US2123832A - Treatment of hides, skins, and leather - Google Patents
Treatment of hides, skins, and leather Download PDFInfo
- Publication number
- US2123832A US2123832A US95280A US9528036A US2123832A US 2123832 A US2123832 A US 2123832A US 95280 A US95280 A US 95280A US 9528036 A US9528036 A US 9528036A US 2123832 A US2123832 A US 2123832A
- Authority
- US
- United States
- Prior art keywords
- acid
- leather
- skins
- acids
- hides
- 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
- 239000010985 leather Substances 0.000 title description 39
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 46
- 239000002253 acid Substances 0.000 description 39
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 31
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 31
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 27
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 23
- 150000007513 acids Chemical class 0.000 description 20
- 238000000034 method Methods 0.000 description 18
- 150000003839 salts Chemical class 0.000 description 18
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 17
- 239000011976 maleic acid Substances 0.000 description 17
- 235000011044 succinic acid Nutrition 0.000 description 17
- 235000011087 fumaric acid Nutrition 0.000 description 16
- 229910052500 inorganic mineral Inorganic materials 0.000 description 16
- 235000010755 mineral Nutrition 0.000 description 16
- 239000011707 mineral Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 15
- 239000001384 succinic acid Substances 0.000 description 15
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 14
- 239000001530 fumaric acid Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 150000001991 dicarboxylic acids Chemical class 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000005554 pickling Methods 0.000 description 9
- -1 ester salts Chemical class 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 238000006386 neutralization reaction Methods 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 235000011941 Tilia x europaea Nutrition 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 239000004571 lime Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000003472 neutralizing effect Effects 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 239000003513 alkali Substances 0.000 description 5
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 238000002791 soaking Methods 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 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 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000020477 pH reduction Effects 0.000 description 4
- 235000021110 pickles Nutrition 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- CHCFOMQHQIQBLZ-UHFFFAOYSA-N azane;phthalic acid Chemical compound N.N.OC(=O)C1=CC=CC=C1C(O)=O CHCFOMQHQIQBLZ-UHFFFAOYSA-N 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 230000003139 buffering effect Effects 0.000 description 3
- 244000309466 calf Species 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 150000002238 fumaric acids Chemical class 0.000 description 3
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- HQWKKEIVHQXCPI-UHFFFAOYSA-L disodium;phthalate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C([O-])=O HQWKKEIVHQXCPI-UHFFFAOYSA-L 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000008233 hard water Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 150000002689 maleic acids Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- 150000003022 phthalic acids Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 150000003444 succinic acids Chemical class 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QISOBCMNUJQOJU-UHFFFAOYSA-N 4-bromo-1h-pyrazole-5-carboxylic acid Chemical compound OC(=O)C=1NN=CC=1Br QISOBCMNUJQOJU-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 229910021538 borax Inorganic materials 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
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 1
- 229940012189 methyl orange Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 230000008674 spewing Effects 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- C14C1/00—Chemical treatment prior to tanning
-
- 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
- C14C1/00—Chemical treatment prior to tanning
- C14C1/08—Deliming; Bating; Pickling; Degreasing
-
- 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
- C14C3/04—Mineral tanning
Definitions
- This invention relates to the use of certain polycarboxylic acids and-their water soluble salts and ester salts in preparinghides and skins for tannages such as mineral andfvegetable tannage,
- tannages, bleaching, neutralizing the leather, fatliquoring the-tanned leather or dyeing the leather, or any combination of these steps may be carried out in the presence of members of the class consisting of phthalic acid, maleic acid, fumaric acid and succinic acid and their water soluble salts which are the ammonium, ethanolamine, and alkali metal salts.
- dicarboxylic acids of the above group and the' water soluble neutral and acid salts thereof are important agents for improving the above steps in leather manufacture when incorporated with the materials ordinarily used therein, and thatleather of improved characteristics will result from their use. Accordingly, it is an object of the invention to improve each of the above steps of leather manufacture in the manner which will be pointed out in the present specification, to the end that leather having a better grain, a better feel, lessened deterioration upon storage or subjection to light and other improved characteristics will result.
- dicarboxylic acids and especially phthalic acid produce a cleaner and firmer grain when the skins are tanned, because their preserving action eliminates the necessity of extreme acidification for the prevention of mold and bacterial growth.
