72results about How to "Delay inactivation" patented technology

The invention relates to a catalyst for converting polycyclic aromatic hydrocarbons into monocyclic aromatic hydrocarbons and a preparation method thereof, mainly solving the problems in the prior art that the conversion level of polycyclic aromatic hydrocarbons is low, the monocyclic aromatic hydrocarbon yield and selectivity are low and the catalyst deactivation rate is high. The problems are better solved by adopting the catalyst and the preparation method thereof. The catalyst comprises 34.5-60wt% of mixture of FAU type zeolite and at least one molecular sieve from MOR, BEA, MFI and MCM-22, 39.5-65wt% of at least one of gamma-alumina, eta-alumina and pseudo-boehmite as a binder and 0.05-0.9wt% of at least one metal from Pt, Pd and Ir. The catalyst can be used in the industrial production of converting heavy polycyclic aromatic hydrocarbons into monocyclic aromatic hydrocarbons.

The present invention provides an alkane dehydrogenation sulfide catalyst, which comprises an active ingredient and a carrier, wherein the active ingredient comprises one or a plurality of elements selected from Fe, Co, Ni, Cu, Zn, Mo, W and Mn, the active ingredient content in the catalyst (calculated as the oxide having the highest valence) is 0.5-40 wt%, the carrier is a mixed oxide or a composite oxide formed from one or a plurality of materials selected from SiO2, Al2O3, ZrO2, La2O3, CeO2, CaO, P2O5, Nb2O5 and MgO, the carrier content is 60-99.5 wt%, and the active ingredient on the surface of the alkane dehydrogenation sulfide catalyst exists in a sulfide form. When the catalyst is adopted for the alkane dehydrogenation reaction, characteristics of high activity, high selectivity, good stability, slow deactivation, low cost and no environment pollution are provided.

The invention discloses a method for preparing an SAPO-34 molecular sieve. The method comprises the following steps of: mixing a silicon source and a phosphorus source; sequentially adding aluminum source serous fluid and an organic amine template agent containing fluoride, and uniformly mixing; aging mixed gel prepared according to the charging sequence for a certain period of time, and raising the temperature to be between 120 and 150 DEG C at the speed of lower than 0.45 DEG C / min; keeping the temperature for a certain period of time, and raising the temperature to 200 DEG C at the speed of lower than 0.30 DEG C / min; performing hydrothermal crystallization at the temperature of 200 DEG C for 24 to 48 hours; controlling the acid strength and the acid density of the synthesized SAPO-34 molecular sieve, and controlling the particle size of the SAPO-34 molecular sieve to be between 2.5 and 3.0 micrometers; and crystallizing the synthesized serous fluid, centrifuging, filtering, washing, drying, roasting, and thus obtaining the SAPO-34 molecular sieve with high crystallinity, suitable acid strength, suitable acid density and a small particle size. The SAPO-34 molecular sieve is used for a reaction of preparing olefin through methanol or dimethyl ether and has high catalytic activity and high ethylene / propylene selectivity.

The invention belongs to the technical field of catalysts, in particular to a preparation method of a catalyst for producing propylene by propane dehydrogenation under the carbon dioxide atmosphere and an application thereof. The preparation method can overcome the shortcomings of low activity, poor stability, high price and the like of the existing catalyst. An HZSM-5 zeolite with high silicon-aluminum ratio is taken as a carrier, zinc oxide is taken as an active component, the impregnation method in the prior art is adopted for preparing the catalyst, the prepration process is simple convenient, and the cost is low. When the catalyst is used for the reaction for producing the propylene by the propane dehydrogenation under the carbon dioxide atmosphere has the advantages of low price, simple process, high reaction activity, high yield of the propylene, good stability, slow inactivation and the like.

The invention pertains to the technical field of catalyst, particularly relating to a method for preparing propylene catalyst by propane dehydrogenation under carbon dioxide atmosphere and an application thereof. The catalysts currently used in the reaction have the disadvantages of low activity, poor stability, high price, etc. HZSM-5 ziolite is treated with high-temperature water vapor, and the ziolite is then taken as a carrier and zinc oxide is taken as an active ingredient to prepare catalyst by the impregnation method of the prior art. The catalyst is applied to the reaction for preparing propylene by propane dehydrogenation under carbon dioxide atmosphere, and the catalyst has the advantages of simple operation, high activity, sound stability, low cost, etc..

