Abstract: A heat generation amount qr/r per unit flow amount of combustible substances supplied to a catalyst is estimated based on upstream and downstream temperature information and supplemental engine information. A deteriorated condition of the catalyst is detected based on a judgement whether or not the estimated heat generation amount is smaller than a predetermined judging value D.

Abstract: The invention relates to equipment for pretreatment of catalysts and/or catalytic testing that makes it possible to establish the material balance of a chemical reaction in the presence of very small amounts of solid catalyst under operating conditions of industrial use.

Abstract: Disclosed herein is a nebulizer capable of performing spraying over a wide flow-rate range from a low flow rate to a high flow rate stably and with high efficiency. Further, the present invention provides a supersonic nebulizer capable of improving the efficiency of spraying by a supersonic region spray gas, and a supersonic array nebulizer wherein a plurality of spray units are placed in array form.

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: A method and apparatus are provided for collecting a sample gaseous mercury, to differentiate between different gaseous mercury components. A quartz denuder module is provided having a coated extended surface for adsorbing reactive gaseous mercury. After collection of a sample, the coating it is heated to desorb the mercury as elemental gaseous mercury, which can then be detected and measured in conventional analyzer. During the sampling phase, as reactive gaseous mercury is removed from the sample flow in the denuder, the sample can then be passed to the analyzer for detection of elemental gaseous mercury. Where particulate mercury may be present, a filter trap can be provided downstream from the denuder. Separate steps can be provided for heating and pyrolysis of particulate mercury, for separate measurement in the analyzer. The pump module can be configured to a past the gas sample through scrubbers, to generate zero air as a flushing gas.

Abstract: The present invention comprises a sample presentation apparatus for mass spectrometry. More particulary, a complex is immoblized on the sample presenting surface.

Abstract: A more efficient combustion or oxidation device for the formation of nitrogen, phosphorus and/or sulfur oxides from a sample containing these elemental constituents is disclosed. The device uses multi-staged addition of an oxidizing agent to enhance oxidation and liberation of nitrogen, phosphorus and/or sulfur oxides for subsequent detection. The oxidation devices of the present invention allow for the injection of larger samples or, the introduction of a greater amount of sample per unit of time which results in a larger amount of analyte being delivered to the detector per unit of time, thereby improving detection limits and detection efficiency.

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

Abstract: An ultrapure water trap is provided for retaining condensed water of water vapor which is formed in a TC oxidative reaction part, and a passage is so connected that an automatic sample injector can collect ultrapure water from the ultrapure water trap for injecting the same into the TC oxidative reaction part. The automatic sample injector dilutes ordinary pure water which is outside this apparatus with the ultrapure water which is retained in the ultrapure water trap, thereby preparing a test solution having ultralow carbon concentration of not more than 50 ppbC in the interior of a TOC meter.

Abstract: This invention provides devices for the measurement of total organic carbon content in water samples. The device has a microfluidic sample cell with a sample channel for receiving a water sample wherein the water sample can be irradiated with UV radiation to oxidize organics to CO2. The sample channel is sufficiently thin in the region irradiated to allow very rapid substantial mineralization of the organics in the sample. A photocatalyst, such as TiO2 or platinized TiO2 can be employed to speed sample oxidation. Substantial mineralization of a sample can be achieved in less than about 30 seconds, significantly decreasing the time required for making a TOC measurement. CO2 generated by sample oxidation can be detected and/or quantitated by various methods, particularly by conductivity measurements or by infrared methods.

Abstract: Ozone-splitting catalytic converters can be monitored through the use of conductivity sensors for detecting ozone. Since such sensors rapidly attain operational readiness have low source sensitivities to other gases, and an adequate service life, they can be used in practical applications. Different methods of operation are capable of optimizing the ratio between ozone sensitivity and transverse axis sensitivity of the sensors.

Abstract: A photothermal absorbance detection apparatus for performing absorbance measurements of analytes in capillaries having non-conductive walls comprises a light source and a conductivity detection device. The conductivity detection device includes an applied voltage source and at least two electrodes disposed adjacent to the walls of a section of capillary. By using the light source to heat the analytes, the resulting change in conductivity of the liquid containing the analytes can be detected in the liquid. A measurement of absorbance can then be obtained as a function of the change in conductivity.

Abstract: Total organic carbon in an aqueous or gaseous sample is measured by admitting the sample and an oxidant gas to a cell transparent to plasma, establishing a relatively low energy plasma in the cell, and measuring the CO2 thus produced using FTIR, NDIR, or conductivity-based techniques.

