摘要:
A microchip apparatus and method provide fluidic manipulations for a variety of applications, including sample injection for microchip liquid chromatography. The microchip is fabricated using standard photolithographic procedures chemical wet etching, with the substrate and cover plate joined using direct bonding. Capillary electrophoresis is performed in channels formed in the substrate. Injections are made by electro-osmotically pumping sample through the injection channel that crosses the separation channel, followed by a switching of the potentials to force a plug into the separation channel.
摘要:
A microchip laboratory system and method provide fluid manipulations for a variety of applications, including sample injection for microchip chemical separations. The microchip is fabricated using standard photolithographic procedures and chemical wet etching, with the substrate and cover plate joined using direct bonding. Capillary electrophoresis and electrochromatography are performed in channels formed in the substrate. Analytes are loaded into a four-way intersection of channels by electrokinetically pumping the analyte through the intersection, followed by switching of the potentials to force an analyte plug into the separation channel.
摘要:
The present invention discloses a method for ascertaining the quality of herbs by applying the techniques of biochip for detecting the presence of biologically active, desired ingredient(s) in the herbs.
摘要:
In conducting liquid chromatographic analysis of a saccharide mixture containing monosaccharides and oligosaccharides, elution is conducted by using two kinds or more of mobile phases to separate the saccharide mixture into individual constituent saccharides followed by conversion thereof into corresponding derivatives by reaction with reagents and detection of the derivatives as contained in a detector cell. The method of the invention is characterized in that the detector cell is cleaned by washing with a cleaning solvent after completion of the detection of each of the saccharide derivatives. The invention also provides an apparatus for efficiently conducting the above-mentioned inventive method comprising an analytical column, a reactor for converting the separated constituent saccharides into the derivatives, detector cell for containing the derivative, a detector for detecting the derivative contained in the detector cell, a solvent-feed means to introduce a cell-cleaning solvent into the cell and a flow channel-switching means.
摘要:
A device for performing a post-column derivatization in connection with liquid chromatography includes a separating column, a detector, an eluent withdrawal unit, connected to an outlet of the separating column, that withdraws eluents from the separating column, a reagent supply unit, arranged between the outlet of the separating column and an inlet of the detector, that supplies reagents to the eluents withdrawn from the separating column and a pump that simultaneously pumps eluents from the eluent withdrawal unit and pumps reagents to the reagent supply unit, wherein the pumping of reagents takes place free of pulsations.
摘要:
A microchip laboratory system and method provide fluid manipulations for a variety of applications, including sample injection for microchip chemical separations. The microchip is fabricated using standard photolithographic procedures and chemical wet etching, with the substrate and cover plate joined using direct bonding. Capillary electrophoresis and electrochromatography are performed in channels formed in the substrate. Analytes are loaded into a four-way intersection of channels by electrokinetically pumping the analyte through the intersection, followed by switching of the potentials to force an analyte plug into the separation channel.
摘要:
A microchip apparatus and method provide fluidic manipulations for a variety of applications, including sample injection for microchip liquid chromatography. The microchip is fabricated using standard photolithographic procedures and chemical wet etching, with the substrate and cover plate joined using direct bonding. Capillary electrophoresis is performed in channels formed in the substrate. Injections are made by electro-osmotically pumping sample through the injection channel that crosses the separation channel, followed by a switching of the potentials to force a plug into the separation channel.
摘要:
An isotope ratio monitoring gas chromatograph-mass spectrometer (irm-GC/MS) unit for generating a chromatogram having improved resolution for peaks representative of individual carbon dioxide isotopes measured when a complex GC amenable organic sample (e.g. petroleum hydrocarbons) is combusted in the presence of a metal catalyst. The present irm-GC/MS unit is similar to known irm-GC/MS units of this type except it uses a capillary combustion tube in the furnace which is connected to the capillary column and has approximately the same inside diameter as that of the capillary column (e.g. 0.25 mm I.D.) whereby any "dead volume" attributable to the combustion tube is substantially eliminated.
摘要:
The invention relates to an apparatus for recovery and buffer exchange and/or concentration of dissolved macromolecules from a mixture of macromolecules. The apparatus includes a liquid chromatography unit and at least one hollow fiber membrane cartridge connected downstream of the liquid chromatography unit.
摘要:
An anlytical equipment and method for the selective detection of individual oxygenated compounds in complex organic mixtures, in particular fuels, comprising, downstream an equipment of chromatographic separation, a cracking reactor, a catalytic hydrogenation microreactor and a FID detector. The cracking reactor is provided with a catalyst under the form of metal elements, made of palladium, inserted inside the capillary tube though which flows the gas under test. Thanks to the present equipment, the analytical process, based on the specific response of oxygenates to the method of flame ionization detection (O-FID), foresees that the cracking reaction takes place at temperatures below 1000 degrees C. and, consequently allows to keep the cracking reactor at stand-by temperatures below 700 degrees C.