The invention relates to a method for converting polycyclic aromatic hydrocarbons into monocyclic aromatic hydrocarbons, mainly solving the problems in the prior art that the conversion level of polycyclic aromatic hydrocarbons is low, the monocyclic aromatic hydrocarbon yield and selectivity are low and the catalyst deactivation rate is high. The problems are better solved by adopting the technical scheme that polycyclic aromatic hydrocarbon mixtures and hydrogen are taken as the raw materials and are contacted with a catalyst in a fixed bend reactor to react under the conditions that the reaction temperature is 335-440 DEG C, the pressure is 4-7MPa, the weight hourly space velocity is 1-3hr<-1> and the hydrogen / hydrocarbon mole ratio is 4.0-8.0 to generate monocyclic aromatic hydrocarbon mixtures. The method can be used in the industrial production of converting heavy polycyclic aromatic hydrocarbons into monocyclic aromatic hydrocarbons.

The invention belongs to the technical field of chemical catalysts, and specifically discloses a catalyst for preparing ethylene through ethane dehydrogenation under a carbon dioxide atmosphere, and a preparation method thereof. The existing catalyst has the shortages of high dosage of chromium, low selectivity of ethylene, low stability, and the like. According to the catalyst disclosed by the invention, small-crystal-grain all-silicon silicalite-1 with an MFI structure is taken as a support, chromium oxide is taken as an active component with a content of 0.3%-5.0%. A soluble chromium salt is taken as a precursor and introduced into the silicalite-1 zeolite by virtue of an impregnation method, and then is prepared into a supported catalyst through roasting during preparation. According to the preparation method disclosed by the invention, the impregnation method is adopted, and the preparation process is simple and convenient. The catalyst is used for a reaction of preparing ethylene through ethane dehydrogenation under a carbon dioxide atmosphere, and has the advantages of being simple in process, high in activity, high in selectivity and stability, and the like.

The invention relates to a silicoaluminophosphate molecular sieve and a preparation method and application thereof. The structure formula of the molecular sieve is (0.2-3.0) R: (Si0.01-0.3Al0.01-1P0.01-0.9 ):(10-400) H2O, and three templates, a silicon source, an aluminum source and a phosphorus source are mixed with water to form gel, and then the silicoaluminophosphate molecular sieve can be obtained by the steps of crystallization and drying. Compared with the preparation methods of the molecular sieve with single template and double templates in the prior art, the invention is taken as a catalyst and is applied to the reaction of light olefins from methanol, can improve the conversion rate of raw materials, delay coking rate, prolong reaction activity time, and improve the selectivities of ethylene and propylene, and simultaneously solve the problem that the synthesis cost of the silicoaluminophosphate molecular sieve is high in the prior art.

The invention relates to a catalyst for converting polycyclic aromatic hydrocarbons into monocyclic aromatic hydrocarbons to produce more dimethylbenzene and a preparation method thereof, mainly solving the problems in the prior art that the conversion level of polycyclic aromatic hydrocarbons is low, the dimenthylbenzene yield and selectivity are low and the catalyst deactivation rate is high. The problems are better solved by adopting the catalyst and the preparation method thereof. The catalyst comprises 30-60wt% of mixture of FAU type zeolite and at least one molecular sieve from MOR, BEA, MFI and MCM-22, 38-69.9wt% of at least one of gamma-alumina, eta-alumina and pseudo-boehmite as a binder, 0.04-0.9wt% of at least one metal from Pt, Pd and Ir and 0.1-1wt% of at least one of Zn, Sn, La, Ce and Mo. The catalyst can be used in the industrial production of increasing production of dimethylbenzene by converting heavy polycyclic aromatic hydrocarbons into monocyclic aromatic hydrocarbons.

The invention relates to a method of producing dimethyl ether liquefied gas by methanol, directly inputting methanol steam to a reaction kettle with compound liquid catalyst, controlling producing temperature at 120-250 deg.C and pressure at 0.2-3.8 MPa, making it pass through a buffer, a condensing tower, a gas-liquid separator, and then input it to liquid gas storage tanks by a compressor, and obtaining the products. It can use 72%-99.9% methanol as raw material, the producing temperature is easy to control, the heat conduction is fast, and the reactor is uniformly used; it uses liquid catalyst, the catalyst is inactivated slowly and easy to make and able to repeatedly use, the corrosion to the device is low, and it can implement continuous production, and make the dimethyl ether products with purity 90-99%.

