Abstract: The invention relates to a method for purifying an alkyl hydroperoxide from dialkyl peroxide thereof, comprising a step of distillation in the presence of alcohol and water followed by extraction of the condensates using a hydrocarbon or a hydrocarbon blend.

Abstract: To provide a method capable of easily and efficiently removing a 2-alkoxyethanol from a mixture containing the 2-alkoxyethanol and a (2-alkoxyethyl) vinyl ether while suppressing a decrease in the yield of (2-alkoxyethyl) vinyl ether. A method for removing a 2-alkoxyethanol, including the step of adding one or more azeotropic solvents selected from the group consisting of alkanes having 7 to 8 carbon atoms and cycloalkanes having 7 to 8 carbon atoms to a mixture containing the 2-alkoxyethanol represented by the following formula (1) R—O—CH2CH2OH??(1) where R represents an alkyl group having 1 to 4 carbon atoms, and a (2-alkoxyethyl) vinyl ether represented by the following formula (2) R—O—CH2CH2O—CH?CH2??(2) where R has the same meaning as R in the formula (1), and subjecting the resulting mixture to azeotropic distillation.

Abstract: The invention relates to a process for the purification of ethanol wherein a dividing wall column is used. In particular, the invention relates to a process for the purification of a feed stream comprising ethanol and impurities such as higher alcohols. The invention further relates to the use of dividing wall in distillation column in an ethanol purification process.

Abstract: A method for upgrading fluid catalytic cracking gasoline includes the following steps: cutting fluid catalytic cracking gasoline into light, medium, and heavy gasoline fractions; subjecting the medium gasoline fraction to an aromatization/hydroisomerization reaction in the presence of a catalyst to obtain a desulfurized medium gasoline fraction; and blending the light gasoline fraction, the desulfurized medium gasoline fraction and the heavy gasoline fraction to obtain upgraded gasoline; where, a cutting temperature of the light and the medium gasoline fractions is 35-60° C., and a cutting temperature of the medium and the heavy gasoline fractions is 70-160° C. The method according to the present invention not only can realize deep desulfurization of fluid catalytic cracking gasoline, but also can improve octane number significantly.

Abstract: The present invention relates to a process for treating secondary components obtained in acrolein and/or (meth)acrylic acid production, comprising the steps of: a) contacting at least one wastewater stream (201) comprising at least a portion of the water of reaction removed in a first stage of a saturation column (101) with at least one process offgas stream (203), b) introducing energy by means of a first heat transferer (103) provided in a first saturation circuit (301) into the first stage of the saturation column (101), c) partly vaporizing the wastewater stream (201) into the process offgas stream (203) and passing the combined gas stream (205) into a second stage of the saturation column (101), d) drawing off a concentrated wastewater stream (207) from the bottom (1011) of the first stage of the saturation column (101) and feeding it to the top (1023) of the second stage of the saturation column (101), e) introducing energy by means of a second heat transferer (105) provided in a second circuit (303) i

Abstract: The present invention provides a process for desulfurizing gasoline fraction by solvent extraction: introducing the gasoline fraction into an extraction tower at a lower-middle part thereof, introducing a solvent into the extraction tower at the top thereof, injecting saturated C5 hydrocarbon into a reflux device at the bottom of the extraction tower, wherein the gasoline fraction which is desulfurized flows out from the top of the extraction tower; the solvent that has extracted sulfide, aromatics and C5 hydrocarbon flows out from the bottom of the extraction tower, and is separated into a C5 hydrocarbon-containing light component, a sulfur-rich component, water and the solvent. The present invention also provides a process for deeply desulfurizing catalytic cracking gasoline, which flexibly combines the process described above and an existing desulfurization technology.

