WO2008066275A1 - Hydrotalcite-zeolite composites and catalysts thereof by nox storage method - Google Patents

Hydrotalcite-zeolite composites and catalysts thereof by nox storage method Download PDF

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Publication number
WO2008066275A1
WO2008066275A1 PCT/KR2007/005810 KR2007005810W WO2008066275A1 WO 2008066275 A1 WO2008066275 A1 WO 2008066275A1 KR 2007005810 W KR2007005810 W KR 2007005810W WO 2008066275 A1 WO2008066275 A1 WO 2008066275A1
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Prior art keywords
zeolite
hydrotalcite
composite
catalyst
nitrogen oxides
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PCT/KR2007/005810
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English (en)
French (fr)
Inventor
Hyun-Sik Han
Gon Seo
Young-San Yoo
Gi-Won Park
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Heesung Catalysts Corporation
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Publication of WO2008066275A1 publication Critical patent/WO2008066275A1/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/92Chemical or biological purification of waste gases of engine exhaust gases
    • B01D53/94Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
    • B01D53/9404Removing only nitrogen compounds
    • B01D53/9409Nitrogen oxides
    • B01D53/9413Processes characterised by a specific catalyst
    • B01D53/9422Processes characterised by a specific catalyst for removing nitrogen oxides by NOx storage or reduction by cyclic switching between lean and rich exhaust gases (LNT, NSC, NSR)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/12Silica and alumina
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/007Mixed salts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/064Crystalline aluminosilicate zeolites; Isomorphous compounds thereof containing iron group metals, noble metals or copper
    • B01J29/068Noble metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/08Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/08Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
    • B01J29/10Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y containing iron group metals, noble metals or copper
    • B01J29/106Y-type faujasite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/08Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
    • B01J29/10Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y containing iron group metals, noble metals or copper
    • B01J29/12Noble metals
    • B01J29/126Y-type faujasite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/18Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
    • B01J29/20Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type containing iron group metals, noble metals or copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/18Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
    • B01J29/20Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type containing iron group metals, noble metals or copper
    • B01J29/22Noble metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/70Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J35/30
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/08Heat treatment
    • B01J37/10Heat treatment in the presence of water, e.g. steam
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00Compounds of aluminium
    • C01F7/78Compounds containing aluminium and two or more other elements, with the exception of oxygen and hydrogen
    • C01F7/784Layered double hydroxide, e.g. comprising nitrate, sulfate or carbonate ions as intercalating anions
    • C01F7/785Hydrotalcite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/20Reductants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/204Alkaline earth metals
    • B01D2255/2047Magnesium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/206Rare earth metals
    • B01D2255/2065Cerium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/207Transition metals
    • B01D2255/20738Iron
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/207Transition metals
    • B01D2255/20746Cobalt
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/207Transition metals
    • B01D2255/20753Nickel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/207Transition metals
    • B01D2255/20761Copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/20Metals or compounds thereof
    • B01D2255/209Other metals
    • B01D2255/2092Aluminium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/50Zeolites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/90Physical characteristics of catalysts
    • B01D2255/91NOx-storage component incorporated in the catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2258/00Sources of waste gases
    • B01D2258/01Engine exhaust gases
    • B01D2258/012Diesel engines and lean burn gasoline engines
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/30After treatment, characterised by the means used
    • B01J2229/42Addition of matrix or binder particles
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/03Particle morphology depicted by an image obtained by SEM
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/12Surface area