The invention relates to a preparation method of a high-efficiency environmental-protection compound ion liquid catalyst used for synthesizing high-quality propene carbonate. The invention has the technical scheme of comprising the following steps of: (1) reacting halogenated alkane and methylimidazole in a reaction kettle according to a proportion; (2) washing by using an ester compound, settling after stirring fully, and stratifying; (3) distilling off the unreacted halogenated alkane, the ester compound and light impurities under a decompression condition; (4) adding a metal halide catalysis aid to obtain a novel compound ion liquid catalyst; and (5) taking propylene oxide and carbon dioxide as raw materials and novel compound ion liquid as the catalyst, and synthesizing the propene carbonate. The invention has the advantages that the cost of the catalyst is low, the inactivation of the catalyst is slow, the service life is long, and the annual use cost is equivalent to 1 / 4 to 1 / 5 of that of a tetraethyl ammonium halide catalyst; and the activity of the catalyst is high, the reaction speed is high, the selectivity is high, and the yield of the propene carbonate can reach 97 to 98 percent.

The present invention relates to a methanol-to-aromatic hydrocarbon catalyst and uses thereof. A purpose of the present invention is mainly to solve the problems of low selectivity and poor catalyst stability in the conversion of methanol into aromatic hydrocarbons in the prior art. The technical scheme of the present invention comprises that a modified mesoporous and microporous compounded molecular sieve is adopted as a catalyst, methanol is adopted as a raw material, and the raw material is subjected to an aromatization reaction at a reaction temperature of 360-500 DEG C under a reaction pressure of 0-1.0 MPa at a raw material mass space velocity of 0.4-8 h<-1> under the effect of the catalyst. With the technical scheme, the problems in the prior art are well solved. The catalyst of the present invention can be used for the industrial production of methanol-to-aromatic hydrocarbon.

The invention relates to a fluidized catalytic method for preparing p-xylene by alkylating aromatic hydrocarbon. By the fluidized catalytic method, the problems of single raw materials, high temperature rise of a reaction bed, poor stability of a catalyst, multiple side reactions of an alkylating reagent and a low utilization rate in the prior art are mainly solved. In the fluidized catalytic method, methanol, dimethyl ether, benzene and toluene are subjected to mixed feeding, and the dimethyl ether is used as the alkylating reagent. Through the technical scheme, the problems are better solved. The fluidized catalytic method can be applied to industrial production of the p-xylene by performing alkylation reaction on the aromatic hydrocarbon.

The invention discloses an alloy catalyst for dehydrogenation of alkane as well as a preparation method and an application of the alloy catalyst. The catalyst comprises three components A, B and C, wherein the component A is one of noble metal element precursors Pt, Pd, Rh and Ir and accounts for 0.1wt%-5wt% of total weight of the catalyst; the component B is one of precursors Sn, Ge and Ga and accounts for 0.1wt%-5wt% of total weight of the catalyst; the component C is a carrier and accounts for 90wt%-99.8wt% of total weight of the catalyst. The metal organic compound is used as a precursor of the component B, and the precursor is very likely to be uniformly dispersed on the surface of the carrier. Then, the active component A is introduced, and finally the alloy catalyst is prepared. Theprepared catalyst has the advantages of small particle size, high dispersibility, high sintering resistance, high catalytic activity and good dehydrogenation performance of light alkane.

The invention discloses a method for synthesizing propylene by using methanol, for solving the problems that in the existing technique for preparing propylene by using methanol, the selectivity of propylene is low and cannot meet the requirement of industrial application and subsequent separation is very difficult. The method disclosed by the invention comprises the following steps of: preparing an intermediate mixture; synthesizing propylene; and separating propylene. According to the method for synthesizing propylene by using methanol, the raw material is a methanol aqueous solution. By the method disclosed by the invention, the problem that in the existing technique for preparing propylene by using methanol, the selectivity of propylene is low can be solved effectively, and therefore, the subsequent separation difficulty is reduced, the production cost is lowered and the economic efficiency of enterprises is improved.

