Abstract: Method of preparing a 1,2-dihydroxy compound of the formula: ##SPC1##Where R is hydrogen or alkyl comprising contacting a naphthalene compound of the formula: ##SPC2##Where R is as heretofore defined with ozone, alkanoic acid and a mineral acid and hydrolyzing the resultant intermediates to form said 1,2-dihydroxy compound.
Abstract: A process is provided for recovery and re-use of dinitrophenols employed as inhibitors of polymerization in the distillation and purification of styrene. The styrene still residues commonly referred to as tar or tars are treated with an aqueous hydroxide at a controlled pH, the phases are separated, the aqueous phase is treated with an acid and an organic solvent at a controlled pH and the resulting organic phase is recycled to a suitable point in the styrene purification system. The recycled solution is a more effective inhibitor than the dinitrophenol originally employed.
Type:
Grant
Filed:
December 26, 1974
Date of Patent:
May 25, 1976
Assignee:
Monsanto Company
Inventors:
Thomas D. Higgins, Jr., Raymond A. Newsom
Abstract: Preparation of cyclohexyl hydroperoxide substantially free of other peroxides by oxidation of cyclohexane containing a cyclohexane soluble cobalt salt in a zoned oxidation process in which an oxygen containing gas is fed to each zone in the oxidation section in an amount in excess of that which will react under the conditions of that zone.
Abstract: Safe ketone peroxide compositions are provided utilizing a novel solvent system which boils smoothly over a wide range of temperatures. In addition, ketone peroxide compositions are prepared by reacting an excess of the ketone with hydrogen peroxide in a homogeneous system, followed by stripping excess ketone and water from the product.
Abstract: New organic peroxides having the formula ##EQU1## may be prepared by reacting a monohydroperoxide selected from R.sub.5 OOH and R.sub.6 OOH with an unsaturated carbonyl compound having the formula ##EQU2## the reaction being carried out in the presence of an acid catalyst at a temperature between about -30.degree.C and +80.degree.C, the molar ratio of the carbonyl compound to the hydroperoxide being between about 1:2 and 1:10. The new organic peroxides are particularly useful for crosslinking plastomers, vulcanizing elastomers, and as initiators for radical polymerizations.
Abstract: A safe peroxide solution composition consisting essentially of a diacyl peroxide having 1-5 carbon atoms in each aliphatic group and an aliphatic hydrocarbon, ketone, ester, ether, or alcohol characterized by a vapor pressure substantially that of the peroxide. Example: Equal parts by weight of diacetyl peroxide and ethyl butyl ketone.
Type:
Grant
Filed:
March 21, 1969
Date of Patent:
May 11, 1976
Assignee:
Pennwalt Corporation
Inventors:
Orville L. Mageli, David C. Noller, Wilbur H. McKellin
Abstract: Cycloaliphatic hydroperoxides are extracted from the reaction mixtures obtained by oxidising the corresponding cycloaliphatic hydrocarbons with the aid of a polar aprotic solvent which is not miscible with the hydrocarbon, said solvent being a polymethylenesulphone or an alkylene glycol carbonate, the alkylene portion containing 2 to 4 carbon atoms.
Abstract: Bis-monoperoxyacetals and bis-monoperoxyketals having the formula ##EQU1## wherein R is selected from the group consisting of C.sub.4 -C.sub.12 tertiary alkyl and C.sub.9 -C.sub.12 tertiary aralkyl and R.sub.1 is selected from the group consisting of hydrogen and C.sub.1 -C.sub.12 alkyl, are effective crosslinking agents for polymers at relatively low cure temperatures.
Abstract: A process for producing a hydroperoxide in highly concentrated form by oxidation of its corresponding liquid hydrocarbon with oxygen or an oxygen-containing gas while simultaneously subjecting the liquid reaction mixture to a carrier gas distillation to remove unreacted hydrocarbon with the carrier gas while withdrawing a portion of the liquid reaction mixture which is enriched in the hydroperoxide.
