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Class 203/65 - Hydroxy aromatic (e.g., Phenol)


Subclass of Class 203 - Distillation: processes, separatory
Definition: Processes in which the organic compound is a hydroxy aromatic,
No. of patents: 110
Last issue date: 11/28/2006


1      
NumberTitleIssue Date
7141641Method and apparatus for production of alkyl aryl ether and diaryl carbonate
A method and apparatus for continuously producing an alkyl aryl ether and a diaryl carbonate by reacting a dialkyl carbonate and an aromatic alcohol in presence of a transesterification catalyst. ...
11/28/2006
6475347High boiling inhibitors for distillable, polymerizable monomers
Disclosed herein are compounds of the structure ##STR1## wherein R1, R2, and R3 are organic radicals of C1 to C20, such that the combination of the three contain at least twelve carbon atoms and R
11/05/2002
6315868Method of separating dimethyl carbonate and methanol
A method of separating methanol and dimethyl carbonate in a distillation column through extractive distillation. The extractive distillation is conducted in the presence of an extractive distillation agent which modifies the azeotropic behavior of the dim...
11/13/2001
6159346Inhibition of 141b decomposition
Inhibition of the formation of unsaturated carbon compounds during the heating of 141b involving the addition of various inhibitors such as dialkylhydroxylamine and/or the use of a vessel made of a nickel alloy....
12/12/2000
6024841Separation of 2-methyl-1-butanol and 3-methyl-1-butanol from 1-pentanol by extractive distillation
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-pe...
02/15/2000
6017423Separation of 3-methyl-2-pentenal from N-butanol by extractive distillation
3-Methyl-2-pentenal cannot be separated from n-butanol by conventioal rectification because of the proximity of their boiling points. 3-methyl-2-pentenal can be readily separated from n-butanol by extractive distillation. Effective agents are 1-methyl-2-p...
01/25/2000
5972172Separation of 1,2,4-trimethylbenzene from 1,2,3-trimethylbenzene by extractive distillation
1,2,4-Trimethylbenzene is difficult to separate from 1,2,3-trimethylbenzene by conventional distillation or rectification because of the proximity of their boiling points. 1,2,4-trimethylbenzene can be readily separated from 1,2,3-trimethylbenzene by extr...
10/26/1999
5968322Process for preparing refined acrylic esters
A process for preparing refined acrylic esters, the process including steps of distilling an acrylic ester containing stream in the presence of hydroquinone or substituted hydroquinone, at a concentration in the range of 200 to 5000 ppmw, wherein the dist...
10/19/1999
5897750Separation of acetone from isopropanol-water mixtures by extractive distillation
Acetone cannot be separated from a mixture of isopropanol and water because of the closeness of their boiling points. Acetone can be easily separated from isopropanol and water by extractive distillation. Effective extractive agents are 1-nitropropane, 3-...
04/27/1999
5879517Method for separating 2-butanol from t-amyl alcohol using certain organic compounds as the agent in extractive distillation
2-Butanol cannot be sparated 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 extractive distillation. Effective agents are butyl ether, benzyl ace...
03/09/1999
5876569Separation of methyl ethyl ketone from ethanol by extractive distillation
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 extractive distillation. Effective agents are methyl benzoate,...
03/02/1999
5873981Recovery of anhydrous acids
A is a process for removing water from an alkanesulfonic acid such as methanesulfonic acid or ethanesulfonic acid by mixing an azeotropic excess of a phenolic compound with water and the alkanesulfonic acid, then boiling off substantially all of the water...
02/23/1999
5840160Separation of 3-carene from limonene by extractive distillation
3-Carene is difficult to separate from limonene by conventional distillation or rectification because of the proximity of their boiling points. 3-Carene can be readily separated from limonene by extractive distillation. Effective agents are o-cresol, 2,6-...
11/24/1998
5830325Separating and removing 1, 1, 1-trifluoroethane by using azeotropic distillation
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...
11/03/1998
5824195Process for distilling crude acrylic silane solution
A process for distilling a crude acrylic silane solution particularly containing impurities in a commercial scale for separating acrylic silane in the presence of a hindered phenol and/or amine as polymerization inhibitor, the process being improved by us...
10/20/1998
5800681Separation of ethanol, isopropanol and water mixtures by extractive distillation
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 isopr...
09/01/1998
5795447Separation of 2-butanol from isobutanol by extractive distillation
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,...
08/18/1998
5789629Separating 3-methyl-1-butanol from 1-pentanol using certain organic compounds as the agent in extractive distillation
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 ag...
08/04/1998
5779862Separation of 2-methyl-1-butanol and 3-methyl-1-butanol from 1-pentanol by azeotropic distillation
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-pe...
07/14/1998
5772853Separation of 1-propanol from t-amyl alcohol by extractive distillation
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 aceta...
06/30/1998
5723024Separation of 2-methyl-1-propanol from 1-butanol by extractive distillation
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 a...