Abstract: There was previously no monitoring method and monitoring apparatus which could measure dioxins at ppt levels and dioxin precursors at ppb levels with high sensitivity.

Abstract: A carbon analyzer, is provided which includes a combustion chamber having a platinum on titania catalyst. The combustion chamber and catalyst are also provided. A method for analyzing carbon-containing specimens with such an analyzer is also provided as well as a method for oxidizing such specimens with a platinum on titania catalyst. A method of conditioning the catalyst is also provided.

Abstract: A photometer including an elongated sample cell having a first end, a second end, and a passageway extending between the first end and the second end. Preferably, a ratio of a length of the sample cell to a lateral dimension of the passageway is at least 100 to 1. A first quartz window assembly is located at the first end of the sample cell and has a first port communicating with the passageway proximate to the first end, and a second quartz window assembly is located at the second end of the sample cell and has a second port communicating with the passageway proximate to the second end. An ultraviolet lamp is positioned to emit ultraviolet light through the first quartz window, the passageway, and the second quartz window, and an ultraviolet detector is positioned to receive the ultraviolet light emanating from the second quartz window. Preferably, the sample cell is operated at about ambient temperature, and the volume of the sample cell is no greater than about 0.

Abstract: A headspace instrument (10, 70) operates to equilibrate a vapor phase of a headspace sample in a sample loop (40, 74). The sample is equilibrated by flow through the headspace between variable volume chambers (28, 50, 86, 90). The volume of the variable volume chambers are changed in coordinated relation so that a constant total volume is always maintained. An aliquot of the equilibrated sample in the sample loop is delivered to an analytical instrument. The headspace instrument enables delivering a vapor sample from a headspace under conditions which do not disturb the thermodynamic equilibrium between the vapor phase and the non-vapor phase of the sample and avoids having the sampling process impact the results of the analysis. Alternative forms of the headspace instrument enable the conduct of concentration dependent processes and absorption and desorption experiments.

Abstract: Thin film thermal oxidative engine oil or other oleaginous liquid deposit device has an oleaginous test liquid placement volume; a heatable depositor surface in liquid communication with the volume; a supply for at least one of an oxidant and another substance which can adversely affect the test liquid; and a relatively thin film forming unit which delivers the test liquid to the depositor surface in a relatively thin film. Thin film thermal oxidative engine oil or other oleaginous fluid deposit method is also provided, which includes providing an oleaginous test liquid in an oleaginous test liquid placement volume; providing a depositor surface and heating said surface; delivering the test liquid as a relatively thin film to the heated depositor surface; providing to the test liquid an oxidizing and/or other substance which can adversely affect the test liquid; and observing any deposits or other activity thereabout. The invention is useful in oil testing.

Abstract: An article, apparatus and method for simulating poisoning and deactivating catalysts with catalyst poison compounds at least one catalyst poison compound selected from the group consisting of a compound comprising phosphorous, a compound comprising zinc compound and a compound comprising phosphorous and zinc.

Abstract: A system for quantitative determination of the local distribution of a quantity to be measured, comprising a planar sensor film, which is applied to a measuring surface, such as the surface of a body organ, a skin area or a cell culture, and whose diffusion properties regarding a parameter to be determined are known. The sensor film contains a luminescent indicator responding to the parameter to be determined with a change of at least one optical property. The system further comprises an excitation and detection unit including means for supplying excitation radiation of at least one wavelength, an imaging detection means, preferably a CCD camera, and an evaluation unit processing the image information obtained from the excitation and detection unit. Further provided is an applicator tube to be placed on the measuring surface, whose rim facing the measuring surface is in elastic contact with the sensor film and is impervious to external radiation interfering with the detection means.

Abstract: An ultratrace detector system for hand-held gas chromatography having high sensitivity, for example, to emissions generated during production of weapons, biological compounds, drugs, etc. The detector system is insensitive to water, air, helium, argon, oxygen, and CO2. The detector system is basically composed of a hand-held capillary gas chromatography (GC), an insulated heated redox-chamber, a detection chamber, and a vapor trap. For example, the detector system may use gas phase redox reactions and spectral absorption of mercury vapor. The gas chromatograph initially separates compounds that percolate through a bed of heated mercuric oxide (HgO) in a silica—or other metal—aerogel material which acts as an insulator.

