6947results about "Molecular sieve catalysts" patented technology

A composition of matter is provided comprising hierarchically ordered crystalline microporous material having well-defined long-range mesoporous ordering of lamellar symmetry. The composition possesses mesopores having walls of crystalline microporous material and a mass of mesostructure between mesopores of crystalline microporous material. Long-range ordering is defined by presence of secondary peaks in an X-ray diffraction (XRD) pattern and / or lamellar symmetry observable by microscopy.

The invention relates to an SSZ-39 molecular sieve and preparation and application thereof.The preparation method comprises the following steps that 1, after water, an alkali source and a template agent are mixed, mesoporous Y zeolite and a silicon source are added, the mixture is stirred to be uniform, and the mixture is aged to be in a white gel shape; (2) transferring the obtained white gel into a reaction kettle, carrying out crystallization treatment, and filtering, washing, drying and calcining a crystallized product to obtain a Na-SSZ-39 molecular sieve; (3) carrying out ammonium ion exchange on the Na-SSZ-39 molecular sieve, filtering, washing, drying and calcining to obtain an H-SSZ-39 molecular sieve; and (4) carrying out copper ion exchange on the H-SSZ-39 molecular sieve, filtering, washing, drying and calcining to obtain the Cu-SSZ-39 catalyst. Aluminum used in the method is provided by mesoporous Y zeolite, the pure-phase SSZ-39 molecular sieve can be synthesized in a wide gel range, the crystallization time is shortened to 24 h, and after copper ion exchange, the pure-phase SSZ-39 molecular sieve shows high denitration activity in the selective catalytic reduction reaction of nitrogen oxide ammonia.

The invention discloses a preparation method of an adsorption and reduction bifunctional catalyst for denitration of tail gas of a diesel vehicle. The preparation method comprises the following steps: uniformly loading a Pd component and a Cu component on the surface of a molecular sieve to prepare a corresponding Pd-based molecular sieve and a corresponding Cu-based molecular sieve; and then coupling the Pd-based molecular sieve and the Cu-based molecular sieve according to a certain proportion by using a solid-phase grinding means to obtain the adsorption and reduction dual-functional Pd-Cu / SSZ-13 catalyst. The adsorption and reduction bifunctional Pd-Cu / SSZ-13 catalyst prepared by the method not only has excellent SCR activity at the temperature of 200 DEG C or above, but also has good PNA capacity at the temperature of 200 DEG C or below, can realize high-efficiency denitration of diesel vehicle tail gas in a full-temperature section, and can be widely applied to a diesel vehicle tail gas after-treatment system.

The invention discloses a method for synthesizing tetrahydrofuran from furfural in one step and a preparation method of a catalyst for the tetrahydrofuran. The catalyst is a bimetallic catalyst, bimetallic is M1 and M2, M1 is Pd, and M2 is selected from one of Pt, Rh, Ru, Ni, Cu, Co, Mn and Ce; the catalyst comprises an active component and a carrier, the bimetallic is the active component, and the carrier is selected from at least one of activated carbon, silicon dioxide, aluminum oxide, magnesium oxide, an S-1 molecular sieve, a ZSM-5 molecular sieve, a Beta molecular sieve, an MOR molecular sieve and a Y molecular sieve; based on the total weight of the catalyst, the loading capacity of M1 is 0.5-3.5%, and the loading capacity of M2 is 0.5-3.5%. The catalyst provided by the invention can be used in a reaction for preparing tetrahydrofuran through furfural hydrogenation, and can improve the conversion rate of furfural and the selectivity of tetrahydrofuran.

An article for joule heating is described, including a three-dimensional substrate on and / or in which a pyrolyzate of a phenolic resin or polymer forms an electrically conductive carbon network. Such articles may be incorporated in structured materials applications, which may include support, sorbent, and or catalyst components. Also described are methods of fabricating such articles and structured materials, and apparatus comprising same, and methods of use of such articles and structured materials and apparatus for conducting material transformation processes requiring input of heat for their performance, such as CO2 adsorption, methane pyrolysis for hydrogen and carbon production, hydrogen-assisted conversion of CO2 to hydrocarbons, including catalytic conversion of CO2 to olefins, catalytic conversion of CO2 to propane (liquefied petroleum gas), and catalytic conversion of CO2 to renewable natural gas, reverse water gas shift reaction, steam ethane cracking, propane cracking, steam methane reforming, and dry methane reforming.

