Abstract: Presently disclosed are high purity unsaturated fatty acid esters with an ester moiety characterized by having from five to seven members in a ring structure, which esters when epoxidized find particular utility as primary plasticizers in flexible polyvinyl halide applications. Also disclosed are processes for making the high purity esters.

Abstract: The invention is directed to a process to prepare an ethanol-derivate compound or compounds by reacting ethanol in the presence of molecular oxygen and a catalyst comprising a gamma-alumina carrier, metal nano-particles wherein the metal is selected from silver, copper or gold. The invention is also directed to processes to prepare such a catalyst.

Abstract: A method is disclosed of coupling and integrating natural gas recovery and separation along with chemical conversion. The method can comprise extracting at least one natural gas component. Non-limiting examples of the extracted component include ethane, propane, butanes, and pentanes. The method can also comprise contacting a natural gas stream with a catalyst under conditions that selectively convert at least one component into at least one product, such as ethylene, acetic acid, polyethylene, vinyl acetate, ethylene vinyl acetate, ethylene oxide, ethylene glycol, and their derivatives, propylene, polypropylene, propylene oxide, propylene glycol, acrylates, acrolein, acrylic acid, butenes, butadiene, methacrolein, methacrylic acid, methacrylates, and their derivatives, which can then be separated from the remaining components.

Abstract: Process for preparing glycidyl esters, wherein carbonate esters of the formula I are reacted in the presence of a homogeneous catalyst with elimination of carbon dioxide to form glycidyl esters of the formula II where R in the above formulae is an organic radical having from 1 to 20 carbon atoms.

Abstract: A process for the preparation of an organic reactive intermediate that contains a combination of epoxy groups, hydroxy groups and unsaturated groups wherein the process can be utilized to control the amounts of each of the functional groups in the final product. The reactive intermediates are prepared from natural triglyceride plant and animal oils containing unsaturation.

Abstract: The present invention relates to a process for producing hydrocarbons from methane, which comprises, in a first stage (i), reacting methane to form ethylene and, in a later stage (ii), reacting the product mixture obtained in stage (i) which comprises ethylene and methane to give higher-value hydrocarbons. In addition, the present invention relates to a plant for producing hydrocarbons from methane in which, in a single plant strand, a plurality of plant units are arranged successively in series comprising: a first reactor A for carrying out a conversion from methane to ethylene a second reactor B for carrying out a conversion from ethylene to higher-value hydrocarbons.

Abstract: A process for preparing epichlorohydrin includes chlorinating glycerol with gaseous hydrogen chloride in a bubble column, by supplying hydrogen chloride, glycerol and a mixture of monochloropropanediol and residues of glycerol recycled from the distillation units connected downstream of the bubble column, dichloropropanol and residues to the bottom of the bubble column, and, close to the top of the bubble column, drawing off the mixture of monochloropropanediol, dichloropropanol, water, residues of glycerol and residues formed there and feeding it to at least one distillation unit, after which the dichloropropanol and water distilled off there are hydrolyzed with sodium hydroxide solution. Unconverted hydrogen chloride drawn off from the top of the bubble column is absorbed with freshly supplied glycerol in a scrubber, and this hydrogen chloride-containing glycerol is supplied at the bottom of the bubble column. Preference is given to increasing the conversion rate by using oxalic acid as a catalyst.

Abstract: Process for preparing a chlorohydrin, wherein a polyhydroxylated aliphatic hydrocarbon whose total metal content, expressed in elemental form, is greater than or equal to 0.1 ?g/kg and less than or equal to 1000 mg/kg is reacted with a chlorinating agent.

Abstract: The present invention provides a novel method for producing hexafluoropropylene oxide, which can attain a high HFPO selectivity without using a phase transfer catalyst. Hexafluoropropylene (HFP), a water-soluble and aprotic organic solvent, and an aqueous solution of an oxidizing agent are introduced into a small space, thereby bringing into contact with each other and reacting hexafluoropropylene with the oxidizing agent to obtain hexafluoropropylene oxide (HFPO).

