US518467A - And henry burk - Google Patents
And henry burk Download PDFInfo
- Publication number
- US518467A US518467A US518467DA US518467A US 518467 A US518467 A US 518467A US 518467D A US518467D A US 518467DA US 518467 A US518467 A US 518467A
- Authority
- US
- United States
- Prior art keywords
- skins
- hides
- tanning
- alumina
- bath
- 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
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 19
- 238000000034 method Methods 0.000 description 19
- 230000008569 process Effects 0.000 description 17
- 230000009471 action Effects 0.000 description 16
- 235000002639 sodium chloride Nutrition 0.000 description 14
- 229910021653 sulphate ion Inorganic materials 0.000 description 14
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 150000001845 chromium compounds Chemical class 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 12
- 230000006872 improvement Effects 0.000 description 10
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 8
- 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 8
- 238000004040 coloring Methods 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 230000009467 reduction Effects 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 4
- -1 chromic acid compound Chemical class 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 3
- 239000010985 leather Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229940072033 potash Drugs 0.000 description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
- 235000015320 potassium carbonate Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229940124024 weight reducing agent Drugs 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000019345 sodium thiosulphate Nutrition 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000009736 wetting Methods 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
- C14C3/04—Mineral tanning
- C14C3/06—Mineral tanning using chromium compounds
Definitions
- Our invention consists of improvements in chrome-tanned leather, and in the process of chrome tanning or tawing hides or skins, the
- object of our invention being to effect a complete reduction of the chromium compound, and so to render the product perfectly insoluble in water, and completely tan the hides or skins.
- the hides or skins at this point can be stacked up or stored, a'ndin fact the beaming and tanning processes can be carried out in one factory, and the skins thus prepared can be sold as an article of manufacture to other manufacturers for coloring and finishing.
- the beam work of our improved process is substantially the same as the beam work in the present chrome tanning process, and the tanning is substantially the same with the exception that the washing is omitted, and immediately after the skins are taken from the reducing bath, they are at once thrown into a solution of sulphate of alumina and chloride of sodium, or their equivalents (when the character of the reducing bath is such that chloride of sodium is formed and absorbed by the skins, the addition of chloride of sodium is omitted) and after remaining in this bath for a short time, they are removed and dried, and allowed to remain in this condition fora few weeks or longer.
- Our invention particularly relates, to this part of the process, and in order. to more clearly explain the process we will give a detailed description.
- the hides or skins are left in the above described bath until they have thoroughly absorbed the chromium compound. They are then removed and drained or pressed out and are then placed in the reducing bath.
- That reducing bath may contain, or be capable of evolving, sulphurous acid, hydrogen sulphide, tartaric acid, oxalic or other suitable acid, or any ferrous salt of iron, cuprous salt of copper or other suitable metallic salt, nascent hydrogen,oranyothersuitable reducingagent.
- the hides or skins are allowed to remainin the reducingbath until all the interaction between the chromium compound and the reducing agent has ceased, whereupon they are taken from the reducing bath, and, without washing, are at once thrown intoasolution of sulphate of alumina, or its equivalent, and common salt (chloride of sodium).
- the salt is omitted from the sulphate of alumina solution.
- the reducing bath is composed of hyposulphite of soda and hydrochloric acid
- the hydrochloric acid combines with the soda thus forming chloride of sodium (or common salt) which is taken up or absorbed by the hides or skins to a considerable extent.
- chloride of sodium or common salt
- the hides or skins are allowed to remain in this sulphate of alumina solution for about two hours, when they are removed, hung upon hooks in a drying room, and allowedto become thoroughly dry. They then remain in this ,condition for about two weeks, or longer, when they are dampened or wet down, staked, and the superfluous flesh removed, then stained, colored, oiled 0E, dried out, and finished in the usual way.
- Linseed oil is largely used for oiling off chrome tanned stock, and we find that after the skins have been finished for some time, a hard varnish frequently appears to form upon the surface of the stock,due to the oxidation of the linseed oil; this oxidation is caused by the liberation of oxygen which takes place when the reduction of the chromium compound proceeds in the finished leather, and the value of the leather is thereby seriously impaired. All these difficulties are avoided by following our process, as the reduction of the chromium compound is continued and the tanning or tawing operation completed by the small amount of oxide of alumina separated from its salt before the stock is subjected to the coloring and finishin g processes. Should skins be dried out from the reducing bath without subjecting them to our sulphate ofalumina solution, it would be impossible to wet them thoroughly and bring them into a proper condition for coloring and finishing. 1
- alum which is a double salt
- the quantity employed should be about twice as much as the proportion herein given for sulphate of alumina.
