US2283540A - Composition for treating leather and process for preparing the same - Google Patents

Composition for treating leather and process for preparing the same Download PDF

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Publication number
US2283540A
US2283540A US270690A US27069039A US2283540A US 2283540 A US2283540 A US 2283540A US 270690 A US270690 A US 270690A US 27069039 A US27069039 A US 27069039A US 2283540 A US2283540 A US 2283540A
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oil
sulfated
value
composition
organic nitrogen
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US270690A
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Gifford D Davis
Ralph E Porter
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National Oil Products Co
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National Oil Products Co
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    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C9/00Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
    • C14C9/02Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes using fatty or oily materials, e.g. fat liquoring
    • 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

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)

Description

Patented May 19, 1942 EYE s'ra'rss COMPOSITION FOR TREATING LEATHER AND PROCESS FOR PREPARING THE SAME No Drawing.
Application April 28, 1939,
Serial No. 270,690
20 Claims.
This invention relates to compositions for treating leather and to processes for preparing the same; more particularly this invention relates to compositions suitable for fatliquoring leather.
It is well known that sulfated oils such as sulfated cod oil, sulfated neats-foot oil, sulfated sperm oil, sulfated castor oil, or sulfated rapeseed oil used for iatliquoring leather should have pH values of between about and about 7.5, preferably between about 5 and about 6, depending upon the particular type of leather to be treated. Such oils ordinarily contain water in the amount of between and 50% of the oil and may contain, in addition, raw oils such as natural or manufactured moellon, and varying amounts of salts and other impurities. Many of these sulfated oils tend to become cloudy at pH values suitable for fatliquoring leather, the clouding being chiefly due to separation of water, raw oil or other substances from the sulfated oil. Cloudy sulfated oils give poor results when used for fatliquoring leather as the oil does not penetrate the leather properly and a spottyproduct may thus result. While these cloudy oils may be cleared by treatment with alkalies such as sodium carbonate or ammonia, the pl-l value of the oil is raised tosuch an extent that when the clear oils are used for iatliquoring leather, the proper take-up thereof is not accomplished, the leather may become harsh, and if dyed leather is being treated, the color thereof may be substantially injured.
The object of this invention is to produce Suliated oils suitable for fatliquorlng leather which are clear and substantially permanently stable at pH values between about 5 and about 7.5.
It has now been found that clear and substantially permanently stable sulfated oils having pI-l values between about 5 and about 7.5 may be prepared by incorporating in a sulfated oil having a pH value between about 5 and about 7.5, a relatively small amount of an organic nitrogen compound selected from the group consisting of organic nitrogen compound selected from the group above set forth.
The organic nitrogen compounds which may be employed in accordance with this invention may be mono-, di-, or poly amides, or thiamides; furthermore, secondary and tertiary as well as primary organic nitrogen compounds of the above types may be used. The following organic nitrogen compounds maybe mentioned as speciiic examples suitable for use in the practice of this invention: urea, acetamide, di-acetamide, tri-acetamide, N-ethylacetamide, acetanilide, thiourea, thiacetamide. thiacetanilide. The particular organic nitrogen compound employed depends to some extent upon the sulfated oil to be treated. Thus, for example, urea has been found suitable for clearing a sulfated cod oil composition or a mixture of sulfated sperm oil and coconut 011 containing water. Under certain conditions of operation it may be found that other organic nitrogen compounds may be more eillcient than urea; it is intended that in practicing this invention, the combination of organic nitrogen compound and sulfated oil found to be most effective under the particular conditions of use should preferably be employed.
The compositions of this invention may be prepared by sulfating an oil such as cod oil in any suitable manner, washing the product with water, partially neutralizing the oil to a pH value between about 2.5 and about 5, preferably between about 2.5 and about 4, so that substantially all of the free sulfuric acid is neutralized, settling the partially neutralized oil in a pan in a warm room and drawing ofi the salt and acid water. The partially neutralized oil thus prepared may be further treatedwith an alkali such as soda or ammonia to adjust its pH value to between about 5 and about 7.5, preferably between about 5 and about 6. The oil may then be treated in accordance with this invention by adding sufficient amounts of an organic nitrogen compound to produce a clear, stable, sulfated oil product. The amount of the organic nitrogen compound added to the oil may vary to some extent, depending somewhat upon the particular oil being treated; it has been found that generally an amount of organic nitrogen compound equivalent to between about 0.5% and about 5% of the final product is suitable. Sumcient water may then be added, if necessary, to adjust the moisture content of the sulfated oil to between about 10% and about preferably between about 25% and about 30%, depending upon the particular type of product, desired. Raw oils,
