Abstract: A process for qualitative or quantitative determination of a reactive chemical contained in a liquid sample by forming doped sol-gel glass pellets from a metal alkoxide, arranging the porous doped sol-gel glass pellets in a glass tube, contacting a liquid sample containing a reactive chemical with the porous doped sol-gel glass pellets contained in the glass tube, and measuring a length of a stained portion of the glass tube resulting from a color change in the sol-gel glass pellets. The sol-gel glass pellets are formed by a gelling step conducted at room temperature in the presence of a colorimetric reagent dopant which produces a color change in the presence of the reactive chemical, and a drying step conducted at not greater than 41.degree. C. The doped sol-gel glass pellets contain the colorimetric reagent dopant encapsulated therein and the encapsulated colorimetric reagent dopant is color changeable in the presence of the reactive chemical in the pores of the doped sol-gel glass pellets.

Abstract: An automated analysis system is provided for the determination of impurities in a liquified hydrocarbon stream. The system employs a hydrocarbon capture vessel for capturing a hydrocarbon sample, a water scrubbing vessel for extracting impurities from the hydrocarbon sample and a titration zone for analyzing the amount of impurities in the aqueous extract.

Abstract: A system for coulometric TCO.sub.2 analysis wherein a sample bottle is pressurized by a head space gas having a CO.sub.2 composition which approximates the dissolved CO.sub.2 concentration in the sample. The head space gas transfers to sample to a pipette. The sample is then transferred to a stripper where the sample is degassed. Two carrier gas lines flush the stripper and transfer the CO.sub.2 to a coulometer.

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 system (10) for in vivo measuring chemical and physical parameters of a patient's blood includes a probe (12), a sensing system (14), and flush interference warning devices (20). The system measures pH, pCO.sub.2, and temperature values, and determines a base excess value using the measured pH and pCO.sub.2. The time rate of change of the base excess value is also determined, as is the time rate of change of temperature. The warning devices are activated, indicating that the measured parameters are likely affected by the presence of flush solution flowing past the probe, when either: (a) the base excess value is less than a predefined threshold base excess; (b) the absolute value of the time rate of change of the base excess value is greater than a predefined threshold time rate of change of base excess; or, (c) the absolute value of the time rate of change of temperature is greater than a predefined threshold time rate of change of temperature.

Abstract: Sensing composition precursors and sensing compositions, useful in sensing the concentration of a gas, e.g., carbon dioxide, in a medium, e.g., blood, are disclosed. In one embodiment, the sensing composition precursor comprises a dispersed aqueous liquid including a sensing component dissolved therein, a polymer precursor, and a hydrophilic dispersing agent selected from hydroxyalkyl celluloses and mixtures thereof in an amount effective to facilitate maintaining the dispersed aqueous liquid.

Abstract: The concentration of an aromatic azole corrosion inhibitor in the water of an aqueous system is monitored by a fluorometric method which is based upon the measurement of the fluorescence intensity of the aromatic azole corrosion inhibitor itself, and the precise determination of concentration permits control of the dosage of such aromatic azole corrosion inhibitor.

Abstract: Methods are disclosed for detecting the effects of cell affecting agents on living cells. The method steps include providing living cells that are retained in a micro flow chamber. The micro flow chamber is adapted for either continuous or intermittent flow of solutions or suspensions in intimate contact with the cells. The solutions or suspensions, which contain a cell affecting agent, are then flowed in intimate contact with the cells and at least one effect of the cell affecting agent on the cells is measured by an appropriate detecting means, which is operatively associated with the micro flow chamber.

Abstract: A process and apparatus are disclosed for the demineralization of ground bone particles or pieces of cancellous or cortical bone. The apparatus includes multiple solution reservoirs which supply solutions to be pumped into one or more columns filled with bone samples to be demineralized. Solvent outflowing from the column(s) can be monitored for pH, calcium ion concentration or conductivity as a basis for determining when demineralization is complete. During the delipidization phase of processing, lipid solute can be monitored by photometry, or a small assay of the eluent can be dropped into deionized water to see whether a precipitate develops. Flow through the apparatus, including the types and amounts of solutions to be flowed through the apparatus, can be manually or computer controlled.

