Abstract: A method is disclosed for removing methyl isocyanate from gaseous effluent streams by contacting the gaseous effluent stream with activated alumina.

Abstract: A color-forming para sulfonamidodiphenylamine dye precursor has one or two sulfonamido groups in positions ortho to the amine --NH-- moiety separating the two phenyl rings of the para sulfonamidodiphenylamine and, in oxidized form, intramolecularly reacts to produce a sulfonamido-substituted phenazine dye. Such color-forming para sulfonamidodiphenylamine dye precursors are useful to produce a dye image by cross-oxidation in an imaging material.

Abstract: Tertiary amine catalyst mixtures comprising at least one hydroxyalkyl piperazine, preferably 2-hydroxyethyl piperazine or 1,4-di-(2-hydroxyethyl) piperazine, and at least one other tertiary amine for increasing the processability of hydroxyalkyl piperazine in controlling the water-isocyanate reaction rate to obtain optimum performance in cellular polyurethane foam formulations and/or enhancing the compatibility of hydroxyalkyl piperazine with other foaming ingredients in flexible polyester polyurethane foam formulation; and a process for producing cellular polyurethanes, such as flexible polyester or polyether polyurethane foam and high resilience polyether polyurethane foam, by effecting the reaction of an organic polyol reactant and an organic polyisocyanate reactant in the presence of a blowing agent and said tertiary amine catalyst mixture, the resulting cellular polyurethanes exhibiting very low residual amine odor.

Abstract: Alkyl amides have been synthesized from cyclic anhydrides, carboxyl acids and their esters by contacting them with an amine carbamic acid salt.

Abstract: A method of decoking (decarbonizing) surfaces of a cracking plant in which the cracking furnace is connected to a heat exchanger for cooling the cracked gas mixture, in which steam and air are admitted as a gas mixture to the cracking furnace and then the gas mixture is conducted through the cooler. The cooling medium is thus passed through the cracking gas cooler during the decoking operation while in a first stage the mixture is fed through the device at such a mass flow rate that the temperature of the deposits on the heat exchange surface is approximately at the temperature corresponding to cracking operations while, in a second stage, the gas flow rate is increased to raise the temperature of the deposits on the heat exchange surfaces of the cooler.

Abstract: Novel ureas of the formula I have herbicidal activity and are suitable in small applied amounts for selectively combating weeds in cultivated crops of soya-bean, maize and cereals. They are advantgeously produced by the isocyanate method and correspond to the formula I ##STR1## wherein R.sub.1 is an unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkynyl, aralkyl, phenyl, acyl or C.sub.1 -C.sub.4 -alkylsulfonyl group or an aminoalkyl group,R.sub.2 is hydrogen, halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy,R.sub.3 is hydrogen, halogen, cyano or trifluoromethyl,R.sub.4 is hydrogen, C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkynyl or C.sub.1 -C.sub.6 -alkoxy,R.sub.5 is hydrogen, C.sub.1 -C.sub.6 -alkyl or C.sub.2 -C.sub.6 -alkenyl, or R.sub.5 together with R.sub.4 and the nitrogen atom to which they are bound also form a 5-6-membered heterocycle, andX is oxygen, sulfur or the sulfinyl or sulfonyl group.

Abstract: 4-aminobutyramide hydrochloride is produced by saponifying 4-(benzylamino)-or-4-(dibenzylamino)-butyronitrile to the corresponding substituted 4-aminobutyramide and subjecting this in the form of the hydrochloride in the presence of an inert solvent and a platinum metal catalyst to a hydrogenation treatment whereby the benzyl group or the two benzyl groups are split off.

Abstract: 4-Vinylcyclohexene-1 is converted to ethylbenzene by contacting the vinylcyclohexene at a temperature ranging from about 100.degree. C. to about 450.degree. C. with a catalyst prepared by impregnating an alumina with an oxide or decomposable salt of Na, K, Rb, Cs, Ca, Sr and/or Ba and calcining the impregnated material at a temperature ranging from about 450.degree. C. to about 750.degree. C.

Abstract: Novel odorants, having the formula ##STR1## wherein R represents sec. butyl, tert. butyl or cyclohexyl. A process for preparing the novel odorants from novel intermediates and fragrance compositions containing the odorants are also taught.

Abstract: Described is a process for preparing several substituted or unsubstituted cycloalkyl acyl alkanoates defined according to the generic structure: ##STR1## wherein R.sub.1 and R.sub.2 taken together complete a cycloalkyl moiety or methyl, dimethyl or trimethyl substituted cycloalkyl moiety containing five or six carbon atoms in the ring and wherein R.sub.3 is C.sub.1 -C.sub.3 lower alkyl and R.sub.4 is methyl or hydrogen by reacting a compound having the generic structure: ##STR2## in an aqueous silver-ion containing solution having a weakly acidic pH at elevated temperatures.

