Abstract: Fatty alcohol containing admixed therewith a small amount on the order of up to 1.0 wt. % of hypophosphorous acid, exhibits markedly reduced oxidation and oxidation-related deterioration such as discoloration and other side effects. This discovery is particularly useful when the fatty alcohol is subjected to reactions such as esterification under conditions which could cause or accelerate undesired oxidation.
Abstract: A method for the on-site reprocessing of isopropyl alcohol used in semiconductor manufacturing, to generate an ultradry and ultrapure isopropyl alcohol. This ultradry and ultrapure isopropyl alcohol is produced through a pervaporation step, followed by double distillation. In the first distillation step, an autonomous azeotropic self-stripping distillation column is used to produce an ultradry and partially purified isopropyl alcohol. In the next step, the isopropyl alcohol is distilled in an overhead product distillation column, to produce an ultrapure and ultradry isopropyl alcohol. Alternatively, if the feed isopropyl alcohol contains less than 2000 ppm water, the pervaporation step may be omitted.The resulting isopropyl alcohol has between a high of 100 parts per million (ppm) and a low of 0.1 ppm of water in the isopropyl alcohol. It also has zero particles per milliliter of a size larger than 2.0 microns, zero to 2 particles per milliliter of a size of 0.5 micron to 2.
Type:
Grant
Filed:
August 2, 1996
Date of Patent:
February 9, 1999
Assignee:
Athens Corporation
Inventors:
John A. Adams, Gerald A. Krulik, Christopher Blatt, David Persichini
Abstract: Methyl ethyl ketone cannot be separated from ethanol by distillation or rectification because of the closeness of their boiling points. Methyl ethyl ketone is readily separated from ethanol by azeotropic distillation. Effective agents are amyl acetate, methyl formate, 2,2-dimethyl butane and 2,3-dimethyl butane.
Abstract: Described is a microbiological method for producing C.sub.9, C.sub.11 and C.sub.13 alkanols defined according to the structures: ##STR1## wherein R.sub.1 is methyl or n-propyl using ketones defined according to the generic structure: ##STR2## as a substrate and using the microorganism: Pseudomonas cepacia ATCC 55792or mutants thereof.
Type:
Grant
Filed:
April 23, 1998
Date of Patent:
February 2, 1999
Assignee:
International Flavors & Fragrances Inc.
Inventors:
Mohamad I. Farbood, Laura E. Kizer, Lynda B. McLean, Mark A. Sprecker
Abstract: A method for producing butyraldehydes, by separating and purifying mixed butyraldehyde products formed by hydroformylation of propylene, into n-butyraldehyde and isobutyraldehyde by using a distillation column, wherein the distillation column is operated under such conditions that the pressure at the top of the distillation column is within a range of from 0.001 to 0.5 kg/cm.sup.2 G, and the pressure at the bottom of the column is within a range of from 0.05 to 1.0 kg/cm.sup.2 G.
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: 4-Methyl-2-pentanol cannot be separated from 3-methyl-1-butanol by distillation because of the closeness of their boiling points. 4-Methyl-2-pentanol can be easily separated from 3-methyl-1-butanol by extractive distillation. Effective agents are dodecane, dimethylformamide and dimethylsulfoxide.
Abstract: Ethanol, isopropanol and water cannot be separated from each other by distillation or rectification because of minimum azeotropes. They are readily separated by extractive distillation. Effective agents are: dimethylsulfoxide for ethanol, phenol for isopropanol.
Abstract: 2-Butanol cannot be separated from isobutanol by distillation or rectification because of the closeness of their boiling points. 2-Butanol is readily separated from isobutanol by extractive distillation. Effective agents are propylene glycol propyl ether, 2-methoxyethanol and ethyl acetate.
Abstract: 3-Methyl-1-butanol is difficult to separate from 1-pentanol by conventional distillation or rectification because of the proximity of their boiling points. 2 Methyl-1-butanol can be easily separated from 1-pentanol by extractive distillation. Effective agents are phenol, anisole and methyl salicylate.
Abstract: 2-Methyl-1-butanol and 3-methyl-1-butanol are difficult to separate from 1-pentanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-butanol and 3-methyl-1-butanol can be easily separated from 1-pentanol by azeotropic distillation. Effective agents are toluene, methyl acetate and tetrahydrofuran.