Abstract: After sintering of a CO sensor using an SnO2-based metal oxide semiconductor, Ir and Pt are added to the sensor at 5˜500 &mgr;g/g SnO2 each, the weight ratio of Ir and Pt being 5˜1/5. This addition is made by impregnating a mixed aqueous solution of an Ir salt and a Pt salt into the SnO2 sintered body and thermally decomposing these salts. Next, an aqueous solution of thiourea is impregnated into the SnO2 sintered body to add thiourea at 0.01˜10 mg/g SnO2 in reduction to simple S element. The temperature and humidity dependency of the CO sensor is suppressed, the CO concentration dependency of the output is increased, and the sensor resistance is brought to a more convenient range of use.

Abstract: The invention relates to a device for pyrolysis gas chromatography, consisting of a carrier gas supply (1), a commercially available gas chromatography (GC) separating capillary (2) and a detector (3), which device is characterized in that upstream of said GC separating capillary (2), a metal capillary (4) connected to a power supply for direct heating is arranged as pyrolyzator and forms an integral part of the carrier gas train, whereby the metal capillary (4) is connected with the GC separating capillary (2) through an interface (6) and the inner diameter of the metal capillary (4) is from 0,32 to 1 mm.

Abstract: The invention concerns an apparatus comprising an intake scoop (2) for the gas sample to be analyzed and, coaxial to said scoop (2): two tubular sleeves (4) defining respectively an intake chamber (5) for an oxygen carrier gas opening into a first combustion chamber (8), and an intake chamber (11) for an oxidant gas opening into a second combustion chamber (9); a pair of electrodes (14) associated with a circuit (21) measuring the conductivity of a combustion zone located in the second combustion chamber (9) and focusing optics (19) focusing the image of the flame generated in the combustion chambers (8, 9) on the input orifice of a spectrophotometer (20); a processor (25) processes the data from the circuit (21) and from the spectrophotometer (20) to deduce therefrom the concentration in the searched elements. The invention is particularly useful for detecting sulphur, phosphorus and organic compounds.

Abstract: The present invention relates to a catalyst characterization apparatus, and in particular to an improved catalyst characterization apparatus which is capable of characterizing the surface of a catalyst more accurately by a volumetric method without requiring a pre-treatment step which may vary the characteristics of the catalyst as well as without exposing the catalyst in air, by combining a dynamic flow type reactor with a volumetric type adsorption apparatus, whereby it is possible to accurately characterize the catalyst during an actual reaction. It is possible to accurately characterize the various catalysts and to characterize the catalyst during the reaction, alternately and/or continuously, by combining a dynamic flow type reactor with a volumetric type characterization apparatus as well as a dynamic flow type characterization apparatus.

Abstract: Elemental analysis of a sample is carried out in an oxygen atmosphere in a combustion reactor and the volume of oxygen required for analysis is determined by means of the algorithm

Abstract: Described is apparatus and a process for analyzing a volatile composition such as a perfume composition located on the surface and/or in the interstices of a planar pliable porous substrate such as a towel section. A planar surface of the substrate which contains the volatile composition is initially juxtaposed adjacent a solid wall (e.g., glass frit) porous to a nonreactive carrier gas such as air, nitrogen or carbon dioxide, and fully and tightly covers the porous section of the wall. The carrier gas is passed through the porous section of the wall and then through the pliable porous substrate section which is adjacent to the wall; after which the carrier gas contains molecules of each component of the volatile composition. The composition-carrier gas mixture is then passed through a trapping substance (e.g., TENAX®) which entraps the molecules of each component of the volatile composition. The volatile composition is then analyzed (e.g.

Abstract: Disclosed are a closed heat-decomposing appliance comprising a heating section with one side closed and other side having common ground portion, screw portion or O-ring-mounted portion and a closed introducing section that allows to connect to this heating section and common ground portion, screw portion or O-ring via O-ring-mounted portion and has cock or valve as a mechanism for closing and introducing the absorbing liquid to absorb the testing components from outside after heat-decomposition, or has packing or septum to introduce the absorbing liquid with needle pipe as well, and a pretreatment method of sample using this appliance.

Abstract: The present invention provides apparatuses and processes for the measurement of hydrogen in aqueous solution at concentrations as low as about 0.1 nM. The present invention is capable of accurately and reproducibly measuring the concentration of dissolved hydrogen in an aqueous solution that also contains other dissolved gases, such as oxygen, carbon monoxide and sulfur compounds, such as hydrogen sulfide. In a presently preferred embodiment of a hydrogen analyzer 38 of the present invention, water containing dissolved hydrogen is equilibrated with a carrier gas by means of gas flow through a mass transfer device 10.

