Abstract: A process for upgrading a hydrocarbon feed to produce light olefins, includes contacting the hydrocarbon feed with steam in the presence of a cracking catalyst in a steam catalytic cracking reactor at reaction conditions sufficient to cause at least a portion of the hydrocarbons in the hydrocarbon feed to undergo one or more cracking reactions to produce a steam catalytic cracking effluent comprising ethylene, propylene, or both, wherein the process is capable of being transitioned between an ethylene-selective mode and a propylene-selective mode; determining whether to produce ethylene or propylene; when producing ethylene, then operating the process in ethylene-selective mode comprises producing more ethylene than propylene; or when producing propylene, then operating the process in propylene-selective mode comprises producing more propylene than ethylene.

Abstract: Methods and systems are provided for producing renewable diesel. Disclosed herein is an example method of method for integration of product separation in renewable diesel production, including: stripping a hydrotreated effluent stream comprising hydrotreated biofeedstock to remove isomerization contaminants and form at least an isomerization feed stream and a first gas stream; contacting an isomerization effluent with the first gas stream such that the isomerization effluent adsorbs at least C4+ hydrocarbons from the first gas stream; and stripping at least a portion of an isomerization effluent in an integrated stripper while separated from the stripping the hydrocarbon stream by a dividing wall to remove hydrocarbons having 10 carbons or less and form at least a product stream and a second gas stream, wherein the product stream comprises renewable diesel.

Abstract: The present disclosure relates generally to processes and systems for producing liquid transportation fuels by converting a feed stream that comprises both isopentane and n-pentane, and optionally, some C6+ hydrocarbons. Isopentane and smaller hydrocarbons are separated to form a first fraction while n-pentane and larger components of the feed stock form a second fraction. Each fraction is then catalytically-activated in a separate reaction zone with a separate catalyst, where the conditions maintained in each zone maximize the conversion of each fraction to olefins and aromatics, while minimizing the production of C1-C4 light paraffins. In certain embodiments, the first fraction is activated at a lower temperature than the second fraction.

Abstract: Processes and systems for C3+ monoolefin conversion. In some examples, the process can include reacting a first mixture that includes C3+ monoolefins and a first oxygenate to produce a first effluent that includes a first ether and <1 wt. % of any first di-C3+ olefin. A first product that includes the first ether and a first byproduct that includes at least a portion of any first di-C3+ olefin and unreacted C3+ monoolefins can be separated from the first effluent. A second olefin mixture, at least a portion of the first byproduct, and a second oxygenate can be combined to produce a second mixture. The second mixture can be reacted to produce a second effluent that includes a second ether and a second di-C3+ olefin. The reaction of the second mixture can produce a greater amount, on a mole basis, of the second di-C3+ olefin than the second ether.

Abstract: A method for producing jet range hydrocarbons may include reacting at least a portion a fatty acid stream comprising C18:1 free fatty acid with ozone in an ozonolysis unit to form at least a C18:1 ozonide intermediate; introducing the C18:1 ozonide intermediate into a reactor, wherein at least a portion of the C18:1 ozonide intermediate is reacted with a reductive agent to produce oxidized products comprising azelaic acid and nonanoic acid; and introducing the oxidized products into a hydrotreating unit, wherein at least a portion of the oxidized products is hydrotreated to produce a paraffin product comprising nonane.

Abstract: A process for cracking olefins to produce propylene, ethylene, or both, includes providing a feed stream that includes mixed butenes and contacting the feed stream with a cracking catalyst at reaction conditions that cause at least a portion of the mixed butenes in the feed stream to react to form propylene, ethylene, or both. The cracking catalyst includes zeolite particles formed from shape selective zeolite particles and an alumina binder. The cracking catalyst further includes at least one transition metal oxide impregnated onto the zeolite particles, where the at least one transition metal oxide can be iron oxide, nickel oxide, or a combinations of these. The cracking catalyst with the iron oxide, nickel oxide, or both increases conversion of mixed butenes to propylene, ethylene, or both alone or in combination with a metathesis upstream of the cracking catalyst, as compared to conventional cracking catalysts.

