GB662356A - Improvements in or relating to the production of acetic anhydride - Google Patents

Improvements in or relating to the production of acetic anhydride

Info

Publication number
GB662356A
GB662356A GB5549/49A GB554949A GB662356A GB 662356 A GB662356 A GB 662356A GB 5549/49 A GB5549/49 A GB 5549/49A GB 554949 A GB554949 A GB 554949A GB 662356 A GB662356 A GB 662356A
Authority
GB
United Kingdom
Prior art keywords
acetic acid
tower
acetone
line
acetic anhydride
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
GB5549/49A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development 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 Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB662356A publication Critical patent/GB662356A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/54Preparation of carboxylic acid anhydrides
    • C07C51/56Preparation of carboxylic acid anhydrides from organic acids, their salts, their esters or their halides, e.g. by carboxylation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/54Preparation of carboxylic acid anhydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/08Acetic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/60Two oxygen atoms, e.g. succinic anhydride

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

<PICT:0662356/IV (b)/1> Acetic anhydride is obtained by a continuous process which comprises pyrolysing acetone to form ketene, immediately quenching the ketene, unconverted acetone and fixed gases so formed to a temperature of 200-300 DEG F. by jet mixing them with a mixture of acetic anhydride and acetic acid, whereby the ketene reacts with the acetic acid to produce acetic anhydride, adding acetic acid to the reaction products and using at least a portion of the resultant mixture of acetic acid and acetic anhydride as the quenching medium. Referring to the drawing acetone is vaporized in vaporizer 2 and then passed through the preheater 4 which is preheated to 1150 DEG F. and then to pyrolysis chamber 6 which may be a single tube or coil of copper or of an alloy such as stainless steel containing a large amount of chromium or of the alloy disclosed in Specification 655,101. The pyrolysis temperature may be from 1150 DEG to 1300 DEG F. with a contact time of 0.3 to 0.5 seconds. The effluent gases from the pyrolysis chamber are immediately quenched to a temperature not exceeding 300 DEG F. in the venturi mixer 8 with a mixture of 75-10 per cent acetic acid and 25-90 per cent acetic anhydride, this quenching mixture being preferably drawn off from tower 10 through line 12. The quenched mixture then passes by line 9 to tower 10 where it is contacted counter-currently with glacial acetic acid introduced through lines 11 and 31. The top section of the tower 10 serves as a fractionation section to separate the acetone and acetic acid, the acetone leaves in the top gases whilst a mixture of acetic acid and acetic anhydride is removed from the bottom of the tower and after passing through cooler 13 is pumped to venturi 8 where it is mixed with the effluent vapours from the chamber 6. Another portion of the bottoms from tower 10 is passed through line 16 to the mid-section of fractionator 17 where the acetic acid and acetic anhydride are separated, the former being recycled to tower 10 through line 28, condenser 29 and line 31 and the latter withdrawn through line 32. Unconverted acetone, some acetic acid and fixed gases (largely methane, carbon monoxide and ethylene) are passed overhead from tower 10 through condenser 19 to separator 20, a portion of the acetone being returned to tower 10 through line 21 as reflux and the remainder returned as feed to the vaporizer 2. Fixed gases containing a small amount of acetone are passed by line 24 to scrubber 25, where they are contacted countercurrently at low temperature with glacial acetic acid introduced through line 26. The acetic acid enriched with acetone is then returned to the middle of tower 10. Specification 627,810 is referred to.
GB5549/49A 1948-10-30 1949-03-01 Improvements in or relating to the production of acetic anhydride Expired GB662356A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US662356XA 1948-10-30 1948-10-30

Publications (1)

Publication Number Publication Date
GB662356A true GB662356A (en) 1951-12-05

Family

ID=22068173

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5549/49A Expired GB662356A (en) 1948-10-30 1949-03-01 Improvements in or relating to the production of acetic anhydride

Country Status (1)

Country Link
GB (1) GB662356A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150044122A1 (en) * 2012-03-28 2015-02-12 Aurotec Gmbh Pressure-regulated multi-reactor system

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150044122A1 (en) * 2012-03-28 2015-02-12 Aurotec Gmbh Pressure-regulated multi-reactor system
US10913048B2 (en) * 2012-03-28 2021-02-09 Aurotec Gmbh Pressure-regulated multi-reactor system

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