Abstract: A method of continuous flow analysis is provided which enables a plurality of color-forming components contained in a sample to be simultaneously analyzed with utmost ease. The method involves irradiating the sample with a measuring light which generates a wavelength having absorption bands with respect to such color-forming components, measuring the absorbance of each of the components in a color-formed state while the components are being adjusted stepwise in their color-forming state, and comparing the resultant absorbances of the components with each other. Preferably, a plurality of measuring cells are used to stepwise adjust the sample in its color-forming state, the measuring cells being connected in tandem such that a color former and/or a masking agent are incorporated in the sample while the latter is being caused to successively flow through these cells so that the sample is adjusted in its color-forming state at each of the measuring cells and measured in respect of its absorbances.

Abstract: A system and method for controlling a microwave heated chemical process is disclosed. Time varying concentrations of some chemical substances within fumes in the microwave oven are monitored to detect concentration variations for which responses are known. Responses to the detected variations are initiated to control the chemical process without terminating the process. Examples of responses include varying microwave radiation energy, initiating safety systems, increased venting of the microwave oven, and so forth.

Abstract: A biosensor based on complexes between biomolecule receptors and colloidal Au nanoparticles, and more specifically, colloid layers of receptor/Au complexes that can be used to detect biomolecule analytes through measuring of binding-induced changes in electrical resistance or surface plasmon resonance. Also disclosed is a method for detecting and analysing carrier-borne chemical compounds with Raman spectroscopy using an improved SERS substrate. Further disclosed is an improved method for detecting compounds in solvents using capillary electrophoresis in conjunction with Raman spectroscopy.

Abstract: A device for the investigation of liquids, in particular of waste water, includes at least one reaction chamber for receiving the liquid to be investigated as well as liquids for analysis from storage containers. The reaction chamber is disposed in a housing while the storage containers are accommodated within the housing or are set up outside. The housing may be positioned in a freely floating manner within the liquid to be investigated or may be set up outside.

Abstract: Methods for diagnosing and screening for ovarian carcinomas in a subject are provided The methods employ the steps of preparing a plasma sample from a blood specimen from the subject, and assaying for the presence of lysophosphatidic acid in the plasma sample. The presence of lysophosphatidic acid in the plasma sample is indicative of ovarian carcinoma in the subject. In a preferred embodiment the plasma sample is prepared under conditions which minimize the release of lysophosphatidic acid from platelets in the blood specimen into the plasma.

Abstract: A method for microwave assisted chemical processes is disclosed that comprises applying sufficient microwave radiation to a temperature-monitored mixture of reagents, with at least one of the reagents being thermally responsive to electromagnetic radiation in the microwave range, and based on the monitored temperature, to maintain the added reagents at or closely about a predetermined temperature while substantially avoiding thermal dilution (or before substantial thermal dilution can occur) that otherwise would have been caused by the addition of the reagents to one another.

Abstract: In a method for infrared-optical determination of the concentration of at least one chemical analyte in a liquid sample, where the liquid sample is passed through a measuring cell and irradiated with infrared radiation of a single narrow waverange and infrared absorption is measured, the analyte being determined is subject to a chemical reaction before measurement, which should leave the other components of the liquid sample unaffected, and the change in infrared absorption caused by the chemical reaction with the analyte is measured as a unique function of the analyte concentration to be determined.

Abstract: A unitized, one step test reagent composition, device and method is presented for the determination of phosphorus in various test sample fluids such as soil extracts. The invention is a modification of the Murphy and Riley methodology which utilizes a molybdate salt and a reducing agent to generate "molybdenum blue" in the presence of phosphate. In addition to the molybdate salt, the test reagent composition includes a chromogenic reducing agent which contributes to the color development and a solid buffer. The composition is preferably incorporated into a matrix such as paper for ease of handling.

Abstract: A method for microwave assisted chemical processes is disclosed that comprises applying sufficient microwave radiation to a temperature-monitored mixture of reagents, with at least one of the reagents being thermally responsive to electromagnetic radiation in the microwave range, and based on the monitored temperature, to maintain the added reagents at or closely about a predetermined temperature while substantially avoiding thermal dilution (or before substantial thermal dilution can occur) that otherwise would have been caused by the addition of the reagents to one another.

