US2983567A - Aldehyde tanning of leather - Google Patents
Aldehyde tanning of leather Download PDFInfo
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- US2983567A US2983567A US729254A US72925458A US2983567A US 2983567 A US2983567 A US 2983567A US 729254 A US729254 A US 729254A US 72925458 A US72925458 A US 72925458A US 2983567 A US2983567 A US 2983567A
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- formaldehyde
- leather
- hide
- water
- acetone
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- 239000010985 leather Substances 0.000 title description 54
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 title 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 214
- 239000000126 substance Substances 0.000 claims description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 11
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 10
- 239000003960 organic solvent Substances 0.000 claims description 9
- 239000010410 layer Substances 0.000 claims description 6
- 239000002344 surface layer Substances 0.000 claims description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 46
- 239000000243 solution Substances 0.000 description 24
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 235000013311 vegetables Nutrition 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 235000017343 Quebracho blanco Nutrition 0.000 description 6
- 241000065615 Schinopsis balansae Species 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 208000005156 Dehydration Diseases 0.000 description 5
- 230000018044 dehydration Effects 0.000 description 5
- 238000006297 dehydration reaction Methods 0.000 description 5
- 239000000284 extract Substances 0.000 description 5
- 230000005484 gravity Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 241000283690 Bos taurus Species 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 235000000396 iron Nutrition 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920006387 Vinylite Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- -1 alkyl ketones Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- UMGLBLXWFVODRF-UHFFFAOYSA-N formaldehyde;4-phenylphenol Chemical compound O=C.C1=CC(O)=CC=C1C1=CC=CC=C1 UMGLBLXWFVODRF-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 101150002688 kremen1 gene Proteins 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920000205 poly(isobutyl methacrylate) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- 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
- C14C3/16—Chemical tanning by organic agents using aliphatic aldehydes
Definitions
- This invention relates to the formaldehyde tanning of leather, and aims to provide such a leather which has the advantages of formaldehyde tanned leathers, without the usual attendant disadvantages of a brittle and cracky grain which resists finishing operations.
- Formaldehyde is a tanning material which is soluble in water and most organic solvents. It is commercially available both in aqueous solution (formalin), in solution in organic solvents, and as polymers which readily depolymerize to yield the active monomer. It is a very active tanning, agent for hide substance, as regards its ability to impart chemical and hydrothermal stability to hide fiber. It is also capable of stabilizing other tannages, such as mineral and vegetable tannages. It has the additional advantage that it yields white tanned leather, and such white leathers yield exceptionally bright colored dyeings.
- the leather produced by the method of this invention is characterized by having more formaldehyde combined with hide substance in the interior of the leather than in the flesh and hide layers. Characteristically, when a standard shrink temperature test is run on leather made in accordance with theinvention, the leather forms a barrel shaped piece instead of an hour-glass shaped piece, as is the case with conventional leathers.
- the preferred method of extracting the water involves immersion in aqueous water-miscible low boiling liquids like methanol, ethanol, the propanols, acetone, etc., which extract the water from and replace it in the. hide.
- aqueous water-miscible low boiling liquids like methanol, ethanol, the propanols, acetone, etc.
- the hide is desolventized by evaporation.
- an add-ant such as butyl carbitol (diethylene glycol monobutyl ether).
- Formaldehyde may be put into the hide substance during such a process of hide dehydration, provided it is not added until the water concentration in the hide is reduced below a point where a typical aqueous astringent tannage occurs.
- a hide comprising about 25% hide substance and water may be extracted with a liquid like acetone, in admixture with some water, to produce a hide containing a liquid comprising about 75% acetone-25% water.
- formaldehyde it is inadvisable to add formaldehyde to the first bath, since the formaldehyde will react with the hide substance.
- the solvent-water ratio is up to 75 %-25 in the hides, it is reasonably safe to add the formaldehyde.