Abstract: This present disclosure relates to catalytic processes for oligomerizing bio-based olefinic mixtures to higher value renewable fuels via a doped Chabazite zeolite catalyst. A stream including a C2-C8 olefin and an oxygenate is fed to an oligomerization process utilizing a doped Chabazite zeolite catalyst resulting in high yields and selectivity of oligomers used to produce bio-based jet fuel and/or diesel fuels depending upon reaction temperatures and pressures. The process also produces iso-octane that is suitable for producing bio-based gasoline. The process tolerates relatively high levels of oxygenates in the olefinic feed and the catalyst is capable of air regeneration.

Abstract: This disclosure relates to hybrid membranes comprising functionalized fillers within a polymer matrix and methods of using the membranes for gas separation applications, such as removal of hydrogen sulfide (H2S) and carbon dioxide (CO2) from natural gas.

Abstract: This disclosure provides improved processes for converting benzene/toluene via methylation with methanol/dimethyl ether for producing, e.g., p-xylene. In an embodiment, a process utilizes a methylation catalyst system comprising a molecular sieve catalyst and an auxiliary catalyst. The auxiliary catalyst comprises a metal element selected from Group 2, Group 3, the lanthanide series, the actinide series, and mixtures and combinations thereof. The auxiliary catalyst may comprise the oxide of the metal element. Deactivation of the molecular sieve catalyst can be reduced with the inclusion of the auxiliary catalyst in the methylation catalyst system.

Abstract: A method of making an active catalyst composition includes mixing at least one support with a vanadium oxide precursor and grinding thereby at least partially embedding the vanadium oxide precursor particles in different layers and surfaces of the at least one support to form a first precursor; mixing the first precursor and a first solvent to form a first mixture; grinding the first mixture and drying at a temperature of 60 to 105° C.; calcining the first mixture after the drying at a temperature of at least 300° C. thereby allowing the vanadium oxide precursor particles embedded in different layers and surfaces of the at least one support to decompose in situ to generate vanadium oxide (VOx) particles embedded in the at least one support and form the first vanadium catalyst; and mixing the first vanadium catalyst with a second vanadium catalyst to form the active catalyst composition.

Abstract: The present disclosure refers to a process of obtaining a biocrude from biomass, where said process comprises the solvothermal liquefaction of the biomass in the presence of a mixture of solvents, until obtaining a gaseous phase, a solid phase, an aqueous liquid phase and an organic liquid phase comprising the biocrude. Wherein the mixture of solvents comprises between 0.5% w/w to 99.5% w/w of water and at least one solvent; and wherein the solvent is selected from alcohols, ketones, aldehydes, or precursors thereof under the processing conditions. The process described herein allows the use of biomass for the production of renewable fuels, as well as obtaining a biocrude with a yield greater than or equal to 30%, with a calorific value between 20 and 35 MJ/Kg and with a sulfur percentage lower than 1% w/w.

Abstract: Processes and apparatuses for converting carbon dioxide into hydrocarbons. Carbon dioxide and coke are reacted in a reaction zone to produce carbon monoxide. The Carbon monoxide and a hydrogen stream are reacted to produce methanol. The methanol is reacted in reaction zone to produce ethylene and propylene. The hydrogen and the oxygen can be produced in an electrolysis zone that separates water into hydrogen and oxygen.

Abstract: Described herein is a catalytic reaction process including introducing one or more gas-phase reactants into a reactor comprising a microporous catalyst having a pore size less than or equal to 2 nm and adjusting the temperature and/or the pressure of the reactor such that one or more of the gas-phase reactants condense within the micropores of the catalyst thereby causing the catalytic reaction to take place in a liquid phase. Additionally, a process for engineering defects on a carboxylate-based metal organic framework (MOF) catalyst is described. The process includes providing a carboxylate-based MOF catalyst; and heating the carboxylate-based MOF catalyst in an inert gas atmosphere at temperatures between about 150° C. and about 900° C.

Abstract: The present invention relates to an oligomerization process implemented in a gas/liquid reactor comprising a headspace recycle loop. The process more particularly relates to the oligomerization of ethylene to linear alpha-olefins such as 1-butene, 1-hexene, 1-octene or a mixture of linear alpha-olefins.

