Abstract: A fuel composition comprising a major amount of hydrocarbons boiling in the gasoline or diesel range and an effective detergent amount of a hydroxyalkyl-substituted amine which is the reaction product of: (a) a polyolefin epoxide derived from a branched chain polyolefin having an average molecular weight of about 400 to 5,000; and (b) an amine having the formula:  wherein R1 and R2 are independently selected from the group consisting of hydrogen and hydrocarbyl of 1 to about 20 carbon atoms and, when taken together, R1 and R2 may form one or more 5- or 6-membered rings containing up to about 20 carbon atoms.

Abstract: A fuel composition comprising a major amount of hydrocarbons boiling in the gasoline or diesel range and an effective detergent amount of a hydroxyalkyl-substituted amine which is the reaction product of: (a) a polyolefin epoxide derived from a branched chain polyolefin having an average molecular weight of about 400 to 5,000; and (b) an nitrogen-containing compound selected from ammonia, a monoamine having from 1 to 40 carbon atoms, and a polyamine having from 2 to about 12 amine nitrogen atoms and from 2 to about 40 carbon atoms.

Abstract: A fuel composition for two-cycle engines comprising a major amount of fuel boiling in the gasoline range and a minor amount of a lubricant composition comprising a base oil of lubricating viscosity and an additive formulation comprising (1) a molybdenum/sulfur complex of a basic nitrogen compound, (2) a carboxylic acid amide, and (3) a succinimide.

Abstract: A fuel composition comprising a major amount of hydrocarbons boiling in the gasoline or diesel range and an effective detergent amount of a hydroxyalkyl-substituted polyamine which is the reaction product of: (a) a polyolefin epoxide derived from a branched chain polyolefin having an average molecular weight of about 400 to 5,000; and (b) a polyamine having from 2 to about 12 amine nitrogen atoms and from 2 to about 40 carbon atoms.

Abstract: A fuel composition comprising a major amount of hydrocarbons boiling in the gasoline or diesel range and about 2,050 to about 10,000 parts per million by weight of a hydrocarbyl-substituted polyoxyalkylene amine having the formula: or a fuel-soluble salt thereof; wherein R is a hydrocarbyl group having from about 1 to about 30 carbon atoms; R1 and R2 are each independently hydrogen or lower alkyl having about 1 to about 6 carbon atoms and each R1 and R2 is independently selected in each —O—CHR1—CHR2— unit; A is amino, N-alkyl amino having about 1 to about 20 carbon atoms in the alkyl group, N,N-dialkyl amino having about 1 to about 20 carbon atoms in each alkyl group, or a polyamine moiety having about 2 to about 12 amine nitrogen atoms and about 2 to about 40 carbon atoms; and x is an integer from about 5 to about 100.

Abstract: A fuel composition comprising a major amount of hydrocarbons boiling in the gasoline or diesel range and an effective detergent amount of a hydroxyalkyl-substituted, five- or six-membered cyclic urea-substituted monoamine or diamine which is the reaction product of:(a) a polyolefin epoxide derived from a branched-chain polyolefin having an average molecular weight of about 400 to 5000;(b) a polyamine having from 3 to 4 amine nitrogen atoms and from 4 to 9 carbon atoms; and thereafter(c) urea.

Abstract: A fuel composition comprising a major amount of hydrocarbons boiling in the gasoline or diesel range and an effective detergent amount of an alkyl-substituted, five- or six-membered cyclic urea-substituted monoamine or diamine which is the reaction product of:(a) a halogenated aliphatic hydrocarbon derived from a branched-chain polyolefin having an average molecular weight of about 400 to 5000;(b) a polyamine having from 3 to 4 amine nitrogen atoms and from 4 to 9 carbon atoms; and thereafter(c) urea.

Abstract: A process for the production of tetra- and trialkylsilanes which comprises reacting(A) an alkylchlorosilane having the formulaR.sub.x SiCl.sub.(4-x)wherein R is an alkyl radical containing from one to three carbon atoms per molecule and x is an integer from 0 to 3, with(B) a trialkylaluminum compound having the formula ##STR1## wherein R.sub.1, R.sub.2 and R.sub.3 are the same or different and represent alkyl radicals containing from 6 to 20 carbon atoms per molecule, in a reaction zone, said reaction being conducted under hydrosilylation conditions. Selectivity to tetra- or trialkylsilanes, respectively, is controlled by the addition of particular alkaline metal salts to the reaction zone.

Abstract: Tetraalkylsilane compounds are produced by contacting an admixture comprising(A) at least one alkylsilane selected from the group consisting of(i) a monoalkylsilane having the formulaR--Si--H.sub.3,(ii) a dialkylsilane having the formulaR--SiH.sub.2 --R.sub.1,(iii) a trialkylsilane having the formulaR--SiH--(R.sub.1).sub.2,and mixtures thereof, wherein R and R.sub.1 each represent an alkyl radical of from one to 20 carbon atoms per molecule, and(B) at least one alpha olefin containing from two to about 20 carbon atoms per molecule, under an inert atmosphere with an oxygenated, platinum-containing catalyst in which the platinum catalyst is selected from the group consisting of (i) a platinum catalyst having a basicity substantially equal to or less than that provided by a platinum-containing catalyst having a triphenylphosphine ligand, or (ii) a heterogeneous platinum-containing catalyst, under hydrosilylation conditions.

