Abstract: A process for producing high octane alkylate is provided. The process involves reacting isobutane and ethylene using an ionic liquid catalyst. Reaction conditions can be chosen to assist in attaining, or to optimize, desirable alkylate yields and/or properties.

Abstract: Techniques are disclosed for increasing the performance of III-N p-channel devices, such as GaN p-channel transistors. Increased performance is obtained by applying compressive strain to the GaN p-channel. Compressive strain is applied to the GaN p-channel by epitaxially growing a source/drain material on or in the GaN. The source/drain material has a larger lattice constant than does the GaN and puts the p-channel under compressive strain. Numerous III-N material systems can be used.

Abstract: The present invention relates to a new process which comprises the steps of hydrotreating, paraffin disproportionation and hydroisomerization to convert biological hydrocarbonaceous oxygenated oils comprising triglycerides into biologically-derived paraffinic jet/diesel fuels, solvents and base oils. A combination of conventional hydrogenation/dehydrogenation catalysts, such as Pt/Al2O3, and conventional olefin metathesis catalysts, such as WO3/SiO2, or inexpensive variations thereof, is generally employed in the paraffin disproportionation step.

Abstract: A molecular sieve material, EMM-17, has in its as-calcined form an X-ray diffraction pattern including the following peaks in Table 11: TABLE 11 d-spacing Relative Intensity (?) [100 × I/I(o)] % 17.4-16.4 1-10 12.6-12.1 1-20 11.8-11.4 60-100 11.2-10.8 5-30 10.7-10.3 30-80? 8.62-8.38 10-40? 6.09-5.96 1-20 5.71-5.61 1-20 4.23-4.17 1-20 4.09-4.03 1-10 3.952-3.901 10-40? 3.857-3.809 5-30 3.751-3.705 1-20 3.727-3.682 1-20 3.689-3.644 1-10 3.547-3.

Abstract: A reverse disproportionation reaction of two hydrocarbon feeds allows production of a reaction mixture containing products with intermediate carbon numbers. The amount of at least one of the products with intermediate carbon numbers is equal to or greater than the amount formed from disproportionation of the hydrocarbon alone. A reverse disproportionation reaction mixture is also described.

Abstract: Processes for the disproportionation and isomerization of a C5 hydrocarbon feed using a liquid catalyst comprising an ionic liquid and a carbocation promoter are described. The ionic liquid is unsupported, and the reactions occur at temperatures below about 200° C.

Abstract: A process of tuning a hydrocarbon product composition is described. The process involves selecting paraffins for reaction. The equilibrium constants for reactions of the selected paraffins can be used to select appropriate feed ratios, or an equilibrium composition as function of C/H molar ratio. A selected feed is reacted to obtain the product. Equilibrium product compositions and non-equilibrium product compositions can be obtained using the process.

Abstract: Processes for the disproportionation and isomerization of a hydrocarbon feed using a liquid catalyst comprising an ionic liquid and a carbocation promoter are described. The ionic liquid is unsupported, and the reactions occur at temperatures below about 200° C.

Abstract: Processes for the disproportionation and isomerization of a C4 hydrocarbon feed using a liquid catalyst comprising an ionic liquid and a carbocation promoter are described. The ionic liquid is unsupported, and the reactions occur at temperatures below about 300° C.

Abstract: Processes for the disproportionation and isomerization of a C7 hydrocarbon feed using a liquid catalyst comprising an ionic liquid and a carbocation promoter are described. The ionic liquid is unsupported, and the reactions occur at temperatures below about 200° C.

Abstract: The disclosure relates to catalytically active carbocatalysts, e.g., a graphene oxide or graphite oxide catalyst suitable for use in a variety of high value chemical transformations.

Abstract: A process for upgrading hydrocarbons comprising removal of C5 hydrocarbons from a feedstock, metathesizing said C5 hydrocarbons to C6+ and C4? hydrocarbons, and upgrading said C4? hydrocarbons is disclosed absent any dehydrogenation.

Abstract: Methods relate to disproportionation of hydrocarbons utilizing a zeolite catalyst. The methods include reacting pentanes in contact with ultrastable zeolite Y having a silica to alumina ratio of less than 80 to disproportionate the pentanes into butanes and hexanes. The ultrastable zeolite Y is defined by having a sodium oxide content of less than 1% by weight.

