GB415427A - Improvements in or relating to the hydration of olefines - Google Patents

Improvements in or relating to the hydration of olefines

Info

Publication number
GB415427A
GB415427A GB231533A GB231533A GB415427A GB 415427 A GB415427 A GB 415427A GB 231533 A GB231533 A GB 231533A GB 231533 A GB231533 A GB 231533A GB 415427 A GB415427 A GB 415427A
Authority
GB
United Kingdom
Prior art keywords
enough
per cent
baked
linseed oil
catalysts
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
GB231533A
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB231533A priority Critical patent/GB415427A/en
Publication of GB415427A publication Critical patent/GB415427A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/03Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
    • C07C29/04Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Catalysts for the production of alcohols from olefines (other than ethylene) and steam are compounded from an oxide of calcium, barium, strontium or magnesium, and if desired boron, and an amount of phosphoric acid more than enough to form the orthophosphates but less than enough to form the metaphosphates of the metals. The catalysts may be used as granules or flakes or on supports such as electrode carbon, and a drying oil may be used in their preparation as described in Specification 404,115. A suitable catalyst may be prepared from 1 mol CaO, 0,5B2O3, 2,6H3PO4, the mixture being evaporated, with the addition of 5 per cent of linseed oil during the final stages. The product is baked at 200 DEG C., tabletted with an additional 3 per cent of linseed oil, and again baked at 200 DEG C. Specifications 407,722, [Group IV], and 408,313 also are referred to.ALSO:Olefines other than ethylene, such as propylene, butene-1 or -2 and isobutylene are reacted with steam in presence of a solid catalyst compounded from an oxide of calcium, barium, strontium or magnesium and, if desired, boron, and an amount of phosphoric acid more than enough to form the orthophosphates of the metals, but less than enough to form the metaphosphates and the normal phosphate of the boron if present. The reaction may be effected at atmospheric or increased pressure. The catalysts may be used as granules or flakes or upon inert supports such as electrode carbon, and a drying oil may be used in their preparation as described in Specification 404,115, [Group III]. The temperature of the reaction may be 100--350 DEG C. and the pressure may be up to 250 atmospheres. A suitable catalyst may be prepared from 1 mol. CaO, 0,5 B2O3, 2,6 H3PO4, the mixture being evaporated with the addition of 5 per cent of linseed oil during the final stages. The product is baked at 200 DEG C., tabletted with an additional 3 per cent of linseed oil and again baked at 200 DEG C. Specifications 407,722 and 408,313 also are referred to.
GB231533A 1933-01-24 1933-01-24 Improvements in or relating to the hydration of olefines Expired GB415427A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB231533A GB415427A (en) 1933-01-24 1933-01-24 Improvements in or relating to the hydration of olefines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB231533A GB415427A (en) 1933-01-24 1933-01-24 Improvements in or relating to the hydration of olefines

Publications (1)

Publication Number Publication Date
GB415427A true GB415427A (en) 1934-08-24

Family

ID=9737384

Family Applications (1)

Application Number Title Priority Date Filing Date
GB231533A Expired GB415427A (en) 1933-01-24 1933-01-24 Improvements in or relating to the hydration of olefines

Country Status (1)

Country Link
GB (1) GB415427A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8558036B2 (en) 2010-11-15 2013-10-15 Saudi Arabian Oil Company Dual phase catalysts system for mixed olefin hydrations
WO2021064733A2 (en) 2019-10-02 2021-04-08 Polaris Solutions Ltd. Method and device for generating a thermal signature

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8558036B2 (en) 2010-11-15 2013-10-15 Saudi Arabian Oil Company Dual phase catalysts system for mixed olefin hydrations
US8865951B2 (en) 2010-11-15 2014-10-21 Saudi Arabian Oil Company Dual phase catalysts system for mixed olefin hydrations
US9056315B2 (en) 2010-11-15 2015-06-16 Saudi Arabian Oil Company Dual phase catalysts system for mixed olefin hydrations
WO2021064733A2 (en) 2019-10-02 2021-04-08 Polaris Solutions Ltd. Method and device for generating a thermal signature

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