- Example I-Additi0n of formaldehyde during hide dehydration Thus, a group of wet cow hides was dehydrated by exposing them to four successive acetone treatments, using a large excess of treating solvent.
- the wet hides were extracted with 81% acetone and water, obtained from a previous second stage of dehydration; the hides, after coming to equilibrium with the fluid, contained acetone and water in the ratio 76-24. They were then treated with 93% acetone, from a previous third stage, and came to equilibrium at 81% acetone-19% water.
- 97% acetone from a previous fourth stage was used on the third stage and a 93% acetone-7% water ratio was obtained at equilibrium.
- Fresh acetone, in the fourth stage increased the acetone-water ratio in the hide to 97-3.
- the 93% acetone-water mixture used in treating the hides in the second stage of dehydration act to rinse out formaldehyde from the surface of the stock.
- the resultant hides, after evaporation of the solvent, can be treated with water to get material which is well tanned in the interior and just barely tanned to untanned at the surface, and which yield barrel shaped shrink pieces at very low temperatures.
- formaldehyde tannage it is preferable to combine the formaldehyde tannage with some other form of tannage, using the formaldehyde to stabilize the other tannage. This can be done in various ways. One way is to treat unfinished leather, already tanned by vegetable extracts or by syntans.
- Example IlFrm'aldehyde tanning 0f tanned leather An unfinished sole leather, 9 irons thick and still porous because of its lack of finish, was dipped into a solution containing 2% formaldehyde, added as a 55% solution It was rinsed with clear isopropanol, and the isopropanol replaced with water. The resultant leather, on finishing, showed much greater resistance to compacting than leather not so treated; where the untreated leather required extensive treatment with fillers to resist compacting, the treated leather finished Well with much less filler.
- Example III-Combined formaldehyde vegetable tan A cow hide was dehydrated as in Example I, adding 2% formaldehyde to the third bath, and rinsing with pure acetone. It was then desolventized by evaporating the acetone; the formaldehyde not rinsed from the surface remained bound to the interior of the hide.
- the dry porous dehydrated hide was treated with a solution comprising Parts by weight Quebracho extract (20% water-80% solids) 5 Dymerex resin (dimerized rosin) 20 Paraffin wax (melting point 50 C.) Acetone at 120 F 65 and allowed to remain minutes to ensure complete impregnation.
- the resultant unfinished leather was about as thick as the original hide (9 to 10 irons), had good abrasion resistance and low water uptake (due to the resin), specific gravity of 0.65. It had a high shrink temperature and gave a barrel shaped test piece. It shows more resistance to compacting than conventional quebracho tanned sole leather.
- Example lV-Combined formaldehyde vegetable tan Example III was repeated, except no formaldehyde was added during the dehydration. Instead the impregnation bath used to treat the dry porous dehydrated hide was modified by removing 5 parts of acetone, and substituting 5 parts of formcel, a solution of 55 parts of formaldehyde in 45 parts of methanol; the rinse solution used was the impregnation solution diluted with 4 parts its weight of acetone.
- the leather was very similar in properties to the leather of Example III, except that it was somewhat more resistant to compacting and had a slightly harder grain surface.
- the combination tanning is preferably combined with the use of impregnants to give the leather additional properties as described in copending application Serial No. 729,238 filed April 18, 1958.
- Example V-Combined formaldehyde vegetable tan Example IV was repeated, except that the rinse consisted of Parts by weight Quebracho extract 5 Dymerex resin 4 Paraffin wax (50 C. melting point) 2 Formcel 1 Acetone 88
- Example Vl-Formaldehyde tanned leather with a surface quebracho tan Example II was repeated, except that the impregnating solution consisted of Parts by weight Dymerex resin 20 Parafiin wax (melting point 50 C.) 10 Methyl formcel (55% formaldehyde, 45% methanol) 5 Distilled fatty acids (oleic-stearic) mixture 2.5
- the rinse solution consisted of 20% of this impregnating solution, acetone.