Abstract: A process for regenerating a spent ionic liquid catalyst including (a) applying a voltage across one or more pairs of electrodes immersed in a spent ionic liquid catalyst comprising conjunct polymer-metal halide complexes to provide freed conjunct polymers and a regenerated ionic liquid catalyst; and (b) separating the freed conjunct polymers from the regenerated ionic liquid catalyst is described. An alkylation process incorporating the regeneration process is also described.

Abstract: A process comprising adjusting a level of conjunct polymers in an ionic liquid catalyst between a low level that favors production of C5+ products boiling at 137.8° C. or below and a higher level that favors production of both C5+ products boiling at 137.8° C. or below and C5+ products boiling above 137.8° C.; wherein the adjusting is done in response to market demand. A process unit, comprising a reactor that operates with an ionic liquid catalyst comprising a low level or a higher level of conjunct polymers, and the alkylation reactor is switched between operating with the low and the higher levels in response to market demand. A process unit, comprising a reactor that operates in an alkylate mode and a distillate mode, and a catalyst regenerator that operates with varying severity to adjust the level of conjunct polymers in response to demand for gasoline or distillate.

Abstract: A process for producing hydrocarbon products, comprising: a) operating a process unit in an alkylate mode wherein greater than 50 wt % of a C5+ hydrocarbon stream from the process unit boils at 137.8° C. or below, b) adjusting one or more process conditions in the process unit, and c) after the adjusting step, operating the process unit in a distillate mode wherein greater than 50 wt % of the C5+ hydrocarbon stream from the process unit boils above 137.8° C. Also, a process unit, comprising: a) an alkylation reactor; and b) a control system that enables the alkylation reactor to be operated in the alkylate mode and in the distillate mode; wherein the alkylation reactor can switch back and forth from operating in the alkylate mode to the distillate mode.

Abstract: A method of converting at least one first alkane to a mixture of at least one low molecular weight alkane (optionally also including additional lower and/or higher molecular weight alkanes) and at least one high molecular weight alkane, comprises: reacting a first alkane in the presence of dual catalyst system comprising a first catalyst (i.e., a hydrogen transfer catalyst) and a second catalyst (i.e., a metathesis catalyst) to produce a mixture of low and high molecular weight alkanes.

Abstract: Methods for producing in a reactor natural gas from heavy hydrocarbons. A mixture of heavy hydrocarbons and a catalyst comprising a transition metal are heated under an anoxic condition in a reactor. Natural gas, e.g., catalytic natural gas, is generated from the heavy hydrocarbons by a disproportionation reaction promoted by the catalyst. The anoxic condition can be created by flowing an anoxic stimulation gas in the reactor.

Abstract: Methods and apparatus for promoting the production of oil and/or gas from organic carbon-rich sedimentary rocks in a subterranean formation. Aspects of the method comprise detecting hydrogen starvation in the formation and remedying the hydrogen starvation.

Abstract: A method for producing a product comprising at least one selected from C2+ hydrocarbons, oxygenates, and combinations thereof from light gas comprising one or more of carbon dioxide, methane, ethane, propane, butane, pentane, and methanol by forming a dispersion of light gas in a liquid feed, wherein the dispersion is formed at least in part with high shear forces and wherein at least one of the liquid feed and the light gas is a hydrogen source. A system for carrying out the method is also presented.

Abstract: The present invention relates to new crystalline molecular sieve SSZ-75 prepared using a tetramethylene-1,4-bis-(N-methylpyrrolidinium) dication as a structure-directing agent, and its use in catalysts for hydrocarbon conversion reactions.

Abstract: A method of converting at least one first alkane to a mixture of at least one low molecular weight alkane (optionally also including additional lower and/or higher molecular weight alkanes) and at least one high molecular weight alkane, comprising: reacting a first alkane in the presence of dual catalyst system comprising a first catalyst (i.e., a hydrogen transfer catalyst and preferably an iridium pincer complex catalyst) and a second catalyst (i.e., a metathesis catalyst) to produce a mixture of low and high molecular weight alkanes.

