Abstract: A method for facilitating removal of mercury from a primary fluid stream of interest which is contaminated with organically-bound, elemental, and ionic mercury species. The stream is analyzed to establish the relative content of the organically-bound, elemental, and ionic mercury species present therein by forming a diverted side stream from the primary stream, and passing the side stream successively through three in series filter stages, the first captures organically bound mercury, the second captures elemental mercury, and the third captures ionic mercury. The side stream flow through the filter stages is continued for a predetermined period, and upon conclusion of the period the quantity of mercury collected at each of the filtration stages is determined. This data is then utilized to determine the capacity of the three different filtration stages required to reduce the mercury content in the mam stream to a desired level.

Abstract: A method for facilitating removal of mercury from a primary fluid stream of interest which is contaminated with organically-bound, elemental, and ionic mercury species. The stream is analyzed to establish the relative content of the organically-bound, elemental, and ionic mercury species present therein by forming a diverted side stream from the primary stream, and passing the side stream successively through three in series filter stages, the first captures organically bound mercury, the second captures elemental mercury, and the third captures ionic mercury. The side stream flow through the filter stages is continued for a predetermined period, and upon conclusion of the period the quantity of mercury collected at each of the filtration stages is determined. This data is then utilized to determine the capacity of the three different filtration stages required to reduce the mercury content in the mam stream to a desired level.

Abstract: Palladium(0)-dibenzylidene acetone complexes Pdx(dba)y, with y/x being from 1.5 to 3, are provided according to the invention at a purity of at least 99.5 wt. %. The use of said Pdx(dba)y complexes according to the invention is for determining their stoichiometry by means of elemental analysis. In the method for the production of Pdx(dba)y complexes from a Pd-containing educt and dibenzylidene acetone (dba) in alcohol, according to the invention a solution of the dba in alcohol pre-heated to more than 40° C. is provided first and then the Pd-containing educt is added to the pre-heated solution upon which the complexes are precipitated by a base.

Abstract: Disclosed are methods of diagnosing, screening and treating individuals at risk of elevated intracranial pressure based on detecting a transient decrease in serum ceruloplasmin and/or serum copper levels in the individual soon after occurrence of a head injury. This early drop in ceruloplasmin or copper level indicates an impending, potentially life threatening, elevation in the individual's intracranial pressure. Also disclosed are diagnostic applications and processes for identifying and producing diagnostic and prognostic assays useful for predicting elevated intracranial pressure, and test kits for performing such tests.

Abstract: A system and method for assessment of a brain status of a subject are disclosed. The brain status comprises a brain disease induced brain dysfunction. An occurrence and/or stage of the brain disease induced brain dysfunction in the subject is determined. The system comprises an apparatus that is adapted to determine the occurrence and/or stage of the brain disease induced brain dysfunction in the subject from random speech of the subject.

Abstract: Palladium(0)-dibenzylidene acetone complexes Pdx(dba)y, with y/x being from 1.5 to 3, are provided according to the invention at a purity of at least 99.5 wt. %. The use of said Pdx(dba)y complexes according to the invention is for determining their stoichiometry by means of elemental analysis. In the method for the production of Pdx(dba)y complexes from a Pd-containing educt and dibenzylidene acetone (dba) in alcohol, according to the invention a solution of the dba in alcohol pre-heated to more than 40° C. is provided first and then the Pd-containing educt is added to the pre-heated solution upon which the complexes are precipitated by a base.

Abstract: A method of manufacture and device for a dual-gate CMOS structure. The structure includes a first plate in an insulating layer and a second plate above the insulating layer electrically corresponding to the first plate. An isolation structure is between the first plate and the second plate.

Abstract: The invention provides a method for determining the content of metallic elements in Fischer-Tropsch waxes by Inductively Coupled Plasma (ICP), wherein digestion of one or more samples of the waxes is carried out in an open vessel microwave digestion system. The invention further provides a sampling protocol for use with the method.

Abstract: The present invention is directed to methods for determining electron transfer rates in systems involving metalloproteins. Metalloprotein/substrate electron transfer rates as well as metalloprotein self exchange rates may be modeled. Such electron transfer rates are useful in smart drug design and enzyme engineering.

Abstract: The present invention is directed, in part, to fluorescein-based ligands for detection of metal ions, and methods of making and using the same.

Abstract: The present application describes methods for conjugating gold to biological molecules and conjugates resulting from the same. The method provides superior gold conjugated biomolecules with higher sensitivity than those made from conventional gold conjugation methods.

Abstract: In accordance with the present invention, an organic additive is characterized in the presence of an acidic metal plating matrix in a metal plating solution by: providing a sample from the metal plating solution; activating a metal-complexing resin with a weak acid to provide an activated metal-complexing resin; eluting the sample through the activated metal-complexing resin to form a treated sample in which a concentration of the acidic metal plating matrix is reduced; and determining a concentration of an organic additive in the metal plating solution by analyzing the treated sample.