Abstract: The silahydrocarbon product containing at least 75 weight percent of saturated silahydrocarbons with the remainder being unsaturated silahydrocarbons is produced by a process in which admixture comprising(A) at least one alpha-olefin containing from 2 to about 20 carbon atoms per molecule, and(B) at least one alkylsilane selected from the group consisting of(i) a dialkylsilane having the formulaR--SiH.sub.2 --R.sub.1(ii) a trialkylsilane having the formula ##STR1## and (iii) mixtures thereof,wherein R and R.sub.1, the same or different, each represent an alkyl radical of from one to 20 carbon atoms per molecule with a catalyst comprising a homogeneous rhodium-containing catalyst or a heterogeneous rhodium-containing catalyst in a halogen-free inert solvent, under hydrosilylation reaction conditions to produce a mixture containing saturated and unsaturated silane hydrocarbons useful as lubricants.

Abstract: A novel ether solution of dinitrobenzophenone and a process for preparing an ether solution of diaminobenzophenone therefrom which comprises subjecting a dinitrobenzophenone dissolved in said ether solvent to hydrogenation in contact with a continuous nickel catalyst to obtain said solution of diaminobenzophenone dissolved in said ether solvent. In a specific embodiment said nickel catalyst is mounted on an inert support. In a still further embodiment, said diaminobenzophenone dissolved in said ether solvent, after removal of water therefrom, is reacted with an aromatic dianhydride to obtain a polyamic acid solution. The polyamic acid solution can be heated at a temperature above 100.degree. C. to drive off water of cyclization and thereby obtain the corresponding polyimide resin.

Abstract: A process for the preparation and recovery of m,m'-dinitrobenzophenone and which comprises reacting benzophenone with nitric acid in oleum; adjusting the reaction product to a water content from 12 to 30 weight percent; and extracting the m,m'-dinitrobenzophenone with a chlorinated hydrocarbon solvent.

Abstract: A one-step solution technique for preparing an aromatic polyimide acid which comprises reacting an aromatic dianhydride with an aromatic diamine in the presence of diglyme and a sufficient amount of a co-solvent to maintain the polyimide acid in solution, said co-solvent having the formula:ROHwhere R is H, an aliphatic branched or straight-chain hydrocarbon having from 1 to 5 carbon atoms or a methoxy substituted aliphatic branched or straight-chain hydrocarbon having from 1 to 5 carbon atoms.

Abstract: A one-step solution technique for preparing an aromatic polyimide acid which comprises reacting an aromatic dianhydride with an aromatic diamine in the presence of propylene glycol methyl ether.

Abstract: A process for preparing dinitrobenzophenones which comprises reacting benzene with ethylene in the presence of an alkylation catalyst to obtain an alkylation product containing unreacted benzene, ethylbenzene, polyethylbenzenes, 1,1-diphenylethane and heavier products, separating benzene, ethylbenzene and polyethylbenzenes from said alkylation product, recovering from the remainder of said alkylation product a fraction whose boiling points fall within the temperature range of about 260.degree. to about 290.degree. C., reacting said fraction with nitric acid at a temperature within the range of about 130.degree. to about 210.degree. C., wherein the molar ratio of nitric acid to said fraction is in the range of about 3:1 to about 8:1, and thereafter reacting the total resulting reaction product with nitric acid in oleum to obtain a nitration product predominating in dinitrobenzophenones.

Abstract: Compounds of the general structural formula, ##STR1## in which R.sup.1 is C.sub.1 to C.sub.4 lower alkyl, cycloalkyl or alkylamino and R.sup.2 is H or lower N-alkylcarbamyl are made from corresponding m-aminophenylacetylenic compounds by conventional methods and are useful as selective herbicides.

Abstract: Compounds of the general structural formula, ##STR1## in which R.sup.1 is C.sub.1 to C.sub.4 lower alkyl, cycloalkyl or alkylamino and R.sup.2 is H or lower N-alkylcarbamyl are made from corresponding m-aminophenylacetylenic compounds by conventional methods and are useful as selective herbicides.

Abstract: A process for preparing m,m'-dinitrobenzophenone which comprises reacting benzophenone with nitric acid in oleum.

Abstract: Acetylene terminated sulfones and oligomers thereof are prepared by reacting a sulfonyldiphenol with a material selected from the group consisting of a meta-dibromobenzene, a para-dibromobenzene and mixtures thereof in the presence of a potassium base to form a bis-bromophenoxydiphenyl sulfone, which is reacted with a substituted terminal acetylene compound containing at least three carbon atoms and an hydroxy group on the carbon atom adjacent to the acetylene group to form an hydroxy-acetylene terminated phenoxydiphenyl sulfone, which is then subjected to base catalyzed cleavage to form the desired acetylene terminated sulfones and oligomers. An hydroxy-arylacetylene terminated sulfone is prepared by reacting a sulfonyldiphenyl with a material selected from the group consisting of meta-dibromobenzene para-dibromobenzene and mixtures thereof in the presence of a sodium base.

Abstract: A process for reducing the amount of ortho nitro aromatic keto compounds in a mixture containing the same which comprises contacting such mixture with oleum.