Abstract: A process for disproportionating isopentane into isomers of hexane and butane that utilizes a fixed bed reactor employing a catalyst composition comprising aluminum halide. The process additionally includes a product separation zone which can be configured to recover and return at least a portion of the isopentane product stream to the inlet of the disproportionation reactor.

Abstract: A porous silicon implant impregnated with a beneficial substance, such as a micromineral required for healthy physiology, is implanted subcutaneously and is entirely corroded away over the following months/year to release the micromineral in a controlled manner. In a second embodiment the implant may have a large number of holes which contain beneficial substance and which are closed by bio-errordable doors of different thickness so as to stagger the release of the beneficial substance over time as the doors are breached.

Abstract: The invention relates to a process for carrying out metathesis reactions, wherein the process is carried out continuously and a ruthenium-containing catalyst is used.

Abstract: A process for the regeneration of spent sulfuric acid including contacting spent sulfuric acid containing acid soluble oils (ASO) with sulfur dioxide to extract at least a portion of the ASO from the spent sulfuric acid into the sulfur dioxide. The sulfuric acid phase having a reduced ASO content and a sulfur dioxide phase containing at least a portion of the ASO may be recovered. The resulting sulfuric acid and sulfur dioxide phases may be further separated to recover ASO, sulfur dioxide, and sulfuric acid.

Abstract: The present invention relates to new crystalline molecular sieve SSZ-75 prepared using a tetramethylene-1,4-bis-(N-methylpyrrolidinium) dication as a structure-directing agent, and its use in catalysts for hydrocarbon conversion reactions.

Abstract: The present invention relates to a process for preparing 2,3-dimethylbutane which comprises contacting in a reaction zone isobutane with a supported catalyst comprising a tungsten hydride and a support comprising an aluminium oxide, so as to form a reaction mixture comprising 2,3-dimethylbutane. The contacting essentially leads to performing a metathesis reaction of the isobutane, with a very high specificity in the formation of 2,3-dimethylbutane. The catalyst is preferably a tungsten hydride grafted onto a support based on aluminium oxide. The support can be chosen from aluminium oxides, mixed aluminium oxides and modified aluminium oxides. The reaction mixture can be isolated and preferably subjected to one or more fractionating operations in order to recover 2,3-dimethylbutane and optionally one or more other components of the reaction mixture, such as C5+ alkanes.

Abstract: Process for the contemporaneous production of fuels and lubricating bases from synthetic paraffinic mixtures, which includes a hydrocracking step in the presence of a solid bi-functional catalyst comprising: (A) a support of an acidic nature consisting of a catalytically active porous solid, including silicon, aluminum, phosphorus and oxygen bonded to one another in such a way as to form a mixed amorphous solid characterized by an Si/Al atomic ratio of between 15 and 250, a P/Al ratio of at least 0.1, but lower than 5, a total pore volume ranging from 0.5 to 2.0 ml/g, with an average pore diameter ranging from 3 nm. to 40 nm, and a specific surface area ranging from 200 to 1000 M2/g; (B) at least one metal with a hydro-dehydrogenating activity selected from groups 6 to 10 of the periodic table of elements, dispersed on said support (A) in an amount of between 0.05 and 5% by weight with respect to the total weight of the catalyst.

Abstract: The present invention provides an improved sulfuric acid catalyzed alkylation process wherein the sulfur content from one or more streams in the alkylation process is recovered by an extraction agent. The extraction agent of the invention comprises ammonia or ammonium hydroxide. Advantageously, the recovered sulfur content is converted to sulfuric acid, such as in a spent acid regeneration (SAR) plant, and recycled to replenish decomposed catalyst in the alkylation process.

Abstract: A catalyst composition includes an oxygen compound of an element selected from Group IVB or Group IVA of the Periodic Table of the Elements; an oxygen compound of an element selected from Group VIB or Group VIA of the Periodic Table of the Elements; and at least about 1% by weight based upon total catalyst weight of fumed silica particles. The catalyst composition is advantageously employed in hydrocarbon conversion processes such as isomerization.

