Abstract: Polymerization grade phosphonitrilic chloride trimer is made by reacting NH.sub.4 Cl and PCl.sub.5 in a solvent (e.g. monochlorobenzene) to form a crude trimer solution, filtering the solution to remove unreacted NH.sub.4 Cl, distilling a portion of the solvent to form a hot concentrate, cooling the concentrate to obtain a precipitate, distilling the precipitate at reduced pressure to first remove a forecut and then a heart-cut of polymerization grade phosphonitrilic chloride trimer.

Abstract: Organic materials are made flame retardant by addition of a polyhalogenated polyphenylene sulfide such as decabromodiphenyl sulfide or 1,4-thiobis(2,4,6-tribromophenyl)-2,3,5,6-tetrabromobenzene alone or in combination with a Group VA metal oxide, e.g. Sb.sub.2 O.sub.3. A process for making the compounds is also disclosed.

Abstract: Compounds with 3,5-dibenzyl-4-hydroxyphenyl substituents have good thermal stability. Organic compositions containing the new additives are protected from oxidative degradation.

Abstract: A magnetic recording media containing a normally liquid polyphosphazene lubricant, e.g. low molecular weight linear or cyclic poly-fluoroalkoxy phosphazene mixtures.

Abstract: A process for making alkyl mercaptans in high yield while minimizing the formation of dialkyl sulfides is conducted by reacting an olefin with hydrogen sulfide in an inert solvent (e.g. CH.sub.2 Cl.sub.2) containing a Lewis Acid catalyst (e.g. BF.sub.3). Best results are obtained when the olefin is added to the hydrogen sulfide solution at a rate that keeps the amount of unreacted olefin below about 0.05 moles per mole of hydrogen sulfide.

Abstract: Metal alkyls such as trimethyl arsine are made in improved yields by reacting a metal halide, e.g. AsCl.sub.3, with a Grignard reagent such as methyl magnesium bromide complexed with a polyether such as di(2-methoxyethyl)ether.

Abstract: Polymer-grade cyclic phosphonitrilic chloride trimer can be obtained from crude cyclic polyphosphonitrilic chlorides by forming a solution of the crude cyclics, water washing the solution, distilling solvent to form a hot concentrate, cooling to form a precipitate and distilling the precipitate to form polymer-grade trimer.

Abstract: Cyclic phosphonitrilic chloride trimer suitable for polymerization to light colored, high molecular weight, linear polyphosphonitrilic chloride can be made by (1) reacting PCl.sub.5 and NH.sub.4 Cl in an inert solvent (e.g. monochlorobenzene) to form a solution of a low molecular weight linear and cyclophosphonitrilic chlorides, (2) evaporating solvent to form a concentrate, (3) adding water and cooling the mixture to precipitate cyclic trimer, (4) separation of the trimer precipitate and (5) distillation of the separated trimer.

Abstract: Polyphosphazene elastomers for use in making low density foam comprising a --P<.dbd.N].sub.n substantially linear backbone randomly substituted with 20-80 mole percent phenoxy, 20-80 mole percent lower alkylphenoxy, 1-50 mole percent alkoxy and 0.5-20 mole percent alkenylphenoxy and the foamed products made therefrom.

Abstract: Color formation in aliphatic amines during storage is prevented by contacting the amines before they develop objectionable color with ethylenediamine tetraacetic acid, salts or ethylenediamine tetraacetic acid, nitrilotris acetic acid, salts of nitrilotris acetic acid, nitrilotris methylenephosphonic acid, salts of nitrilotris methylenephosphonic acid, 8-hydroxy-quinoline or mixtures of the above compounds.

Abstract: A process for making an alkali metal alkoxide (e.g. sodium alkoxide) of a halogen-substituted alcohol (e.g. fluorine-substituted alcohols) by dispersing an alkali metal (e.g. sodium) in a cycloalkane (e.g. cyclohexane) containing a phenol (e.g. o-allylphenol) and adding the resultant dispersion to an ether (e.g. THF) solution of a halogen-substituted alcohol. The resultant alkali metal haloalkoxide solution contains phenoxides and can be reacted with a phosphonitrilic chloride polymer to introduce haloalkoxide and phenoxide substituents.

Abstract: A prosthesis for subcutaneous implantation such as a mammary implant used in reconstructive surgery is made from a polyphosphazene elastomer (e.g. polyfluoroalkoxy phosphazene) sac containing a silicone gel. The sac is essentially impermeable to the silicone gel fill and overcomes a gel migration problem encountered with implants made using polysiloxane sacs.