- Phthalic acid in saturated solution has a pH of 2.2, which is low enough for any acidification in modern leather manufacture. 'It has considerable advantages over mineral acids in operations involving hide substance. A most important characteristic for this purpose is its bufiering capacity, making it very valuable where gradual acidification is required. This is important not only in pickling operations but also in all other operations of leather manufacture due to the necessity of protecting the collagens against destruction during the relatively great changes in hydrogen ion concentration to which the hide is subjected.
- the dicarboxylic acids of the above class have greater buifering capacity due to the availability of the second hydrogen ion, at least doubling the buffering range.
- alkali metal salts of dicarboxylic acids, and particularly sodium acid phthalate advantage is taken of the reverse effect in accomplishing a gentle and limited neutralization.
- Phthalic acid has two buffering 'maxima at 2.92 and 5.41 respectively.
- Sodium phthalate or other alkali metal phthalates when used in chrome tannage or other mineral tannages, operates to set the chrome or other metal and thus to convert the hide or skin into leather. When so used it avoids the development of a drawn grain and produces fuller fianks with more uniform distribution during subsequent fat-liquoring, as compared with conventional neutralizing agents. Similar results are obtained by the use of maleic acid, fumaric acid and succinic acid in the form of their alkali metal salts.
- dicarboxylic acids have the additional important property, especially when applied in water solution, of bleaching vegetable and mineral tanned leather.
- fat-liquoring or stuffing compositions the addition of polycarboxylic acids andwtheir salts, especiallysodium phthalate, impart greater stability against auto-oxidation and rancidification of the finished leather and prevents spewing and rancidification during storage by reason of their resistance to the action of light. Better distribution of the fat-liquor or stuffing composition. fuller feel and a finer grain are also produced.
- the present invention provides a class of organic polybasic acids all of which may be used, either in the free state or in the form of their neutral or acid water soluble salts, in each of the steps of leather manufacture.
- organic polybasic acids all of which may be used, either in the free state or in the form of their neutral or acid water soluble salts, in each of the steps of leather manufacture.
- the employment of these materials throughout the process wherever changes of acidity or alkalinity are to be made will result in a finished leather of much better characteristics, for there is never a sudden or drastic change of pH with its resulting uneven action on the outer and inner layers of the hides being treated.
- the acid ammonium salts, the corresponding free acid or the sodium, potassium or triethanolamine salts may be used in the presence or absence of other salts such as ammonium sulfate and other acids such as lactic acid, formic acid or mineral acids such as boric acid or sulfuric acid.
- this blast can be removed as follows: after transferring the stock to the bate paddle or drum, phthalic, maleic, fumaric or succinic acid is added until the bate liquor reacts acid to methyl orange and remains acid for 3 minutes.
- the bate may then be added and no difficulties will be experienced, since all the lime blast is sufficiently dissolved and the obstacle to proper enzyme action is removed.
- This method is successful even in the case of thin skins, such as sheep and goatskins where it is necessary to carry some. lime into the bate, for the organic dicarboxylic acids of the above described class do not inhibit thebating action. On the contrary, they perform the double function of removing the raspy feel of the blasted hides and at the same time reducing the pH of the leather to a range most suitable for the subsequent bating step.
- EXAMPLE 2 Eating In this step, phthalic acid, maleic acid, fumaric acid and succinic acid and the ammonium, ethanolamine and alkali metal salts thereof form an-excellent mediumfor control of. the operation, since they automatically provide a proper control 1 of the hydrogen ion concentration.
- the right salt of the right-dicarboxylic acid a bate of any desired pH within the ordinary bating range may. be maintained.
- calf-skins are bated in the production of upper leather by the following procedure: 100 pounds of the calf-skins are paddled for 30 to 45 minutes in a solution containing 2 /2 pounds of ammonium phthalate to which fine-fourth pound of: a concentrated proteolytic enzyme preparation such as pancreatic enzymate has been added, the temperature being maintained at F. At the end of this period an examination of the hide will show that all keratinous substances have been removed and that the skin has reached a proper degree of lime depletion and has a clean and clear grain.
