US2057959A - Process of removing the odor from bleached alkali metal salts of fatty acids - Google Patents
Process of removing the odor from bleached alkali metal salts of fatty acids Download PDFInfo
- Publication number
- US2057959A US2057959A US706162A US70616234A US2057959A US 2057959 A US2057959 A US 2057959A US 706162 A US706162 A US 706162A US 70616234 A US70616234 A US 70616234A US 2057959 A US2057959 A US 2057959A
- Authority
- US
- United States
- Prior art keywords
- bleached
- odor
- soaps
- soap
- pressure
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 title description 15
- 235000014113 dietary fatty acids Nutrition 0.000 title description 5
- 229930195729 fatty acid Natural products 0.000 title description 5
- 239000000194 fatty acid Substances 0.000 title description 5
- 150000004665 fatty acids Chemical class 0.000 title description 5
- 229910052783 alkali metal Inorganic materials 0.000 title description 4
- -1 alkali metal salts Chemical class 0.000 title description 4
- 239000000344 soap Substances 0.000 description 43
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 25
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 14
- 235000011121 sodium hydroxide Nutrition 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 238000004061 bleaching Methods 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 150000002927 oxygen compounds Chemical class 0.000 description 6
- 230000001603 reducing effect Effects 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- 239000003925 fat Substances 0.000 description 5
- 235000019197 fats Nutrition 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 230000009965 odorless effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical class OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910000286 fullers earth Inorganic materials 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D13/00—Making of soap or soap solutions in general; Apparatus therefor
- C11D13/02—Boiling soap; Refining
- C11D13/06—Bleaching of soap or soap solutions
Definitions
- the present invention relates to the removal of theodor adhering to the alkali metal salts of fatty acids on account of the bleaching process.
- the mixture thus obtained is heated either extern'ally or by indirect steam or by introducing steam into the pressure vessel; the pressure is thus raised and for instance increased to about 2 atmospheres toabout 6 atmospheres. Only in rare cases a still higher pressure is required, which may be increased to 15 atmospheres.
- the temperatures to be applied are generally between about 120 C. and 180 C. A working at a temperature of about 160 C. and under a pressure of about 6 atmospheres has proved to be particularly suitable.
- the salts of sulfurous acid, hyposulfurous acid and hydrosulfurous acid and the derivatives of these acids furthermore the sulfoxylates and thiosulfates either per se or several in comare the alkali metal salts, the salts of the alkaline earth metals and the zinc salts.
- thermore ammonia and the derivatives thereof thermore ammonia and the derivatives thereof,
- the effect of the process may still be improved by adding to the bleached soaps an alkaline substance besides the oxygen compound of sulfur having a reducing action.
- alkaline substances there may be used, besides caustic soda, other alkaline-reacting substances, such as the alkaline salts and ammonium salts of the carbonic acid, phosphorous acid, acetic acid or boric acid, fur- It may be pointed out that the present process is applicable not only to such soaps as have been bleached with active chlorine, but also to such for instance with peroxides, persulfates or the like.
- soaps which have been prepared from already bleached fats it being of no moment whether the fats have been bleached with chemicals or with adsorbents, such as fullers earth, active charcoal, silicic acid gel.
- (1) 5000 kilos of curd soap are prepared in the usual manner from dark waste fat in an iron vessel provided with a stirring device. Itis ad vantageous, if desired, repeatedly, to grain this soap and to separate the underlye. The soap is then bleached by causing the bleaching solution, at 0., to flow into the filled soap, while the stirring device is running.
- the bleaching solution is prepared from the usual chlorine lye with about grams of active chlorine per liter by dilution with twice to three times the quantity of water. After about 6 to 12 per cent. of the,
- the bleached soap paste is introduced into a pressure vessel having a capacity of about 8 tons. There is then added 2 parts per thousand of sodium bisulfite calculated upon the weight of the fat and neutralized by means of lye. After the lid has been closed, the mass is heated for 4 to 5 hours to about 150 C. under a pressure of 3 to 5 atmospheres. as the soap is odorless, it is reconducted into the first vessel and further treated as usual. In cases where the chlorine odor adheres particularly firmly to the soap, it is advisable to use, besidesv sodium hydrosulfite, formaldehyde-sodium-sulfoxylate or this substance only.
- An aqueous solution of 80 kilos of soda bleaching lye, 10 kilos of caustic soda and 200 kilos of water is then caused to run into the mixture in the course of one hour, while intimately mixing, care having to be taken that by the supply of open steam the soap paste is kept during the bleaching operation at a temperature of between 80 C. and C.
- the mixture is stirred until the active chlorine has been consumed.
- the material is then grained and the bleached soap is subjected to a subsequent treatment with pressure.