Abstract: Phosphopeptides which significantly reduce bone loss or weakening are provided by the invention. Also provided is a method for treating or preventing any condition associated with bone loss or weakening by administering the phosphopeptides by oral or injectable means.

Abstract: A method of extracting anionic species from a solid or liquid medium by contacting the medium with an extract solvent of supercritical carbon dioxide and a positively charged complexant ligand for solubilizing and extracting the anionic species form the medium.

Abstract: The present invention provides a new method for detecting the presence of gynecological carcinomas in a patient. The method, which comprises detecting the presence of lysophosphatidic acid in a plasma sample of the patient, is useful for detecting ovarian carcinoma, cervical carcinoma, endometrial carcinoma, and peritoneal carcinoma. In a preferred embodiment the method comprises: providing a blood specimen from the patient, obtaining a plasma sample for the blood specimen under conditions which minimize the release of lysophosphatidic acid from the platelets in the blood specimen into the plasma, extracting lipids from the plasma, and detecting the presence of lysophosphatidic acid in the lipid extract. A new method for extracting lysophosphatidic acid from a biological fluid is also provided.

Abstract: A portable apparatus for detecting the presence of at least one methylxanthine chemical species such as caffeine or theophylline in a beverage comprises a first portion comprising an effective concentration of phosphodiesterase enzyme, a second portion comprising cyclic AMP, and means for indicating inhibition of degradation of the cyclic AMP by the phosphodiesterase due to the presence of the methylxanthine species. A method for determining the presence of at least one methylxanthine chemical species in a beverage comprises contacting at least one test portion of the beverage with effective concentrations of at least one phosphodiesterase enzyme and cyclic AMP, and further contacting the test portion with means for indicating the inhibition of the degradation of the cyclic AMP by the phosphodiesterase due to the presence of the methylxanthine species.

Abstract: A method and apparatus for analysing a chemical species in a fluid are disclosed. The apparatus includes filtering apparatus (15, 17) upstream and downstream of the sample preparation section (3). The fluid is diverted from a line (1) by an arrangement of pumps (27) and valves through the upstream filter (15) to the digester (11) and through the downstream filter (17) out to the analyser/detector system (5). The pumps (27) and valve arrangement allows the purging of the sample preparation section (3) and backflushing of the filters (15, 17), the inlet line (7) and the outlet line (13).

Abstract: A method for the detection of chemical agent present in a material comprising exposing a calixarene, having redox active substituents on its para rim, to a solution or suspension derived by admixture of all or some of the material with a liquid measuring any change in electrical behavior of the calixarene during or after exposure to the solution or suspension as compared to a reference condition, and relating such change in electrical behavior to the presence of chemical agent. Preferably, the calixarene exposed to the solution or suspension is a calix?4!arene or general formula (J), wherein Y.sup.1 to Y.sup.4 are independently selected from hydrogen, alkyl, alkenyl, aryl, aralkyl or a redox active substituent and R.sup.1 to R.sup.4 are independently selected from hydrogen, alkyl, alkenyl, aryl, aralkyl, or a polymerisable moiety, wherein at least one of Y.sup.1 to Y.sup.4 is a redox active substituent.

Abstract: Viscous, liquid hexafluoroisopropanol-siloxane polymers having the basic structure: ##STR1## wherein R.sub.1 is a monovalent hydrocarbon radical selected from the group consisting of C.sub.1 -C.sub.6 alkyl groups; cyclohexyl groups and phenyl groups;R.sub.2 is ##STR2## wherein m=1 to 4; and n is an integer greater than 1, are useful for rapid, reversible vapor sorption, especially for hydrogen bond accepting vapors.

