Abstract: Method which makes it possible to define, over time, the concentration of the species in a reaction medium from the infrared profiles of the products resulting from the monitoring of the reaction and from the HPLC data, without precalibration of the devices.

Abstract: A method and an apparatus for efficiently analyzing an organic macromolecular component contained in a sample with high precision are provided. The method and the apparatus for analyzing the organic macromolecular component are based on a flow analysis method with a measuring system including a sample introduction section, a preparation section, and a measuring section, and include the steps of supplying a sample together with a carrier solution into the measurement system through the introduction section, leading the sample to the preparation section and separating an organic macromolecular component from the sample, and leading the separated organic macromolecular component to the measuring section for analysis.

Abstract: A method and apparatus for efficiently analyzing an organic macromolecular component contained in a sample with high precision are provided. The method and apparatus for analyzing the organic macromolecular component are based on a flow analysis method with a measuring system including a sample introducing section, a preparing section, and a measuring section, composed of steps of supplying a sample with a carrier solution into the measurement system through the introducing section, leading the sample to the preparing section and separating an organic macromolecular component in the sample, and leading the separated organic macromolecular component to the measuring section and analyzing. Herein, the step of separating the organic macromolecular component includes steps of the organic macromolecular component in the sample being adsorbed on a resin and introducing an eluant into the preparing section and eluting the organic macromolecular component adsorbed on the resin.

Abstract: A system for conducting high-temperature liquid chromatographic analysis includes a mobile phase transport tube configured to operably convey mobile phase from a source to respective chromatographic instruments in the system, a pre-heater apparatus operably coupled to the mobile phase transport tube for heating the mobile phase to a desired temperature, a chromatographic column operably coupled to the pre-heater apparatus, and including temperature-maintaining means for maintaining the column at a pre-determined temperature and a counter-flow heat exchanger operably exchanging heat from outlet mobile phase to inlet mobile phase through conductive heat transfer means. In a particular embodiment, the mobile phase passing through the chromatographic column is maintained in a substantially adiabatic environment.

Abstract: A chromatographic chip is formed of a plate member, a plurality of grooves formed on the plate member, and silica gel having monolithic bimodal pore structure formed in at least one of the grooves. The monolithic bimodal pore structure includes through pores and mesopores smaller than those of the through pores.

Abstract: The present invention provides an on-chip packed reactor bed design that allows for an effective exchange of packing materials such as beads at a miniaturized level. The present invention extends the function of microfluidic analysis systems to new applications including on-chip solid phase extraction (SPE) and on-chip capillary electrochromatography (CEC). The design can be further extended to include integrated packed bed immuno- or enzyme reactors.

Abstract: A sanitary static seal for the fixed end of a chromatography column is described. The seal is in the form of an “L” or a “U” so as to form a seal against at least one major surface of the frit or screens and the outer peripheral edge of the frit or screen. In this way, any bypass is prevented and the potential for dead spaces such as O-ring grooves is eliminated thereby reducing the potential for bacteria or mold growth in the system. The gasket maybe formed separately and placed on the edge of the frit or screen or it may be molded in place.

Abstract: A microfluidic system is provided for separating components of many fluid samples in a parallel fashion through an array of capillary conduits. The system includes capillary conduits for receiving fluid samples, and for effecting separation of substituents of the sample by passing the sample through a corresponding array of capillary separation conduits containing a solid separation medium. The microfluidic circuit is made of three or more substrate layers and preferably includes etched channels in different layers that are dimensioned relative to one another to provide for retaining the solid composition within the capillary separation conduits. The system also includes an array of detector flow cells in fluid communication with the capillary separation conduits, and an array of high pressure connectors for connecting discrete capillary tubes to the fluid passages in the microfluidic circuit for introducing and removing the fluid samples from the system.

Abstract: A system for conducting high-temperature liquid chromatographic analysis includes a mobile phase transport tube configured to operably convey mobile phase from a source to respective chromatographic instruments in the system, a pre-heater apparatus operably coupled to the mobile phase transport tube for heating the mobile phase to a desired temperature, a chromatographic column operably coupled to the pre-heater apparatus, and including temperature-maintaining means for maintaining the column at a pre-determined temperature and a counter-flow heat exchanger operably exchanging heat from outlet mobile phase to inlet mobile phase through conductive heat transfer means. In a particular embodiment, the mobile phase passing through the chromatographic column is maintained in a substantially adiabatic environment.

Abstract: A method of using microwave-induced dielectric polarization to enhance the diffusivity of a liquid or a supercritical fluid mobile phase in chromatography, while having essentially no effect on other physical properties of the mobile phase.

