A process and a preparation plant prepares methacrolein from formaldehyde and propionaldehyde, in presence of water and a homogeneous catalyst based at least on an acid and a base. A reaction mixture is introduced into a methacrolein workup plant and separated in a first distillation column, into a first distillation mixture in a gas phase at the top and a second distillation mixture in a liquid phase at the bottom. The first distillation mixture is condensed and, in a first phase separator, the organic phase and the aqueous phase of the condensate are separated from one another. The aqueous phase is introduced into a second distillation column, that is not part of the methacrolein workup plant, and is separated into a third distillation mixture in a gas phase at the top and a fourth distillation mixture at the bottom. The third distillation mixture is introduced into the methacrolein workup plant.

A process can treat a gaseous material mixture obtained by catalytic conversion of synthesis gas that contains at least alkenes, possibly alcohols and possibly alkanes, and also possibly nitrogen as inert gas and unconverted components of the synthesis gas, comprising hydrogen, carbon monoxide and/or carbon dioxide. After catalytic conversion of synthesis gas, separation of the product mixture obtained in this reaction into a gas phase and a liquid phase is performed by at least partial absorption of the alkenes, possibly of the alcohols and possibly of the alkanes, in a high boiling point hydrocarbon or hydrocarbon mixture as an absorption medium, separation as the gas phase of the gases not absorbed into the absorption medium, separating an aqueous phase from the organic phase of the absorption medium, preferably by decanting, and desorption of the alkenes, possibly of the alcohols and possibly of the alkanes, from the absorption medium.

A process can produce alcohols having at least two carbon atoms by catalytic conversion of synthesis gas into a mixture containing alkanes, alkenes, and alcohols. Alkenes are converted into corresponding alcohols in a subsequent step by hydration of the alkanes. Before the hydration and after the catalytic conversion, gas and liquid phases may be separated. Specific catalysts can be employed that have a markedly higher selectivity for alkenes than for alkanes. These catalysts comprise grains of non-graphitic carbon having cobalt nanoparticles dispersed therein. The cobalt nanoparticles have an average diameter d.sub.p from 1 to 20 nm, and an average distance D between nanoparticles is from 2 to 150 nm. The combined total mass fraction of metal ω in the grains ranges from 30% to 70% by weight of the total mass of the grains of non-graphitic carbon, wherein 4.5 dp/ω>D≥0.25 dp/ω.

An apparatus, system, and method to purify produced water from a wellbore using heat energy recovery. The apparatus comprises a wellbore with a wellhead attached to the wellbore; at least one energy recapture device connected to the wellhead of the wellbore with produced water, wherein the at least one energy recapture device captures heat energy of the production fluids including produced water, and at least one distillation device connected to a heat recovery device wherein the at least one distillation device uses at least a portion of the energy from the heat energy recovery device to heat a volume of the produced water in the distillation device to remove contaminants from the produced water to create purified water. The method comprises steps to use the apparatus and the system comprises a control panel that operates at least one energy recapture device.

The invention relates to a process for the production of 1,4-butanediol comprising the preparation of a fermentation broth comprising 1,4-butanediol from renewable sources and water, separation of a liquid fraction comprising said 1,4-butanediol and water from one or more solid fractions, said liquid fraction comprising 2-pyrrolidone in an amount higher than 80 ppm, one or more passages of the resulting liquid fraction through a bed comprising one or more cation-exchange resins thereby providing an output pH of said liquid fraction from 4 to 2, one or more passages of the resulting liquid fraction through a bed comprising one or more anion-exchange resins thereby providing an output pH of said liquid fraction from 8 to 11, and the distillation of the liquid fraction thereby provided so as to obtain a composition having a concentration of said 1,4-butanediol higher than 99.0% by weight and comprising 2-pyrrolidone in an amount lower than 6 ppm. The resulting composition should exhibit an APHA color value after ageing of less than 30.

A system of concentrating and separating waste solvent liquid includes a distillation tower, an extracting distillation unit, an extract agent recovery unit, and a vapor permeation film unit. The scheme of centrifugal distillation is specifically employed to collocate with vapor permeation to effectively concentrate the content of isopropanol in the waste solvent liquid to generate a final produce with ultra high concentration of isopropanol, and constantly recovers the extract agent. The system is able to be quickly settled to a steady state of operation with low power consumption because the extracting distillation unit has smaller size. Since no liquid is left in the extract agent recovery unit, operation risk is greatly reduced. In addition, the input feed is almost processed, overall efficiency is thus improved. The vapor permeation film unit further removes considerably little content of water from the organic solvent to increase the content of isopropanol up to 99.9% or more.

A system of concentrating and separating waste solvent liquid includes a distillation tower, an extracting distillation unit, an extract agent recovery unit, and a vapor permeation film unit. The scheme of centrifugal distillation is specifically employed to collocate with vapor permeation to effectively concentrate the content of isopropanol in the waste solvent liquid to generate a final produce with ultra high concentration of isopropanol, and constantly recovers the extract agent. The system is able to be quickly settled to a steady state of operation with low power consumption because the extracting distillation unit has smaller size. Since no liquid is left in the extract agent recovery unit, operation risk is greatly reduced. In addition, the input feed is almost processed, overall efficiency is thus improved. The vapor permeation film unit further removes considerably little content of water from the organic solvent to increase the content of isopropanol up to 99.9% or more.

System and method for producing 1-butene are disclosed. The method includes dehydrogenating butane to form a mixture comprising butene isomers. 1-butene is separated from the mixture using a system that includes a membrane. The system also includes an isomerizing unit for isomerizing cis-2-butene and trans-2-butene to form additional 1-butene.

Disclosed is a method of purifying a stream of crude hydrochlorofluoroolefin refrigerant produced by the reaction of 1,1,3,3 tetrachloropropene (R1230za) or 1,1,1,3,3-pentachloropropane (R240fa) with HF. The process includes a step of removing the cis-(Z) isomer by distillation of the crude refrigerant stream prior to a step of reacting the crude refrigerant stream with a base. The reaction with the base is a necessary step in production of the refrigerant and is done to remove HF and residual HCl from the crude refrigerant stream. Removal of the cis-(Z) isomer before the reaction with the base reduces the amount of toxic flammable trifluoropropyne (TFP) that is produced as a side-reaction during the reaction with the base. In addition, temperature control during the reaction with the base is less critical to minimizing the TFP production if the cis-(Z) isomer is first removed.

A filtering device is used for obtaining a chemical liquid by purifying a liquid to be purified and includes an inlet portion, an outlet portion, a filter A, at least one filter B different from the filter A, and a flow path that includes the filter A and the filter B arranged in series and extends from the inlet portion to the outlet portion. The filter A has a porous membrane made of ultra-high-molecular-weight polyethylene and a resin layer disposed to cover at least a portion of the surface of the porous membrane, and the resin layer includes a resin having a neutral group or an ion exchange group.