US2591218A - Guanide-formaldehyde condensation products for tanning and bleaching leather - Google Patents
Guanide-formaldehyde condensation products for tanning and bleaching leather Download PDFInfo
- Publication number
- US2591218A US2591218A US110021A US11002149A US2591218A US 2591218 A US2591218 A US 2591218A US 110021 A US110021 A US 110021A US 11002149 A US11002149 A US 11002149A US 2591218 A US2591218 A US 2591218A
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- US
- United States
- Prior art keywords
- leather
- guanide
- tanning
- condensation products
- bleaching
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Classifications
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- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C3/00—Tanning; Compositions for tanning
- C14C3/02—Chemical tanning
- C14C3/08—Chemical tanning by organic agents
- C14C3/18—Chemical tanning by organic agents using polycondensation products or precursors thereof
Definitions
- This invention relates to the treatment of skins and/or hides or leather and more particularly, to a process for obtaining white leather.
- a further objectyof the present invention is the provision of an agent which will whiten chrome tanned leather.
- Another object of the present invention is the provision of a new tanning and bleaching agent.
- Still another object of the present invention is to provide a leather tanning and bleaching agent which may be used alone or in conjunction with other tanning agents such as, mineral, vegetable, and synthetic tanning. agents.
- Example 1 126 parts (1 mol) of acetoguanide and 243 parts (3 mols) of 37% aqueous formaldehyde solution are refluxed for 30 minutes and cooled to 40 C. 74 parts of 50% sodium hydroxide solution are then slowly added with stirring and cooling to prevent the temperature of the mixture from rising above 50 C. The reaction mixture is then refluxed for 20 minutes longer, and a clear stable solution of acetoguanide-formaldehyde resin is obtained.
- Example 2 Example 1 is repeated using a resin prepared as follows: 28.5 (0.23 mol) of acetoguanide, 60.8 (0.75 mol) of 37% aqueous formaldehyde solu-- 'tion and 20 parts concentrated sulfuric acid are heated together at 90 C. and then quickly cooled. A clear stable solution of resin is obtained.
- My new tanning agents include formaldehyde condensation products of guanides of the following general formula:
- R is an alkyl hydrocarbon having from 1-3 carbon atoms or an aryl hydrocarbon of from 6-8 carbon atoms.
- the condensation products are prepared by condensing from about 1 to about 3 mols of formaldehyde with each mol of the guanide under either acid or alkaline conditions.
- Formaldehyde-yielding materials such as paraformaldehyde and hexamethylenetetramine may be substituted for the formaldehyde of the examples as may other aldehydes including acetaldehyde, paraldehyde, furfural, and the like.
- guanides themselves may be readily prepared from dicyandiamide and the particular acid corresponding to the R group.
- the acetoguanide of the examples was prepared by refluxing 48 parts of glacial acetic acid with 33.6 parts of dicyandiamide until reaction ceased. Water was added to the reaction mixture, and the acetoguanide which precipitated out was filtered off.
- the water-soluble condensation products here described are acid-sensitive. In aqueous solution they may be converted to the insoluble or hydrophobe state by the addition of acid, with conse quent precipitation of a solid white resin. Since the chrome salts in leather tanned therewith will generate sulfuric acid when brought intocontact with water, it is possible by the process of the present invention to capitalize on the acidsensitivity of the condensation products on the one hand, and the capacity of the chrometanned leather to generate sulfuric acid in the presence of water on the other, for the bleaching or whitening of green chrome-tanned leather.
- the bleaching process of the present invention may be carried out simply by drumming chromed leather in a water solution of one of the described guanide condensation products. Varying concentrations, e. g., from about 1% to about 50% by weight of solid resin based on the shaved weight of the stock, may be used in the process and my invention is in no sense limited to the use of any particular concentration. I prefer to use from about 5% to about 25% resin, on the same basis.