The invention discloses a supported nickel catalyst for preparing 1, 3-propylene glycol through hydrogenation of 3-hydroxypropionaldehyde as well as a preparation method and application of the supported nickel catalyst, and relates to the technical field of catalysts. The modified long-chain multi-carbon inducer is used, and a special long-chain molecular structure and a branched chain group of the inducer can effectively and selectively adsorb and occupy a micropore impregnation site; the preparation method has the beneficial effects that more active component nickel species are obviously promoted to be dispersed in main reaction confinement spaces such as mesopores and macropores and interact with the carrier to form effective active sites, and active component steeping liquor is inhibited from entering micropore channels due to capillary action; the active site failure caused by agglomeration of nickel species in micropores in the subsequent drying and roasting process of the catalyst precursor is avoided, the efficient and directional reaction is ensured, the generation of by-products is greatly reduced, the pressure is relieved for the subsequent product rectification separation, and the final product purity is improved. The catalyst provided by the invention can still keep an excellent catalytic effect when the air speed of a 3-hydroxypropionaldehyde solution is increased to 6.5 h <-1 >.

The invention relates to the technical field of molecular sieves, in particular to a catalyst hydrogen type H-ZSM-5 molecular sieve for cyclohexanol preparation through cyclohexene hydration as well as a preparation method and application of the catalyst hydrogen type H-ZSM-5 molecular sieve. The molecular sieve is based on organic amine as a template agent, a ZSM-5 molecular sieve is prepared through boron isomorphous substitution, sodium ion is exchanged into protons through acid exchange, meanwhile, boron is removed, the hydrogen type H-ZSM-5 molecular sieve with the acid property is prepared, and the hydrogen type H-ZSM-5 molecular sieve serves as a catalyst to be used for a reaction for preparing cyclohexanol through cyclohexene hydration. The method comprises the following steps: adding a boron-containing reagent into synthetic gel for preparing a ZSM-5 molecular sieve for preparing cyclohexanol by hydrating cyclohexene, synthesizing the ZSM-5 molecular sieve by adopting a hydrothermal crystallization method, removing an organic template agent through programmed roasting, exchanging boron and sodium in an acid exchange process, and filtering and washing to obtain the hydrogen-type H-ZSM-5 molecular sieve. The obtained hydrogen type H-ZSM-5 molecular sieve is used as a catalyst for a reaction of preparing cyclohexanol by cyclohexene hydration, so that the yield of cyclohexanol reaches about 11.5%.

The present application relates to a phosphorus-aluminum sol, a preparation method therefor, and a use thereof as a binder in a hydrocarbon oil conversion catalyst. The present application also relates to a hydrocarbon oil conversion catalyst, a preparation method therefor, and a hydrocarbon oil catalytic conversion method using the catalyst. The phosphorus-aluminum sol provided by the present application has an appropriate colloidal particle size, a high degree of polymerization, high stability, and good adhesion, when used in a catalyst containing a molecular sieve, such as an FCC catalyst, the phosphorus-aluminum sol can reduce the blockage of molecular sieve pores, and when synergizing with other matrix materials in the catalyst, the phosphorus-aluminum sol can improve hydrothermal stability, catalytic performance and mechanical strength of the catalyst.

