Abstract: A reactor for subjecting multiple reactant samples to controlled conditions with respect to pressure, temperature, and time. All individual samples in a single test run are exposed to the same temperature and pressure profiles but can be independently and selectively quenched at different times during the test run.

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: The invention relates to a method for applying samples to be analyzed by gas chromatography using a sampling tube, which has a section which contains the adsorbing agent and narrows essentially conically towards a bore which is free of adsorbing agent and has a reduced diameter, in such a manner that the flow rate of a gas which is guided through towards the narrowed section on the outlet side is at least approximately equal to the inlet-side flow rate, liquid or gaseous starting sample material being guided through the sampling tube towards the narrowed section, so that substances to be analyzed are adsorbed on the adsorbing agent, the sampling tube being flushed with drying gas, which is guided through the sampling tube in the same direction as the starting sample material, until the liquid phase, which is contained in the sampling tube, or the starting sample material is essentially removed, and the adsorbed sample being desorbed by means of a carrier gas which is introduced through the sampling tube from

Abstract: An apparatus and method for assaying an asphalt-containing composite material by irradiating the sample using a radiation source having a tunable preselected wavelength selected to closely approximate the absorbance wavelength of a particular material or materials found in the composite material to reduce the overall time and temperatures ordinarily needed to combust and assay such samples.

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: A furnace includes an enclosure and a hearth plate within the enclosure for supporting combustible material. The furnace further includes a first heater element adjacent the hearth plate for initial combustion of the combustible material, a filter disposed above the hearth plate for filtering uncombusted products of combustion of the combustible material, and a second heater element adjacent the filter for final combustion of the uncombusted products of combustion filtered by the filter. A filter bypass path has an inlet located in a lower portion of the enclosure and an outlet located between the filter and the second heater.

Abstract: A gas-sampling tube for a flue-gas analysis apparatus having therein a particle filter and a measured gas line downstream of it. A heating jacket comprising an electric heater is located in the gas-sampling tube and extends axially co-extensive with the measured gas line and the particle filter, and in surrounding relation to them.

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.

Abstract: The present invention and its claims encompass principles, methods, apparatus, and applications for detection, quantification, and monitoring of responses of gases, vapors, aerosols, and mixtures thereof to initiators of exothermic reactions. While the invention can be utilized for any concentration level, the intended, normal utilization is for gases in which the concentrations of species capable of participating in exothermic chemistry are too low to support self-sustaining exothermic reactions leading to detonations or deflagrations as well as for gases in which other factors prevent the exothermic reaction chemistry from becoming self-sustaining. This abstract shall not be construed to define or limit in any way the scope of the invention, which is measured by the appended claims.

Abstract: An electrically heatable hollow-body furnace with a secondary surface on which an analyte of a sample can be condensed prior to being atomized. The furnace is constructed in two sections which are capable of being electrically heated independently of one another. The secondary surface is defined by a surface of one of the sections. A process for atomizing an analyte of a sample to be examined, utilizing the device according to the following steps: introducing the sample into a hollow-body furnace having a secondary surface, condensing the analyte on the secondary surface and atomizing the analyte.

Abstract: The invention relates to a method for the quantitative determination of deuterium in samples containing hydrogen, and to a reduction oven for reducing gaseous or liquid substances containing hydrogen, which may be coupled directly to an isotope ratio mass spectrometer (IRMS), thereby permitting an online-coupled, reliable deuterium determination which can be automatized.

Abstract: The object of this invention is to provide an atomic absorptiometer and a metal specimen atomic vapor generation apparatus used in the atomic absorptiometer, which enable a light absorption measurement based on the Zeeman effect highly capable of background correction and eliminate the need for the troublesome work of dismounting a magnet. For this purpose, the following configuration is employed. First, the specimen, hydrochloric acid, and sodium borohydride are delivered and mixed by the peristaltic pump 10 to produce a metallic hydride. The generated gas-liquid mixture solution is separated by the separator 12 into a specimen gas and liquids. The separated specimen gas is introduced into the heating section 30. Electricity is supplied from the power source 28 to the specimen heating section 30 where the specimen gas introduced is heated and separated into hydrogen and a specimen metal vapor to be measured.