Abstract: The present invention is directed to a method of assaying for the presence or absence of a metal-ligand chelate in a sample containing either a metal-ligand chelate or a free ligand. The method includes (a) reacting the sample with a luminophore to obtain either a metal-ligand-luminophore chelate and/or a ligand-luminophore adduct; (b) detecting the electromagnetic spectrum of the reaction product; (c) matching the electromagnetic spectrum of the reaction product with an electromagnetic spectrum metal-ligand chelate luminophore chelate or the electromagnetic spectrum of a ligandluminophore adduct; (d) correlating a match of the electromagnetic spectrum of the reaction product and the electromagnetic spectrum of the metalligand-luminophore chelate with the presence of a metal-ligand chelate, or correlating a match of the electromagnetic spectrum of the reaction product and the electromagnetic spectrum of the ligand-luminophore adduct with the absence of a metal-ligand chelate.

Abstract: A method of measuring the concentration of metal ions in a sample comprising the steps of: providing a sample comprising a nonpolar, liquid hydrocarbon, suspected of containing a metal ion; adding a dye such as a spirobenzopyran dye or bathocuproine and a reducing agent to the sample; wherein the dye forms a complex with the metal ion; wherein the complex has a spectral shift in light absorbance relative to the dye; observing the spectral shift; and calculating the concentration of the metal ion in the sample.

Abstract: A method, a device, and a test kit for performing this method for determining the volume of a sample of the liquid. In the method, a specific concentration of a chromophoric indicator is provided in this liquid, a sample is separated from the liquid, the optical absorption of the separated sample is measured, and the volume of the separated sample is determined by correlation of the measured optical absorption with the concentration of indicator in this liquid. Ions that generate a color in the sample by complexing with a specific ligand are used as the indicator to stain the liquid.

Abstract: A combinatorial method for discovering or optimizing materials is disclosed. The method uses solution-based components that are mixed and dispensed into regions on a substrate for drying and/or heat-treating. The drying and/or heat-treating produces materials that can be tested for a desired property.

Abstract: The present invention is drawn to a method of performing a one-pot organic reactions including carbon monoxide as reactant, without the use of an external CO gas source, wherein a reaction mixture containing a solid or liquid CO releasing compound, a non-metal substrate and a metal catalyst is exposed to an energy source to release carbon monoxide from the CO releasing compound and wherein carbon atoms of the released carbon monoxide form a bond with the non-metal substrate compound. The present invention is further drawn to a method of preparing chemical libraries and a kit for organic reactions.

Abstract: Sensors and methods of monitoring for the presence of gas phase materials by detecting the formation of films based on the gas phase material are disclosed. Advantageously, some gas phase materials preferentially deposit on specific surfaces. As a result, selective detection of those gas phase materials can be obtained by detecting films deposited on those detection surfaces. Examples of gas phase materials that may be detected include RuO4, IrO4 and RhO4.

Abstract: The present invention relates to sensors for the determination of organometallic compounds comprising the following elements: a) an inorganic, organic or polymeric support, insoluble in the sample to analyze b) an indicator which reversibly reacts with the organometallic compound and whose reaction product gives a characteristic absorption, reflection or emission band in the range 150-15000 nm and which is physically trapped, adsorbed, absorbed, dissolved or chemically linked in an electrostatic or covalent way to the support c) an optical sensor which measures the absorption, reflection or emission of the functionalized support at the characteristic wavelength and transforms it in the concentration of the organometallic present in the solution. Also described is the method for the determination of the concentration of organometallic compounds by the on line use of a sensor as above defined.

Abstract: A method for assaying a pharmaceutical product containing a Fe-Sugar complex is described herein. The assay comprises in one embodiment measurement of the molecular weight of the Fe-Sugar complex. The method described herein is robust, reproducible and can serve as a quality assurance method for pharmaceutical purposes.

Abstract: A method of assaying metal proteinate samples to determine compliance with European Union standard definitions for such products.

Abstract: A method and apparatus for non-invasive extraction and/or detection of chemicals such as heavy metals, drugs such as cocaine and analytes such as blood glucose has been developed. A patch or hydrogel containing a reagent such as N-methyl pyrrole, or a similar compound, is used to extract the chemical or analyte to be measured through the skin or hair. This method is most useful for detecting analytes which are generally present in relatively constant blood concentrations. The method is particularly useful for the detection of heavy metals such as lead, lithium, copper, iron, and has been demonstrated to be useful with drugs such as cocaine and acetominaphen, and metabolic analytes like blood glucose. In the preferred embodiment, the method involves the use of the water miscible solvent N-methyl pyrrolidone (NMP) in an aqueous solution which is incorporated into an adsorbent pad or hydrogel.

