Abstract: A process for hydrogenating an unsaturated organic compound which comprises contacting the same with hydrogen in the presence of a catalyst composed of a support containing (1) (A) a Group IIB metal compound selected from the group consisting of zinc and cadmium compounds, (B) a combination of said zinc and cadmium compounds or (C) a combination of at least one of said Group IIB metal compounds with at least one Group IIA metal compound selected from the group consisting of magnesium, calcium, strontium and barium compounds, (2) alumina and (3) aluminum phosphate and carrying nickel thereon.

Abstract: The novel compound having the structural formula ##STR1## is disclosed, as well as its use by pre-emergent application to control noxious grasses and some broadleaf weeds in cool season crops such as rape, sugar beets and flax.

Abstract: The combustible component of a gas stream of low heating value is combusted using less than a stoichiometric amount of oxygen with minor production of carbon monoxide due to the use of an oxygenation catalyst comprising at least three metals in a perovskite-type crystal structure. This combusted gas can be directly vented to the atmosphere after energy has been extracted from it for a useful purpose.

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 novel class of compounds which are useful as plant growth regulators is disclosed, having the general structural formula: ##STR1## In which R is C.sub.1 to C.sub.4 alkyl, alkenyl or aklynyl to which may be attached phenyl, pyridyl, benzoyl, phenoxy, halophenoxy, halobenzoyl, N-phenylcarbamyl, N-alkylcarbamyl, N-trifluoromethylthiadiazolylcarbamyl, carboxy, carbalkoxy or halo substituents,R.sup.1 is H, C.sub.1 to C.sub.3 alkyl, alkenyl or alkynyl to which may be attached phenyl, halophenyl or phenoxy groups, acetyl, or R and R.sup.1 together may be C.sub.2 to C.sub.4 alkylene,Ar is phenyl or benzoyl,R.sup.2 is C.sub.1 to C.sub.4 alkyl, alkoxy, alkylene, alkylamino or alkylthio, phenoxy, benzyloxy, carbalkoxy, acetyl, methylenedioxy, trifluoromethyl, nitro, halo or cyano and n may be zero or an integer from 1 to 4, with the provision that at least one position ortho to the point of attachment of a phenyl ring of the Ar structure must be unsubstituted,R.sup.

Abstract: A process for selectively producing aldehydes, particularly acetaldehyde, which comprises introducing into a reaction zone (1) methanol, (2) carbon monoxide, (3) hydrogen, (4) cobalt, (5) iodine and (6) a specific phosphorus-containing ligand and then subjecting the contents of said reaction zone to an elevated temperature and an elevated pressure for a time sufficient to convert methanol to said aldehydes.

Abstract: A process for selectively producing aldehydes, particularly acetaldehyde, which comprises introducing into a reaction zone (1) methanol, (2) carbon monoxide, (3) hydrogen, (4) cobalt, (5) iodine and (6) a ligand containing atoms from Group VB of the Periodic Table separated by a sterically constrained carbon-carbon bond and then subjecting the contents of said reaction zone to an elevated temperature and an elevated pressure for a time sufficient to convert methanol to said aldehydes.

Abstract: A process for hydrogenating an unsaturated organic compound which comprises contacting the same with hydrogen in the presence of a catalyst composed of a support containing alumina and aluminum phosphate carrying nickel thereon.

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: A novel composition of matter capable of being cured to a solid resinous material obtained as a result of the reaction of (1) a coal derivative comprising a mixture of monocyclic, polycyclic, multifunctional carboxylic acids, resulting from the interaction of coal with nitric acid with (2) an oxirane, and a process for producing a solid resinous material therefrom by heating the same under pressure.

Abstract: A process for hydrogenating unsaturated carboxylic acids and esters of unsaturated carboxylic acids such as fatty acids which comprises reacting the unsaturated composition with hydrogen in contact with a catalyst prepared from a layered complex nickel silicate which has been prepared in a multi-stage procedure comprising reduction in a hydrogen atmosphere, oxidation in an atmosphere containing molecular oxygen and then again reduction in a hydrogen atmosphere.

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.

Abstract: A process for selectively producing alcohols, particularly ethanol, which comprises introducing into a reaction zone (1) methanol, (2) carbon monoxide, (3) hydrogen, (4) cobalt, (5) iodine, (6) ruthenium and (7) a ligand containing atoms from Group VA of the Periodic Table separated by a sterically constrained carbon-carbon bond, and then subjecting the contents of said reaction zone to an elevated temperature and an elevated pressure for a time sufficient to convert methanol to said ethanol.

Abstract: A process for selectively producing ethanol which comprises introducing into a reaction zone methanol, hydrogen, carbon monoxide, a cobalt tricarbonyl complex and an iodine promoter and then subjecting the contents of said reaction zone to an elevated temperature and an elevated pressure for a time period sufficient to convert methanol to ethanol.

Abstract: This invention relates to a method for selectively removing molybdenum values from a spent catalyst and producing a fresh molybdenum-containing catalyst. Such a method preferably contacts anhydrous gaseous hydrogen chloride at an elevated temperature with the metal containing catalyst which is substantially free of carbonaceous material to selectively remove molybdenum therefrom, and producing a fresh molybdenum-containing catalyst by depositing molybdenum from the vapor phase onto a fresh support in the presence of air. At least 50 weight percent and generally as much as 95 weight percent of the molybdenum is removed while other metals such as iron, titanium, cobalt and nickel along with the supporting alumina or silica are not affected.

Abstract: Aluminum trihydrocarbyls are prepared by reacting an organo magnesium compound with a mixture of chlorinated and brominated aluminum compounds. There is thus obtained a mixture of aluminum trihydrocarbyls and a magnesium halide containing both chloride and bromine. The aluminum trihydrocarbyls are then recovered from the mixture. They may be used in the preparation of an alpha olfin polymerization catalyst as hereinafter described.

Abstract: A novel catalyst system comprising (1) a cobalt carbonyl, a hydrido cobalt carbonyl or a cobalt-containing material convertible to a cobalt carbonyl or a hydrido cobalt carbonyl, (2) a tertiary organo Group VA compound of the Periodic Table, (3) an iodine compound and (4) a ruthenium compound and to a process for selectively producing ethanol which comprises introducing into a reaction zone (1) methanol, (2) hydrogen, (3) carbon monoxide, (4) a cobalt carbonyl, a hydrido cobalt carbonyl or a cobalt-containing material convertible to a cobalt carbonyl or a hydrido cobalt carbonyl, (5) a tertiary organo Group VA compound of the Periodic Table, (6) an iodine compound and (7) a ruthenium compound and then subjecting the contents of said reaction zone to an elevated temperature and an elevated pressure for a time sufficient to convert methanol to ethanol.

Abstract: Quaternary ammonium thiomolybdates are prepared in a two-phase reaction system by contacting an aqueous solution of a thiomolybdate salt with a solution of a quaternary ammonium salt in a water-immiscible organic solvent. For example, mixing a solution of dicocodimethylammonium chloride in toluene with an aqueous solution of potassium thiomolybdate results in a toluene solution containing dicocodimethylammonium thiomolybdate.

Abstract: Novel quaternary ammonium thiomolybdates are prepared by contacting an aqueous solution of a thiomolybdate salt with a solution of a water-insoluble quaternary ammonium salt in a water-immiscible organic solvent. For example, mixing a solution of dicocodimethylammonium chloride in toluene with an aqueous solution of potassium thiomolybdate results in a toluene solution containing dicocodimethylammonium thiomolybdate. These quaternary ammonium thiomolybdates find use as additives in motor oils and greases to enhance their antifriction characteristics.