- a concentrated proteolytic enzyme preparation such as pancreatic enzymate
- Such a skin will show uniformity after tanning with no undertone or cast and with a strong and pliable grain.
- pounds of hides are charged to a solution containing 500 g. of phthalic acid and are run for 10 minutes in order to reduce the pH of the outer layers of the hide. 200 gra ns of papaine are then introduced and the hides are paddled in this bate from 45 minutes to 1 hour at 90 F.
- Phthalic acid, maleic acid and the other acids of the present invention, or properly selected mixtures of these with their salts will show a different action from other acids, and particularly from mineral acids in bating.
- they When used in the above described manner they will neutralize the outside layer of leather to the desired pH for enzyme action while leaving the inside at a different pH and so prevent over-bating and the resulting difliculties from loose flanks.
- the amount of neutralization with alkali for subsequent tannage is greatly reduced, and can be dispensed with in some tannages, thereby avoiding a drawn grain and obtaining leather having the above described characteristics.
- 100 pounds of bated sheepskins are washed in a paddle wheel for one hour and are then transferred to a pickle liquor containing 10% sodium chloride and 2% phthalic acid, which is maintained at room temperatures, An amount of pickle liquor equal to 6 times the weight of the wet skins is used, and the skins remain in the pickle liquor for'6 hours or longer, and preferably over-night. It will then be found that the skins have taken up approximately 1.7% of the phthalic acid, based on the weight of the bated skins, and have attained a pH of about 2.9.
- - maleic or succinic acids or a mixture thereof may be substituted for the phthalic acid in the above process.
- Mixtures of the acids of the present invention with other acids such as sulfuric acid may also be used in pickling processes, where a very low pH is not objectionable.
- phthalic acid is probably themost valuable pickling agent among the acids of the present invention, as it is selfregulating and requires no accurate control, but it is apparent that maleic acid, fumaric acid and succinic acid may be substituted if desired. All of these acids possess the great advantage that they may be brought into direct contact with the human skin without damage thereto, which makes them much easier to handle than strong mineral acids, and they cannot damage the skins to be pickled under any circumstances. Being solid acids, they are easy to store, handle and ship which is another great advantageover the mineral acids.
- alkalies are used to reduce the acidity of the chrome solution and thus cause the resulting basic chrome salt to combine with the animal fibers and produce leather.
- alkali salts of dicarboxylic acids of the present invention are used for this purpose,'with or without the addition of other alkaline reacting agents, they give a distinctive color to the resulting leather and improve the cut thereof.
- calf skins are tumbled in 75% of their weight of water together with of sodium chloride for one-half hour, and then a 33% basic chrome so-- lution containing a total of 2% chromium oxide is added in three portions, one hour apart.
- a solution containing 3% of sodium phthalate, based on the weight of the hides, is added in three portions, one-half hour apart, the; first portion being added shortly after the last addition of chrome to the solution.
- the mixture is run for several hours until the desired heat resistance is'obtained, after which the completely tanned calf skins are removed, washed and are ready for fat-liquoring.
- the total amount of ammonium, ethanolamine, or alkali metal salt of the dicarboxylic acid to be used depends upon the final acidity of the leather desired and upon the original basicity of the chrome solution.
- bated calf skins are paddled in a liquor containing from 3 to l of their weight of sodium .bi-
- chromate together with 2 /2% of their weight of phthalic or succinic acid Preferably this acid is added in three portions, the first. immediately after solution of the chrome in the water containing the hides, but it is also possible'to add 'all the acid at one time by reason of its relatively mild acidity.
- the skins are run in the above bath until a uniform yellow color is obtained throughout the leather. They are then horsed up overnight with exclusion of light and are then ready for the fixing bath.
- This bath may consist, in accordance with the present invention, of a solution containing from to of sodium thiosulfate and approximately 3 to 5% of maleic or succinic acid, based on the weight'ofthe skins. If necessary, additional amounts of these acids, or of phthalic or fumaric acids may be added during the treatment of the hides in order to produce a uniform blue color therein.
- alkalies such as sodium bicarbonate, ammonium bicarbonate,
- the neutral salts of the dicarboxylic acids of the present invention are excellent neutralizing agents for use in place of the alkalies above mentioned. They have a mild and gentle neutralizing action by reason of their relatively low pH and great bufiering capacity and yet a thorough neutralization can be obtained by soaking the hides in solutions containing these substances.