Abstract: A method for microwave assisted chemical processes is disclosed that comprises applying sufficient microwave radiation to a temperature-monitored mixture of reagents, with at least one of the reagents being thermally responsive to electromagnetic radiation in the microwave range, and based on the monitored temperature, to maintain the added reagents at or closely about a predetermined temperature while substantially avoiding thermal dilution (or before substantial thermal dilution can occur) that otherwise would have been caused by the addition of the reagents to one another.

Abstract: A device for determining at least one petroleum characteristic of a geologic sediment sample placed in a boat, said device including a first heater heating said sample in a non-oxidizing atmosphere, a measuring component determining hydrocarbon-containing products released after feeding the sample into said first heater, a second subsequent heater heating said sample in an oxidizing atmosphere, a measuring component determining the amount of CO.sub.2 contained in effluents discharged from the two heaters, said CO.sub.2 measuring means include a cell for measuring continuously CO.sub.2 throughout heating of the first and second heaters and a measuring component determining the amount of CO contained in the effluents discharged from the two heaters, and thereby allowing determination of said petroleum characteristic.

Abstract: A method is proposed for the contiuous determination of gaseous oxidation products from industrial process, drinking and/or waste water, particularly for determining the TOC value, at least the organically bound carbon contained in a test solution to be investigated being oxidatively transformed and the gaseous oxidation products are supplied to a measuring unit, where at least the organically bound carbon is detected, the test solution being continuously pumped into a microreactor, where it is heated to a predetermined temperature and the organic compounds in the test solution are continuously oxidatively transformed under a temperature and pressure increased in a defined manner.

Abstract: A dye couple compound is provided for use in a test device containing a reagent system for detecting the presence or quantity of an analyte in a sample. The reagent system comprises one or more enzymes which, in the presence of the analyte, produce an oxidizing agent in quantities indicative of the quantity of analyte in the sample. The compound of choice is meta?3-methyl 2-benzothiazolinone hydrozone!N-sulfonyl benzenesulfonate monosodium.

Abstract: Apparatus and methods for the measurement of total organic carbon, total inorganic carbon and total carbon of water are described. The ample is acidified and split into an inorganic carbon stream and a total carbon stream. The inorganic carbon in the inorganic stream is oxidized and both the organic and inorganic carbon in the total carbon stream is oxidized. The resulting carbon dioxide is measured in each stream using carbon dioxide sensors employing a gas permeable membrane dividing deionized water from the oxidized sample water and a pair of micro-conductivity and temperature sensors.

Abstract: The present invention relates to a system, apparatus, and process to reduce the oxidized mercury in an exhaust gas to elemental mercury and to prevent its reoxidation by congeneric components in the exhaust gas prior to the photometric measurement of said elemental mercury. In the process, the sample stream flows through a reactor heated to preferably about 800.degree. C. in which a stream of hydrogen is introduced directly into a hot portion thereof. The congeneric oxidized mercury species, i.e, HgCl.sub.2, and HgO are thermally reduced quantitatively to elemental mercury. The hydrogen reacts in situ with oxygen to form water vapor and with chlorine to form hydrochloride gas. The hydrochloride gas is effectively absorbed by the water vapor and consequently prevents the reoxidation of elemental mercury. The concentration of total mercury in a stream can then be determined by the intensity of radiation absorbed by a UV spectrometer.

Abstract: An apparatus for sequentially pyrolyzing a plurality of samples held in sample tubes comprises a substantially vertical passage through which tubes carrying the samples may be passed; an upper gas-tight valve for closing off the upper end of the passage; a lower gas-tight valve for holding a sample tube in the passage; a distribution valve directing purge gas and carrier gas to the top end of the passage and for passing pyrolyzed sample from the bottom of the passage to an analytical device; and an electrical heating element for heating the passage to temperatures at which a sample will be pyrolyzed.