i. e., oils which have not been subjected to solubilizing treatments may be added to the oil if desired. It cloudiness has been induced by the addition of water or raw oils, additional amounts of an organic nitrogen compound may be added to the oil in order to produce the desired clarity; this, however, is ordinarily unnecessary. The finished product thus obtained is a brilliantly clear, stable, sulfated oil having a pH value of between about and about 7.5, preferably between about 5 and about 6.
The above method of preparation may bewaried somewhat. If desired, the oil may be neutralized to a pH value of between about 5 and about 7.5 before panning. The organic nitrogen compound may be added to the oil before neutralization or may be introduced into the 011 after water, raw oils or both have been added. The organic nitrogen compound may be added to the oil in a substantially pure condition or in the form of a solution or suspension in a liquid medium compatible with the oil; thus, for example, when using urea as the organic nitrogen compound, it may be added to the oil in the form of an aqueous solution thereof. Other modifications may also be made without departing from the scope of this invention.
This invention is also applicable to the treatment of sulfated oils containing water, raw oils or both which have become cloudy on standing. It has been found that the addition of between about 0.5% and about 5% of an organic nitrogen compound to such cloudy oils effects an immediate clarification of the oils and produces products which remain substantially permanently stable for long periods of time.
In some instances, it may be desirable to incorporate a reducing agent such as sodium bisulflte in the oil along with the organic nitrogen compound, since it has been found the presence of such reducing agents tends to increase the stability of the cleared sulfated oils; generally, an amount of reducing agent equivalent to between about 0.25% and about 1% of the final product is suitable.
The following examples are illustrative of this invention. Amounts are given in parts by weight.
Example I A composition comprising a mixture of sulfated sperm oil and coconut oil containing about 30% water and having a pH of about 5.8 became very cloudy and an appreciable amount of water separated after standing for a short time. About 3 parts of urea were added to about'97 parts of this composition. The mixture was then stirred and warmed gently. The composition cleared to form a brilliantly clear product, all the separated water being taken up again by the 011. Furthermore, the product remained clear after repeated freezings and thawings. The addition of the urea to the composition did not raise the pH value to any substantial extent.
Example II A composition comprising about 58 parts of a sulfated cod oil, 19 parts of a natural moellon, 19 parts of a manufactured moellon made by blowing warm air through raw cod oil and containing about 25% water, and about 4 parts of urea was formed. The pH value was adjusted to 5.9 with soda; the composition thus obtained remained clear and stable. A composition containing the above ingredients in the same relative proportions but containing no urea clouded at a pH value of 5.9 in a short time.
Example III A composition comprising about 78 parts of a mixture of sulfated sperm oil and coconut oil, 10 parts of a sulfated mixture of coconut fatty acids and castor oil, 9 parts of water and 3 parts of urea was formed. The pH value was adjusted to 5.7 withsoda; the composition thus obtained remained clear and stable. A composition containing the above ingredients in the same relative proportions but containing no urea clouded at a pH value of 5.7 in a short time.
Example IV A composition comprising 97 parts of a mixture of sulfated sperm oil and coconut oil containing about 30% water and 3 parts of acetamide was formed. The pH value was adjusted to 5.8 with soda; the composition thus obtained remained clear and stable. The mixture of sulfated sperm oil and coconut oil containing about 30% water but containing no acetamide clouded at a pH value of 5.8 in a short time.
Example V A composition comprising 97 parts of a mixture of sulfated sperm oil and coconut oil containing about 30% water and 3 parts of acetanilide was formed. The pH value was adjusted to 5.8 with soda; the composition thus obtained remained clear and stable. The mixture of sulfated sperm oil and coconut oil containing about 30% water but containing no acetanilide clouded at a pH value of 5.8 in a short time.
Example VI A composition comprising 97 parts of a mixture of sulfated sperm oil and coconut oil containing about 30% water and 3 parts of thiourea was formed. The pH value was adjusted to 5.8 with soda; the composition thus obtained remained clear and stable. The mixture of sulfated sperm oil and coconut oil containing about 30% water but containing no thiourea clouded at a pH value of 5.8 in a short time.
