1067results about "Preparation by oxidation reactions" patented technology

The present invention relates to a method of producing methanol from a methane source by oxidizing methane under conditions sufficient to a mixture of methanol and formaldehyde while minimizing the formation of formic acid and carbon dioxide. The oxidation step is followed by treatment step in which formaldehyde is converted into methanol and formic acid which itself can further be converted into methanol via catalytic hydrogenation of intermediately formed methyl formate.

The invention discloses a method of converting carbon dioxide to methanol and / or dimethyl ether using any methane source or natural gas consisting of a combination of steam and dry reforming, in a specific ratio to produce a 2:1 molar ratio of hydrogen and carbon monoxide with subsequent conversion of the CO and H2 mixture exclusively to methanol and / or dimethyl ether. This method is termed the BI-REFORMING™ process. Dehydrating formed methanol allows producing dimethyl ether (DME) using any suitable catalytic method, including use of solid acid catalysts. When recycling formed water into the bi-reforming step the conversion of carbon dioxide with methane produces exclusively dimethyl ether without any by-product formation and complete utilization of hydrogen

A reaction product and an imide compound can be separated from a reaction mixture obtained by reacting a substrate in the presence of the imide compound having an imide unit represented by the following formula (1): wherein X represents an oxygen atom, a hydroxyl group or an acyloxy group by (A1) a solvent-crystallization step for crystallizing the imide compound with at least one solvent selected from the group consisting of a hydrocarbon, a chain ether and water, (A2) a cooling-crystallization step for crystallizing the reaction product by cooling, or (B) an extraction step for distributing the reaction product into a phase of a water-insoluble solvent and the imide compound into a phase of an aqueous solvent, respectively by using the aqueous solvent containing at least water and the water-insoluble solvent separable from the aqueous solvent. Further, the imide compound and the metal catalyst can be separated from a mixture containing the imide compound and the metal catalyst by (C) a solvent-crystallization step for crystallizing the imide compound by using a solvent for crystallization, (D) an absorption step for absorbing the metal catalyst by an absorption treatment, or (E) an extraction step for distributing the imide compound into a phase of a water-insoluble solvent and the metal catalyst into a phase of an aqueous solvent, respectively by using the aqueous solvent containing at least water and the water-insoluble solvent separable from the aqueous solvent.

The invention relates to a new process in which under the catalytic action of metal porphyrin the cyclohexane can be selectively oxdated by air and made into cyclohexanol and cyclohexanone. Under the condition of 2-10 atm air, reaction temp. is 125-150 deg.C, it selects and uses micro-oxo double metal porphyrin and single metal porphyrin or their solid carrier as main catalyst, and uses transition metal salt or oxide as co-catalyst, the metal porphyrin can high-effectively and high-selectively catalyze oxidation of cyclohexane by using air in the biological concentratino as biological enzyme. The dose of metal porphyrin is small and said metal porphyrin can be repeatedly used, and said catalyst dose also is small, its catalystic effect is good, said catalyst can be used for making homogeneous catalysis, and after it is solid-carried, it also can be used for making heterogeneous catalysis.

The invention belongs to the technical field of catalysis and relates to a method for preparing a monatomic cobalt catalyst by roasting silicon dioxide pellets and immobilizing metalloporphyrin. The method is realized by adopting the following technical scheme: namely stirring and dispersing nano silicon dioxide particles, dropwise adding 3-aminopropyl triethoxy silane, so as to obtain amino modified SiO2 pellets, then linking monocarboxyl metalloporphyrin (CoTPCPP) onto an amino modified SiO2 carrier through organic complexing, carbonizing porphyrin through high-temperature calcination in an inert atmosphere, and loading highly dispersed cobalt atoms onto the amino modified SiO2 pellets, thus an amino modified silicon dioxide pellet loaded monatomic cobalt catalyst is obtained. The monatomic dispersion catalyst has high catalytic activity and stability on a molecular oxygen selective ethylbenzene catalytic oxidation reaction in absence of solvent; meanwhile, a preparation method is simple, and product quality can be easily controlled, so that the monatomic dispersion catalyst is applicable to the fields of alkane selective oxidation reactions and synthesis of medical intermediates.

