GB666206A - An improved process for neutralizing capillary active, sulphonated products - Google Patents
An improved process for neutralizing capillary active, sulphonated productsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/42—Separation; 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.
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)
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 |
-
1947
- 1947-08-12 GB GB22396/47A patent/GB666206A/en not_active Expired
Cited By (2)
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3176622B2 (en) | Process for producing glyceride sulfate partial ester | |
US5312932A (en) | Process for the continuous production of partial glyceride sulfates | |
US4816188A (en) | Process for the preparation of saturated/unsaturated mixed fatty acid ester sulfonates | |
GB614044A (en) | Detergent composition | |
KR840007535A (en) | Method for Controlling the Viscosity of Concentrated High Viscosity Industrial Surfactants | |
US5304664A (en) | Process for the production of highly sulfated fatty acids and fatty acid derivatives | |
Stirton et al. | Sodium salts of alkyl esters of a-sulfo fatty acids. Wetting, lime soap dispersion, and related properties | |
JPH05502221A (en) | Process for producing salt of sulfonated fatty acid glycerol ester | |
GB666206A (en) | An improved process for neutralizing capillary active, sulphonated products | |
GB1022663A (en) | Washing agents | |
GB632447A (en) | Improvements in or relating to the production of neutral phthalates | |
US2644831A (en) | Alkali metal and ammonium sulfates of hydroxy ethers | |
GB908774A (en) | Process for preparing soluble sporicidally active solid polyglyoxals | |
US2165997A (en) | Process of preparing fire-extinguishing foam | |
US2195187A (en) | Production of sulphonation derivatives | |
GB1204514A (en) | Process for the manufacture of alkali paraffin sulphonate solutions containing small amounts of alkali sulphate | |
GB1190023A (en) | Composition for a Liquid Biodegradable Detergent Product | |
GB723925A (en) | Process for preparing all-purpose detergent compositions | |
JP3425247B2 (en) | Concentration method of surfactant solution | |
US2493445A (en) | Method for stabilizing sulfated products | |
SU523136A1 (en) | The method of obtaining surfactants | |
US2660588A (en) | Neutralization of sulphonated organic esters | |
SU112641A1 (en) | The method of obtaining primary alcohols by the oxidation of liquid paraffins | |
GB584219A (en) | Wetting-out treatment of fibrous materials | |
GB1049770A (en) | Production of omega aminoketocarboxylic acids |