Example VII A composition comprising 96.5 parts of a mixture of sulfated sperm oil and coconut oil containing about 30% water, 3 parts of urea and 0.5 part of sodium bisulfite was formed. The pH value was adjusted to 5.8 with soda; the composition thus obtained remained clear and stable for 10 months when it was used. A mixture of sulfated sperm oil and coconut oil containing about 30% water but containing no urea and sodium bisulfite clouded at a pH value of 5.8 in a short time.
The above examples clearly show that the addition of the organic nitrogen compounds to sulfated oils produces substantially permanently clear products having pH values within the range suitable for treating leather. The chemical action of these compounds on the sulfated oils is somewhat obscure due to the extremely complicated and varied character of the oils treated in accordance with this invention. Thus the oils before sulfation may contain degradation products such as dior mono-glycerides and fatty acids as well as other substances of a more or less complicated nature. In addition, the sulfuric acid treatment ordinarily causes the formation of various hydrolytic decomposition products, thereby increasing the complexity of the chemical mixture being dealt with. The compounds which may be used in accordance with this invention may be either basic as in the case of urea, or neutral as in the case of acetamide: yet these compounds act in an entirely similar manner when added to sulfated oils in accordance with this invention. In view of the above, it will be seen it is impossible to advance any theory to explain the action of the organic nitrogen compounds used; in some cases the organic nitrogen compound may react with some of the constituents of the sulfated oil, and in others it may remain in its original condition. However, in either event, the purpose of this invention, namely, the production of a clear, substantialhr permanently stable sulfated oil, is accomplished by incorporating an organic nitrogen compound in the sulfated oil.
It has also been found that compositions prepared in accordance with this invention are suitable for treating textiles; for example, for softening textiles. This invention is therefore intended to include compositions for treating textiles and methods for preparing the same in which the problem is presented of maintaining the pH value of the sulfated oil between about and about 7.5 while also reserving the clarity of the sulfated oil.
It will be evident from the above description that the compositions prepared in accordance with this invention display considerable improvement over those heretofore employed, since they may be stored for considerable periods of time without becoming cloudy, and may be used to treat leather without in any way detrimentally affecting the leather being treated.
The term sulfated oils used throughout the specification and in the claims is intended to refer. to the sulfated oils in general use in the leather and other industries, and which ordinarily contain water, inorganic salts and, in some cases, raw oils and other substances; these oils are more commonly referred to as sulfonated oils.
Since certain changes in carrying out the above process and certain modifications in the composition which embody the invention may be made without departing from its scope, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
Having described our invention, what we claim as new and desire to secure by Letters Patent, is:
l. A process of treating fibrous material which comprises contacting said material with a sulfated oil having a pH value between about 5 and about 7.5, and containing 'a relatively small amount of an organic nitrogen compound selected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
2. A process of fatliquoring leather which comprises treating the leather with an emulsion of a sulfated oil having a pH value between about 5 and about 6, and containing between about 0.5% and about 5% of an organic nitrogencompound selected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
3. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and 7.5, and containing a relatively small lected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
4. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing a relatively small amount of an organic nitrogen compound selected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
5. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 7.5, and containing between about 10% and about 50% water and a relatively small amount of an organic nitrogen compound selected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
6. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing between about 0.5% and about 5% of an organic nitrogen compound selected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
7. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing a relatively small amount of acompound selected from the group consisting of urea, and reaction products thereof with constituents of the sulfated oil.
8. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about, 6, and containing a relatively small amount of a compound selected from the group consisting of thiourea, and reaction products thereof with constituents of the sulfated oil.