Abstract: Solvent regeneration to recover a polar hydrocarbon (HC) selective solvent substantially free of hydrocarbons (HCs) and other impurities from a solvent-rich stream containing selective solvent, heavy HCs, and polymeric materials (PMs) generated from reactions among thermally decomposed or oxidized solvent, heavy HCs, and additives is provided. A combination of displacement agent and associated co-displacement agent squeezes out the heavy HCs and PMs from the extractive solvent within a solvent clean-up zone. Simultaneously, a filter equipped with a magnetic field is positioned in a lean solvent circulation line to remove paramagnetic contaminants. The presence of the co-displacement agent significantly enhances the capability of the displacement agent in removing the heavy HCs and PMs from the extractive solvent.

Abstract: A method for purifying used antifreeze is disclosed. An antifreeze recycling systems uses a simple-distillation apparatus adapted to distill clean antifreeze from used antifreeze. A novel scraper blade is used in the simple-distillation apparatus. Also, antifreeze recycling methods that minimize waste and generate nontoxic, landfillable waste are provided. An antifreeze product produced by the present method, and a nontoxic, landfillable sludge product produced by the present method, are disclosed.

Abstract: Product propylene oxide in a reaction mixture resulting from the reaction of propylene, oxygen and hydrogen or from the reaction of propylene and hydrogen peroxide is separated from propylene and/or propane by extractive distillation using methanol and/or water extractive distillation solvent.

Abstract: In the water purification process, apparatus, and method, contaminated water vapor is exposed to liquid solvent, which causes a transfer of contaminants from the contaminated water vapor to the liquid solvent. In an advantageous embodiment, this latter step is followed by a second purification step where the decontaminated water in liquid phase is exposed to water vapor which causes a transfer of solvent remaining in the decontaminated water to the water vapor. The energy freed during the condensation of the vapor can advantageously be used for evaporation of the liquids, optionally by compressing the vapors prior to condensation thereof within heat exchangers.

Abstract: A process for the recovery of substantially pure alkyl alkanoate, such as ethyl acetate, from an impure feedstock. The impure feedstock is contacted with a selective hydrogenation catalyst in the presence of hydrogen in a selective hydrogenation zone maintained under selective hydrogenation conditions effective for selective hydrogenation of impurities containing reactive carbonyl groups thereby to hydrogenate the impurities to the corresponding alcohols. After recovery from the selective hydrogenation zone of a selectively hydrogenated reaction product mixture including the alkyl alkanoate and the corresponding alcohols, this is distilled in one or more distillation zones so as to produce substantially pure alkyl alkanoate therefrom which is recovered.

Abstract: A method of treating cleaning solvent used to clean mechanical parts. The method includes adding to the cleaning solvent a treating composition selected from the group of C.sub.5 -C.sub.14 alcohols, C.sub.2 -C.sub.8 dials, C.sub.10 -C.sub.14 polyols, and C.sub.4 -C.sub.14 glycol ethers, and mixtures thereof. A further embodiment includes the foregoing plus adding a clarifying agent from the group of aromatic, aliphatic and alkaryl sulfonic acids and sulfonic acid salts, esterified polyols, and alkyl phenol formaldehyde resins capped with alkoxy groups. The solvent is vaporized and condensed to effect recycling thereof without adding substituted quantities of treating composition to the solvent.

Abstract: Acetaldehyde may be effectively removed from a contaminated methanol stream using a distillation method wherein a solvent stream containing a relatively heavy polar compound such as water or propylene glycol is utilized as an extractive distillation solvent. Following the separation of the polar compound from the bottoms stream obtained by extractive distillation, the purified methanol may be recycled for use as a reaction solvent in an olefin epoxidation process.

Abstract: The disclosure relates to separating 1,1,1-trifluoroethane (HFC-143a from fluorocarbon impurities by using extractive distillation with an extractive agent comprising an alcohol. Examples of suitable extractive agents comprise at least one member from the group of methanol, butanol, ethanol, propanol, their isomers and cyclic compounds thereof, among others.

