Abstract: In a method for efficiently analyzing a posttranslational modification of a protein using no enzyme, a protein or peptide to be analyzed is reacted with an acid (a thioester or hydrazine) under certain conditions. This makes it possible to detect variously modified states of a protein or peptide, whereby the identification of each specific modifying group and the position of each modified amino acid can be efficiently analyzed using a chemical method and a mass spectrometric apparatus.

Abstract: A system for detecting the occurrence of anomalies, includes a plurality of spaced apart nodes, with each node having adjacent nodes, each of the nodes having one or more sensors associated with the node and capable of detecting anomalies, and each of the nodes having a controller connected to the sensors associated with the node. The system also includes communication links between adjacent nodes, whereby the nodes form a network. Each controller is programmed to query its adjacent nodes to assess the status of the adjacent nodes and the communication links.

Abstract: An apparatus and method for delivering repetitive, precision, low volume liquid dispensing from a dispensing orifice of a non-contact liquid dispensing apparatus. An elongated communication passageway of the dispensing apparatus is defined by interior walls having one end in fluid communication with a system fluid reservoir and an opposite end terminating at the dispensing orifice. A system fluid is placed in the communication passageway extending substantially continuously from the system fluid reservoir to the dispensing orifice. A relatively small volume of gaseous fluid is aspirated through the dispensing orifice, and into the communication passageway in a manner such that the gaseous fluid extends substantially continuously across the transverse cross-sectional dimension of the communication passageway.

Abstract: A test composition and device are described for determining levels of cyanuric acid in water, especially water in swimming pools and spas. The invention is especially characterized by avoiding the use of melamine as part of the test composition.

Abstract: An acid test kit uses an indicator paper in a transparent tube which is easily and temporarily inserted in a Schrader-valve at a compressor suction inlet of a refrigeration system. The simplicity, yet sufficient accuracy, of the kit permits several different ways of holding the paper in the tube through a friction fit. One way is to sandwich the paper between a tapered holder which is folded to provide a nose for actuating the Schrader valve. Another way is to provide the paper on or over a cylindrical member. A method for using the test kit including allowing vapor refrigerant from the system to pass through the tube to the atmosphere.

Abstract: A method for measuring cystine supersaturation of a patient urine sample as an indicator of the patient's risk for cystine stone formation has been found. A method for collecting a patient urine sample for assessment of cystine concentration and cystine supersaturation has also been found.

Abstract: A test strip for confirming a desired proportion of components in dialysate, including a first medium capable of indicating the concentration of bicarbonate ion, and a second medium capable of indicating the concentration of glucose. The test strip defines a first region impregnated with the first medium, and a second region impregnated with the second medium. The test strip optionally includes a third medium capable of indicating the pH of the dialysate. The third medium is impregnated at a third region on the test strip. Alternatively, the test strip comprises a bicarbonate test pad attached to the first region, a glucose test pad attached to the second region, and optionally a pH test pad attached to the third region. The glucose test pad is impregnated with the first medium, the glucose test pad is impregnated with the second medium, and the pH test pad is impregnated with the third medium.

Abstract: Method and apparatus used to calculate the hydrogen sulfide and carbon dioxide loading of both rich and lean amine solutions used to remove acidic gas components from sour or production gases in order to produce a sweet or sales gas for transmission purposes. The amine solution is divided into three(3) liquid streams carrying different proportions of heat stable salts, hydrogen sulfide and carbon dioxide. Conductivity measurements are made on each of the streams and are converted to acid loading values for the amine. The acid loading values of the amine are used to obtain the hydrogen sulfide and carbon dioxide loading for the amine solution.

Abstract: There is disclosed an apparatus and method for detecting and measuring volatile acidic or basic components including ammonia, ammonium, or volatile amines (compound) in a gas or liquid state fluid. Specifically, the present invention provides a PTFE-carrier solid phase indicator film having an ammonia-sensitive indicator dye embedded therein, such that the dye moiety changes color or spectral properties upon exposure to the compound to be detected.