Multiphasic reactions, especially those reactions using a phase transfer catalyst, are conducted in microchannel apparatus. Advantageously, these reactions can be conducted with two, planar microlayers of reactants in adjacent laminar flow streams. Microchannel apparatus and methods for conducting unit operations such as reactions and separations in microchannel apparatus is also described. Microchannel apparatus can provide advantages for controlling reactions and separating products, solvents or reactants in multiphase reactions.

In the presence of an imide compound (e.g., N-hydroxyphthalimide) shown by the formula (2):wherein R1 and R2 independently represents a hydrogen atom, a halogen atom, an alkyl group, an aryl group, a cycloalkyl group; or R1 and R2 may bond together to form a double bond or an aromatic or non-aromatic ring; Y is O or OH and n=1 to 3;or the imide compound and a co-catalyst (e.g., a transition metal compound), an adamantane derivative having a functional group such as a nitro group, an amino group, a hydroxyl group, a carboxyl group, a hydroxymethyl group and an isocyanato group is oxidized with oxygen. According to the above method, an adamantane derivative having a hydroxyl group together with a functional group such as a nitro group, an amino group, a hydroxyl group, a carboxyl group, a hydroxymethyl group and an isocyanato group is efficiently obtained.

The invention relates to regenerative, solid sorbents for adsorbing carbon dioxide from a gas mixture, including air, with the sorbent including a modified polyamine and a solid support. The modified polyamine is the reaction product of an amine and an epoxide. The sorbent provides structural integrity, as well as high selectivity and increased capacity for efficiently capturing carbon dioxide from gas mixtures, including the air. The sorbent is regenerative, and can be used through multiple cycles of adsorption-desorption.

The invention discloses a catalyst for preparing methane by low-temperature oxidization of methane and a preparation method and application thereof. The catalyst consists of a molecular sieve carrier and an active ingredient supported on the carrier; and the active ingredient comprises copper oxide or copper oxide and noble metal compound active ingredient, wherein the mass ratio of the molecular sieve to the copper in the copper oxide to the noble metal is 100:1-5:0-1. The molecular sieve serves as the carrier, and the preparation method for the catalyst comprises the following steps of: mixing a precursor copper acetate of the basic active ingredient or / and a metal precursor of the noble metal active ingredient in a certain ratio to prepare solution; and soaking the molecular sieve in the solution to allow the metals of the active ingredient to be supported on the carrier, and washing, drying and baking to prepare the catalyst. The catalyst can catalyze the methane oxidation at low temperature to prepare the methanol; a catalytic reaction system is simple; and the yield and selectivity of the target product methanol are high.

A process is disclosed for the preparation of zinc alkyl chain growth products via a catalysed chain growth reaction of an alpha-olefin on a zinc alkyl, wherein the chain growth catalyst system employs a group 3-10 transition metal, or a group 3 main group metal, or a lanthanide or actinide complex, and optionally a suitable activator. The products can be further converted into alpha-olefins by olefin displacement of the grown alkyls as alpha-olefins from the zinc alkyl chain growth product, or into primary alcohols, by oxidation of the resulting zinc alkyl chain growth product to form alkoxide compounds, followed by hydrolysis of the alkoxides.

Organic molecules are partially oxidized in that the gas phase on supported and immobilized photocatalysts deposited having a nanostructure. the photocatalysts are semiconductors such as titanium dioxide and are preferentially coated onto a substrate by flame aerosol coating.

A catalyst of synthesizing benzaldehyde and benzyl alcohol by methylbenzene, its manufacturing method and application. The active component is zirconium, or transit metals, alkaline metal, alkaline-earth metals, metals of IIIAíóIVA and VA Group in the Periodic Table. The method comprises solving a zirconium compound or a zirconium compound and a compound of an element as the active component, adding a precipitator; drying, burning, pulverizing to particles. In reactions, a gas containing oxygen is the oxygen source, such as oxygen and air, an organic solution wouldn't be used. The catalyzing reaction is 180-195 degree C, the pressure is 0.8-1.2Mpa. when the conversion rate of methylbenzene is 13.0úÑ, the total selectivity of benzaldehyde and benzyl alcohol is 86.6úÑ. In the method, the catalyst is easy to be separated and could be recyclable, the reaction condition is mild.

