GB651275A - A process of producing ethyl alcohol - Google Patents

A process of producing ethyl alcohol

Info

Publication number
GB651275A
GB651275A GB4067/48A GB406748A GB651275A GB 651275 A GB651275 A GB 651275A GB 4067/48 A GB4067/48 A GB 4067/48A GB 406748 A GB406748 A GB 406748A GB 651275 A GB651275 A GB 651275A
Authority
GB
United Kingdom
Prior art keywords
ethylene
phosphoric acid
temperature
bed
support
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
GB4067/48A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB651275A publication Critical patent/GB651275A/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)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

<PICT:0651275/IV (b)/1> Ethyl alcohol is continuously prepared by the hydration of ethylene by passing a mixture of ethylene and water vapour at elevated temperature and pressure into intimate contact with a catalyst bed made up of a solid porous support containing absorbed phosphoric acid, of a concentration of at least 70 per cent, the acid having been supplied to the support in a more dilute form and been concentrated in situ on the support. The solid support for the phosphoric acid may be any strong, porous material having good absorptivity for aqueous phosphoric acid. The preferred material is a calcined diatomaceous earth, preferably the product sold under the trade name "Celite". The solid supporting material is impregnated with an aqueous solution of phosphoric acid, preferably of concentration between 55 and 65 per cent to form the catalyst bed which is then heated, preferably by recycling heated ethylene gas through the system under pressure until its temperature reaches 175-200 DEG C. Steam is then gradually mixed with the ethylene and the temperature is raised until when the desired operating ratio of steam to ethylene is established a temperature of 270-280 DEG C. is reached. The average temperature of the bed is controlled between 270 DEG and 310 DEG C., preferably between 290 DEG and 300 DEG C. In the Figure, various curves show how a given concentration of phosphoric acid may be attained at any given temperature by using one of the many combinations of pressure and water vapour-ethylene molecular ratio. As the reaction progresses some phosphoric acid is lost from the bed and to maintain the efficiency of the catalyst it is desirable to add further amounts of phosphoric acid to the bed, the quantity added depending on the amount of ethyl alcohol formed. The ethylene used in the process may be obtained from the catalytic or thermal cracking of petroleum hydrocarbons. If the ethylene is contaminated with acetylene the reactants should be copper-free and should be conducted to the catalyst bed out of contact with any copper surfaces to avoid the formation of cuprene.
GB4067/48A 1947-08-25 1948-02-11 A process of producing ethyl alcohol Expired GB651275A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US651275XA 1947-08-25 1947-08-25

Publications (1)

Publication Number Publication Date
GB651275A true GB651275A (en) 1951-03-14

Family

ID=22060510

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4067/48A Expired GB651275A (en) 1947-08-25 1948-02-11 A process of producing ethyl alcohol

Country Status (1)

Country Link
GB (1) GB651275A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769847A (en) * 1951-10-03 1956-11-06 Ici Ltd Catalysts for the hydration of olefines and dehydration of alcohols
US3855307A (en) * 1967-02-20 1974-12-17 Monsanto Co Catalysis

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2769847A (en) * 1951-10-03 1956-11-06 Ici Ltd Catalysts for the hydration of olefines and dehydration of alcohols
US3855307A (en) * 1967-02-20 1974-12-17 Monsanto Co Catalysis

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