Definitions

  • the present invention relates to a hydrotalcite-zeolite composite comprising
  • hydrotalcite substituted with transition metals a method of producing the
  • oxidizing substances such as oxygen, nitrogen
  • urea serving as a reductant, to exhaust gases to reduce the nitrogen oxides
  • This method is a method of removing nitrogen oxides by
  • Rea-SCR urea-selective catalytic reduction
  • ammonia has strong reducing ability and thus can efficiently reduce
  • urea injection apparatus such as a urea injection apparatus, a hydrolysis reactor, a storage apparatus,
  • a social infrastructure such as a sales network for a urea
  • nitrogen oxides are stored in barium oxide supported in alumina,
  • the injected fuel is decomposed into reducing
  • oxides are removed by the injection of fuel, and thus additional facilities for
  • the performance of an NSR catalyst is primarily evaluated by the amount of the
  • the NSR catalyst must have
  • an automobile purification catalyst contain a large amount of water and are
  • SUBSTITUTE SHEET compounds are formed into sulfur dioxide through a combustion process of fuel
  • barium oxide which is a conventional
  • the amount of nitrogen oxides stored in the catalyst is greatly decreased.
  • the storage materials are less poisoned by sulfur dioxide
  • zeolite-hydrotalcite composite which stores nitrogen oxides in pores thereof or between crystal planes thereof in an oxidation atmosphere without forming a nitrate, and desorbs nitrogen dioxide in a reduction atmosphere. Since the zeolite-hydrotalcite composite is used as a material for storing nitrogen dioxide, it is expected that the breaking of the structure of the zeolite-hydrotalcite composite due to the repeated state change will be prevented, and synergistic effect of using the advantages of two kinds of
  • the surface area of the zeolite-hydrotalcite composite measured using a
  • FIG. 1 is a schematic block diagram showing a process of preparing a zeolite-
  • FIG. 2 is a graph showing an X-ray diffraction pattern of zeolite Y, synthesized
  • FIG. 3 is a graph showing an X-ray diffraction pattern of hydrotalcite
  • FIG. 4 is a graph showing X-ray diffraction patterns of a zeolite Y-hydrotalcite
  • FIG. 5 is scanning electron micrographs of the zeolite Y-hydrotalcite composite
  • FIG. 6 is a graph showing nitrogen dioxide temperature-desorption curves of a
  • the present invention provides a method of producing a zeolite-hydrotalcite
  • composite including: preparing a zeolite stock solution and a hydrotalcite stock
  • the present invention provides the method of producing a zeolite-
  • hydrotalcite composite further including: supporting one or more platinum group
  • the zeolite is ANA zeolite, BEA zeolite, MFI zeolite,
  • MOR zeolite or zeolite Y.
  • the hydrotalcite is substituted with a transition metal
  • the hydrothermal reaction is conducted at a
  • the platinum group metal is supported on the zeolite-
  • hydrotalcite composite such that the amount thereof is 0.1 ⁇ 4.0%.
  • the composite of the present invention includes zeolite and hydrotalcite.
  • zeolite stock a zeolite stock
  • the zeolite stock solution and the hydrotalcite stock solution are mixed and then
  • a zeolite precursor solution and a hydrotalcite precursor solution are provided. Therefore, a zeolite precursor solution and a hydrotalcite precursor solution.
  • FIG. 1 schematically
  • hydrotalcite composite in which zeolite and hydrotalcite are simultaneously
  • an NSR catalyst in order to reduce nitrogen dioxide, desorbed in a reducing atmosphere, an NSR catalyst must be supported with precious metals, such as platinum, palladium, rhodium and the like.
  • the NSR catalyst is supported with the precious metals thorough impregnation, coprecipitation or evaporation, calcined, and then reduced. Through this process, the precious metals are supported on the zeolite-hydrotalcite composite, and thus act as active spots for reducing and removing nitrogen dioxide.
  • barium oxide which is chiefly used as a
  • oxides are stored in the zeolite-hydrotalcite composite in a state in which the
  • nitrogen oxides are coordinated with alkali earth metal ions or transition metal
  • zeolite-hydrotalcite composite has excellent durability.
  • hydrotalcite-zeolite composite is defined in
  • hydrotalcite-zeolite composite catalyst For example, HT-NaY(2.0) is a
  • hydrotalcite-zeolite composite in which Na+-containing zeolite Y is mixed with
  • hydrotalcite at a ratio of 2:1. If the hydrotalcite-zeolite composite is substituted
  • the element symbol of the transition metal is additionally
  • Y stock solution prepared by mixing 8.2 g of silica, 9.4 g of sodium hydroxide,
  • the solid product was washed, filtered, and then dried at a
  • FIG. 2 shows
  • Hydrotalcite for storing and removing nitrogen dioxide, present in exhaust gases
  • the yield of the synthesized hydrotalcite was 87% based on alumina
  • FIG. 3 shows the X-ray diffraction
  • Zeolite Y-hydrotalcite composites were prepared by mixing the zeolite Y stock
  • Example 2 hydrothermally reacting the mixed solution. Specifically,
  • zeolite Y-hydrotalcite composites (HT-NaY(0.5) and HT-NaY(2.0)
  • FIG. 4 shows X-ray
  • hydrotalcite appeared at diffraction angles of 1 L7°and 23.2°and diffraction
  • FIG. 5 shows the shapes of the prepared zeolite Y-hydrotalcite composites
  • hydrotalcite (Example 2) is much smaller than that of the zeolite Y (Example 1 ).
  • BET Brunauer-Emmett-Telle
  • zeolite Y-hydrotalcite composites is a composite of zeolite Y and hydrotalcite.
  • NaY(LO) composite was calcined in an electric furnace at a temperature of
  • zeolite Y composite was measured using a weight type adsorber.
  • An analcime zeolite-hydrotalcite composite was prepared using an analcime
  • zeolite stock solution a hydrotalcite stock solution was prepared using
  • hydrotalcite appeared weak at diffraction angles of 11.7°, 23.2°, 34.8°and
  • hydrotalcite composite has micropores, each of which is formed of a ring of
  • a mordenite zeolite-hydrotalcite composite was prepared by mixing a mordenite

