

Abstract: There are provided a method for manufacturing a modified aluminosilicate by which a hydroquinone is highly selectively manufactured by reaction of a phenol with hydrogen peroxide, a modified aluminosilicate, and a method for manufacturing an aromatic dihydroxy compound by using the modified aluminosilicate, under industrially advantageous conditions. The method for manufacturing a modified aluminosilicate of the present invention includes a first step of treating an aluminosilicate with an acid, a second step of primarily calcining the treated material obtained in the first step at 550° C. to 850° C., and a third step of contacting the calcined material obtained in the second step with a liquid. containing one or more elements selected from the group consisting of Group 4 elements and. Group 5 elements on. the periodic table, and then drying and secondarily calcining the resultant. The modified aluminosilicate included in the present invention.

Abstract: A device for collecting and transferring liquid samples having a detachable sample collecting portion includes an elongated body with a liquid collecting portion disposed at one end and a handling portion disposed at the other end separated by a frangible portion. The sample collecting portion includes an inner surface configured to be wetted by the sample. After collection, the sample is transferred into a separate housing by inserting the sample collecting portion filled with sample into a confining cavity and subsequently breaking the sample transfer device along the frangible portion. The liquid sample is extracted from the collecting portion using known means to drive and control flow in fluidic devices including rotation, capillary pressure or pneumatics. The separate housing may be part of a device capable to process the liquid sample to provide for a system for handling liquid samples.

Abstract: Disclosed is an assay device comprising a high density of wells aligned thereon.

Abstract: A microfluidic channel and a preparation method and an operation method thereof. The microfluidic channel includes: a channel structure, including a channel for a liquid sample to flow through and a channel wall surrounding the channel. The channel wall includes an electrolyte layer made of an electrolyte material; and a control electrode layer, at a side of the electrolyte layer away from the channel. The control electrode layer overlaps with the electrolyte layer with respect to the channel.

Abstract: The present disclosure discloses a method for driving a microfluidic chip including controlling a first electrode that currently carries a droplet to be electrically connected to a first power supply by a first switch circuit connected to the first electrode; after controlling the first electrode to be in electrical connection to the first power supply for a first period of time, controlling the first electrode to be in electrical connection to a second power supply for a second period of time; and after the second period of time, continuing to control the first electrode to keep disconnected from two power supplies.