Allied Chemical Corporation

Alliedsignal Inc.

Other

Buffalo Color Corporation

Morris B Berenbaum

Richard E Eibeck

Henry R Nychka

Bernard F Sukornick

James O Peterson

Thomas P Izod

Martin A Robinson

Richard F Sweeney

Francis E Evans

James T Yardley

Harry E Ulmer

Charles J Cole

Frederick R Hopf

John H Bonfield

Paul W Harris

Karen M Bland

Michael D Swerdloff

Louis G Anello

Jon I Williams

Himangshu R Bhattacharjee

Morton H Litt

Donald R Taylor

Kenneth B Gilleo

Allen W Sogn

John D Hewes

A fluorinated cation exchange resin catalyst is prepared by contacting a polymer containing pendant acid groups, particularly the radical --SO.sub.3 X with elemental fluorine in the presence of a water-free halogenated hydrocarbon liquid and thereafter converting the resulting pendant --SO.sub.3 X radical to a free acid.

Preparation of strong and super acid catalysts using elemental fluorine

This invention relates to a process for removal of spinning solvents from solution spun fibers by extraction with an extraction solvent such as a polyether.

Method for removal of spinning solvent from spun fiber

A new class of sulfonated 2-(2'-hydroxyaryl)-2H-benzotriazole compounds and method for using them and other sulfonated hydroxyaryl benzotriazoles on nylon fibers to improve stain resistance and dye lightfastness has been discovered. A process is provided for improving stain resistance of nylon fibers by treatment with sulfonated aromatic-formaldehyde condensate and fluorinated dry soil resist agents.

Sulfonated 2-(2'-hydroxyaryl)-2H-benzotriazoles and/or sulfonated

A process for preparing a co-poly(amide/peptide) by reacting polymeric or oligomeric polypeptides and polymeric or oligomeric polyamides in the presence of an effective amount of one or more aryl phosphoryl azide compounds.

Process for preparing co-poly(amides/peptides)

Fluoroorganic compounds are prepared by reacting a haloorganic starting material in which at least one halo atom is replaceable with a fluorine atom by metathetical exchange, with calcium fluoride in the presence of a crown ether and an anhydrous, polar, basic organic solvent which complexes with the calcium ion and contains no --OH groups, at a temperature and for a period of time adequate to effect fluorination.

Preparation of fluoroorganic compounds with calcium fluoride

Sulfonation of anthraquinone by a sulfur trioxide component including SO.sub.3 or oleum in a liquid sulfur dioxide solvent. When a mercury catalyst is used to give alpha anthraquinone sulfonate products, most of the mercury is left in the reactor or recovered with unreacted anthraquinone by precipitation with water after vaporization of the sulfur dioxide. High sulfuric acid and mercury pollution are thus avoided.

Sulfonation of anthraquinone in sulfur dioxide solvent

Chlorofluorinated carboxylic acids may be effectively produced by an oxychlorofluorination process by reacting a gaseous mixture of a starting material selected from a saturated aliphatic carboxy containing compound, a saturated aliphatic carboxylic acid halide and a saturated aliphatic aldehyde in which all atoms are selected from C, H and O, and corresponding hydrohalogenated compounds in which the halo atoms are selected from chloro and fluoro, or mixtures thereof, an oxygen-containing gas, a chlorinating agent selected from the group consisting of HCl and Cl.sub.2 and mixtures thereof, and HF, in the presence of a Deacon catalyst supported by a stable, inert metal salt carrier.

Process for the production of chlorofluorinated carboxylic acids

A stabilized heat exchange medium is disclosed including a fluorocarbon, an absorbant and a tribasic phosphite stabilizer. The preferred absorbants are assymetrical furan derivatives containing at least 1 oxygen with a single bond to an adjacent carbon, and is most preferably an alkyl tetrahydrofurfuryl ether. The fluorocarbon contains 1 or 2 carbons, 1 or 2 hydrogens and the remainder chlorine and fluorine. The tribasic phosphites are of the formula (R.sub.1 'O)(R.sub.2 'O)(R.sub.3 'O)P, wherein R.sub.1 ', R.sub.2 ' and R.sub.3 ' are each independently alkyl, alkenyl, phenyl, alkylene phenyl, alkylene alkylphenyl or alkylphenyl.

Stabilized heat activated heat exchange absorption pair

Chlorofluorinated aliphatic ketones may be effectively produced by an oxychlorofluorination process by reacting a gaseous mixture of a starting material selected from an aliphatic ketone and a halogenated aliphatic ketone in which the halogen atoms are selected from chlorine and fluorine, or mixtures thereof, an oxygen-containing gas, a chlorinating agent selected from the group consisting of HCl and Cl.sub.2 and mixtures thereof, and HF, in the presence of a Deacon catalyst supported by a stable, inert metal salt carrier.

Process for the production of chlorofluorinated aliphatic ketones

Chlorofluorinated acyclic hydrocarbons may be produced produced by a commercially viable oxychlorofluorination process by reacting a gaseous mixture of a starting material selected from an acyclic hydrocarbon containing up to four carbon atoms and an acyclic hydrohalocarbon containing up to four carbon atoms in which the halo atoms are selected from chloro and fluoro, or mixtures thereof, an oxygen-containing gas, a chlorinating agent selected from the group consisting of HCl and Cl.sub.2 and mixtures thereof, and HF, in the presence of a Deacon catalyst supported by a stable, inert metal salt carrier.

Process for the production of chlorofluorinated acyclic hydrocarbons

Chlorofluorinated cycloaliphatic hydrocarbons may be effectively produced by an oxychlorofluorination process by reacting a gaseous mixture of a starting material selected from a cycloaliphatic hydrocarbon and a cycloaliphatic hydrohalocarbon in which the halo atoms are selected from chloro and fluoro, or mixtures thereof, an oxygen-containing gas, a chlorinating agent selected from the group consisting of HCl and Cl.sub.2 and mixtures thereof, and HF, in the presence of a Deacon catalyst supported by a stable, inert metal salt carrier.

Process for the production of chlorofluorinated cycloaliphatic

Chlorofluorinated aromatic hydrocarbons may be effectively produced by an oxychlorofluorination process by reacting a gaseous mixture of a starting material selected from an aromatic hydrocarbon and an aromatic hydrohalocarbon in which the halo atoms are selected from chloro and fluoro, or mixtures thereof, an oxygen-containing gas, a chlorinating agent selected from the group consisting of HCl and Cl.sub.2 and mixtures thereof, and HF, in the presence of a Deacon catalyst supported by a stable, inert metal salt carrier.

Process for the production of chlorofluorinated aromatic hydrocarbons

A flame resistant organic polymer which decomposes into fragments containing acidic and/or basic groups and the process for making same comprising treating an organic polymer which decomposes into said fragments with from about 0.5 to about 25 weight percent of a compound which contains at least one functional radical selected from --0--, --S-- and --N-- and at least one carboxyl or mercapto group which is able to dissociate in water to provide a free positively charged ion.

Growing community of inventors

Summit, NJ, United States of America

Morris B Berenbaum