Abstract: Process for producing a chlorohydrin by reaction between a multihydroxylated-aliphatic hydrocarbon, an ester of a multihydroxylated-aliphatic hydrocarbon, or a mixture thereof, and a chlorinating agent, according to which the multihydroxylated-aliphatic hydrocarbon, the ester of a multihydroxylated-aliphatic hydrocarbon, or the mixture thereof used contains at least one solid or dissolved metal salt, the process comprising a separation operation to remove at least part of the metal salt.

Abstract: The present invention relates to a process for producing polyhydroxyalkanoate oligomers and/or polymers of reduced molecular weight, which comprises reacting at least one polyhydroxyalkanoate (PHA) with at least one carbonate salt at a temperature of from 50° C. to 300° C., preferably from 120° C. to 200° C. The above reaction allows a controlled degradation of the PHA chains which yields oligomers and/or polymers having a controlled molecular weight, which can be modulated in view of the specific application for which the oligomers and/or polymers are intended. Moreover, during the reaction carbon dioxide evolves which produces a foamed material which can be easily processed on an industrial scale.

Abstract: A process for producing an epoxide such as a cycloaliphatic diepoxide by the reaction of an olefin such as a cycloaliphatic diene with hydrogen peroxide (H2O2) as an oxidant in the presence of a catalytic system under pH control for example at a pH of less than about 5. The present invention is advantageously used for the epoxidation of olefinic compounds such as olefins and aliphatic or aromatic dienes.

Abstract: Process for manufacturing a chemical: chlorohydrins, epoxides, diols, diols derivatives, epoxy derivatives or mixtures thereof, in an industrial plant, comprising a step of chemical reaction for manufacturing the chemical and at least one step selected from the group consisting of storage, supply, removal, transfer, chemical treatment and physical treatment of compounds used or produced in such process, in which at least one aqueous effluent is generated, this aqueous effluent containing at least one of overhead waters, surface waters, ground waters, waters from drinking water distribution networks, waters from industrial water distribution networks, plant cleaning waters, or waters used for heating and cooling the plant, this aqueous effluent containing at least one compound other than water and exhibiting at least one of the following features, a water solubility at 25° C. greater than or equal to 0.01 g/kg of water and a boiling point at 1013 mbar, greater than or equal to ?100° C.

Abstract: An economical one-step process is provided for the preparation of epoxides by oxidation of olefins in a homogeneous gas phase reaction, wherein the olefin is reacted in a flow reactor with a gas mixture of ozone and NO2 and/or NO as oxidants without use of a catalyst, and wherein ozone and NO2 and/or NO are mixed in a mixing chamber connected upstream to the flow reactor. The process is characterized in that the olefin in the reaction zone of the flow reactor is reacted at a reaction temperature of approximately 150° C. to approximately 450° C. and a pressure of 250 mbar to 10 bar with the gas mixture of the oxidant, that the carrier gas flow containing the olefin is heated in a preheating zone of the flow reactor to a temperature of 250° C. to 650° C.

Abstract: A process for stereoselective synthesis of a compound of Formula (X) or Formula (X?) wherein: R1 is an aryl group substituted with one to three substituent groups, wherein each substituent group of R1 is independently C1-C5 alkyl, C2-C5 alkenyl, C2-C5 alkynyl, C1-C5 alkoxy, C1-C5 alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, C1-C5 alkoxycarbonylamino, aminosulfonyl, C1-C5 alkylaminosulfonyl, C1-C5 dialkylaminosulfonyl, halogen, hydroxy, carboxy, cyano, trifluoromethyl, trifluoromethoxy, nitro, or C1-C5 alkylthio wherein the sulfur atom is oxidized to sulfoxide or sulfone, and R2 and R3 are each independently hydrogen or C1-C5 alkyl.

Abstract: A process for the preparation of a catalyst for the use in a hydrocarbon conversion reaction, said catalyst containing a titanium zeolite and carbonaceous material, the catalyst containing said carbonaceous material in an amount of from 0.01 to 0.5% by weight based on the total weight of titanium zeolite contained in the catalyst, the process comprising (i) preparing a catalyst containing the titanium zeolite and (ii) depositing carbonaceous material on the catalyst according to (i) in an amount of from 0.01 to 0.5% by weight based on the total weight of titanium zeolite contained in the catalyst by contacting said catalyst, prior to using the catalyst in said hydrocarbon conversion reaction, with a fluid containing at least one hydrocarbon in an inert atmosphere, to obtain the carbonaceous material containing catalyst, wherein in (ii), the catalyst is not contacted with an oxygen containing gas.