- the wet hide was immersed for one hour in lukewarm water containing 10% of a powdered bisulfite-quebracho extract, at pH 3 to 4. After this immersion, the hide was drained and dried.
- the resultant leather had a surface color and character about identical with conventional quebracho tanned sole leather. However, it was much more water resistant than either conventional leather or the leather of Example III, since the hydrophilic quebracho was present only in the surface layers of the leathers. As a result, only the surface was wettable, an ideal situation, since the surface must be wettable for rolling in the finishing operation, whereas a hydrophobic interior makes the leather highly resistant to penetration by water.
- Leathers can be made with a wide variety of impregnants; substantially all natural and synthetic resin,-cellulose derivatives, soluble waxes and natural and synthetic rubbers can be used, provided they can be put into solution. Preferably those which can be put into mutual solution with formaldehyde are used for the practice of this invention.
- Example VII A series of resins was tested on pieces of hide dehydrated as above without the use of formaldehyde. In each case the formula used was as follows:
- Bakelite OKR 5254 p phenyl phenol formaldehyde resin
- Parlon S chlorinated rubber 7 Resin only partly soluble. Results uncertain. Orange shellac 25 Heavy color. Polyviny formal 28 Excellent color. it second cellulose butyrate 25 Good color. Polyisobutyl methacrylate 24 Do. Beckamine P 196 (urea formaldehyde resin) 22 Do. Epon 1001 (bisphenol epichlohydrin condensation product) 28 Oumar Resin 0 (conlnarone resin). 24 Piccolyte 450$ (coumarone indene 31 Firm.
- Example VIII Stock dehydrated as in Example IV, without the use of formaldehyde, was immersed ina solution consisting of at 40 C. for minutes. The temperature is not controlling; it may vary from room temperature to the boiling point.
- the stock was rinsed with a mixture of 1 part by weight of the above solution to 4 of acetone for 10 minutes. It was then treated with water containing very small quantities of surfactant, tanning agents, dyes and acids, to complete the tannage.
- a sole leather characterized by having a specific gravity of substantially under 1.0 and the excellent finishing characteristics of its grain surface, comprising cow hides of full thickness, the interior fibers of which are tanned with sufiicient formaldehyde to render them resistant to compacting under pressure, and the grain fibers of which are reacted with so much less formaldehyde that grain crackiness is avoided.
- a sole leather comprising cowhide, the interior fibers of which are tanned with sufficient formaldehyde to render the leather resistant to compacting under rolling pressure, and the grained surface of which contains substantially less reacted formaldehyde than the interior of the leather and is tanned with a hydrophilic vegetable tan which renders the surface easily wettable to facilitate finishing operations.
- the method of tanning with formaldehyde which comprises treating hide substance with an impregnating solution consisting essentially of formaldehyde in an organic solvent containing insufficient water to cause tannage of the hide substance by the formaldehyde, treating the hide substance with an organic solvent for formaldehyde containing substantially less formaldehyde than in the impregnating solution to substantially reduce the formaldehyde content of the surface layers and then treating the hide substance with water to cause the formaldehyde to react with the hide substance, to produce a leather having substantially more formaldehyde combined with hide substance in the interior of the leather than in the outer layers thereof.
- the method of tanning with formaldehyde which comprises treating porous untanned hide substance with an impregnating solution consisting essentially of formaldehyde in an organic solvent containing insufficient Water to cause tannage of the hide substance by the formaldehyde, treating the wet hide substance with an organic solvent for formaldehyde containing substantially less formaldehyde than in the impregnating solution to substantially reduce the formaldehyde content of the surface layers and then reacting the formaldehyde with the hide substance, to produce a leather having substantially more formaldehyde combined with hide substance in the interior of the leather than in the outer layers thereof.
Landscapes
- 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
mur w.
