39results about How to "Avoid hydrogenation" patented technology

A process for purifying a crude furan 2,5-dicarboxylic acid composition (cFDCA) by hydrogenation of a FDCA composition dissolved in a hydrogenation solvent such as water, and hydrogenating under mild conditions, such as at a temperature within a range of 130° C. to 225° C. by contacting the solvated FDCA composition with hydrogen in the presence of a hydrogenation catalyst under a hydrogen partial pressure within a range of 10 psi to 900 psi. A product FDCA composition is produced having a low amount of tetrahydrofuran dicarboxylic acid, a low b*, and a low amount of 5-formyl furan-2-carboxylic acid (FFCA).

A process for purifying a crude furan 2,5-dicarboxylic acid composition (cFDCA) by hydrogenation of a FDCA composition dissolved in a hydrogenation solvent such as water, and hydrogenating under mild conditions, such as at a temperature within a range of 130° C. to 225° C. by contacting the solvated FDCA composition with hydrogen in the presence of a hydrogenation catalyst under a hydrogen partial pressure within a range of 10 psi to 900 psi. A product FDCA composition is produced having a low amount of tetrahydrofuran dicarboxylic acid, a low b*, and a low amount of 5-formyl furan-2-carboxylic acid (FFCA).

The process of selectively hydrogenating and desulfurizing inferior gasoline includes selectively hydrogenating and desulfurizing inferior gasoline, separating oil from gas, eliminating mercaptan and other steps. In the step of selectively hydrogenating and desulfurizing inferior gasoline, one kind of high activity hydrogenating and desulfurizing catalyst in the upstream and one kind of low activity hydrogenating and desulfurizing catalyst in the downstream are applied. The hydrogenating and desulfurizing has the great amount of heat produced in the hydrogenating and desulfurizing reaction well utilized, so that the present invention has lowered hydrogen consumption, high heat efficiency, prevention of over hydrogenation, inhibition of saturating hydrogenation of olefin and lowered octane value loss.

The invention discloses a composite molten steel slag washing agent based on LF (ladle furnace) refining waste slag and a preparation method thereof. The composite molten steel slag washing agent consists of 65 to 95% of LF refining slag, 10 to 30% of active lime and 5 to 15% of industrial soda. The LF refining slag is composed of 50 to 60% of CaO, 25 to 35% of Al2O3, 4 to 8% of SiO2, 4 to 7% of MgO, 0.5 to 1.0% of MnO and FeO, 0.005 to 0.02% of P2O5, and 0.01 to 0.3% of S; the active lime includes 90 to 94% of CaO, and HCl with activity of 350 to 380 ml / 4N and granularity of 0.5 to 3.0 mm; and the industrial soda includes 99.2% of Na2CO3 with granularity of 0.5 to 1.0 mm. The preparation method comprises the following steps of: processing the LF refining slag and the active lime into the powder with the granularity of 0.5 to 3.00 mm; uniformly mixing and stirring the materials according to the percentage, dry-pressing and moulding the materials with granularity of 25 to 35 mm and applying the waterproof packaging to the materials. On the condition that the adding quantity is 4 to 6 kg / t, the desulfurization rate of the invention achieves more than 30%, the reduction rate of the total oxygen content is more than 25% and the qualified rate of the thermal top forge is improved from 80% to 95%, so that the invention realizes the resource recycling of the LF refining waste slag and is beneficial to the energy-saving and emission reduction of the iron and steel enterprises.

A coupling method for preparing ª†-butyrolactone and cyclohexanone, carrying out integral reaction with the mixture of cyclohexanol and anhydride under the condition of gas phase, existence of additional hydrogen or no additional hydrogen, proper temperature and hydrogen catalyst. The invention is characterized compared with current technology by the integral reaction of hydrogenation and dehydrogenation, low energy consumption, no need for hydrogenation or hydrogen recovery, low producing cost, high selectivity and recovery rate, simple preparing process and easy-to-operate.