Abstract: The invention relates to a method for producing hydrocarbons having a modified carbon skeleton by reacting aliphatic hydrocarbons a) with themselves, b) with another aliphatic hydrocarbon or c) with aromatic alkyl substituted hydrocarbons, in the presence of a metal organic catalyst or the hybrid thereof, at a temperature of between 20–400° C. and a pressure of between 0.2–100 bars, wherein the reaction takes place in the presence of hydrogen.

Abstract: A novel hydrocarbon disproportionation process is provided and includes contacting a hydrocarbon feed comprising at least one paraffin with a disproportionation catalyst comprising a support component, a metal, and a halogen in a disproportionation reaction zone under disproportionation reaction conditions.

Abstract: Hydrocarbon or oxygenate conversion process in which a feedstock is contacted with a non zeolitic molecular sieve which has been treated to remove most, if not all, of the halogen contained in the catalyst. The halogen may be removed by one of several methods. One method includes heating the catalyst in a low moisture environment, followed by contacting the heated catalyst with air and/or steam. Another method includes steam-treating the catalyst at a temperature from 400° C. to 1000° C. The hydrocarbon or oxygenate conversion processes include the conversion of oxygenates to olefins, the conversion of oxygenates and ammonia to alkylamines, the conversion of oxygenates and aromatic compounds to alkylated aromatic compounds, cracking and dewaxing.

Abstract: A catalyst and process is disclosed to selectively upgrade a paraffinic feedstock to obtain an isoparaffin-rich product for blending into gasoline. The catalyst comprises a support of a sulfated oxide or hydroxide of a Group IVB (IUPAC 4) metal, a first component comprising at least one Group III A (IUPAC 13) component, and at least one platinum-group metal component which is preferably platinum.

Abstract: A catalyst and process is disclosed to selectively upgrade a paraffinic feedstock to obtain an isoparaffin-rich product for blending into gasoline. The catalyst comprises a support of a tungstated oxide or hydroxide of a Group IVB (IUPAC 4) metal, a first component of at least one lanthanide element, yttrium or mixtures thereof, which is preferably ytterbium or holmium, and at least one platinum-group metal component which is preferably platinum.

Abstract: A novel hydrocarbon disproportionation process is provided and includes contacting a hydrocarbon feed comprising at least one paraffin with a disproportionation catalyst comprising a support component, a metal, and a halogen in a disproportionation reaction zone under disproportionation reaction conditions.

Abstract: The present invention relates to a process for manufacturing alkanes, comprising, as main stage, a reaction resulting from bringing methane into contact with at least one other starting alkane (A) in the presence of a catalyst based on a metal M capable of catalyzing a metathesis of alkanes. The reaction results in the formation of at least one or two final alkanes (B) having a number of carbon atoms less than or equal to that of the starting alkane (A) and at least equal to 2. Preferably the catalyst comprises a hydride of a metal M grafted to and dispersed over a solid support. The metal M may be chosen from transition metals, lanthanides and actinides. The present invention also relates to the use of a catalyst capable of catalyzing a metathesis of alkanes in 3 reaction resulting from bringing methane into contact with at least one other starting alkane (A).

Abstract: The invention relates to a method for producing hydrocarbons having a modified carbon skeleton by reacting aliphatic hydrocarbons a) with themselves, b) with another aliphatic hydrocarbon or c) with aromatic alkyl substituted hydrocarbons, in the presence of a metal organic catalyst or the hybrid thereof, at a temperature of between 20-400° C. and a pressure of between 0.2-100 bars, wherein the reaction takes place in the presence of hydrogen.

Abstract: The present invention relates to new mesoporous inorganic solids in the form of primary and/or secondary inorganic particles of D10≧1 &mgr;m and D50≧3 &mgr;m, preferably from D10≧2 &mgr;m and D50≧10 &mgr;m the size of which can go up to 10 mm, wherein the microporous volume (pores of size less than or equal to 2 &mgr;m) represents at most 10% of the total porous volume up to 300 nm.

Abstract: A process of contacting at least one feed hydrocarbon, containing three to about seven carbon atoms per molecule, and ethylene in a hydrocarbon-containing fluid in the presence of a catalyst composition to provide at least one product hydrocarbon isomer containing about four to about nine carbon atoms per molecule is provided. The at least one feed hydrocarbon can be selected from paraffins, isoparaffins, and the like and combinations thereof. The catalyst composition contains a hydrogen halide component, a sulfone component, and a metal halide component.