03/03/1998
5720857Separation of 1,2,4-trimethylbenzene from 1,2,3-trimethylbenzene by azeotropic distillation
1,2,4-Trimethylbenzene is difficult to sepparate from 1,2,3-trimethylbenzene because of the proximity of their boiling points. They are readily separated by azeotropic distillation. Effective agents are 1-propanol, methyl formate and 1-nitropropane....
02/24/1998
5709781Separation of 1-butanol from 2-pentanol by extractive distillation
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, ...
01/20/1998
5705038Separation of phellandrene from limonene by extractive distillation
Phellandrene is difficult to separate from limonene by conventional distillation or rectification because of the proximity of their boiling points. Phellandreneecan be readily separated from limonene by extractive distillation. Effective agents are o-cres...
01/06/1998
5693194Separation of butyraldehyde from ethanol by extractive distillation
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-...
12/02/1997
5659095Composition for inhibiting the polymerization of aromatic vinyl monomers
A polymerization inhibitor composition for inhibiting the polymerization of aromatic vinyl monomers at elevated temperatures comprising: (a) a benzofuroxan derivative of the formula ##STR1## wherein R is C1 -C4 alkyl or alkoxy; R
08/19/1997
5648573Compositions and methods for inhibiting vinyl aromatic monomer polymerization
The polymerization of a vinyl aromatic monomer such as styrene is inhibited by the addition of a composition of a benzoquinone derivative and a hydroxylamine compound....
07/15/1997
5602294Separation of o-xylene from p-xylene and m-xylene by extractive distillation
o-Xylene cannot be separated from p-xylene and m-xylene by conventional distillation or rectification because of the proximity of their boiling points. o-Xylene can be readily separated from mixtures of p-xylene and m-xylene by extractive distillation. Ef...
02/11/1997
5597455Separation of 3-carene and limonene by extractive distillation
3-Carene and limonene cannot be separated from each other by rectification because of the closeness of their boiling points. They are readily separated by extractive distillation. Effective agents are: diethylene glycol phenyl ether, nonyl phenol, triprop...
01/28/1997
5582693Separation of 3-carene and limonene by azeotropic distillation
3-Carene and limonene cannot be separated from each other by rectification because of the closeness of their boiling points. They are readily separated by azeotropic distillation. Effective agents are: cyclopentanol, 2-nitropropane, ethyl formate amyl ace...
12/10/1996
5580427Separation of butyraldehyde from ethanol by azeotropic distillation
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,...
12/03/1996
5562863Methods and compositions for inhibiting vinyl aromatic monomer polymerization
Vinyl aromatic monomer polymerization methods utilizing a composition of 2,6-di-tert-butyl-4-methylphenol and a substituted benzoquinonediimide compound are disclosed. Preferably, the composition is employed in an amount of 1 part to 10,000 parts per mill...
10/08/1996
5470443Separation of isopropanol from 2-butanone by extractive distillation
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-cr...
11/28/1995
5470440Method for inhibiting vinyl aromatic monomer polymerization
Vinyl aromatic monomer polymerization methods utilizing a composition of 2,6-di-tert-butyl-4-methylphenol and a substituted benzoquinonediimide compound are disclosed. Preferably, the composition is employed in an amount of 1 part to 10,000 parts per mill...
11/28/1995
5458741Separation of benzene from close boiling hydrocarbons by extractive distillation
Benzene is difficult to separate from cyclohexane or cyclohexene by conventional distillation or rectification because of the close proximity of their boiling points. Benzene can be readily separated from cyclohexane or cyclohexene by using extractive dis...
10/17/1995
5453167Separation of xylenes by extractive distillation
p-Xylene cannot be separated from m-xylene by distillation or rectification because of the proximity of their boiling points. p-Xylene can be separated from m-xylene by means of extractive distillation. Effective agents are 3-ethylphenol and isopropyl pal...
09/26/1995
5453166Separation of ethanol from 2-butanone by extractive distillation
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 d...
09/26/1995
5445716Separation of ethanol from isopropanol by extractive distillation
Ethanol is difficult to separate from isopropanol by conventional distillation or rectification because of the proximity of their boiling points. Ethanol can be readily separated from isopropanol by extractive distillation. Effective agents are dipentene,...
08/29/1995
5443697Separation of heptane from 1-heptene by extractive distillation
Heptane is difficult to separate from 1-heptene by conventional distillation or rectification because of the proximity of their boiling points. Heptane can be readily separated from 1-heptene by extractive distillation. Effective agents are diacetone alco...
08/22/1995
5441608Separation of xylenes by extractive distillation
p-Xylene cannot be separated from m-xylene by distillation or rectification because of the proximity of their boiling points. p-Xylene can be separated from m-xylene by means of extractive distillation. Effective agents are 3-ethylphenol and 1,1,2-trichlo...
08/15/1995
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