The invention provides a multipurpose environment-friendly cleaning paste and a preparation method thereof. The multipurpose environment-friendly cleaning paste comprises, by weight, 5-15% of stearic acid, 4-10% of palm oil, 4-10% of coconut oil, 0.8-2% of sodium hydroxide, 0.1-0.5% of potassium hydroxide, 0.2-0.8% of soda ash, 0.8-2% of peregal O, 0.8-2% of tween-20, 0.8-2% of tween-80, 5-15% of carnauba wax, 15-20% of water-soluble silicone oil, 8-15% of OP-10, 0.2-0.8% of preservative, 0.1-0.5% of essence and 20-45% of purified water. The multipurpose environment-friendly cleaning paste has the unique advantages of being green, environment-friendly, free of corrosion and foreign smell and strong in detergency, sterilizing, polishing, waxing and saving water and time. Besides, the multipurpose environment-friendly cleaning paste removes dust, leaves no trace and is long in duration time, simple to manufacture, practical and simple and convenient to operate and use.

The invention relates to a catalyst system for preparing cyclohexene by benzene selective hydrogenation, and a method for preparing cyclohexene by benzene selective hydrogenation. The method for preparing cyclohexene by benzene selective hydrogenation is implemented by catalyzing with the catalyst system composed of nanometer Ru catalyst, alkaline substance M, zinc salt and water. The nanometer Ru catalyst with microcrystalline size of 3-6 nm is prepared from NaOH, RuCl3 and polyethylene glycol (PEG) by co-current co-precipitation method. The alkaline substance M can be hydroxide, oxide or alkaline organic substance of alkali metal, alkaline earth metal, transition metal or rare earth metal. The zinc salt can be zinc sulfate, zinc nitrate or zinc chloride. Ru catalyst / M / zinc salt weight ratio is 1:(0-10):(20-30), and Ru / water weight ratio is 0.5-1%. At 150 DEG C and 5.0 MPa, after reaction for 15-25 min, when the benzene conversion rate is 40-60%, cyclohexene selectivity is 75-85%, and cyclohexene yield is 35-50%.

A coupling method for preparing 2-methylfuran and cyclohexanone, carrying out integral reaction with the mixture of furfuraldehyde and anhydride under the condition of gas phase, existence of additional hydrogen or no additional hydrogen, proper temperature and hydrogen catalyst. The invention is characterized by the low energy consumption, no need for hydrogenation or hydrogen recovery, low producing cost, high selectivity and productivity, simple preparing process and easy-to-operate.

The invention discloses a preparation method of a bi-functional catalyst of a (Ru / MeOx)@MeOx core-shell structure. The method is characterized in that a center suitable for surface catalyzing is formed by core phase Ru / MeOx and shell phase m-MeOx. A ruthenium-based catalyst prepared by the method has high dispersing performance, so that benzene is dissociated and absorbed more easily at a lower temperature to improve the conversion rate of the benzene;the cyclohexene is allowed to be desorbed on a shell by a hydrophilic m-MeOx shell phase to prevent further hydrogenation and improve the selectivity of the cyclohexene, the loss of activated species can be reduced by the core-shell structure to allow the catalyst to be more stable, the mass transfer resistance can be reduced, the excellent composite performance can be applied to part of hydrogenation cyclohexene reaction of benzene, and extremely high selectivity and yield are obtained. The preparation method is simple, the conditions are mild, the repeating is easy, and the method is suitable for large-scale industrial production.

A rubber composition comprising (1) a diene rubber, (2) a highly saturated rubber, and (3) a block copolymer that comprises a diene polymer block A and a hydrogenated diene polymer block B and has a primary structure selected from the following structures: (A-B)X, (A-B)X-A, and B-(A-B)X (wherein X is an integer of 1 or above) wherein the rubber composition contains 0.1 to 25 parts by mass of the block copolymer (3) with respect to 100 parts by mass of the total amount of the diene rubber (1) and the highly saturated rubber (2). Such a rubber composition exhibits improved dispersibility between its rubber components, i.e., diene rubber and highly saturated rubber, and improved adhesion at the interface between the rubber phases. The rubber composition also shows high tensile property as well as high flexing property.

