GB666206A - An improved process for neutralizing capillary active, sulphonated products - Google Patents

An improved process for neutralizing capillary active, sulphonated products

Info

Publication number
GB666206A
GB666206A GB22396/47A GB2239647A GB666206A GB 666206 A GB666206 A GB 666206A GB 22396/47 A GB22396/47 A GB 22396/47A GB 2239647 A GB2239647 A GB 2239647A GB 666206 A GB666206 A GB 666206A
Authority
GB
United Kingdom
Prior art keywords
alcohols
neutralizing
sulphonated
product
solvent
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
GB22396/47A
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.)
Colgate Palmolive AS
Original Assignee
Colgate Palmolive AS
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 Colgate Palmolive AS filed Critical Colgate Palmolive AS
Publication of GB666206A publication Critical patent/GB666206A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07C303/42Separation; Purification; Stabilisation; Use of additives

Landscapes

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

Abstract

A process for neutralizing sulphonated mono-or diglycerides of higher fatty acids having at least 8 carbon atoms in the molecule, is characterized by adding the crude sulphonation product to an inert organic solvent for the sulphonation product in which solvent there is suspended a neutralizing agent slightly soluble or insoluble in the said solvent. The crude sulphonation product is applied to the suspension of the neutralizing agent in the form of a thin jet. Any organic solvent may be used which does not react in an undesirable way with the sulphonating agent under the neutralizing conditions, for example aliphatic alcohols such as methyl alcohol, ethyl alcohol, propyl alcohols, butyl alcohols and amyl alcohols, polyhydric aliphatic alcohols such as ethylene glycol and glycerols, ketones such as acetone and methyl ethyl ketone, ethers such as dimethyl ether, diethyl ether and diisopropyl ether, but ethyl and propyl alcohols are preferred. Hydrocarbons and halogenated hydrocarbons are suitable solvents but less satisfactory than the alcohols. Mixtures of solvents may be used. The organic solvents may contain water or water may be emulsified with water-immiscible organic solvents. As neutralizing agents may be used any substance of alkaline reaction and only slightly soluble or insoluble in the organic solvent, examples of which are the hydroxides such as calcium and magnesium hydroxide, oxides such as calcium and magnesium oxides and salts having an alkaline reaction such as phosphates or sulphites and carbonates and/or bicarbonates such as sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, ammonium carbonate and ammonium bicarbonate. Preferably the neutralized sulphonated product should be soluble in the organic solvent and the neutralized sulphonated product should be precipitated together with unused neutralizing agent. The sulphonated product may be obtained from the solution by evaporation of the solvent after filtration though the latter is not essential. In the example a mixture of sulphonated coconut oil monoglycerides is poured as a thin jet into a suspension of sodium bicarbonate in ethanol. At approximately 25 DEG C. water formed by the neutralization will be absorbed by the sodium sulphate produced, which is insoluble in the alcohol.
GB22396/47A 1946-05-01 1947-08-12 An improved process for neutralizing capillary active, sulphonated products Expired GB666206A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DK666206X 1946-05-01

Publications (1)

Publication Number Publication Date
GB666206A true GB666206A (en) 1952-02-06

Family

ID=8152117

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22396/47A Expired GB666206A (en) 1946-05-01 1947-08-12 An improved process for neutralizing capillary active, sulphonated products

Country Status (1)

Country Link
GB (1) GB666206A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4832876A (en) * 1987-09-14 1989-05-23 Colgate-Palmolive Company Process for the manufacture of higher fatty monoglyceride monosulfate detergents
US4950440A (en) * 1987-09-14 1990-08-21 Colgate-Palmolive Company Process for the manufacture of high fatty acid monoglyceride monosulfate detergents

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4832876A (en) * 1987-09-14 1989-05-23 Colgate-Palmolive Company Process for the manufacture of higher fatty monoglyceride monosulfate detergents
US4950440A (en) * 1987-09-14 1990-08-21 Colgate-Palmolive Company Process for the manufacture of high fatty acid monoglyceride monosulfate detergents

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