Abstract: A method and apparatus are provided for collecting a sample gaseous mercury, to differentiate between different gaseous mercury components. A quartz denuder module is provided having a coated extended surface for adsorbing reactive gaseous mercury. After collection of a sample, the coating it is heated to desorb the mercury as elemental gaseous mercury, which can then be detected and measured in conventional analyzer. During the sampling phase, as reactive gaseous mercury is removed from the sample flow in the denuder, the sample can then be passed to the analyzer for detection of elemental gaseous mercury. Where particulate mercury may be present, a filter trap can be provided downstream from the denuder. Separate steps can be provided for heating and pyrolysis of particulate mercury, for separate measurement in the analyzer. The pump module can be configured to a past the gas sample through scrubbers, to generate zero air as a flushing gas.

Abstract: A method and apparatus for detection of multiple target nucleic acids and/or antigens such as hormones, antibodies, or nerve agents in a sample, involves presenting the sample to a plurality of reporter binding sites wherein each reporter binding site comprises two partially hybridized molecules. A first of the two hybridized molecules is bound to the binding site and is complementary to a target nucleic acid or antigen, and it will therefore hybridize to the target nucleic acid or antigen and cause the release of the second hybridized molecule into the sample. The second hybridized molecule comprises a reporter nucleic acid sequence, which uniquely identifies the target nucleic acid or antigen. Subsequent PCR amplification of the unique reporter nucleic acid sequence using labeled primers results in multiple labeled copies of the unique nucleic acid sequence.

Abstract: Gases flow to individual gas analysis cells. The cells are sequentially aligned with an infrared detector, which senses the composition and quantities of the gas components. Each elongated cell is tapered inward toward the center from cell windows at the ends. Volume is reduced from a conventional cell, while permitting maximum interaction of gas with the light beam. Reduced volume and angulation of the cell inlets provide rapid purgings of the cell, providing shorter cycles between detections. For coal and other high molecular weight samples, from 50% to 100% oxygen is introduced to the tubes. Cells are suspended from adjustable holders on a frame which is spaced from a table. The table is moved by a linear motor and a fixed platen. Sides of the table are shielded to prevent electromagnetic and magnetic motor interference with detected results. The entire table, cells, mounting plate and linear motor are mounted in a housing with aligned holes for the analysis energy source and detector.

Abstract: The invention relates to a sample application device for a gas chromatograph, having an evaporator (1) which can be cooled, can be heated in a temperature-controlled manner, is provided with a carrier-gas feed and has a valve head (11) for holding an exchangeable sampling tube (27), a receiving chamber (4) for the sampling tube (27), a column exit (18) and, if appropriate, a splitter exit (31). In this device, a pyrolyser tube (20), which is coupled to the carrier-gas feed and is held by the valve head (11), is arranged in the receiving chamber (4), in which there is a heating coil (26) into which the sampling tube (27) can be fitted and to which current can be applied by means of a heating conductor (25) which is guided outwards through the valve head (11).

Abstract: A flame ionization detector burner, includes a housing having a generally cylindrical flame cavity therein extending along a generally longitudinal axis of the housing and a housing exterior with intake passageways communicating between the housing exterior and the flame cavity for passing fuel, air and sample flows into the flame cavity and an exhaust passage communicating between the housing exterior and the flame cavity for passing exhaust gasses out of the flame cavity. A burner carried in the housing cavity receiving the fuel, air, and sample flow generates a flame to ionize the sample. An ion collector plate spaced away from the burner carried in the time cavity collects sample ions and provides an electrical output representative of the sample ions to the housing exterior via an electrical feedthrough between the flame cavity and the housing exterior. The housing includes at least two cylindrical sidewalls removably joined together along the general longitudinal axis of the housing.

Abstract: Apparatus and methods for determining the content of total organic carbon, total inorganic carbon, total carbon and total heteroorganic carbon in water are disclosed. In a preferred comprehensive embodiment, the water sample is split into a first stream and a second stream. Inorganic carbon in the first stream, if any, is determined by acidifying the sample, measuring the electrical conductivity using a temperature and conductivity sensor, and removing the ionic species. Organic carbon in the first stream is then substantially completely oxidized in a U.V. oxidation reactor to carbon dioxide and possibly other oxidation products, and the electrical conductivity of the effluent- stream is measured using another temperature and conductivity sensor. At least a portion of the carbon dioxide in the first stream is transferred through a carbon dioxide permeable membrane into the second strewn. The second stream then passes into another temperature and conductivity sensor and conductivity is measured.