Abstract: A tetradendate amide based macrocyclic ligand and its Fe(III) complex which act as activators of hydrogen peroxide. The synthetic methodology to develop the ligands is new, simple and provides better yield for each step of the ligand synthesis. The Fe(III)-complexes and hydrogen peroxide together are can perform several environmentally benign oxidation reactions. Organic dye bleaching, bleaching of pulp and paper effluent and N-oxide synthesis may be performed using the newly developed catalyst and hydrogen peroxide. Alcohol oxidation and alkene epoxidation may also be performed using the catalysts and hydrogen peroxide.

Abstract: Compounds, compositions, systems and methods for the chemical and electrochemical modification of the electronic structure of graphene and especially epitaxial graphene (EG) are presented. Beneficially, such systems and methods allow the large-scale fabrication of electronic EG devices. Vigorous oxidative conditions may allow substantially complete removal of the EG carbon atoms and the generation of insulating regions; such processing is equivalent to that which is currently used in the semiconductor industry to lithographically etch or oxidize silicon and thereby define the physical features and electronic structure of the devices. However graphene offers an excellent opportunity for controlled modification of the hybridization of the carbon atoms from sp2 to sp3 states by chemical addition of organic functional groups.

Abstract: Process for preparing a chlorohydrin, comprising the following steps: (a) a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture thereof whose alkali metal and/or alkaline earth metal content is less than or equal to 5 g/kg, a chlorinating agent and an organic acid are reacted so as to give a mixture containing at least chlorohydrin and by-products (b) at least part of the mixture obtained in step (a) is subjected to one or more treatments in steps subsequent to step (a) (c) at least one of the steps subsequent to step (a) consists in oxidation at a temperature greater than or equal to 800° C.

Abstract: Process for preparing glycidyl esters, wherein carbonate esters of the formula I are reacted in the presence of a homogeneous catalyst with elimination of carbon dioxide to form glycidyl esters of the formula II where R in the above formulae is an organic radical having from 1 to 20 carbon atoms.

Abstract: Process for preparing a chlorohydrin, comprising the following steps: (a) a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture thereof is reacted with a chlorinating agent and an organic acid so as to give a mixture containing the chlorohydrin and esters of the chlorohydrin (b) at least part of the mixture obtained in step (a) is subjected to one or more treatments in steps subsequent to step (a) (c) polyhydroxylated aliphatic hydrocarbon is added to at least one of the steps subsequent to step (a), so as to react, at a temperature greater than or equal to 20° C., with the esters of the chlorohydrin, so as to form, at least partly, esters of the polyhydroxylated aliphatic hydrocarbon.

Abstract: The present invention relates to a process for producing glycidol from glycerol carbonate as a raw material with a high yield. The process for producing glycidol according to the present invention includes the steps of (1) reducing a content of a salt having a weak acidity in glycerol carbonate to 1500 ppm by mass or less; and (2) obtaining the glycidol from the glycerol carbonate.

Abstract: Apparatus, methods, and processes are provided for a tube reactor including multiple, substantially parallel reaction tubes arranged within a tube reactor shell, the reaction tubes spaced apart such that a thermal fluid can flow between the tubes and transfer heat between the tubes and the thermal fluid during operation; an inlet head defining an inlet head space, where the inlet head space is in fluid communication with an inlet end of the reaction tubes, and an outlet head including an outlet head shell and at least one insert positioned within an outlet head space defined by the outlet head, where the insert defines a reduced volume outlet head space relative to that defined by the outlet head, and where the reduced volume outlet head space is in fluid communication with an outlet end of the reaction tubes and in fluid communication with a reactor outlet.