The invention discloses a Pt-loaded hierarchical pore HY molecular sieve double-effect catalyst and a preparation method and application thereof.The preparation method comprises the steps that firstly, an acid solution and an HY molecular sieve are mixed, heated and stirred, and the hierarchical pore HY molecular sieve is obtained; then, Pt salt is loaded on the hierarchical pore HY molecular sieve through an impregnation method, and the hierarchical pore HY molecular sieve is dried, calcined and then reduced. The concentration of the acid solution is not higher than 0.1 mol / L; the catalyst is used for hydrocracking of polyethylene or polypropylene. According to the Pt-loaded hierarchical pore HY molecular sieve double-effect catalyst disclosed by the invention, Pt atoms have excellent C-H bond activation capability, meanwhile, the hierarchical pore HY molecular sieve carrier has an open connection mesoporous structure and an acid site, and the mesoporous structure constructed by acid pickling and dealumination is beneficial to diffusion of a reaction intermediate and improvement of the yield of a liquid product; more orifice acid can be exposed by surface erosion, so that the initial cracking of reaction raw materials is facilitated, and the catalytic performance is improved.

Methods for upgrading heavy aromatic waste streams, such as polystyrene, to chemical feedstocks are disclosed. The process involves feeding waste streams to a first pyrolysis zone followed by hydrogenation. The hydrogenation effluent is processed to recover ethylene, propylene, benzene, ethylbenzene, or their precursors. Optionally, the effluents are separated into light and heavy streams. The light stream from the first pyrolysis effluent is sent to hydrogenation, while the heavy stream is either removed, recycled to the first pyrolysis zone, or fed to a second pyrolysis zone. The light stream from the hydrogenation effluent is processed to recover the same chemicals, and the heavy stream is similarly managed. If present, the second pyrolysis effluent is separated into light and heavy streams, with the light stream processed to recover chemicals and the heavy stream managed as before.

The invention discloses a metal particle Ni supported catalyst based on fly ash. The preparation method comprises the following steps: firstly, carrying out alkali fusion on fly ash to prepare powder; dissolving the powder and Ni (NO3) 2.6 H2O in a mixed solution of distilled water and absolute ethyl alcohol, adding polyethylene glycol, and performing ultrasonic stirring to obtain uniform dispersion liquid; and finally, continuously performing ultrasonic stirring on the dispersion liquid, performing hydrothermal reaction, cooling, performing centrifugal separation, drying, calcining, cooling and grinding to obtain the catalyst. The coal ash derivative zeolite is adopted as a carrier of the catalyst, Ni is loaded on the carrier to improve the specific surface and effective active sites of the carrier, the effective catalytic specific surface area of the catalyst is effectively improved, and the catalytic activity is improved, so that a stable and safe catalyst material for preparing methane through CO2 hydrogenation with high activity and selectivity is obtained; the space time yield of methane is high.

The application provides a method for grading diesel deep hydrodesulfurization catalysts, which comprises the following steps: loading catalysts containing AlPO4-5 phosphorus aluminum molecular sieves and catalysts containing ETS-10 titanium silicon molecular sieves in the upper and lower parts of a fixed bed hydrogenation reactor respectively according to a loading mass ratio of 1:3-3:1, so that diesel is subjected to hydrodesulfurization reaction through catalysts containing AlPO4-5 phosphorus aluminum molecular sieves first and then through catalysts containing ETS-10 titanium silicon molecular sieves; the carrier of the catalysts containing AlPO4-5 phosphorus aluminum molecular sieves comprises AlPO4-5 phosphorus aluminum molecular sieves and aluminum oxide powder, the carrier of the catalysts containing ETS-10 titanium silicon molecular sieves comprises ETS-10 titanium silicon molecular sieves and aluminum oxide powder, and the active components of the two kinds of catalysts respectively comprise a combination of two or three of nickel oxide, molybdenum oxide and cobalt oxide. The sulfur content of the hydrogenated diesel obtained through the method can be as low as 10 μg / g or below.