- the new tanning agents of the present invention may be used either alone or in conjunction with other tanning agents such as oils, vegetable tannins, alum, chrome, syntans, formaldehyde and the like.
- tanning agents such as oils, vegetable tannins, alum, chrome, syntans, formaldehyde and the like.
- the guanide resins can be used directly to obtain a white tanned leather or they may be used to whiten leather tanned by some other agent.
- white tanned skins obtained by treatment with the guanide condensation products described in the present specification may be further tanned by means of other type agents such as those listed above.
- a process which comprises impregnating skins and hides with an aqueous solution of a water-dilutable, acid-sensitive condensation product of 1 mol of a guanide of the formula:
- R is selected from the group consisting of alkyl radicals of from 1 to 3 carbon atoms and aryl radicals of from 6 to 8 carbon atoms with from about 1 to about 3 mols of formaldehyde.
- a process which comprises impregnating skins and hides with an aqueous solution of a Water-dilutable, acid-sensitive condensation prodnot of 1 mol of acetoguanide with from about .1 to about 3 mols of formaldehyde.
- a process which comprises impregnating skins and hides first with an aqueous solution of a water dilutable, acid-sensitive condensation product of 1 mol of a guanideof the formula:
- R is selected from the group consisting of alkyl radicals of from 1 to 3 carbon atoms and aryl radicals of from 6-8 carbon atoms with from about 1 to about 3 mols of formaldehyde, said leather being obtained by the process of claim 1.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Description
Patented Apr. 1, 1952 GUANIDE-FORMALDEHYDE CONDENSATION PRODUCTS FOR TANNING AND BLEACH- ING LEATHER Jack T. Thurston, Riverside, Conn., assignor ,to American Cyanamid Company, New York, N. Y., a corporation of Maine No Drawing. Application August 12, 1949, Serial No. 110,021
10 Claims.
This invention relates to the treatment of skins and/or hides or leather and more particularly, to a process for obtaining white leather.
It is an object of the present invention to provide a bleaching agent for tanned hides and/or skins.
It is another object of the present invention to provide a tanning agent which will tan skins and/or hides white.
A further objectyof the present invention is the provision of an agent which will whiten chrome tanned leather.
Another object of the present invention is the provision of a new tanning and bleaching agent.
Still another object of the present invention is to provide a leather tanning and bleaching agent which may be used alone or in conjunction with other tanning agents such as, mineral, vegetable, and synthetic tanning. agents.
The above and other objects are attained by treating hides and/or skins or tanned leather with a water-soluble formaldehyde condensation product of a guanide, and particularly of acetoguanide.
The invention will be described in greater detail in conjunction with the following specific examples in which proportions are given in parts by weight. These examples are not intended to limit the scope of the invention; they are merely illustrative.
Example 1 126 parts (1 mol) of acetoguanide and 243 parts (3 mols) of 37% aqueous formaldehyde solution are refluxed for 30 minutes and cooled to 40 C. 74 parts of 50% sodium hydroxide solution are then slowly added with stirring and cooling to prevent the temperature of the mixture from rising above 50 C. The reaction mixture is then refluxed for 20 minutes longer, and a clear stable solution of acetoguanide-formaldehyde resin is obtained.
100 parts of chrome tanned leather are drummed for one hour with 100 parts of a 5% solution of the resin prepared as described above. The leather is then rinsed, fat liquored and dried, the final leather product being a white full leather having good characteristics.
Example 2 Example 1 is repeated using a resin prepared as follows: 28.5 (0.23 mol) of acetoguanide, 60.8 (0.75 mol) of 37% aqueous formaldehyde solu-- 'tion and 20 parts concentrated sulfuric acid are heated together at 90 C. and then quickly cooled. A clear stable solution of resin is obtained.