Abstract: The present invention provides a method and apparatus for rapid measurement of a fluid bulk analyte, requiring only microscale volumes. Several fluid bulk analytes can be measured simultaneously and, for biological samples, the cell content can also be measured simultaneously. The invention comprises reporter beads for chemical analysis of fluid bulk properties such as pH, oxygen saturation and ion content. Each reporter bead comprises a substrate bead having a plurality of at least one type of fluorescent reporter molecules immobilized thereon. The fluorescent properties of the reporter bead are sensitive to a corresponding analyte. Reporter beads are added to a fluid sample and the analyte concentration is determined by measuring fluorescence of individual beads, for example in a flow cytometer. Alternatively, reporter molecules which change absorbance as a function of analyte concentration can be employed.

Abstract: Methods and apparatus for monitoring and controlling pH, phosphate, and sodium to phosphate ratio in boiler systems operating with captive alkalinity chemistry are described. The methods for monitoring and controlling these parameters include the steps of determining the phosphate concentration via FIA, determining the pH, and using these values to determine the sodium to phosphate ratio. These values are then compared to the optimum values for the boiler system being treated; on the basis of this comparison, adjustments to the feed rate of water treatment chemicals being added to the system are then made. The apparatus includes a device for determining phosphate concentration via FIA, a device for determining pH, a means for determining sodium to phosphate ratio and a device for adjusting the feed rate of water treatment chemicals being added to the system. The device for adjusting the chemical feed rate is computer controlled.

Abstract: Using a mixed sample of a plurality of phosphoric acid compounds different in chemical structure as a sample for measurement, a .sup.31 P nuclear magnetic resonance signal obtained through polarization transfer between .sup.17 O and .sup.31 P is observed and signals obtained without polarization transfer are eliminated, whereby .sup.31 P nuclear magnetic resonance signal spectrum of an .sup.17 O-labeled phosphoric acid is selectively observed. For this purpose, a double resonance NMR detector capable of exciting .sup.17 O and .sup.31 P at the same time is connected to an NMR spectrometer, and using a pulse train which permits observation of a .sup.31 P nuclear magnetic resonance signal obtained through polarization transfer between .sup.17 O and .sup.31 P, a .sup.31 P nuclear magnetic resonance signal from the .sup.17 O-labeled phosphoric acid is observed, and signals for .sup.17 O-unlabeled .sup.31 P are eliminated.

Abstract: An apparatus to detect and measure the amount of phosphorus in phosphorus-containing compounds comprises a burning chamber with a housing having an integral combustion chamber. A flammable reducing agent such as hydrogen is introduced into the combustion chamber along with a sample containing phosphorus admixed with air or oxygen. At least a portion of any phosphorus in the sample will be converted into phosphorus monoxide (PO) by the combustion. The resulting phosphorus monoxide is immediately drawn into a low-pressure, ambient temperature reaction chamber and reacted with ozone to convert the phosphorus monoxide to chemiluminescent phosphorus dioxide. A light-measuring device then measures the intensity of the light released from the chemiluminescent phosphorus dioxide.

Abstract: Traditional methods for measuring the phosphorylation state of cellular proteins have relied on .sup.32 P-orthophosphate labeling of cells in culture. The problems associated with radioactive isotopes have therefor prohibited phosphorylation studies on whole animals and humans. The present invention provides a unique technique that allows quantitative attachment of probes (e.g. fluorophors or biotin) to phospho-proteins and peptides by activating phospho-amino acids. the phosphorylation state of cellular proteins derived from human tissues can now be measured. This method can be used for early detection of cancer and diabetes and also for the identification of pharmaceutical agents.

Abstract: A detecting agent for hydride gases (arsine, phosphine, silane, diborane, selenium hydride etc.) which comprises at least one member selected from molybdic acid, a salt thereof, a molybdenum-containing acid (molybdophosphoric acid, etc.) and a salt thereof, and optionally a cupric salt each as a discoloring component being supported on an inorganic carrier (silica, alumina, silica-alumina, zirconia, etc.). The above detecting agent can detect the above hydride gases contained in the exhaust gas discharged from a semiconductor manufacturing process, with high accuracy, selectivity and sensitivity at a high discoloring rate without being influenced by other gases such as hydrogen gas.