Abstract: An analyzer system for improving quality of a reaction product, wherein a liquid sample must be maintained at an elevated temperature to prevent precipitation of titratable species, comprises a heated sample and dilution section, an autotitrator and a programmable controller. In operation a liquid sample to be analyzed is withdrawn from a reactor and maintained at reactor temperature while being diluted. The diluted sample is then cooled and passed to an autotitrator for analysis. The analyzer system includes a programmable controller for automatic unattended dilution of successive samples.

Abstract: A sheath is used to house a conventional pH sensor within the sheath's interior. The sheath is exposed to a descending spray within a sulfur dioxide (SO.sub.2) absorber. A fill port collects a portion of the spray and the sheath accumulates the collected spray as a slurry sample within its interior. The pH sensor becomes immersed in the sample slurry. Slurry is discharged from the interior by way of drain notches and drain holes. Discharged sample slurry descends to enter a bulk slurry to allow recycling. A steady state of slurry collection and slurry discharge is reached such that the sample slurry is continuously refreshed. Elevation of the sheath over the bulk slurry prevents slurry from the bulk from entering into the slurry sample.

Abstract: A pH-indicating material capable of undergoing a clearly visually detectable color transition at a desired pH, e.g., at a pH at or below about 5.6 and/or at a pH at or above about 7.6. When the pH-indicating material is wetted on its surface with liquid animal dross, particularly animal urine, such as cat urine, the pH-indicating material will undergo a clearly visible color transition at a urine-problematic pH, e.g., acidic or alkaline. The pH-indicating material is maintained on an inert carrier, separate from the cat litter material itself, so that the cat litter material does not chemically interfere with the urine pH-induced color transition provided by the dye(s) in the coating material, and so that the color transition is an exclusive result of the pH of the contacting animal urine, without pH interference from the litter material.

Abstract: An automated analysis system for the determination of impurities in a liquified hydrocarbon stream. The system employs a hydrocarbon capture vessel for capturing a hydrocarbon sample, a water scrubbing vessel for extracting impurities from the hydrocarbon sample and a titration zone for analyzing the amount of impurities in the aqueous extract.

Abstract: For optical determination of the catalytic enzyme activity of a sample by means of enzyme reactants which are split under the influence of the enzyme to be measured, the enzyme reactant is placed at the end of an optical fiber and brought into contact with the sample to be determined. The measurements are carried out by observing the rate of change in spectral characteristics of the enzyme reactant, or its reaction products, resulting from the enzyme reaction. The method permits measurements of undiluted blood and in-vivo determinations of enzyme activities.

Abstract: A method of chemically modifying the poly (methyl methacrylate) (hereinafter "PMMA") clad surface of an optical fiber to introduce amino groups. N-butyl lithium in a suitable organic solvent with ethylene diamine is applied to the clad surface of the optical fiber in a substantially oxygen-free atmosphere, such as nitrogen, at approximately 10.degree. C. to 40.degree. C. for about one to two hours. A pH-sensitive dye with isothiocyanate functionality can be bounded to the modified clad surface resulting in a pH sensor based on fiber optics.

Abstract: An analyzer system for improving quality of a reaction product, wherein a liquid sample must be maintained at an elevated temperature to prevent precipitation of titratable species, comprises a heated sample and dilution section, an autotitrator and a programmable controller. In operation a liquid sample to be analyzed is withdrawn from a reactor and maintained at reactor temperature while being diluted. The diluted sample is then cooled and passed to an autotitrator for analysis. The analyzer system includes a programmable controller for automatic unattended dilution of successive samples.

Abstract: Bromide ion content in a photographic developer is an important variable to be controlled by photoprocessors who process color reversal material or color negative film. The bromide content of such developers can be determined by titration with silver ion, using tetraiodophenolsulfonephthalein (TIPS) or other suitable adsorption indicator, after the developer has been acidified with an organic acid such as citric acid. This titrimetric method can be adapted for use in a test kit which is designed for use by photoprocessors who otherwise lack the chemical sophistication to readily conduct analysis by titration, or who have the necessary sophistication, but wish to gain the benefits and convenience available from use of a test kit specifically designed for conducting the analytical method.