The invention discloses a production method for pre-melted slag for small-batch electroslag remelting. The production method comprises the steps that firstly, a slag melting bag with the volume being300 kg is selected and used; secondly, pre-melted slag raw materials are taken to be preheated and baked in a slag baking furnace; thirdly, the baked pre-melted slag raw materials with the weight being smaller than or equal to 300 kg in the second step are placed in the slag melting bag in the first step, a double-pole series connection electroslag furnace is used for arc strike for slag melting in the slag melting bag, and after slag melting is over, the slag liquid is poured into a steel tank to be cooled and solidified; and fourthly, slag blocks solidified in the third step are crushed through a small crusher, and the slag blocks serve as pre-melted slag for electroslag remelting after being weighed. The double-pole series connection electroslag furnace is utilized for slag melting in the slag melting bag, production of small-batch pre-melted slag with the weight being smaller than or equal to 300 kg is achieved, and the problem that pre-melted slag for the small-batch test steel grade is hard to produce and purchase is solved. The method is simple, convenient to use and worthy of popularization and application.

The invention relates to a production method for effectively controlling gas content in beam blank. The production method comprises processes of raw material pre-treating, converter smelting, deoxidation alloying, and refining, wherein the materials maintain dry, the process of adding slag charge is moved forward to avoid adding material operation 3 minutes before the terminal point; the process of modifying converter slag is moved backward, synthesis slag is added on top of the steel slag after the converter furnace has been stocked with steels other than going into the converter furnace with the steel water, synthesis slag is subjected to a ultra-high-temperature baking by utilizing the steel slag to maximumly reduce the water in the synthesis slag and the crystal water contained by the synthesis slag; electrode powder replaces carbon powder to match with carbon in the refining process to reduce the effect of carbon matching on molten steel hydrogenation. The production method can effectively control hydrogen addition in production process, reduces the hydrogen content in molten steel, makes the hydrogen content in the steel stay in a range of 1 to 3 ppm, reduces casting blank pinhole defects, and improves casting blank yield rate.

The invention particularly relates to a nitrogen-filling electroslag process for a cavity of a nitrogen-containing steel hollow blank, which is different from a common process in which nitrogen is added into an electrode blank of nitrogen-containing steel and then electroslag is carried out. The process is characterized in that nitrogen is not added during smelting of an electrode blank, a nitrogen-free hollow electrode blank is adopted, nitrogen is injected from a reserved hole during electroslag, nitrogen is added into steel through the physical and chemical reaction of nitrogen and steel slag, the nitrogen flow is controlled according to the nitrogen content of different steel types, and alloying of the nitrogen element is completed in the electroslag remelting process. The process can be applied to common electroslag equipment only, and a special pressurizing electroslag furnace high in price does not need to be arranged. Due to the fact that the blank is a hollow blank, the hot spot is not in the center of a molten pool, the shape of an electroslag molten pool is greatly improved, the molten pool tends to be in a flat state, the consistency of internal and external crystalline states of an ingot is higher, redundant nitrogen overflows from the periphery to form a protective atmosphere, oxygen increasing and hydrogen increasing of molten steel are avoided, the alloying target of the nitrogen element can be easily achieved, and the quality of the electroslag ingot can be improved.

An article and method of manufacture of a catalyst. The article includes a nanoparticle of a noble metal based on material with a primary alkylamine layer disposed on the surface of the nanoparticle catalyst. The alkylamine layer of at least about one monolayer establishes a minimum level of selectivity for hydrogenation reactions.