- the salts of phthalic, maleic, fumaric and succinic acids are also valuable agents for the neutralization of tanned leather which has been bleached with a syntan such as a sulfonated diaryl methane. They may be used with much greater safety than the conventional neutralizing agents of the type above mentioned and present the important advantage that re-darkening of the leather does not occur as is sometimes the case when free alkalies are used.
- the method of adjusting the hydrogen ion concentration of the hides, skins or leather which comprises introducing therein a suitable compound comprising a member of the group consisting of phthalic acid, maleic acid, 'fumaric acid and succinic acid and their water soluble salts.
- the method of washing and deliming hides and skins which comprises soaking them in an aqueous solution containing a neutral or acid salt of a compound, selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
- the method of removing lime blast resulting from the washing of limed skins in hard water which comprises soaking the blasted skins in an aqueous solution containing a compound, selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
- a method of controlling the hydrogen ion concentration of a hating preparation during the bating of hides or skins which comprises incorporating therein a compound containing the radical of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
- a method of pickling hides and skins which comprises soaking them in an aqueous solution containing an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumarlc acid and succinic acid.
- a method of mineral tannage which comprises impregnating hides and skins with a solution of a mineral tanning agent and introducing into the hide or skin a compound containing the radical of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and 'succinic acid.
- a method of chrome tannage which comprises impregnating hides and skins with a solution of a water soluble chromate and introducing into the hide or skin a compound containing the radical of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
- a method of neutralizing leather preparatory to finishing operations which comprises soaking it in a solution containing a neutral or acid salt of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
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
I Patented July 12, 1938 PATENT OFFICE TREATMENT F RIDES, SKINS, AND
LEATHER No lirawing.
8 Claims.
This invention relates to the use of certain polycarboxylic acids and-their water soluble salts and ester salts in preparinghides and skins for tannages such as mineral andfvegetable tannage,
formaldehyde tannage, tannage with synthetic tanning agents and thelike, as well as in the tanning and finishing operations themselves. In accordance therewith, any of the steps of washing the limed hides, deliming, bating, pickling,
tannages, bleaching, neutralizing the leather, fatliquoring the-tanned leather or dyeing the leather, or any combination of these steps, may be carried out in the presence of members of the class consisting of phthalic acid, maleic acid, fumaric acid and succinic acid and their water soluble salts which are the ammonium, ethanolamine, and alkali metal salts.
, We have found that the dicarboxylic acids of the above group and the' water soluble neutral and acid salts thereof are important agents for improving the above steps in leather manufacture when incorporated with the materials ordinarily used therein, and thatleather of improved characteristics will result from their use. Accordingly, it is an object of the invention to improve each of the above steps of leather manufacture in the manner which will be pointed out in the present specification, to the end that leather having a better grain, a better feel, lessened deterioration upon storage or subjection to light and other improved characteristics will result.
The four acids which constitute the class dealt acid, maleic acid and fumaric acid is obtained,
and upon treatment of this solution with me-' 'tallic zinc a part or all of the maleic and fumaric acids are reduced to succinic acid. On the other hand, they distinguish from all other dicarboxylic acids by their pH values in aqueous solutions and by thesolubility of their salts, and particularly by the remarkable advantages we have found them to possess in leather manufacture as will now be explained.
buffering for pH adjustment, setting of mineral Application August 10, 1936, Serial No. 95,280
' We have found that these acids and their water soluble salts have very desirable cleansing and deliming properties on hides and skins, and produce a desirable pH for further operations.
By reason of the bufiering range which is possessed by these acids and their salts, and especially by phthalic acid and its salts, they are very useful in the bating of skins with enzymes such asproteolytic enzymes.
In pickling, particularly with sheepskins, dicarboxylic acids and especially phthalic acid produce a cleaner and firmer grain when the skins are tanned, because their preserving action eliminates the necessity of extreme acidification for the prevention of mold and bacterial growth.
Much stronger acidification is necessary for pickling if sulfuric acid or other mineral acids are used.