Abstract: A flow injection nonaqueous solvent neutralization titration process and system is provided. The predetermined quantity of a known titrant is used to derived calibration values based on different predetermined concentrations of a desired component in a sample. The quantity of the titrant agent in excess of an amount necessary to completely react with the sample is added and then subsequently the amount of the unreactant titrant agent is determined. From this value, the calibration values that have been stored, for example, in a look-up table can be used to determine the actual concentrations of the desired component in the sample.

Abstract: A chemical test kit and method for detecting the presence of impurities in an oil sample is provided. The test kit is comprised of two flexible translucent or transparent containers, each with at least one breakable capsule mounted within it. One of the flexible containers has a means for separating an aqueous layer from an oil layer. The capsules contain reagents capable of extracting the impurity to be detected from the oil into an aqueous layer and indicating the presence of a threshold concentration of the impurity. The method involves the steps of introducing an oil sample into a first flexible container, breaking the capsule within it by squeezing the flexible container in the vicinity of the capsule, transferring the aqueous layer to the second container, and breaking the capsule within the second container in the same manner. A chemical reaction occurs in the second container indicating whether the impurity is present at a given threshold concentration.

Abstract: A method for determining the concentration of an acidic metal carbonyl hydride in an organic liquid by measuring the conductivity or pH of the liquid. The air addition to a continuous air demetallating unit may be controlled by feedback from the conductivity or pH measurement of the effluent.

Abstract: An automatic titration device for use in either batch processing or a continuous processing mode to identify quantitative fluid properties. The device consists of a plurality of reservoirs each connected to a respective plurality of pumps. A central computer controls individual pump speeds and therefore the pump output mix through a delivery tube that delivers fluid mixture through an ultrasonic mixer to a mixing tube whereupon a color detector is disposed to detect indicator color changes of the liquid for providing indication back to the central computer for calculation of fluid presence, fluid equivalent points, and related fluid properties.

Abstract: An automatic analytical apparatus in which a series of operations ranging from the sampling into a treating receptacle, pretreatment, analysis and discharge of a fluid sample to the preparation for the next analysis are repeated automatically in order, wherein the time-dependent variation of the composition is traced successively. This permits the presence of the composition variation or the course of the composition variation to be confirmed or the composition variation to be controlled, automatically.

Abstract: The present invention relates to a chromogenic benzoisothiazolone polymer derivative for measuring the presence or appearance of thiols in an aqueous system.

Abstract: A test device having the following meritorious effects is obtained in accordance with the present invention by using at least one composition selected from the group consisting of ink compositions for detecting glucose, for detecting protein, for detecting urobilinogen, and for detecting occult blood in a body fluid, and for detecting the pH thereof:a) The test device is stable during storage in atmospheric air for a long period of time, presenting no discoloration phenomenon;b) The test device has high sensitivity coupled with excellent measurement performance;c) The regions for detecting glucose and the other body fluid ingredients and the pH can be formed directly on the surface of the test device by printing, allowing the test device to be formed by mass production and the process steps to be reduced; andd) The ink compositions for detecting glucose, etc. are stable, and can be handled easily.

Abstract: A method and apparatus are is disclosed for determining whether respiratory gas is present in a gaseous sample. The sample is brought into contact with an indicator which yields an indication within a diagnostically effective period of time of the presence in the sample of carbon dioxide in concentration of at least 2% while an indication of the presence of carbon dioxide or other trace acidic gas in a sample of ambient air is delayed beyond a predetermined period of time. The method and apparatus of the present invention have particular utility in determining the correct placement of an endotracheal catheter in a patient or in the direction of apnea.

Abstract: A method and apparatus for operating a limestone wet scrubbing flue gas desulfurization apparatus comprises first and second pH measuring devices connected respectively to a recirculation line in the scrubber and above the liquid holdup tray in the scrubber. The difference in the pH values measured at these two locations in the system is used to adjust the amount of air supplied to the sump or reaction tank of the scrubber to maximize oxidation in the scrubber and to avoid wasted airflow.