Abstract: A synthesis of an energetic prepolymer used as a high-energy binder for an insensitive and high performance explosive is disclosed. More specifically, provided are a novel compound 2-nitratoethyl oxirane expressed by formula III, a novel compound poly(2-nitratoethyl oxirane) expressed by formula IV, obtained by polymerization of 2-nitratoethyl oxirane used as a monomer and a preparation method thereof. The compound, used as an energetic prepolymer and a monomer for preparation thereof can substitute for existing poly(glycidyl nitrate) (PGN) which has been known to be a promising one having the best performance among existing energetic prepolymers, but which has a problem to be self-decomposed after synthesis of polyurethane elastomer, to solve this problem.

Abstract: A production method of propylene oxide, wherein hydrogen, oxygen and propylene are reacted by a multistep process in a mixed solvent of acetonitrile and water, in the presence of a layered precursor of Ti-MWW and a catalyst comprising palladium supported on a carrier.

Abstract: The present invention relates to a process for producing glycidol from glycerol carbonate by subjecting the glycerol carbonate to decarboxylation reaction in the presence of a solvent containing no active hydrogen. In the process, glycidol can be produced from glycerol carbonate as a raw material of the glycidol with a high selectivity.

Abstract: The present invention relates to a process for producing glycidol from glycerol carbonate by subjecting the glycerol carbonate to decarboxylation reaction in the presence of a solvent containing no active hydrogen. In the process, glycidol can be produced from glycerol carbonate as a raw material of the glycidol with a high selectivity.

Abstract: The present invention relates to a gas-liquid dispersion device which is used in a column wherein a gas-liquid mixed fluid flows upward which comprises a liquid as a continuous phase and a gas as a dispersed phase, characterized in that the gas is dispersed effectively into the liquid, so that a sufficient contact between the gas and the liquid can be attained. The device is characterized in that (A) the plate has at least one hole through which the gas and the liquid pass, (B) one end of the conduit is connected to the hole at a lower surface of the plate so that the conduit extends downward from the plate, (C) at least one passage for the gas is provided through a side surface of the conduit, and (D) at least one passage for the liquid is provided in a lower part of the conduit.

Abstract: The invention relates to a glycerol-based product comprising at least one nitrogen-containing compound and of which the total content of nitrogen-containing compound expressed as elemental nitrogen (N) is less than or equal to 1 g of nitrogen (N)/kg of product, to a process for obtaining glycerol, and to its use in the manufacture of dichloropropanol and of derived products such as epichlorohydrin and products derived from epichlorohydrin.

Abstract: An improved method of operating an alkylene oxide production process to achieve and maintain a desired alkylene oxide production parameter is shown and described. The method comprises adjusting one of an overall catalyst chloriding effectiveness parameter or reaction temperature to obtain the desired alkylene oxide production parameter.

Abstract: In this disclosure, a system is described, comprising a shear device with at least one inlet and at least one outlet and a mixing vessel with at least one inlet and at least one outlet, wherein an inlet of the shear device is in fluid communication with an outlet of the mixing vessel. In certain embodiments, the shear device and the mixing vessel form a loop for fluid communication. Also disclosed herein is a method of high shear oxidation, comprising mixing an oxidant with a substrate to form a substrate-oxidant mixture and applying shear to the substrate-oxidant mixture to form a product. The product includes ethylene oxide, propylene oxide, terephthalic acid, phenol, acrylonitrile, maleic anhydride, phthalic anhydride, nitric acid, caprolactam, oxidized polyethylene, oxidized polypropylene, oxidized polyethylene copolymers, and oxidized polypropylene copolymers. Suitable oxidant includes air, oxygen, ozone, peroxide, organic peroxide, halogen, oxygen-containing gas, and halogen-containing gas.

Abstract: A gas mixer is disclosed which includes a vessel (10) (e.g., pipe) containing a stream (12) of a first hydrocarbon-containing gas. The mixer includes a hollow pipe (14) located internal to the vessel containing a stream of a second gas, e.g., an oxygen-containing gas stream such as a stream of pure oxygen gas or air enriched with oxygen. The internal pipe further includes a mixer tip (30) at the peripheral end thereof. The mixer tip includes a body having an internal passage for conducting the second gas out of the pipe and an opening introducing the second gas stream into the first gas stream in a radial plane at an acute angle relative to the longitudinal axis of the pipe. The pipe further includes a deflector (20) on its external surface in longitudinal alignment with the opening of the mixer tip. The deflector serves to deflect any entrained particles within the first gas stream away from the mixing zone where the two streams mix, minimizing the risk of ignition of the hydrocarbon-containing gas.