The new process of synthesizing acetic acid with methane consists of two reaction steps, including the first step of reacting methane, oxygen and hydrogen bromide or hydrobromic acid on catalyst to produce CH3Br, CO and H2O; and the second step of reacting CH3Br, CO and H2O on catalyst to prepare acetic acid. During the reaction of synthesizing methanol and dimethyl ether, the first step of oxybromizing reaction may have the reacting gas composition regulated and different catalyst adopted to reach the aim of creating CH3Br and H2O in high selectivity; and methanol and dimethyl ether may be then produced through hydrolysis on one other kind of catalyst. In the process of preparing acetic acid or methanol and dimethyl ether, HBr as the circular reaction medium is regenerated and returned to the reactor for reuse.

The invention discloses a preparation method and an application of a load type nano-gold catalyst. The preparation method comprises the following steps of: (1) adding 2.0g of halloysite nanotube carrier, 2.05 to 6.15mL of chlorogold acid solution with a concentration of 10g / L and 40 to 120mL of deionized water to a 250mL flask with three necks; (2) putting the flask into an oil bath with the temperature of 60 DEG C; adjusting the pH of the solution to 8 to 12 by using 4.0M ammonia water; then carrying out stirring reflux at 95 DEG C-105 DEG C for 1 hour; filtering; rinsing for 5 minutes by using 10 to 20mL of 4.0M ammonia water; washing twice with 15 to 20mL of hot water; drying for 1 to 2 hours at 100 DEG C; and finally roasting for 3 to 4 hours in air at 300 DEG C to obtain the load type nano-gold catalyst. The invention has the advantages of simple and convenient preparation method, uniformly dispersed gold particles and high loading efficiency. The catalyst provided by the invention can be used for cyclohexene oxidation of cyclonene and cyclohexenol, with the advantages of mild reaction condition, good activity and selectivity and less catalyst utilization quantity.

Methanol is produced as a storable and transportable carbon-based energy carrier using at least two different methods. To produce a first methanol portion, water is electrolyzed, preferably using energy from renewable energy sources such as solar or wind power, to produce hydrogen. The hydrogen is then reacted with carbon dioxide to produce the first methanol portion. To produce a second methanol portion, methane is reacted with oxygen. A controller can advantageously be used to control the amount of chemicals in each reaction.

The present invention is a method for oxyfunctionalizing, that is, introducing oxygen functionality to, a polyolefin such as polypropylene and poly(ethylene-alt-propylene). The polyolefin is contacted with an oxygen source such as a persulfate and catalytic amounts of a metal porphyrin complex under mild conditions to yield an oxyfunctionalized polymer that has a polydispersity that is very similar to that of the starting polymer.

The invention discloses a metal organic framework material of a Fe porphyrin ligand, a preparation method therefor and an application thereof, and belongs to the technical field of crystalline materials. A chemical formula of the Fe porphyrin ligand is FeL, wherein L is am organic ligand, namely 5, 15-bipyridine-10 and 20-dicarboxyphenyl ironporphyrin. In a closing condition, a crystal of the metal organic framework material is obtained by the organic ligand, namely 5, 15-bipyridine-10, 20-dicarboxyphenyl ironporphyrin and iron nitrate nonahydrate by virtue of thermal reaction in a solution of N,N-dimethylformamide and acetic acid. The metal organic framework material has an iron porphyrin catalytic property, and can be used for selective catalysis of cycloalkane.

