Abstract: In an embodiment, a process of making C2+ hydrocarbons comprises contacting a feed comprising a methane steam reforming gas and an additional carbon dioxide with a manganese oxide-copper oxide catalyst to produce a product syngas in a contacting zone under isothermal conditions at a temperature of 620 to 650° C.; and converting the product syngas to C2+ hydrocarbons in the presence of a Fischer-Tropsch catalyst; wherein the methane steam reforming gas has an initial H2:CO volume ratio greater than 3; wherein the product syngas has a H2:CO volume ratio of 1.5 to 3; and wherein the contacting further comprises removing water.

Abstract: A compound has Structure I: where R1 and R2 independently are C2-C12 alkyl groups, R3 and R3? independently are H or CH3, X1 is a C4-C28 alkyl or alkenyl group, and R4 is H or a N,N-bis((meth)acryloylalkyl)-amide group having Structure II: where R5 and R6 independently are C2-C12 alkyl groups, and R3? and R3?? independently are either H or CH3.

Abstract: In one aspect, the present invention provides a method for recycling natural gas during a reformer startup in a methanol plant. The method comprises recycling natural gas from a point before entry into the natural gas saturator where the natural gas is recycled until the natural gas reaches a desired temperature.

Abstract: A process for ammonia-urea production where: liquid ammonia produced in an ammonia section is fed to a urea section directly at the ammonia synthesis pressure, and where the liquid ammonia is purified at high pressure with the steps of: cooling the liquid ammonia (20) obtaining a cooled liquid ammonia stream (21), separating a gaseous fraction (22) comprising hydrogen and nitrogen from said cooled liquid ammonia, obtaining purified liquid ammonia (23) at a high pressure, and reheating said purified liquid ammonia (23) after separation of said gaseous fraction, obtaining a reheated purified ammonia (24) having a temperature suitable for feeding to the urea synthesis process. The application also deals with an ammonia-urea plant comprising an ammonia cooler, a liquid-gas separator and an ammonia re-heater and with a method for revamping existing ammonia-urea plants.

Abstract: A method for preparing a polyoxymethylene dimethyl ether carbonyl compound and/or methyl methoxyacetate as intermediates for producing ethylene glycol, which comprises passing a raw material: polyoxymethylene dimethyl ether or methylal together with carbon monoxide and hydrogen gas through a reactor carrying an acidic molecular sieve catalyst, and performing a reaction to prepare a corresponding product under an appropriate condition where no other solvent is added, in which the process of the reaction is a gas-liquid-solid three-phase reaction, the raw material of polyoxymethylene dimethyl ether or methylal has a high conversion rate, each product has a high selectivity, the catalyst has a long service life, additional solvents are not required to be used, and reaction conditions are relatively mild.

Abstract: Catalyst compositions, methods of making catalysts, and methods of conducting Fischer-Tropsch (FT) reactions are described. It has been discovered that a combination of large crystallite size and high porosity results in catalysts and FT catalyst systems with high stability and low methane selectivity.

Abstract: In a process for producing biphenyl compounds, a Cn aromatic hydrocarbon may be hydroalkylated to give C2n cycloalkylaromatic compounds and byproduct Cn saturated cyclic hydrocarbons. The C2n cycloalkylaromatic compounds are dehydrogenated to provide the biphenyl compounds. The Cn saturated cyclic hydrocarbons may also be dehydrogenated back to the corresponding Cn aromatic hydrocarbon, which may be recycled to provide additional feed. Although both the intermediate C2n cycloalkylaromatic compounds and the byproduct Cn saturated cyclic hydrocarbons should be dehydrogenated, at least part of the dehydrogenation of the Cn saturated cyclic hydrocarbons should take place in the absence of C2n or greater hydrocarbons. Thus, dehydrogenation of the byproduct Cn saturated cyclic hydrocarbons should take place at least in part separately from dehydrogenation of the C2n cycloalkylaromatic compounds.

Abstract: The invention relates to a process to prepare 2-chloro-3,3,3-trifluoropropene (HCO-1233xf) or 2-chloro-1,1,12-tetrafluoropropane (HCFC-244bb) using dichloro-trifluoropropanes and/or trichloro-difluoropropanes, and to prepare 2-chloro-3,3,3-trifluoropropene (HCO-1233xf) using various 242 and 243 isomers.

Abstract: The process for producing amino acids from volatile fatty acid (VFA) molecules, referred to as precursors, produced by anaerobic fermentation from fermentable biomass, comprises at least the following steps: a) extracting the volatile fatty acid (VFA) molecules, without stopping the fermentation, via an extraction means chosen from means that are, at least, insoluble in the fermentation medium, b) collecting, outside the fermentation reactor, the volatile fatty acid (VFA) molecules once they have been extracted, c) synthesizing, by halogenation, using a type of volatile fatty acid (VFA) chosen from the volatile fatty acids collected in step b) and defined according to the desired type of amino acid, a given ?-halo acid, d) synthesizing from this ?-halo acid a defined amino acid.