Abstract: A process for disproportionating isoparaffins and paraffins in the presence of at least one initiator is disclosed. The product from the disproportionation contains a gasoline range material having a higher octane-rating than the isoparaffins and paraffins in the feed and a diesel range material having a higher cetane number than the isoparaffins and paraffins in the feed.

Abstract: A process for preparing a C4- product stream and a C6+ product stream is disclosed. The process involves contacting a C5 containing paraffinic feedstock with a catalyst that includes a hydrogenation/dehydrogenation catalyst and an olefin metathesis catalyst under conditions which dehydrogenate the paraffins to olefins. The olefins are then metathesized and rehydrogenated to provide a product stream. A C4- fraction and a C6+ fraction can each be isolated from the product stream. The C4- fraction can be used, for example, in an alkylation reaction to provide compounds useful in gasoline compositions. Unconverted C5 paraffins can be recycled. The C6+ fraction can be used, for example, as solvents. Alternatively, they can be isomerized to form gasoline additives, or can be converted to aromatic compounds via reforming, for example, using conventional reforming techniques, preferably using the AROMAX™ process or traditional rheniforming conditions.

Abstract: A process for the manufacture of alkanes comprising a cross-metathesis reaction between at least one starting alkane (A) and one organometallic compound (B) fixed to an inorganic support and comprising a metal bonded to at least one hydrocarbon-comprising radical. The reaction leads to the formation of at least one other alkane (C) which is a higher or lower homologue of the starting alkane (A), by cleavage of the hydrocarbon-comprising radical with the metal of the organometallic compound (B) and recombination of the radical with at least one other radical originating from a cleavage of the starting alkane (A). The metal of the compound (B) preferably is selected from transition metals, lanthanides and actinides, and the hydrocarbon-comprising radical of the compound (B) preferably is selected from alkyl, alkylidene and alkylidyne radicals.

Abstract: A novel i-pentane disproportionation process is provided and includes contacting i-pentane with an acidic disproportionation catalyst in the presence of a lower paraffin co-feed and, optionally, in the presence of an initiator.

Abstract: A process for partially converting well gas to saleable products on site by disproportionation of the alkanes in the well gas into higher and lower molecular weight alkanes.

Abstract: A process for the disproportionation of pentane to alkanes containing fewer carbon atoms per molecule and alkanes containing more atoms per molecule in the presence of a catalyst composition containing hydrogen fluoride (HF), titanium tetrafluoride (TiF4) and sulfolane.

Abstract: A process for the metathesis of linear or branched starting alkanes involves, first, grafting metal atoms in the form of hydrides to a solid oxide, such that the grafted metal atoms are dispersed over the solid oxide, which effects a solid catalyst, and second, reacting the starting alkanes over the solid catalyst.

Abstract: Salable hydrocarbon products prepared by reacting a light hydrocarbon gaseous stream with a gaseous oxidant to produce carbon oxides and hydrogen, which is contacted in a hydrocarbon synthesis zone to produce a product stream comprising salable hydrocarbon products. That product stream is separated into a gaseous fraction and at least one fraction of salable hydrocarbon products. The light hydrocarbon gaseous stream is formed by separating a light hydrocarbon gaseous feed comprising alkanes into a lighter fraction and a heavier fraction and contacting that heavier fraction in a disproportionation zone to convert a significant portion of the alkanes in the heavier fraction by disproportionation into both higher and lower alkanes, then at least part of the lighter fraction and the lower alkanes form the light hydrocarbon gaseous stream.

Abstract: Hydrocarbon conversion processes using a new family of crystalline manganese phosphate compositions is disclosed. These compositions have an extended network; which network can be a one-, two-, or three-dimensional network. The composition has an empirical formula of:(A.sup.a+).sub.v (Mn.sup.b+)(M.sup.c+).sub.x P.sub.y O.sub.zwhere A is a templating agent such as an alkali metal, M is a metal such as Al, Fe.sup.3+ and "b" is the average manganese oxidation state and varies from greater than 3.0 to about 4.0.