- the bleached soap paste is introduced into a pressure vessel; an aqueous solutionof 3 kilos of sodium bisulfite, 1 kilo of sodium hydrosulfite and 6 kilos of caustic soda is added and after the lid has been closed the paste is treated for 3 to 5 hours at a temperature of about 160 C. and under a pressure of 6 atmospheres.
- the soap improved-with regard to its odor is then worked up as usual.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
Patented Oct. 20, 136
FATE
Fr es PROCESS OF REMOVING THE ODOR FROM BLEACHED AL LIETAL SALTS 0F FATTY ACIDS Waldemar Kling, Frankfort-on-the-Main-Griesheim, Germany, assignor to I. G. Far-bonindustrie Aktiengesellschaft, Frankfort-on-the- Main, Germany No Drawing. Application January 10, 1934, Serial No. 706,162. ImGermany January 18, 1933 6 Claims. (crew-16) The present invention relates to the removal of theodor adhering to the alkali metal salts of fatty acids on account of the bleaching process.
It has already been attempted to render odorless the soaps bleached with hypochlorite, i. e. alkali metal salts of fatty acids which show the known odor resembling carbol or iodoform by boiling them, while simultaneously. using oxygen compounds of sulfur having a reducing action. The eifect obtained was, however, completely insufficient. It has, furthermore, been proposed to eliminate the smelling substances by blowing steam through the soap at a temperature of 200 C. or above, while applying pressure. This method has likewise not been successful, as it has been sufiicient only for removing the readily volatile odor carriers but not those which are bound to alkali and are consequently sparingly volatile, as is the case with the bodies causing the carbol odor. y A 1 It has also been suggested to eliminate the odor by heating the bleached soaps with alkali, while applying. pressure. This process, however, involves the danger that the bleached soaps discolor and assume a yellow to dark brown coloration. I have now found that the bleached soap can be rendered odorless in a satisfactory manner by heating it in the presence of oxygen compounds of sulfur having a reducing action with application of raised pressure. This treatment may be carried out as follows: the bleached'soap is introduced, if desired after having been grained and converted into a soap glue, into a pressure vessel and mixed with thenamed-substances. The mixture thus obtained is heated either extern'ally or by indirect steam or by introducing steam into the pressure vessel; the pressure is thus raised and for instance increased to about 2 atmospheres toabout 6 atmospheres. Only in rare cases a still higher pressure is required, which may be increased to 15 atmospheres. The temperatures to be applied are generally between about 120 C. and 180 C. A working at a temperature of about 160 C. and under a pressure of about 6 atmospheres has proved to be particularly suitable.
- bination with one another.
As agents capable of removing the odor there are used the salts of sulfurous acid, hyposulfurous acid and hydrosulfurous acid and the derivatives of these acids, furthermore the sulfoxylates and thiosulfates either per se or several in comare the alkali metal salts, the salts of the alkaline earth metals and the zinc salts. In most cases thermore ammonia and the derivatives thereof,
either per se or mixed with one another.
soaps as have been bleached with other metals,
Particularly useful only very small quantities of these agents are sufficient, for instance about A part to about 10 parts per thousand of the soap material to be treated. The height of the pressure, the kind and degree of purity of the fatty material to be used 0 for saponifica tion have an influence upon the quantity of the reducing agent to'be applied. In order to counteract a premature and. unnecessary consumption of the reducing agent, it may be advantageous to remove the air from the seat: material and the vessel by blowing in steam.
The effect of the process may still be improved by adding to the bleached soaps an alkaline substance besides the oxygen compound of sulfur having a reducing action. As alkaline substances there may be used, besides caustic soda, other alkaline-reacting substances, such as the alkaline salts and ammonium salts of the carbonic acid, phosphorous acid, acetic acid or boric acid, fur- It may be pointed out that the present process is applicable not only to such soaps as have been bleached with active chlorine, but also to such for instance with peroxides, persulfates or the like.
Furthermore, there may be treated according to the present process the soaps which have been prepared from already bleached fats, it being of no moment whether the fats have been bleached with chemicals or with adsorbents, such as fullers earth, active charcoal, silicic acid gel.
Accordingto the new process it is possible in all cases to render the soaps odorless in a satisfactory manner, even palm kernel oil soaps to which, as is known, the carbol odor adheres very tenaciously, without there occurring 9. discoloration of the bleached soaps.
