GB799038A - Continuous sulphonation of organic liquids - Google Patents

Continuous sulphonation of organic liquids

Info

Publication number
GB799038A
GB799038A GB2701955A GB2701955A GB799038A GB 799038 A GB799038 A GB 799038A GB 2701955 A GB2701955 A GB 2701955A GB 2701955 A GB2701955 A GB 2701955A GB 799038 A GB799038 A GB 799038A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
reaction zone
sulphur trioxide
sulphonation
continuously
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
GB2701955A
Inventor
Geoffrey Place
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.)
Hedley Thomas & Co Ltd
Thomas Hedley and Co Ltd
Original Assignee
Hedley Thomas & Co Ltd
Thomas Hedley and 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 Hedley Thomas & Co Ltd, Thomas Hedley and Co Ltd filed Critical Hedley Thomas & Co Ltd
Priority to GB2701955A priority Critical patent/GB799038A/en
Publication of GB799038A publication Critical patent/GB799038A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B45/00Formation or introduction of functional groups containing sulfur
    • C07B45/02Formation or introduction of functional groups containing sulfur of sulfo or sulfonyldioxy groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/02Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
    • C07C303/04Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups
    • C07C303/06Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups by reaction with sulfuric acid or sulfur trioxide

Landscapes

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

Abstract

Organic liquids are continuously sulphonated or sulphated by continuously introducing a stream of the organic liquid into a reaction zone, without any addition of sulphuric or other acid, and intimately mixing said liquid with a continuously introduced stream of a mixture of sulphur trioxide vapour and inert gas, which contains between 3 and 40 per cent by volume of sulphur trioxide vapour, the molecular ratio of sulphur trioxide to organic liquid being between 1.0:1 to 1.5:1, the temperature in the reaction zone being 32-60 DEG C., the pressure 0 to 100 p.s.i.g. and the mean residence time of the reactants in the reaction zone being not more than 10 minutes. The reactants may be intimately mixed in a reactor as described in Specification 799,039. Suitable liquids which may be subjected to the sulphonation or sulphation process are alkylbenzenes having from 9 to 20 carbon atoms in the alkyl group, fatty alcohols containing from 9 to 20 carbon atoms, ethylene oxide condensation products in which from one to ten mols. of ethylene oxide are condensed with one mol. of any of the following: alkyl phenols having 8-20 carbon atoms in the alkyl group, fatty alcohols having 9-20 carbon atoms, fatty acids having 9-20 carbon atoms, fatty acid alkanolamides having 9-20 carbon atoms in the fatty acid residue and 2-4 carbon atoms in the alkanol group. An example is given of the sulphonation of an alkyl benzene derived from alkylating benzene with a propylene tetramer. Specification 680,613 also is referred to.
GB2701955A 1955-09-21 1955-09-21 Continuous sulphonation of organic liquids Expired GB799038A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2701955A GB799038A (en) 1955-09-21 1955-09-21 Continuous sulphonation of organic liquids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2701955A GB799038A (en) 1955-09-21 1955-09-21 Continuous sulphonation of organic liquids

Publications (1)

Publication Number Publication Date
GB799038A true GB799038A (en) 1958-07-30

Family

ID=10252856

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2701955A Expired GB799038A (en) 1955-09-21 1955-09-21 Continuous sulphonation of organic liquids

Country Status (1)

Country Link
GB (1) GB799038A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3259645A (en) * 1962-12-12 1966-07-05 Chemithon Corp Continuous sulfonation process

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3259645A (en) * 1962-12-12 1966-07-05 Chemithon Corp Continuous sulfonation process
US3350428A (en) * 1962-12-12 1967-10-31 Chemithon Corp Continuous sulfonation process

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