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Geology (AREA)
  • Combustion & Propulsion (AREA)
  • Biomedical Technology (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Catalysts (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
PCT/KR2007/005810 2006-11-29 2007-11-19 Hydrotalcite-zeolite composites and catalysts thereof by nox storage method WO2008066275A1 (en)

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KR1020060118939A KR100827788B1 (ko) 2006-11-29 2006-11-29 하이드로탈사이트-제올라이트 복합체 및 이를 이용한 질소산화물 흡장형 촉매
KR10-2006-0118939 2006-11-29

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Cited By (11)

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ES2341637A1 (es) * 2008-12-22 2010-06-23 Consejo Superior De Investigaciones Cientificas (Csic) Materiales composites micro- y nano-estructurados basados en hidroxidos dobles laminares de tipo hidrotalcita y silicatos de la famili de las arcillas.
GB2483801A (en) * 2010-09-17 2012-03-21 Magnesium Elektron Ltd Synthetic hydrotalcite
CN102049262B (zh) * 2009-10-28 2013-01-02 中国石油化工股份有限公司 一种清洁型co耐硫变换催化剂的制备方法
JP2016107262A (ja) * 2014-11-27 2016-06-20 国立大学法人佐賀大学 エンドトキシン及び/又はサイトカインの吸着体及びその製造方法、これを配合した皮膚外用製剤及び経口投与用製剤、並びにエンドトキシン及び/又はサイトカインの吸着除去方法
JP2016120488A (ja) * 2014-12-24 2016-07-07 国立大学法人佐賀大学 有害気相物質の除去のための吸着体及びその製造方法、有害気相物質除去材、並びに有害気相物質の除去方法
CN109833861A (zh) * 2017-11-28 2019-06-04 中国石油天然气股份有限公司 硅胶载体的改性制备方法
CN109833857A (zh) * 2017-11-28 2019-06-04 中国石油天然气股份有限公司 一种烯烃催化用载体硅胶的制备方法
CN109833860A (zh) * 2017-11-28 2019-06-04 中国石油天然气股份有限公司 一种硅胶载体的制备方法
CN114768754A (zh) * 2022-04-29 2022-07-22 福州城建设计研究院有限公司 一种吸附选择性的Mg/Al层状双金属氢氧化物成型吸附颗粒的制备、再生方法和应用
CN115845907A (zh) * 2022-12-16 2023-03-28 四川大学 一种低温scr催化剂及其制备方法和应用
CN114768754B (zh) * 2022-04-29 2024-05-14 福州城建设计研究院有限公司 一种吸附选择性的Mg/Al层状双金属氢氧化物成型吸附颗粒的制备、再生方法和应用

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KR101011830B1 (ko) * 2009-09-30 2011-01-31 상명대학교 산학협력단 질소산화물 분해용 혼합금속산화물 촉매
CN109833917B (zh) * 2017-11-28 2022-02-01 中国石油天然气股份有限公司 一种催化剂负载用硅胶载体的制备方法
CN113713838B (zh) * 2021-11-04 2022-01-04 中汽研(天津)汽车工程研究院有限公司 一种柴油车用整体式氧化型催化剂的制备方法

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