Abstract: An apparatus for moving a series of boats loaded with samples into one end of a furnace, testing each sample by heating it to the point where the gases to be analyzed are released and discarding the boat with the remaining ashes, while maintaining the sample and the gasses emitted by the sample free from atmospheric contamination in the furnace. The sample is initially positioned in the furnace by use of a pushing mechanism in the form of a rod driven by a step motor. The boat remain in position after the gasses are driven from the sample, until another sample is introduced. The boat with the new sample pushes the boat with the ashes of the previous sample towards a means for automatic extraction of the boat from the furnace.

Abstract: The present invention enables siloxanes which have a detrimental effect on the quality of products during semiconductor production to be efficiently removed from silicon compound gases, and enables minute amounts of siloxanes in these gases to be accurately measured to a few ppb, thus allowing for improvements in quality control by offering silicon compound gases of high purity. Diatomaceous earth M filled into a removal column 2 is heated by heating means provided on the removal column 2, while an inert gas such as nitrogen or helium is fed from an inert gas delivery pipe 13 via a pressure regulator 5 and an entry valve 6 into the removal-column 2, and is allowed to flow out through an outlet valve 8 in order to thermally activate the diatomaceous earth M. After activation, the removal column is cooled to a temperature of 60-0° C.

Abstract: An improved apparatus and method is disclosed utilizing hydrogen absorption in combination with photolysis and/or electrolysis for in situ generation, i.e., without the need for adding chemical oxidizing agents, or enhancement of oxidizing conditions used to promote oxidation of organic compounds to form carbon dioxide, and the use of the same in connection with high-accuracy determination of even extremely low levels of organic and/or inorganic carbon compounds both in flowing aqueous streams and in bulk solutions.

Abstract: A method for the determination of total organic carbon in an aqueous sample by trapping the organic matter on a sorbent which is carbon free and analyzing the sorbent by combustion and determination of total CO2 by IR.

Abstract: The present invention provides for a hydride formation analytical apparatus which forms hydrides of target components contained in a sample liquid and then analyzes them. The hydride formation analytical apparatus comprises a sample-introducing part, a reagent-introducing part, a reaction part, a gas-liquid separating part and a detecting part, wherein an acid-feeding part and a reducing agent-feeding part are part of the reagent-introducing part; the hydride gas of the sample is formed by the aid of the acid and the reducing agent fed into the above reaction part; and this is introduced into the detecting part for analysis.

Abstract: A method and apparatus for determining nitrification effectiveness of activated sludge in an aqueous solution, includes supplying equivalent quantities of an activated sludge, an aqueous solution, and a gas containing oxygen to each of first and second reaction vessels; simultaneously delivering a nitrification inhibitor to only the second reaction vessel; performing a bacterial respiration reaction in the vessels for either a preselected period of time or continuously in which case the materials are supplied per unit of time so that the bacterial respiration reaction in the first reaction vessel, where oxygen consumption as a result of total bacterial respiration occurs and includes oxygen consumption as a result of endogenous respiration, oxygen consumption as a result of nitrification, and oxygen consumption as a result of degradation of carbon compounds, may be compared with the respiration reaction in the second reaction vessel where oxygen consumption includes oxygen consumption as a result of endogenou

Abstract: A method and apparatus are disclosed for the near simultaneous detection of light emitted from ozone induced chemiluminescence of nitrogen and sulfur species capable of undergoing ozone induced chemiluminescence in a single instrument. A sample containing sulfur and/or nitrogen is first subjected to an oxidative/reductive process which generates ozone reactive nitrogen and sulfur species which are then forwarded to an specially designed ozone/detector chamber. The ozone relative species are brought in contact with ozone in the special chamber and the chemiluminescence of the nitrogen species and the sulfur species are measured and quantitated.

Abstract: A kit is provided for testing a gas produced from a sample for an absolute amount of a hydrogen sulfide. The kit includes a vessel for receiving the sample to be tested. The vessel includes one or more gas flow passages through which gas within the vessel can leave the vessel. The kit also includes one or more testing tubes. Each testing tube includes a lumen through which gas can flow. The lumen includes a column of medium observable from outside the testing tube and has a length which changes in appearance in proportion to the amount of hydrogen sulfide which has passed through the testing tube. Graduations are included on the one or more testing tubes for indicating the length of the column of medium whose appearance has changed. The kit also includes a coupling mechanism for coupling the one or more testing tubes with the one or more gas flow passages such that gas leaving the vessel passes through the one or more testing tubes.

