US1985439A - Method of chrome tanning of leather - Google Patents
Method of chrome tanning of leather Download PDFInfo
- Publication number
- US1985439A US1985439A US636191A US63619132A US1985439A US 1985439 A US1985439 A US 1985439A US 636191 A US636191 A US 636191A US 63619132 A US63619132 A US 63619132A US 1985439 A US1985439 A US 1985439A
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- United States
- Prior art keywords
- salt
- acid
- skins
- lbs
- chrome
- Prior art date
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- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 title description 27
- 238000000034 method Methods 0.000 title description 18
- 239000010985 leather Substances 0.000 title description 4
- 150000003839 salts Chemical class 0.000 description 31
- 239000002253 acid Substances 0.000 description 27
- 239000003513 alkali Substances 0.000 description 25
- 239000000243 solution Substances 0.000 description 18
- 235000015217 chromium(III) sulphate Nutrition 0.000 description 10
- 239000011696 chromium(III) sulphate Substances 0.000 description 10
- 150000007513 acids Chemical class 0.000 description 8
- GRWVQDDAKZFPFI-UHFFFAOYSA-H chromium(III) sulfate Chemical compound [Cr+3].[Cr+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRWVQDDAKZFPFI-UHFFFAOYSA-H 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000013019 agitation Methods 0.000 description 7
- ZMESHQOXZMOOQQ-UHFFFAOYSA-N 1-(naphthalen-1-ylmethyl)naphthalene Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZMESHQOXZMOOQQ-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- -1 oxymethylene salicylic acid Chemical compound 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 3
- 239000001263 FEMA 3042 Substances 0.000 description 3
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 3
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 159000000007 calcium salts Chemical class 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000012266 salt solution Substances 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 239000001117 sulphuric acid Substances 0.000 description 3
- 235000011149 sulphuric acid Nutrition 0.000 description 3
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 3
- 229940033123 tannic acid Drugs 0.000 description 3
- 235000015523 tannic acid Nutrition 0.000 description 3
- 229920002258 tannic acid Polymers 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- UJPKMTDFFUTLGM-UHFFFAOYSA-N 1-aminoethanol Chemical class CC(N)O UJPKMTDFFUTLGM-UHFFFAOYSA-N 0.000 description 1
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- OPUAWDUYWRUIIL-UHFFFAOYSA-N methanedisulfonic acid Chemical compound OS(=O)(=O)CS(O)(=O)=O OPUAWDUYWRUIIL-UHFFFAOYSA-N 0.000 description 1
- 229960004011 methenamine Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HNDXKIMMSFCCFW-UHFFFAOYSA-N propane-2-sulphonic acid Chemical compound CC(C)S(O)(=O)=O HNDXKIMMSFCCFW-UHFFFAOYSA-N 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- KIEOKOFEPABQKJ-UHFFFAOYSA-N sodium dichromate Chemical compound [Na+].[Na+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KIEOKOFEPABQKJ-UHFFFAOYSA-N 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- ZVUUCUFDAHKLKT-UHFFFAOYSA-M sodium;2,4,6-trinitrophenolate Chemical compound [Na+].[O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O ZVUUCUFDAHKLKT-UHFFFAOYSA-M 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 235000010269 sulphur dioxide Nutrition 0.000 description 1
- 239000004291 sulphur dioxide Substances 0.000 description 1
- 235000013311 vegetables Nutrition 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
- C14C3/28—Multi-step processes
Definitions
- This invention relates to a novel and highly advantageous process of chrome tanning of leather.
- the essential feature of the invention is that by introducing a salt of the type mentioned we obtain a source of free alkali.
- the free alkali arises from the fact that a combination of the acid with the hide substance leaves the base which was previously associated with theorganic acid free to neutralize sulfuric acid which was previously combined with the chrome.
- the chromic salt is thus rendered more basic and in consequence of this is able to tan the pelts completely.
- the organic acid gives a supplementary tannage.