The invention discloses a preparation method of a mesoporous Zn-ZSM-5 molecular sieve for preparing aromatic hydrocarbon from methanol, and belongs to the technical field of synthesis of inorganic materials. Aiming at the problems that a conventional mesoporous Zn / ZSM-5 molecular sieve catalyst Zn blocks orifices, the mesoporous structure is disordered, the molecular sieve solid yield is low, a molecular sieve framework is seriously damaged and the like, the preparation method comprises the following steps: uniformly mixing zinc gluconate with an aluminum source, a silicon source and a template agent, putting the mixture into a closed reaction container, carrying out hydrothermal crystallization, and sequentially washing, drying and roasting to obtain the mesoporous Zn / ZSM-5 molecular sieve catalyst. The sodium type molecular sieve is obtained; the preparation method comprises the following steps: carrying out multiple ion exchange on a sodium type molecular sieve by using an ammonium chloride solution, and sequentially carrying out suction filtration, washing, drying and roasting to obtain the mesoporous Zn-ZSM-5 molecular sieve. According to the preparation method of the methanol-to-aromatic hydrocarbon Zn / ZSM-5 molecular sieve provided by the invention, the obtained molecular sieve is used in the methanol-to-aromatic hydrocarbon process, and has the characteristics of high carbon deposition resistance, high aromatic hydrocarbon selectivity, low Zn wastage rate and the like.

The invention discloses a Fe-Beta molecular sieve for N2O catalytic decomposition and a preparation method of the Fe-Beta molecular sieve. According to the method, chitosan and metal Fe < 3 + > ions are complexed to form a chitosan Fe < 3 + > complex, and then the complex, a silicon source, an aluminum source and a template agent are used as raw materials to prepare the Fe-Beta molecular sieve in one step through a hydrothermal method. Hydroxyl, amino and other groups rich in a chitosan molecular chain can effectively complex metal Fe < 3 + > ions to form a stable chitosan Fe < 3 + > complex, and the stable chitosan Fe < 3 + > complex is used as a Fe source to realize uniform dispersion of Fe species in the molecular sieve and effectively reduce formation of FexOy clusters and Fe2O3 nanoparticles, so that the N2O decomposition catalytic performance of the Fe-Beta molecular sieve is improved. Inorganic alkali metal ions are not introduced, so that a large amount of ammonia-nitrogen wastewater generated in a subsequent tedious ammonium exchange process can be avoided, the synthesis period is effectively shortened, and energy consumption, material consumption and environmental pollution are reduced.

The invention provides a Pt-Sn bimetallic catalyst and a preparation method and application thereof.The preparation method comprises the steps that 1, a Y molecular sieve is placed in a mixed solution of KOH and methyl alcohol, centrifugation and washing are conducted till the Y molecular sieve is neutral after stirring, drying and roasting are conducted, and a non-acid KY molecular sieve is obtained; the silica-alumina ratio of the Y molecular sieve is 3-100; 2) taking the non-acidic KY molecular sieve as a carrier, and loading Sn by adopting an atomic layer deposition technology to obtain a Sn-modified non-acidic KY molecular sieve; and 3) loading Pt by using the Sn-modified non-acidic KY molecular sieve as a carrier and adopting an atomic layer deposition technology to obtain the Pt-Sn bimetallic catalyst. According to the preparation method provided by the invention, spatial distribution of Pt and Sn is accurately regulated and controlled by combining an atomic layer deposition technology, so that the electronic state of Pt species is adjusted, alkane is promoted to be dehydrogenated into an olefin intermediate, and the aromatization catalytic activity and the aromatic hydrocarbon selectivity of alkane are improved.

The invention discloses a method for performing tar steam reforming by coupling low-temperature plasma with a nickel-loaded hydrogen type molecular sieve composite catalyst. The method comprises the following steps: preparing the nickel-loaded hydrogen type molecular sieve composite catalyst; the mass of Ni in the nickel-loaded hydrogen type molecular sieve composite catalyst accounts for 5-30% of the mass of the catalyst; introducing tar and water vapor into a dielectric barrier discharge plasma reactor filled with the nickel-loaded hydrogen type molecular sieve composite catalyst; starting the dielectric barrier discharge plasma reactor, and carrying out a tar steam reforming reaction; wherein the temperature of the tar steam reforming reaction is 150-525 DEG C, and the power of the tar steam reforming reaction is 30-90 W. The catalyst disclosed by the invention is coupled with a low-temperature plasma technology, so that good tar reforming performance, target product selectivity and system stability are realized.

