GB716770A - Method of purifying a cuprous salt catalyst in the synthesis of acrylonitrile - Google Patents

Method of purifying a cuprous salt catalyst in the synthesis of acrylonitrile

Info

Publication number
GB716770A
GB716770A GB30424/52A GB3042452A GB716770A GB 716770 A GB716770 A GB 716770A GB 30424/52 A GB30424/52 A GB 30424/52A GB 3042452 A GB3042452 A GB 3042452A GB 716770 A GB716770 A GB 716770A
Authority
GB
United Kingdom
Prior art keywords
catalyst
polymerization products
acrylonitrile
synthesis
vessel
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
GB30424/52A
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.)
BASF Schweiz AG
Original Assignee
Ciba AG
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 Ciba AG filed Critical Ciba AG
Publication of GB716770A publication Critical patent/GB716770A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/08Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds
    • C07C253/12Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds to compounds containing carbon-to-carbon triple bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

<PICT:0716770/IV (b)/1> In the synthesis of acrylonitrile from hydrocyanic acid and acetylene using a cuprous salt catalyst at 70-100 DEG C., polymerization products dissolved in the hot catalyst are separated by cooling at least part of the catalyst to a temperature below 70 DEG C. and at which the catalyst is still substantially liquid; the separated polymerization products are removed and the purified catalyst reheated for further use in the synthesis. Preferably the catalyst is cooled to about 40 DEG C. and then reheated in two stages, firstly to 50-55 DEG C. to coagulate the polymerization products, and then to reaction temperature. The whole of the catalyst may be treated at once, or a portion (e.g. one-tenth) may be withdrawn continuously or periodically for purification. As shown, hydrocyanic acid enters at 1 into reaction vessel R containing a catalyst composed of water, cuprous chloride, ammonium chloride, copper powder, and concentrated hydrochloric acid; acetylene introduced at 2 circulates through pipes 4 and acrylonitrile is dissolved out with water in tower W; a portion of the catalyst passes continuously through pipes 6 to vessel D1 maintained at 40 DEG C. and then to vessel D2 maintained at 50-55 DEG C., from which precipitated polymerization products are removed.ALSO:<PICT:0716770/III/1> In the synthesis of acrylonitrile from hydrocyanic acid and acetylene using a cuprous salt catalyst at 70-100 DEG C polymerization products dissolved in the hot catalyst are separated by cooling at least part of the catalyst to a temperature below 70 DEG C. and at which the catalyst is still substantially liquid; the separated polymerization products are removed and the purified catalyst reheated for further use in the synthesis. Preferably the catalyst is cooled to about 40 DEG C. and then reheated in two stages, firstly to 50-55 DEG C. to coagulate the polymerization products, and then to reaction temperature. The whole of the catalyst may be treated at once, or a portion (e.g. one-tenth) may be withdrawn continuously or periodically for purification. As shown, hydrocyanic acid enters at 1 into reaction vessel R containing a catalyst composed of water, cuprous chloride, ammonium chloride, copper powder, and concentrated hydrochloric acid; acetylene introduced at 2 circulates through pipes 4 and acrylonitrile is dissolved out with water in tower W; a portion of the catalyst passes continuously through pipes 6 to vessel D1 maintained at 40 DEG C. and then to vessel D2 maintained at 50-55 DEG C., from which precipitated polymerization products are removed.
GB30424/52A 1951-12-07 1952-12-01 Method of purifying a cuprous salt catalyst in the synthesis of acrylonitrile Expired GB716770A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH716770X 1951-12-07

Publications (1)

Publication Number Publication Date
GB716770A true GB716770A (en) 1954-10-13

Family

ID=4531185

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30424/52A Expired GB716770A (en) 1951-12-07 1952-12-01 Method of purifying a cuprous salt catalyst in the synthesis of acrylonitrile

Country Status (1)

Country Link
GB (1) GB716770A (en)

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