A process for endothermic dehydrogenation including contacting a catalyst material in a moving bed reactor having at least one reaction zone, the moving bed reactor comprising a heat exchanger containing a heating medium, wherein the catalyst material and the heating medium do not contact one another, and wherein at least 50% of the delta enthalpy of the at least one reaction zone is provided by the heat exchanger; and contacting a feedstock comprising hydrocarbons with the catalyst material in the at least one reaction zone of the moving bed reactor under reaction conditions to convert at least a portion of the hydrocarbons to a first effluent comprising a product comprising alkenes, alkynes, cyclic hydrocarbons, and/or aromatics.

Systems and methods for the electrochemical conversion of COT to multi-carbon products are provided. Each system and method comprises a sequence of multiple, independently optimized electrochemical reaction steps that take place in separate reaction chambers.

Systems and methods are provided for performing steam cracking on a feed while using direct heating of the reaction environment. The heating of the reaction environment can be achieved in part by transporting heat transfer particles from a heating zone to cracking zone. This can be performed in a fluidized bed reactor, a moving bed reactor, a riser reactor, or another type of reactor that can allow for catalyst movement and regeneration during operation.

A process for endothermic dehydrogenation including contacting a catalyst material in a moving bed reactor having at least one reaction zone, the moving bed reactor comprising a heat exchanger containing a heating medium, wherein the catalyst material and the heating medium do not contact one another, and wherein at least 50% of the delta enthalpy of the at least one reaction zone is provided by the heat exchanger; and contacting a feedstock comprising hydrocarbons with the catalyst material in the at least one reaction zone of the moving bed reactor under reaction conditions to convert at least a portion of the hydrocarbons to a first effluent comprising a product comprising alkenes, alkynes, cyclic hydrocarbons, and/or aromatics.

A process for endothermic dehydrogenation including contacting a catalyst material in a moving bed reactor having at least one reaction zone, the moving bed reactor comprising a heat exchanger containing a heating medium, wherein the catalyst material and the heating medium do not contact one another, and wherein at least 50% of the delta enthalpy of the at least one reaction zone is provided by the heat exchanger; and contacting a feedstock comprising hydrocarbons with the catalyst material in the at least one reaction zone of the moving bed reactor under reaction conditions to convert at least a portion of the hydrocarbons to a first effluent comprising a product comprising alkenes, alkynes, cyclic hydrocarbons, and/or aromatics.

An electrochemical conversion method for converting at least a portion of a first mixture comprising hydrocarbon to C.sub.2+ unsaturates by repeatedly applying an electric potential difference, V(.sub.1), to a first electrode of an electrochemical cell during a first time interval .sub.1; and reducing the electric potential difference, V(.sub.1), to a second electric potential difference, V(.sub.2), for a second time interval .sub.2, wherein .sub.2.sub.1. The method is beneficial, among other things, for reducing coke formation in the electrochemical production of C.sub.2+ unsaturates in an electrochemical cell. Accordingly, a method of reducing coke formation in the electrochemical conversion of such mixtures and a method for electrochemically converting carbon to C.sub.2+ unsaturates as well as an apparatus for such methods are also provided.

Surface modification agents may be included in emulsified acidic treatment fluids to leave surfaces in carbonate formations water wet after acidizing operations. A method of acidizing a subterranean formation, comprising: providing a treatment fluid in the form of an invert emulsion, wherein the treatment fluid comprises: a hydrocarbon phase comprising an oil-soluble liquid and an emulsifier; and an aqueous acidic phase comprising water, an acid, and a surface modification agent; and introducing the treatment fluid into a wellbore.

A process is described for obtaining high-purity 1-butene starting from C.sub.4 hydrocarbon mixtures containing isobutene, n-butane, isobutane, 1,3-butadiene, 1-butene, 2-butenes and also optionally C.sub.3 and C.sub.5 hydrocarbons, comprising the following stages: conversion of isobutene effected in a double stage, wherein each stage consists of one or more reactors followed by a distillation column for the recovery of the reaction product; recovery of the excess alcohol; recovery of 1-butene using at least two distillation columns; characterised in that it also uses a further conversion stage, consisting of one or more reactors in series, for completing the isobutene removal.

A process and system for preparing C.sub.2 to C.sub.5 hydrocarbons includes introducing a feed stream containing hydrogen gas and a carbon-containing gas selected from carbon monoxide, carbon dioxide, and mixtures thereof into a first reaction zone, contacting the feed stream and a hybrid catalyst in the first reaction zone, introducing a reaction zone product stream into a water removal zone that is downstream from the first reaction zone, and introducing a product stream from the water removal zone into a second reaction zone, resulting in a final stream comprising C.sub.2 to C.sub.5 hydrocarbons. The hybrid catalyst includes a methanol synthesis component and a microporous solid acid component; the microporous solid acid component is a molecular sieve having 8-MR access. The water removal zone removes at least a portion of water from the reaction zone product stream.

A process and system for preparing C.sub.2 to C.sub.5 hydrocarbons includes introducing a feed stream containing hydrogen gas and a carbon-containing gas selected from carbon monoxide, carbon dioxide, and mixtures thereof into a first reaction zone, contacting the feed stream and a hybrid catalyst in the first reaction zone, introducing a reaction zone product stream into a water removal zone that is downstream from the first reaction zone, and introducing a product stream from the water removal zone into a second reaction zone, resulting in a final stream comprising C.sub.2 to C.sub.5 hydrocarbons. The hybrid catalyst includes a methanol synthesis component and a microporous solid acid component; the microporous solid acid component is a molecular sieve having 8-MR access. The water removal zone removes at least a portion of water from the reaction zone product stream.