Abstract: An apparatus and method for treating chemical production plant process condensate and low pressure purge gas such that a contaminant-rich stream is recoverable from the condensate and purge gas, wherein the contaminants are substantially removed from the condensate by steam stripping and subsequent rectification in a relatively low pressure stripping/rectification tower. The tower overhead is then condensed, and any non-condensed gases are subjected to water scrubbing, along with the low pressure purge gas to further recover contaminates from the non-condensed gas. A portion of the condensed overhead and scrubbing water containing contaminates is returned to the top of the rectification section of the tower as reflux and the balance being withdrawn as a concentrated stream for reuse in the plant. The apparatus may be used in conjunction with existing low pressure equipment, avoiding costly major modifications, and is particularly adapted to use in conjunction with ammonia and methanol plants.
Abstract: 1-Propanol cannot be separated from t-amyl alcohol by distillation or rectification because of the closeness of their boiling points. 1-Propanol is readily separated from t-amyl alcohol by azeotropic distillation. Effective agents are heptane, ethyl acetate and tetrahydrofuran.
Abstract: 4-Methyl-2-pentanol cannot be separated from 3-methyl-1-butanol by distillation because of the closeness of their boiling points. 4-Methyl-2-pentanol can be easily separated from 3-methyl-1-butanol by azeotropic distillation. Effective agents are m-xylene and cumene.
Abstract: 1-Propanol and t-amyl alcohol cannot be separated by distillation or rectification because of the closeness of their boiling points. 1-Propanol is readily separated from t-amyl alcohol by extractive distillation. Effective agents are dipentene, amyl acetate and 1,4-dioxane.
Abstract: 3-Methyl-1-butanol cannot be separated from 1-pentanol by distillation or rectification because of the closeness of their boiling points. 3-Methyl-1-butanol is readily separated from 1-pentanol by azeotropic distillation. Effective agents are methylcyclohexane, methyl formate and tetrahydrofuran.
Abstract: Ethanol, isopropanol and water cannot be separated from each other by rectification because of the presence of minimum azeotropes. They are readily separated by azeotropic distillation. Effective agents are cyclopentane for ethanol from water, methyl acetate for isopropanol from water.
Abstract: 3-Methyl-1-butanol cannot be separated from 1-pentanol by distillation or rectification because of the closeness of their boiling points. 3-Methyl-1-butanol is readily separated from 1-pentanol by extractive distillation. Effective agents are butyl benzoate, 2-undecanone and diethylene glycol methyl ether.
Abstract: 2-Butanol cannot be separated from t-amyl alcohol by distillation or rectification because of the closeness of their boiling points. 2-Butanol is readily separated from t-amyl alcohol by azeotropic distillation. Effective agents are methyl acetate, ethyl propionate and octane.
Abstract: The process claimed enables three separate streams to be obtained, from mixtures containing methanol, ethanol, n-propanol, isobutanol, water and other both low- and high-boiling compounds, of which one is anhydrous basically consisting of methanol and ethanol (I), one containing most of the n-propanol present in the mixture fed (II), together with small quantities of methanol, ethanol, isobutanol and water, and one containing most of the isobutanol and high-boiling compounds present in the above mixture (III), by the use of three rectifying columns, stream (I) being taken from a lateral point of the first column, stream (II) obtained from the head of the second column, stream (III) obtained from the bottom of the second column.
Abstract: An MTBE recycle stream (which consists mainly of TBA and methanol) contaminated with residual amounts of tertiary butyl hydroperoxide, ditertiary butyl peroxide and allyl tertiary butyl peroxide can be effectively catalytically treated under mild conversion conditions with a silica-supported nickel, copper, chromium, iron catalyst in order to substantially completely decompose the peroxide contaminants and to thereby provide a treated MTBE recycle stream which is not only substantially free from contaminating quantities of such peroxides, but which also contains an enhanced amount of methyl tertiary butyl ether.
Abstract: T-Amyl alcohol is difficult to separate from 2-methyl-1-propanol by conventional distillation or rectification because of the proximity of their boiling points. T-Amyl alcohol can be easily separated from 2-methyl-1-propanol by azeotropic distillation. Effective agents are triethyl amine, ethyl ether and acetone.
