Abstract: Compositions including silicone surfactants of the type used in manufacturing urethane foams and certain siloxane-oxyalkylene copolymers which act as cell openers when employed in combination with silicone surfactants in urethane foam manufacture are disclosed and claimed, as are urethane foam compositions including such cell operers, a method of preparing urethane foams using such cell operers, and urethane foams prepared by the method.

Abstract: Silicone surfactants having a siloxane backbone and a mixture of high and low atomic mass oxyalkylene pendant groups, these polyether pendants having average atomic masses of 1500-6000 and 300-750 respectively. The surfactants of the invention operate in polyurethane foam compositions to provide stable foams over a range of surfactant concentrations while still producing product foams having relatively constant breathability. Also disclosed and claimed are polyurethane foam compositions which include the surfactants, a method of making polyurethane foam using the surfactants, and polyurethane foam made by the method.

Abstract: An acid-sulfolane catalyzed process of preparing cyclic alkylated compounds such as indanes by reacting a monovinyl aromatic compound with an olefinic compound, such reaction further improved by the addition of a lanthanide oxide, or Group VI A elements and/or oxides or a mixture of such oxides.

Abstract: An improved process for preparing high yields of 4,4'-difluorobiphenyl comprised of reacting a p-halofluorobenzene Grignard reagent with a p-halofluorobenzene coupling reagent in the presence of a palladium chloride triphenylphosphine catalyst.

Abstract: In a process for reacting an aromatic compound (preferably chlorobenzene) with free chlorine in the presence of a catalyst comprising a zeolite of the L family (zeolite L) under such reaction conditions as to obtain a product comprising 1,4-dichlorobenzene, the improvement comprises employing ammonium ion-exchanged zeolite of the L family.

Abstract: 1,2-dichlorobenzene is isomerized to 1,4-dichlorobenzene in the presence of a catalyst comprising (a) at least one of AlCl.sub.3 and AlBr.sub.3 and (b) at least one of iodine, alkaline earth metal halides and sulfates and lanthanide halides. Benzene and/or dichlorobenzene is chlorinated with free chlorine in the presence of a catalyst composition comprising (a) at least one suitable metal halide (preferably AlCl.sub.3, SbCl.sub.5 or FeCl.sub.3) and (b) free iodine and/or at least one organic iodo-compound (preferably methyl iodide of p-iodochlorobenzene), so as to obtain a reaction product comprising 1,4-dichlorobenzene. A preferred catalyst composition comprises (a) at least one of AlCl.sub.3 and AlBr.sub.3, (b) free iodine and (c) at least one of alkaline earth metal halides, alkaline earth metal sulfates and lanthanide halides.

Abstract: 1,2-dichlorobenzene is isomerized to 1,4-dichlorobenzene in the presence of a catalyst comprising (a) at least one of AlCl.sub.3 and AlBr.sub.3 and (b) at least one of iodine, alkaline earth metal halides and sulfates and lanthanide halides. Benzene and/or dichlorobenzene is chlorinated with free chlorine in the presence of a catalyst composition comprising (a) at least one suitable metal halide (preferably AlCl.sub.3, SbCl.sub.5 or FeCl.sub.3) and (b) free iodine and/or at least one organic iodo-compound (preferably methyl iodide or p-iodochlorobenzene), so as to obtain a reaction product comprising 1,4-dichlorobenzene). A preferred catalyst composition comprises (a) at least one of AlCl.sub.3 and AlBr.sub.3, (b) free iodine and (c) at least one of alkaline earth metal halides, alkaline earth metal sulfates and lanthanide halides.

Abstract: Monohalobenzene compounds are iodinated with an iodination reagent selected from the group consisting of (i) iodine monochloride and (ii) I.sub.2 /Cl.sub.2 mixtures having a mol ratio of about 1:3-5:1, in the presence of a catalyst selected from the group consisting of MoCl.sub.5, FeCl.sub.3, lanthanide chlorides and mixtures thereof. Preferably one of chlorobenzene and fluorobenzene is at least partially converted to at least one of para-iodochlorobenzene and para-iodofluorobenzene. Various other aromatic compounds, preferably di- and trichlorobenzene, xylenes, nitrobenzene and ethyl benzoate, are iodinated with an iodination reagent selected from the group consisting of (i) iodine monochloride and (ii) I.sub.2 /Cl.sub.2 mixtures having a mol ratio of about 1:3-5:1, in the presence of a catalyst comprising FeCl.sub.3 and, optionally, a lanthanide chloride.

Abstract: An improved process for the removal of by-product amounts of undesirable aromatic hydrocarbon compounds from a mixture comprised of such compounds and predominantly tetramethyltetrahydronaphthalene is provided. In accordance with the process the mixture is contacted with a concentrated sulfuric acid solution whereby the undesirable aromatic hydrocarbons are dissolved therein and the acid phase containing said hydrocarbons is removed from the mixture.

Abstract: Hydrocarbon solutions containing iodine or iodine-containing impurities are rendered essentially color-free by distillation in the presence of small amounts of a hydrocarbon soluble organometallic compound.

Abstract: The alkylation of para-substituted isopropyl benzenes with dipentenes employing an aluminum halide catalyst system produces novel tetracyclic compounds.

Abstract: Hydrocarbon solutions containing iodine or iodine-containing impurities are rendered essentially color-free by distillation in the presence of small amounts of a hydrocarbon soluble organometallic compound.

Abstract: The self condensation of monovinyl aromatic compounds to acyclic dimers, the cross-reaction of monovinyl aromatic compounds with olefins in the presence of acid catalysts to produce cyclialkylated aromatic compounds, and the production of cyclialkylated aromatic compounds by reaction of olefins with acyclic dimers of monovinyl aromatic compounds in the presence of acid catalysts is improved by employing a tetrahydrothiophene 1,1-dioxide solvent.

Abstract: A process is provided for preparing polymethylbenzenes by simultaneously contacting (a) a phenolic compound, preferably phenol, with (b) a methylating agent, preferably methanol, in the presence of (c) zinc aluminate as catalyst, under such conditions as will result in the at least partial conversion of the reactants to either pentamethylbenzene or hexamethylbenzene or a mixture of both.

Abstract: The alkylation of aromatic compounds with olefinic compounds is catalyzed by catalyst consisting essentially of aluminum halide and elemental iodine.

Abstract: In the production of 1,1-dimethyl-6-hydroxyindans through the reaction of phenols with isoprene or 2,3-dimethyl-1,3-butadiene in the presence of phosphoric acid, an improvement is comprised of using a phosphoric acid concentration of about 100% instead of 85% or less and also of the distillation of the product mixture from a solution containing phosphoric acid of about 95% concentration.

Abstract: The alkylation of aromatic compounds with olefins can be conducted more efficiently in the presence of certain catalysts.

Abstract: Novel sulfinates and sulfonates are provided comprising salts of 3-cyano-3-alkenesulfinic acids and salts of 3-carbamoyl-3-alkenesulfonic acids and process for preparing these novel compounds. The compounds of the invention are useful as comonomers or termonomers in the preparation of polymers, particularly polymers which are useful in fiber and textile applications.

Abstract: A process for obtaining at least one tert-butyltoluene comprising reacting isobutylene and isobutane in the presence of hydrogen fluoride and then separating said toluene from the hydrocarbon product.

Abstract: Monovinyl aromatic polymers are modified by reacting with elemental alkali metal and a conjugated diene to produce polymers having branches containing olefinic unsaturation. The olefinically unsaturated branches provide reactive sites which are readily reacted with various substances to obtain numerous variations in the properties of the monovinyl aromatic polymers.