Abstract: A method for determining hydrogen content in a compound is disclosed. This method generally comprises heating the sample to sufficient temperatures to effect pyrolytic conversion of any hydrogen containing compounds in the sample to hydrogen gas, and measuring the hydrogen content evolved by this conversion. In a preferred embodiment, this is carried out in a tube furnace inerted and purged with a noble gas. An apparatus for determining hydrogen content in a compound is also disclosed.

Abstract: Apparatus and methods for the measurement of total organic carbon, total inorganic carbon and total carbon of water are described. The sample is acidified and split into an inorganic carbon stream and a total carbon stream. The inorganic carbon in the inorganic stream is oxidized and both the organic and inorganic carbon in the total carbon stream is oxidized. The resulting carbon dioxide is measured in each stream using carbon dioxide sensors employing a gas permeable membrane dividing deionized water from the oxidized sample water and a pair of micro-conductivity and temperature sensors.

Abstract: The present invention relates to a method for determining at least one petroleum characteristic of a geologic sediment sample heated in a non-oxidizing atmosphere and an oxidizing atmosphere. The sample is heated to a first temperature value below 200.degree. C. for a predetermined period of time and then to a second temperature value ranging between 600 and 850.degree. C. according to a temperature gradient between 0.2.degree. C. and 50.degree. C./min. Carbon dioxide and carbon monoxide are continuously measured during the temperature stages in order to determine at least one petroleum characteristic, wherein said petroleum characteristic comprises a quantity of organic oxygen, inorganic oxygen, total organic carbon, or inorganic carbon.

Abstract: Apparatus and methods for the measurement of total organic carbon, total inorganic carbon, total carbon and total heteroorganic carbon of deionized water are described. In a preferred embodiment, the sample is split into a first stream and a second stream. Inorganic carbon in the first stream is measured using a temperature and conductivity cell, and then the organic carbon in the first stream is oxidized in a U.V. oxidation module. The resulting carbon dioxide is transferred through a carbon dioxide permeable membrane into the second stream. The second stream then passes into a second temperature and conductivity cell for the measurement of total carbon.

Abstract: A method of evaluating at least on type of pollution characteristic in a soil sample contaminated by hydrocarbon compounds, a method wherein the soil sample is first heated in a non-oxidizing atmosphere, then in an oxidizing atmosphere. The method comprises several temperature rise stages from which at least five quantities Q.sub.0, Q.sub.1, Q.sub.2, Q.sub.3 and Q.sub.4 are measured, wherein the quantities represent concentrations of hydrocarbon compounds in the soil sample. At least one type of pollution characteristic of the sample is determined from quantities Q.sub.0, Q.sub.1, Q.sub.2, Q.sub.3 and Q.sub.4.

Abstract: A DNA sequencing, mapping, and diagnostic process which includes the steps of labeling nucleotide segments or peptide nucleic acids (PNAs) with one or more atoms of specific stable or long-lived radioactive isotopes of a selected element that do not normally occur in DNAs, ODNs or PNAs such that the nucleotide segment or PNA has specific stable or long-lived radioactive isotope of a specified selected element at a terminal or an interior position; hybridizing the labeled nucleotide segment or PNA to complementary nucleic acid segments or PNAs which are fixed on a hybridization surface; and, using mass spectrometric techniques, including RIS, to analyze the presence and position of the labeled hybridized nucleotide segments or PNAs which are bound to the fixed nucleotide segments or PNAs.

Abstract: A method and apparatus for analysing a chemical species in a fluid are disclosed. The apparatus includes filtering apparatus (15, 17) upstream and downstream of the sample preparation section (3). The fluid is diverted from a line (1) by an arrangement of pumps (27) and valves through the upstream filter (15) to the digester (11) and through the downstream filter (17) out to the analyser/detector system (5). The pumps (27) and valve arrangement allows the purging of the sample preparation section (3) and backflushing of the filters (15, 17), the inlet line (7) and the outlet line (13).

