Abstract: A process for the production of syngas, the process comprising (i) reacting at least a portion of carbon dioxide with hydrogen within an initial reactor to produce an initial product stream including carbon monoxide, water, unreacted carbon dioxide, and unreacted hydrogen; and (ii) reacting at least a portion of the unreacted carbon dioxide and unreacted hydrogen within a reactor downstream of the first reactor to thereby produce a product stream including carbon monoxide, water, unreacted carbon dioxide, and unreacted hydrogen.

Abstract: It has been discovered that mixed-alcohol production can utilize the waste tail gas stream from the pressure-swing adsorption section of an industrial hydrogen plant. Some variations provide a process for producing mixed alcohols, comprising: obtaining a tail-gas stream from a methane-to-syngas unit (e.g., a steam methane reforming reactor); compressing the tail-gas stream; separating the tail-gas stream into at least a syngas stream, a CO2-rich stream, and a CH4-rich stream; introducing the syngas stream into a mixed-alcohol reactor operated at effective alcohol synthesis conditions in the presence of an alcohol-synthesis catalyst, thereby generating mixed alcohols; and purifying the mixed alcohols to generate a mixed-alcohol product.

Abstract: The present disclosure provides a composition including trifluoroacetyl iodide, at least one organic impurity and at least one inorganic impurity. The at least one organic impurity includes at least one of: difluoroiodomethane, pentafluoroiodoethane, iodomethane, iodopropane, dichlorotetrafluoroethane, dichlorotrifluoroethane, trichlorotrifluoroethane, methyltrifluoroacetate, trifluoroacetic anhydride, difluorobutane and methyl propane. The at least one inorganic impurity includes at least one of: hydrogen iodide, hydrogen chloride, iodine and hydrogen triiodide.

Abstract: Methods for utilizing carbon dioxide to produce multi-carbon products are disclosed. The systems and methods of the present disclosure involve: reducing CO2 to produce a first product mixture comprising an alcohol product mixture comprising one or more alcohols and a paraffin product mixture comprising one or more paraffins; dehydrating the alcohol product mixture to form an olefin product mixture comprising one or more olefins; oligomerizing the olefin product mixture to form a higher olefin product mixture comprising unsaturated paraffins and optionally aromatics; and reducing the higher olefin product mixture to form a higher hydrocarbon product mixture comprising unsaturated paraffins and optionally aromatics. Catalyst materials and reaction conditions for individual steps are disclosed to optimize yield for ethanol or jet fuel range hydrocarbons.

Abstract: There are provided systems and methods for using fuel-rich partial oxidation to produce an end product from waste gases, such as flare gas. In an embodiment, the system and method use air-breathing piston engines and turbine engines for the fuel-rich partial oxidation of the flare gas to form synthesis gas, and reactors to convert the synthesis gas into the end product. In an embodiment the end product is methanol.

Abstract: A catalytic carbon capture material is provided. The catalytic carbon capture material includes a microporous polymer including a Tröger's base moiety, and a transition metal is coordinated within the microporous polymer. The catalytic carbon capture material selectively captures carbon dioxide (CO2) and also is a catalyst that simultaneously converts the captured carbon dioxide into one or more carbon dioxide-based products. A method of making the catalytic carbon capture material and a method of selective carbon dioxide capture and conversion are also provided.

Abstract: Compound are described comprising a perfluorinated group bonded to at least one terminal photoinitiator group with an organic linking group comprising at least one amide moiety. The compound typically comprises the (e.g. Michael addition) reaction product of i) a compound comprising an acryl group and a photoinitiator group; and ii) an amino functional perfluorinated compound. Also described is a composition comprising at least one free-radically polymerizable (e.g. fluorinated) monomer, oligomer, or combination thereof; and the described fluorinated photoinitiator compound and methods.

Abstract: A dehydrohalogenation product includes a hydrochlorofluorocarbon mixture of a fluoroolefin of formula RCX=CZQ and a halofluoroalkane of formula RCXYCZQT. R is a perfluorinated alkyl group and X, Z, and Q are independently H or halogen. One of Y and T is H and the other is Cl, Br, or I. About 80% or greater of the hydrochlorofluorocarbon mixture is the fluoroolefin. The dehydrohalogenation product also includes a caustic agent and a solvent. In some embodiments, the dehydrohalogenation product is free of any catalyst, including any phase transfer catalyst.

Abstract: The present invention describes improved processes for the synthesis of high value chemical products from low carbon syngas. In one aspect, a process for the production of chemicals is provided. The process comprises the following: feeding a feedstock comprising hydrogen and carbon monoxide to a liquid fuel production reactor, wherein the liquid fuel production reactor comprises a catalyst, thereby producing a product, wherein the product comprises a liquid phase and a solid phase, and wherein the liquid phase comprises C5-C23 hydrocarbons and oxygenated hydrocarbons, and wherein the solid-phase comprises C24-C45 aliphatic hydrocarbons, and wherein the liquid phase is between 51 percent by volume and 99 percent by volume of the product.

Abstract: Production of fuels from low carbon electricity and from carbon dioxide by the use of a solid oxide electrolysis cell (SOEC) and Fischer-Tropsch is shown. Fischer-Tropsch is an exothermic reaction that can be used to produce steam. Steam produced from the Liquid Fuel Production (LFP) reactor system, where the Fischer-Tropsch reaction occurs, is used as feed to the SOEC. The higher temperature steam improves the efficiency of the overall electrolysis system. The integration of the LFP steam improves the efficiency of the electrolysis because the heat of vaporization for the liquid water does not have to be supplied by the electrolyzer.