Abstract: A liquid chromatography column distributor spreads liquid over the internal cross sectional area of the column to facilitate separation of the liquid in the column into its constituent components for analysis, particularly where the volume of liquid is small and the rate of flow through the column is high. The distributor is useful for small volumes, less than 100 micro liters. The distribution is preferably done in two or more stages by two or more plates arranged in series. This arrangement keeps the flow paths short and volumes of channels in the plate carrying the liquid small. The distributor may be used in a high performance liquid chromatography (HPLC) in which liquid flows at high rates through the column. The distributor is constructed to protect the liquid sample from damage.

Abstract: An apparatus and method for electrochemically modifying the retention of a species on a chromatography material is disclosed. The apparatus comprises a housing having an effluent flow channel adapted to permit fluid flow therethrough. The effluent flow channel comprises chromatography material. The apparatus further comprises first and second electrodes positioned such that at least a portion of the chromatography material is disposed between the first and second electrodes, and fluid flow through the apparatus is between, and in contact with, the first and second electrodes.

Abstract: A system for conducting high-temperature liquid chromatographic analysis includes a mobile phase transport tube configured to operably convey mobile phase from a source to respective chromatographic instruments in the system, a pre-heater apparatus operably coupled to the mobile phase transport tube for heating the mobile phase to a desired temperature, a chromatographic column operably coupled to the pre-heater apparatus, and including temperature-maintaining means for maintaining the column at a pre-determined temperature and a counter-flow heat exchanger operably exchanging heat from outlet mobile phase to inlet mobile phase through conductive heat transfer means. In a particular embodiment, the mobile phase passing through the chromatographic column is maintained in a substantially adiabatic environment.

Abstract: A process, a method and apparatus are provided for testing and analyzing oil's physical and chemical characteristics and contaminants found in oil. A process separates contaminants prior to testing of oil's chemical and physical characteristics and includes manufacturing and operation parameters, and visual techniques for analysis. An apparatus is provided to separate and remove contaminants into magnetic, non-magnetic and liquids for further testing and analysis. This is accomplished using magnetic fields, filtration and condensing systems. The testing of oil's chemical and physical characteristics as well as contaminants is done using a plurality of tests such as viscosity, blotter, opacity and images for contaminants. A method is provided to prepare blotter and filtration systems, to remove fluid contaminants from particles and to include process parameters, trending and graphical analysis of images via software programming.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed, where the polymer sample, solvent, liquid chromatograph column and/or mobile phase eluant is heated to temperatures of at least 75 degrees Celsius during the sample injection or elution process. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.

Abstract: In a chromatograph comprising a pump, a sample injecting unit, a column, a photo-diode array detector and a data processing unit having a spectrum library of registered spectrums of known components, a spectrum selected in advance from the spectrum library is compared with a spectrum of each of peaks in an actual sample. Thereby, it is possible to reduce the number of spectrum comparisons required for identification, and it is further possible to perform identification quickly since the identification can be performed during analysis.

Abstract: A microfluidic system is provided for separating components of many fluid samples in a parallel fashion through an array of capillary conduits. The system includes capillary conduits for receiving fluid samples, and for effecting separation of substituents of the sample by passing the sample through a corresponding array of capillary separation conduits containing a solid separation medium. The microfluidic circuit is made of three or more substrate layers and preferably includes etched channels in different layers that are dimensioned relative to one another to provide for retaining the solid composition within the capillary separation conduits. The system also includes an array of detector flow cells in fluid communication with the capillary separation conduits, and an array of high pressure connectors for connecting discrete capillary tubes to the fluid passages in the microfluidic circuit for introducing and removing the fluid samples from the system.

Abstract: In a liquid chromatograph mass spectrometer, chromatogram data is obtained by carrying out alternately a mass scanning in a positive ion detection mode and a mass scanning in a negative ion detection mode, obtaining the chromatogram data in every positive and negative polarities through summing up the mass spectrum data obtained at the respective mass scannings, and adding the data of both polarities. Since the chromatograms in both polarities are averaged, even if there is a level difference therebetween, a chromatogram in a normal form can be obtained.

Abstract: An ion separation instrument includes an ion source coupled to at least a first ion mobility spectrometer having an ion outlet coupled to a mass spectrometer. In one embodiment, the ion source includes a molecule separation instrument operable to separate ions in time according to a molecular characteristic such as ion retention time. The resultant instrument is thus operable to provide molecular information separated in time as functions of retention time, ion mobility and ion mass/charge. In another embodiment, the ion separation instrument includes first and second ion mobility instruments disposed in a cascade arrangement between the ion source and mass spectrometer, wherein the two ion mobility instruments are operable to separate ions in time each according to different ion mobility functions.