Abstract: An apparatus for measuring material outgassed from an object. The apparatus has a chamber containing the object, a condensed material detector (e.g. a quartz microbalance), a heater for heating the object and chamber, and a cooler for cooling the detector. The chamber is sealed from the ambient atmosphere and the detector is located within the chamber. The chamber may contain a vacuum or a gas at ambient atmospheric pressure. Material outgassed from the object is distributed throughout the chamber by vapor transport and is incident upon the detector, where it condenses. Since the detector is the only cooled surface in contact with the vapors, it collects nearly all the outgassed material. This provides high sensitivity to outgassing. The chamber may also include a mechanical stirring device for aiding vapor transport, or may be oriented so that a thermal convection current is established.

Abstract: To determine the total organic carbon content of a flowing liquid in a continuous process, water and oxidizing agents enter lower ports in a multi-stage column and flow upwardly through residence chambers as they are mixed. Spaced apart along the upper path of the liquid, there are helical reaction grooves relatively shallow and containing at least one helical groove to cause rapid motion of the liquid. An ultraviolet lamp extends downwardly through the center of the column so that the outer confining surface of the helical grooves is the outer surface of the ultraviolet lamp, causing the liquid to move rapidly in intimate contact with the ultraviolet lamp to receive intense radiation. The stages are separate and interchangeable so that selected sizes may interconnect. The residence chambers may have different sizes to permit different lengths of residence time and thus permit tailoring of the reaction to the expected organic carbon content and possible side reactions with other impurities in the water.

Abstract: Apparatus and processes for water impurity analysis and for impurity analysis of various other liquids as well. More particularly, the present invention concerns apparatus and processes for chemical oxidant and catalyst enhanced total organic carbon analysis of liquid samples for determination of the level of organic contamination of the samples. In particular the present invention concerns a novel reactor for TOC anlysis in which carbon, particularly organic carbon is oxidized to CO.sup.2 gas for further measurement by a CO.sub.2 gas detector, preferably a non-dispersive infrared analyzer. The invention also concerns a process for TOC analysis wherein by measuring the CO.sub.2 gas created by combining carbon with oxygen (either in the water, with a carrier gas of oxygen (O.sup.2), or a chemical oxidant, such as sodium persulfate, the carbon in the water sample is determined. A process and apparatus are employed for TOC analysis in which UV light having a wave length in the range of from about 3.8 to about 4.

Abstract: A device for evaluating at least one pollution characteristic of natural soils contaminated by hydrocarbon compounds, said device comprising a first heater heating said sample in a non-oxidizing atmosphere, a measuring device determining an amount of hydrocarbon compounds released after feeding the sample into said first heater, a sample transfer device transferring the sample from the first heater into a second heater operating in an oxidizing atmosphere, a CO.sub.2 measuring device determining CO.sub.2 contained each effluent discharged from the two heaters, said CO.sub.2 measuring device measuring continuously the CO.sub.2 throughout the heating cycle of the first and the second heaters and including a device measuring CO contained in each effluent discharged from the two heaters, a temperature controller controlling the temperature of samples waiting to be fed into said heating means, and a device determining the pollution characteristic.

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

Abstract: Disclosed is a method and apparatus for sampling and determining the presence of certain substances, such as residues of contaminants in containers. The method includes steps of: injecting compressed air into said containers in order to displace at least a portion of the contents thereof; evacuating a sample of the container contents so displaced by applying suction thereto; and analyzing the sample evacuated to determine the presence or absence of the certain residues therein. The compressed air is injected through a nozzle into an opening in the containers to displace a portion of the container contents and form a sample cloud outside of the container. The sample cloud is then at least partially evacuated by suction and the sample is analyzed for the presence of contaminants such as nitrogen containing compounds or hydrocarbons. The sample cloud may be split into first and second portions.

Abstract: An analytical instrument measures carbon content of a liquid sample. The instrument includes a sample inlet, a reagent inlet, a rinsing solution inlet, a reaction chamber, a waste outlet and a syringe pump. A multiple port valve has a plurality of ports which are coupled to the sample inlet, the reagent inlet, the rinse solution inlet, the reaction chamber and the waste outlet. The valve also includes a primary port coupled to the syringe pump and selectively fluidically couplable to each of the remaining ports.