The invention discloses a monatomic catalyst capable of retaining surface defects of a catalyst as well as a preparation method and application of the monatomic catalyst, and belongs to the field of catalysis. The monatomic catalyst comprises an active metal component, a doping element and a carrier, the carrier is a semiconductor material rich in surface defects. The preparation method adopts a light-induced migration-conversion strategy. The monatomic catalyst which is obtained by the preparation method and retains the surface defects of the semiconductor material is applied to the fields of photocatalysis, thermocatalysis and electrocatalysis, and shows excellent performance.

The invention discloses a cracking dechlorination catalyst as well as a preparation method and application thereof. The cracking dechlorination catalyst comprises zeolite, an adsorbent and a carrier, the zeolite is selected from at least one of an MFI structure, an FAU structure and an MEL structure; the adsorbent is selected from at least one of metal oxide and carbonate; and the carrier is selected from one of a carbon material and carbide. The invention provides a catalyst for one-step catalytic cracking-dechlorination of waste plastics, which can realize oil recovery and chlorine impurity removal in one step in catalytic cracking of chlorine-containing waste plastics.

The invention discloses a catalyst for catalyzing ethane to prepare ethylene or an oxygen-containing compound as well as a preparation method and application of the catalyst, and belongs to the field of catalysts. On the basis of ERB-1 and MCM-22, a large number of hydroxyl structures are formed through post-treatment of nitric acid or ammonium nitrate; a titanium source and molecular sieve silicon hydroxyl are subjected to a dehydrohalogenation reaction in a titanium halide gas form to form a Ti-O-Si bond, so that titanium successfully enters a molecular sieve framework and is uniformly distributed. Au or Pd is anchored by a framework Ti, Au or Pd is loaded by using a deposition-precipitation method, and the introduced Ti species can provide a better environment for further dispersing Au or Pd by changing isoelectric points on the surface of a molecular sieve carrier, so that the size of Au or Pd nanoparticles is controlled; secondly, due to the high specific surface area of the MWW molecular sieve, the gold precursor can be effectively dispersed, and agglomeration is inhibited; compared with an MWW molecular sieve of pure Si, Au or Pd nanoparticles can be dispersed and anchored by introducing a framework Ti, so that an Au and Pd-based catalyst which is about 2nm in size and good in dispersion is prepared.

Transalkylation processes using catalysts comprising three dimensional 12 membered ring zeolites with a combination of small and large pores are described. These catalysts have increased conversion of alkylphenols to phenol, cresols, and alkylbenzenes from coal-derived liquid streams compared to catalysts consisting of HZSM-5 zeolite.

The invention relates to the technical field of catalysts, in particular to a plasma silver nanocluster coated mesoporous molecular sieve TS-1 photocatalyst as well as a preparation method and application thereof. The preparation method comprises the following steps: 1, synthesizing mesoporous molecular sieve TS-1 powder; and 2, mixing the mesoporous molecular sieve TS-1 and CH3OH to prepare a suspension, injecting an AgNO3 aqueous solution into the suspension, and carrying out ultraviolet irradiation, filtration, washing and freeze drying to obtain the plasma silver nanocluster coated mesoporous molecular sieve TS-1 photocatalyst. The obtained electron-rich Ag cluster / mTS-1 shows an Ag-Ag coordination number (CN = 2.0 + / -0.1) lower than that of a mesoporous molecular sieve TS-1 (CN = 2.9 + / -0.2) loaded with Ag nanoparticles, so that the electron-rich Ag cluster / mTS-1 has higher CO2 adsorption and activation performance. In addition, the silver nanoclusters are firmly anchored on the surface of the mesoporous molecular sieve TS-1, so that the mesoporous molecular sieve TS-1 has high stability, and therefore, the mesoporous molecular sieve TS-1 shows high-stability CO2-to-CO photocatalytic conversion activity under simulated sunlight irradiation, and the yield of CO within 4 hours is 350 [mu] mol g <-1 >.