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.
WILLIAM M. NORRIS, OF PRINCETON, NEW JERSEY, AND HENRY BURK, OF PHILADELPHIA, PENNSYLVANIA.
TAWED SKIN AND PROCESS OF MAKING SAME.
SPECIFICATION forming part of Letters Patent No. 518,467, dated April 17,1894.
Application filed January 23, 1893. Serial No.459,441. (No specimens.)
Tanning the Same, of which the following is a specification.
Our invention consists of improvements in chrome-tanned leather, and in the process of chrome tanning or tawing hides or skins, the
object of our invention being to effect a complete reduction of the chromium compound, and so to render the product perfectly insoluble in water, and completely tan the hides or skins. We are thus enabled to completely tan the hide or skin and permit the stoppage of work upon the skins immediately after tanning, and before coloring and finishing, so that it is not essential as in the old process as at present employed, to immediately proceed with the operation of coloring and finishing after tanning, for during the interval between the tanning step and the coloring step, we allow the hide or skin itself to complete the tanning. The hides or skins at this point can be stacked up or stored, a'ndin fact the beaming and tanning processes can be carried out in one factory, and the skins thus prepared can be sold as an article of manufacture to other manufacturers for coloring and finishing.
The beam work of our improved process is substantially the same as the beam work in the present chrome tanning process, and the tanning is substantially the same with the exception that the washing is omitted, and immediately after the skins are taken from the reducing bath, they are at once thrown into a solution of sulphate of alumina and chloride of sodium, or their equivalents (when the character of the reducing bath is such that chloride of sodium is formed and absorbed by the skins, the addition of chloride of sodium is omitted) and after remaining in this bath for a short time, they are removed and dried, and allowed to remain in this condition fora few weeks or longer.
Our invention particularly relates, to this part of the process, and in order. to more clearly explain the process we will give a detailed description. We first tan or taw the skins by subjecting them to abath of bichromate of potash or other analogous salt dissolved in water, to which an acid is added, such as hydrochloric or sulphuric acid, using for each one hundred pounds of raw hides or skins about five pounds of bichromate of potash or its equivalent, and two and one half pounds of hydrochloric acid, or its equivalent. The hides or skins are left in the above described bath until they have thoroughly absorbed the chromium compound. They are then removed and drained or pressed out and are then placed in the reducing bath. That reducing bath may contain, or be capable of evolving, sulphurous acid, hydrogen sulphide, tartaric acid, oxalic or other suitable acid, or any ferrous salt of iron, cuprous salt of copper or other suitable metallic salt, nascent hydrogen,oranyothersuitable reducingagent. The hides or skins are allowed to remainin the reducingbath until all the interaction between the chromium compound and the reducing agent has ceased, whereupon they are taken from the reducing bath, and, without washing, are at once thrown intoasolution of sulphate of alumina, or its equivalent, and common salt (chloride of sodium). When the character of the reducing bath is such that chloride of sodium is formed and absorbed by the hides or skins during the action of said reducing bath, the salt is omitted from the sulphate of alumina solution. For example, when the reducing bath is composed of hyposulphite of soda and hydrochloric acid, the hydrochloric acid combines with the soda thus forming chloride of sodium (or common salt) which is taken up or absorbed by the hides or skins to a considerable extent. For each one hundred pounds of hides or skins about six pounds of sulphate of alumina and an equal amount of salt, may conveniently be employed. The hides or skins are allowed to remain in this sulphate of alumina solution for about two hours, when they are removed, hung upon hooks in a drying room, and allowedto become thoroughly dry. They then remain in this ,condition for about two weeks, or longer, when they are dampened or wet down, staked, and the superfluous flesh removed, then stained, colored, oiled 0E, dried out, and finished in the usual way. The
usual process of fat liquoring may be omitted, as stock treated by our process is so soft, flexible and pliable, and at the same time free from stretch, that the fat liquor is unnecessary.