Abstract: An apparatus and method for electrochemically modifying the retention of a species on a chromatography material is disclosed. The apparatus comprises a housing having an effluent flow channel adapted to permit fluid flow therethrough. The effluent flow channel comprises chromatography material. The apparatus further comprises first and second electrodes positioned such that at least a portion of the chromatography material is disposed between the first and second electrodes, and fluid flow through the apparatus is between, and in contact with, the first and second electrodes.

Abstract: This invention provides a RP-HPLC method, for the determination of logPoct values, which combines ease of operation and high accuracy, and which has been shown to work for a set of 36 molecules largely comprised of drugs. The general features of the method are: i) compound sparing (≦1 mL of a 30-50 &mgr;g/mL solution needed), ii) rapid determinations (20 minutes on average), iii) low sensitivity to impurities, iv) wide lipophilicity range (6 logPoct units), v) good accuracy, vi) excellent reproducibility. A linear free energy relationship (LFER) analysis, based on solvation parameters, shows that the method encodes the same information obtained from a shake-flask logPoct determination. The value generated via this method is referred to as ElogPoct.

Abstract: Methods and devices for stop flow detection and measurement of radioactivity in liquid samples are provided. In some embodiments, the invention includes precise positioning of fractions within a flow cell detection area. Novel flow cells and methods providing for flushing samples with gas are also provided.

Abstract: A flowmeter for accurately measuring the flowrate of fluids in high pressure chromatography systems. The flowmeter is a porous bed of a material, the porous bed having a porosity in the range of about 0.1 to 0.6 and a pore size in the range of about 50 nm to 1 &mgr;m, disposed between a high pressure pumping means and a chromatography column. The flowmeter is provided with pressure measuring means at both the inlet and outlet of the porous bed for measuring the pressure drop through the porous bed. This flowmeter system provides not only the ability to measure accurately flowrates in the range of &mgr;L/min to nL/min but also to provide a signal that can be used for a servo loop or feedback control system for high pressure pumping systems.

Abstract: Methods for calculating Log P values for organic compounds are disclosed. The methods allow identification of compounds in a library with a desired Log P value. The method can be used to minimize the number of compounds in a given combinatorial or lead generation library which need to be further characterized and/or assayed. The Log P value is preferably obtained while the purity of the compounds is being determined. Preferably, the Log P value is correlated to the retention time on an HPLC column, such that the retention time equals the Log P value.

Abstract: An improved system, device and method for characterizing a fluid sample that includes injecting a fluid sample into a mobile phase of a flow characterization system, and detecting a property of the fluid sample or of a component thereof with a flow detector comprising a mechanical resonator, preferably one that is operated at a frequency less than about 1 MHz, such as a tuning fork resonator.

Abstract: A porous polymer particle includes an alkali-resistant polymer substrate having bonded thereto through a spacer a nitrogen-containing heterocyclic group containing a quaternary ammonium structure.

Abstract: High-performance liquid chromatography (HPLC) methods and systems are disclosed that combine sequential, serial injection of a plurality of samples into mobile-phases supplied in parallel to two or more chromatographic columns, such that staggered, parallel separation of the plurality of samples is effected. Because injection of samples is relatively fast as compared to separation, substantial efficiencies are gained with respect to overall sample throughput. The disclosed HPLC methods and systems are preferably applied in connection with combinatorial chemistry, combinatorial material science and more particularly, combinatorial synthesis and screening of polymeric materials.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.

Abstract: A flowmeter for accurately measuring the flowrate of fluids in high pressure chromatography systems. The flowmeter is a porous bed of a material, the porous bed having a porosity in the range of about 0.1 to 0.6 and a pore size in the range of about 50 nm to 1 &mgr;m, disposed between a high pressure pumping means and a chromatography column. The flowmeter is provided with pressure measuring means at both the inlet and outlet of the porous bed for measuring the pressure drop through the porous bed. This flowmeter system provides not only the ability to measure accurately flowrates in the range of &mgr;L/min to nL/min but also to provide a signal that can be used for a servo loop or feedback control system for high pressure pumping systems.

Abstract: A method of measuring a concentration and a molecular weight distribution of glue or gelatin contained in an electrolyte, which comprises high performance liquid chromatography combined with column switching.