ALDEHYDE TANNING OF LEATHER Seymour S. Kremen and Robert Lee Southwood, Cincinnati, Ohio, assignors to Leather Research Corporation, New York, N.Y., a corporation of Delaware No Drawing. Filed Apr. 18, 1958, Ser. No. 729,254
Claims. (Cl. 894.33)
This invention relates to the formaldehyde tanning of leather, and aims to provide such a leather which has the advantages of formaldehyde tanned leathers, without the usual attendant disadvantages of a brittle and cracky grain which resists finishing operations.
Formaldehyde is a tanning material which is soluble in water and most organic solvents. It is commercially available both in aqueous solution (formalin), in solution in organic solvents, and as polymers which readily depolymerize to yield the active monomer. It is a very active tanning, agent for hide substance, as regards its ability to impart chemical and hydrothermal stability to hide fiber. It is also capable of stabilizing other tannages, such as mineral and vegetable tannages. It has the additional advantage that it yields white tanned leather, and such white leathers yield exceptionally bright colored dyeings.
The onefactor that has limited the use. of formaldehyde has been the difficulty of obtaining proper distribution through the vertical cross-section of the hides being tanned. Where the leather is of any substantial thickness, the surface is generally over-tanned with respect to the interior. The result is usually a leather with a brittle and cracky grain, which resists all efforts to work it into the desired commercially smooth surface. As a result, formaldehyde tanning has been restricted commercially to thin leather, such as glove leathers, of thicknesses under about 4 inch 4 inch is called an iron in the leather trade).
According to our invention, we can obtain formaldehyde tanned thicker leathers which have the desirable properties obtained with formaldehyde tanning, without the brittle and cracky grain, by treating porous dry untanned hide substance with an impregnating solution of formaldehyde in an organic solvent containing insufiicient water to give the typical astringent reaction between hide substance and aqueous formaldehyde, then rinsing the hide substance with a similar formaldehyde solvent containing substantially less formaldehyde than the impregnating solution, and then treating the hide substance with water to cause the formaldehyde to completely react with and tan the hide substance. Preferably, both the impregnating solvent and the rinsing solvent are Watermiscible; the lower alkyl ketones and alcohols are preferred solvents.
The leather produced by the method of this invention is characterized by having more formaldehyde combined with hide substance in the interior of the leather than in the flesh and hide layers. Characteristically, when a standard shrink temperature test is run on leather made in accordance with theinvention, the leather forms a barrel shaped piece instead of an hour-glass shaped piece, as is the case with conventional leathers.
This standard shrink temperature test is described in American Chemical Society Monograph No. 101, Mc- Laughlin and 'Iheis, The Chemistry of Leather Manufacture, Reinhold Publishing (New York) 1945, at page 783. A piece of leather 0.5 x 3" is clamped and set in a bath of acidulated water (for vegetable tanned leather) or aqueous glycerol (other leathers) and the bath temperature raised in standard fashion. As the test proceeds, the leather first swells as it absorbs the liquid and then, at the shrink temperature, starts to shrink. Since the lesser tanned leathers will shrink first, a conventional leather test piece which has more tan near the outside, will yield a finished test piece whose cross-section is hour-glass shaped, whereas leathers made in accordance with this invention yield pieces which are barrel shaped in cross-section.
It should be noted that formaldehyde, once it impregnates, is diificult to rinse from the interior of the hides, being Washed out well for only about .02 inch from the surface (this approximates one iron=% inch). Obviously, leather which is thinner than about 3 irons, will not show the notable difference between interior and surface characteristic of the present invention.
Where ordinary thick leathers, such as sole leathers, have specific gravities of 1.0 or more, it is possible to produce formaldehyde tanned sole leathers, in which some impregnant is used to give the leather other desirable properties, with a specific gravity as low as 0.65, and still have a leather which is resistant to compacting by the pressure applied by the rollers used in the finishing operation. In general, thinner formaldehyde tanned leathers made in accordance with this. invention will have specific gravities of the order of 0.75 or less.