Abstract: An oxidation reactor having particular utility in a system for measuring carbon in an aqueous sample. A first chamber and second chamber are separated by a hydrogen-permeable electrode, each chamber having a separate electrolysis cell. The hydrogen-permeable electrode acts as the anode of one cell and the cathode of the other cell. The sample stream flows into one chamber and the electrolysis cell produces oxygen from the water at one optically transparent electrode and in combination with short wave ultraviolet light oxidizes organic carbon to CO.sub.2 and produces hydrogen at the other electrode which passes through the hydrogen-permeable electrode into the second chamber. The electrolysis cell in the second chamber produces oxygen at hydrogen-permeable electrode to react with the hydrogen that passes through the hydrogen-permeable electrode to form water, thereby maintaining the maximum concentration gradient of hydrogen across the hydrogen-permeable electrode to improve hydrogen transferring efficiency.

Abstract: The invention concerns a device for automatically injecting substances solubilised or diluted in a solvent for a gaseous phase chromatographic analysis column (14), wherein it includes a concentration/calcination chamber (10), a vaporization chamber (12) in contact with the chromatographic column (14), a sample support (16) moving in the concentration/calcination chamber between a first position in which the sample is in the concentration/calcination chamber and a second position in which the sample is in the vaporization chamber, as well as a system (18) for scavenging the two chambers with a vector gas.

Abstract: An improved measurement cell and circuit for measuring the electrical characteristics of a liquid sample during exposure to radiation includes a glass cell formed of a main tube extending generally parallel to an elongated lamp emitting the radiation, and a pair of electrodes disposed axially within the sample tube. In the preferred embodiment, the ends of the cell are formed of glass twinbore tubing fused to the glass main tube, the bores retaining ends of the electrodes. Inlet and outlet tubes and a temperature sensing well may also be fused to the main tube. In an implementation for measurement of TOC in water by oxidation to CO.sub.2, the source comprises a low pressure mercury vapor lamp, and the electrodes are formed of solid Ti with catalytic TiO.sub.2 surfaces.

Abstract: This invention provides a process for determining the nitrogen content of a sample involving (a) combusting the sample in a combustion reactor in the presence of oxygen, which oxygen is introduced into the combustion reactor in pulse form; (b) reducing the resulting combustion gases by flowing them in a flow of helium or other noble carrier gas through a Cu-containing reduction reactor; (c) performing the steps of (i) making anhydrous in a water trap the reduced gases, (ii) flowing the reduced gases through a gas-chromatographic column in order to carry out a gas-chromatographic separation of N.sub.2 from CH.sub.4 possibly present within the reduced gases, and (iii) removing CO.sub.2 from the reduced gases using a CO.sub.2 trap, with the proviso that step (i) immediately precedes step (ii); and (d) analyzing the resulting gases by detecting thermal conductivity.

Abstract: An apparatus which mounts a sample in a vacuum chamber, heats the sample, and analyzes the gas generated from the sample. A loading lock mechanism, enables the vacuum chamber to be maintained at a vacuum even when a measurement is not conducted, and even when a sample is introduced/discharged in/from the chamber, thereby minimizing the background noises and increasing detection performance.

Abstract: An inorganic carbon removing part defined by has a double tube structure formed by an inner tube of polytetrafluoroethylene having continuous pores and an outer tube of resin. An acidified sample solution is guided into the inner tube and an alkalified sample solution is guided into the outer tube, and inorganic carbon contained in the acidified sample solution is outwardly moved toward the alkalified sample solution to be removed. The acidified sample solution, from which inorganic carbon is removed, is injected into a combustion tube, so that a carbon component contained in the sample solution is converted into carbon dioxide and detected by a detecting part. Since the alkalified sample solution contains purgeable organic carbon components of the same concentration as the acidified sample solution, the content of total organic carbon is correctly measured with no loss of the purgeable organic carbon components.

Abstract: A system and method are provided for minimizing the effects of background signals in masking signals indicating the presence of substances to be detected such as contaminants in materials moving rapidly along a conveyor. The contaminants detected may include nitrogen containing compounds and hydrocarbons. The system and method of the present invention minimizes the number of falsely positive indications of the presence of such substances due to background signals and changes in background signals. The substances detected are divided into first and second sample portions and the respective portions are heated. The first heated portion is reacted with ozone to generate radiation by chemiluminescence having characteristic wavelengths related to substances in the first portion. The second portion heated is also reacted with ozone to generate radiation by chemiluminescence having characteristic wavelengths related to substances in the second portion.