Abstract: A thermostat array including an array of two or more capillary columns (10) or two or more channels in a microfabricated device is disclosed. A heat conductive material (12) surrounded each individual column or channel in array, each individual column or channel being thermally insulated from every other individual column or channel. One or more independently controlled heating or cooling elements (14) is positioned adjacent to individual columns or channels within the heat conductive material, each heating or cooling element being connected to a source of heating or cooling, and one or more independently controlled temperature sensing elements (16) is positioned adjacent to the individual columns or channels within the heat conductive material. Each temperature sensing element is connected to a temperature controller.

Abstract: A liquid chromatography-electrospray ionization mass spectrometry method is capable of separating and identifying different prostaglandin isomers, including PGD2 and PGE2. Unlike traditional gas chromatography methods, little sample preparation and no derivatization are required. The chromatography is performed under acidic conditions that are optimal for separating the isomers. A basic sheath flow liquid is added to the chromatographic eluent, resulting in high ionization efficiency when the electrospray ionization is performed in negative ion mode. Additionally, by altering the energy at which the ionization is performed, tandem mass spectra of the two isomers can be made to differ as a result of the different relative energies of the two isomers.

Abstract: A flowmeter for accurately measuring the flowrate of fluids in high pressure chromatography systems. The flowmeter is a porous bed of a material, the porous bed having a porosity in the range of about 0.1 to 0.6 and a pore size in the range of about 50 nm to 1 &mgr;m, disposed between a high pressure pumping means and a chromatography column. The flowmeter is provided with pressure measuring means at both the inlet and outlet of the porous bed for measuring the pressure drop through the porous bed. This flowmeter system provides not only the ability to measure accurately flowrates in the range of &mgr;L/min to nL/min but also to provide a signal that can be used for a servo loop or feedback control system for high pressure pumping systems.

Abstract: To economically perform preparatory chromatography, a plurality of pumps each having a corresponding one of a plurality of pistons and a corresponding one of a plurality of cylinders are driven by one motor to draw and pump solvent simultaneously into corresponding columns. To form a gradient the pumps are connected to two-way valves that are connected alternately to a first solvent and a second solvent, whereby the time said valve is in a first position controls the amount of solvent drawn from said first reservoir into said pumps and the amount of time in said second position controls the amount of said second solvent drawn into said pumps and the solvent is mixed in the pumping systems. The detectors are photodiodes mounted to light guides in the flow cells that generate signals related to light absorbance and communicate with a controller, whereby said controller receives signals indicating solute between the light guides and causes collection of solute.

Abstract: An improved method for measuring the chromatographic properties, such as excluded volume, of hydrophobic polymer substrates is disclosed. Use of 0.05-1 micron sized crosslinked ionically-charged polymer particles, especially emulsion-form or ground polymer particles, as a large-molecule probe, allows environmentally friendly aqueous-based solvent systems to be used as mobile phases to characterize hydrophobic polymer supports for use in analytical or preparative scale chromatographic applications. This method eliminates the use of non-polar organic solvents that is required when conventional non-polar large-molecule probes (such as polystyrene) are used to characterize chromatographic media.

Abstract: High-performance liquid chromatography (HPLC) methods and systems are disclosed that combine parallel chromatographic separation of a plurality of samples with a detection technique that involves post-separation treatment of the plurality of samples to enhance one or more properties of the sample or of a component thereof, followed by detection of the one or more enhanced properties. Selective, tunable detection schemes are achievable, and are particularly advantageous as applied in connection with combinatorial chemistry, combinatorial material science and more particularly, combinatorial synthesis and screening of polymeric materials.

Abstract: Single pass methods and systems for measuring the total masses of individual compounds present in fluid samples in real time, and particularly for fluid samples prepared in microtiter plate format are provided. Individual compounds are isolated by fluid separation column (14). Portions of the individual compounds isolated by column (14) are analyzed by mass spectrometer (16), which determines their concentration on the basis of their molecular weights, and an evaporative light scattering detector (24), (which determines the total masses of each of the isolated compounds passing therethrough). Total collected masses of the individual compounds are calculated by determining the amount and portion of the isolated compounds diverted into evaporative light scattering detector (24) during a period of fraction collection.

Abstract: Ionic species in an aqueous sample stream are analyzed by (a) chromatographically separating the ionic species in the presence of an aqueous eluent solution comprising electrolyte to form a chromatographic effluent, (b) suppressing the electrolyte in the chromatography effluent by flowing the same through a suppressor (e.g., a membrane suppressor) to form a suppressed effluent, (c) detecting the ionic species in the suppressed effluent, and (d) regenerating the suppressor by flowing a mixture of a gas stream and a regenerant liquid stream through the suppressor. The gas stream may be generated by flowing the detected suppressed effluent through an electrolytic gas generator which electrolyzes water in the effluent to hydrogen and oxygen gas. Also, pressurized gas may be directed into a reservoir of regenerant liquid for flow from said reservoir to said regenerant flow channel.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.

