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489 results about "Liquid fraction" patented technology

Catalytic multi-stage process for hydroconversion and refining hydrocarbon feeds

A multi-stage catalytic hydrogenation and hydroconversion process for heavy hydrocarbon feed materials such as coal, heavy petroleum fractions, and plastic waste materials. In the process, the feedstock is reacted in a first-stage, back-mixed catalytic reactor with a highly dispersed iron-based catalyst having a powder, gel or liquid form. The reactor effluent is pressure-reduced, vapors and light distillate fractions are removed overhead, and the heavier liquid fraction is fed to a second stage back-mixed catalytic reactor. The first and second stage catalytic reactors are operated at 700-850.degree. F. temperature, 1000-3500 psig hydrogen partial pressure and 20-80 lb./hr per ft.sup.3 reactor space velocity. The vapor and light distillates liquid fractions removed from both the first and second stage reactor effluent streams are combined and passed to an in-line, fixed-bed catalytic hydrotreater for heteroatom removal and for producing high quality naphtha and mid-distillate or a full-range distillate product. The remaining separator bottoms liquid fractions are distilled at successive atmospheric and vacuum pressures, low and intermediate-boiling hydrocarbon liquid products are withdrawn, and heavier distillate fractions are recycled and further upgraded to provide additional low-boiling hydrocarbon liquid products. This catalytic multistage hydrogenation process provides improved flexibility for hydroprocessing the various carbonaceous feedstocks and adjusting to desired product structures and for improved economy of operations.
Owner:HEADWATERS CTL

Apparatus and Process for Production of Biogas

A process and an apparatus for the manufacture of biogas and a solids fraction from an organic waste feedstock is provided. The process involves thermal hydrolysis of the organic waste feedstock at a temperature from about 100 to about 220° C., a pressure from about 5 to about 20 bars, for a period of time from about 15 minutes to 4 hours, to produce a hydrolysate. The hydrolysate undergoes anaerobic digestion at a temperature from about 25 to 60° C., for a period of time from about 1 to 35 days to produce a biogas stream and a digestate. The digestate is separated into a solids fraction and a liquid fraction, and a portion of the solids fraction is recycled for further anaerobic digestion. The biogas stream, characterized as having a methane content from between 55 to 80% by volume, and the solids fraction, are recovered. The apparatus includes a receiving bin for receiving and supplying organic waste feedstock to a thermal hydrolysis reactor. The thermal hydrolysis reactor for processing the organic waste feedstock at a temperature from about 100 to about 220° C., a pressure from about 5 to about 20 bars, for a period of time from about 15 minutes to 4 hours to produce a hydrolysate. An anaerobic digester for processing the hydrolysate at a temperature from about 25 to 60° C., for a period of time from about 1 to 35 days to produce the biogas and a digestate, and a solids thickening tank for separating the digestate into the solid fraction, a liquid fraction and a secondary biogas fraction.
Owner:GEMINI CORP

Testing device for competitive adsorption of supercritical CO2 and CH4 in shale and testing method of device

The invention provides a testing device for competitive adsorption of supercritical CO2 and CH4 in shale and a testing method of the device. The device comprises an injection pump system, a long core holder, a back-pressure valve, a differential pressure gauge, a temperature control system, a liquid fraction collector, a gas meter and a gas chromatograph instrument. The testing method comprises an evaluation method of CH4 single component gas in a shale core and an evaluation method of CH4 gas, converted by the supercritical CO2, in the shale core. According to the device and method, the detection conditions of a laboratory test that the supercritical CO2 displaces CH4 adsorbed in the shale under the high temperature and high pressure conditions of a stratum are met through a multifunctional long core displacement method, and then the purpose of evaluating the efficiency that the supercritical CO2 displaces the adsorbed CH4 is achieved; by using the combined long core, the gas injection volume is large, the errors are decreased, and the formation condition is truly restored; the cracked long core can simulate the competitive adsorption process of the fractured supercritical CO2 and the CH4 under the true shale reservoir condition; the injected CO2 is in the supercritical state, and an experiment is performed in a step-by-step depressurizing mode, and the depletion exploitation process of a stratum can be truly simulated.
Owner:SOUTHWEST PETROLEUM UNIV
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