Abstract: An improved method is disclosed for the selective synthesis of low molecular weight olefins, particularly C.sub.2 and C.sub.3 olefins inclusive, which method comprises the steps of passing a CO and H.sub.2 synthesis gas stream over a catalyst at a temperature and pressure and for a time sufficient to generate the desired olefinic products, wherein the improvement consists in using as a catalyst ruthenium on a support selected from the group consisting of a manganese oxide, other manganese-containing oxides or mixtures of various manganese oxides. The weight loading of the ruthenium may range from about 0.01 to about 15 wt. % based on the total catalyst weight. The operating conditions of the instant process are the standard Fischer-Tropsch synthesis reaction parameters, preferably an H.sub.2 /CO mole ratio of from about 10 to about 0.1, a space velocity of from about 100 hr.sup.-1 to about 50,000 hr.sup.-1, a temperature of from about 100.degree. C. to about 500.degree. C.

Abstract: An improved method for the enhanced synthesis of paraffinic hydrocarbons with chain lengths of from 2 to 6 carbon atoms inclusive with reduced methane formation which method comprises the steps of passing a synthesis gas stream comprising CO and H.sub.2 over a catalyst at a temperature and pressure for a time sufficient to generate the desired C.sub.2 -C.sub.6 paraffinic product, wherein the catalyst comprises from about 0.01 to about 15 wt. % nickel on a support selected from the group consisting of tantalum oxides, niobium oxides, and other tantalum or niobium containing oxides and mixtures thereof. The nickel average crystallite size is preferably less than 5 nm (50 A). The supported nickel catalyst has a BET surface area of from about 10 to 60 m.sup.2 /g.

Abstract: An apparatus is disclosed for generating a multiple phase dispersion and distributing said multiple phase dispersion as globules in a suspension phase. The apparatus comprises a conduit for introducing a first fluid under pressure into a first zone including a porous fluid dispersing layer. This first zone is in fluid communication with a second zone through the porous fluid dispersing layer. The second zone has introduced into it a second fluid under pressure through inlets. The first fluid is dispersed as bubble-like micro droplets in the second fluid by passage from the first zone through the fluid dispersing layer into the fluid in the second zone. An outlet zone is in contact with the second zone and comprises a perforated nonporous layer having an outer and inner surface and includes a porous flow distribution layer substantially in contact with the inner second zone facing surface of the nonporous layer.

Abstract: This invention relates to unique supported potassium (or rubidium) - Group VIII-metal cluster catalysts which are useful in CO/H.sub.2 reactions (Fischer-Tropsch synthesis reactions). The novel catalysts of the instant invention are prepared by depositing well characterized potassium (or rubidium) - Group VIII-metal carbonyl cluster complexes onto high surface area supports. Following a subsequent reduction, the precursor bimetallic cluster complexes are decomposed on the support surface forming a potassium (or rubidium) promoted Group VIII-metal cluster catalyst in which the potassium (or rubidium) and Group VIII metals are intimately associated. These unique, highly promoted cluster catalysts have been found to demonstrate high Group VIII-metal dispersions and enhanced Fischer-Tropsch activities and selectivities for producing olefinic and paraffinic hydrocarbons.

Abstract: Hydrocarbon conversion processes wherein hydrocarbon feedstreams are contacted with heteronuclear noble metal catalysts are improved by the use of supported heteronuclear noble metal cluster catalysts prepared from novel supported heteronuclear noble metal cluster complexes. The heteronuclear noble metal cluster complexes used as catalyst precursors are selected from the group consisting of(pyridine).sub.2 Pt[Ir.sub.6 (CO).sub.15 ],(pyridine).sub.2 Pt[Ir.sub.2 (CO).sub.7 ],((C.sub.6 H.sub.5).sub.3 P).sub.2 Pt[IR(CO).sub.3 P(C.sub.6 H.sub.5).sub.3 ].sub.2,(pyridine).sub.2 Pt[Ru.sub.3 (CO).sub.12 ]((C.sub.6 H.sub.5).sub.3 P).sub.2 Rh(CO)[Ir(CO).sub.4 ],(pyridine).sub.2 Pt[Rh(CO).sub.2 (P(C.sub.6 H.sub.5).sub.3).sub.2 ].sub.2.