The present invention discloses a supported gold nano-particles catalyst and the preparation method of the same, which comprises Au, Ce, Zr, Al and Si; wherein Au is the main active component and has a mass percent of 0.1~4.0%; Ce and Zr are the assistant active component and has a mass percent of 3~57%, wherein the mol ratio of Ce to Zr is 1~10; Al and Si are the carrier and has a mass percent of 40~97%. The catalyst is prepared by a sequential immersion method, wherein the alumina or silicon oxide carrier is firstly impregnated by an aqueous liquid containing cerous nitrate and zirconium nitrate and then the gold component is impregnated. The present invention has the advantages of that: the preparation method is simple, the stability is excellent and the cost is low. For the reaction of preparing cyclohexanone and cyclohexanol by cyclohexane oxygenation, the catalyst of the present invention can obtain high ketone alcohol selectivity even under the condition of a high conversion, besides the peroxide content in the product is very low. For example, when the conversion of cyclohexane is 12.8%, the ketone alcohol selectivity is up to 92.6% and the peroxide content is only 0.7%.

A method for forming propylene wherein ethylene is employed as a primary feed material in a combination of steps comprising dehydration, skeletal isomerization, and metathesis to form a versatile product mix that can contain one or more of propylene, gasoline, MTBE, and propylene oxide.

LDH-osmate of the formula [MII(1-x)MIIIx(OH)2][OsO42-]x / 2.zH2O wherein MII is a divalent cation selected from the group consisting of Mg2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+ and Ca2+ and MIII is a trivalent ion selected from the group consisting of Al3+, Cr3+, Mn3+, Fe3+ and Co3+, and x is the mole fraction having integral value ranging from 0.2 to 0.33, and z is the number of water molecules and ranges from 1 to 4, useful as, a catalyst, and a process for the preparation thereof and use thereof to manufacture vicinal diols.

Production of methanol includes supplying into a reactor a hydrocarbon-containing gas, supplying into the reactor an oxygen-containing as gas, carrying out in the reactor an oxidation of the heated hydrocarbon-containing gas by oxygen of the oxygen-containing gas, and supplying into the reactor a cold hydrocarbon-containing gas to be mixed directly with a mixture of the heated hydrocarbon-containing gas and the oxygen-containing gas at a later stage of the reaction to produce also formaldehyde.

The invention belongs to the chemical field of nano materials, and in particular relates to a graphene loaded metal nano composite material, and a preparation method and application thereof. The invention discloses the graphene loaded metal nano composite material. Under the dispersion and bearing action of graphene, the composite material can be uniformly distributed; the size of the composite material is about 10-100nm. The composite material mainly consists of graphite and simple metal inorganic salt which serve as raw materials, water serving as a solvent, hydrazine hydrate serving as a reducing agent and a proper amount of a surfactant, and is reacted to obtain graphene loaded metal nano particles. The graphene loaded metal nano composite material has the advantages of low cost, high efficiency, energy conservation and the like, and embodiments excellent catalysis activity in benzyl oxidization, so that a low-cost, environment-friendly and high-efficiency nano composite material catalyst is supplied to industrial production.

A process for selectively oxidizing alkyl cyclohexane by air under the catalysis of mu-oxygen bimetal porphyrin, single-metal porphyrin, or their solid carried substance to become alkyl cyclohexanol and alkyl cyclohexanone is disclosed. Said alkyl cyclohexane may be methyl cyclohexane, ethyl cyclohexane, isopropyl cyclohexane, etc. Its advantages are low cost, high catalytic performance, low reaction temp (less than 200 deg.C) and high transform rate.

The present invention is selectively catalytic air oxidation and substitution of toluene to form aldehyde and alcohol. Under the conditions of 2-10 atm air pressure, 25-180 deg.c temperature and 0.1-1 MPa reaction pressure, and in the presence of catalyst comprising module-metalloporphyrin oxide or solid carried metalloporphyrin as main catalyst and salt or oxide of transition metal as co-catalyst, toluene is oxidized with air into benzaldehyde and benzyl alcohol or oxidized and substituted into substituted benzaldehyde and substituted benzyl alcohol. The present invention has less catalyst consumption, high catalytic efficiency, low reaction temperature and pressure, easy-to-control oxidation depth, product with high purity and being easy separated. The catalyst may be used in homogeneous catalysis or solid carried for inhomogeneous catalysis.