Abstract: Low molecular weight organophosphazene oligomers, especially cyclic oligomers, can be cross-linked by siloxane bridges to form solid high molecular weight polymers.

Abstract: Olefin mixtures containing vinyl, vinylidene and internal olefins are upgraded in value by removing the vinylidene olefin content and lowering the internal olefin content by selective reaction with a sulfur halide such as S.sub.2 Cl.sub.2 followed by reaction with aqueous alkali metal hydrosulfide and optionally alkali metal sulfide. The reaction mixture is distilled to remove mainly vinyl and a reduced amount of internal olefins. The distillation residue is an effective extreme pressure additive for lubricating oil.

Abstract: A polyphosphazene hydraulic fluid that remains solids-free on storage at temperatures down to -30.degree. C. over an extended period can be made by reacting a solution of sodium phenoxide, sodium m-methylphenoxide, sodium p-methylphenoxide and sodium trifluoroethoxide with a small stoichiometric excess of cyclic phosphonitrilic chloride oligomer, mainly trimer, and then reacting the remaining replaceable chlorine atoms with a solution of sodium trifluoroethoxide.

Abstract: A process for the production of diphenolic compounds having a divalent bridge. A first disubstituted phenol is reacted with an aldehyde in the presence of a secondary amine and excess alcohol to form an ether intermediate. The ether intermediate is reacted with a phenol having an open ortho or para position to form a diphenolic.

Abstract: The reaction of alkali metal with aromatic hydroxy compounds is promoted by inclusion of an alcohol in the reaction mixture. The alkali metal aryloxide formed can be reacted with phosphonitrilic chloride polymers to make polyaryloxyphosphazenes.

Abstract: Polyetheroxy-substituted polyphosphazenes having reduced mono and polyetheroxy alkanol, alkali metal and halide contaminants that are suitable for use in making solid electrolytes are made by dissolving the impure polyphosphazene in an inert solvent (e.g. tetrahydrofuran) and mixing this solution with a cycloalkane (e.g. cyclohexane) to precipitate the polyetheroxy-substituted polyphosphazene with reduced etheroxy alkanol content. This can be dissolved in water and contacted with an anion exchange material to remove residual halide anions. The purified polyetheroxy-substituted polyphosphazene is then recovered by distilling off the water.

Abstract: Polymer-grade cyclic phosphonitrilic halide trimer can be obtained by (i) reacting ammonium halide with phosphorus pentahalide in an inert solvent containing pyridine, substituted pyridines or mixtures thereof or hydrogen halide complexes thereof, (ii) washing the solvent phase with an aqueous alkali metal hydroxide and (iii) crystallizing cyclic trimer and/or distilling the cyclic trimer to obtain polymer-grade trimer.

Abstract: Shampoo containing a di-C.sub.6-18 primary alkyl methylamine oxide hair conditioning agent, e.g. didecylmethylamine oxide, is very effective in improving hair body and flyaway control.

Abstract: A process for purifying crude brominated aromatic compounds such as decabromodiphenyl oxide containing impurities. The crude brominated aromatic compound undergoes a single processing step of grinding in the presence of heated air. The temperature is sufficient to effect substantial removal of impurities and yet remains below the melting point of the brominated aromatic compound.

Abstract: A process which enhances conversion and speeds the reaction rate for the preparation of esters. Methyl acrylate and a hindered phenol are reacted (i) in the presence of an alkali metal alkaline catalyst that provides a phenolate anion and (ii) in the presence of an agent which solubilizes the phenolate to enhance the reaction rate. Excellent yields of methyl ester are obtained in a rapid reaction and by-products are minimal. The invention includes a preparation of methyl .beta.-(3,5-dialkyl-4-hydroxyphenyl)propionates by reaction of a hindered phenol with methyl acrylate in the presence of an alkaline catalyst and dimethyl sulfoxide present in an amount sufficient to advance the reaction rate.

Abstract: Cyclic phosphonitrilic halides are formed rapidly and in high yield in a controllable multi-step process including the step of reacting a nitrogenous base (e.g. pyridine) with a phosphorus tetrahalide (e.g. phosphorus pentachloride) in a suitable inert liquid reaction medium (e.g. monochlorobenzene) to form a complex and in a subsequent step reacting this complex with an ammonium halide (e.g. ammonium chloride) at a temperature above about 90.degree. C. up to the reflux temperature of the reaction medium to form cyclic phosphonitrilic halides, mainly trimer.

Abstract: Cyclic phosphonitrilic halide trimer is made in high yield and at a rapid rate by adding NH.sub.3 or ammonium halide to a pyridine-hydrogen halide complex and adding phosphorus pentahalide and a solvent for the trimer (e.g. monochlorobenzene) and heating the mixture to above 90.degree. C. to form trimer which dissolves in the solvent and then separating the trimer-solvent phase from the residue phase of pyridine-hydrogen halide complex and recovering trimer from the solvent phase and recycling the pyridine-hydrogen halide phase to a subsequent procedure conducted in the same manner. The process can also be adapted to produce linear species in high yield also.

Abstract: Polyetheroxy-substituted polyphosphazenes useful in making solid electrolytes are purified by dissolving the impure polyphosphazene in water at a low temperature (e.g. below 40.degree. C.) and heating the water solution to a temperature high enough to cause the purified polyphosphazene to precipitate (e.g. above 50.degree. C.).

Abstract: Ether disulfonates or mixtures of ether monosulfonates and ether disulfonates are disclosed as useful surfactants in the recovery of oil.

Abstract: Process for compounding polyphosphazene gum by (a) mixing a composition comprising a curable polyphosphazene gum, filler, plasticizer and other conventional components but without any curing agent to form a non-curing masterbatch, (b) mixing a composition comprising a polyphosphazene gum and an excess amount of curing agent, at least 10 times that required to cure the phosphazene gum in this mixture and optionally containing other conventional components to form a concentrate and (c) blending the non-curing masterbatch from (a) with sufficient concentrate from (b) to provide an amount of curing agent sufficient to cure the entire resultant mixture.