Abstract: A catalyst composition comprising a complex of catalytic oxides of iron, bismuth, molybdenum, cobalt, cerium, antimony, at least one of nickel or magnesium, and at least one of lithium, sodium, potassium, rubidium, or thallium, and characterized by the following empirical formula: AaBbCcFedBieCofCegSbhMomOx wherein A is at least one of Cr, P, Sn, Te, B, Ge, Zn, In, Mn, Ca, W, or mixtures thereof B is at least one of Li, Na, K, Rb, Cs, Tl, or mixtures thereof C is least one of Ni, Mg or mixtures thereof a is 0 to 4.0 b is 0.01 to 1.5 c is 1.0 to 10.0 d is 0.1 to 5.0 e is 0.1 to 2.0 f is 0.1 to 10.0 g is 0.1 to 2.0 h is 0.1 to 2.0 m is 12.0 to 18.0 and x is a number determined by the valence requirements of the other elements present. The catalyst is useful in processes for the ammoxidation of an olefin selected from the group consisting of propylene, isobutylene or mixtures thereof, to acrylonitrile, methacrylonitrile and mixtures thereof, respectively.

Abstract: A method of preparing a V.sub.a Sb.sub.b M.sub.m N.sub.n O.sub.x catalyst useful in the ammoxidation of a C.sub.2 -C.sub.5 hydrocarbon to its corresponding .alpha., .beta. unsaturated nitrile comprising heating an aqueous mixture comprising V.sub.2 O.sub.5 and Sb.sub.2 O.sub.3 at a temperature above about 100.degree. to 250.degree. C., preferably 110.degree. to 175.degree. C., most preferably 120.degree. to 160.degree. C., under autogenous pressure with agitation to form a catalyst precursor, drying the catalyst precursor and calcining the catalyst precursor to form the finished catalyst.

Abstract: A process for the destruction of organic wastes and ammonia from acrylonitrile plant wastewater, comprising contacting volatilized wastewater with a catalyst at an elevated temperature so as to convert volatile organic compounds and ammonia to a mixture comprising hydrogen, nitrogen and carbon dioxide which are separated and removed from the stream, yielding a purified aqueous stream, substantially free of organic compounds and ammonia.

Abstract: The process for the ammoxidation of a C.sub.3 to C.sub.5 paraffinic hydrocarbon to its corresponding .alpha.,.beta.-unsaturated hydrocarbon comprising reacting the C.sub.3 to C.sub.5 paraffinic hydrocarbon with ammonia and oxygen in a fluid bed reactor at a temperature of between 250.degree. C. to 600.degree. C. in the presence of a catalyst having the empirical formula as follows:V.sub.v Sb.sub.m A.sub.a D.sub.d O.sub.xwherein A when present is Sn and/or Ti;D when present is one or more of Li, Mg, Na, Ca, Sr, Ba, Co, Fe, Cr, Ga, Ni, Zn, Ge, Nb, Zr, Mo, W, Cu, Te, Ta, Se, Bi, Ce, In, As, B, Al, P and Mn; andwherein v is 1, m is 0.5-75, a is 0 to 25, d is 0 to 25, and x is determined by the oxidation state of the cations present,and a minor quantity of an halogen-containing component, preferably characterized by the following formula:R--X or X.sub.2where R=Hydrogen, C.sub.1 -C.sub.20 alkyland X=F, Cl, Br, I or mixtures thereof.

Abstract: Maleic acid, maleic anhydride or other hydrogenatable precursor are catalytically hydrogenated to 1,4-butanediol and tetrahydrofuran. It has been discovered that high yields of 1,4-butanediol are achieved when the hydrogenation catalyst comprises palladium, silver and rhenium on a carbon support and is prepared by the steps of(i) impregnating a carbon support with a source of palladium, silver and rhenium, wherein the source of palladium, silver and rhenium is at least one solution,(ii) after each impregnation step, drying the impregnated carbon support to remove solvent,(iii) heating the impregnated carbon support at a temperature of about 120.degree. C. to about 350.degree. C. under reducing conditions.The palladium in the catalyst is present in the form of crystallites having a particle size of less than 10 nm.

Abstract: A process for the manufacture of a Pd/Au/alkali metal catalyst, preferably a fluid bed catalyst used in the production of vinyl acetate comprising impregnating a microspheroidal support with a hydroxy-free metal salt solution of Pd and Au substantially free of barium and halide, reducing said salts to deposit Pd and Au on said support surface and impregnating said support with a halide-free metal salt of an alkali metal (preferably potassium).

Abstract: Disclosed is a process for making acetic acid which comprises oxidizing ethane with molecular oxygen in a reaction zone at a pressure of at least 100 psig while the reactants are in contact with a solid catalyst having the elements and relative atomic proportions indicated by the empirical formula:VP.sub.a M.sub.b O.sub.xwhere M is one or more optional element selected from Co, Cu, Re, Fe, Ni, Nb, Cr, W, U, Ta, Ti, Zr, Zn, Hf, Mn, Pt, Pd, Sn, Sb, Bi, Ce, As, Ag, and Au,whereina is 0.5 to 3,b is 0 to 1, andx is a number determined by the valence requirements of the other elements in the catalyst, andwherein said catalyst contains crystalline vanadyl pyrophosphate.

