GB888772A - Method of producing alumina - Google Patents

Method of producing alumina

Info

Publication number
GB888772A
GB888772A GB8937/58A GB893758A GB888772A GB 888772 A GB888772 A GB 888772A GB 8937/58 A GB8937/58 A GB 8937/58A GB 893758 A GB893758 A GB 893758A GB 888772 A GB888772 A GB 888772A
Authority
GB
United Kingdom
Prior art keywords
alumina
homogenization
slurry
boiling range
spray
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
GB8937/58A
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid 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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB888772A publication Critical patent/GB888772A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00Compounds of aluminium
    • C01F7/02Aluminium oxide; Aluminium hydroxide; Aluminates
    • C01F7/34Preparation of aluminium hydroxide by precipitation from solutions containing aluminium salts
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/10Solid density
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/12Surface area

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

Hydrated alumina is precipitated from an aqueous solution of an aluminium compound at pH 7-10,5 and the resultant slurry subjected to comminution to reduce the particle size and render it more uniform ("homogenization"), whereby the apparent bulk density after spray drying is increased, e.g. to 0,3-1.5 gms./c.c. When the precipitation pH remains below 10, aging of the slurry at pH 10-11 is essential The alumina precipitate may be obtained by acidifying sodium aluminate solution with a mineral acid, e.g. nitric acid, or with aluminium sulphate solution. The precipitation may be conducted at 70 DEG -130 DEG F. and the amount of solids in the mixture is generally from 4-9%. Preferably the alumina is aged after formation at pH 10-11 for at least 15 minutes at 90 DEG -130 DEG F.: aging at lower pH values is also described. The alumina may, if desired, be filtered and washed prior to the homogenization, and in the flow sheet (not shown) two filters are employed with an intermediate reslurry tank to which a flocculant such as glue or polyacrylamide may be added. The homogenization may be performed with a homogenizing valve operating at 500-3,000 p.s.i.g., or by grinding or milling. After homogenization, the slurry may be dried in a tray dryes or rotating kiln, but is prefreably spray-dried, e.g. at 500 DEG -1,000 DEG F., to a moisture content of 15-40%, whereby microspheres are produced which, after pelleting, may be fully dehydrated by calcination at 1,100 DEG -1,350 DEG F. Catalytic materialr may be added to the slurry before homogenization or may be incorporated after drying. Platinic chloride may be employed, with or without subsequent treatment with hydrogen sulphide or ammonium sulphide and, as activator therewith, hydrogen fluoride, hydrogen chloride or aluminium chloride, to provide 0,1-0,8% of platinum and up to 3% of halogen in the catalyst; the alumina may be impregnated or coated with 8-20% of molybdena; catalysts may comprise 10-25% of molybdena and 1-5% of cobalt oxide (supplied as ammonium molybdate and cobalt nitrate) or 10-30% of chromic oxide or tungstic or palladium oxide. In one example, a hydrodesulphurization catalyst is prepared by adding ammonium molybdate and cobalt nitrate during the formation of the alumina and, after spray-drying, mixed with 1% of graphite, formed into pellets and calcined at 1,260 DEG F. It is then used (a) in the desulphurization of a gas oil with a boiling range of 480 DEG -630 DEG F.; (b) in desulphurization, nitrogen removal and olefin saturation of a thermal naphtha with a boiling range of 196 DEG -430 DEG F. and (c) in desulphurizing a heavy vacuum gas oil with a boiling range of 480 DEG -860 DEG F. Specification 737,429 is referred to.
GB8937/58A 1957-05-17 1958-03-20 Method of producing alumina Expired GB888772A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US888772XA 1957-05-17 1957-05-17

Publications (1)

Publication Number Publication Date
GB888772A true GB888772A (en) 1962-02-07

Family

ID=22214020

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8937/58A Expired GB888772A (en) 1957-05-17 1958-03-20 Method of producing alumina

Country Status (1)

Country Link
GB (1) GB888772A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2202850A1 (en) * 1972-10-12 1974-05-10 Laporte Industries Ltd Pseudoboehmite alumina prodn - by controlled reaction of aluminium sulphate and sodium aluminate solns
US4124699A (en) * 1973-03-14 1978-11-07 Rhone Progil Alumina-based bodies with large pores, produced by agglomeration
US4313923A (en) * 1980-12-29 1982-02-02 Filtrol Corporation Method of producing pseudoboehmites
US4332782A (en) * 1980-07-28 1982-06-01 Filtrol Corporation Method of producing pseudoboehmite
EP0692305A1 (en) 1994-07-13 1996-01-17 Rhone-Poulenc Chimie Alumina catalyst for the treatment of sulfur containing gasses, use of these catalysts for the treatment and treatment process for these gasses
US5800797A (en) * 1993-12-09 1998-09-01 Catalysts & Chemicals Industries Co., Ltd. Process for producing alumina and apparatus therefor
JP2003519617A (en) * 2000-01-10 2003-06-24 アルベマール・コーポレーシヨン Process for producing aluminum hydroxide with improved thermal stability

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2202850A1 (en) * 1972-10-12 1974-05-10 Laporte Industries Ltd Pseudoboehmite alumina prodn - by controlled reaction of aluminium sulphate and sodium aluminate solns
US4124699A (en) * 1973-03-14 1978-11-07 Rhone Progil Alumina-based bodies with large pores, produced by agglomeration
US4332782A (en) * 1980-07-28 1982-06-01 Filtrol Corporation Method of producing pseudoboehmite
US4313923A (en) * 1980-12-29 1982-02-02 Filtrol Corporation Method of producing pseudoboehmites
US5800797A (en) * 1993-12-09 1998-09-01 Catalysts & Chemicals Industries Co., Ltd. Process for producing alumina and apparatus therefor
EP0692305A1 (en) 1994-07-13 1996-01-17 Rhone-Poulenc Chimie Alumina catalyst for the treatment of sulfur containing gasses, use of these catalysts for the treatment and treatment process for these gasses
JP2003519617A (en) * 2000-01-10 2003-06-24 アルベマール・コーポレーシヨン Process for producing aluminum hydroxide with improved thermal stability

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