Other

The United States of America As Represented by the United States

Becton Dickinson and Company Limited

Reynolds Metals Company

Arch Development Corporation

Solomon Zaromb

Joseph R Stetter

Dennis J Martell

Isaac Ray

William R Penrose

Lawrence Spritzer

Takaaki Otagawa

Melvin W Findlay, Jr

Daniel B Lawson

Ralph M Bozen

To alleviate and possibly even reverse global warming while providing a liquid fuel to replace petroleum, apparatus and methods are disclosed for capturing COfrom an air mixture and converting it to a useful substance, especially a methanol-containing fuel, utilizing preferably an MgO-loaded cartridge, which is converted partly into MgCOas it captures COby a carbonation reaction and is reconverted into MgO by a calcination reaction while emitting a stream of substantially pure CO. The emitted COstream is reacted with hydrogen or water to yield a methanol-containing fuel or other useful chemical agent. The hydrogen is preferably derived from water electrolysis using inexpensive solar or wind driven electricity thereby also reducing the cost of such electricity by providing an economical energy storage means. Said air mixture may be the effluent from an internal combustion engine of a motor vehicle or from other fossil fuel burning sources or from the ambient atmosphere. The catalytic combination of hydrogen with COto form methanol can provide a new global environmentally beneficial fuel whose burning will not contribute to any net increase in the atmospheric COburden.

Apparatus and methods for carbon dioxide capture and conversion

Apparatus and methods for detecting the presence of an airborne chemical or biological analyte utilise:a substantially gas- and liquid-impermeable container; means for introducing a substantially analyte-free collection liquid into said container; means for rapidly sampling ambient air and transferring said analyte therefrom into said collection liquid, said sampling means comprising an air intake means and and an air venting means; and-means for removing from said container an analyte-enriched collection liquid; wherein said volume of air passes through a substantially horizontal air inlet and upwardly through a substantially vertical collector electrode tube with means for applying an electric field between said tube and a co-axial spiked wire- or rod-shaped discharge electrode.

Aerosol collection apparatus and methods

Apparatus and methods for detecting the presence of an airborne chemical or biological analyte utilize: Efficient wet electrostatic precipitation with efficient collection of captured particles into a tiny liquid volume are achieved by the use of a liquid flow system comprising a programmable reversible pump with a reversible filter and appropriate liquid connections and valves. Injection of water sprays into the air stream and onto the interior walls of the collector electrode permits thorough wetting of interior surfaces and efficient removal of residual captured particles.

Aerosol collection apparatus and method

Air is sampled at a rate in excess of 100 L/min, preferably at 200-300 L/min, so as to collect therefrom a substantial fraction, i.e., at least 20%, preferably 60-100%, of airborne particulates. A substance of interest (analyte), such as lead, is rapidly solubilized from the the collected particulates into a sample of liquid extractant, and the concentration of the analyte in the extractant sample is determined. The high-rate air sampling and particulate collection may be effected with a high-throughput filter cartridge or with a recently developed portable high-throughput liquid-absorption air sampler. Rapid solubilization of lead is achieved by a liquid extractant comprising 0.1-1 M of acetic acid or acetate, preferably at a pH of 5 or less and preferably with inclusion of 1-10% of hydrogen peroxide. Rapid determination of the lead content in the liquid extractant may be effected with a colorimetric or an electroanalytical analyzer.

Apparatus and methods for monitoring the concentrations of hazardous airborne substances, especially lead

The presence of carcinogens in air, soils, and other areas is detected by combining liquid-assisted air sampling with means for testing liquid samples for mutagenicity. Hazardous or illicit substances or pathogens which may be buried in the ground or otherwise concealed or present in contaminated food at various stages of food processing are detected using a two-line probe such that one of the lines directs exhaust air from the sampler onto suspect surfaces so as to dislodge and blow off droplets, particles or insects therefrom while the other line draws some of them into the sampler. Variants of said two-line probe can also serve to collect lead, hexavalent chromium or other harmful substances and bacterial, fungal or viral pathogens from crumbling walls or floors. Liquid-assisted air sampling can also serve to capture disease-transmitting insects and detect and identify insect-borne pathogens.

Methods for the detection of harmful substances or traces thereof

Apparatus for the detection of harmful substances or traces thereof

Apparatus and methods for detecting selected chemical compounds in air or other gas streams at room or ambient temperature includes a liquid-free humidity-resistant amperometric sensor comprising a sensing electrode and a counter and reference electrode separated by a solid electrolyte. The sensing electrode preferably contains a noble metal, such as Pt black. The electrolyte is water-free, non-hygroscopic, and substantially water-insoluble, and has a room temperature ionic conductivity &gE;10,(ohm-cm),, and preferably &gE;0.01 (ohm-cm),. The conductivity may be due predominantly to Ag&plus; ions, as in Ag,WO,.4AgI, or to F&minus; ions, as in Ce,Ca,F,. Electrical contacts serve to connect the electrodes to potentiostating and detecting circuitry which controls the potential of the sensing electrode relative to the reference electrode, detects the signal generated by the sensor, and indicates the detected signal.

