Untitled record
Abstract
This record has no abstract on file.
Term
Term ended
Expired 27 May 1952, 74.3 years ago.
- Priority and filed
- Granted
- Expired
- Today
7 claims: 6 independent, 1 dependent
- 1Having thus described the invention, what is 110 1,068,708
- 22 claimed as new and desired to be secured by Letters Patent is:1. A medium for wetting, permeating, and producing foam and dispersion which comprises the 5 true sulphonates of primary lauric and primary myristic alcohols. 2. A medium for wetting, permeating, and producing foam and dispersion comprising true sulphonates of the alcohols obtained from cocoanut 10 oil.
- 4A medium for wetting, permeating, and pro ducing foam and dispersion comprising true sulphonates of the lower boiling alcohols obtained from cocoanut oil.
- 5A true sulphonate of primary myristyl alcohol. , SO
- 6A true sulphonate of primary octadecyl alcohol.
- 7A medium for wetting, permeating and producing foam and dispersion comprising a mixture of true sulphonates of primary myristyl alcohol 85 and primary Octadecyl alcohol. HEINRICH BERTSCH. 100 105 110 115 120 125 13 Γ » 135 140 145 150
Independent claims6
23 paragraphs in 1 section, as filed
Patented July 31, 1934
1,968,796
UNITED STATES PATENT OFFICE
1,968,796
AGENT FOR WETTING, EMULSIFYING, ETC.
Heinrich Bertsch, Chemnitz, Germany, assignor, by mesne assignments, to American Hyalsol Corporation, Wilmington, Del., a corporation of Delaware
No Drawing. Original application March 6, 1930, Serial No. 433,815. Divided and this application May 27, 1932, Serial No. 614,053. In Germany March 6, 1929
Claims.
The present invention relates to agents or media adapted for wetting, emulsifying and like purposes. This application is a division of Ser. No. 433,815, filed March 6, 1930, relating to the prepI aration of these agents.
More particularly, the instant invention comprehends sulphuric reaction products of the fatty alcohols such as those obtained from cocoanut and palm nut oils. The phrase “sulphuric reac10 tion products” as used herein, includes sulphuric acid esters, sulphonic acids and mixtures or combinations of the same in any desired proportion.
The principal object of the present invention is to provide agents of the above nature which are 15 excellently adapted for the many purposes herein later set forth, and which are producible from raw ma.tPTia.ls at low cost by a minimum number of operations.
These agents are most conveniently produced 20 by reacting sulphuric acid or its equivalent with fatty alcohols, such as those produced from cocoanut oil by esterifying the fatty acids derived therefrom with lower aliphatic alcohols and reducing the mixture of esters to alcohols. Instead 25 of using the whole mixture of alcohols from the cocoanut oil, it is preferred to employ only the lower boiling portion thereof such as the first 50 to 60% of a distillate collected during distillation of the mixture. This portion of the distillate 30 consists principally of lauric alcohol.
The higher boiling fraction of the distillate consists mainly of myristic and octodecyl alcohols. The sulphuric reaction products obtainable from this fraction are also satisfactory for the purposes 35 for which the product is intended but not to as high a degree as those derived from the lower boiling fraction.
In the production of the product, the whole distillate or either fraction thereof may be treated 40 with any sulphonating or sulphating agent including concentrated or fuming sulphuric acid, sulphur trioxide, or chlorosulphonic acid, either alone or, if desired, together with a dehydrating media of organic or inorganic nature.
.- The nature of the reaction product as to whether it is an ester, a sulphonate or a mixture thereof is obviously dependent upon the intensity of the sulphonation or sulphating conditions, such as the character and quantity of the sulphonating 50 or sulphating agent and the temperature maintained during the reaction.
Herein follow some examples of methods by which the products of the present invention may be prepared. It is to be understood, however, that 55 the sulphuric reaction products as disclosed and (Cl. 252—1) .
claimed herein may be produced by other processes from lauric and related fatty alcohols.