- Example 5 500 lbs. of bated steer hides are pickled with 5 lbs. sulphuric acid and 50 lbs. salt in 60 gallons water to show a pH between 3 and 4.
- Example 8 100 lbs. of bated calfskins are pickled and penetrated with partially basic chromic sulphate as described in Example 1, whereupon 5 gallons of a solution of the sodium salt of the product of condensation of oxymethylene salicylic acid and resorcinol in slightly acid solution,. containing /2 continued for a further period of one to two hours. The skins are piled on a horse overnight and well washed the following morning when they should be fully tanned.
- Example 9 100 lbs. of pickled sheepskins shown a pH of 3 /24 are agitated in a drum in 10 gals. of a 5% brine solution and 1 gal. of a partially basic chromic sulphate solution added containing between 2 and 2% lbs. chromic oxide in the form of basic sulphate of 60-67% acidity by the Schorlemmer scale.
- the skins are agitated until penetration is complete, then 5 gals. of a solution of sodium picrate containing 2 lbs. of the dry salt is added.
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
UNITED STATES PATENT OFFICE METHOD or CHROME TANNING 0F LEATHER Thomas Blackadder, St. Davids, Pa., assignor to ltiihm & Haas Company, Philadelphia, Pa.
No Drawing. Application October}, 1932, Serial 110,636,191
12 Claims.
This invention relates to a novel and highly advantageous process of chrome tanning of leather.
When pelts are converted to leather by tanning with the aid of compounds of chromium two general methods are followed for the purpose of effecting the conversion. Firstly, the pelts after proper processing to remove hair and other extraneous matter are soaked in a solution of chromic acid which is taken up and later reduced in situ by immersing the pelt in a reducing bath, commonly a solution of hyposulphite or of bisul phite of sodium; or secondly, the pelts after proper processing are pickled, that is steeped in a solution of acid and salt and then immersed in a solution of'a chromium salt, e. g., of chrome alum or of a partially basic chromium sulphate prepared by reducing sodium bichromate with glucose in presence of sulphuric acid or with sulphur dioxide or other suitable reducing agent.
In both methods the object in view is the presentation to the hide substance of a chromic salt in a suitable degree of basicity so that combination occurs between the hide substance and the basic chrome salt.
With the first method we are not at present concerned. In the second method it is common knowledge that, when the pelts after proper processing are brought in contact with the chromic salt solution, these chromic salts must be of suflicient acidity to prevent immediate combination to any appreciable degree as otherwise a tanned condition would be set up on the outer surfaces of the pelt which would prevent proper penetration of the chromic salt to the inner parts. This is taken care of in practice by pickling the processed raw pelts, prior to their treatment with a partially basic chromic salt; or by the use of a fully acid chrome salt such as chrome alum. In order now that true tannage may occur it is necessary to reduce the acidity of the chromic salt in contact with the pelt. This is accomplished generally by the addition to the chromic salt solution, still containing the pelts, of an alkali such as soda ash or bicarbonate of soda or of borax. It has also been suggested to add a potential source of alkali such as hexamethylene tetramine or other aldehyde ammonia compounds.
According to the present invention the reduction in acidity is caused in a unique and very convenient manner by the addition to the chromic salt solution, still containing the pelts, of a salt of an acid which will combine with the hide substance.
Acids which combine with hide substance, in
other words tanning acids comprise a variety of acids which have the common feature of combining with hide substance and renderingit imputrescible. Among these acids there are several distinct groups namely, natural tanning acids present in vegetable extracts, typified by tannic acid; the condensed sulfonic acids of aromatic hydrocarbons or of phenols, typified by dinaphthyl methane disulfonic acid or by diphenylol methane disulfonic acid; condensation products of polyhydric phenols with dibasic acids typified by the condensation product of oxymethylene salicylic acid and resorcinol; individual acids such as picric acid.