Phthalic acid in saturated solution has a pH of 2.2, which is low enough for any acidification in modern leather manufacture. 'It has considerable advantages over mineral acids in operations involving hide substance. A most important characteristic for this purpose is its bufiering capacity, making it very valuable where gradual acidification is required. This is important not only in pickling operations but also in all other operations of leather manufacture due to the necessity of protecting the collagens against destruction during the relatively great changes in hydrogen ion concentration to which the hide is subjected.
Compared with other organic'acids used in leather manufacture, the dicarboxylic acids of the above class have greater buifering capacity due to the availability of the second hydrogen ion, at least doubling the buffering range. In the use of alkali metal salts of dicarboxylic acids, and particularly sodium acid phthalate, advantage is taken of the reverse effect in accomplishing a gentle and limited neutralization. Phthalic acid has two buffering 'maxima at 2.92 and 5.41 respectively.
Sodium phthalate or other alkali metal phthalates, when used in chrome tannage or other mineral tannages, operates to set the chrome or other metal and thus to convert the hide or skin into leather. When so used it avoids the development of a drawn grain and produces fuller fianks with more uniform distribution during subsequent fat-liquoring, as compared with conventional neutralizing agents. Similar results are obtained by the use of maleic acid, fumaric acid and succinic acid in the form of their alkali metal salts.
The above mentioned dicarboxylic acids have the additional important property, especially when applied in water solution, of bleaching vegetable and mineral tanned leather.
In fat-liquoring or stuffing compositions the addition of polycarboxylic acids andwtheir salts, especiallysodium phthalate, impart greater stability against auto-oxidation and rancidification of the finished leather and prevents spewing and rancidification during storage by reason of their resistance to the action of light. Better distribution of the fat-liquor or stuffing composition. fuller feel and a finer grain are also produced.
From the above it will be seen that the present invention provides a class of organic polybasic acids all of which may be used, either in the free state or in the form of their neutral or acid water soluble salts, in each of the steps of leather manufacture. The employment of these materials throughout the process wherever changes of acidity or alkalinity are to be made will result in a finished leather of much better characteristics, for there is never a sudden or drastic change of pH with its resulting uneven action on the outer and inner layers of the hides being treated.
In the following examples the methods whereby the group of substances constituting, the subject matter of the invention are used inleather manufacture'will be illustrated in greater detail by a description and discussion of. each of the It will be found that these steps, although discussed separately, will conindividual steps.
stitute a single unitary process giving final products of improved characteristics. Accordingly, it should be understood that the invention includes the combination of any two or more of these novel steps collectively as well as the novel features of each individual step, and this is sought to be protected by the appended claims.
- 1 EXAMPLE 1 Washing and deliming adjustment of the pH for the following hating step is obtained.
instead of ammonium phthalate, the acid ammonium salts, the corresponding free acid or the sodium, potassium or triethanolamine salts may be used in the presence or absence of other salts such as ammonium sulfate and other acids such as lactic acid, formic acid or mineral acids such as boric acid or sulfuric acid.
When hard water difliculties are encountered, for example when the water supply of the tanner contains carbonates, bicarbonates and sulfates which would react with lime to form insoluble compounds, the steady flow of water in the washing operation which is ordinarily used before hating may cause the surface of the skins to become blasted. This phenomenon is known in the tanneryas lime blast. In accordance with the present invention, this blast can be removed as follows: after transferring the stock to the bate paddle or drum, phthalic, maleic, fumaric or succinic acid is added until the bate liquor reacts acid to methyl orange and remains acid for 3 minutes. The bate may then be added and no difficulties will be experienced, since all the lime blast is sufficiently dissolved and the obstacle to proper enzyme action is removed. This method is successful even in the case of thin skins, such as sheep and goatskins where it is necessary to carry some. lime into the bate, for the organic dicarboxylic acids of the above described class do not inhibit thebating action. On the contrary, they perform the double function of removing the raspy feel of the blasted hides and at the same time reducing the pH of the leather to a range most suitable for the subsequent bating step.
EXAMPLE 2 Eating In this step, phthalic acid, maleic acid, fumaric acid and succinic acid and the ammonium, ethanolamine and alkali metal salts thereof form an-excellent mediumfor control of. the operation, since they automatically provide a proper control 1 of the hydrogen ion concentration. By choosing the right salt of the right-dicarboxylic acid a bate of any desired pH within the ordinary bating range may. be maintained.