To obtain porous untanned hide substance, it is necessary to extract the water from untanned hides. The preferred method of extracting the water involves immersion in aqueous water-miscible low boiling liquids like methanol, ethanol, the propanols, acetone, etc., which extract the water from and replace it in the. hide. When sufficient Water has been replaced so that the Water left will not damage the hide during evaporation, the hide is desolventized by evaporation. Such a process is described in the copending Kremen and Southwood application Serial No. 535,755 filed September 21, 1955, now U.S. Patent No. 2,917,833, where the extracting liquid is mixed with an add-ant such as butyl carbitol (diethylene glycol monobutyl ether).
Formaldehyde may be put into the hide substance during such a process of hide dehydration, provided it is not added until the water concentration in the hide is reduced below a point where a typical aqueous astringent tannage occurs. Thus, a hide comprising about 25% hide substance and water may be extracted with a liquid like acetone, in admixture with some water, to produce a hide containing a liquid comprising about 75% acetone-25% water. In such a system, it is inadvisable to add formaldehyde to the first bath, since the formaldehyde will react with the hide substance. However, once the solvent-water ratio is up to 75 %-25 in the hides, it is reasonably safe to add the formaldehyde.
Example I-Additi0n of formaldehyde during hide dehydration Thus, a group of wet cow hides was dehydrated by exposing them to four successive acetone treatments, using a large excess of treating solvent. The wet hides were extracted with 81% acetone and water, obtained from a previous second stage of dehydration; the hides, after coming to equilibrium with the fluid, contained acetone and water in the ratio 76-24. They were then treated with 93% acetone, from a previous third stage, and came to equilibrium at 81% acetone-19% water. 97% acetone from a previous fourth stage was used on the third stage and a 93% acetone-7% water ratio was obtained at equilibrium. Fresh acetone, in the fourth stage, increased the acetone-water ratio in the hide to 97-3.
In the practice of our invention with such a process, we have added 0.5, 1.0, 2.5 and 5.0% of formaldehyde (in the form of 55% formaldehyde solution in methanol) in methanol, the balance being isopropanol.
based on solution weight, to the 93% acetone-water mixture used in treating the hides in the second stage of dehydration. The 97% third stage bath, and the pure acetone used in the fourth stage, act to rinse out formaldehyde from the surface of the stock. The resultant hides, after evaporation of the solvent, can be treated with water to get material which is well tanned in the interior and just barely tanned to untanned at the surface, and which yield barrel shaped shrink pieces at very low temperatures.
Somewhat less formaldehyde is needed when the formaldehyde is added to the third bath, and the pure acetone of the fourth bath is used as a rinse, to get equivalent tannage. By using higher concentrations of formaldehyde (2.5% to 5%) in the third bath, and rinsing only with pure acetone, a fair degree of surface tannage is obtained. Similar results may be obtained with lower amounts of formaldehyde in the third bath, and very low amounts of formaldehyde (0.1% or less) in the final rinse. Care must be taken, however, to avoid too much formaldehyde in the surface, or grain crackiness will result.
It is preferable to combine the formaldehyde tannage with some other form of tannage, using the formaldehyde to stabilize the other tannage. This can be done in various ways. One way is to treat unfinished leather, already tanned by vegetable extracts or by syntans.
Example IlFrm'aldehyde tanning 0f tanned leather An unfinished sole leather, 9 irons thick and still porous because of its lack of finish, was dipped into a solution containing 2% formaldehyde, added as a 55% solution It was rinsed with clear isopropanol, and the isopropanol replaced with water. The resultant leather, on finishing, showed much greater resistance to compacting than leather not so treated; where the untreated leather required extensive treatment with fillers to resist compacting, the treated leather finished Well with much less filler.
It showed a barrel shaped cross-section when exposed to the shrink temperature test.
