A method for processing pentanes obtained from a DIB unit is disclosed. The process can include separating a first stream containing pentanes obtained from a DIB unit, in a separation column to obtain a second stream comprising iso-pentane and a third stream comprising n-pentane and neo-pentane; and subjecting the third stream to a butane isomerization unit producing a fourth stream containing iso-pentane, n-pentane, and neo-pentane.

This invention relates to a method for preparing 1,4-cyclohexane dicarboxylic acid (CHDA). More specifically, this invention relates to a method for preparing 1,4-cyclohexane dicarboxylic acid having a high rate of trans isomers, without an isomerization reaction step.

Steam cracking of ethane, a non-catalytic thermochemical process, remains the dominant means of ethylene production. The severe reaction conditions and energy expenditure involved in this process incentivize the search for alternative reaction pathways and reactor designs which maximize ethylene yield while minimizing cost and energy input. According to the present invention, ethylene yields as high as 68% were obtained with a quartz open tube reactor without the use of a catalyst or a cofed stream of oxidizing agents. The open tube reactor design promotes simplicity, low cost, and negligible coke formation. Reactor designs can be optimized to improve the conversion of ethane to ethylene via non-oxidative dehydrogenation, an approach which shows promise for decentralized production of ethylene from natural gas deposits.

Various processes for preparing aldaric acids, aldonic acids, uronic acids, and/or lactone(s) thereof are described. For example, processes for preparing a C.sub.2-C.sub.7 aldaric acid and/or lactone(s) thereof by the catalytic oxidation of a C.sub.2-C.sub.7 aldonic acid and/or lactone(s) thereof and/or a C.sub.2-C.sub.7 aldose are described.

A photoreactor having computer actuated input/output ports is operated by introducing reactant through an input port and collecting product through an output port, and upon closure of the input and output ports, treating photocatalyst within the photoreactor to remove intermediates limiting performance of the photocatalyst. Once the photocatalyst is regenerated, introduction of reactant to the photoreactor through the input port and collection of product from the output port can be resumed. The automated process does not require removal of catalyst from the photoreactor and significantly improves process economics.

A method for the aromatization of hydrocarbons, comprising: introducing a feed stream to an aromatization catalyst in a fixed bed reactor wherein the feed stream comprises a hydrocarbon having 2 to 4 carbon atoms, converting the hydrocarbon having 2 to 4 carbon atoms to form an outlet stream comprising an aromatic hydrocarbon; wherein the feed stream is introduced at a GHSV of greater than or equal to 4,000 milliliters per gram of catalyst per hour(ml.Math.g.sup.−1 Cat.Math.h.sup.−1), and a pressure of greater than or equal to 0.4 MPa. The feed stream can comprise hydrogen in an amount of at least 0.1 volume percent (vol %) up to 20 vol % based upon total volume of the feed stream.

A MXene support for a noble metal that forms a catalyst having active sites comprising single metal-layer nanostructures. The catalyst is stable under conditions for methane conversion to higher hydrocarbons and provides reduced coke formation. The results show a supported metal catalyst using the MXene where Pt atoms form one or more layers of atoms on the surface of the Mo.sub.2TiC.sub.2T.sub.x support after it is reduced at 750° C. The catalyst shows high selectivity for C.sub.2-hydrocarbons with reduced coke formation, which can cost effectively convert methane into other valuable products.

The present invention relates to a catalyst for producing olefins from dehydrogenation of alkane having 2 to 5 carbon atoms and a method for producing olefins using said catalyst, wherein said catalyst comprises a hierarchical zeolite nanosheet having a silica to alumina (SiO.sub.2/AI.sub.2O.sub.3) ratio more than 120 and group X metal(s) in a range of 0.3 to 5% by weight. The catalyst according to the conversion of precursor to yields and high olefins selectivity.

A dehydrogenation catalyst for producing propylene by a dehydrogenation reaction of propane, the dehydrogenation catalyst including a platinum element and an element M1 and may contain an element M2 as active components, wherein the element M1 is one or more elements selected from the group consisting of a gallium element, a cobalt element, a copper element, a germanium element, a tin element and an iron element, the element M2 is one or more elements selected from the group consisting of a lead element and a calcium element, and the platinum element and the element M1 form an alloy.

The present disclosure generally relates to a process for converting a hydrocarbon feed including introducing a hydrocarbon feed comprising a C.sub.1+ alkane to a catalyst composition in a reactor, the catalyst composition comprising a Group 6-Group 15 metal supported on a support; and irradiating the hydrocarbon feed and the catalyst composition with electromagnetic energy in the reactor at reactor conditions to produce a product comprising a C.sub.2+ alkane, wherein the C.sub.2+ alkane of the product is heavier than the C.sub.1+ alkane in the hydrocarbon feed.