Abstract: A method for enhancing detection sensitivity of suspected trace amounts of organic analytes and particularly semivolatile organic analytes extractable from a sample by an organic solvent carrier matrix and subsequent extraction and analysis of said trace organic analytes by SPME wherein the improvement comprises exchanging the organic solvent carrier matrix containing the trace organic analytes for an aqueous carrier matrix before performing SPME fiber extraction and detection of the trace organic analytes.

Abstract: Sample water is supplied to an oxidative decomposer, heated to 90.degree. C. under presence of a photooxidation catalyst, and irradiated with ultraviolet radiation by a low pressure mercury lamp while being supplied with air, to cause photooxidative decomposition reaction. After the reaction, nitric acid ions are measured with an absorption photometer at a wavelength of 220 nm. Then, a color developer is added to the sample water, and the colored solution is employed for measurement of phosphoric ions with the absorption photometer at a wavelength of 880 nm.

Abstract: A method and apparatus for detecting the presence of a vapor of an alkyl ester of phosphoric acid, particularly tributylphosphate, in ambient air. A sample of ambient air is heated to convert any alkyl ester of phosphoric acid to an alkene. The heated sample of air is then passed to a sample loop. Carrier air periodically carries a fixed volume of sample from the sample loop through a chromatographic column to a photoionization detector which detects the presence and amount of the alkene in the sample.

Abstract: Compounds and methods for single step, covalent labeling of the phosphate group of an organic substance under aqueous conditions are described. The labeling compound includes any kind of detectable signal group covalently bound to an imidazole moiety, which can be imidazole or a substituted imidazole.

Abstract: The invention relates to a method and an apparatus for individually detecting in ambient air a predetermined gaseous warfare agent, namely a poison gas of the class of organic sulfuric or phosphorous substances, and a predetermined interfering compound, e.g. another poison gas. First, light O.sub.2 reaction ions are generated from water and are added in a measuring chamber to a mixture of the agent and the ambient air. As a result, the O.sub.2 reaction ions will deposit on the heavy molecules of the agent in a spatially non-uniform distribution to generate quasi-molecular ions. An electrical field alternating about a zero line and having a predetermined basic frequency and an amplitude is generated within the measuring chamber. The resulting quasi-molecular ion current is measured and resulting current signals are processed. For distinguishing the agent from the interfering compound, an initial experiment is made for a standardized measuring chamber.

Abstract: A general purpose technique called extractive hydrogenation analysis, useful for both trace component and imaging analysis of samples containing organic matter. In processes according to the invention, organic matter is thoroughly decomposed in the presence of a hydrogenation catalyst under substantially aqueous conditions into products, and one or more of the products is then detected.

Abstract: The instant invention is a method for converting particulate silicon into monocrystalline silicon suitable for the determination of contaminates present in the particulate silicon. The method uses a silicon vessel, with known levels of the contaminates to be determined, to contain the particulate silicon. The silicon vessel, containing the particulate silicon, is float-zone processed to form a monolithic unit of monocrystalline silicon. The concentration of contaminates in the monocrystalline silicon can then be determined by the more sensitive analytical methods known for analysis of monolithic, monocrystalline silicon. The instant method is especially useful for measuring very low levels of aluminum, boron, phosphorous, and carbon in particulate silicon.

Abstract: The determination of the halogen content in a substance is carried out by oxidative combustion of the sample under a continuous flow of gas, in the presence of oxygen, the gases coming out of the combustion reactor being then carried by gas flow to analysis equipment.

Abstract: A safe analytical technique for determining the concentration amount of dibutyl and monobutyl phosphate degradation products in the TBP-dodecane solvent used in solvent extraction processes. This method of chemical analysis eliminates the use of diazomethane, which is toxic and explosive, thereby providing a safer laboratory technique for routine analyses required to monitor production solvent extraction processes. The solvent sample to be analyzed is spiked with mass labelled, deuterated dibutyl and monobutyl phosphates, which act as internal standards. After adding a silylating agent, bistrimethylsilyltrifluoracetamide, the sample is injected into a gas chromatograph/mass spectrometer, which measures the ratio between the labelled internal standard and the naturally occurring material to obtain a quantitative result.