Abstract: Emulsions are prepared utilizing an emulsification device comprising an enclosure having orifices thereby permitting flow of a fluid through the enclosure along one of its axis, of any cross-section profile perpendicular to its axis for fluid flow, which enclosure is packed with a material which causes the flow of fluids to be broken down into many fine streams which fine streams, being in intimate contact one with the other, remix rapidly and repeatedly, resulting in the formation of the desired emulsion. The fluids which are mixed in the packed enclosure are fed to the enclosure by fluid feeding means such as pumps or by gravity feed tanks and conduits communicatively attached to the packed enclosure. The fluids fed into the packed enclosure are introduced into the enclosure in close proximity one to another so as to insure maximum intermixing of the different fluids.

Abstract: This invention relates to the use of liquid membrane technology in preparing medicinals. The medicinals prepared by this invention may be ingested and may be utilized as traps for toxins present in the GI (gastrointestinal) tract, or as slow-release compositions of drugs, or as reactors. In the trap embodiment, the liquid membrane encapsulated medicinal is an emulsion comprising an exterior phase which is immiscible with the liquids present in the GI tract and permeable to the toxins therein, and an interior phase which is immiscible with the exterior phase and comprises a reagent capable of converting said toxin into a nonpermeable form. In addition, hydrophilic adsorbents, such as a hydrophilic carbon or a silica gel, may be encapsulated in the emulsions of the instant invention.

Abstract: The present invention relates to liquid membrane capsules which rupture when contacted with biliary or pancreatic secretions in the intestine thereby releasing their contents in the intestine so the contents become fully available for the treatment of disease at that location in the animal or patient. Particularly, the rupturable liquid membrane capsules containing urease are used for the treatment of chronic uremia. The liquid membrane capsules comprise an internal aqueous phase which contains an oil insoluble medicinal of choice, some complexing agent, dietary supplement or enzyme particularly suited for the intended treatment. This internal aqueous and oil insoluble phase is encapsulated in a nonaqueous external phase comprising a biologically inert oil component, and a material which will complex with the biliary and/or pancreatic secretions in the intestine thereby causing the rupture of the external phase resulting in the release of the internal phase in the intestine.

Abstract: The instant invention relates to an improved process for oxygenating blood comprising: contacting said blood with oxygen-containing bubbles, said bubbles being coated with a liquid membrane, said liquid membrane phase permitting the permeation of oxygen into the blood whereby at least a portion of said oxygen passes through said membrane and into said blood; removing said liquid membrane coated bubbles as a three phase foam comprising gas bubbles coated with said liquid membrane suspended in blood; and coalescing said foam comprising gas bubbbles to form three separate bulk phases comprising the liquid membrane phase, a gaseous phase and a blood phase, wherein the improvement comprises a liquid membrane phase comprising a biologically non-retainable liquid halocarbon compound. These liquid membrane formulations having a membrane phase comprising a biologically non-retainable liquid halocarbon compound exhibit improved coalescing characteristics.

Abstract: N,N-dichloro-N-acyl compounds such as N,N-dichlorocarbamates, sulfonamides, amidosulfonamides selectively react with conjugated dienes to yield the corresponding 1,4-adducts, i.e. N-chloro-N-chlorocrotyl compounds. The N-chloro group of these adducts can be selectively reduced by aqueous sodium sulfite. Both the original and reduced adducts are effective fungicides, herbicides and bacteriocides.

Abstract: N,N-dichloro-N-acyl compounds, such as N,N-dichlorocarbamates, sulfonamides and amidosulfonamides selectively react with conjugated dienes to yield the corresponding 1,4-adducts, i.e. N-chloro-N-chlorocrotyl compounds. The N-chloro group of these adducts can be selectively reduced by aqueous sodium sulfite. Both the original and the reduced adducts are novel compositions useful as biologically active compounds and vulcanizing agents. The bis-N-chlorocrotyl carbamates and their N-chloro derivatives are particularly claimed compositions.

Abstract: N,N-dichloro-N-acyl compounds, such as N,N-dichlorocarbamates, sulfonamides and amidosulfonamides selectively react with conjugated dienes to yield the corresponding 1,4-adducts, i.e. N-chloro-N-chlorocrotyl compounds. The N-chloro group of these adducts can be selectively reduced by aqueous sodium sulfite. Both the original and the reduced adducts are novel compositions useful as biologically active compounds and vulcanizing agents. The N-chlorocrotyl sulfamides and their N-chloro derivatives are particularly claimed compositions.