Abstract: The present disclosures and inventions relate to a method including the steps of: a) introducing a natural gas; b) reforming the natural gas; wherein the reforming step comprises contacting the natural gas with steam to produce a syngas; c) converting the syngas to a product mixture comprising an olefin, carbon dioxide, and hydrogen; wherein the converting step comprises contacting the syngas with a Co/Mn catalyst; and d) converting at least some process hydrogen and at least some process and/or external carbon dioxide to syngas by a reverse water gas shift reaction, and recycling such reverse water gas shift reaction produced syngas to before step c).

Abstract: Hydroxycarboxylic acids, e.g., 3-hydroxypropionic acid, and/or their ammonium salts are dehydrated to their corresponding unsaturated carboxylic acids, e.g., acrylic acid, by a process that uses a catalyst comprising ammonium bisulfate. The use of ammonium bisulfate reduces or eliminates the problems associated with processes that use sulfuric acid as a dehydrating catalyst, e.g, excess sulfuric acid consumption and/or recovery.

Abstract: This disclosure relates to a ligand compound, a catalyst system for olefin oligomerization, and a method for olefin oligomerization using the same. The catalyst system for olefin oligomerization according to the present invention has excellent catalytic activity, and yet, exhibits high selectivity to 1-hexene and 1-octene, thus enabling efficient preparation of alpha-olefin.

Abstract: Alternative continuous downstream processes for the production of 5-acetamido-N,N?-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide (“Compound A”) are described. Compound A is a key intermediate in the production of iodixanol and iohexol, which are two of the biggest commercially available non-ionic x-ray contrast media agents.

Abstract: The present disclosures and inventions relate to a method comprising: a) introducing a natural gas; b) reforming the natural gas; wherein the reforming step comprises contacting the natural gas with steam to produce a syngas; c) converting the syngas to a product mixture comprising at least one olefin and a byproduct comprising a paraffin and a gasoline; wherein the converting step comprises contacting the syngas with a Co/Mn catalyst; and d) converting the byproduct to syngas.

Abstract: Analgesic compounds for treatment of pain or fever, comprising a bicyclopentane moiety linked to an amine, combinations of the compounds with opioid analgesic drugs, and methods for treating pain or fever by administering the compounds.

Abstract: Techniques for synthesizing methanol are provided. In an exemplary embodiment, the processes include obtaining a syngas mixture from an integrated carbon dioxide hydrogenation process and a methane steam reforming process, and contacting the syngas mixture with a methanol catalyst to obtain a product stream comprising methanol.

Abstract: An alternative acetylation process for the synthesis of 5-acetamido-N,N?-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide (“Compound A”), an intermediate in the industrial preparation of non-ionic X-ray contrast agents, is described. The process can be performed on an industrial scale to produce Compound A with improved purity and improved yields compared to the established processes.

Abstract: Process for scrubbing a crude mixture which is obtained in the nitration of toluene after separating off the nitrating acid and comprises dinitrotoluene, nitric acid, nitrogen oxides and sulfuric acid, which comprises two scrubbing steps (WS-I) and (WS-II), wherein i) in a first scrubbing step (WS-I), the crude mixture is extracted with a scrubbing acid I comprising nitric acid, nitrogen oxides and sulfuric acid in a scrub comprising at least one extraction stage, where the scrubbing acid discharged from the first extraction stage (WS-I-1) of the first scrubbing step (WS-I) has a total acid content of from 10 to 40% by weight and a content of from 80 to 350 ppm of hydrocyanic acid, giving a prescrubbed crude mixture, ii) in a second scrubbing step (WS-II), the prescrubbed crude mixture comprising dinitrotoluene is extracted with a scrubbing acid II in a scrub comprising at least one, preferably at least 2, extraction stage(s), where the scrubbing acid discharged from the first extraction stage (WS-II-1) of th

Abstract: The present invention provides a bifunctional catalyst of the formula (1): wherein: each R1 is independently selected from an optionally substituted alkyl group, an optionally substituted cycloalkyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, an optionally substituted aralkyl group and an optionally substituted alkaryl group; Z represents a divalent organic linking moiety optionally containing one or more stereocenters; and EWG represents an electron-withdrawing group.

Abstract: Compounds that stimulate fibroblast growth factor production, and thus cell growth are provided. Also provided are compositions comprising the compounds and methods of using the compounds. The compounds can be used to treat wounds, to expand cell populations, such as hematopoietic cells, or to grow tissue in vitro, among other uses.