Humidity-resistant ambient-temperature solid-electrolyte amperometric sensing apparatus and methods

A portable high-throughput liquid-absorption air sampler [PHTLAAS] has an asymmetric air inlet through which air is drawn upward by a small and light-weight centrifugal fan driven by a direct current motor that can be powered by a battery. The air inlet is so configured as to impart both rotational and downward components of motion to the sampled air near said inlet. The PHTLAAS comprises a glass tube of relatively small size through which air passes at a high rate in a swirling, highly turbulent motion, which facilitates rapid transfer of vapors and particulates to a liquid film covering the inner walls of the tube. The pressure drop through the glass tube is &lt;10 cm of water, usually &lt;5 cm of water. The sampler's collection efficiency is usually &gt;20% for vapors or airborne particulates in the 2-3.mu. range and &gt;50% for particles larger than 4.mu.. In conjunction with various analyzers, the PHTLAAS can serve to monitor a variety of hazardous or illicit airborne substances, such as lead-containing particulates, tritiated water vapor, biological aerosols, or traces of concealed drugs or explosives.

High-throughput liquid-absorption air-sampling apparatus and methods

A system for detecting trace concentrations of an analyte in air includes a preconcentrator for the analyte and an analyte detector. The preconcentrator includes an elongated tubular container comprising a wettable material. The wettable material is continuously wetted with an analyte-sorbing liquid which flows from one part of the container to a lower end. Sampled air flows through the container in contact with the wetted material with a swirling motion which results in efficient transfer of analyte vapors or aerosol particles to the sorbing liquid and preconcentration of traces of analyte in the liquid. The preconcentrated traces of analyte may be either detected within the container or removed therefrom for injection into a separate detection means or for subsequent analysis.

High-throughput liquid-absorption preconcentrator sampling methods

Apparatus and methods for detecting selected chemical compounds in air or other gas streams at room or ambient temperature includes a liquid-free humidity-resistant amperometric sensor comprising a sensing electrode and a counter and reference electrode separated by a solid electrolyte. The sensing electrode preferably contains a noble metal, such as Pt black. The electrolyte is water-free, non-hygroscopic, and substantially water-insoluble, and has a room temperature ionic conductivity .gtoreq.10.sup.-4 (ohm-cm).sup.-1, and preferably .gtoreq.0.01 (ohm-cm).sup.-1. The conductivity may be due predominantly to Ag+ ions, as in Ag.sub.2 WO.sub.4.4AgI, or to F- ions, as in Ce.sub.0.95 Ca.sub.0.05 F.sub.2.95. Electrical contacts serve to connect the electrodes to potentiostating and detecting circuitry which controls the potential of the sensing electrode relative to the reference electrode, detects the signal generated by the sensor, and indicates the detected signal.

Humidity-resistant ambient-temperature solid-electrolyte amperometric

A process for recovering zinc/rich and iron-rich fractions from the baghouse dust that is generated in various metallurgical operations, especially in steel-making and other iron-making plants, comprises the steps of leaching the dust by hot concentrated sulfuric acid so as to generate dissolved zinc sulfate and a precipitate of iron sulfate, separating the precipitate from the acid by filtration and washing with a volatile liquid, such as methanol or acetone, and collecting the filtered acid and the washings into a filtrate fraction. The volatile liquid may be recovered distillation, and the zinc may be removed from the filtrate by alternative methods, one of which involves addition of a sufficient amount of water to precipitate hydrated zinc sulfate at 10.degree. C., separation of the precipitate from sulfuric acid by filtration, and evaporation of water to regenerate concentrated sulfuric acid. The recovery of iron may also be effected in alternative ways, one of which involves roasting the ferric sulfate to yield ferric oxide and sulfur trioxide, which can be reconverted to concentrated sulfuric acid by hydration. The overall process should not generate any significant waste stream.

Hydrometallurgical process for recovering iron sulfate and zinc sulfate

High throughput liquid absorption preconcentrator sampling instrument

A method of gathering a library of response patterns for one or more sensor arrays used in the detection and identification of chemical components in a fluid includes the steps of feeding samples of fluid with time-spaced separation of known components to the sensor arrays arranged in parallel or series configurations. Modifying elements such as heating filaments of differing materials operated at differing temperatures are included in the configurations to duplicate operational modes designed into the portable detection systems with which the calibrated sensor arrays are to be used. The response patterns from the known components are collected into a library held in the memory of a microprocessor for comparison with the response patterns of unknown components.

Method and system for gathering a library of response patterns for

A method capable of detecting low concentrations of a pollutant or other component in air or other gas, utilizing a combination of a heating filament having a catalytic surface of a noble metal for exposure to the gas and producing a derivative chemical product from the component, and an electrochemical sensor responsive to the derivative chemical product for providing a signal indicative of the product. At concentrations in the order of about 1-100 ppm of tetrachloroethylene, neither the heating filament nor the electrochemical sensor is individually capable of sensing the pollutant. In the combination, the heating filament converts the benzyl chloride to one or more derivative chemical products which may be detected by the electrochemical sensor.

Method for detecting toxic gases

A system for detecting trace concentrations of an analyte in air and includes a preconcentrator for the analyte and an analyte detector. The preconcentrator includes an elongated tubular container in which is disposed a wettable material extending substantially the entire length of the container. One end of the wettable material is continuously wetted with an analyte-sorbing liquid, which flows to the other end of the container. Sample air is flowed through the container in contact with the wetted material for trapping and preconcentrating the traces of analyte in the sorbing liquid, which is then collected at the other end of the container and discharged to the detector. The wetted material may be a wick comprising a bundle of fibers, one end of which is immersed in a reservoir of the analyte-sorbing liquid, or may be a liner disposed on the inner surface of the container, with the sorbing liquid being centrifugally dispersed onto the liner at one end thereof. The container is preferably vertically oriented so that gravity effects the liquid flow.

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Hinsdale, IL, United States of America

Solomon Zaromb