Abstract: The instant invention relates to a method for preparing high activity supported nickel catalysts. The method comprises the deposition of nickel nitrate on a carrier, typically an inert inorganic refractory oxide, by techniques known in the art followed by careful heating to a temperature of between 100.degree. to 270.degree. C., avoiding any excursions into temperatures beyond the stated maxima, in a flowing nonreactive gas atmosphere for a time sufficient to convert substantially all of the nickel nitrate into nickel oxide. When using an H.sub.2 containing atmosphere the maximum temperature is 220.degree. C. The supported nickel oxide resulting from the above procedure is then reduced to a supported nickel metal catalyst in a reducing atmosphere at a temperature ranging from about 230.degree. C. to 400.degree. C.

Abstract: This invention relates to the use of chelated lithium hydridoaluminates or hydridoborates in hydride reductions of inorganic substrates. Novel or improved reductions are obtained at increased rates or selectivities in hydrocarbon media to recover metals.

Abstract: This invention relates to unique supported potassium (or rubidium)-Group VIII-metal cluster catalysts which are useful in CO/H.sub.2 reactions (Fischer-Tropsch synthesis reactions). The novel catalysts of the instant invention are prepared by depositing well characterized potassium (or rubidium)-Group VIII-metal carbonyl cluster complexes onto high surface area supports. Following a subsequent reduction, the precursor bimetallic cluster complexes are decomposed on the support surface forming a potassium (or rubidium) promoted Group VIII-metal cluster catalyst in which the potassium (or rubidium) and Group VIII metals are intimately associated. These unique, highly promoted cluster catalysts have been found to demonstrate high Group VIII-metal dispersions and enhanced Fischer-Tropsch activities and selectivities for producing olefinic and paraffinic hydrocarbons.

Abstract: Chelated lithium aluminum compounds are prepared by mixing a lithium aluminum compound such as a lithium aluminum hydride with a chelating agent wherein the agent contains at least one nitrogen atom. The chelating agent is a tertiary polyamine or aminoether. The resultant chelate is used for a variety of processes such as separations, catalytic reactions, substitution reactions, reductions, electrochemical reactions, and also as an oil and fuel additive.

Abstract: Novel heterogeneous silylhydrocarbyl phosphine transition metal complex catalysts and intermediates therefor are prepared by (a) the selective monoaddition of silane having chlorine, alkoxy or acyloxy groups to an .alpha.,.omega.-diene, (b) followed by the addition of a phosphine to the resulting .omega.-alkenyl silanes to form the corresponding silylalkyl phosphines, (c) which are then covalently anchored as such or in the form of their transition metal complexes via condensation of their reactive silane substituents with hydroxy groups of silica and metal oxides, (d) optionally followed by complexing the free phosphine groups of anchored silylalkyl phosphines with transition metal compounds.

Abstract: This invention relates to a class of heterogeneous catalysts. More particularly, it pertains to catalysts consisting of group VIII metals dispersed on oxide carriers selected from the group consisting of Ti, V, Nb and Ta and mixtures thereof, and zirconium titanate and BaTiO.sub.3, it having been discovered that these oxide carriers are capable of exerting remarkable effects on the properties of the Group VIII metals so dispersed. Among the strong effects on the properties of supported Group VIII metals which these carriers have been observed to bring about are the suppression of the capacity of the Group VIII metals to chemisorb hydrogen at room temperature, the suppression of the capacity of the Group VIII metals to chemisorb carbon monoxide at room temperature and profound alterations in the activity and/or selectivity of various Group VIII metals in reactions such as the dehydrocyclization of n-heptane and the hydrogenolysis of ethane.These catalyst compositions which exhibit suppression of H.sub.

Abstract: This invention relates to the use of chelated sodium hydridoaluminates or hydridoborates in hydride reductions of inorganic substrates. Novel or improved reductions are obtained at increased rates or selectivities in hydrocarbon media to recover metals.

Abstract: A method of preparation and application of a composition comprising specified microorganisms in combination with surfactants for a synergistic dispersal of oil slicks.