Abstract: The invention pertains to a method for generating the fluorescence of polyanionic fluorophores in low dielectric media with fluorescence activation produced by specific quaternary onium compounds. The method may be used for measuring an analyte and may be useful in sensor devices.

Abstract: A sensor device includes ultra-large pore crystalline material M41S as a selective detecting element, and a measuring element for quantifying physical, chemical or biological events which occur within the crystalline material. The crystalline material may also contain an additional selective detecting component within its pores.

Abstract: A method for detecting the presence of a vapor of an alkyl ester of phosphoric acid, particularly tributylphosphate, in ambient air. A sample of ambient air is heated to convert any alkyl ester of phosphoric acid to an alkene. The heated sample of air is then passed to a sample loop. Carrier air periodically carries a fixed volume of sample from the sample loop through a chromatographic column to a photoionization detector which detects the presence and amount of the alkene in the sample.

Abstract: A process for measurement of low levels of phosphonates in brine waters wherein the phosphonate samples are acidified with hydrochloric acid promptly upon removal from an oil or gas well to prevent phosphonate precipitation or adsorption. The hydrochloric acid acidified phosphonate is digested in the presence of an oxidizing agent at elevated temperature and pressure for sufficient time to oxidize substantially all of the phosphonate to orthophosphate. The phosphorous containing compound is extracted with an organic extractant, preferably selected from the group consisting of methyl iso-butyl ketone/cyclohexane mixture and ethyl acetate, followed by color development for absorption spectrophotometry.

Abstract: A method for flow injection analysis of total inorganic phosphate contained in an aqueous system such a cooling tower or boiler is described which uses a reducing agent and preservative composition therefore as the carrier for the sample to be analyzed, thereby creating a facile process which permits conversion of the various polyphosphates to orthophosphate and development of the molybdenum blue complex color reaction at 60.degree.-95.degree. C. and under 2-10 psi. This method has less stringent pressure and temperature requirements than those employed heretofore, thus permitting the use of more reliable and economic devices for measuring total inorganic phosphate in the field.

Abstract: Inositol phosphates and/or derivatives thereof are analytically separated, whereby a quaternary amine is mixed with an aqueous solution containing one or more inositol phosphates and/or derivatives thereof. The aqueous solution obtained is fed to an analytical column containing a solid non-polar phase and the different constituents thereof are detected.

Abstract: A novel method quantitatively analyzes certain organophosphorus compounds present in mixtures of the organophosphorus compounds, a Group VIII metal and an inert solvent using gas chromatography techniques. The method involves the conversion of a catalytically-active form of the Group VIII metal to a cyano complex prior to gas chromatography analysis. Compositions are also described which are useful in the gas chromatography analysis.

Abstract: A method of detecting the initial concentration of a water-treatment chemical present in a diluted aqueous system, by (1) incorporating into the aqueous system, a mixture including a known amount of the active ingredient and a known amount of an ultra-violet sensitive compound having the formula (I): ##STR1## wherein halogen is chlorine or bromine; X is ##STR2## and a and b, independently are 0 or 1; M is hydrogen or an alkaline metal ion; and (2) detecting the concentration of the compound of formula I, by exposing to ultra-violet light a sample of the aqueous system so treated.

Abstract: An ion mobility spectrometer, ionization detector and mass spectrometer is described having a reaction region, and a region for introducing a sample gas, liquid or solid samples into the reaction region and an electrolyte in the reaction region of an alkali salt heated to a predetermined temperature, such as room temperature to 1000.degree. C., to provide a chemical reaction between the alkali atoms, cations or complement anions with the sample to provide product ions. The invention provides a non-radioactive ionization source for ionization of a broad class of compounds.

Abstract: A triiodide-phosphoric acid stain when applied to either moist or dry fiber samples produces a range of colors indicative of the fiber species and the degree of refining of the fiber. The stain is made from an aqueous triiodide solution of about 0.6M in potassium iodide and about 0.1M in iodine and is mixed with an acid solution about 77 percent by weight of phosphoric acid in a ratio of about 1 to 100 v/v of triiodide to acid just prior to its application to the fiber samples to be stained.