Abstract: A process for the production of a high purity first diol from a product stream comprising two or more C2 to C7 diols, said process comprising the steps of: (i) providing the product stream to a first distillation column; (ii) providing an extractant selected from the group of C3 to C6 sugar alcohols and mixtures thereof to the first distillation column; (iii) operating the first distillation column to obtain a first bottoms stream comprising at least a first diol and the extractant; (iv) providing the first bottoms stream to a second distillation column operating to obtain a second top stream comprising the first diol and diols with atmospheric boiling points at least 10° C. higher than the first diol, and (v) providing the second top stream to a third distillation column to obtain a third top stream comprising the first diol; wherein the product stream comprises 0.1 to 10 wt % of diols with atmospheric boiling points at least 10° C.

Abstract: A method for preparing C2 to C5 paraffins including introducing a feed stream of hydrogen gas and a carbon-containing gas selected from carbon monoxide, carbon dioxide, and mixtures thereof into a reaction zone of a reactor. Converting the feed stream into a product stream that includes C2 to C5 paraffins in the reaction zone in the presence of a hybrid catalyst. The hybrid catalyst including a microporous catalyst component; and a metal oxide catalyst component. The metal oxide catalyst component including a metal component present on a metal oxide support material. The metal oxide support material includes at least one oxide of a metal selected from Group 4 of the IUPAC periodic table of elements. The product stream has a C3/C2 carbon molar ratio greater than or equal to 4.0.

Abstract: Processes for producing high biogenic concentration Fischer-Tropsch liquids derived from the organic fraction of municipal solid wastes (MSW) feedstock that contains a relatively high concentration of biogenic carbon (derived from plants) and a relatively low concentration of non-biogenic carbon (derived from fossil sources) wherein the biogenic content of the Fischer-Tropsch liquids is the same as the biogenic content of the feedstock.

Abstract: A process for preparing glycols from a lignocellulosic solid biomass involves contacting the biomass with an organic solvent comprising a low boiling point alcohol and a pre-treatment acid at a temperature in a range from 80 to 220° C. and a pressure in a range from 1 to 50 bara. The resulting mixture, having less than wt. % water, is separated into a pre-treated solid residue comprising cellulose and a liquid stream comprising dissolved lignin. The pre-treated solid residue is subjected to a hydrogenolysis reaction. generating a glycols stream, a lights stream, comprising a first portion of organic solvent, and a heavies stream. At least part of the liquid stream is separated to produce a second portion of organic solvent and a lignin stream. At least part of the first and second portions of organic solvent is recycled to the contacting step.

Abstract: A method of reducing carbon dioxide (CO2) including contacting a catalyst and the CO2 and irradiating the catalyst and the CO2 with visible light. Upon irradiating the CO2 is reduced to a conversion product. The catalyst includes Fe2TiO5 in the form of nanosheets. The nanosheets have an average width of 200 nanometers (nm) to 800 nm and form a hierarchical structure.

Abstract: A method for the synthesis of methanol, wherein a carbonaceous energy source flow is supplied to a synthesis gas reactor arrangement for obtaining a synthesis gas flow having hydrogen and carbon oxides, wherein the synthesis gas flow is supplied to a thermal recovery apparatus for recovering heat from the synthesis gas flow and then to a synthesis gas compressor for pressure increase. The synthesis gas flow is supplied at least in part to a first reactor stage of a methanol reactor arrangement for partial conversion to methanol, a residual gas flow having unreacted carbon oxides being obtained from the methanol reactor arrangement, which residual gas flow is supplied to a recycling compressor for increasing its pressure, the pressure-increased gas flow being supplied to the methanol reactor arrangement for partial conversion to methanol, a recovery flow from an unreacted residual gas being supplied to the first reactor stage of a hydrogen recovery arrangement to obtain a H-recycling flow.

Abstract: A process for the production of methanol from hydrogen and carbon monoxide includes contacting the hydrogen and carbon monoxide with a liquid in at least one bubble or loop or jet loop reactor. The liquid comprises at least one solvent, an alcohol and/or an amine as a nucleophilic promoter, optionally an additional base and a catalyst, the catalyst comprising a transition metal and at least one Lewis base ligand. At least one device is provided for heat removal from the reactor. Methanol is formed as a product.

Abstract: A method is provided for manufacturing vinyl chloride monomer (VCM), the method comprises subjecting ethylene dichloride (EDC) to thermal cracking to yield a VCM-containing gaseous product, in which method an amount of thermal energy required to heat a stream of EDC-containing process fluid to temperature(s), at which cracking reactions occur, is produced and transferred to said EDC-containing process fluid using a rotary apparatus (100). A VCM production unit and use of the rotary apparatus in production of vinyl chloride monomer from EDC through thermal cracking, are further provided.

Abstract: A reaction system includes a wellbore extending from a surface into a subterranean heat source. The reaction system further includes a reaction chamber configured to be maintained at a reaction temperature using heat from the subterranean heat source. The reaction system further includes one or more inlet conduits. The inlet conduits are configured to provide one or more feed streams to the reaction chamber. The reaction system also includes outlet conduits configured to allow flow of one or more product streams.

Abstract: Disclosed is a preparation system and a preparation method for high-quality xylitol crystals. The preparation system comprises a blending tank, a heat exchanger, a decolorization tank, an ion exchange system, a microporous filter, a first evaporator, a first crystallization kettle, a first centrifuge, a fluidization drying bed, a xylitol dissolution tank, a second evaporator, a second crystallization kettle, a second centrifuge, a hot air drying tank, and a cold air fluidization bed sequentially connected through pipelines. Liquid outlet of the first centrifuge is connected with first inlet of the blending tank. Liquid outlet of the second centrifuge is connected with first inlet of the xylitol dissolution tank. The blending tank is provided with second inlet for receiving xylitol hydrogenation solution. The xylitol dissolution tank is provided with water inlet for pure water. The material output from a product outlet of the cold air fluidization bed is xylitol crystal product.