The invention relates to a silicon-aluminium phosphate molecular sieve synthesized by a composite template agent, and a preparation method and application thereof. The structural formula of the molecular sieve is (0.2-3.0)R: (Si0.1-0.3Al0.1-1P0.01-0.9): (10-400)H2O, wherein R is a tetraethyl ammonium hydroxide / diethylamine composite template agent, and the composite template agent is x tetraethyl ammonium hydroxide+(1-x) diethylamine, wherein x is equal to between 0 and 1. Compared with the prior art, the composite template agent (tetraethyl ammonium hydroxide / diethylamine) has low synthesis cost for synthesizing the silicon-aluminium phosphate molecular sieve and is easy for industrial production, and when used as a catalyst in the preparation of low-carbon olefin from methanol, the template agent has slow reaction cocking rate and deactivation rate, and long activity time and service life, and has the advantages of high feed stock conversion, high selectivity for low-carbon alkene such as ethylene, propylene, and the like.

A macroreticular cationic exchange resin is prepared from styrene or substituted styrene, divinylbenzene and atoleine through copolymerizing and sulfonating. It can be used to synthesize the catalyst for synthesizing diphenol A by ionic exchange. Said catalyst has high activity and selectivity and long service life.

The invention specifically provides an alkylation catalyst and application thereof, belonging to the field of catalysts. The alkylation catalyst comprises a modified IM-5 molecular sieve and a binder, wherein the modified IM-5 molecular sieve has a mesoporous area of 150 m<2> / g or above and a mesoporous volume of 0.5 cm<3> / g or above. The catalyst provided by the invention has the advantages of slow inactivation rate, high catalytic activity and good selectivity; e.g., when the catalyst is used under a high space velocity condition, activity stability of the catalyst is still long, and the catalyst still has a high benzene conversion rate in a reaction at low temperature. Thus, the catalyst can be used under the high space velocity condition, has high catalysis efficiency, is reactable at a low temperature, shows good activity stability, reduces energy consumption of alkylation and has prolonged service life.

The invention provides a synthesis method of 3-methyl-2-butene-1-aldehyde diisopentenyl acetal. The synthesis method comprises the following step: in the presence of a supported catalyst, carrying outan alcohol-aldehyde condensation reaction on isopentenal and isopentenol to realize high-activity high-selectivity synthesis of the 3-methyl-2-butene-1-aldehyde diisopentenyl acetal. The catalyst provided by the invention improves the activity of reactants and the selectivity of the product, can obtain high yield, avoids the problem of equipment corrosion, prolongs the service life of equipment,has obvious environmental protection benefits, is environment-friendly, and is beneficial to industrial mass production.

The invention relates to a catalyst for converting sulphur-containing polycyclic aromatic hydrocarbon into mononuclear aromatic and a preparation method thereof and mainly aims at solving the problems that the conversion level of the sulphur-containing polycyclic aromatic is low, the yield of the mononuclear aromatic is low, the selectivity is low and the catalyst deactivation rate is high in the prior art. The catalyst for converting the sulphur-containing polycyclic aromatic hydrocarbon into the mononuclear aromatic comprises the following components in percentage by weight: 30-65% of a mixture of FAU-type zeolite and a ZSM-12 molecular sieve, 33.5-69.8% of at least one selected from gamma-alumina, eta-alumina and pseudo boehmite, which serves as a binding agent, 0.1-0.5% of at least one metal selected from Pt, Pd and Ir, and 0.1-1% of at least one metal selected from La, Ce and Sn. By adopting the technical scheme, the problems are relatively well solved, and the catalyst for converting the sulphur-containing polycyclic aromatic hydrocarbon into the mononuclear aromatic can be applied to the industrial production of converting the sulphur-containing polycyclic aromatic hydrocarbon into the mononuclear aromatic.

The invention discloses a metal catalyst for dehydrogenation of light alkane and a preparation method and application thereof. The catalyst comprises a component A, a component B and a component C, wherein the component A is one of noble metals including Pt, Pd, Rh and Ir and accounts for 0.1-5wt% of the total weight of the catalyst; the component B is Sn or Ge and accounts for 0.1-5wt% of the total weight of the catalyst; and the component C is a carrier and accounts for 90-99wt% of the total weight of the catalyst. The preparation method of the catalyst is characterized in that the surface organometallic chemistry that is molecular science is utilized to accurately control the structure, particle size and dispersity of an alloy catalyst; a high-dispersity metal nano-cluster catalyst withuniform component and particle size can be prepared; the effective adjustment and control of synthesizing-structure-performance of the metal alloy catalyst can be achieved. The catalyst prepared by the method is high in light alkane dehydrogenation performance; and a technical source is supplied to the development of a new generation of catalyst for alkane dehydrogenation.