Abstract: 2-Methyl-1-propanol is difficult to separate from 2-methyl-1-butanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-propanol can be readily separated from 2-methyl-1-butanol by extractive distillation. Effective agents are hexyl formate, 2-heptanone and dipropyl amine.
Abstract: Disclosed is a method for decomposing formate esters, free acids and peroxides in a tertiary butyl alcohol stream to produce noncondensible gas products which comprises reacting said tertiary butyl alcohol stream or a methyl tertiary butyl alcohol stream containing formate esters over a catalyst comprising a non-noble Group VIII metal and a metal of Group IB on a support comprising an inert composition mixed with a hydrotalcite-like composition.
Abstract: 2-Methyl-1-propanol is difficult to separate from 2-butanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-propanol can be readily separated from 2-butanol by extractive distillation. Effective agents are hexyl acetate, dimethyl phthalate and p-xylene.
Abstract: 2-Methyl-1-propanol is difficult to separate from 1-butanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-propanol can be readily separated from 1-butanol by extractive distillation. Effective agents are ethyl benzene, amyl acetate and propoxypropanol.
Abstract: T-Amyl alcohol and 2-methyl-1-propanol are difficult to separate by conventional distillation or rectification because of the proximity of their boiling points. T-Amyl alcohol can be easily separated from 2-methyl-1-propanol by extractive distillation. Effective agents are N,N-dimethylacetamide, cyclohexyl amine and glycerol.
Abstract: 2-Methyl-1-propanol is difficult to separate from 1-butanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-propanol can be easily separated from 1-butanol by azeotropic distillation. Effective agents are isobutyl acetate, methyl cyclohexane and 2-nitropropane.
Abstract: 1-Butanol is difficult to separate from 2-pentanol by conventional distillation or rectification because of the proximity of their boiling points. 1-Butanol can be easily separated from 2-pentanol by extractive distillation. Effective agents are anisole, ethyl nonanate and butyl ether.
Abstract: Butyraldehyde cannot be separated from ethanol by conventional distillation or rectification because they form a minimum boiling azeotrope. Butyraldehyde can be readily separated from ethanol by extractive distillation. Effective agents are 2-propanol, m-xylene and dimethylsulfoxide.
Abstract: 2-Methyl-1-propanol is difficult to separate from 2-butanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-propanol can be easily separated from 2-butanol by azeotropic distillation. Effective agents are sulfolane, acetonitrile and acetal.
Abstract: 2-Methyl-1-butanol is impossible to separate from 3-methyl-l-butanol because they both boil at 130.degree. C. 2-Methyl-1-butanol can be readily separated from 3-methyl-1-butanol by extractive distillation. Effective agents are o-xylene, 3-carene and 1-methoxy-2-propanol.
Abstract: A process for forming, isolating and purifying xanthophyll crystals, preferably lutein from marigold flower petals, zeaxanthin from wolfberries or capsanthin and capsorubin from red pepper, is disclosed. A xanthophyll diester-containing plant extract is saponified in a composition of propylene glycol and aqueous alkali to form xanthophyll crystals. Crystallization is achieved without the use of added organic solvents. The crystals are isolated and purified. The substantially pure xanthophyll crystals so obtained are suitable for human consumption and can be used as a nutritional supplement and as an additive in food.
Abstract: 2-Methyl-1-propanol is difficult to separate from 2-methyl-1-butanol by conventional distillation or rectification because of the proximity of their boiling points. 2-Methyl-1-propanol can be readily separated from 2-methyl-1-butanol by azeotropic distillation. Effective agents are tetrahydrofuran, methyl acetate and toluene.
Abstract: An apparatus and method for treating chemical production plant process condensate such that a contaminant-rich stream and a relatively pure aqueous stream is separately recoverable from the condensate, wherein the contaminants are substantially removed from the condensate by steam stripping and subsequent rectification in a relatively low pressure stripping/rectification tower. The tower overhead is then condensed, and any non-condensed gases are subjected to water scrubbing to further recover contaminates from the non-condensed gas. A portion of the condensed overhead and scrubbing water containing contaminates is returned to the top of the rectification section of the tower as reflux and the balance being withdrawn as a concentrated stream for reuse in the plant. The apparatus may be used in conjunction with existing low pressure equipment, avoiding costly major modifications, and is particularly adapted to use in conjunction with ammonia and methanol plants.