Abstract: A method is disclosed for determining whether respiratory gas is present in a gaseous sample by which the sample is brought into contact with an indicator which yields an indication within a diagnostically effective period of time of the presence in the sample of carbon dioxide in concentration of at least 2% while an indication of the presence of carbon dioxide in a sample of ambient air would be delayed beyond a predetermined period of time. The method has particular utility in determining the correct placement of an endotracheal catheter in a patient or in the detection of apnea.

Abstract: A method for measuring the concentration of hydroxides in alkaline solutions in a remote location using the tendency of hydroxides to absorb carbon dioxide. The method includes the passing of carbon dioxide over the surface of an alkaline solution in a remote tank before and after measurements of the carbon dioxide solution. A comparison of the measurements yields the absorption fraction from which the hydroxide concentration can be calculated using a correlation of hydroxide or pH to absorption fraction.

Abstract: A process is provided for the quantitative selective complexometric analysis of a sample. First and second aliquot parts of a sample containing N-phosphonomethyl-glycine, N-carboxymethyl-N-phosphonomethyl-glycine or N,N-bis-phosphonomethyl-glycine; or N-phosphonomethyl-glycine and N,N-bis-phosphonomethyl-glycine; or N-phosphonomethyl-glycine and N-carboxymethyl-N-phosphonomethyl-glycine are taken. The first aliquot part is titrated with a bismuth volumetric solution at a Ph=1.8-2.5 in the presence of a methylethymol blue indicator. The second aliquot part is titrated with a copper volumetric solution at a Ph=8-10 in the presence of a murexide indicator. Two end point values are obtained and compared. The difference between these two values result in the determination of the content of N-phosphonomethyl-glycine in the sample.

Abstract: A titrating system includes a pulse length modulator for controlling a drive train including a DC drive motor to supply a given dosage of a titrating agent to a specimen. The pulse length modulator is so designed that the drive motor is supplied with DC-current pulses having a constant amplitude, the lengths of the pulses being a function of the start-up characteristic of the drive apparatus. In order to produce the simultaneous dosing of two different titration agents, at least two dosing arrangements and at least two drive trains are provided, thereby affording a joint control-train pair for the alternate selection of the drives. By virtue of the combination of several control-train pairs, a large number of simultaneously selectable pairs of supply devices can be provided. In a preferred embodiment, the pulse length modulator supplies to the electromechanical drive apparatus DC voltage pulses having a generally constant amplitude.

Abstract: Method for making a probe with a plurality (one or more) of optical fiber sensors containing colorimetric chemical indicators in gaps in the fibers, the fibers bent to provide good light transmission qualities. Apparatus for making a probe with a plurality of such optical fiber sensors. A probe with a plurality of such optical fiber sensors. A vacuum chuck for holding the ends of such fibers.

Abstract: A carbon dioxide indicator for use in determining the proper placement of endotracheal tubes. The indicator is comprised of a pH-sensitive dye suspended in a predominantly hydrophilic polymer matrix. The indicator may be placed inside a tube or connector to form an indicator device. When the pH-sensitive dye changes color due to CO.sub.2 and moisture in exhaled air, the color change is visible from outside the device.

Abstract: A method for analyzing water or other liquid, in particular rain water, comprises the steps of providing a collector comprising at least first and second volumetric cells and a mechanism for causing water to flow selectively into the cells and for causing water to flow selectively from the cells. Water is caused to flow into a first one of the cells while it is prevented from flowing into the other one of the cells. The water collected in the first cell is caused to flow to a property determining cell when the first cell has been filled to a predetermined volume, and simultaneously water is prevented from flowing into the first cell while it is now permitted to flow into the second volumetric cell. The water collected in the second cell is then permitted to flow to a property determining cell when the second cell has been filled to a predetermined volume, and simultaneously the water is prevented from flowing to the second cell while it is now permitted to flow to the first cell.

Abstract: The invention provides a nonenzymatic method useful for the semiquantitative determination of glucose, a test composition and test device. Glucose concentration in an aqueous test sample can be determined by preparing a test solution by contacting an aqueous test sample and a dihydroxide component, at an initial pH above 6.5, capable of forming a complex with glucose which complex formation releases a proton, and determining the final pH of the test solution. The invention also provides a self-indicating device format which allows the determination of glucose concentration by merely counting the number of pads which have changed color. No comparison to a color chart is required. The glucose test of the present invention is free of the interferences found in enzymatic glucose tests.