9. A clear and substantially permanently stable sulfatedoil having a pH value between about I 5 and about 6, and containing a relatively small amount of a compound selected from the group consisting of acetamide, and reaction products thereof with constituents of the sulfated oil.
10. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing between about 25% andabout 30% water and between about 0.5 and abbut 5% of a compound selected from the group consisting of urea, and reaction products thereof with constituents of the sulfated oil.
11. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing between about 25% and about 30% water and between about 0.5 and about 5% of a compound selected from the group consisting of thiourea, and reaction products thereof with constituents of the sulfated 011.
12. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing between about 25% and about 30% water and between amount of an organic nitrogen compound se- 76.
about 0.5 and about 5% of a compound selected 14. A clear and substantially permanently stable sulfated oil having a pH value between about 5 and about 6, and containing relatively small amounts of sodium bisulfite and an organic nitrogen compound selected from the group consisting of amides, thiamides, and reaction products thereof with constituents of the sulfated oil.
15. In a process of preparing a sulfated oil having a pH value between about 5 and about 7.5 suitable for treating fibrous material, involving treating an oil with sulfuric acid and neu tralizing the treated oil to the desired pH value, the improvement which comprises incorporating in the sulfated oil a relatively small amount of an organic nitrogen compound selected from the group consisting of amides and thiamides.
16. In a process of preparing a sulfated oil having a pH value of between about 5 and about 6 suitable for treating leather, involving treating an oil with sulfuric acid, neutralizing the treated oil to the desired pH value, and adjusting its moisture content so that the final product contains between about 25% and about 30% water, the improvement which comprises incorporating in the sulfated oil an amount of urea equivalent to between about 0.5% and about 5% of the 1 water, the improvement which comprises in ter, the improvement which comprises incorporating in the sulfated oil an amount of thiourea equivalent to between about 0.5% and about 5% of the final product.
18. In a process of preparing a sulfated oil having a pH value of between about 5 and about 6 suitable for treating leather, involving treating an oilwith sulfuric acid, neutralizing the treated oil to the desired pH value, and adjusting its moisture content so that the final product contains between about 25% and about 30% corporating in the sulfated 011 an amount of acetamide equivalent to between about 0.5% and about 5% of the final product.
19. A process of clearing a cloudy sulfated oil having a pH value between about 5 and about 17.5, which comprises introducing into said oil an organic nitrogen compound selected from the group consisting of amides and thiamides.
20. A process of clearing a cloudy sulfated oil having a pH value between about 5 and about 6, and containing between about 25% and about 30% water, which comprises introducing into said oil an amount of a reducing agent equivalent to between about 0.25% and about 1% of the final product, and an amount of an organic nitrogen compound selected from the group consisting of amides and thiamides equivalent to between about 0.5% and about 5% of the final product.
G. D. DAVIS. RALPH E. PORTER.
US270690A 1939-04-28 1939-04-28 Composition for treating leather and process for preparing the same Expired - Lifetime US2283540A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2445975A (en) * 1946-05-08 1948-07-27 American Cyanamid Co Solubilized alkaryl sulfonate composition
US2630408A (en) * 1948-01-30 1953-03-03 Nopco Chem Co Fat composition
US5415789A (en) * 1994-09-20 1995-05-16 Citra Science Ltd. Leather cleaner and conditioner
US5415787A (en) * 1994-09-20 1995-05-16 Citra Science Ltd. Leather cleaner and conditioner
US5415788A (en) * 1994-09-20 1995-05-16 Citra Science Ltd. Leather cleaner and conditioner
US20060150342A1 (en) * 2002-09-12 2006-07-13 Basf Akiengesellschaft Stuffing agent for leather based on mixtures of modified, native oils with alcoxylated alkanols, use thereof and method for treating leather

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2445975A (en) * 1946-05-08 1948-07-27 American Cyanamid Co Solubilized alkaryl sulfonate composition
US2630408A (en) * 1948-01-30 1953-03-03 Nopco Chem Co Fat composition
US5415789A (en) * 1994-09-20 1995-05-16 Citra Science Ltd. Leather cleaner and conditioner
US5415787A (en) * 1994-09-20 1995-05-16 Citra Science Ltd. Leather cleaner and conditioner
US5415788A (en) * 1994-09-20 1995-05-16 Citra Science Ltd. Leather cleaner and conditioner
WO1996009413A1 (en) * 1994-09-20 1996-03-28 Citra Science Ltd. Leather cleaner and conditioner
US20060150342A1 (en) * 2002-09-12 2006-07-13 Basf Akiengesellschaft Stuffing agent for leather based on mixtures of modified, native oils with alcoxylated alkanols, use thereof and method for treating leather

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