Abstract: In a chromatograph comprising a pump, a sample injecting unit, a column, a photo-diode array detector and a data processing unit having a spectrum library of registered spectrums of known components, a spectrum selected in advance from the spectrum library is compared with a spectrum of each of the peaks in an actual sample. Thereby, it is possible to reduce the number of spectrum comparisons required for identification, and it is further possible to perform identification quickly since the identification can be performed during analysis.

Abstract: A method for analyzing a multichannel chromatogram is realized for accurately resolving overlapping peaks on a multichannel chromatogram to permit analysis of the composition of a sample. First, components of overlapping peaks are specified. A data matrix Dij is determined, and compressed in the wavelength direction to obtain a data matrix vector Di. By compressing three-dimensional data in the wavelength direction, noise components cancel with each other to obtain noise free two-dimensional data Di&bgr;. Next, the two-dimensional data is deconvoluted, final standard deviation s0 is registered, and the deconvoluted two-dimensional data is reconvoluted to a retention intensity matrix. A quantitative spectral intensity matrix is computed, components are identified, and the identified components are quantified. The quantified data is displayed on a screen.

Abstract: A liquid chromatograph and a column packing material effectively condensing cationic specimen and exhibiting a high resolution. The liquid chromatograph includes a pre-focusing column (30, 40) having a volume of less than 2.0 milliliters and packed with a column packing material, in which a porous support is coated by a silicone polymer having a Si—R—X (R is a spacer part, X is a sulfonic group) bond and a Si—R′ (R′ is a hydrophilic group) bond, wherein the specimen to be analyzed is supplied to the pre-focusing column in the state dispersed in a solvent for condensation. The condensed specimen is then separated in a separation column (16, 43) used for separating the specimen dispersed in the solvent, and the separated specimen is analyzed by a detector (17, 41).

Abstract: Methods and devices for stop flow detection and measurement of radioactivity in liquid samples are provided. In some embodiments, the invention includes precise positioning of fractions within a flow cell detection area. Novel flow cells and methods providing for flushing samples with gas are also provided.

Abstract: The present invention relates to a method for analyzing mixtures of components by a process selected from the group consisting of flow based separation processes and flow analysis processes. The method comprising the steps of: obtaining measurement signals by measuring process conditions at a plurality of positions throughout the system; applying signal processing to the measurement signals, said signal processing comprising multivariate data analysis for condensing the plurality of measurement signals to a smaller number of main signals being non-correlated; logging said main signals; and displaying said main signals versus time, where changes of said system conditions are indicated by one or more of the displayed main signals; detecting any error occurrence during an on going process, and determining what part of said system cause said error.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.

Abstract: An analytical apparatus for measuring a low concentration of a constituent in a stream at a parts per billion level is provided. The apparatus comprises a sample loop having a predetermined volume for receiving a sample from the stream, a purifier for producing substantially pure carrier liquid from a sample of the stream, a first and a second multi-path valve, a preconcentrator column for absorbing and increasing the concentration of the low concentration constituent, an eluent, and a detector. In one embodiment, the apparatus is an ion chromatograph and may be used to analyze ions at concentrations as low as about 10 to about 1 part per billion. A method for analyzing a stream for a low concentration constituent present in a stream at a parts per billion level is also provided. The invention also includes methods for single- and multi-point calibration of a detector in an analytical apparatus for measuring a low concentration of a constituent in a stream at a parts per billion level.

Abstract: A high-throughput liquid chromatography system capable of parallel separations for increased sample throughput is described. The system comprises valves allowing for the use of multiple liquid chromatography columns and a single injector and pumping system while also minimizing extraneous plumbing and hardware. The system is capable of injecting individual samples and directing them to one of a multiplicity of columns followed by selective output to a detector. The system described allows for up to 16 columns, but the number may vary according to the application. The system may be run in an isocratic or gradient mode. Whereas currently available multi-probe systems incorporate a separate injector for each column, the invention described here uses only one injector and is independent of column number. This removes injector variability along with reducing the amount of pluming and mechanical parts in the system allowing for better separations while providing a more robust system.

Abstract: Rapid characterization and screening of polymer samples to determine average molecular weight, molecular weight distribution and other properties is disclosed. Rapid flow characterization systems and methods, including liquid chromatography and flow-injection analysis systems and methods are preferably employed. High throughput, automated sampling systems and methods, high-temperature characterization systems and methods, and rapid, indirect calibration compositions and methods are also disclosed. The described methods, systems, and devices have primary applications in combinatorial polymer research and in industrial process control.