Abstract: The present invention provides a method of detecting trace anions in solutions at a parts per billion (ppb) concentration level or less using existing anion detection technology, by employing a novel sample preparation method conducted prior to injection into a detection unit. The method includes the steps of: adding a precipitant to at least a portion of the solution; evaporating the solution, whereby a trace anion-rich solution is formed; and detecting the level of the trace anions in the trace anion-rich solution to at least a ppb concentration level. As such, any existing detection unit designed for measuring anions, known to those skilled in the art, can be used without modification. This results in a cost and time effective method of detecting trace anions in solution at a ppb concentration level. The invention also provides a system for effectuating the novel method of the present invention.

Abstract: A device for analyzing sample solutions such as whole blood based on coagulation and agglutination which requires no external power source or moving parts to perform the analysis. Single disposable cartridges for performing blood typing assays can be constructed using this technology.

Abstract: Detection of an evolving or diffusing gaseous substance emanating from an irradiated or thermolyzed layer of polymeric composition in semiconductor processing or similar processes is disclosed. The evolving or diffusing gaseous substance is detected by spatially disposing from the irradiated or thermolyzed layer a detector layer that includes a compound having leaving groups that are sensitive to the gaseous substance being detected.

Abstract: The present invention relates to a modular analyzer system for the analysis of at least two or more chemical components contained in pickle liquor solution. The analyzer modules include a strong acid analysis module, a weak acid analysis module, an oxidizer analysis module, and a metal ion analysis module. These four modules may be used in any combination, including the use of more than one of the same type of analysis module.

Abstract: A fluorescence-based method for highly sensitive and selective detection of molecules of basic gases, such as dimethyl methylphosphonate (DMMP), Sarin, Soman and other chemical warfare agents, is proposed. The method employs the effect of strong fluorescence change in a solvatochromic dye isolated in a matrix of the hydrogen bond acidic polymer. In one preferred embodiment the dye and polymer matrix are chosen such that the hydrogen-bond interaction between them results in depression of the fluorescence yield of the sensitive material prior its interaction with the molecules of basic gases. The interaction between the molecule of basic gases and the acidic polymer matrix breaks the hydrogen bond of the dye with the polymer matrix “releasing” the dye and returning it back into the state with a low solute-solvent interaction. That results in strong enhancement of the dye florescence quantum yield and shift of the dye fluorescent spectrum in the direction of shorter wavelengths.

Abstract: A food quality indicator device an indicator compound provided on a substrate. The indicator compound changes color due to the presence of volatile compounds, such as volatile bases, in spoiled food, even when the food is frozen. Alternatively, the indicator compound detects the presence of an unwanted amine-producing biological agent, such as bacteria or fungi. The indicator compound is typically contained within a polymeric matrix disposed on the substrate. Examples of suitable indicator compounds include halogenated azo dyes, sulfonated xanthene dyes, and sulfonated hydroxy-functional triphenylmethane dyes.

Abstract: A process and testing liquid is provided for detecting acidic fluxing agent residue on electronic components. The testing liquid preferably contains a reactive dye or pigment that changes color when brought into contact with the contaminants on the electronic components; the testing liquid is subsequently removed from the electronic components by washing. The respective surfaces of the electronic components that show the corresponding color change contain contaminants. Preferably, the testing liquid contains the dye Nile blue and a surfactant.

Abstract: The invention relates to a method for detecting an acid or base in an environment, measuring the concentration of an acid or base in an environment, or measuring the pH of an environment, by contacting the environment containing the acid or the base with a sensor, wherein the sensor is composed of an index of refraction transducer having an outer surface; at least one compound having at least one functional group of a Lewis acid, a Lewis base, a Bronsted acid, a Bronsted base, or a combination thereof, wherein the compound is on or near the outer surface of the transducer, wherein the functional group can interact with the acid or base in the environment to induce a change in index of refraction on or near the outer surface of the transducer, with the provisos that (i) the compound does not undergo a color change when contacted with the acid or base, and (ii) when there are naturally occurring functional groups, no transducer attached compounds, and exactly one overlayer, then the overlayer is not poly(vinyl

Abstract: The invention relates to a system and a method for detecting antifreezing substances in a hermetic compressor.