For my purpose salts of aromatic sulfonic acids are particularly suitable, altho other acid bodies can also be used. These acids have a very strong afiinity for hide substance. The type of acid is not of major importance, so long as the acid shows an afiinity for the hide substance markedly greater than the aflinity shown by inorganic acids such as hydrochloric, sulphuric or phosphoric. The type of base combined with the acid in the form of a salt may be either an alkali such as potassium, sodium or ammonium, or an alkali earth such as calcium. The preferred alkali earth is calcium, but barium and strontium, although they give inferior results, may also be employed.
The essential feature of the invention is that by introducing a salt of the type mentioned we obtain a source of free alkali. The free alkali arises from the fact that a combination of the acid with the hide substance leaves the base which was previously associated with theorganic acid free to neutralize sulfuric acid which was previously combined with the chrome. The chromic salt is thus rendered more basic and in consequence of this is able to tan the pelts completely. At the same time the organic acid gives a supplementary tannage.
The invention is illustrated by the following examples', but it is understood that it is not confined thereto.
Emample 1 100 lbs. of bated calfskins are pickled in 1 lb. sulphuric acid 10 lbs. salt 12 gals. water.
2 lbs. of the dry salt is added. Y Agitation is continued for a further period of one to two hours. The skins may lie in the liquor overnight or be piled down overnight and then washed with water when it will be found that they are very evenly tanned throughout.
Example 2 lbs. of pickled sheepskins showing a pH of less than 3 as is normally the case with sheepskins from either domestic or foreign pulleries, are agitated in 10 gals. of a 5% brine solution and soda ash added, a few ounces at a time until the pH value of the skins is between 3 and 4'.
To the skins, still in the brine, add 1 gal. of a partially basic chromic sulphate solution containing between 1 and 1% lbs. chromic oxide in the form of basic sulphate of 60% acidity by the Schorlemmer scale. I
The skins are agitated until the chromic sulphate has penetrated whereupon 5 gallons of a solution of the sodium salt of diphenylol dimethyl methane monosulphonic acid containing 2 lbs. of the dry salt is added.
Agitation is continued for two hours longer and the skins are left in the liquor for a further period of eight hours and then washed with water. The skins will then be found to be thoroughly tanned.
Example 3 100 lbs. kidskins are pickled and penetrated.
with partially basic chromium sulphate as described in Example 1, whereupon 5 gallons of a solution of the calcium salt of dinaphthyl methane disulphonic acid, containing 2 lbs. of the dry calcium salt is added. Agitation is continued for a further period of one to two hours. The skins may .lie in the liquor overnight or be piled down overnight and then washed with water when it will be found that they-are very evenly tanned throughout.
Example 5 Example 6 500 lbs. of bated steer hides are pickled with 5 lbs. sulphuric acid and 50 lbs. salt in 60 gallons water to show a pH between 3 and 4.
To the skins in this liquor is added 5 gallons of a partially basic chromic sulphate solution containing between 9-9/; lbs. chromic oxide in the form of basic sulphateof 60% acidity by the Schorlemmer scale.
The skins are agitated until the chromic sulphate has penetrated, whereupon 25 gallons of a solution of the sodium salt of diphenylolmethane disulphonic acid containing 10 lbs. of the dry salt is added. Agitation is continued for a further period of one to two hours. The skins may lie .in the liquor overnight or be piled down overnight and then washed with water when it will be found that they are very evenly tanned throughout.
Example 7 100 lbs. of pickled sheepskins are penetrated with partially basic chromic sulphate as described in Example 1, whereupon 5 gallons of a solution of the ammonium salt of diphenylol-monomethylmethane disulphonic acid containing 2 lbs. of the dry salt is added. Agitation is continued for a further period of one to two hours. The skins are piled on a horse overnight and well washed the following morning when they should be fully tanned.
, Example 8 100 lbs. of bated calfskins are pickled and penetrated with partially basic chromic sulphate as described in Example 1, whereupon 5 gallons of a solution of the sodium salt of the product of condensation of oxymethylene salicylic acid and resorcinol in slightly acid solution,. containing /2 continued for a further period of one to two hours. The skins are piled on a horse overnight and well washed the following morning when they should be fully tanned.