Abstract: A device for reacting fluids comprising: a reactor; a first inlet for transporting a first fluid into the reactor; a first tube system contained within the reactor and connected to and communicating with the first inlet for receiving the first fluid from the first inlet, the first tube system comprising at least one first tube in the form of a ring, the at least one first tube comprising outlets for releasing the first fluid into the reactor; a second inlet for transporting a second fluid into the reactor; and a second tube system contained within the reactor and connected to and communicating with the second inlet for receiving the second fluid from the second inlet, the second tube system comprising at least one second tube in the form of a ring, the at least one second tube comprising outlets for releasing the second fluid into the reactor; wherein at least one first tube and at least one second tube are concentric, and the outlets for releasing the first fluid from the at least one first tube and

Abstract: A process and apparatus for recovering dichlorohydrins from a mixture comprising dichlorohydrins, water, one or more compounds selected from esters of dichlorohydrins, monochlorohydrins and/or esters thereof, and multihydroxylated-aliphatic hydrocarbon compounds and/or esters thereof, and optionally one or more substances comprising chlorinating agents, catalysts and/or esters of catalysts while minimizing formation of heavies is disclosed.

Abstract: Process for manufacturing dichloropropanol via reaction between glycerol and/or monochloropropanediol and a chlorinating agent in a reactor which is supplied with one or more liquid streams, in which the sum of the glycerol and monochloropropanediol contents in all the liquid streams introduced into the reactor is less than 50 wt % and in which all the liquid streams introduced into the reactor comprise at least one liquid recycling stream, the recycling stream forming at least 10 wt % of all the liquid streams introduced into the reactor.

Abstract: A process for producing propylene oxide, which comprises: supplying a solution containing a peroxide selected from the group consisting of hydrogen peroxide and organic hydroperoxide having 2 or more of carbon atoms as a raw material and propylene to an epoxidation step to react the peroxide with propylene, and controlling a concentration of methyl hydroperoxide in the solution to be supplied to the epoxidation step.

Abstract: A process for making propylene oxide from propylene is disclosed. The process comprises reacting propylene, oxygen, and hydrogen in the presence of a catalyst and a solvent to produce a reaction mixture comprising propylene oxide. Separation of propylene, oxygen, hydrogen, and propylene oxide from the reaction mixture results in a residual mixture comprising methanol. A portion of the residual mixture is recycled to the reaction. A portion of the residual mixture is distilled to generate a distilled methanol stream, which is recycled to the reaction.

Abstract: The present invention relates to a catalyst system which is a mixture of at least two catalytic species, the first catalytic species being a dehydrogenation catalyst and the second catalytic species being an epoxidation catalyst and comprising silver. The present invention also relates to a process for the production of epoxides, in particular a process for the production of an epoxide from an alkane or a mixture comprising an alkane and an alkene, which process comprises contacting said alkane or mixture comprising said alkane and said alkene and a source of oxygen with such a catalyst system comprising a mixture of at least two catalytic species, the first catalytic species providing dehydrogenation activity and the second catalytic species providing epoxidation activity and comprising silver.

Abstract: Process for manufacturing epichlorohydrin comprising the following steps: a) in a liquid reaction medium, a mixture of 1,3-dichloro-2-propanol and 2,3-dichloro-1-propanol, in which the 1,3-dichloro-2-propanol content is at least 10 wt %, is reacted with at least one basic compound in order to form epichlorohydrin and a salt; and b) at least one part of the liquid reaction medium from step a) is subjected to a settling operation in which at least a first fraction containing most of the epichlorohydrin which was contained in the part of the reaction medium from step a) before the settling operation and a second fraction containing most of the salt which was contained in the part of the reaction medium from step a) before the settling operation are separated.