Abstract: In the nitration of phenol with nitric acid, decantation of the residual acid, and steam distillation of ortho-nitrophenol to leave an aqueous distillation residue of para-nitrophenol, a cleaner purer crystalline para-nitrophenol product is obtained by cooling the hot distillation residue when it contains at least 0.5% of sodium bisulphite and is at pH 5.4 to 6.4.
Abstract: High-purity dicumyl peroxide is obtained by mixing a melted crude dicumyl peroxide containing not less than 50% of dicumyl peroxide with an aqueous solution of surfactant, emulsifying the resulting mixture, and cooling the emulsion to a temperature lower than the temperature for solidifying dicumyl peroxide.
Abstract: Meta-and/or paradiisopropylbenzene dihydroperoxides are continuously produced by oxidizing meta-and/or paradiisopropylbenzenes in liquid phase through contact with oxygen or a gas containing oxygen, while keeping the concentration of meta-and/or paradiisopropylbenzene monohydroperoxides of the oxidation product solution in a range of 20 to 40% by weight.
Abstract: 2,5-BIS-(1',1'-Dimethylbutyl)hydroquinone and a process for the production thereof which comprises reacting hydroquinone with 2-methyl-1-pentene.
Abstract: Disclosed is a process for making ortho- and para-chlorophenols by treating alpha-cumylchloride with an aqueous hydrogen peroxide solution. The two products can be separated by distillation.
Abstract: A process for alkylating the ortho-position of a phenol compound which comprises bringing a phenol compound containing at least one hydrogen atom at its ortho-position and an alcohol into contact with a catalyst in the gaseous phase, said catalyst being selected from the group consisting ofA. a mixture of iron oxide and silica in which the atomic ratio of Fe to Si is 100 : 0.03 - 200, andB. a mixture of iron oxide, silica and chromium oxide in which the atomic ratio of Fe to Si to Cr is 100 : 0.1 - 5 : 0.1 - 5.
Abstract: Compounds of the general formula ##EQU1## WHERE M IS 1 OR 2 [E.G., 2,2-DI-(T-OCTYLPEROXY) PROPANE]; AND IMPROVED PROCESSES USING THESE COMPOUNDS AS INITIATORS FOR THE POLYMERIZATION OF ETHYLENICALLY UNSATURATED MONOMERS (SUCH AS STYRENE) AND AS CURING CATALYSTS FOR CURING UNSATURATED POLYESTER RESIN COMPOSITIONS.
Abstract: Impurities, that is, by-products, in an oxidation product solution obtained by oxidation of diisopropylbenzene by molecular oxygen or in the oxidation product solution freed from diisopropylbenzene dihydroperoxide, are removed by extracting the by-products such as carbinols, ketones and styrenes from the solution with a mixture of an aqueous alkaline solution and at least one of alcohols having 1 to 3 carbon atoms such as methanol, ethanol, and isopropanol, as an extracting reagent at a temperature of 20.degree. to 80.degree.C.
Abstract: Dihydric phenols are produced preferentially in high yields by having monohydric phenols or phenyl ethers oxidized by an organic peracid using, as a catalyst, at least one member selected from the group consisting of peracid stabilizers, polycarboxylic acids containing N or OH and possessed of a structure from which heavy metal ion-chelating property can theoretically be assumed, magnesium salts, sodium salts and potassium salts thereof, sodium salt, potassium salt and lower alkyl esters of phosphoric acid, and sodium salt and lower alkyl esters of pyrophosphoric acid.
Abstract: Method for the production of hydroperoxides of hydrocarbons having no aliphatic or cycloaliphatic tertiary carbon atoms wherein such hydrocarbons are oxidized in the liquid phase with molecular oxygen in the presence of a tertiary alcohol and a tertiary hydroperoxide. This method gives high hydroperoxide selectivities at high conversion levels and at high conversion rates.
Abstract: Method for the production of hydroperoxides of hydrocarbon having no aliphatic or cycloaliphatic tertiary carbon atoms, wherein such hydrocarbons are oxidized in the liquid phase with molecular oxygen in the presence of a stabilizing agent. This method gives high hydroperoxide selectivities at high conversion levels.