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.

The present disclosure relates to a detection method for congeners of short-chain chlorinated paraffins as well as a device for realizing the detection method. The detection method includes the following steps: adding an internal standard substance to a test sample; subjecting the test sample to a separation process using a comprehensive two-dimensional gas chromatograph formed by connecting a non-polar or weak-polar column and a medium-polar column in series via a modulator; and detecting the sample by a mass analyzer employing a negative chemical ion source after the separation process. The method according to the present disclosure enables accurate qualitative analysis as well as accurate quantitative measurement for short-chain chlorinated paraffins. The detection is extremely accurate yet can be easily carried out with simple operations.

The present disclosure relates to a detection method for congeners of short-chain chlorinated paraffins as well as a device for realizing the detection method. The detection method includes the following steps: adding an internal standard substance to a test sample; subjecting the test sample to a separation process using a comprehensive two-dimensional gas chromatograph formed by connecting a non-polar or weak-polar column and a medium-polar column in series via a modulator; and detecting the sample by a mass analyzer employing a negative chemical ion source after the separation process. The method according to the present disclosure enables accurate qualitative analysis as well as accurate quantitative measurement for short-chain chlorinated paraffins. The detection is extremely accurate yet can be easily carried out with simple operations.

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.

Certain embodiments described herein are directed to systems and methods that can be used to analyze species in a fluid stream. In some configurations, a sorbent tube effective to directly sample aromatics and/or polyaromatics in a fluid stream is described.

A method for analyzing a drilling fluid receiving a drilling fluid sample from a flow of the drilling fluid at a surface of a borehole being drilled in a subterranean formation and extracting, using a gas extraction and sampling system, a dissolved gas from the drilling fluid sample. The method includes determining, using a gas chromatograph, a concentration over time of at least one chemical species of a dissolved gas from the drilling fluid sample and generating an area per concentration curve based on the concentration over time. The method includes determining, using a gas extraction and sampling system, at least one concentration value of the at least one chemical species of the dissolved gas from the drilling fluid sample and correcting bias caused by the gas extraction and sampling system, wherein correcting the bias comprises modifying the at least one concentration value based on the area per concentration curve.

A method to simulate distillation of a petroleum stream by gas chromatography can include separating the petroleum stream with a gas chromatograph as a function of boiling point; passing the separated petroleum stream through a vacuum ultraviolet detector to yield data comprising a vacuum ultraviolet signal as a function of boiling point; integrating the vacuum ultraviolet signal as a function of boiling point over two or more wavelength ranges to derive relative concentrations of two or more components of the separated petroleum stream that correspond to the two or more wavelength ranges.

Disclosed is an organic carbon detector that can be used with a liquid chromatography equipment such as a size exclusion chromatography. The organic carbon detector contains a carbon oxidization subsystem and a stripping and CO.sub.2 detection subsystem arranged and detachably connected with each other in said order. The carbon oxidization subsystem contains a microfluidic agent injection module (1), an inorganic carbon removal module (2), a microfluidic ultraviolet oxidation module (3) and a vacuum pumping system (4), configured to remove inorganic carbons and oxidize organic carbons. The stripping and CO.sub.2 detection subsystem contains a stripping module (7) and a CO.sub.2 detector (12), using a carrier gas to transfer the organic carbon converted gas to the CO.sub.2 detector (12). Also disclosed is a method of using the organic carbon detector in water quality monitoring.

The present invention is generally related to the analysis of chemical compositions of hydrocarbons and hydrocarbon blends. This method applies specifically to the problem of analyzing extremely complex hydrocarbon-containing mixtures when the number and diversity of molecules makes it impossible to realistically identify and quantify them individually in a reasonable timeframe and cost. The advantage to this method over prior art is the ability to separate and identify chemical constituents and solvent fractions based on their solvent-solubility characteristics, their high performance liquid chromatographic (HPLC) adsorption and desorption behaviors, and their interactions with stationary phases; and subsequently identify and quantify them at least partially using various combinations of non-destructive HPLC, destructive HPLC, and stand-alone detectors presently not routinely used for HPLC but reconfigured to obtain spectra on the fly. This analytical method is especially useful for, but not limited to, asphalt binders and asphalt binder blends, modified asphalts, asphalt modifiers, asphalt additives, polymer-modified asphalts, asphalts containing rejuvenators and softening agents, asphalts containing recycled products, aged asphalts, and air-blown asphalts, which may contain wide varieties of different types of additives and chemistries, and forensic applications, and environmental pollutant identification.

This method allows for prediction of subsurface fluid properties (e.g., phase or API gravity) using gas chromatogram data of a small-volume extract. Small volume equates to microliter scale volume (or milligram scale weight) from a subsurface rock sample, where a fluid test may not be available for analysis. The method may also be applied to petroleum liquid samples where drilling fluid or other contaminants preclude accurate direct property measurement. Gas chromatographic data is calibrated to measured petroleum properties; preferably local oils from the same petroleum system, however, a general global calibration can also be used.