For example, calf-skins are bated in the production of upper leather by the following procedure: 100 pounds of the calf-skins are paddled for 30 to 45 minutes in a solution containing 2 /2 pounds of ammonium phthalate to which fine-fourth pound of: a concentrated proteolytic enzyme preparation such as pancreatic enzymate has been added, the temperature being maintained at F. At the end of this period an examination of the hide will show that all keratinous substances have been removed and that the skin has reached a proper degree of lime depletion and has a clean and clear grain.
Such a skin will show uniformity after tanning with no undertone or cast and with a strong and pliable grain.
As another example, pounds of hides are charged to a solution containing 500 g. of phthalic acid and are run for 10 minutes in order to reduce the pH of the outer layers of the hide. 200 gra ns of papaine are then introduced and the hides are paddled in this bate from 45 minutes to 1 hour at 90 F. Phthalic acid, maleic acid and the other acids of the present invention, or properly selected mixtures of these with their salts will show a different action from other acids, and particularly from mineral acids in bating. When used in the above described manner they will neutralize the outside layer of leather to the desired pH for enzyme action while leaving the inside at a different pH and so prevent over-bating and the resulting difliculties from loose flanks.
Exaurm 3 Pickling After the bating step, skins are pickled in acid solutions to prevent mold and bacterial growth and enable them to be stored. We have found that skins treated with phthalic acid, maleic acid, fumaric acid and succlnic acid have excellent storing properties and that subsequent tanning of the skins so pickled will yield leather having good color, fine texture, strong fiber and a clear and clean grain. This result is obtained because the above organic acids are all inhibitors of mold and bacterial growth, and by their use a satisfactory pickle is obtained at a much higher pH value than would be necessary with mineral acid. Accordingly, the amount of neutralization with alkali for subsequent tannage is greatly reduced, and can be dispensed with in some tannages, thereby avoiding a drawn grain and obtaining leather having the above described characteristics. As an example, 100 pounds of bated sheepskins are washed in a paddle wheel for one hour and are then transferred to a pickle liquor containing 10% sodium chloride and 2% phthalic acid, which is maintained at room temperatures, An amount of pickle liquor equal to 6 times the weight of the wet skins is used, and the skins remain in the pickle liquor for'6 hours or longer, and preferably over-night. It will then be found that the skins have taken up approximately 1.7% of the phthalic acid, based on the weight of the bated skins, and have attained a pH of about 2.9.
Where skins requiring a lower pH for subsequent acid tannages are required, for example Where an acid syntan tannage is to be used,
- maleic or succinic acids or a mixture thereof may be substituted for the phthalic acid in the above process. Mixtures of the acids of the present invention with other acids such as sulfuric acid may also be used in pickling processes, where a very low pH is not objectionable.
In thepickling ofsheepskins, phthalic acid is probably themost valuable pickling agent among the acids of the present invention, as it is selfregulating and requires no accurate control, but it is apparent that maleic acid, fumaric acid and succinic acid may be substituted if desired. All of these acids possess the great advantage that they may be brought into direct contact with the human skin without damage thereto, which makes them much easier to handle than strong mineral acids, and they cannot damage the skins to be pickled under any circumstances. Being solid acids, they are easy to store, handle and ship which is another great advantageover the mineral acids.
' EXAMPLE 4 Setting mineral tannages and the like, alkalies are used to reduce the acidity of the chrome solution and thus cause the resulting basic chrome salt to combine with the animal fibers and produce leather. When the alkali salts of dicarboxylic acids of the present invention are used for this purpose,'with or without the addition of other alkaline reacting agents, they give a distinctive color to the resulting leather and improve the cut thereof.
As an example of the one-bath process, calf skins are tumbled in 75% of their weight of water together with of sodium chloride for one-half hour, and thena 33% basic chrome so-- lution containing a total of 2% chromium oxide is added in three portions, one hour apart. A solution containing 3% of sodium phthalate, based on the weight of the hides, is added in three portions, one-half hour apart, the; first portion being added shortly after the last addition of chrome to the solution. The mixture is run for several hours until the desired heat resistance is'obtained, after which the completely tanned calf skins are removed, washed and are ready for fat-liquoring.