Another way to combine tannages is to impregnate untanned hide substance with both formaldehyde and other tanning agents; thus Example III-Combined formaldehyde vegetable tan A cow hide was dehydrated as in Example I, adding 2% formaldehyde to the third bath, and rinsing with pure acetone. It was then desolventized by evaporating the acetone; the formaldehyde not rinsed from the surface remained bound to the interior of the hide.
The dry porous dehydrated hide was treated with a solution comprising Parts by weight Quebracho extract (20% water-80% solids) 5 Dymerex resin (dimerized rosin) 20 Paraffin wax (melting point 50 C.) Acetone at 120 F 65 and allowed to remain minutes to ensure complete impregnation.
, The hide was drained and immersed in a solution comprising 1 part by weight of above.
4 parts by weight of acetone at 120 F.
After 10 minutes, the hide was withdrawn, then immersed 'in water for several hours and dried.
The resultant unfinished leather was about as thick as the original hide (9 to 10 irons), had good abrasion resistance and low water uptake (due to the resin), specific gravity of 0.65. It had a high shrink temperature and gave a barrel shaped test piece. It shows more resistance to compacting than conventional quebracho tanned sole leather.
It is somewhat better practice to dehydrate without formaldehyde, and add both tans together; thus Example lV-Combined formaldehyde vegetable tan Example III was repeated, except no formaldehyde was added during the dehydration. Instead the impregnation bath used to treat the dry porous dehydrated hide was modified by removing 5 parts of acetone, and substituting 5 parts of formcel, a solution of 55 parts of formaldehyde in 45 parts of methanol; the rinse solution used was the impregnation solution diluted with 4 parts its weight of acetone.
The leather was very similar in properties to the leather of Example III, except that it was somewhat more resistant to compacting and had a slightly harder grain surface.
The combination tanning is preferably combined with the use of impregnants to give the leather additional properties as described in copending application Serial No. 729,238 filed April 18, 1958.
Example V-Combined formaldehyde vegetable tan Example IV was repeated, except that the rinse consisted of Parts by weight Quebracho extract 5 Dymerex resin 4 Paraffin wax (50 C. melting point) 2 Formcel 1 Acetone 88 Example Vl-Formaldehyde tanned leather with a surface quebracho tan Example II was repeated, except that the impregnating solution consisted of Parts by weight Dymerex resin 20 Parafiin wax (melting point 50 C.) 10 Methyl formcel (55% formaldehyde, 45% methanol) 5 Distilled fatty acids (oleic-stearic) mixture 2.5
Acetone 62.5
and the rinse solution consisted of 20% of this impregnating solution, acetone. After the final immersion in water to activate the formaldehyde tan, the wet hide was immersed for one hour in lukewarm water containing 10% of a powdered bisulfite-quebracho extract, at pH 3 to 4. After this immersion, the hide was drained and dried. The resultant leather had a surface color and character about identical with conventional quebracho tanned sole leather. However, it was much more water resistant than either conventional leather or the leather of Example III, since the hydrophilic quebracho was present only in the surface layers of the leathers. As a result, only the surface was wettable, an ideal situation, since the surface must be wettable for rolling in the finishing operation, whereas a hydrophobic interior makes the leather highly resistant to penetration by water.
Leathers can be made with a wide variety of impregnants; substantially all natural and synthetic resin,-cellulose derivatives, soluble waxes and natural and synthetic rubbers can be used, provided they can be put into solution. Preferably those which can be put into mutual solution with formaldehyde are used for the practice of this invention.
