GB1035644A - Improvements relating to the preparation of synthetic crystalline zeolites - Google Patents

Improvements relating to the preparation of synthetic crystalline zeolites

Info

Publication number
GB1035644A
GB1035644A GB4567262A GB4567262A GB1035644A GB 1035644 A GB1035644 A GB 1035644A GB 4567262 A GB4567262 A GB 4567262A GB 4567262 A GB4567262 A GB 4567262A GB 1035644 A GB1035644 A GB 1035644A
Authority
GB
United Kingdom
Prior art keywords
na2o
al2o3
pore size
zeolite
preparation
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
GB4567262A
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 GB1035644A publication Critical patent/GB1035644A/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)

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 zeolite of formula Na2O.Al2O3.2SiO2.nH2O (where n is 0-8) and pore size 4.5 <\>rA, designated Z-12L-Na, is prepared by ageing a reaction mixture, of composition such that Na2O/Al2O3 is 0.84 to 3.1, SiO2/Al2O3 is 0.88 to 1.8, and H2O/Na2O is 6.4 to 25, at 20-60 DEG C. for at least 2 hours (up to e.g. 72 hrs.), then heating at elevated temperatures, e.g. at 50-120 DEG C., until the zeolite crystallizes and is recovered. Material used may be a mixture of the oxides Na2O, Al2O3, SiO2 and H2O, or of materials whose compositions are mixtures of such, e.g. sodium silicate, sodium aluminate, or alumina; or may be clay, e.g. kaolin or halloysite, precalcined at 500-900 DEG C. for 2-18 hrs. and treated with NaOH solution containing 3.8 to 13.5% Na2O such that there are 0.7 to 2.6 parts calcined clay and 6.4 to 25 parts H2O per part Na2O. The wet zeolite may be activated by heating at 350 DEG C. for a few hours, or converted to Z-12L-Ca, of pore size 5.5 <\>rA, by treating with CaCl2. The preparation of Z-12-Na, of pore size 4 <\>rA, is also described, in which the ageing step is omitted. The two Na zeolites have similar X-ray diffraction patterns, but Z-12L-Na will absorb CHClF2 (molecular diameter 4.0 <\>rA) whereas Z-12-Na will not.
GB4567262A 1961-12-12 1962-12-03 Improvements relating to the preparation of synthetic crystalline zeolites Expired GB1035644A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15889561A 1961-12-12 1961-12-12

Publications (1)

Publication Number Publication Date
GB1035644A true GB1035644A (en) 1966-07-13

Family

ID=22570183

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4567262A Expired GB1035644A (en) 1961-12-12 1962-12-03 Improvements relating to the preparation of synthetic crystalline zeolites

Country Status (1)

Country Link
GB (1) GB1035644A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4606899A (en) * 1985-03-27 1986-08-19 Air Products And Chemicals, Inc. Synthesis of maximum aluminum X zeolites
WO2013151070A1 (en) * 2012-04-03 2013-10-10 旭硝子株式会社 Method for purifying fluoroolefin, and method for producing fluoroolefin
JP2013241390A (en) * 2012-04-27 2013-12-05 Asahi Glass Co Ltd Method for purifying fluoroolefin, and method for producing fluoroolefin
JP2013241389A (en) * 2012-04-25 2013-12-05 Asahi Glass Co Ltd Method for drying fluid containing fluoroolefin, and method for producing fluoroolefin

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4606899A (en) * 1985-03-27 1986-08-19 Air Products And Chemicals, Inc. Synthesis of maximum aluminum X zeolites
WO2013151070A1 (en) * 2012-04-03 2013-10-10 旭硝子株式会社 Method for purifying fluoroolefin, and method for producing fluoroolefin
JPWO2013151070A1 (en) * 2012-04-03 2015-12-17 旭硝子株式会社 Method for purifying fluoroolefin and method for producing fluoroolefin
JP2013241389A (en) * 2012-04-25 2013-12-05 Asahi Glass Co Ltd Method for drying fluid containing fluoroolefin, and method for producing fluoroolefin
JP2013241390A (en) * 2012-04-27 2013-12-05 Asahi Glass Co Ltd Method for purifying fluoroolefin, and method for producing fluoroolefin

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