Abstract: Novel sulfamoyl-substituted phenethylamine derivatives which exhibit .alpha.-adrenergic blocking action and are useful as an antihypertensive agent and an agent for the treatment of congestive heart failure.

Abstract: The catalytic dehydrogenation of at least one dehydrogenatable organic compound which has at least one ##STR1## grouping is carried out in the presence of a zinc silicate catalyst and in the substantial absence of free oxygen.

Abstract: 3-Nitro-acetoacetanilides of the formula ##STR1## in which R.sup.1, R.sup.2 and R.sup.3 independently of one another represent hydrogen, alkyl, cycloalkyl or aryl, it being possible for two of the said radicals to form a cycloaliphatic ring together with the carbon atom on which they are substituents, andR.sup.4 and R.sup.5 independently of one another denote hydrogen, alkyl, aralkyl, aryl, alkoxy, alkylthio, aralkoxy, aralkylthio, aryloxy, arylthio, halogen, nitro or amino disubstituted by alkyl, aralkyl or aryl, andR.sup.4 and R.sup.5, when they are adjacent, can be parts of a fused cycloaliphatic or aromatic ring,are described as well as methods for its preparation such as by reaction of an acetoacetic acid compound with a 3-nitro-aniline under condensation conditions, or, by reaction of an enamine with 3-nitro-phenyl isocyanate. The 3-nitro-acetoacetanilides are useful intermediates in the preparation of coupling components for color photography.

Abstract: Esters of alkoxylated long chain fatty alchols with halo acetic acid are contacted with tertiary amines incorporating a long chain aliphatic group to produce a class of novel quaternary ammonium compounds. These product compounds have utility as fabric softeners and as hair conditioners.

Abstract: .alpha.-Ketocarboxylic acid N-acylamides of the formulaR.sup.1 --CO--CO--NH--CO--R.sup.2in whichR.sup.1 is an optionally substituted aliphatic radical with up to 12 carbon atoms, an optionally substituted cycloalkyl radical with 3 to 10 carbon atoms, an optionally substituted heterocyclic radical, andR.sup.2 is an optionally substituted aliphatic radical with up to 8 carbon atoms or an optionally substituted phenyl radical,are prepared by reacting an acyl cyanide of the formulaR.sup.1 --CO--CNwith a carboxylic acid anhydride of the formulaR.sup.2 --CO--O--CO--R.sup.2in the presence of a strong acid, and then adding water to the reaction mixture. The products can be used directly in the synthesis of known herbicides.

Abstract: The present invention relates to the use of telluroxides as mild and selective oxidizing agents serving to oxidize certain functions, notably >C.dbd.S groups, in the presence of other relatively easily oxidized functions which remain unaffected; telluroxides of interest as oxidizing agents include, for example, compounds of the formula: ##STR1## wherein R and R.sup.1, which may be the same or different, each represent an optionally substituted aryl or heterocyclic group; or R and R.sup.1 together with the tellurium atom therebetween represent a heterocyclic ring, which may contain one or more further heteroatoms, and which may carry substituents and/or fused aromatic rings.

Abstract: Described are the uses for augmenting or enhancing the aroma of perfume compositions and colognes of the compounds having the structures: ##STR1## wherein "R" represents isopropyl, phenethyl, allyl, cyclohexyl, hydroxyl alkyl or alkoxy alkyl.

Abstract: The catalytic oxidative dehydrogenation of at least one dehydrogenatable organic compound which has at least one ##STR1## grouping is carried out in the presence of a zinc titanate catalyst. The selectivity of the zinc titanate catalyst may be improved by a promoter at least one member of which is selected from the group consisting of chromium, antimony, bismuth, aluminum, phosphorus, indium, tin, lanthanum and cerium.

Abstract: A novel disproportionation catalyst comprising the product resulting from the combination of elemental sulfur and a disproportionation catalyst consisting essentially of a refractory oxide containing molybdenum oxide or tungsten oxide.

Abstract: The process relates to the recovering of essentially pure acetylene from the gaseous out-put stream from a coal to acetylene conversion process. A plasma arc generator or other high energy type reactor can be used for the conversion to coal. The gaseous out-put stream is initially treated in an acid gas removal stage by absorbing HCN and H.sub.2 S in an organic solvent such as N-methyl pyrrolidone and scrubbing with a caustic agent such as NaOH to remove CO.sub.2. In a second stage, the gaseous out-put stream is scrubbed with the organic solvent to provide a sweet gas treatment and remove essentially pure acetylene as a product. In a third stage, the second stage gases are first hydrogenated, then desulferized and then methanated. The out-put from the third stage is recycled to the coal to acetylene conversion process. In a fourth stage, the organic solvent from said second stage is refined and recycled to the first stage and/or second stage.