It is a well known fact that hides and skins themselves have reducing power, and also attract and separate the oxides of alumina, chromium and iron from their salts. By our process we allow the hides or skins tohave an opportunity to complete the reduction of the chromium compound, which is only partially accomplished by the reducing agent in the bath, and we also afford an opportunity for the separation of some oxide of alumina from its salt, and so. complete the tanning or tawing process. By saturating the hides or skins with an excess of sulphate of alumina they are in condition to become thoroughly wet again, which is absolutely essential in order that they should be colored and finished. The usual method of procedure at the present time among chrome-tanners is to first saturate the skins with a chromium compound prepared by adding hydrochloric acid to an aqueous solution of bichromate of potash, and
then reducing this chromium compound by a bath prepared by adding hydrochloric acid to an aqueous solution of hyposulphite of soda. The skins are removed from this reducing bath, washed, and, without drying out, are subjected to the usual staining, fat-liquoring, coloring and finishing operations. We find that in working this process the reduction of the chromium compound is not complete, and
proceeds slowly in the stock after being finished, the result being often disastrous. The oxygen liberated appears to form compounds with the oils and the other materials used in the coloring and finishing processes, causing the stock to shrink and become spotted, thus seriously impairing its commercial value. We also find that in the reducing bath considerable of the chromium compound is washed out of the stock, and the reduction proceeds in the bath and not in the skins. In this way the skins are not thoroughly tanned, which causes them to crack and become hard after being finished.
Linseed oil is largely used for oiling off chrome tanned stock, and we find that after the skins have been finished for some time, a hard varnish frequently appears to form upon the surface of the stock,due to the oxidation of the linseed oil; this oxidation is caused by the liberation of oxygen which takes place when the reduction of the chromium compound proceeds in the finished leather, and the value of the leather is thereby seriously impaired. All these difficulties are avoided by following our process, as the reduction of the chromium compound is continued and the tanning or tawing operation completed by the small amount of oxide of alumina separated from its salt before the stock is subjected to the coloring and finishin g processes. Should skins be dried out from the reducing bath without subjecting them to our sulphate ofalumina solution, it would be impossible to wet them thoroughly and bring them into a proper condition for coloring and finishing. 1
It will be understood that alum, which is a double salt, may be used instead of sulphate of alumina, in which case, however, the quantity employed should be about twice as much as the proportion herein given for sulphate of alumina.
Having thus described our invention, we claim and desire to secure by Letters Patent- 4 1. The within described improvements in the art of tanning or tawing hides or skins, consisting in first subjecting such hides or skins to the action of a solution of a chromic acid compound; second to the action of a reducing bath, and third, to the action of another and different mineral tanning ortawing bath, as and for the purpose set forth.
2. The within described improvement in the art of tanning or tawing hides or skins, said improvement consisting in subjecting the skins first, to the action of a solution of the chromic acid compound, second, to the action of a reducing bath, and third, to the action of a bath containing sulphate of alumina, substantially as specified.
3. The within described improvement in the art of tanning or tawing hides or skins, by the chrome process, said improvement consisting in subjecting the skins first, to the action of a solution of a chromic acid compound, second to the action of a reducing bath, and third to the action of a bath containing sulphate of alumina, and chloride of sodium, substantially as specified.
4. The within described improvement in the art of tanning or tawing hides or skins by the chrome process, said improvement consisting in first, subjecting the skin or hides to the action of a solution of a chromic acid compound, second, to the action of a reducing bath, third to the action of a bath containing sulphate of alumina, and fourth permitting the skins to become dry, and to remainin the dry condition until the chromium compound is reduced, and sufficient oxide of alumina separated from the salt to complete the tanning, substantially as specified.
5. The within described improvement in the art of tanning or tawing hides or skins by the chrome process, said improvement consisting in subjecting the skins first, to the action of asolution of achromic acid compound, second to the action of areducing bath, third to the action of a bath containing sulphate of alumina and chloride of sodium, and fourth permitting the skins to become dry and to remain in the dry condition, until the chromium compound is reduced and sufficient oxide of alumina is separated from the salt of alumina, to complete'the tanning, substantially as specified.
6. As a new article of manufacture a dry chrome tanned hide or skin saturated with a metallic salt susceptible of removal by washing to render the hide or skin capable of absorbing water in the subsequent treatment,
substantially as described.
7. As a new article of manufacture a dry chrome tanned hide or skin uncolored. and unfinished, and containing sulphate of alumina capable of removal by washing and serving to permit the thorough Wetting of the hide or skin as a preliminary to the subsequent treatment, substantially as specified.
In testimony whereof we have signed our names to this specification in the presence of two subscribing witnesses.
WVILLIAM M. NORRIS.
HENRY BURK.
Witnesses:
JOSEPH H. KLEIN, HENRY HOWSON.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US518467A true US518467A (en) | 1894-04-17 |
Family
ID=2587268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US518467D Expired - Lifetime US518467A (en) | And henry burk |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US518467A (en) |
-
0
- US US518467D patent/US518467A/en not_active Expired - Lifetime
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