The invention provides a multipurpose environment-friendly cleaning paste and a preparation method thereof. The multipurpose environment-friendly cleaning paste comprises, by weight, 5-15% of stearic acid, 4-10% of palm oil, 4-10% of coconut oil, 0.8-2% of sodium hydroxide, 0.1-0.5% of potassium hydroxide, 0.2-0.8% of soda ash, 0.8-2% of peregal O, 0.8-2% of tween-20, 0.8-2% of tween-80, 5-15% of carnauba wax, 15-20% of water-soluble silicone oil, 8-15% of OP-10, 0.2-0.8% of preservative, 0.1-0.5% of essence and 20-45% of purified water. The multipurpose environment-friendly cleaning paste has the unique advantages of being green, environment-friendly, free of corrosion and foreign smell and strong in detergency, sterilizing, polishing, waxing and saving water and time. Besides, the multipurpose environment-friendly cleaning paste removes dust, leaves no trace and is long in duration time, simple to manufacture, practical and simple and convenient to operate and use.

The invention belongs to the technical field of organic synthesis and chemical catalysis, and discloses a large-steric-hindrance N-heterocyclic carbene palladium complex, a preparation method thereof, application of the large-steric-hindrance N-heterocyclic carbene palladium complex to efficient catalysis of C-N coupling reaction at room temperature, and a synthesis method of Sonidegib based on the large-steric-hindrance N-heterocyclic carbene palladium complex. According to the structure of the large-steric-hindrance nitrogen heterocyclic carbene palladium complex, diphenyl imidazole serves as a main ligand framework, functionalized allyl serves as an auxiliary ligand, and the functionalized allyl is introduced beside a metal center of a catalyst to serve as the auxiliary ligand, so that the large-steric-hindrance nitrogen heterocyclic carbene palladium complex has remarkably improved catalytic activity and stability and can be applied to efficient catalysis of C-N coupling reaction; and especially, the catalyst can efficiently catalyze C-N coupling reaction at room temperature, and the yield can reach 99%. The invention also provides a three-step method for synthesizing the Sonidegib at room temperature by taking aryl / aliphatic amine and aryl chloride as reactants under the catalysis of a palladium catalytic system, the synthesis method provided by the invention has few steps, and the total yield can be up to 74.5%.

In a nuclear fuel rod a cladding tube is provided having a closed inner space and manufactured from at least one of the materials in the group zirconium and a zirconium-based alloy, and a pile of nuclear fuel pellets arranged in the inner space in the cladding tube. The nuclear fuel pellets fill part of the inner space. A fill gas is arranged in the closed inner space to fill the rest of the inner space. The internal pressure of the fill gas in the nuclear fuel rod amounts to at least 2 bar (abs) or at least 10 bar (abs). The fill gas contains a proportion of inert gas a proportion of carbon monoxide that is greater than 3 volume percent of the fill gas or greater than 2 volume percent of the fill gas.

The invention relates to a ruthenium-carbon catalyst as well as a preparation method and application thereof. The ruthenium-carbon catalyst comprises an activated carbon carrier, ruthenium nanoparticles and a cocatalyst, the ruthenium nanoparticles and the cocatalyst are loaded on the activated carbon carrier, and the cocatalyst is a compound containing phosphorus and iron and capable of being coordinated with ruthenium ions; in the ruthenium-carbon catalyst, the mass content of the ruthenium nanoparticles is 1%-6%. According to the ruthenium-carbon catalyst, the activated carbon serves as a carrier, ruthenium nano-particles in a specific proportion are loaded, meanwhile, a phosphorus and iron containing compound capable of being coordinated with ruthenium ions is loaded to serve as a cocatalyst, the ruthenium-carbon catalyst can be used for catalyzing carbonyl selective hydrogenation, and then the selectivity and the reaction conversion rate of carbonyl selective hydrogenation are improved; for example, the catalyst is used for selective hydrogenation catalysis of carbonyl groups of unsaturated aldehydes to produce unsaturated alcohols. The ruthenium-carbon catalyst is used for selective hydrogenation of carbonyl of citral to prepare nerol and geraniol, the reaction conversion rate reaches 95%-100%, and the selectivity to nerol and geraniol reaches 90%-99%.

