US2044919A - Lime, magnesia- and acid-resisting sulphonates produced from unsaturated fatty alcohols - Google Patents

Lime, magnesia- and acid-resisting sulphonates produced from unsaturated fatty alcohols Download PDF

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Publication number
US2044919A
US2044919A US608846A US60884632A US2044919A US 2044919 A US2044919 A US 2044919A US 608846 A US608846 A US 608846A US 60884632 A US60884632 A US 60884632A US 2044919 A US2044919 A US 2044919A
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fatty alcohols
unsaturated fatty
acid
lime
magnesia
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Expired - Lifetime
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US608846A
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Schrauth Walther
Hueter Richard
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"unichem" Chemikalien Handels A-G
UNICHEM CHEMIKALIEN HANDELS A
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UNICHEM CHEMIKALIEN HANDELS A
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    • 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
    • C07C303/24Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfuric acids
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/01Wetting, emulsifying, dispersing, or stabilizing agents
    • Y10S516/03Organic sulfoxy compound containing

Definitions

  • the present invention relates to wetting and dispersing agents and has for an object to provide an improved process of producing sulphates and/or sulphonates of fatty alcohols.
  • the product-neutralized by ordinary means is completely soluble in a 50% solution of epsom Application May 2, 1932, Serial In Germany May 2, 1931 salts and in water of 50% hardness. It is neither salted out by a 12% solution of Glaubers salt nor by a 20% solution of sodium chloride, and. withstands boiling with sulphuric acid of 1% strength. Under the same circumstances a sulphate and/or sulphonate produced in the same manner, though at 30", is salted out or decomposed.
  • the reaction product possesses the same properties as the products obtained in Example 1, and may be produced free of sodium sulphate by dissolving in spirit, butyl alcohol and the like and subsequent further vaporization.
  • the pure product may also be obtained by extracting the non-neutralized sulphation and/or sulphonation mixture without previous concentration by vaporization.
  • unsaturated fatty alcohols is used in the claims to define the oleyl alcohol and its homologues hereinbefore mentioned and with which the present invention is particularly concerned.
  • a process for the production of soap-like products comprising the gradual addition of unsaturated fatty alcohols to concentrated sulphuric acid which is pre-cooled to a temperature only slightly above the melting-point of the alcohols.
  • a process, according to claim 1, comprising the sulphonation of unsaturated fatty alcohols in presence of additional indifferent agents lowering the melting-point of said alcohols.
  • the process for the production of sulphuric acid reaction products which comprises mixing oleyl alcohol and carbon-tetra-chloride in a proportion of the order of 1 to l and reacting with I point of the alcohol and gradually adding thereto the alcohol while maintaining the materials at approximately the same temperature.
  • a process for the production oi soap-like products comprising gradually adding unsaturated fatty alcohols to a concentrated sulphating agent which has been pre-cooled to a temperature substantially below the melting point. of the alcohols but insufliciently low to cause solidlflcation of the alcohols before contact and reaction with the acid occurs.
  • a process for the production of soap-like products comprising mixing concentrated sulphuric acid with unsaturated fatty alcohols in the presence of an inert diluent which produces a mixture having a melting point below that of the alcohols, and reacting the acid and the alcohols at a temperature only slightly above the melting point of the alcohol-diluent mixture.
  • the steps comprising cooling a concentrated sulphating agent to'a temperature below the melting point of the unsaturated fatty alcohol employed and gradually adding the alcohol to the cooled mass while maintaining the mass at approximately the same temperature, said temperature being sufllciently high to prevent solidification of the alcohol being introduced.
  • the step comprising gradually adding an unsaturated fatty alcohol to concentrated sulphuric acid which has been precooled to a temperature adapted to cause the alcohol to enter the solution at a temperature within the range below or only slightly above the melting point of the alcohol.