Typical of other resins useful are the following:
Example VII A series of resins was tested on pieces of hide dehydrated as above without the use of formaldehyde. In each case the formula used was as follows:
Parts by weight Resin 20 Formcel (55% formaldehyde, 45% methanol) Acetone 75 In each case, the dehydrated hide was immersed in the solution of resin and then rinsed in a rinse comprising Parts by weight Original solution 20 Acetone 80 Resin Uptake, Comments percent )4 second nitrocellulose 16 Very pale color. Manila gum MA 24 Clorafin 42-8 (Chlorinated parafiin 42%) 22 Leather softer than Dymerex. Vinyllte VAGH (Polyvinyl choloride resin with hydroxyl groups) 27 Good color. Vinylite VYLF (Copolymer of vinyl chloride and vinyl acetat 25 Do. Bakelite OKR 5254 (p phenyl phenol formaldehyde resin) 28 Parlon S (chlorinated rubber) 7 Resin only partly soluble. Results uncertain. Orange shellac 25 Heavy color. Polyviny formal 28 Excellent color. it second cellulose butyrate 25 Good color. Polyisobutyl methacrylate 24 Do. Beckamine P 196 (urea formaldehyde resin) 22 Do. Epon 1001 (bisphenol epichlohydrin condensation product) 28 Oumar Resin 0 (conlnarone resin). 24 Piccolyte 450$ (coumarone indene 31 Firm.
25 Dirty color. 28 27 The example indicates that in general, resins can be used as a general class as well as elastomers, to impregnate hide substance by the process of the invention.
Example VIII Stock dehydrated as in Example IV, without the use of formaldehyde, was immersed ina solution consisting of at 40 C. for minutes. The temperature is not controlling; it may vary from room temperature to the boiling point.
The stock was rinsed with a mixture of 1 part by weight of the above solution to 4 of acetone for 10 minutes. It was then treated with water containing very small quantities of surfactant, tanning agents, dyes and acids, to complete the tannage.
While only a few examples of the technique for practicing the invention have been shown, it is obvious that the examples can be multiplied indefinitely and variations in the technique made without departing from the scope of the invention. It is only necessary that the stock be 6 impregnated with formaldehyde and that the bulk of the formaldehyde be rinsed from the surface so that the stock be more heavily tanned with formaldehyde in the interior than in the outer layers. While the invention has been described as applicable to leather from cattle hides, it may obviously be applied to the preparation of other types of hides and skins provided the hides are thick enough, ,4 inch or more, to produce leathers in which the difference between the interior and the exterior surfaces are noticeable.
What is claimed is:
1. A formaldehyde tanned leather of a thickness of at least 15 inch in which the interior of the leather contains substantially more formaldehyde combined with hide substance than do the outer layers and which leather produces a barrel-shaped cross section when a test section is immersed in water heated to the temperature at which the leather begins to shrink and is then withdrawn and permitted to dry.
2. A sole leather characterized by having a specific gravity of substantially under 1.0 and the excellent finishing characteristics of its grain surface, comprising cow hides of full thickness, the interior fibers of which are tanned with sufiicient formaldehyde to render them resistant to compacting under pressure, and the grain fibers of which are reacted with so much less formaldehyde that grain crackiness is avoided.
3. A sole leather comprising cowhide, the interior fibers of which are tanned with sufficient formaldehyde to render the leather resistant to compacting under rolling pressure, and the grained surface of which contains substantially less reacted formaldehyde than the interior of the leather and is tanned with a hydrophilic vegetable tan which renders the surface easily wettable to facilitate finishing operations.
4. The method of tanning with formaldehyde which comprises treating hide substance with an impregnating solution consisting essentially of formaldehyde in an organic solvent containing insufficient water to cause tannage of the hide substance by the formaldehyde, treating the hide substance with an organic solvent for formaldehyde containing substantially less formaldehyde than in the impregnating solution to substantially reduce the formaldehyde content of the surface layers and then treating the hide substance with water to cause the formaldehyde to react with the hide substance, to produce a leather having substantially more formaldehyde combined with hide substance in the interior of the leather than in the outer layers thereof.
5. The method of tanning with formaldehyde which comprises treating porous untanned hide substance with an impregnating solution consisting essentially of formaldehyde in an organic solvent containing insufficient Water to cause tannage of the hide substance by the formaldehyde, treating the wet hide substance with an organic solvent for formaldehyde containing substantially less formaldehyde than in the impregnating solution to substantially reduce the formaldehyde content of the surface layers and then reacting the formaldehyde with the hide substance, to produce a leather having substantially more formaldehyde combined with hide substance in the interior of the leather than in the outer layers thereof.