The invention discloses a platinum-tungsten bimetallic catalyst for PET depolymerization and a method for directional depolymerization of PET by the platinum-tungsten bimetallic catalyst, and belongs to the technical field of solid waste recycling, the platinum-tungsten bimetallic catalyst for PET depolymerization is prepared by a deposition-precipitation method, a mesoporous molecular sieve MCM-48 is used as a carrier to load platinum-tungsten bimetallic, the molar ratio of platinum to tungsten is 1: (0.5-2), the molecular sieve MCM-48 is a mesoporous molecular sieve MCM-48, and the mesoporous molecular sieve MCM-48 is a mesoporous molecular sieve MCM-48 carrier. And the platinum loading capacity is 4-6 wt%. By utilizing the platinum-tungsten bimetallic catalyst, one-pot depolymerization of PET can be realized to prepare p-toluic acid and p-xylene, the platinum-tungsten bimetallic catalyst can be used for multiple times through reduction regeneration, the catalytic activity is high, and the PET depolymerization method under catalysis of the platinum-tungsten bimetallic catalyst is suitable for recycling and upgrading of PET wastes in various forms and has wide application prospects. The technical problems of efficient depolymerization and directional conversion of the waste PET are solved, and a sustainable technical path is provided for resource recycling of the PET.

The invention relates to the technical field of SCR denitration catalyst preparation, in particular to a denitration and dioxin removal core-shell structure catalyst and a preparation method thereof.The denitration and dioxin removal core-shell structure catalyst comprises 50-65 wt% of a core layer, 25-35 wt% of a shell layer and 5-15 wt% of an auxiliary layer, and the core layer is CeMoLaSnOx microspheres; the shell layer is a porous SiO2-TiO2 (at) ZSM-5 composite carrier; and the auxiliary agent layer is a Fe-Co-Ni-Y oxide. The prepared denitration and dioxin removal core-shell structure catalyst has good sulfur resistance and water poisoning resistance, effectively overcomes the defects that a traditional denitration catalyst is poor in low-temperature activity, prone to sulfur poisoning, low in dioxin degradation efficiency and the like, and can be widely applied to collaborative purification of low-temperature flue gas generated in waste incineration, steel sintering and the like.

The invention provides a preparation method of a catalyst for preparing glycollic acid by oxidizing ethylene glycol, which comprises the following steps: impregnating a carrier in an impregnation liquid containing active metal salt, auxiliary metal salt and a polyhydroxy compound in equal volume, drying, roasting and reducing to obtain the catalyst for preparing glycollic acid by oxidizing ethylene glycol, wherein the active metal salt is selected from Pt salt and Pd salt, or Pt salt and Ru salt; the auxiliary metal salts are selected from any two of Sn, Ce, Ga, Bi, La, Mn and Rb salts; the carrier is a mixture of a mesoporous molecular sieve and an amorphous inorganic porous material. The catalyst prepared by the method can be used for preparing glycollic acid by high-activity and high-selectivity oxidation of ethylene glycol under mild, green and alkali-free conditions under the condition of low catalyst dosage.

The invention discloses a catalyst for catalytic synthesis of 2, 5-furandicarboxylic acid as well as a preparation method and application of the catalyst, and the preparation method of the catalyst comprises the following steps: (1) obtaining a molecular sieve modified by nitrogen species as a catalyst carrier; and (2) mixing transition metal salt with the molecular sieve modified by nitrogen species, and roasting at high temperature to obtain the transition metal oxide catalyst coated with the nitrogen modified molecular sieve. The 2, 5-furandicarboxylic acid is prepared by using 5-hydroxymethylfurfural as a raw material and using the catalyst for catalytic oxidation in a containing atmosphere, the method is simple to operate and mild in condition, the catalyst has high stability and good reusability, and the production process of the 2, 5-furandicarboxylic acid is economical and environment-friendly.