Abstract: A chemical analysis method for the determination of a base (or an acid) in a nonaqueous liquid (such as a polyol) which method can be automated and placed on-line in a chemical production facility. The instant invention includes two steps. The first step is to mix an acid-base indicator (for example, bromocresol green) with the non-aqueous liquid to produce a colored reaction product between the base or acid and the acid-base indicator. The second step is to determine the intensity of the color of the colored product.

Abstract: The invention relates to a polymer composition comprising pH-sensitive fluorescent dyes, to an ionic strength-independent optical sensor for pH value determination that contains the composition in the form of a membrane on a transparent support material, and to an optical process, according to the fluorescence method, that renders possible highly accurate pH value determination independently of the ionic strength of the test solution. The process is especially suitable for the determination of the pH value of physiological solutions, especially for the determination of the pH value of blood.

Abstract: In an HF alkylation process where an acid catalyst regeneration column separates HF acid from ASO and water to provide regenerated catalyst for a catalyst circulation stream, and where buildup of ASO in the catalyst circulation stream is encountered, an improved control scheme uses an on-line analyzer/controller to maintain desired concentrations of HF acid, or ASO or water in the catalyst circulation stream. In one embodoment, a continuously flowing catalyst slip stream is piped to the analyzer/controller for simultaneously determining concentration of HF acid, ASO and water, and in a preferred embodiment the ASO concentration is maintained at a desired low level by manipulating temperature of a stripping fluid charged to a lower section of the column. An alternate manipulated variable is temperature of the acid catalyst feed to the regenerator column. Alternate controlled variables are the HF acid, and water concentration in the catalyst circulation stream.

Abstract: A process for the preparation of an analytical sample characterized by depositing and separating solely the impurity to be analyzed from phosphoric acid; a process for analysis of the impurity characterized by depositing and separating solely the impurity from phosphoric acid and applying the separated material to analysis; a process for preparation of high grade phosphoric acid characterized by depositing and separating solely the impurity from phosphoric acid to be purified; a process for the fabrication of a semiconductor device characterized by using phosphoric acid, the impurity content of which is not more than 10−3 Bq/mL, defined by the concentration of a contained radioactive element selected from the group consisting of Pb, Bi and Po, as a processing solution.

Abstract: An indicator system provides a visual indication of the cumulative level of an airborne contaminant. The indicator is a transparent sheath with support medium having an acidic surface and treated with a color pH indicator. As a basic contaminant is adsorbed by the medium, the medium color changes. As additional contaminant is adsorbed, the color front progresses the length of the indicator. The indicator system may be used with an adsorptive filter system to predict the life of adsorption bed assemblies. A sample flow is taken upstream of the adsorption beds and is passed through the indicator. Preferably, the flow rate is calibrated so that the rate of the color change in the indicator is proportional to the rate of depletion of the adsorption bed. By monitoring the indicator, an accurate prediction of adsorption bed life may be made.

Abstract: A process for extracting inorganic ionic contaminants from a front surface of a silicon wafer for chemical analysis. The wafer is placed in a container upon a support which holds the wafer in a generally level orientation and isolates the wafer to inhibit air circulation over the front surface. Air circulation can introduce contaminants to the extraction fluid, causing a false measurement of contaminants on the wafer. A layer of extraction fluid is deposited upon only the front surface of the wafer and held for a period of time so that contaminants on the front surface are extracted into the layer of fluid. A portion of the layer of fluid is collected by a sampling device for subsequent analysis.

Abstract: A reagent for pH-metric acid number determination in a petroleum oil with low acid numbers (AN≦0.03 mg KOH/g oil) includes a salt of a strong base and a weak acid, and, an alkali in a mixture of water and an alcohol. The salt of a strong base and a weak is, preferably, sodium benzoate in a concentration of 0.02 to 0.1 M. The alcohol is, preferably, isopropanol in a concentration of from 50% to 80% by volume. The alkali is, preferably, an hydroxide and, most preferably, potassium hydroxide. The alkali should be adjusted to provide a pH′o, which is the pH of an equivalence-point on a titration curve of a strong acid added to a test portion of sodium benzoate, water and isopropanol.