References Cited in the file of this patent UNITED STATES PATENTS 2,582,298 Ushakofi' Jan. 15, 1952 2,766,134 Davis Oct. 9, 1956 2,781,241 Ushakoif Feb. 12, 1957 2,824,816 Somerville et a1. Feb. 25, 1958 FOREIGN PATENTS 118,155 Australia Mar. 2, 1944 482,286 Great Britain Mar. 23, 1938 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 2,983,567 May 9 1961 Seymour S. Kremen et al.
at error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below Column 4, line 45, for "Example II" (SEAL) Attest:
ERNEST W. SWIDER DAVID L. LADD Attesting Officer Commissioner of Patents USCOM M DC read Example III -a
Claims (1)
- 4. THE METHOD OF TANNING WITH FORMALDEHYDE WHICH COMPRISES TREATING HIDE SUBSTANCE WITH AN IMPREGNATING SOLUTION CONSISTING ESSENTIALLY OF FORMALDEHYDE IN AN ORGANIC SOLVENT CONTAINING INSUFFICIENT WATER TO CAUSE TANNAGE OF THE HIDE SUBSTANCE BY THE FORMALDEHYDE, TREATING THE HIDE SUBSTANCE WITH AN ORGANIC SOLVENT FOR FORMALDEHYDE CONTAINING SUBSTANTIALLY LESS FORMALDEHYDE THAN IN THE IMPREGNATING SOLUTION TO SUBSTANTIALLY REDUCE THE FORMALDEHYDE CONTENT OF THE SURFACE LAYERS AND THEN TREATING THE HIDE SUBSTANCE WITH WATER TO CAUSE THE FORMALDEHYDE TO REACT WITH THE HIDE SUBSTANCE, TO PRODUCE A LEATHER HAVING SUBSTANTIALLY MORE FORMALDEHYDE COMBINED WITH HIDE SUBSTANCE IN THE INTERIOR OF THE LEATHER THAN IN THE OUTER LAYERS THEREOF.
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US729254A US2983567A (en) | 1958-04-18 | 1958-04-18 | Aldehyde tanning of leather |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US729254A US2983567A (en) | 1958-04-18 | 1958-04-18 | Aldehyde tanning of leather |
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US2983567A true US2983567A (en) | 1961-05-09 |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB482286A (en) * | 1936-09-23 | 1938-03-23 | George Freeman Lloyd | Improved process of tanning skins and hides and the product thereof |
US2582298A (en) * | 1949-10-01 | 1952-01-15 | Secotan Inc | Formed shoe uppers and the like |
US2766134A (en) * | 1954-03-31 | 1956-10-09 | John H Davis | Method for restoring original appearance of impregnated leather by dissolving the impregnant on the surface of the leather |
US2781241A (en) * | 1951-12-24 | 1957-02-12 | Secotan Inc | Method of treating animal skins |
US2824816A (en) * | 1954-05-13 | 1958-02-25 | Rohm & Haas | Method for treating leather |
-
1958
- 1958-04-18 US US729254A patent/US2983567A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB482286A (en) * | 1936-09-23 | 1938-03-23 | George Freeman Lloyd | Improved process of tanning skins and hides and the product thereof |
US2582298A (en) * | 1949-10-01 | 1952-01-15 | Secotan Inc | Formed shoe uppers and the like |
US2781241A (en) * | 1951-12-24 | 1957-02-12 | Secotan Inc | Method of treating animal skins |
US2766134A (en) * | 1954-03-31 | 1956-10-09 | John H Davis | Method for restoring original appearance of impregnated leather by dissolving the impregnant on the surface of the leather |
US2824816A (en) * | 1954-05-13 | 1958-02-25 | Rohm & Haas | Method for treating leather |
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