My new tanning agents include formaldehyde condensation products of guanides of the following general formula:
t 19 N HO-A i l-NH:
in which R is an alkyl hydrocarbon having from 1-3 carbon atoms or an aryl hydrocarbon of from 6-8 carbon atoms. 7 The condensation products are prepared by condensing from about 1 to about 3 mols of formaldehyde with each mol of the guanide under either acid or alkaline conditions.
Formaldehyde-yielding materials such as paraformaldehyde and hexamethylenetetramine may be substituted for the formaldehyde of the examples as may other aldehydes including acetaldehyde, paraldehyde, furfural, and the like.
The guanides themselves may be readily prepared from dicyandiamide and the particular acid corresponding to the R group. Thus the acetoguanide of the examples was prepared by refluxing 48 parts of glacial acetic acid with 33.6 parts of dicyandiamide until reaction ceased. Water was added to the reaction mixture, and the acetoguanide which precipitated out was filtered off.
The water-soluble condensation products here described are acid-sensitive. In aqueous solution they may be converted to the insoluble or hydrophobe state by the addition of acid, with conse quent precipitation of a solid white resin. Since the chrome salts in leather tanned therewith will generate sulfuric acid when brought intocontact with water, it is possible by the process of the present invention to capitalize on the acidsensitivity of the condensation products on the one hand, and the capacity of the chrometanned leather to generate sulfuric acid in the presence of water on the other, for the bleaching or whitening of green chrome-tanned leather.
The bleaching process of the present invention may be carried out simply by drumming chromed leather in a water solution of one of the described guanide condensation products. Varying concentrations, e. g., from about 1% to about 50% by weight of solid resin based on the shaved weight of the stock, may be used in the process and my invention is in no sense limited to the use of any particular concentration. I prefer to use from about 5% to about 25% resin, on the same basis.
The new tanning agents of the present invention may be used either alone or in conjunction with other tanning agents such as oils, vegetable tannins, alum, chrome, syntans, formaldehyde and the like. Thus the guanide resins can be used directly to obtain a white tanned leather or they may be used to whiten leather tanned by some other agent. Similarly, white tanned skins obtained by treatment with the guanide condensation products described in the present specification may be further tanned by means of other type agents such as those listed above.
It is an advantage of the guanide resins of the present invention that they maybe precipitated V and dissolved under pH conditions which are suitable for leather work.
I claim:
1. A process which comprises impregnating skins and hides with an aqueous solution of a water-dilutable, acid-sensitive condensation product of 1 mol of a guanide of the formula:
in which R is selected from the group consisting of alkyl radicals of from 1 to 3 carbon atoms and aryl radicals of from 6 to 8 carbon atoms with from about 1 to about 3 mols of formaldehyde.
2. A process which comprises impregnating skins and hides with an aqueous solution of a Water-dilutable, acid-sensitive condensation prodnot of 1 mol of acetoguanide with from about .1 to about 3 mols of formaldehyde.
, 3. A process which comprises impregnating skins and hides first with an aqueous solution of a water dilutable, acid-sensitive condensation product of 1 mol of a guanideof the formula:
no-o N N 11MB in which R is selected from the group consisting of alkyl radicals of from 1 to 3 carbon atoms and aryl radicals of from 6-8 carbon atoms with from about 1 to about 3 mols of formaldehyde, said leather being obtained by the process of claim 1.
10. White tanned leather obtained by the process of claim 9 wherein the guanide is acetoguanide.
guanide JACK T. THURSTON.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,197,357 Widmer Apr. 16, 1940 7 2,309,187 Grim et al v Jan. 26, 1943 2,316,741 Dawson Apr. 13, 1943 OTHER REFERENCES Textile Finishing, by Marsh, pub1948 by Chapman and Hall,- Ltd., London, England, pp. 390, 404.