Abstract: A tertiary butyl hydroperoxide reaction product is distilled to provide a tertiary butyl alcohol distillation fraction containing tertiary butyl alcohol and a heavier fraction containing unreacted tertiary butyl hydroperoxide, and reaction by-products boiling below tertiary butyl alcohol, the tertiary butyl alcohol fraction is charged to a vacuum distillation column for separation into a vaporized overhead tertiary butyl alcohol fraction that is cooled to obtain a liquefaction product containing a minor amount of vaporized tertiary butyl alcohol and a major amount of a liquified tertiary butyl alcohol, andthe tertiary butyl alcohol vapors are dissolved in water to form an aqueous solution of tertiary butyl alcohol from which the tertiary butyl alcohol is recovered.
Abstract: From a synthesis gas which contains hydrogen and carbon oxides, methanol is produced on copper-containing catalysts under pressures in the range from 20 to 20 bars and at temperatures in the range from 200 to 350.degree. C. The synthesis gas is passed through a first synthesis reactor, which consists of a shaft reactor and contains a fixed bed of a copper-containing catalyst. The reaction in the shaft reactor is carried out adiabatically and without a recycling of synthesis gas. Together with recycle gas, the gas mixture which has not been reacted in the first synthesis reactor is passed through a second synthesis reactor, which contains a copper-containing catalyst, which is disposed in tubes and is indirectly cooled through boiling water. 10 to 30% of the carbon oxides of the synthesis gas are reacted in the shaft reactor to form methanol.
Abstract: A process for separating a mixture containing mainly ethyl tertio-butyl ether (ETBE), ethanol and C.sub.4 hydrocarbons includes introducing the mixture to be separated into a debutanizer from which the C.sub.4 hydrocarbons are recovered overhead with a fraction of the ethanol, and purified ETBE is recovered as a bottom product; a side stream of an ethanol-rich phase is extracted and sent to a permeation zone in which the dense film of the membrane is constituted by a N,N-dimethylaminoethyl methacrylate polymer (DMAEMA) or a copolymer of DMAEMA with N-vinylcaprolactam (NVCL) and/or with N-vinyl pyrrolidone (NVP); the ethanol-depleted retentate from this permeation zone is returned to the debutanizer and the permeate contains mainly separated ethanol.The process can be integrated into an ETBE production process, in which the ethanol separated during the permeation step is recycled to the etherification reactor. The debutanizer may be replaced by a catalytic distillation column.
Abstract: A process for separating a first component of a process stream from a second component of a process stream in a single vessel has been developed. The separation process uses an apparatus having a distillation zone to separate a first component from a second component of a process stream, thereby producing a distillation zone overhead stream enriched in the first component, and a membrane separation zone containing a membrane capable of selectively removing additional amounts of the second component from the distillation overhead stream. The benefit is the production of a high purity process at lower capital equipment costs.
Abstract: Butyraldehyde cannot be separated from ethanol by conventional distillation or rectification because they form a minimum boiling azeotrope. Butyraldehyde can be readily separated from ethanol by azeotropic distillation. Effective agents are ethyl formate, hexane and isopropyl ether.
Abstract: In the multistage distillation of a methyl tertiary butyl ether reaction product comprising methyl tertiary butyl ether, tertiary butyl alcohol, methanol, isobutylene and water, the methyl tertiary butyl ether reaction product is separated in a primary methyl tertiary butyl ether distillation column into a lower boiling methyl tertiary butyl ether fraction and a higher boiling aqueous tertiary butyl alcohol fraction; the lower boiling aqueous tertiary butyl alcohol fraction is separated in a tertiary butyl alcohol distillation column into a vaporized overhead tertiary butyl alcohol fraction and a higher boiling water fraction; cooling water is charged to the reflux condenser for the tertiary butyl alcohol distillation column to liquify the vaporized, overhead tertiary butyl alcohol fraction and to convert the cooling water to wet steam, and the wet steam is independently charged to the reboiler for the primary methyl tertiary butyl ether distillation zone to supply the heat necessary for the distillation to b
Type:
Grant
Filed:
June 16, 1995
Date of Patent:
October 15, 1996
Assignee:
Texaco Development Corporation
Inventors:
Stuart J. Parker, Arlen G. Sliger, Rei-Yu J. Hwan
Abstract: A process is disclosed for separating a mixture of methanol and tetrahydrofuran into its components. The separation is carried out in the liquid or gaseous phase through an organophilic membrane, for example, a plasma polymerization membrane.