Abstract: A method and apparatus for detecting the presence of a vapor of an alkyl ester of phosphoric acid, particularly tributylphosphate, in ambient air. A sample of ambient air is heated to convert any alkyl ester of phosphoric acid to an alkene. The heated sample of air is then passed to a sample loop. Carrier air periodically carries a fixed volume of sample from the sample loop through a chromatographic column to a photoionization detector which detects the presence and amount of the alkene in the sample.

Abstract: A dye couple compound is provided for use in a test device containing a reagent system for detecting the presence or quantity of an analyte in a sample. The reagent system comprises one or more enzymes which, in the presence of the analyte, produce an oxidizing agent in quantities indicative of the quantity of analyte in the sample. The compound of choice is meta[3-methyl 2-benzothiazolinone hydrozone]N-sulfonyl benzenesulfonate monosodium.

Abstract: An efficient method for the microfabrication of electronic devices which have been adapted for the analyses of biologically significant analyte species is described. The techniques of the present invention allow for close control over the dimensional features of the various components and layers established on a suitable substrate. Such control extends to those parts of the devices which incorporate the biological components which enable these devices to function as biological sensors. The materials and methods disclosed herein thus provide an effective means for the mass production of uniform wholly microfabricated biosensors. Various embodiments of the devices themselves are described herein which are especially suited for real time analyses of biological samples in a clinical setting. In particular, the present invention describes assays which can be performed using certain ligand/ligand receptor-based biosensor embodiments.

Abstract: The content of decomposable organic carbon compounds present in a gaseous phase is determined down to the parts per billion (10.sup.-9) range and in special cases down to the parts per trillion (10.sup.-12) range. The gaseous sample material being tested is introduced into a limited quantity of water wherein the organic compounds are photolytically decomposed. The decomposition products are ascertained in the carrier gas and/or in the limited quantity of water.

Abstract: An electrochemical detection cell (320), which is usable either for potentiometric or electrolytic conductivity detection, has a capillary (305), which controls electrolyte flow. A gas stream containing detectable substances is input through a non-wettable plastic capillary (306). A reaction zone (310) through which both gas and liquid flow is internally wettable. Reference electrode (309) and either electrode (311) or (312) may be used for potentiometric detection. Sensor electrodes (311) and (312), both in the reaction zone, are used for conductivity detection. The electrolyte is fed through the capillary (305) gravimetrically from a reservoir, and the gas stream is supplied by a pyrolysis furnace. The mechanism of ionization in the gas phase ionization detector (GPELCD) is described.

Abstract: Sealable container assemblies include containers for materials which are to be microwave heated, such as in digesting or extracting operations, made of thermoplastic material, such as fluoropolymer, that is strengthened by reinforcing means that may be a fiber reinforced thermoplastic of high tensile strength, such as polyetherimide, with reinforcing continuous fibers in a matrix of such thermoplastic, which fibers are very preferably in the shape of a sleeve or sleeves and are of glass or other heat resistant and microwave transmissive material. The containers may be strengthened by incorporating the fiber reinforced thermoplastic in a wall or walls of the container or preferably by inserting the container into a reinforcement, which is a sleeve or collar of the reinforced thermoplastic. In both such constructions the reinforcing means protects the container against radial failure due to pressure that is generated by the microwave heating of the container contents.

Abstract: An apparatus for testing peroxide concentration in a gaseous sterilant. A preferred embodiment of the apparatus includes a condenser for condensing the gaseous sterilant into a liquid condensate; an aliquot collector of predetermined volume to receive the condensate; a reaction chamber containing a catalyst for dissociating the peroxide; and a pressure monitor for detecting pressure changes in the reaction chamber as a function of time. The pressure monitor of this apparatus is capable of detecting a threshold pressure and an upper pressure and it includes a timer to measure time change between detection of the threshold pressure and the upper pressure.

Abstract: A method and apparatus for extracting hydrocarbon gas from drilling fluid samples utilizes microwave energy as the source for heating a sample, containing water, sufficiently to cause the extraction of the hydrocarbon gases therefrom. Either a batch or a continuous operation can be realized using this method.

