GB972831A - Crystalline zeolite y' - Google Patents

Crystalline zeolite y'

Info

Publication number
GB972831A
GB972831A GB4320360A GB4320360A GB972831A GB 972831 A GB972831 A GB 972831A GB 4320360 A GB4320360 A GB 4320360A GB 4320360 A GB4320360 A GB 4320360A GB 972831 A GB972831 A GB 972831A
Authority
GB
United Kingdom
Prior art keywords
hours
ranges
iii
zeolite
maintaining
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
GB4320360A
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
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB972831A publication Critical patent/GB972831A/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)
    • C01B33/2853Zeolitic 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 Y

Abstract

A synthetic crystalline zeolitic sodium aluminosilicate having a composition expressed as oxides of 0.9\sB0.2Na2O=Al2O3=5 to 6 SiO2=0 to 9 H2O and having a specified X-ray diffraction pattern is prepared by forming an aqueous sodium aluminosilicate mixture, the major source of silica being aqueous colloidal silica sol, having a composition expressed in terms of oxide-moleratios falling within one of the following ranges: <TABS:0972831/C1/1> (where III is a preferred example of I and IV and V are preferred examples of II), maintaining the reactant mixture at ambient (12 DEG to 38 DEG C.) temperature for at least 20 hours but not more than 40 hours for Range I and III and for at least 16 hours but not more than 40 hours for Ranges II, IV and V, heating the reaction mixture to 90 DEG to 105 DEG C. and maintaining the elevated temperature until the zeolite Y1 crystallizes, and separating the crystals. For composition Ranges I and III crystallization may be for 3 to 8 days, while ranges II, IV and V require 24 hours to 65 hours. Zeolite Y1 may be activated by heating to effect hydration water loss, e.g. as high as 450 DEG C. in air, vacuum, or other gas, preferably 350 DEG C. at 10-5 mm. Hg, when it will absorb at least 30 wt. per cent O2 at 100 mm. Hg and - 183 DEG C. In examples reaction mixtures are prepared from sodium aluminate, caustic soda and colloidal silica. Specifications 777,233 and 909,266 are referred to.
GB4320360A 1959-12-28 1960-12-15 Crystalline zeolite y' Expired GB972831A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US86206259A 1959-12-28 1959-12-28

Publications (1)

Publication Number Publication Date
GB972831A true GB972831A (en) 1964-10-21

Family

ID=25337534

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4320360A Expired GB972831A (en) 1959-12-28 1960-12-15 Crystalline zeolite y'

Country Status (4)

Country Link
AT (1) AT269813B (en)
BE (1) BE598582A (en)
DE (1) DE1467179B2 (en)
GB (1) GB972831A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5601798A (en) * 1993-09-07 1997-02-11 Pq Corporation Process for preparing zeolite Y with increased mesopore volume
US5646082A (en) * 1993-06-24 1997-07-08 Cosmo Research Institute Crystalline aluminosilicate, process for producing the same, and catalyst employing the same for catalytic cracking of hydrocarbon oil
CN110255569A (en) * 2019-07-01 2019-09-20 杨鈜博 A method of directly production prepares white carbon black from quartz mineral powder

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5646082A (en) * 1993-06-24 1997-07-08 Cosmo Research Institute Crystalline aluminosilicate, process for producing the same, and catalyst employing the same for catalytic cracking of hydrocarbon oil
US5705142A (en) * 1993-06-24 1998-01-06 Cosmo Research Institute Process for producing a crystalline aluminosilicate
US5601798A (en) * 1993-09-07 1997-02-11 Pq Corporation Process for preparing zeolite Y with increased mesopore volume
CN110255569A (en) * 2019-07-01 2019-09-20 杨鈜博 A method of directly production prepares white carbon black from quartz mineral powder

Also Published As

Publication number Publication date
AT269813B (en) 1969-04-10
BE598582A (en) 1961-04-14
DE1467179A1 (en) 1969-02-06
DE1467179B2 (en) 1972-05-04

Similar Documents

Publication Publication Date Title
GB1011771A (en) Process for the preparation of crystalline zeolite y
GB1005949A (en) Molecular sieve adsorbents
JPS57123815A (en) Production of crystalline aluminosilicate zeolite
US3436174A (en) Synthetic mordenite and preparation thereof
GB1023283A (en) Crystalline zeolite l
GB868846A (en) Improvements in and relating to zeolites
GB1279485A (en) Process for preparing high silica faujasite
GB961215A (en) Process for making crystalline zeolites
GB909265A (en) Synthetic crystalline zeolite
EP0190903A3 (en) A crystalline zeolite composition having a cancrinite-like structure and a process for its preparation
GB870440A (en) Process for producing sodium zeolite a
GB897670A (en) Crystalline zeolite
GB972831A (en) Crystalline zeolite y&#39;
GB1035645A (en) Preparation of zeolites
FR1264290A (en) Process for the catalytic preparation of ethylene glycol
GB1188584A (en) Process for the preparation of Synthetic Zeolite Molecular Sieves
GB841812A (en) &#34;improvements in and relating to zeolites&#34;
US3433588A (en) Method for the preparation of 4 angstrom unit zeolites
GB1341984A (en) Production of synthetic zeolites of faujasite structure
GB1223592A (en) Process for the preparation of aluminosilicate ion exchange materials
GB1066258A (en) Improved process for preparing crystalline zeolites
GB1297927A (en)
GB1035644A (en) Improvements relating to the preparation of synthetic crystalline zeolites
GB1035646A (en) Preparation of zeolites
JPS5617920A (en) Manufacture of synthetic crystalline aluminosilicate zeolite