The present invention includes a first flow path through which a sample gas flows, a first analyzer that is provided in the first flow path to measure total hydrocarbon concentration in the sample gas, a second flow path through which the sample gas flows, a non-methane non-ethane cutter that is provided in the second flow path to remove the hydrocarbon components other than the methane and the ethane in the sample gas, a second analyzer that is provided downstream of the non-methane non-ethane cutter in the second flow path to measure the total methane ethane concentration of the methane and the ethane in the sample gas, and a calculation part that calculates the concentration of the hydrocarbon components other than the methane and the ethane in the sample gas with use of the total hydrocarbon concentration by the first analyzer and the total methane ethane concentration by the second analyzer.

A method for separating diastereomers of pristane. A pristane sample is prepared, and then injected into a chromatographic instrument equipped with a chiral chromatographic column, where a stationary phase of the chiral chromatographic column has a preset pore size. The pristane diastereomers in the pristane sample are separated by the chiral chromatographic column, and the components produced by the separation of the pristane diastereomers sequentially enter a mass spectrometer for detection and analysis.

Apparatus for monitoring the quality of gas in a process stream at a subsea location comprises: a container for permanent installation at the location; one or more devices for analysing gas quality, said devices being located in the container; and means for supplying a sample of gas from the process stream to the said one or more devices; wherein the pressure within the container is maintained at or near to atmospheric pressure. The invention also extends to a method of monitoring the quality of gas in a process stream at a subsea location.

The disclosed system and method improve measurement of trace volatile chemicals, such as by Gas Chromatography (GC) and Gas Chromatography/Mass Spectrometry (GCMS). A first trapping system can include a plurality of capillary columns in series and a focusing column fluidly coupled to a first detector. The first trapping system can retain and separate compounds in a sample, including C3 hydrocarbons and compounds heavier than C3 hydrocarbons (e.g., up to C12 hydrocarbons, or compounds having a boiling point around 250° C.), and can transfer the compounds from the focusing column to the first detector. A second trapping system can receive compounds that the first trapping system does not retain, and can include a packed trap, a polar column and a PLOT column fluidly coupled to one or more second detectors. The second trapping system can remove water from the sample and can separate and detect compounds including C2 hydrocarbons and Formaldehyde.

An improved liquid vaporization and conditioning system, and associated method, for efficiently vaporizing a liquid sample for accurately determining the constituent components thereof providing enhanced flow rate, pressure and thermal control, the improvement including a combination of a resistance temperature detector, a sweeping bend to, an in-line thermal break, a flow buffering input manifold, enhanced multi-path heater vaporizer construction with four heater units, a vaporizer output mixing manifold and control elements providing a capability for partial shutdown in the event of compromised heating or flow anomalies without risk of flow loss/volume capacity beyond a permissible threshold and an improved, modular heat vaporizer enclosure.

A system can flush a drilling fluid sample with a hydrocarbon blend, which includes a determined concentration of at least one chemical species to generate a flushed drilling fluid sample. The system can extract a dissolved gas from the flushed drilling fluid sample. The system can determine a concentration over time of at least one chemical species of the dissolved gas. The system can generate an area per concentration curve based on the concentration over time of the at least one chemical species. The system can determine at least one concentration value of the at least one chemical species. The system can modify the at least one concentration value based on the area per concentration curve. The system can then correct bias caused by the gas extractor and fluid sampling system.

Modified thermoplastic hydrocarbon thermoplastic resins are provided, as well as methods of their manufacture and uses thereof in rubber compositions. The modified thermoplastic resins are modified by decreasing the relative quantity of the dimer, trimer, tetramer, and pentamer oligomers as compared to the corresponding unmodified thermoplastic resin polymers, resulting in a product that exhibits a greater shift in the glass transition temperature of the elastomer(s) used in tire formulations. This translates to better viscoelastic predictors of tire tread performance, such as wet grip and rolling resistance. The modified thermoplastic resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the modified thermoplastic resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, snow performance, and wet braking performance.

A system, device, and a method for determining a compound content in transformer oil are provided. The method includes positioning a syringe filled with transformer oil in the device to transfer the oil to a vial using the device. The device includes a stand, a threaded rod, a handle, a disc, and a syringe holder. The threaded rod is movable in a vertical direction by rotation of the handle and is configured to apply pressure via the disc on a plunger of the syringe positioned in the syringe holder to maintain an airtight connection between the vial and the device. The compound content is determined using a gas chromatograph by analyzing an aliquot extracted from a headspace gas of the vial.

The invention is directed to a furnace suited for oxidation of a gaseous starting mixture comprising one or more sulphur compounds to obtain an oxidized gas mixture and reduction of the oxidized gas mixture to obtain a gaseous mixture of reduced sulphur compounds comprising an interior furnace space, an inlet conduit for the gaseous starting mixture, an inlet for supply of an oxygen comprising gas, a ceramic comprising outlet conduit provided with an inlet opening for the mixture of reduced sulphur compounds, an inlet for hydrogen and heating means, wherein the inlet opening of the outlet conduit is comprised of more than one opening which openings fluidly connect the interior furnace space and the interior of the outlet conduit.

The present disclosure provides compositions, methods, and systems for identifying marked hydrocarbon fluids. These compositions, methods, and systems utilize a gas chromatography marker including a pyrrolidinone. The methods and systems can identify the presence or absence of the gas chromatography marker and/or the pyrrolidinone. The compositions, methods, and systems can optionally utilize a spectroscopic marker.