The total amount of ammonium, ethanolamine, or alkali metal salt of the dicarboxylic acid to be used depends upon the final acidity of the leather desired and upon the original basicity of the chrome solution.
erations.
As an example of the two bath process, bated calf skins are paddled in a liquor containing from 3 to l of their weight of sodium .bi-
chromate together with 2 /2% of their weight of phthalic or succinic acid. Preferably this acid is added in three portions, the first. immediately after solution of the chrome in the water containing the hides, but it is also possible'to add 'all the acid at one time by reason of its relatively mild acidity.
The skins are run in the above bath until a uniform yellow color is obtained throughout the leather. They are then horsed up overnight with exclusion of light and are then ready for the fixing bath.
This bath may consist, in accordance with the present invention, of a solution containing from to of sodium thiosulfate and approximately 3 to 5% of maleic or succinic acid, based on the weight'ofthe skins. If necessary, additional amounts of these acids, or of phthalic or fumaric acids may be added during the treatment of the hides in order to produce a uniform blue color therein.
When all the chrome has been fixed in the skins they are removed from the bath, horsed up, and washed with cold running water in a wheel until a pH of approximately 4-5 is obtained, and are then ready for further operations.
EXAMPLE 5 Neutralization of finished leathers After chrome tannage, the chrome salts in the leather sometimes hydrolyze and keep the pH at a value which may be too low for subsequent op- This is particularly true when leather is stored for several days after the chrome tannage.
In practice the prior art has used alkalies, such as sodium bicarbonate, ammonium bicarbonate,
borax and the like to raise the pH of chrome- In mineral tannages Such as chrome tammge tralize the surface of theleather and produce a drawn grain. Moreover, they tend to neutralize the looser parts of the hides, for example, the flanks to a greater degree than the denser parts. This over neutralization results in turn, in too great a penetration during the subsequent fatliquoring or stufling of the leather and produces over-lubrication of these parts.
We have found that the neutral salts of the dicarboxylic acids of the present invention, such as sodium and ammonium phthalates and maleates, are excellent neutralizing agents for use in place of the alkalies above mentioned. They have a mild and gentle neutralizing action by reason of their relatively low pH and great bufiering capacity and yet a thorough neutralization can be obtained by soaking the hides in solutions containing these substances.
The salts of phthalic, maleic, fumaric and succinic acids are also valuable agents for the neutralization of tanned leather which has been bleached with a syntan such as a sulfonated diaryl methane. They may be used with much greater safety than the conventional neutralizing agents of the type above mentioned and present the important advantage that re-darkening of the leather does not occur as is sometimes the case when free alkalies are used.
We have found that the subsequent dyeing of the leather is also-greatly influenced by the neutralization step.' When the leather is neutralized deeply the penetration oi. acid dyestufls is also deepened and the dyes do not tend to collect on used, for the surface of the leather becomes overneutralized, with the resulting difliculties noted above, when this is attempted. Salts of the dicarboxylic acids of the present invention, on the other hand, have a definite upper limit of alkalinity and will never over-neutralize any part of the leather no matter how long it remains in contact with them. Accordingly; they may be employed for such times and in such concentrations that the entire thickness of the leather is neutralized, and may even be added to the dyebath if desired.
What we claim is:
1. In the treatment of hides, skins and leather by a process including any oi-the steps of washing limed hides, deliming, hating, pickling, setting of mineral tannages, bleaching, fat-liquoring or dyeing with acid dyes, the method of adjusting the hydrogen ion concentration of the hides, skins or leather which comprises introducing therein a suitable compound comprising a member of the group consisting of phthalic acid, maleic acid, 'fumaric acid and succinic acid and their water soluble salts.
2. The method of washing and deliming hides and skins which comprises soaking them in an aqueous solution containing a neutral or acid salt of a compound, selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
3. The method of removing lime blast resulting from the washing of limed skins in hard water which comprises soaking the blasted skins in an aqueous solution containing a compound, selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
4. A method of controlling the hydrogen ion concentration of a hating preparation during the bating of hides or skins which comprises incorporating therein a compound containing the radical of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
5. A method of pickling hides and skins which comprises soaking them in an aqueous solution containing an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumarlc acid and succinic acid.
