GB983395A - A method of producing molecular sieve bodies - Google Patents

A method of producing molecular sieve bodies

Info

Publication number
GB983395A
GB983395A GB3395161A GB3395161A GB983395A GB 983395 A GB983395 A GB 983395A GB 3395161 A GB3395161 A GB 3395161A GB 3395161 A GB3395161 A GB 3395161A GB 983395 A GB983395 A GB 983395A
Authority
GB
United Kingdom
Prior art keywords
kaolin
zeolite
alkali metal
shaping
silica
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3395161A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US58199A external-priority patent/US3119659A/en
Priority claimed from US58200A external-priority patent/US3119660A/en
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB983395A publication Critical patent/GB983395A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/20Silicates
    • C01B33/26Aluminium-containing silicates, i.e. silico-aluminates
    • C01B33/28Base exchange silicates, e.g. zeolites
    • C01B33/2807Zeolitic silicoaluminates with a tridimensional crystalline structure possessing molecular sieve properties; Isomorphous compounds wherein a part of the aluminium ore of the silicon present may be replaced by other elements such as gallium, germanium, phosphorus; Preparation of zeolitic molecular sieves from molecular sieves of another type or from preformed reacting mixtures
    • C01B33/2815Zeolitic silicoaluminates with a tridimensional crystalline structure possessing molecular sieve properties; Isomorphous compounds wherein a part of the aluminium ore of the silicon present may be replaced by other elements such as gallium, germanium, phosphorus; Preparation of zeolitic molecular sieves from molecular sieves of another type or from preformed reacting mixtures of type A (UNION CARBIDE trade name; corresponds to GRACE's types Z-12 or Z-12L)
    • 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
    • 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

Abstract

A crystalline zeolitic molecular sieve is produced by shaping acturated kaolin-type clay into a preformed body which is reacted as part of an aqueous reactant system until crystals of zeolitic molecular sieve are produced in the body. The aqueous reactant system contains in the aggregate, water and oxide of aluminium, silicon and alkali metal in the proportions required to form crystals of the desired zeolitic molecular sieve. Reference is made to the production of synthetic zeolites X, Y, L, D, T, R, A. The kaolin-type clay is actuated by thermal treatment at a temperature between 550-850 DEG C., before or after shaping. Bodies may be shaped from mixtures of raw kaolin and at least 10% reactive kaolin and subsequently fired for at least one hour to make them reactive. The shaping and forming step may be accomplished by moulding, extruding, tumbling, drum-rolling, casting, slip-casting, disc-forming, belt-forming, prilling, tableting and briquetting. Certain materials may be combined with the kaolin-type substance prior to shaping. For example, in the production of silica rich zeolites, silica in the form of colloidal silica solution, silica gel, silicic acid and alkali metal silicates may be included in the mixture to be shaped. It is easier to incorporate the silica when small amounts of organic gelling or thickening agents are used in the mixture to be shaped. Resins of the water-soluble ethylene oxide type are especially useful, when these are added, a heating step at 200-700 DEG C. is conducted after shaping to wholly or partly carbonize the resin in the shaped body. Alumina over and above that supplied by the reactive kaolin can be added by incorporating aluminium trihydrate, activated alumina, gamma alumina or alkali metal aluminate in the kaolin material prior to shaping. Alkali metal hydroxide in amounts of at least 0.1 mol. of alkali metal oxide per mol. of silica may also be incorporated in the kaolin material prior to shaping. Incorporation of 1.30% of combustible diluents in the raw kaolin-type materials improves the purity of the zeolitic body and forms macroporis. Diluents which can be used are sawdust, powdered carbon, lamp black, powdered coke, methyl or ethyl cellulose or other organic resins, wood flour and starch. After the forming or shaping step the bodies are dried so that the moisture content is less than 30 weight per cent. Digestion and crystallization of the shaped body may now be accomplished by treating the reaction system in a single step or in two separate steps. The first step takes place at a temperature of from room temperature to 55 DEG C. for 3-80 hours. In the second step, which need not of necessity employ a reaction mixture of the same composition as that used in the first step, the reaction temperature is preferably maintained between 75-175 DEG C. for 1-40 hours until crystals of the desired product form in situ. The aqueous reactant system, made up of the ambient liquid and the shaped body have on an aggregate an initial overall composition defined in terms of oxide-mol. ratios as follows: M2O/SiO2 = a SiO2/Al2O3 = b H2O/M2O = c. The ambient liquor contains proportions of silica and alumina, added in the form of materials specified above, and alkali metal oxide, in amounts needed to achieve the overall initial reactant composition, e.g. for sodium zeolite if M = Na a = 0.5-1.5 b = 1.0-2.5 c = 10-100. In the preparation of silica rich zeolite shapes having an SiO2/Al2O3 ratio greater than 3, e.g. sodium zeolite 7, the product purity can be improved by first contacting reactive kaolin powder with 0.1-5 mols. per mol. of alumina of a suitable aqueous reactant, e.g. a water-soluble alkali metal salt, in a predigestive step. In another aspect of the invention, high purity zeolite bodies are produced from a mixture of finely-divided kaolin-type material, either raw or reactive, and fine crystals of a pure zeolite. In determining the quantity of reactant required to provide the proper values of a, b and c (as defined above), the composition of the added zeolite is not included in the determination. The crystalline zeolite does not need to be the same as the final product, unless alkali metal hydroxides are used to form the shaped objects. The amount of zeolite incorporated in the to be shaped is from 30-80 weight per cent, unless an alkali metal hydroxide is incorporated when the preferred percentage is 5-80 weight per cent. On firing to produce the reactive kaolin, the firing temperature must be adjusted to the thermal stability limit of the particular zeolite. After crystallization, the zeolite bodies are filtered and washed until the effluent wash-water has a pH of between 9-12. Thereafter, the bodies are dried at a temperature between 25-150 DEG C. The zeolite is characterized by X-ray diffraction or adsorption measurements. Specifications 777,232, 777,233, 841,812, 868,846, 909,264, 909,266, 912,936 and 972,831 are referred to.
GB3395161A 1960-09-26 1961-09-22 A method of producing molecular sieve bodies Expired GB983395A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58199A US3119659A (en) 1960-09-26 1960-09-26 Process for producing molecular sieve bodies
US58200A US3119660A (en) 1960-09-26 1960-09-26 Process for producing molecular sieve bodies

Publications (1)

Publication Number Publication Date
GB983395A true GB983395A (en) 1965-02-17

Family

ID=26737346

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3395161A Expired GB983395A (en) 1960-09-26 1961-09-22 A method of producing molecular sieve bodies

Country Status (4)

Country Link
AT (1) AT255383B (en)
BE (1) BE608291A (en)
GB (1) GB983395A (en)
SE (1) SE302954B (en)

Also Published As

Publication number Publication date
BE608291A (en) 1962-01-15
SE302954B (en) 1968-08-12
AT255383B (en) 1967-07-10

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