GB1044983A - Improvements in and relating to zeolites - Google Patents

Improvements in and relating to zeolites

Info

Publication number
GB1044983A
GB1044983A GB694764A GB694764A GB1044983A GB 1044983 A GB1044983 A GB 1044983A GB 694764 A GB694764 A GB 694764A GB 694764 A GB694764 A GB 694764A GB 1044983 A GB1044983 A GB 1044983A
Authority
GB
United Kingdom
Prior art keywords
zeolite
na2o
reaction mixture
metal
al2o3
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
GB694764A
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering 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 Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB1044983A publication Critical patent/GB1044983A/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

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)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A process for the preparation of crystalline Type Y zeolite having the following molar ratio of constituents in its dehydrated form 0.9\sB0.2 Na2O: Al2O3: XSiO2 where X has a value from 3 to 7, comprises preparing an aqueous reaction mixture containing Na2O, SiO2 and Al2O3, the molar ratios of the constituents being within the following ranges. <TABS:1044983/C1/1> and heating the reaction mixture to a crystallization temperature of 180 DEG to 250 DEG F. for at least 24 hours and recovering the crystallized Type Y zeolite product. The reactants may be mixed at ambient temperature and then the reaction mixture may be maintained at 50-140 DEG F. for 1-15 hours prior to heating to the crystallization temperature. The product crystals, after separation from the mother liquor and thorough washing, may be activated by heating to 300-450 DEG C. to remove water of hydration to give an anhydrous product suitable for use as an adsorbent. The zeolites may be subjected to ion-exchange with metal cations of Groups I to VIII and the rare earth metals to give products suitable for use as catalysts. The ion-exchanged zeolites may be further modified by impregnation with noble metals, e.g. Pd, Pt, Rh, Mo, Cr, V, Co, Ni, Cu, Ag or Mn.ALSO:Crystalline Type Y zeolite having the following molar ratio of constituents in its dehydrated form 0.9 \sB 0.2 Na2O : Al2O3 : XSiO2 where X has a value from 3 to 7 is prepared by preparing an aqueous reaction mixture containing Na2O1 SiO2 and Al2O3, the molar ratio of constituents being within the following range: .SiO2/Al2O3.3.0 - 9.5 .Na2O/SiO2.0.20 - 0.27 .H2O/SiO2.3 - 10 and heating the reaction mixture to a crystallization temperature of 180 DEG -250 DEG F. for at least 24 hours and recovering the crystallized Type Y zeolite product. The zeolite may be subjected to ion exchange with a metal cation e.g. of Group I to VIII and the rare earth metals or a hydrogen containing cation e.g. ammonium to reduce the Na content (Na2O) to less than 10% by wt. based on the weight of zeolite crystals to give products useful as catalysts for hydrocarbon conversion processes. The ion-exchanged zeolites can be further modified for certain applications e.g. hydrocracking by impregnation with a suitable metal e.g. Pd, Pt, Rh, Mo, Cr, V, Co, Ni, Cu, Ag or Mn. Preferably the zeolite are first decationized by base exchange with NH14 or H ions and then heated with the appropriate metal salt or ammonium complex of the metal e.g. ammonium chloroplatinate and palladium chloride and the catalyst will generally contain 0.01 to 5.0 wt per cent of the metal.
GB694764A 1963-04-30 1964-02-19 Improvements in and relating to zeolites Expired GB1044983A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US27704263A 1963-04-30 1963-04-30

Publications (1)

Publication Number Publication Date
GB1044983A true GB1044983A (en) 1966-10-05

Family

ID=23059173

Family Applications (1)

Application Number Title Priority Date Filing Date
GB694764A Expired GB1044983A (en) 1963-04-30 1964-02-19 Improvements in and relating to zeolites

Country Status (6)

Country Link
CA (1) CA922487A (en)
CH (1) CH483995A (en)
DE (1) DE1295533B (en)
GB (1) GB1044983A (en)
NL (1) NL6402217A (en)
SE (1) SE301139B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USH282H (en) 1982-12-27 1987-06-02 W. R. Grace & Co. High silica/alumina ratio faujasite type NaY

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5785944A (en) * 1996-07-31 1998-07-28 Chevron U.S.A. Inc. Preparation of Y zeolite
US6756029B2 (en) 1999-08-11 2004-06-29 Petroleo Brasileiro S.A.-Petrobras Molecular sieves of faujasite structure

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1098927B (en) * 1957-08-26 1961-02-09 Union Carbide Corp Process for making crystalline zeolitic molecular sieves
DE1098929B (en) * 1958-04-14 1961-02-09 Union Carbide Corp Process for making crystalline zeolitic molecular sieves

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USH282H (en) 1982-12-27 1987-06-02 W. R. Grace & Co. High silica/alumina ratio faujasite type NaY

Also Published As

Publication number Publication date
CA922487A (en) 1973-03-13
CH483995A (en) 1970-01-15
NL6402217A (en) 1964-11-02
DE1295533B (en) 1969-05-22
SE301139B (en) 1968-05-27

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