Abstract: An ether sulfinate/sulfonate or disulfonate having the following formula: ##STR1## wherein: R is a hydrocarbon group having from about 6 to about 24 carbon atoms,Y is SO.sub.2 M or SO.sub.3 M,Z is hydrogen or a methyl group, andM is an alkali metal, alkylammonium or ammonium cation and mixtures of each of said sulfinate/sulfonate and said disulfonate with an ether monosulfonate having the following formula:ROCH.sub.2 CH(Z)CH.sub.2 SO.sub.3 Mwherein:R is a hydrocarbon group having from about 6 to about 24 carbon atoms,Z is hydrogen or a methyl group, andM is an alkali metal, alkylammonium or ammonium cation.

Abstract: Alkali metal salts and alkaline earth metal salts of acyloxybenzenesulfonate are prepared by sulfonating an aryl ester of an organic acid with gaseous sulfur trioxide to produce a sulfonation reaction mixture containing acyloxybenzenesulfonic acid, neutralizing the sulfonation reaction mixture with alkali metal hydroxide or alkaline earth metal hydroxide to produce an alkali metal salt or alkaline earth metal salt of an acyloxybenzenesulfonic acid and thereafter recovering from the reaction mixture the acyloxybenzenesulfonic acid salt product thus formed.

Abstract: Vinylidene olefins which contain the olefinic unit ##STR1## are isomerized in high yield to form di-substituted internal olefins containing the olefinic unit --CH.dbd.CH-- by heating to 150.degree.-350.degree. C. in contact with an iron carbonyl catalyst. Only minor amounts of tri-substituted internal olefins which contain the olefinic unit ##STR2## are formed.

Abstract: A reactive fire retardant mixture useful in the preparation of polyurethane foams. The mixture contains a halogenated imide-containing polyol having the formula: ##STR1## and the corresponding ether having the formula: ##STR2## wherein R is a hydrocarbon group having the valance n+2 and is selected from the group consisting of benzene groups, naphthalene groups and alicyclic hydrocarbon groups containing 5 to 10 carbon atoms, R' is an aliphatic hydrocarbon group containing 3-12 carbon atoms, X is selected from the group consisting of bromine and chlorine, n is an integer from 1-6 and p is an integer from 2-6. They are prepared by reacting an alcohol (e.g. isopropyl alcohol), a halogenated dicarboxylic anhydride (e.g. tetrabromophthalic anhydride) and an aminopolyol (e.g. 2-amino-2-ethyl-1,3-propanediol).

Abstract: Residual alkali metal salt (e.g. NaCl) is removed from an alkali metal alkoxide and/or aryloxide-polyphosphonitrilic halide reaction product by neutralizing the reaction solution with acid and water extracting the salt using a lower water-soluble alcohol (isopropanol) to effect rapid phase separation.

Abstract: A process for making an alkali metal alkoxide (e.g. sodium alkoxide) of a halogen-substituted alcohol (e.g. fluorine-substituted alcohols) by dispersing an alkali metal (e.g. sodium) in a cycloalkane (e.g. cyclohexane) and adding the resultant dispersion to an ether (e.g. THF) solution of a halogen-substituted alcohol. The resultant alkali metal haloalkoxide solution can be reacted with a phosphonitrilic chloride polymer to introduce haloalkoxide substituents.

Abstract: Polyphosphazenes containing 20-80 mole percent phenoxy, 20-80 mole percent alkylphenoxy and 2-30 mole percent alkoxy substituents possess low glass transition temperature while still exhibiting good smoke values in standard tests.

Abstract: A reactive fire retardant mixture useful in the preparation of polyurethane foams. The mixture contains a halogenated imide-containing polyol having the formula: ##STR1## and the corresponding ether having the formula: ##STR2## wherein R is a hydrocarbon group having the valance n+2 and is selected from the group consisting of benzene groups, naphthalene groups and alicyclic hydrocarbon groups containing 5 to 10 carbon atoms, R' is an aliphatic hydrocarbon group containing 3-12 carbon atoms, X is selected from the group consisting of bromine and chlorine, n is an integer from 1-6 and p is an integer from 2-6. They are prepared by reacting an alcohol (e.g. isopropyl alcohol), a halogenated dicarboxylic anhydride (e.g. tetrabromophthalic anhydride) and an aminopolyol (e.g. 2-amino-2-ethyl-1,3-propanediol).