The invention relates to the field of preparation of molecular sieves and particularly relates to modified IM-5 molecular sieves, a preparation method therefor, an application of the modified IM-5 molecular sieves and an alkylation reaction method for toluene and methanol. The preparation method for the modified IM-5 molecular sieves comprises the steps of subjecting a modifier solution to contactwith H-IM-5 molecular sieves, and then, roasting a solid material obtained through contact, wherein the modifier solution contains quaternary ammonium cations, quaternary phosphonium cations and at least one lanthanide metal compound and is alkaline, and the contact temperature is 70 DEG C to 200 DEG C. According to the modified IM-5 molecular sieves provided by the invention, on the basis of overall weight of the modified IM-5 molecular sieves, by oxides, the phosphorus content is 0.1wt% to 15wt%, and the content of lanthanide metal element is 0.1wt% to 20wt%. By applying the modified IM-5 molecular sieves provided by the invention to an alkylation reaction for the toluene and the methanol, the modified IM-5 molecular sieves have the advantages that the deactivation rate is low, the catalytic activity is high, and the selectivity of dimethylbenzene and trimethylbenzene is good.

The invention specifically provides an alkylation method, belonging to the field of alkylation. The alkylation method comprises a step of allowing benzene to contact with methanol in the presence of a catalyst containing a modified IM-5 molecular sieve, wherein the modified IM-5 molecular sieve has a mesoporous area of 150 m<2> / g or above and a mesoporous volume of 0.5 cm<3> / g or above. The catalyst used in the invention has the advantages of slow inactivation rate, high catalytic activity and good selectivity; e.g., when the catalyst is used under a high space velocity condition, activity stability of the catalyst is still long, and the catalyst still has a high benzene conversion rate in a reaction at low temperature. Due to the advantages of the catalyst, the alkylation reaction of benzene with methanol has the advantages of high benzene conversion rate, good selectivity of target products, i.e., xylene and 1,2,4-trimethylbenzene, etc.; and since the catalyst is not prone to inactivation, the alkylation reaction has a long operation period and is especially suitable for industrial application.

The invention specifically provides a modified IM-5 molecular sieve and a preparation method and application thereof, belonging to the field of modification of molecular sieves. The modified IM-5 molecular sieve has a mesoporous area of 150 m<2> / g or above and a mesoporous volume of 0.5 cm<3> / g or above. The modified IM-5 molecular sieve has a large mesoporous area and a large mesoporous volume, so a reactant can more easily contact with an acid center and a product can be rapidly diffused from active center to places out of a catalyst; thus, side reactions are prevented, and the activity, selectivity and service life of the catalyst are improved; e.g., when the modified IM-5 molecular sieve is applied to an alkylation reaction of benzene and methanol, the catalyst has the advantages of a slow inactivation rate, a high benzene conversion rate and high target product selectivity. The modified IM-5 molecular sieve can be used under a high space velocity condition, has high catalysis efficiency, is reactable at a low temperature, shows good activity stability, reduces energy consumption of alkylation, prolongs the service life of the catalyst and is suitable for industrial application.

The invention discloses an aluminum oxide carrier, a preparation method of a catalyst containing the aluminum oxide carrier, and application of the catalyst. The aluminum oxide carrier is prepared from the following raw materials of aluminum stone, methylcellulose and an ingredient A. The invention also discloses the preparation method of the aluminum oxide carrier, and the catalyst containing thealuminum oxide carrier. The catalyst is prepared from the following raw materials of 40 to 55 mass parts of the aluminum oxide carriers (preferably 45 mass parts of the aluminum oxide carriers), 10 to 30 mass parts of an ingredient B and 1 to 10 mass parts of an ingredient C. The invention also discloses the preparation method of the catalyst containing the aluminum oxide carrier. The catalyst has dehydrogenation activity and has the advantages of high selectivity, slow inactivation, high carbon accumulation resistant capability and the like in the dehydrogenation reaction process.

The invention relates to a fluidized catalytic method of p-xylene by methylation of aromatic hydrocarbon, and mainly solves the problems of high temperature rise of a reaction bed, poor catalyst stability, more side reaction of an alkylation reagent and low utilization rate in the prior art. According to the technical scheme, dimethyl ether and aromatic hydrocarbon are used as mixing feeds and dimethyl ether is used as the methylation reagent. The technical scheme greatly solves the problems and can be applied in the industrial production of p-xylene by methylation reaction of aromatic hydrocarbon.