Abstract: A process is provided whereby phenol is separated from 1-phenyl ethanol, acetophenone or mixtures by extractive distillation with sulfolane as extractive distillation agent which decreases phenol volatility relative to 1-phenyl ethanol and acetophenone.
Type:
Grant
Filed:
June 5, 1995
Date of Patent:
July 23, 1996
Assignee:
ARCO Chemical Technology, L.P.
Inventors:
Tim T. Wong, Stephen H. Harris, Thomas S. Zak, Te Chang
Abstract: A first alkanol having from 1 to 3 carbon atoms can be separated off from other organic compounds of higher carbon number from the group comprising other alcohols, polyalcohols, ethers, oxo compounds, esters of carboxylic acids and of carbonic acid, haloaliphatics, amines, amides, hydrocarbons, carboxylic acids and nitriles, which in each case have at least 1 carbon atom more than the first alkanol, where in the case of halogenoaliphatics, halogen substituents are counted as further carbon atoms, by permeation on membranes, if a water content from 1 to 30% by weight, preferably from 5 to 15% by weight, based on the amount of mixture and water, is maintained.
Type:
Grant
Filed:
June 7, 1994
Date of Patent:
April 2, 1996
Assignee:
Bayer Aktiengesellschaft
Inventors:
Wolf Mehl, Wolfgang Scheinert, Ingo Janisch, Andreas Groschl
Abstract: An apparatus and method for treating chemical production plant process condensate such that a contaminant-rich stream and a relatively pure aqueous stream is separately recoverable from the condensate, wherein the contaminants are substantially removed from the condensate by steam stripping and subsequent rectification in a relatively low pressure stripping/rectification tower. The tower overhead is then condensed with a portion of the condensed overhead being returned to the top of the rectification section of the tower as reflux and the balance being withdrawn as a concentrated stream for reuse in the plant. In a second embodiment, separate stripping and rectification towers operate in series whereby the overhead of the stripping tower is delivered to the lower section of the rectification tower and the rectification bottoms are returned to the top of the stripping tower.
Abstract: A method of separating a liquid mixture wherein the liquid mixture is heated; the heated liquid mixture is supplied to a pervaporation membrane module to separate a permeable component of the liquid; a portion of non-permeated liquid is circulated through a circulation pipe into a liquid mixture feeding pipe before a heater, and the remaining portion of the non-permeated liquid is extracted to the outside of the system, and wherein the temperature of the liquid in the liquid mixture feeding pipe in which the non-permeated liquid has been mixed with the liquid mixture or in the circulation pipe for the non-permeated liquid, is measured, and when the measured temperature is out of a predetermined range, new supply of the liquid mixture and/or extraction of the non-permeated liquid is stopped.
Type:
Grant
Filed:
November 28, 1994
Date of Patent:
February 27, 1996
Assignees:
Mitsubishi Chemical Corporation, Mitsubishi Kasei Engineering Company
Abstract: Isopropanol is difficult to separate from 2-butanone by conventional distillation or rectification because of the proximity of their boiling points. Isopropanol can be readily separated from 2-butanone by extractive distillation. Effective agents are o-cresol, ethylene glycol and nitroethane.
Abstract: Ethanol is impossible to separate from 2-butanone by conventional distillation or rectification because of the minimum boiling azeotrope between these two. Ethanol can be readily separated from 2-butanone by extractive distillation. Effective agents are dipromyl amine, phenol and dimethylsulfoxide.
Abstract: From a mixture containing methanol, ethanol, n-propanol, isobutanol water and other high-boiling and low-boiling compounds, the claimed process enables three separate streams to be obtained, one an anhydrous stream of methanol or methanol and ethanol (I), one containing most of the n-propanol present in the feed mixture (II), and one containing most of the isobutanol present in the feed mixture (III), by using three fractionating columns.
Abstract: 3-Methyl-2-butanol, 2-pentanol and 1-butanol are difficult to separate by conventional distillation or rectification because of the proximity of their boiling points. Mixtures of these three can be readily separated from each other by azeotropic distillation. Effective agents are hexyl acetate, hexane and 3-methyl pentane.