The invention belongs to the technical field of organic synthesis and chemical catalysis, and discloses a large-steric-hindrance N-heterocyclic carbene palladium complex, a preparation method thereof,an application of the complex in efficient catalysis of a C-N coupling reaction under a room-temperature air condition, and a synthesis method of sonidegib based on the complex. According to the large-steric-hindrance N-heterocyclic carbene palladium complex, diphenyl imidazole serves as a main ligand framework, functionalized allyl serves as an auxiliary ligand, the functionalized allyl is introduced beside a metal center of a catalyst to serve as an auxiliary ligand, the catalytic activity and stability are remarkably improved, the large-steric-hindrance N-heterocyclic carbene palladium complex can be applied to efficient catalysis of a CN coupling reaction, particularly, the CN coupling reaction can be efficiently catalyzed under the room temperature condition, and the yield can reachup to 99%. The invention also provides a method for synthesizing sonidegib by taking aryl / aliphatic amine and aryl chloride as reactants and a three-step method at room temperature under the catalysisof a palladium catalytic system, the synthetic method has few steps, and the total yield can reach 74.5%.

The invention relates to a preparation method and application of a Pt nanoparticle-loaded biochar catalyst, and belongs to the technical field of catalysts. According to the catalyst, biochar is takenas a carrier, and Pt nanoparticles are loaded; Pt nanoparticles are used as active sites, the loading capacity of the Pt nanoparticles is 1-10wt.%, and the particle size of the Pt nanoparticles is 1-3nm. The carrier and the Pt nanoparticles are combined through an impregnation method, the operation is simple, the cost is low, the Pt nanoparticles are uniformly distributed on the carrier, the sizeof the Pt nanoparticles is small, and the utilization rate is higher.

This invention relates to a novel synergistic reversible solid / semi-solid organic composition, said composition comprising (a) at least one saturated long chain fatty acid and / or its glycerol esters and (b) one or more liquid neutral organic compounds, said ingredients (a) and (b) being present in a ratio between 0.1 to 40% by weight, and a process for producing said synergistic reversible solid / semi-solid organic composition by mixing the ingredients (a) and (b) defmed above in a ratio between 0.1 to 40% by weight, at a temperature between 2 to 50° C. and at a pressure in the range of 200 torr to 2500 torr.

The invention discloses a preparation method of an aluminum-calcium multifunctional slag washing material, and belongs to the technical field of steel smelting. The preparation method of the aluminum-calcium multifunctional slag washing material comprises the following steps: S1, preparing raw materials; S2, drying; and S3, mixing. In the step S1, the raw materials comprises, by mass, 5%-20% of Al, 10%-40% of Al2O3, 30%-50% of CaO and 5%-20% of an additive; in the step S2, the CaO is put into a drying box and dried; and in the step S3, the Al and the Al2O3 are crushed until the particle size is less than 5mm, the CaO is crushed until the particle size is less than 60mm, and the additive is added for mixing. According to the preparation method, finished products and the raw materials do not contain polluting elements, so that the safety and the environmental protection property are remarkable; and a high-temperature melting environment is not needed in the preparation process, so that the energy digestion is reduced, and safety is further improved.

The invention provides a metal-site-free method for preparing aromatic hydrocarbon by hydrocracking aromatic polymer and heavy aromatic hydrocarbon by dissociating hydrogen through an oxide, which comprises the following steps of: reacting the aromatic polymer with a catalyst in the presence of hydrogen at the temperature of below 350 DEG C; and rectifying and separating reaction products to obtain aromatic hydrocarbons. The catalyst contains at least one of niobium oxide, niobium phosphate, a niobium-silicon mixed oxide, a niobium-aluminum mixed oxide and a porous carbon-niobium material.