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

Description

Patented June 23, 1936 UNITED STATES PATENT OFFICE LIME, MAGNESIA- AND ACID-RESISTING SULPHONATES PRODUCED FROM UNSAT- URATED FATTY ALCOHOLS No Drawing.
10 Claims.
The present invention relates to wetting and dispersing agents and has for an object to provide an improved process of producing sulphates and/or sulphonates of fatty alcohols.
The nature and objects of the invention will be understood from the following description:
It has been found that by the sulphation and/or sulphonation of oleyl alcohol and its homologues, products are obtained with properties varying according to the method of production employed. Depending upon whether the sulphation and/or sulphonation is performed at high temperatures or under substantial cooling, the sulphates and/or sulphonates possess different degrees of stability against inorganic products such as limeand magnesia-compounds, further against acids, salts with salting out eifects, etc. Products of astonishing resistance against the aforementioned substances are obtained if unsaturated fatty alcohols are sulphated and/or sulphonated at temperatures lower than or only slightly above the melting-point of fatty alcohols. Indeed, complete sulphation and/or sulphonation to an extent adapted to obtain clear solubility in water may not be successfully achieved by the methods employed up to the present time, the reason being that the fatty alcohols solidify at the temperaturesdesirable for the reaction and only an incomplete reaction takes place with sulphuric acid. It was found, however, that these difficulties can be eliminated either by thorough pre-cooling of the sulphuric acid and then gradually adding the fatty alcohol to the pre-cooled acid, or by adding agents which reduce the melting-point of the fatty alcohol thereby admitting a reduction of the temperature to 5 without involving solidification. The products produced are of great capillarlty, and may be used as agents for wetting, steeping, dispersing, levelling and washing purposes. They may be employed in acidic or alkaline washing liquors, as well as in baths containing for instance bitter salt or alum. The use of the aforementioned products also prevents the formation of lime deposits and detrimental effects due to the precipitation of such lime-soap deposits on the fibre.
Examples 1. kg. of sulphuric acid (about 96-98%) are cooled down to 6 and 100 kg. of oleyl alcohol (iodine number of about are gradually added in such a manner as not to raise the temperature of the reaction mixture above 0.
The product-neutralized by ordinary means is completely soluble in a 50% solution of epsom Application May 2, 1932, Serial In Germany May 2, 1931 salts and in water of 50% hardness. It is neither salted out by a 12% solution of Glaubers salt nor by a 20% solution of sodium chloride, and. withstands boiling with sulphuric acid of 1% strength. Under the same circumstances a sulphate and/or sulphonate produced in the same manner, though at 30", is salted out or decomposed.
2. To common oleyl alcohol kg.) solidification point of 19, there is added an equal quantity of carbon tetrachloride and the mass is sulphated and/or sulphonated by addition of 60 parts of sulphuric acid monohydrate at 5 and then at 0. After being stirred for three hours at the same temperature and subsequent neutralization, the mixture is evaporated to a salvelike consistency.
The reaction product possesses the same properties as the products obtained in Example 1, and may be produced free of sodium sulphate by dissolving in spirit, butyl alcohol and the like and subsequent further vaporization.
The pure product may also be obtained by extracting the non-neutralized sulphation and/or sulphonation mixture without previous concentration by vaporization.
The expression unsaturated fatty alcohols is used in the claims to define the oleyl alcohol and its homologues hereinbefore mentioned and with which the present invention is particularly concerned.
We claim:-
1. A process for the production of soap-like products, comprising the gradual addition of unsaturated fatty alcohols to concentrated sulphuric acid which is pre-cooled to a temperature only slightly above the melting-point of the alcohols.
2. A process, according to claim 1, comprising the sulphonation of unsaturated fatty alcohols in presence of additional indifferent agents lowering the melting-point of said alcohols.
3. The process for the production of sulphuric acid reaction products of oleyl alcohol which comprises cooling concentrated sulphuric acid to a temperature approximating -6 C. and gradually adding thereto oleyl alcohol while maintaining the temperature below 0 C.
4. The process for the production of sulphuric acid reaction products, as defined in claim 3, wherein the proportion of alcohol and sulphuric acid approximates 100 to 75.
5. The process for the production of sulphuric acid reaction products which comprises mixing oleyl alcohol and carbon-tetra-chloride in a proportion of the order of 1 to l and reacting with I point of the alcohol and gradually adding thereto the alcohol while maintaining the materials at approximately the same temperature.
'7. A process for the production oi soap-like products comprising gradually adding unsaturated fatty alcohols to a concentrated sulphating agent which has been pre-cooled to a temperature substantially below the melting point. of the alcohols but insufliciently low to cause solidlflcation of the alcohols before contact and reaction with the acid occurs.
8. A process for the production of soap-like products comprising mixing concentrated sulphuric acid with unsaturated fatty alcohols in the presence of an inert diluent which produces a mixture having a melting point below that of the alcohols, and reacting the acid and the alcohols at a temperature only slightly above the melting point of the alcohol-diluent mixture.
9. In the production of sulphated unsaturated fatty alcohols, the steps comprising cooling a concentrated sulphating agent to'a temperature below the melting point of the unsaturated fatty alcohol employed and gradually adding the alcohol to the cooled mass while maintaining the mass at approximately the same temperature, said temperature being sufllciently high to prevent solidification of the alcohol being introduced.
10. In the production of sulphates of unsaturated fatty alcohols, the step comprising gradually adding an unsaturated fatty alcohol to concentrated sulphuric acid which has been precooled to a temperature adapted to cause the alcohol to enter the solution at a temperature within the range below or only slightly above the melting point of the alcohol.
' WALTHER SCI-IRAU'IH.
RICHARD HUETER.
US608846A 1931-05-02 1932-05-02 Lime, magnesia- and acid-resisting sulphonates produced from unsaturated fatty alcohols Expired - Lifetime US2044919A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5037992A (en) * 1989-12-18 1991-08-06 The Procter & Gamble Company Process for sulfating unsaturated alcohols
WO1991013057A1 (en) * 1990-03-01 1991-09-05 The Procter & Gamble Company Co-sulfation of ethoxylated alcohols and unsaturated fatty alcohols

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5037992A (en) * 1989-12-18 1991-08-06 The Procter & Gamble Company Process for sulfating unsaturated alcohols
WO1991013057A1 (en) * 1990-03-01 1991-09-05 The Procter & Gamble Company Co-sulfation of ethoxylated alcohols and unsaturated fatty alcohols

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