Abstract: The present invention provides a general assay methodology suitable for the detection of organic analytes which are neither aldehydes nor ketones and for inorganic substances. The methodology utilizes prepared sensitized films of derivatizing agents and specific developer solutions for the selective and controlled formation of light scattering crystals whose presence serves as a qualitative and/or quantitative measure of the individual analyte of interest in the sample.

Abstract: There are disclosed polyethylene evaporation covers and a method of analysis that uniquely solve the problem of contamination of CKMB test elements when phosphorous test elements are incubated in the same incubator. The solution is to have the surface of the evaporation cover the contacts the test element, be non-porous polyethylene.

Abstract: A process and an apparatus for the detection of molecular or ionic species, comprising:(a) contacting a gaseous or liquid medium containing the species to be detected with a film comprising at least one monomolecular layer of amphiphilic compound chosen from among the tetracyanoquinodimethane (TCNQ) charge transfer complexes and the tetracyanoquinodimethane (TCNQ) salts, which conduct electricity or are precursors of electricity conducting charge transfer complexes and(b) determining the variation of one of the physical properties of the film.It is in particular possible to use layers of TCNQ alkyl-pyridinium, TCNQ alkyl-quinolinium, for detecting iodine, nitrogen oxides and fluoric compounds.

Abstract: A method and apparatus for determining the phosphorus content which can be volatilized in a solid carbon sample. The sample is heated in the presence of steam to produce a vaporous steam containing volatile phosphorus. Next, the vaporous stream is passed through a zinc oxide layer whereby the voliatle phosphorus is retained. A colored solution is formed upon adding to the zinc oxide layer a vanadate-molybdate reagent. Finnally, the intensity of the colored solution is determined by a spectrophotometer; and the phosphorus content is determined by comparison with a standard intensity graph.

Abstract: A reagent for determining quantitatively the amount of phosphorous in bodily fluids which comprises a surface active agent, a strong acid, ammonium molybdate, a heavy metal chelating compound, and anti-oxidant, and deionized water is described. A method of using such a reagent is also described.

Abstract: A device for treating water to reduce the concentration of cations or anions therein includes a water-tight container (4) of flexible material, designed to be able to lie substantially flat (FIG. 3) when empty and having an aperture (5) for the introduction of liquid, a strainer (7) extending across the aperture, and a closure (6) for the aperture, and a quantity of ion-exchange material (b 8) occupying a minor proportion of the available interior volume of the container. A soil extraction outfit and a soil testing outfit are described, which incorporate the water treatment device.

Abstract: A solid detecting reagent for gaseous hydrides and a gaseous hydride detecting method are disclosed, said reagent comprising a basic copper carbonate as a color changing component and undergoing color change upon contact with at least one gaseous hydride selected from the group consisting of arsine, phosphine, diborane, hydrogen selenide, germane, monosilane, disilane and dichlorosilane. The reagent is applicable to all of these gaseous hydrides and, upon contact therewith, rapidly changes from an initial blue color to a black color, said black color standing for a long period of time.

Abstract: A reagent of the type comprising an acid, a molybdate salt, a non-ionic surfactant, and polyvinylpyrrolidone (PVP). The reagent is characterized in that it further comprises an enhancing amount of at least one sugar alcohol. Also, a method for assaying inorganic phosphorus of the type which comprises mixing a sample of biological fluid with a reagent and measuring the absorbance of the resulting solution. The method is characterized in that the above reagent is employed therein. The method can further be characterized in that the measurement can be made via a rate technique.

Abstract: A device for treating water to reduce the concentration of cations or anions therein includes a water-tight container (4) of flexible material, designed to be able to lie substantially flat (FIG. 3) when empty and having an aperture (5) for the introduction of liquid, a strainer (7) extending across the aperture, and a closure (6) for the aperture, and a quantity of ion-exchange material (b 8) occupying a minor proportion of the available interior volume of the container. A soil extraction outfit and a soil testing outfit are described, which incorporate the water treatment device.