Abstract: The present invention is related with bioplasticizers or primary oleochemical plasticizers and the improved process for obtaining thereof. It refers primarily to epoxydized oleochemical plasticizers produced from vegetable oils, as substitute of traditional petrochemical plasticizers. The process starts with the epoxydized product of natural oils, such as sunflower, linseed, Jatropha curcas, soybean, etc., which are transesterified with an alcohol such as ethylic or methylic, in the presence of a catalyst such as sodium methoxide or sodium hydroxide in order to produce an alkylic esters mixture of the fatty acids that were present in the oil or oil mixture used as raw material in the epoxydized oil production.

Abstract: The present invention relates to a process for producing glycidol from glycerol carbonate as a raw material with a high yield. The process for producing glycidol according to the present invention includes the steps of (1) reducing a content of a salt having a weak acidity in glycerol carbonate to 1500 ppm by mass or less; and (2) obtaining the glycidol from the glycerol carbonate.

Abstract: Compounds useful as plasticizers and the synthesis thereof are disclosed. In general, the invention includes mixed alkyl/aryl diesters where the aryl and alkyl ester moieties are attached to a cyclic structure at vicinal carbons. The invention also includes synthetic processes of making such compounds.

Abstract: A process for making propylene oxide from propylene is disclosed. The process comprises reacting propylene, oxygen, and hydrogen in the presence of a catalyst, a solvent, and a buffer to produce a reaction mixture comprising propylene oxide. Separation of light components from the reaction mixture gives a heavy residue comprising the buffer. The buffer is precipitated from the heavy residue by a precipitating agent.

Abstract: A reactor system comprising: a reactor vessel, and positioned inside the reactor vessel, an absorbent and a catalyst positioned downstream from the absorbent; a process for reacting a feed; and a process for preparing a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine.

Abstract: The present invention provides a process for producing highly pure fluoro-compounds by making use of N-(2-chloro-1,1,2-trifluoroethyl)diethylamine. The process produces little or no chlorinated by-products.

Abstract: This invention relates to a process for synthesizing Atazanvir, including novel intermediates and novel steps to various intermediates along the synthetic pathway.

Abstract: A novel compound represented by the following formula (1) or a salt thereof: wherein symbol “A” represents a saturated heterocyclic group, a 5-membered heteroaromatic group having two heteroatoms in the ring, a group represented by the formula A1 (R2, R3, and R4 represent hydrogen atom, hydroxyl group, etc.), etc., B represents a group represented by the formula B1 (R11 represents hydrogen atom, hydroxyl group, etc.), etc., R1 represents an alkyl group, and symbol “n” represents an integer of 2 to 6, which has a parathyroid hormone depressing action and showing low toxicity, and a medicament containing the compound or salt thereof as an active ingredient.

Abstract: A catalytically active oxide mixture as well as a process for the production thereof and the use thereof.

Abstract: Process for preparing a chlorohydrin, wherein: (a) a polyhydroxylated aliphatic hydrocarbon, an ester of a polyhydroxylated aliphatic hydrocarbon or a mixture thereof is reacted with a chlorinating agent so as to give a mixture containing chlorohydrin, chlorohydrin esters and water, (b) at least a fraction of the mixture obtained in step (a) is subjected to a distillation and/or stripping treatment so as to give a part concentrated with water, with chlorohydrin and with chlorohydrin esters, (c) at least a fraction of the part obtained in step (b) is subjected to a separating operation in the presence of at least one additive so as to give a portion concentrated with chlorohydrin and with chlorohydrin esters and containing less than 40% by weight of water.

Abstract: The present descriptive report refers to a patent of invention of primary PVC plasticizers composed of epoxidized ethyl and/or isoamyl esters of vegetable oil fatty acids and to the compounds of PVC plasticized with epoxidized bioesters, belonging to the technical field of polymer additives, developed from renewable sources such as vegetable oils and sugar cane, to reduce the cost and improve the properties of PVC compounds. The epoxidized bioesters are suitable to be added to at least one PVC resin and are obtained from a transesterification reaction of at least one type of vegetable oil with ethanol or isoamylic alcohol and subsequent epoxidation, presenting oxirane index equal to or less than 8.