Abstract: A method of determining the reaction efficiency of a CVD process reactor by which a reactive gas combination entering the reactor deposits a solid reaction product as a thin film onto a substrate. The composition of the reactive gas combination is measured by an acoustic cell which is disposed downstream from the outlet port of the reactor to determine the reactor's efficiency. Determination of the reactor's efficiency allows the growth rate of the thin film to be determined as well as associated rates of the products which have been exhausted from the reactor.

Abstract: The present invention relates to sensors for the determination of organometallic compounds comprising the following elements:

Abstract: This invention generally relates to the detection, determination, and quantitation of certain ions and small molecules involving the quenching of a fluorescent label attached to a macromolecule, often due to fluorescence energy transfer to a colored inhibitor or certain metal ions bound to the macromolecule.

Abstract: Apparatus (1) for testing items of metal such as jewelry comprises a housing (3) which is closed at one end (3a) and partly open at the other end (3b). Sealed within the housing is an insert comprising a reservoir (5) containing a testing chemical and an applicator (7). The applicator extends into the reservoir (5) and projects from the housing through its partly open end (3b). The outer surface of the applicator (7) projecting from the housing forms a tip which is used to apply the testing chemical to the surface of the metal under test.

Abstract: This invention generally relates to the detection, determination, and quantitation of certain ions and small molecules involving the quenching of a fluorescent label attached to a macromolecule, often due to fluorescence energy transfer to a colored inhibitor or certain metal ions bound to the macromolecule.

Abstract: A method for detecting a substance in a liquid sample involves precipitating a substance from the liquid sample and filtering it from the liquid sample. The precipitate is then tested for the substance of interest by contacting the precipitate with a dye that forms a visible reaction when exposed to the substance. A releasing agent may be used after filtering the precipitate and prior to testing the precipitate with a dye. In another embodiment, the sample is filtered without the prior use of a precipitating agent.

Abstract: The present invention relates to a method of detecting harmful components selected from the group consisting of volatile inorganic hydrides, volatile inorganic halides and organometallic compounds. The harmful components can be detecting by bringing it into contact with a crystalline cupric hydroxide. The harmful components can be detected based on the color change of the copper hydroxide.

Abstract: The present invention provides a highly effective method for determining very low concentrations of heavy metals such as lead, cadminum, mercury, and copper in body fluids. Ratios of d-5'-N/Pyr-5'-N activities which display greater deviation and stronger correlation with blood heavy metal concentrations than absolute Pyr-5'-N activities alone, are utilized to provide a highly sensitive, internally controlled biomarker of low-level lead overburden, for example.

Abstract: The present invention provides a method of improving the sensitivity and accuracy of a lead assay. The method enhances the recovery of lead during isolation of the lead from interfering compounds by maintaining the lead in a sample solution and making the recovered lead available for detection by the assay. An enhancing reagent complexes with the lead isolated in the sample solution. The enhancer includes a chelator having a lead equilibrium binding constant in the range of about 4 log K to about 13 log K. A kit for performing such a lead assay is also provided.

Abstract: The present invention provides a method of improving the sensitivity and accuracy of a lead assay. The method enhances the recovery of lead during isolation of the lead from interfering compounds by maintaining the lead in a sample solution and making the recovered lead available for detection by the assay. An enhancing reagent complexes with the lead isolated in the sample solution. The enhancer includes a chelator having a lead equilibrium binding constant in the range of about 4 log K to about 13 log K. A kit for performing such a lead assay is also provided.

Abstract: Detection of lead present in a sample, comprising the steps of: (a) adding a lead recovery agent to an assay solution containing lead from the sample; (b) adding to the assay solution a disulfide enzyme which is inhibited in the presence of lead; and (c) correlating the activity of the disulfide enzyme to the amount of lead in the sample. The lead recovery agent enhances the sensitivity and accuracy of the assay such that the assay can be readily automated for detection of lead in whole blood using commercially available automation systems.

Abstract: The invention provides method and kits for detecting a metallic cation in a sample of a body fluid. The preferred method and kits include the use of at least two different types of antibodies having different specificities. In the preferred method, the sample of body fluid can be contacted with an effective amount of a capture antibody specific for a naturally occurring polypeptide that can bind the metallic cation to form a first antigen-antibody complex. An effective amount of an antibody specific for an epitope on a metallic cation-naturally occurring polypeptide complex or an antibody specific for a metallic cation is added to the first antigen-antibody complex to form a second antigen-antibody complex. The amount of the metallic cation in the sample of body fluid is determined by detecting the amount of the second antigen-antibody complex.