Abstract: Methods and systems for hydrodeoxygenating a bio-derived feedstock during the production of renewable diesel and generating renewable power as part of the hydrodeoxygenation (HDO) process are provided herein. One method includes providing an HDO catalyst within either a shell or tube side of an isothermal HDO reactor including a shell-and-tube configuration and exposing a bio-derived feedstock to the HDO catalyst within the isothermal HDO reactor to form an HDO reactor effluent. The method also includes flowing a water stream through the opposite side of the isothermal HDO reactor as compared to the side including the HDO catalyst to remove the heat of reaction between the bio-derived feedstock and the HDO catalyst, where the removal of the heat of reaction using the water stream forms steam. The method further includes flowing the steam through a steam turbine to provide for the generation of renewable power.

Abstract: An aspect of the present disclosure relates to a process for preparing a composite hydroalkylation catalyst including: (a) effecting impregnation of a hydrogenation metal on an inorganic oxide to form a metal impregnated inorganic oxide; (b) effecting calcination of the metal impregnated inorganic oxide to obtain a calcined metal impregnated inorganic oxide; (c) preparing a composite mixture comprising a molecular sieve, the calcined metal impregnated inorganic oxide and a binder; (d) preparing an extruded catalyst; and (e) effecting calcination of the extruded catalyst to obtain the composite hydroalkylation catalyst. The composite hydroalkylation catalyst prepared using this process affords dramatic improvement in conversion of mononuclear aromatic hydrocarbon and the yield of the hydroalkyled mononuclear aromatic hydrocarbon (e.g. CHB).

Abstract: Disclosed herein are processes and reaction systems for controlling a temperature of an oligomerization reaction zone using a heat exchange system.

Abstract: Provided is a method of producing a porous molded body, the method including: the step of obtaining a molded body by molding a raw material that contains from 1 part by mass to 100 parts by mass of a bicarbonate compound (A) represented by AHCO3 (wherein, A represents Na or K) and from 0 parts by mass to 99 parts by mass of a compound (B) represented by BnX (wherein, B represents Na or K; X represents CO3, SO4, SiO3, F, Cl, or Br; and n represents an integer of 1 or 2 as determined by the valence of X) (provided that a total amount of (A) and (B) is 100 parts by mass); and the step of obtaining a porous molded body by performing a heat treatment of the molded body in a temperature range of from 100° C. to 500° C. and an atmosphere that contains water vapor in an amount of from 1.0 g/m3 to 750,000 g/m3 and thereby thermally decomposing not less than 90% by mass of the bicarbonate compound (A).

Abstract: A method of removing CO from a mixture of CO and saturated and unsaturated hydrocarbons CO to CO2 is provided. In one embodiment, the method is to contact feed stream with an oxygen transfer agent; and then oxidize at least a portion of the CO to CO2 to produce a stream enriched in CO2. The saturated and unsaturated hydrocarbons in the feed are not further oxidized during the oxidation. The oxygen transfer agent includes at least one of: i) water; ii) at least one reducible metal oxide; iii) at least one reducible chalcogen; or mixtures thereof. In another embodiment, the CO is converted to methane. The unsaturated hydrocarbons in the feed are not hydrogenated. In both of these alternatives, the CO2 or methane are then removed. Systems for removing the CO are also provided.

Abstract: The invention relates to a process for preparing a catalyst for alkane oxidative dehydrogenation and/or alkene oxidation, which catalyst is a mixed metal oxide catalyst containing molybdenum, vanadium, niobium and optionally tellurium, wherein the process comprises: a) preparing a catalyst precursor containing molybdenum, vanadium, niobium and optionally tellurium; b) optionally contacting the catalyst precursor obtained in step a) with oxygen and/or an inert gas at an elevated temperature; c) contacting the catalyst precursor obtained in step a) or step b) with a gas mixture comprising ammonia and water, which gas mixture further comprises oxygen and/or an inert gas, at an elevated temperature; and d) optionally contacting the catalyst precursor obtained in step c) with an inert gas at an elevated temperature.