Abstract: The present invention provides a method by which harmful trace gases in a gaseous mixture containing as such harmful halogen gases, halogenated hydrogen gases, acid gases, oxidizing gases, basic gases, organic acid gases, especially halogen gases or halogenated hydrogen gases, are detected by using tetraphenylporphyrin (TPP) and quantitated from a calibration curve constructed therefrom, where the range of detectable concentration is made adjustable so that harmful gas can be detected and quantitated over a broad range of concentration. Furthermore, this invention also provides a method for extending the accessible range of gas concentration by adjusting the sensitivity of the detector material via control of tetraphenylporphyrin concentration in matrix polymer of the detector material, by controlling the gas concentration range via measurement at a specific wavelength(s), and by the use of a plurality of detector materials with pre-set assay sensitivity.

Abstract: The instant invention provides for a method of inhibiting prenyl-protein transferases and treating cancer which comprises administering to a mammal a prenyl-protein transferase inhibitor which is efficacious in vivo as an inhibitor of geranylgeranyl-protein transferase type I (GGTase-I). The invention also provides for a method of inhibiting farnesyl-protein transferase and geranylgeranyl-protein transferase type I by administering a compound that is a dual inhibitor of both of those prenyl-protein transferases. The invention also provides for a method of identifying such a compound, the method comprising a modified inhibitory assay that incorporates a modulator anion that alters the in vitro potency of prenyl-protein transferase inhibitors in a way that predicts their potency in vivo, thus providing convenient identification of compounds that possess such in vivo activity.

Abstract: This invention provides a method for determining the concentration of a gas to be detected by a gas detector using a gas reactive pigment, wherein the dynamic range of the detectable concentration can be controlled. The method comprising bringing a gas to be detected such as a halogen gas, a hydrogen halide gas or the like into contact with a gas detector placed in a detection area and comprising a gas reactive pigment tetraphenylporphyrin or a derivative thereof represented by the general formula (1) or a metal complex of tetraphenylporphyrin or a derivative thereof represented by the general formula (2); and irradiating said gas detector with a detection beam and measuring a color change in said gas detector to determine the concentration of said gas to be detected, wherein the measurement is carried out in the temperature range from 40 to 80.degree. C. of said detection area; and a detection apparatus for carrying out the said method are disclosed.

Abstract: A method for determining the concentration of acid-gases in an amine-regeneration system, such as is typically found in a natural gas refining plant, having a device for measuring the pH of the system from which the concentration of the acid-gases complexed and the amine can be calculated using an empirically-derived relationship between acid-gas concentration and pH. The invention also includes a system for controlling amine regeneration based upon the above described determining method.

Abstract: An indicator system provides a visual indication of the cumulative level of an airborne contaminant. An indicator has a transparent sheath with support medium treated with acid and a pH indicator, as the contaminant is adsorbed, the color changes along the medium. The indicator system may be used with an adsorptive filter system to predict the life of adsorption bed assemblies. A sample flow is taken upstream of the adsorption beds and is calibrated with a flow meter and valve. By monitoring the indicator, an accurate prediction of adsorption bed life may be made.

Abstract: The present invention provides a method by which harmful trace gases in a gaseous mixture containing as such harmful halogen gases, halogenated hydrogen gases, acid gases, oxidizing gases, basic gases, organic acid gases, especially halogen gases or halogenated hydrogen gases, are detected by using tetraphenylporphyrin (TPP) and quantitated from a calibration curve constructed therefrom, where the range of detectable concentration is made adjustable so that harmful gas can be detected and quantitated over a broad range of concentration. Furthermore, this invention also provides a method for extending the accessible range of gas concentration by adjusting the sensitivity of the detector material via control of tetraphenylporphyrin concentration in matrix polymer of the detector material, by controlling the gas concentration range via measurement at a specific wavelength(s), and by the use of a plurality of detector materials with pre-set assay sensitivity.