Abstract: Single or multi-cell reservoir sensors with single illumination sources and one or more detectors per cell unit have an arrangement whereby a gaseous, vapor or liquid sample enters the cell body and interacts with a sensing solution to detect and quantify a given species. Entrance of the sample into the sensor is through an opening in the cell body which may be covered with a membrane to contain the sensing reagent and to presort the species entering the cell. Reservoir cells can be used with organic, inorganic or biochemical sensing materials. A variety of sensors as alcohol, drugs of abuse, organic halides, cyanide and inorganic ions are provided.

Abstract: For the simultaneous measurement of two parameters of a liquid or gaseous sample, in a fluorescence measuring device in which the influence of the aging processes of the indicator substance and the fluctuations in the light intensity of the excitation light source are to be avoided, it is proposed that the change in the first parameter to be measured is obtained from the change in the ratio of two intensity values, determined for different wavelengths of the excitation and emission spectrum of the indicator substance, and the change of a second parameter is obtained from the change in the decay time t of the fluorescence radiation of the same indicator substance from the group of aromatic hydrocarbons, the aromatic heterocycles and the metal organic complexes.

Abstract: The ionic strength or the specific gravity of an aqueous liquid is determined by mixing the liquid with a reagent composition which contains at least one pH buffer substance but no polyelectrolyte polymer, or at least one pH buffer substance and/or at least one complex former, determining the pH of the mixture, and evaluating the determined value.

Abstract: A method and apparatus for assessing the odor intensity of combustion gas produced from an internal combustion engine in which the odor intensity of combustion gas is obtained from the pH-value of an aqueous solution prepared from odor-producing substances, based on a predetermined relationship between pH-value and odor intensity. The odor intensity thus obtained strongly correlates with organoleptically evaluated odor intensity. Since the odor intensity of the gas is determined from the pH-value, the precision and the reliability of the odor intensity measurement are enhanced.

Abstract: The molar concentration of chloroformate in an organic chloroformate solution is determined by adding an excess of a monohydroxyaromatic compound, water and a catalytic amount of a 4-dialkylaminopyridine such as 4-dimethylaminopyridine, titrating with aqueous base and taking as the end point the volume of base which achieves complete conversation of chloroformate groups to monoaromatic carbonate groups, as shown by a rapid rise in the pH of the aqueous phase of more than two points to a value in the range of 7-9. This method is particularly applicable to the determination of bischloroformate molar concentration in systems to be converted to cyclic polycarbonate oligomers. Conversion may be effected by condensation in the presence of a trialkylamine and aqueous base in the amount of about 3 moles per mole of bischloroformate.

Abstract: The invention relates to a quantitative assay for an analyte which comprises contacting a sample containing an analyte with a solid phase support to immobilize said analyte, following by indirectly quantitating the presence of bound analyte by titrating the unoccupied binding sites with a titrating protein which is detectably labeled.

Abstract: A sensor system for determining the pH or carbon dioxide concentration of a liquid medium comprising, in combination, a pH-insensitive fluorescent indicator and a PH-sensitive fluorescent indicator which act in concert or a single fluorescence indicator which emits fluorescent signals of different wavelengths in different carriers, which system(s) produce diverging signals, the ratio of which provides an accurate and stable determination of the parameter being measured. A method for determining pH and CO.sub.2 concentration is also disclosed.

Abstract: A method for determining the concentration of an acidic metal carbonyl hydride in an organic liquid by measuring the conductivity or pH of the liquid. The air addition to a continuous air demetallating unit may be controlled by feedback from the conductivity or pH measurement of the effluent.