Abstract: The process of preparing higher aluminum alkyls by olefin chain growth on alkyl aluminum is improved by using on-line flow-through calorimetry to determine the aluminum concentration of a process stream, such as the aluminum alkyl feed stream, by reacting a sample portion of the process stream with a molar excess of alcohol and measuring the change in temperature. The aluminum concentration of the stream can then be adjusted as required to maintain it within a selected range.

Abstract: A swab is impregnated with a test reagent such that a test for a specific substance can be effected by rubbing the impregnated swab over the surface to be tested and then viewing the swab for a reagent reaction. A method for testing for a substance includes impregnating a swab with a reagent, and rubbing the swab over a surface suspected of containing the substance. If the substance is present in the surface, a reaction with the substance produces an easily detectable color on the swab tip.

Abstract: A method for purifying an aqueous intrinsic factor solution which contains R-protein is disclosed. The method involves adding to the intrinsic factor solution an amount of colloidal silica to disperse lipid emulsion, an amount of cobinamide sufficient to bind substantially all of the R-protein in the solution and an amount of an intrinsic factor affinity resin sufficient to bind the intrinsic factor in the solution, washing the bound cobinamide and the R-protein from the resin, eluting the intrinsic factor from the resin, and dialyzing the eluted intrinsic factor. The purified intrinsic factor possesses less than 0.004 percent cross reactivity with cobinamides, and at least 95 percent of the proteins in the purified material can bind cobalamins. A conjugate of microparticles and the purified intrinsic factor is also disclosed, as is a kit for conducting an assay for cobalamins which includes a conjugate of microparticles and purified intrinsic factor.

Abstract: A portable test kit for colorimetric analysis of trace levels of dithizone-complexing metal cations including lead, is provided. The test kit includes storage tubes each of which contains the reagents and apparatus required for a single test, and has sufficient volumetric capacity to serve as a vessel for the formation and extraction of colored, metal cation-dithizonate complex. Use of the test kit involves a novel and unique sampling technique for capturing a portion of a colored liquid within a container for viewing of the color. Also provided is an improved method for analyzing for trace levels of such metal cations.

Abstract: There is disclosed a measurement reagent for a human Cu.Zn-superoxide dismutase (SOD) which comprises an anti-human Cu.Zn-SOD monoclonal antibody labelled with an enzyme, a method for measuring a human Cu.Zn-SOD which comprises measuring the human Cu.Zn-SOD with the measurement reagent for the human Cu.Zn-SOD, and an anti-human Cu.Zn-SOD monoclonal antibody by the enzyme-linked immunosorbent assay according to the sandwich method, a diagnostic test drug for a human cancer of the stomach which comprises the measurement reagent and a method for diagnosing and testing a human cancer of the stomach which comprises measuring the human Cu.Zn-superoxide dismutase with the measurement reagent, and an anti-human Cu.Zn-superoxide dismutase monoclonal antibody by the enzyme-linked immunosorbent assay according to the sandwich method.

Abstract: A method for detecting the presence of carboxylic acids in a specimen is provided. A specimen is contacted with a developing system containing a metal salt reactive with carboxylic acids present in the specimen to form metal-carboxylic acid complexes. Any such complexes are colorimetrically detected by their activity in catalyzing oxidation of a chromogen such as guaiac. The method is useful in detecting intestinal helminth infestation.

Abstract: A gas concentration measuring method comprises irradiating a sample gas with ultraviolet light in the presence of oxygen, thereby converting a specific gas for detection contained in the sample gas into fine oxide particles by photochemical reaction, irradiating the sample gas having the fine oxide particles contained therein with light, and detecting scattered light emitted from the fine oxide particles contained in the sample gas.

Abstract: A method of analyzing a volatile, air or moisture sensitive or pyrophoric, liquid, organometallic compound for an impurity comprising inserting a sample of the compound into an exponential dilution flask, allowing substantially the entire sample to vaporize, and analyzing the vapor by plasma spectroscopy; or decomposing the sample by dropwise addition into frozen aqueous acid, diluting the decomposed sample with water, and analyzing the diluted, decomposed sample by plasma spectroscopy.

Abstract: The presence of volatile metal carbonyls, e.g., nickel tetracarbonyl and iron pentacarbonyl, in fluid streams can be measured simultaneously by a gas chromatograph using squalane as the stationary liquid phase and a constant current, electron capture detector.

Abstract: An extractant system comprising (a) a high molecular weight alkylaromatic sulfonic acid and (b) a chelating amine having a pKa of from about 3 to about 9 in a solvent which is essentially immiscible with water, said system being useful for the selective extraction of desired metals, e.g., cobalt, nickel or copper ions from aqueous acidic ore leach liquors.