The invention relates to the field of biomass energy and chemical industry, in particular to an efficient methanol preparation method based on biomass graded catalytic conversion and cycle coupling. The method comprises the following steps: in a graded catalytic oxidation reaction system, mixing a biomass raw material with a composite vanadium-based catalyst, water, oxygen and circulating methanol for reaction to generate a gas-liquid mixture containing methyl formate; recycling methyl formate by using a gradient variable-pressure rectification separation system; carrying out an interface hydrogenation reaction under the action of a copper-zinc-LTA hierarchical pore catalyst to generate methanol; finally, part of methanol is purified and recycled through membrane separation. The method realizes efficient conversion from biomass to methanol, has the advantages of mild reaction conditions, low energy consumption, high yield and good catalyst stability, and opens up a new path for industrialization of preparation of methanol from biomass.

The invention discloses a shape-selective isomerization catalyst as well as a preparation method and application thereof. The catalyst comprises a ten-membered ring aluminum phosphate molecular sieve, a noble metal active component and a metal oxide auxiliary active component. The ten-membered ring aluminum phosphate molecule is selected from at least one of SAPO-11, MeAPO-11, SAPO-41 and MeAPO-41, and the ten-membered ring aluminum phosphate molecule is selected from at least one of SAPO-11, the noble metal active component is selected from at least one of Pt and Pd; the metal oxide auxiliary agent is selected from at least one of CeO2, Nb2O5 and Ta2O5. Compared with the catalyst prepared in the prior art, the catalyst prepared by the method provided by the invention has higher activity and isomer yield in the isomerization reaction of long-chain n-alkanes.

The invention discloses two aluminosilicate molecular sieves with super-macroporous structures, the synthetic state schematic chemical composition of the molecular sieves is rROH: a (OH <-> or F <->): xAl2O3: SiO2: wH2O, the schematic chemical composition of the molecular sieves after roasting is (HAlO2) x.SiO2, the molecular sieves are NJU120-1, and after roasting of the NJU120-1, the molecular sieves have the molecular weight of 250,000-350,000. A framework structure composed of a T (Si, Al) O4 tetrahedron has a 22 * 10 * 10 membered ring three-dimensional pore channel system, the molecular sieve is NJU120-2, and after the NJU120-2 is roasted, the framework structure composed of the T (Si, Al) O4 tetrahedron has a 22 * 12 * 10 membered ring three-dimensional pore channel system. The preparation method is reasonable in design, is a novel germanium-free, high-silicon or pure-silicon and fully-connected super-macroporous molecular sieve material, not only has very important practical application value in the fields of catalysis, adsorption separation and the like, but also has very important theoretical significance for enriching molecular sieve structure families.

The invention discloses a preparation method and application of a monatomic catalyst for catalytic degradation of ethanethiol, and belongs to the technical field of organic sulfur pollutant treatment.The atomic-scale dispersion of Ce species is achieved through HY molecular sieve FAU type topological structure constraint and cerium loading capacity limitation, the catalyst shows atomic-scale active sites, and the catalytic degradation of ethanethiol is achieved. The conversion path of ethanethiol can be accurately regulated and controlled, and efficient degradation of ethanethiol is realized; the topological confinement effect guarantees the stability of the monatomic catalyst, and the HY molecular sieve pore channel restrains migration of Ce atoms and inhibits agglomeration of Ce metal, so that the monatomic catalyst shows good anti-sintering ability, and at the same time, sulfur poisoning and carbon deposition rate are slowed down.

The invention discloses a preparation method of an in-situ nano manganese dioxide and zeolite composite material and application of the composite material in removal of metal ions and micropollutants in water, and belongs to the field of drinking water source water treatment. The preparation method of the in-situ nano manganese dioxide and zeolite composite material comprises the following steps: 1, pretreating natural zeolite; 2, preparing acid-treated zeolite; and 3, preparing the in-situ nano manganese dioxide and zeolite composite material. According to the invention, an impregnation-calcination method is adopted, MnO2 is loaded in situ on the pore channels and the surface of the acid-treated zeolite, and uniform growth of nanometer and sub-nanometer layered manganese dioxide is realized based on the nanometer pore channel structure of the zeolite. According to the structure, the reactivity of various oxidants represented by monopersulfate is stimulated, macromolecules and background substances with the same electric property are excluded through the confinement effect, interference of non-target objects on the oxidation process is reduced, and a new thought and technical support are provided for solving the problem of combined pollution of drinking water.