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: Acid/base measuring sensor systems consisting of arrays of basic sensor cells are described which are constructed based on the chemical/electrical response characteristics of poly(aromatic amines). Protonation (doping) or deprotonation (de-doping) of the --N.dbd.sites in the polymers leads to characteristic conductivity vs. concentration curves which can be calibrated to produce reliable, instantaneous readings of the acid/base concentrations at various points in the working environment.

Abstract: A scheme for monitoring the performance of a gas-phase filter in which upstream and downstream detection surfaces are exposed to upstream and downstream air so that molecular contamination may respectively form non-volatile residue thereon, and the performance of the air filter is determined based on the ratio of the amount of non-volatile residue respectively forming on the upstream and downstream detection surfaces. In another embodiment, a first electrical signal is provided representative of the amount of non-volatile residue forming on the upstream detection surface, a second electrical signal is provided representative of the amount of non-volatile residue forming on the downstream detection surface, and the performance of the air filter is determined in real-time based on the first and second electrical signals that are provided.

Abstract: A method for continuously measuring particulate nitrate in a gas sample, comprising the steps of passing the gas sample through an inertial impactor with a 50% cut off at 2.5 microns, removing ambient pollutant gases from the gas with diffusion denuders, passing the gas through a first path so as to contact the gas with a coated filter so as to convert particulate nitrate to nitric acid vapor or passing the gas through a second path so as to contact the gas with coated filters to trap particulate nitrate and ammonia, and measuring nitric acid vapor and residual ambient pollutant gases produced from the first path and residual ambient pollutant gases produced from the second path with a chemiluminescent monitor, the difference in the signal produced from the gases from the two paths being a measurement of the particulate nitrate in the gas sample.

Abstract: The total base number of an oil sample of measured volume is determined by solvating the oil sample, adding a predetermined amount of acidic species to the solvated sample to react the acidic species with any basic species contained in the oil sample, extracting the remaining acidic species into an extractant phase, separating the extractant phase from the oil sample, and measuring the acidic species content of the extractant phase to determine the quantity of basic species in the oil sample. The same technique may be used to determine the total acid number of an oil sample by adding a predetermined amount of basic species to the sample and measuring the basic species content of the extractant phase.

Abstract: A device for measuring free acid concentrations in a solution bearing an ionic constituent therein, forms a test sample of the solution and measures the concentration of the ionic constituent in solution in the test sample. The device measures conductivity of the test sample and calculates the concentration of free acid in the test sample based on the conductivity and the concentration of the ionic constituent in solution.

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: A process for measuring and controlling at an aim point the neutralization of an organic acid in an organic polymer solution using a near-infrared analyzer.

Abstract: A halogenated hydrocarbon (HHC) detector is formed from a silent discharge (also called a dielectric barrier discharge) plasma generator. A silent discharge plasma device receives a gas sample that may contain one or more HHCs and produces free radicals and excited electrons for oxidizing the HHCs in the gas sample to produce water, carbon dioxide, and an acid including halogens in the HHCs. A detector is used to sensitively detect the presence of the acid. A conductivity cell detector combines the oxidation products with a solvent where dissociation of the acid increases the conductivity of the solvent. The conductivity cell output signal is then functionally related to the presence of HHCs in the gas sample. Other detectors include electrochemical cells, infrared spectrometers, and negative ion mobility spectrometers.

Abstract: In an analytical method for trace amounts of silicic acid in pure water of the present invention, swollen gel which has been swollen with pure water sufficiently is used as granular solid which adsorbs colored silicic acid species. A small amount of swollen gel is aliquotted volumetrically, and then the gel is added to a sample solution. Colored silicic acid species is adsorbed and concentrated on a small amount of the granular solid. Therefore, trace amounts of silicic acid can be determined with high sensitivity.