Abstract: A method of analysis in which a first fluid is delivered to a sensing position at a controlled first rate of flow through a fluid junction. Fluid including this first fluid is pumped to the sensing position at a rate of flow greater than the first rate, whereby to aspirate further fluid into the first fluid at the fluid junction. A condition of the fluid is sensed at the sensing position. Associated analytic apparatus includes first and second pumps (1, 2). The first pump has a pair of ports and the second pump has at least one port. A conduit (4, 5) provides fluid flow communication from a first of the ports of the first pump (1) to the port of the second pump (2). A fluid junction (3) in the conduit (4, 5) is spaced from the second pump for admitting a further fluid to the conduit. A sensor (13) is associated with the conduit (5) to sense a condition of the fluid in the conduit at least at a sensing position between the fluid junction (3) and the second pump (2).

Abstract: A test device and method of determining the presence and concentration of proteins, such as albumin or Bence Jones proteins, in a test sample. The test device includes a carrier matrix incorporating a reactant system capable of interacting with proteins to produce a visually or instrumentally detectable and/or measurable response. The carrier matrix of the device can include commonly used bibulous matrices, such as filter paper, or a nonbibulous protein-permeable strip, membrane or layer of a polymerized urethane-containing composition. In addition, a reactant system, including a dual indicator reagent system, such as bromophenol blue, methyl orange and, if necessary, a suitable buffer, is incorporated into the carrier matrix to provide improved color resolution and increased sensitivity to proteins, thereby affording a more accurate and trustworthy protein assay of test samples, such as urine.

Abstract: A method for measuring trace amounts of analyte substance(s), which utilize a pH electrode is disclosed. This method is by far simpler than conventional optical detecting systems. The apparatus for practicing the method is also disclosed. By the use of pH electrode, the apparatus is compact, inexpensive and easy to operate, and hence usable in small-size and medium-size hospitals or clinical laboratories and by patient's bedside.

Abstract: The ionic strength or the specific gravity of an aqueous liquid is determined by mixing the liquid with a reagent composition which contains at least one pH buffer substance but no polyelectrolyte polymer, or at least one pH buffer substance and/or at least one complex former, determining the pH of the mixture, and evaluating the determined value.

Abstract: A blood chemical sensor has a blood gas sensitive dye contained in a hydrogel matrix, the combination of dye and gel being mounted on the end of an optical fiber. The hydrogel is freeze-dried to facilitate packaging and handling.

Abstract: A test device and method of determining the presence and concentration of proteins, such as albumin or Bence Jones proteins, in a test sample. The test device includes a carrier matrix incorporating a reactant system capable of interacting with proteins to produce a visually or instrumentally detectable and/or measurable response. The carrier matrix of the device can include commonly use bibulous matrices, such as filter paper, or a nonbibulous protein-permeable strip, membrane or layer of a polymerized urethane-containing composition. In addition, a reactant system, including a dual indicator reagent system, such as bromophenol blue, methyl orange and, if necessary, a suitable buffer, is incorporated into the carrier matrix to provide improved color resolution and increased sensitivity to proteins, thereby affording a more accurate and trustworthy protein assay of test samples, such as urine.

Abstract: A fluorescent optical probe employed for the analysis of the concentration of an analyte (or material to be analyzed) in a fluid, employs a permeable, transparent polymeric matrix in which a fluorophor is immobilized, with the polymeric material being directly exposed to the fluid being analyzed. The composite material of the probe may be made up of a homogeneous matrix of transparent polymer, fluorescent compound, catalyst(s) and reagents(s) and is employed to measure analyte concentration in a fluid in the environment surrounding the material. For analyzing oxygen, the fluorophor may be 9,10-diphenyl anthracene and the polymer matrix may be poly (dimethyl siloxane), or silicone, with the presence of oxygen quenching the fluorescence of 9,10-diphenyl anthracene.

Abstract: A gravimetric method for determining the iodine adsorption number of carbon black is disclosed. The concentration of an accurately weighed iodine solution is determined by titrating with a standardized titrant and determining the concentration of the iodine solution by the weight of the standardized titrant needed to reach the titration endpoint. An appropriate amount of accurately weighed iodine solution is mixed with an accurately weighed amount of carbon black, and the mixture is equilibrated. The concentration of the resulting supernatant is determined by determining the weight of the standardized titrant needed to reach the titration endpoint. The iodine adsorption number is then determined based on the gravimetrically determined concentrations of the solutions. Preferably, the method is semi-or fully automated, and an apparatus for accomplishing the same is disclosed.