6. A method of mineral tannage which comprises impregnating hides and skins with a solution of a mineral tanning agent and introducing into the hide or skin a compound containing the radical of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and 'succinic acid.
'1. A method of chrome tannage which comprises impregnating hides and skins with a solution of a water soluble chromate and introducing into the hide or skin a compound containing the radical of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
3. A method of neutralizing leather preparatory to finishing operations which comprises soaking it in a solution containing a neutral or acid salt of an organic dicarboxylic acid selected from the group consisting of phthalic acid, maleic acid, fumaric acid and succinic acid.
ALPHONS O. JAEGER. RICHARD HERRLINGER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95280A US2123832A (en) | 1936-08-10 | 1936-08-10 | Treatment of hides, skins, and leather |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95280A US2123832A (en) | 1936-08-10 | 1936-08-10 | Treatment of hides, skins, and leather |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2123832A true US2123832A (en) | 1938-07-12 |
Family
ID=22251120
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US95280A Expired - Lifetime US2123832A (en) | 1936-08-10 | 1936-08-10 | Treatment of hides, skins, and leather |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2123832A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2693996A (en) * | 1949-11-28 | 1954-11-09 | Fuchs George Hugo Von | Water resistant leather and process of making the same |
| US4221564A (en) * | 1978-05-20 | 1980-09-09 | Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) | Water-insoluble alkali metal aluminosilicates and polycarboxylic acids in the tanning process for the production of leather |
| US4229175A (en) * | 1977-04-02 | 1980-10-21 | Basf Aktiengesellschaft | Lime-free and sulfide-free liming process |
| US4396387A (en) * | 1979-11-11 | 1983-08-02 | Motov David L | Method for preparing titanium tanning agent and use thereof in leather tanning process |
-
1936
- 1936-08-10 US US95280A patent/US2123832A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2693996A (en) * | 1949-11-28 | 1954-11-09 | Fuchs George Hugo Von | Water resistant leather and process of making the same |
| US4229175A (en) * | 1977-04-02 | 1980-10-21 | Basf Aktiengesellschaft | Lime-free and sulfide-free liming process |
| US4221564A (en) * | 1978-05-20 | 1980-09-09 | Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) | Water-insoluble alkali metal aluminosilicates and polycarboxylic acids in the tanning process for the production of leather |
| US4396387A (en) * | 1979-11-11 | 1983-08-02 | Motov David L | Method for preparing titanium tanning agent and use thereof in leather tanning process |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11001902B2 (en) | Production of leather | |
| US4443221A (en) | Tanning method | |
| US3254938A (en) | Leather tanning | |
| JPS6354040B2 (en) | ||
| US2123832A (en) | Treatment of hides, skins, and leather | |
| US4715861A (en) | Economy chrome tanning process with aldehyde-acids and keto-acids | |
| AU607525B2 (en) | A high-extraction chrome tanning process | |
| US4314803A (en) | Tanning method | |
| US2157969A (en) | Method for producing hides with the aid of mold tryptases | |
| US4211529A (en) | Chrome-tanning | |
| US3960481A (en) | Process for tanning leather | |
| US2212750A (en) | Method of treating hides, skins, and pelts | |
| US2127304A (en) | Tanning | |
| US2264414A (en) | Tanning with complex basic zirconium sulphates | |
| US2071567A (en) | Combination tanning process | |
| US3493318A (en) | Tanning composition made from a basic chrome sulfate and a tris(hydroxyacetato)chromiate | |
| US1541819A (en) | Method of and liquor for producing tanned leather | |
| US2004473A (en) | Production of leather | |
| US3102772A (en) | Process of after-tanning with chromium werner type complex | |
| US1256974A (en) | Process of tanning fish-skins. | |
| US411932A (en) | Tanning process | |
| US2019568A (en) | Process of tanning | |
| US2228133A (en) | Treatment of hides and skins | |
| US3114589A (en) | Rapid tanning sole leather using polyoxysaccharide bisulfites | |
| AT156344B (en) | Process for the production of pelts ready for tanning. |