Abstract: Organometallic compounds such as tricarbonyl-(.eta..sup.4 -1,3-cyclo-hexadiene)lron(O) display an infrared spectrum which varies according to the solvent polarity, pH and similar factors. By comparing the wavenumber position and shape of the peak of a test spectrum with reference spectra by interpolation or extrapolation, information is obtained about the test sample, even a quantitative analysis in some cases. More than one organometallic compound may be used in one experiment (for double checking), and/or a mixture of analytes may be investigated, for obtaining information about the combination.

Abstract: A method and system to optimize the acid strength and level of total organic carbon (TOC) of process streams in which specific hydrocarbons are extracted from hydrocarbon mixtures by sulfuric acid.

Abstract: A porous cellulose tape impregnated with powdered silica or other gas adsorbent carries a coloring reagent of silver perchlorate or silver para-toluenesulfonate and a light-resistance enhancer of para-toluenesulfonic acid which are dissolved in glycol. When the tape is exposed to a sample gas, the silane contained in it dissolves in the glycol. The resulting reduction of the silver perchlorate or silver para-toluenesulfonate forms a colloid of silver as a trace of their reaction. The concentration of silane, which is proportional to the colloid of silver formed, can be determined by measuring the optical concentration of the reaction trace. The absence of strong acid detrimental to cellulose assures the determination of silane concentration with a high degree of sensitivity, without impairing the mechanical strength in the cellulose tape.

Abstract: The present invention provides a method for measuring the amount of free sulfurous acid and bound sulfurous acid in a sample using a bacterium belonging to Thiobacillus thiooxidans or Thiobacillus ferrooxidans of in which the sample is treated with acid and/or alkali to give free sulfurous acid alone in the sample. Then, the total amount of free sulfurous acid in the sample is measured by an oxidation reaction of free sulfurous acid to sulfuric acid using a bacterium belonging to Thiobacillus thiooxidans or Thiobacillus ferrooxidans.

Abstract: The total base number of an oil sample of measured volume is determined by solvating the oil sample, adding a predetermined amount of acidic species to the solvated sample to react the acidic species with any basic species contained in the oil sample, extracting the remaining acidic species into an extractant phase, separating the extractant phase from the oil sample, and measuring the acidic species content of the extractant phase to determine the quantity of basic species in the oil sample. The same technique may be used to determine the total acid number of an oil sample by adding a predetermined amount of basic species to the sample and measuring the basic species content of the extractant phase.

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: Trioxane derivatives represented by the formula (I): ##STR1## wherein A and RA are the same with or different from each other, and represent a substituted or unsubstituted aliphatic hydrocarbon group, respectively, or represent R.sub.1 --X.sub.1 --or R.sub.2 --X.sub.2 --in which X.sub.1 and X.sub.2 represent independently a divalent organic residue, and R.sub.1 and R.sub.2 represent independently carboxyl group, amino group, hydroxyl group or mercapto group, and Z represents hydrogen atom, halogen atom, methyl group, ethyl group or propyl group, or carboxyl, amino, hydroxyl or mercapto group through a divalent organic residue, and process for the preparation thereof, as well as method for chemiluminescence comprising mixing the trioxane derivatives and a base.

Abstract: A method for optical measurement of bilirubin which comprises reacting a bilirubin-containing sample with a zinc compound, a coloring agent and bilirubin oxidase in a buffer, wherein a stable green pigment having a large molecular extinction coefficient is formed by the action of the zinc compound and thereby bilirubin in the sample can be measured specifically, and a reagent useful therefor. Said method and the reagent are useful for clinical test of total bilirubin and direct bilirubin in serum.

Abstract: Measurements of acids in air can be greatly falsified by the content of carbon dioxide in the air in spite of the low solubility of carbon dioxide in water and its low dissociation constant. When the measurements are made after a simple absorption of the acid residues in the air in an absorption solution. The air separated from the absorption solution on its way to measurement is cleaned of carbon dioxide by exposure to silica gel and soda-lime and then is used to clean the absorption solution of carbon dioxide in a similar exposure of air to the liquid. The measurement of the acidity of the solution thus cleaned of carbon dioxide provides reliable measurements of strong acid residues in air and can be carried out on a continuous basis.