Example 9 100 lbs. of pickled sheepskins shown a pH of 3 /24 are agitated in a drum in 10 gals. of a 5% brine solution and 1 gal. of a partially basic chromic sulphate solution added containing between 2 and 2% lbs. chromic oxide in the form of basic sulphate of 60-67% acidity by the Schorlemmer scale.
The skins are agitated until penetration is complete, then 5 gals. of a solution of sodium picrate containing 2 lbs. of the dry salt is added.
Agitation is continued for 2 hours longer and the skins are left in the liquor for a further period of 8 hours, then washed with water, when they will be found to be thoroughly tanned.
Example 10 100 lbs. of pickled sheepskins are penetrated with a partially basic chromic sulphate solution as described in Example 9, then 5 gals. of a solution of the sodium salt of tannic acid containing the equivalent of 2 lbs. of tannic acid is added.
Drumming is continued for 2 hours longer, and the skins left in the liquor for a further period of 8 hours, then washed with water, when they will be found to be thoroughlytanned.
It is understood that the invention is in no way to be confined to the specific examples given but that wide deviations are possible without departing from the spirit of the invention, the scope of which is to be determined only by the claims which follow. No modification is claimed to the exclusion of any other modification.
lbs. of the dry salt is added. Agitation is- What I claim is:
1. In' a process of chrome tanning the step which comprises the application to the hide, previously treated with a partially basic chromic salt, of the potassium salt of diphenyloldimethylmethane mono sulphonic acid.
2. In a process of chrome tanning the step which comprises the application to the hide, previously treated with a partially basic chromlc salt, of the sodium salt of dinaphthylmethane disulphonic acid.
3. In a process of chrome tanning the step which comprises the application to the hide, previously treated witha partially basic chromic salt, of the calcium salt of dinaphthylmethane disulphonic acid.
4. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath conta'ning a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a synthetic tanning acid.
5. In a process of chrome tannfng, the steps which comprise immersing hides and skins in a bath, containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a tanning acid.
6. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of an aromatic sulphonic acid.
'7. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a hydroxy aromatic sulphonic acid.
8. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a condensed aromatic sulphonic acid.
9. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a condensed naphthalene sulphonic acid.
10. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chromesalt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a condensed phenol sulphonic acid.
11. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of diphenyloldimethylmethane mono sulphonic acid.
-12. In a process of chrome tanning, the steps which comprise immersing hides and skins in a bath containing a partially basic chrome salt and thereafter adding to the bath, one of the group consisting of alkali and alkali earth salts of a dinaphthylmethane disulphonic acid,
THOMAS BLACKADDER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US636191A US1985439A (en) | 1932-10-04 | 1932-10-04 | Method of chrome tanning of leather |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US636191A US1985439A (en) | 1932-10-04 | 1932-10-04 | Method of chrome tanning of leather |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1985439A true US1985439A (en) | 1934-12-25 |
Family
ID=24550841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US636191A Expired - Lifetime US1985439A (en) | 1932-10-04 | 1932-10-04 | Method of chrome tanning of leather |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1985439A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2733977A (en) * | 1956-02-07 | Process of tanning with salt of ampho- | ||
| US3166073A (en) * | 1963-05-29 | 1965-01-19 | Ethicon Inc | Quinone, aldehyde and chrome tanned articles and their production |
| US3166074A (en) * | 1963-05-29 | 1965-01-19 | Ethicon Inc | Aldehyde, chrome and polyhydric alcohol tanned collagen articles and their production |
-
1932
- 1932-10-04 US US636191A patent/US1985439A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2733977A (en) * | 1956-02-07 | Process of tanning with salt of ampho- | ||
| US3166073A (en) * | 1963-05-29 | 1965-01-19 | Ethicon Inc | Quinone, aldehyde and chrome tanned articles and their production |
| US3166074A (en) * | 1963-05-29 | 1965-01-19 | Ethicon Inc | Aldehyde, chrome and polyhydric alcohol tanned collagen articles and their production |
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