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GB924938A - Process for preparing synthetic crystalline zeolites - Google Patents

Process for preparing synthetic crystalline zeolites

Info

Publication number
GB924938A
GB924938A GB2587060A GB2587060A GB924938A GB 924938 A GB924938 A GB 924938A GB 2587060 A GB2587060 A GB 2587060A GB 2587060 A GB2587060 A GB 2587060A GB 924938 A GB924938 A GB 924938A
Authority
GB
United Kingdom
Prior art keywords
zeolite
hours
calcined
parts
calcination
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
GB2587060A
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.)
WR Grace and Co
Original Assignee
WR Grace and Co
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
Application filed by WR Grace and Co filed Critical WR Grace and Co
Publication of GB924938A publication Critical patent/GB924938A/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
    • C01B33/2838Zeolitic 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 faujasite type, or type X or Y (UNION CARBIDE trade names; correspond to GRACE's types Z-14 and Z-14HS, respectively)
    • C01B33/2846Zeolitic 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 faujasite type, or type X or Y (UNION CARBIDE trade names; correspond to GRACE's types Z-14 and Z-14HS, respectively) of type X

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

A synthetic crystalline zeolite, the same as that designated zeolite X in Specification 777,233, is prepared by ageing a calcined kaolinitic clay in an aqueous solution of sodium hydroxide and hydrous silica and thereafter heating the solution at 50 DEG C. to the boiling point to produce the zeolite, the weight ratio of the reactant, at least during the heating step being 9-20 parts H2O, 0,2-0,4 parts SiO2 and 0,9-2 parts Na2O per part of calcined clay. Calcination may be effected at 500 DEG -800 DEG C. for 1-18 hours and the ageing may be effected at 20 DEG -40 DEG C. The term "hydrous silica" includes in this context sodium silicate, and this is the preferred reactant. According to Example (1) kaolin calcined at 700 DEG C. for 2 hours was aged as a slurry in of sodium hydroxide and silicate at 25 DEG C. for 72 hours after which it was refluxed at 100 DEG C. for 10 hours and the zeolite recovered by filtering and washing. Further Examples 2, 4, 5 and 6 exemplify the effect of calcination timer and temperatures, whilst Example 7 exemplifies the use of calcined halloysite. Example 3 is comparative, the aging step being omitted and the product being sodalite. Ion exchanged forms of the zeolite X may be obtained by conventional means.
GB2587060A 1959-11-04 1960-07-25 Process for preparing synthetic crystalline zeolites Expired GB924938A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US85075759A 1959-11-04 1959-11-04

Publications (1)

Publication Number Publication Date
GB924938A true GB924938A (en) 1963-05-01

Family

ID=25309028

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2587060A Expired GB924938A (en) 1959-11-04 1960-07-25 Process for preparing synthetic crystalline zeolites

Country Status (1)

Country Link
GB (1) GB924938A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105967196A (en) * 2016-05-05 2016-09-28 江西理工大学 Method for synthesis of sodalite from kaolinite

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105967196A (en) * 2016-05-05 2016-09-28 江西理工大学 Method for synthesis of sodalite from kaolinite

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