Abstract: Propylene oxide is recovered through the use of an additive in a distillation solution, resulting in suppressed side reactions and reduced loss of product. Propylene oxide is produced by oxidizing ethylbenzene in a liquid phase with molecular oxygen to a obtain a reaction liquid containing ethylbenzene hydroperoxide; distilling the reaction liquid to obtain a concentrated solution of ethylbenzene hydroperoxide; further mixing and reacting the concentrated solution with propylene to obtain a mixed solution containing propylene oxide; and distilling the mixed solution to separate and recover propylene oxide. At least one compound selected from aliphatic saturated alcohols having 2 to 4 carbon atoms, allyl alcohol, saturated aliphatic hydrocarbons having 6 or 7 carbon atoms, benzene, ethers, ketones, nitriles, amines, pyridines, diamines, and aminoalcohols is added to the mixed distillation solution in an amount of 0.01-100 parts by weight per 100 parts by weight of propylene oxide.

Abstract: A method is provided for the separation by extractive distillation of hydrocarbon impurities from propylene oxide wherein t-butyl alcohol/water is used as extractive distillation solvent.

Abstract: A mixture of (a) at least one N-alkyl-2-pyrrolidone (preferably N-methyl-2-pyrrolidone) and (b) at least one glycol compound (preferably ethylene glycol or tetraethylene glycol) is used as solvent in the extractive distillation of a feed mixture of cycloalkane(s) (in particular cyclohexane) and close-boiling alkane(s).

Abstract: A mixture of (a) at least one saturated C5-C9 alcohol (preferably cyclohexanol) and (b) at least one sulfolane (preferably unsubstituted sulfolane, cyclotetramethylene sulfone) is used as solvent in the extractive distillation of a feed mixture of cycloalkane(s) in particular cyclohexane) and close-boiling alkane(s). A novel composition of matter contains (a) and (b), as defined above, and optionally also (c) water.

Abstract: A process for purifying diethoxymethane from a mixture containing ethanol and, optionally, water. The process involves the addition of an amount of water, DEM, or an appropriate mixture of any two or three of water, DEM and ethanol that is effective in moving the mixture into the two liquid phase region on an equilibrium tie-line which crosses the critical distillation boundary without the need for additional azeotrope-forming agents such as cyclohexane.

Abstract: The separation of homozeotropic mixtures of a paraffin or paraffins of 6-14 carbon atoms and an alcohol or alcohols of 4-8 carbon atoms is conducted in two rectification steps. In a first step, rectification is carried out in the presence of water as the azeotropic agent, and the resultant distillate, after condensation, is separated into two liquid phases. The thus-obtained organic phase is rectified in a further step without the addition of water, and the head product consisting of an alcohol/paraffin mixture is recycled into the first step. The paraffin or paraffins and the alcohol or alcohols are obtained in the lower section of the individual rectifying step or steps. The water which may be present in the starting mixture is removed from the cycle. Low-boiling paraffins and/or low-boiling alcohols are suitable as additional azeotropic agents.

Abstract: A method of purification of crude .beta.-phenylethyl alcohol to give a highly pure .beta.-phenylethyl alcohol suitable as a perfume, which comprises subjecting the crude .beta.-phenylethyl alcohol to azeotropic distillation in the presence of an azeotropic solvent selected from water, an alkylene glycol, an alkylene glycol monoalkyl ether and a mixture of two or more kinds of these solvents, or extractive distillation in the presence of an extractive solvent selected from glycerine, an alkylene glycol, a polyalkylene glycol, an alkylene glycol monoalkyl ether, a polyalkylene glycol monoalkyl ether and a mixture of two or more kinds of these solvents.

Abstract: In a process of extractive distillation, the combination of operating with two liquid phases in at least the uppermost trays of the column, preferably while maintaining the column operation at substantially an optimum reflux ratio, results in increased efficiencies and minimum requirements for selective solvent.

Abstract: Process for removing hydrochloric acid and other impurities which are contained in vinyl chloride monomer, by treatment in a distillation zone, comprising the addition to crude vinyl chloride, in the course of distillation thereof, of at least one alcohol selected from the group of C.sub.4 to C.sub.10 tertiary aliphatic alcohols and C.sub.3 to C.sub.10 primary or secondary alcohols with unsaturation in the alpha position, and rectifying the vinyl chloride monomer from the resulting mixture.