Abstract: A process is provided for the oxydehydrogenation of saturated carboxylic acids with oxygen in the presence of iron phosphorus oxide catalysts containing promoters selected from the group Ag, Al, B, Cd, Co, Cr, Cu, Ga, Ge, In, Mn, Ni, Te, Th, Ti, Tl, U, V, Zn, Zr, rare earths and mixtures thereof.

Abstract: The selective leaching of metal ions from various iron oxide and manganese oxide containing ores employs intermediary solutions. The leaching processes are based upon a redox acid leach step employing stabilized cuprous ions and, in one instance, a combination thereof with ferrous ions. Leaching is conducted at low temperatures, up to about 90.degree. C. and low pressures, up to about 1.5 MPa and at a pH of about 1.5 to 2.5. Nickel and cobalt recoveries from the ores, employing these processes, will usually equal or exceed 90 percent. The intermediary solutions comprise stabilized acidic cuprous ions Cu.sup.+ L wherein L is a stabilizing ligand selected from the group consisting of CO, XRCN and Cl.sup.-, X being --H or --OH and R being aliphatic having from one to about four carbon atoms. In at least one process, ferrous ions are introduced for a separate leaching step.

Abstract: A system for controlling the vertical movement of a drillstring and which is removably interconnected with a conventional drill rig. The system includes at least one fluidic cylinder and piston assembly removably connected at an upper end to a support, such as the rig's traveling block assembly, and at a lower end to the drillstring. A pump is operatively connected to the cylinder and piston assembly and a control valve device is provided to control the flow of the fluid to and from the cylinder and piston assembly. A computing device is in operative communication with a data measurement system and the control valve device and is used to automatically control the movement of the drillstring in response to data, such as WOB, received from the data measurement system.

Abstract: A process is provided for the production of aliphatic acetate esters and gaseous alkanes comprising contacting acetic acid and synthesis gas in the vapor phase at elevated temperature and pressure in the presence of a catalyst containing the mixed oxides of ruthenium and nickel, and optionally an alkali metal oxide and the oxides of cobalt, cadmium, zinc or mixtures thereof. Other carboxylic acids may be substituted for acetic acid as desired.

Abstract: A process for recovery of vanadium and molybdenum from a feed material containing compounds of these metals by reacting at an effective pH an aqueous solution of vanadate and molybdate anions with a quaternary ammonium surfactant dissolved in an organic solvent which is immiscible with water and separating a vanadate anion rich phase from a molybdate anion rich phase.

Abstract: Hydrogen is produced from hydrogen sulfide by a 3-step, thermochemical process comprising:(a) contacting hydrogen sulfide with carbon dioxide to form carbonyl sulfide and water,(b) contacting the carbonyl sulfide produced in (a) with oxygen to form carbon monoxide and sulfur dioxide, and(c) contacting the carbon monoxide produced in (b) with water to form carbon dioxide and hydrogen.

Abstract: Bismuth molybdate catalysts formed from a precatalyst slurry which uses an organic liquid or mixture of an organic liquid and water as the liquid medium of the slurry exhibit superior catalytic properties.

Abstract: A process for the manufacture of a phosphorus/vanadium/metal oxide catalyst suitable for the oxidation of butane to maleic anhydride can be prepared by reacting in an aqueous medium a vanadium compound, inorganic acid and metal oxide, then adding orthophosphoric acid to form a soluble vanadium phosphorus metal oxide catalyst, removing the acidified water and adding an aliphatic alcohol, removing the alcohol and recovering under vacuum the solid phosphorus vanadium metal oxide catalyst.

Abstract: An element selected from Groups IA, IB, IIB, IIIA and IIIB is incorporated into an iron bismuth molybdate oxide complex catalyst by impregnation.

Abstract: Oxide complex catalysts comprising Fe-Sb-Bi-O.sub.x promoted with a wide variety of different elements have been found to be especially useful in the ammoxidation of olefins to nitriles such as acrylonitrile and methacrylonitrile. Not only are the desired nitriles obtained with high yields when these catalysts are used, but also the production of unwanted liquid byproducts such as acrolein, acrylic acid and acetonitrile is significantly reduced.

Abstract: The invention is an oxidation catalyst which contains at least a Group IIA or Group IIB element or manganese plus as required elements, chromium, bismuth and molybdenum. The catalysts can optionally contain a number of other elements and are useful for various oxidation reactions, especially the ammoxidation of propylene or isobutylene to obtain acrylonitrile or methacrylonitrile, the oxidation of propylene or isobutylene to obtain acrolein or methacrolein and the oxidative dehydrogenation of olefins containing 4 or 5 carbon atoms to obtain the corresponding diolefin.

Abstract: Cyclohexanone and/or cyclohexanol can be ammoxidized in the liquid phase to heterocyclic compounds by contacting the cyclohexanone and/or cyclohexanol with various oxidation catalysts in the presence of molecular oxygen and ammonia.

Abstract: A process is described for the recovery and purification of an olefinic nitrile, such as methacrylonitrile, from mixtures of said olefinic nitrile with hydrogen cyanide, acetonitrile, acrylonitrile, and carbonyl compounds, which result from the ammoxidation of an olefin, such as isobutylene. The mixtures of olefinic nitrile are fed to an extractive distillation column at a point above the middle of the column, a vapor sidestream is removed at a point below the middle of the extractive distillation column said sidestream containing substantially all of the hydrogen cyanide, acetonitrile and carbonyl compounds and then concentrating the hydrogen cyanide, acetonitrile and carbonyl compounds in a stripping pot.