Abstract: A cement admixture comprised of a mixture of certain alkyl ether oxyalkylene adducts with certain oxyalkylene glycols to provide cement compositions of mortar and concrete which inhibit drying shrinkage while permitting substantial air entrainment and enhanced compressive strength.

Abstract: A process for alkoxylating phenols is disclosed. The process comprises reacting a carbonyl-functionalized phenol with an alkylene oxide in the presence of a substantially non-crystalline double metal cyanide (DMC) catalyst. The process offers fast reaction times at low catalyst levels, reduced problems with condensation side reactions, and low-color, low-viscosity, low-polydispersity alkoxylated phenols. The process enables efficient preparation of alkoxylated carbonyl-functonalized phenols that are especially valuable in the surfactant industry.

Abstract: Polyethers of polyhydric compounds are prepared by the liquid phase reaction of polyhydric compound and the reaction being carried out with separate liquid phases comprised of a polar polyhydric compound phase and an organic polyether containing phase.

Abstract: Microemulsion cleaner compositions are disclosed. The cleaners comprise a terpene, a secondary or tertiary C.sub.4 -C.sub.5 alcohol, a surfactant, and water. Compared with commercial formulations, cleaners of the invention are low in water, high in hydrocarbon, and have excellent degreasing capability. The secondary or tertiary C.sub.4 -C.sub.5 alcohol coupling solvent, compared with other alcohols, significantly reduces the amount of surfactant required to produce a stable, effective microemulsion cleaner. The compositions are particularly valuable as metal degreasers.

Abstract: The present invention provides a process for the production of dialkyl peroxides by reaction of an alcohol and/or an olefin with an organic hydroperoxide, using a solid acidic zeolite catalyst.

Abstract: The invention relates to a cement composition containing a shrinkage reducing amount of an alkyl ether derivative of an aliphatic polyhydroxy compound of the formula:Q--[(A).sub.n --OR].sub.xwherein Q is a C.sub.3 -C.sub.12 aliphatic hydrocarbon group, R is hydrogen or C.sub.1 -C.sub.10 alkyl, at least one R being the C.sub.1 -C.sub.10 alkyl group, A is C.sub.2 -C.sub.4 oxyalkylene, n is 0-10, and x is 3-5.

Abstract: The present invention provides a process the production of dialkyl peroxides by reaction of an alcohol and/or an olefin with an organic hydroperoxide, using an acidic resin catalyst, especially a highly cross-linked hydrophobic acidic resin catalyst.

Abstract: The present invention relates to a diesel fuel which contains a synergistic combination of an organic peroxidic additive such as ditertiary butyl peroxide in combination with a propylene or butylene glycol monoalkyl ether or polyol, the combination of additives providing for reduced fuel emissions and improved fuel economy.

Abstract: An integrate process is provided for the production of ditertiary butyl peroxide wherein isobutane oxidate containing tertiary butyl alcohol and tertiary butyl hydroperoxide is reacted in the presence of an aqueous acidic catalyst, the reaction mixture is phase separated, the aqueous catalyst is recovered and recycled, and the product peroxide is recovered from the organic phase by water extraction.

Abstract: The present invention relates to a low sulfur diesel fuel which contains a dialkyl and a trialkyl derivative of glycerol in amount sufficient to reduce particulate matter emissions.

Abstract: A process for preparing trisubstituted ureas is disclosed. A nitroarene is reacted with carbon monoxide and a secondary amine in the presence of a Group VIII transition metal catalyst and optionally one or more promoters selected from primary amines, halide ion-containing compounds, and chelating phosphorus and nitrogen compounds.

Abstract: A process for recovering both an amine and a volatile acid from an amine salt is disclosed. In the process, the amine salt is reacted with a non-volatile acid to liberate the volatile acid. Thermal decomposition of the resulting amine/non-volatile acid salt liberates the amine.

Abstract: A selective process for the preparation of diphenylmethane bis(dialkylureas) is disclosed. An alkyl phenylcarbamate or an N,N-dialkyl-N'-phenylurea is reacted with a methylene bis(alkyl carbamate) in the presence of an acid catalyst. The use of a staged addition of phenylcarbamate or phenylurea to the methylene bis(carbamate) and the use of a ramped temperature program are the keys to good selectivity to MDI dimer products.

Abstract: A selective process for the preparation of diphenylmethane diisocyanate precursors is disclosed. An alkyl phenylcarbamate or an N,N-dialkyl-N'-phenylurea is reacted with a methylene bis(alkyl carbamate) in the presence of an acid catalyst. The use of a staged addition of phenylcarbamate or phenylurea to the methylene bis(carbamate) and the use of a ramped temperature program are the keys to good selectivity to MDI dimer products.

Abstract: Olefins are epoxidized by hydrogen peroxide in the presence of an organorhenium oxide catalyst and an alkyl aryl secondary alcohol solvent. High yields of epoxides with minimal non-selective loss of either hydrogen peroxide or olefin are realized. The epoxidation may comprise one step of an integrated process wherein an oxidant mixture is generated by molecular oxygen oxidation of the alkyl aryl secondary alcohol and used directly in the epoxidation without further purification or extraction.

Abstract: A process for producing tetrahydrofuran, 1,4-butanediol, and 2-methyl-1,3,-propanediol is disclosed. A mixture containing 4-hydroxybutanal and 3-hydroxy-2-methylpropanal is hydrogenated in the presence of a transition metal supported on a weakly acidic ion-exchange resin or zeolite-type material to give tetrahydrofuran as the major product, and 1,4-butanediol and 2-methyl-1,3-propanediol as minor products. High yields of 2-methyl-1,3-propanediol can be obtained.

Abstract: Prochiral ethylenically unsaturated substrates are converted to chiral epoxides by reaction with optically active hydroperoxides in the presence of transition metal catalysts. For example, chiral glycidol is obtained by asymmetric epoxidation of allyl alcohol using optically active ethyl benzene hydroperoxide and a titaniuym alkoxide/tartrate catalyst. The chiral epoxide products are versatile synthetic intermediates.

Abstract: A process for making aryl-, heteroaryl-, or cycloalkyl-substituted alkyl urethanes is disclosed. The urethanes are prepared by electrophilic carbamylation of aromatic compounds with alkylene bis(carbamic acid esters) or the equivalent in the presence of an acidic catalyst and a polar aprotic solvent. The alkyl urethanes may be cracked to give the corresponding substituted alkyl isocyanates.

Abstract: Olefins are oxidized to epoxide compounds by contacting the olefins with organic hydroperoxides in the presence of rhenium catalysts comprised of perrhenate anions and organopnicogen-containing cations. High yields of epoxides are attained, particularly when the olefin substrate bears an aromatic substituent.

Abstract: Olefins are oxidized to epoxide compounds by contacting the olefins with organic hydroperoxides in the presence of oxorhenium porphyrin complex catalysts. High yields of epoxides are attained, particularly when the olefin substrate bears an aromatic substituent.