Claims (1)
1. A PROCESS WHICH COMPRISES IMPREGNATING SKINS AND HIDES WITH AN AQUEOUS SOLUTION OF A WATER-DILUTABLE, ACID-SENSITIVE CONDENSATION PRODUCT OF 1 MOL OF A GUANIDE OF THE FORMULA:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US110021A US2591218A (en) | 1949-08-12 | 1949-08-12 | Guanide-formaldehyde condensation products for tanning and bleaching leather |
Applications Claiming Priority (1)
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US110021A US2591218A (en) | 1949-08-12 | 1949-08-12 | Guanide-formaldehyde condensation products for tanning and bleaching leather |
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US2591218A true US2591218A (en) | 1952-04-01 |
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US110021A Expired - Lifetime US2591218A (en) | 1949-08-12 | 1949-08-12 | Guanide-formaldehyde condensation products for tanning and bleaching leather |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2717356A (en) * | 1951-03-28 | 1955-09-06 | Erie Resistor Corp | Temperature and voltage control capacitors |
DE1052628B (en) * | 1952-05-03 | 1959-03-12 | Basf Ag | Process for the production of leather |
DE975207C (en) * | 1952-04-25 | 1961-09-28 | Boehme Fettchemie G M B H | Tanning of hides and skins |
DE976279C (en) * | 1952-07-22 | 1963-06-06 | Cassella Farbwerke Mainkur Ag | Tanning agent for animal skins and hides |
DE1153858B (en) * | 1952-03-18 | 1963-09-05 | Jacques Wolf & Co | Process for treating leather |
DE1185763B (en) * | 1953-09-18 | 1965-01-21 | Boehme Fettchemie Gmbh | Process for tanning hides and skins |
DE977577C (en) * | 1952-08-01 | 1967-05-18 | Basf Ag | Process for impregnating leather |
DE1289941B (en) * | 1953-06-01 | 1969-02-27 | Boehme Chemie Gmbh | Water-soluble condensation products from dicyandiamide, oxo compounds and salts of sulphurous acid for tanning skins or pelts |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2197357A (en) * | 1935-09-28 | 1940-04-16 | Ciba Products Corp | Condensation products of amino-triazine, aldehyde, and alcoholic group-containing compounds and processes of making same |
US2309187A (en) * | 1941-10-14 | 1943-01-26 | American Cyanamid Co | Treatment of hides |
US2316741A (en) * | 1942-07-25 | 1943-04-13 | American Cyanamid Co | Leather manufacture |
-
1949
- 1949-08-12 US US110021A patent/US2591218A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2197357A (en) * | 1935-09-28 | 1940-04-16 | Ciba Products Corp | Condensation products of amino-triazine, aldehyde, and alcoholic group-containing compounds and processes of making same |
US2309187A (en) * | 1941-10-14 | 1943-01-26 | American Cyanamid Co | Treatment of hides |
US2316741A (en) * | 1942-07-25 | 1943-04-13 | American Cyanamid Co | Leather manufacture |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2717356A (en) * | 1951-03-28 | 1955-09-06 | Erie Resistor Corp | Temperature and voltage control capacitors |
DE1153858B (en) * | 1952-03-18 | 1963-09-05 | Jacques Wolf & Co | Process for treating leather |
DE975207C (en) * | 1952-04-25 | 1961-09-28 | Boehme Fettchemie G M B H | Tanning of hides and skins |
DE1052628B (en) * | 1952-05-03 | 1959-03-12 | Basf Ag | Process for the production of leather |
DE976279C (en) * | 1952-07-22 | 1963-06-06 | Cassella Farbwerke Mainkur Ag | Tanning agent for animal skins and hides |
DE977577C (en) * | 1952-08-01 | 1967-05-18 | Basf Ag | Process for impregnating leather |
DE1289941B (en) * | 1953-06-01 | 1969-02-27 | Boehme Chemie Gmbh | Water-soluble condensation products from dicyandiamide, oxo compounds and salts of sulphurous acid for tanning skins or pelts |
DE1185763B (en) * | 1953-09-18 | 1965-01-21 | Boehme Fettchemie Gmbh | Process for tanning hides and skins |
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