Example 1
A mixture of fatty alcohols consisting prin- 60 cipally of lauric alcohol is obtained from cocoanut oil by esterification of the fatty acids with ethyl alcohol, reduction of the ethyl ester, distillation of the reduced product and collection of the first 50 to 60% of the distillate. This mixture in a 65 quantity of 100 kgs. is melted at a temperature of about 30° C. and treated with 50 kgs. of chlorosulphonic acid at the said temperature.
Example 2 γθ
A mixture of alcohols obtained as described in the above example, in a quantity of 100 kgs. is treated with 70 kgs. of fuming sulphuric acid at a temperature of 100° C.
The reaction products of the above processes 75 are directly neutralized by means of soda lye and then separated by known methods from inorganic impurities, such as sodium sulphate or sodium chloride.
The true sulphonic acids of the fatty alcohols 80 obtained by energetic sulphonation at elevated temperatures, as has been described in Example 2 above, are extremely valuable in the treatment of fibrous material, for the reason that they do not split off sulphuric acid even during the drying 85 and calendering of the textile at elevated temperatures. Ordinary or unstable sulphuric reaction products of fats and oils used for sizing purposes break up splitting off sulphuric acid, with the result that frequently the fibers are 90 injured.
The products of the present invention, and in particular those obtained from the mixture composed largely of lauric alcohol are very stable, are very soluble in water, and are excellent for 95 moistening and foaming purposes in many commercial processes, such as those employed in the textile, leather, pharmaceutical, ceramic and metal working industries. The products are also suitable for use in manufacturing insecticides 100 and dust binding agents and as a foaming agent in fire extinguishers, in which case 5% of the product is added to a 10% solution of sodium bicarbonate to be reacted in the extinguisher with sulphuric acid. In fact the products are useful 105 in substantially all processes wherein there is involved moistening, permeating, emulsifying, cleaning, softening, introducing active substances or forming protective colloids.
Every citation, both ways
| Document | Relation | Office | Cited during |
|---|---|---|---|
| US2934451A | Cited by | United States of America | Search report |
| US4612991A | Cited by | United States of America | Search report |
| US3003971A | Cited by | United States of America | Search report |
| US2956947A | Cited by | United States of America | Search report |
28 members in 6 offices; this record represents the family
Members28
| Document | Office | Kind | |
|---|---|---|---|
| GB308824A | United Kingdom | A | |
| GB317039A | United Kingdom | A | |
| NL24700C | Netherlands (Kingdom of the) | C | |
| NL31966C | Netherlands (Kingdom of the) | C | |
| NL32123C | Netherlands (Kingdom of the) | C | |
| NL32138C | Netherlands (Kingdom of the) | C | |
| NL35808C | Netherlands (Kingdom of the) | C | |
| FR671456A | France | A | |
| FR679186A | France | A | |
| FR37134E | France | E | |
| GB318610A | United Kingdom | A | |
| GB341978A | United Kingdom | A | |
| FR38048E | France | E | |
| GB350432A | United Kingdom | A | |
| FR38628E | France | E | |
| GB354851A | United Kingdom | A | |
| GB358535A | United Kingdom | A | |
| CH153812A | Switzerland | A | |
| NL32127C | Netherlands (Kingdom of the) | C | |
| US1968793A | United States of America | A | |
| US1968794A | United States of America | A | |
| US1968796AThis record | United States of America | A | |
| US1968797A | United States of America | A | |
| DE619182C | Germany | C | |
| US2114042A | United States of America | A | |
| DE659277C | Germany | C | |
| DE686332C | Germany | C | |
| DE736400C | Germany | C |
Numbers
- Publication, DOCDB
- 1968796
- Publication, EPODOC
- US1968796
- Application
- 61405332
- Application, DOCDB
- 61405332
- Application, EPODOC
- US19320614053
Classification
- CPC, 2
- C07C305/00
- A62D1/0071
- IPC, 2
- A62D1 02
- C07C305 00