Abstract: In a gas scavenging unit for gas chromatography analysis of gas generated in a thermal analyzer, the thermal analyser is equipped with a gas scavenging unit for scavenging gas generated in the thermal analyzer without usage of a carrier gas and no influence of a switching valve exists in the case of multi-stage sampling. For scavenging, there can be provided multiple sampling flow paths each have an aperture placed between the sample and the carrier gas outlet of the thermal analyzer, a flow regulator, a flow path switching valve, and a suction unit which is connected to the switching valve. The gas generated in the thermal analyzer is suctioned by the suction unit through a sampling flow path which is changed with the flow path switching valve. The appropriate volume of gas is scavenged to the GC analysis without any influence of the flow (rate) of the carrier gas even when the scavenging is done through switching to multiple scavengers.

Abstract: By heating a wire and positioning the wire against a specimen, the specimen may be pyrolyzed to release a pyrolysate therefrom. The pyrolysate is collected in a hood and carried to a membrane separator from which the pyrolysate may be spectrochemically analyzed. The heated wire may be repeatedly indexed for replacing the adulterated portion of the wire with a clean portion of the wire for each subsequent pyrolysis and spectrochemical analysis of the pyrolysate therefrom. A pyrolysis instrument includes a movable probe supporting the heated wire with the probe being preferably joined to a remote membrane separator flexibly joined thereto.

Abstract: The determination of the halogen content in a substance is carried out by oxidative combustion of the sample under a continuous flow of gas, in the presence of oxygen, the gases coming out of the combustion reactor being then carried by gas flow to analysis equipment.

Abstract: Containers for materials which are to be microwave heated such as in digesting or extracting operations, are made of thermoplastic material, such as a fluoropolymer, e.g., TEFLON.RTM. PFA, that is strengthened by reinforcing means that may be a fiber reinforced thermoplastic of high tensile strength, such as polyetherimide, e.g., ULTEM.RTM., with reinforcing continuous fibers in a matrix of such thermoplastic, which fibers are preferably of glass or other heat resistant and microwave transmissive material. The containers may be strengthened by incorporating the fiber reinforced thermoplastic in a wall or walls of the container or by inserting the container into a reinforcement, which is a sleeve or collar of the reinforced thermoplastic. In both such constructions the reinforcing means protects the container against peripheral or radial failure due to pressure that is generated by the microwave heating of the container contents.

Abstract: A purgeable organic carbons analyzer for measuring the content of purgeable organic carbons (POC) in a water sample using barium hydroxide as the CO.sub.2 absorbing agent in a CO.sub.2 absorber.

Abstract: Carbon particulate concentration of diesel exhaust or other sampled gas is measured by collecting the particulate on a high efficiency filter or other collector while measuring the amount of sampled gas passing through the filter. Particulate collection occurs along an open ended collection flow path. The collected particulate is then heated in an oxygen rich environment to oxidize carbon within the particulate to carbon dioxide. The amount of resulting carbon dioxide is measured along a closed measurement flow path to derive a corresponding measurement of the amount of collected particulate. Particulate concentration is calculated by comparing the amount of carbon particulate with the measured amount of sampled gas. A computer controls automatic switching of operation along the collection and measurement flow paths for respective particulate collection and measurement cycles.

Abstract: A sample autoloader loads a sample into a furnace and removes a sample from the furnace. The sample autoloader includes a sealing plate for sealing the furnace. The sample autoloader also includes a mechanism for pushing a sample into the furnace and removing a sample from the furnace. The sample autoloader may include a hotel which stores sample containers for automatic loading and a container which receives spent sample containers.

Abstract: A method for separating and analyzing the hydrocarbons, particularly heavy hydrocarbons, contained in sedimentary rocks, comprising:A) loading a sample tube with the sample of sedimentary rock and one or more inert solvents;B) preheating the sample tube;C) removing the solvent and the hydrocarbons previously contained in the rock;D) condensing the vapour and feeding it to a separation and analysis device.The invention also comprises an apparatus for implementing separating and analyzing method.