The following examples serve to illustrate the invention, but they are not intended to limit it thereto:
(1) 5000 kilos of curd soap are prepared in the usual manner from dark waste fat in an iron vessel provided with a stirring device. Itis ad vantageous, if desired, repeatedly, to grain this soap and to separate the underlye. The soap is then bleached by causing the bleaching solution, at 0., to flow into the filled soap, while the stirring device is running. The bleaching solution is prepared from the usual chlorine lye with about grams of active chlorine per liter by dilution with twice to three times the quantity of water. After about 6 to 12 per cent. of the,
chlorine lye, calculated upon the saponiiied fat, 55
has been consumed, the bleached soap paste is introduced into a pressure vessel having a capacity of about 8 tons. There is then added 2 parts per thousand of sodium bisulfite calculated upon the weight of the fat and neutralized by means of lye. After the lid has been closed, the mass is heated for 4 to 5 hours to about 150 C. under a pressure of 3 to 5 atmospheres. as the soap is odorless, it is reconducted into the first vessel and further treated as usual. In cases where the chlorine odor adheres particularly firmly to the soap, it is advisable to use, besidesv sodium hydrosulfite, formaldehyde-sodium-sulfoxylate or this substance only.
(2) 1000 kilos of dark grease are saponified by means of caustic soda and the soap paste is grained twice. instance with a solution of sodium hydrochlorite. The soap curd is converted into a soap paste by the addition of kilos of calcined soda and water. The soap paste contains 40 per cent. of fatty acid and is heated to C. There is then added as much caustic soda solution (about 20 kilos of 40 B.) as the paste can take up without a separation into soap and lye occurring. An aqueous solution of 80 kilos of soda bleaching lye, 10 kilos of caustic soda and 200 kilos of water is then caused to run into the mixture in the course of one hour, while intimately mixing, care having to be taken that by the supply of open steam the soap paste is kept during the bleaching operation at a temperature of between 80 C. and C. After the addition of the bleaching solution the mixture is stirred until the active chlorine has been consumed. The material is then grained and the bleached soap is subjected to a subsequent treatment with pressure.
The bleached soap paste is introduced into a pressure vessel; an aqueous solutionof 3 kilos of sodium bisulfite, 1 kilo of sodium hydrosulfite and 6 kilos of caustic soda is added and after the lid has been closed the paste is treated for 3 to 5 hours at a temperature of about 160 C. and under a pressure of 6 atmospheres. The soap improved-with regard to its odor is then worked up as usual.
As soon The mass is then bleached, for
I claim:
1. The process of removing the carbolic or iodoform odor from bleached plastic soaps which comprises heating said bleached soaps under a pressure of about 2 to 16 atmospheres at about C. to about 180 C. in the presence of a small amount of a salt of an oxygen compound of sulfur having a reducing action sufficient to remove the odor.
2. The process of removing the carbolic or iodoform odor from bleached plastic soaps which comprises heating said bleached soaps under a pressure of about 6 atmospheres to about C. in the presence of about part to about 10 parts per thousand of an oxygen compound of sulfur having a reducing action.
3. The process of removing the carbolic or iodoform odor from bleached plastic soaps which comprises heating said bleached soaps under a pressure of about 2 to 16 atmospheres at about 120 C. to about C. in the presence of a small amount of sodium sulfite sufiicient to remove the odor.
4. The process of removing the carbolic or iodoform odor from bleached plastic soaps which comprises heating said bleached soaps under a pressure of about 2 to 16 atmospheres at about 120 C. to about 180 C. in the presence of a small amount of sodium hydrosulfite sufiicient to remove the odor.
5. The process of removing the carbolic or iodoform odor from bleached plastic soaps which comprises heating said bleached soaps under a pressure of about 2 to 16. atmospheres at about 120 C. to about 180 C. in the presence of a small amount of sodium formaldehyde sulfoxylate suflicient to remove the odor.
6. The process of removing the carb-olic or iodoform odor from bleached plastic soaps which comprises heating said bleached soaps under a pressure of about 2 to 16 atmospheres at about 120 C. to about 180 C. in the presence of a small amount of a salt of an oxygen compound of sulfur having a reducing action suflicient to remove the odor and an alkaline substance.
WALDEMAR KLING.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2057959X | 1933-01-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2057959A true US2057959A (en) | 1936-10-20 |
Family
ID=7982964
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US706162A Expired - Lifetime US2057959A (en) | 1933-01-18 | 1934-01-10 | Process of removing the odor from bleached alkali metal salts of fatty acids |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2057959A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2483414A (en) * | 1945-01-03 | 1949-10-04 | Lever Brothers Ltd | Process of bleaching fats and oils and making soap therefrom |
| US2755294A (en) * | 1951-11-09 | 1956-07-17 | Lever Brothers Ltd | Bleaching of soaps and soapstocks |
-
1934
- 1934-01-10 US US706162A patent/US2057959A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2483414A (en) * | 1945-01-03 | 1949-10-04 | Lever Brothers Ltd | Process of bleaching fats and oils and making soap therefrom |
| US2755294A (en) * | 1951-11-09 | 1956-07-17 | Lever Brothers Ltd | Bleaching of soaps and soapstocks |
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