US983005A - Process of making sole-leather. - Google Patents

Process of making sole-leather. Download PDF

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Publication number
US983005A
US983005A US23841704A US1904238417A US983005A US 983005 A US983005 A US 983005A US 23841704 A US23841704 A US 23841704A US 1904238417 A US1904238417 A US 1904238417A US 983005 A US983005 A US 983005A
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United States
Prior art keywords
solution
hide
sodium
leather
chromic acid
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Expired - Lifetime
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US23841704A
Inventor
John Alexander Tanner
Louis L Green
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Individual
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Priority to US23841704A priority Critical patent/US983005A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C3/00Tanning; Compositions for tanning
    • C14C3/02Chemical tanning
    • C14C3/04Mineral tanning

Definitions

  • My invention relates to a process of making sole leather, and provide a new and improved process of this description.
  • the hide from which the sole leather is to be made is first nnhaired and then preferably immersed in a solution of sodium chlorid. It is allowed to remain in this solution for several hours, the length of time depending of course upon the characteristics of the hide used.
  • the hide is taken from the sodium chlorid solution, and the surplus liquid allowed to drain on”.
  • the hide is then placed in a chromic acid solu tion.
  • This solution is made in any desired manner, but preferably from chromic acid crystals and water in the proportion oi two ounces of crystals to five gallons of water.
  • the hide may be placed directly in this chromic acid solution without being treated with sodium chlorid if desired, but, as before stated, it is preferably previously immersed in the sodium chlorid solution. 0 the chromic acid solution made from the crystals a small amount of potassium chrome alum or sodium chrome alum may be added.
  • the hide is preferably allowed to remain in the chromic acid solution until it is only partially impregnated, and the color shows about one-fourth through from the grain and flesh sides, leaving about one-half the thickness of the hide at the center nncolored.
  • the hide is then removed and placed in a reducing solution such, for example, as a solution of thiosulfate of sodium, and is allowed to remain in this solution until the surface shows the dingy, greenish color.
  • a reducing solution such as a solution of thiosulfate of sodium
  • the hide is then removed before the central part is impregnated with the solution and the surplus material allowed to drain off.
  • the hide is then placed in a tannic acid solution which may be the ordinary bark or extract solution, and of the ordinary strength of such solution, and the tanning finished the same as in any of the tanning processes Where such tannic acid solution is used.
  • the tannic solution follows the other solutions into the pores of the hide, and the interval between the impregnation wit-h the other solutions and the action of the tannic solution is thus reduced to a minimum.
  • the driving ahead of the other solutions also keeps the material porous so that the tannic solution may rapidly and easily impregnate the pores of the skin.
  • the change of the skin from the chromic acid and thiosulfate of sodium so lution to the tannic acid solution should not be delayed too long, for if it is the resulting leather will be hard and brittle.
  • I may also add under ordinary conditions sodium chrome alum or sodium bichromate, etc., to the chromic acid solution, as I find that the presence of these materials benefits the action and tends to open up the pores and make the hide more spongy.
  • the proportion of these parts may be varied, depending upon the conditions. I may, for example, add one or two ounces of the material to, say, five gallons of the solution.
  • the thiosulfate of sodium is then used, the proportions being two pounds of thiosulfate of sodium to ten gallons of water.
  • the hide preferably remains in this solution until partly saturated, being removed before the central part becomes impregnated.
  • the hide is then immersed in the tanning solution.
  • the length of time required for the material to be impregnated in the proper degree with the solution will, of course, depend upon the material itself, and will vary as this material varies.

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

JOHN ALEXANDER nannies,
OF BOSTON, MASSACHUSETTS; LOUIS L. GREEN ADMIN- ISTRATOR 0F SAID TANNEB, DECEASED.
PROCESS OF MAKING SOLE-LEATHER.
No Drawing.
' Suffolk and State of Massachusetts, have invented a certain new and useful Improvement in Processes of lvlaking Sole-Leather,
of which the following is a specification.
My invention relates to a process of making sole leather, and provide a new and improved process of this description. The hide from which the sole leather is to be made is first nnhaired and then preferably immersed in a solution of sodium chlorid. It is allowed to remain in this solution for several hours, the length of time depending of course upon the characteristics of the hide used. The hide is taken from the sodium chlorid solution, and the surplus liquid allowed to drain on". The hide is then placed in a chromic acid solu tion. This solution is made in any desired manner, but preferably from chromic acid crystals and water in the proportion oi two ounces of crystals to five gallons of water. The hide may be placed directly in this chromic acid solution without being treated with sodium chlorid if desired, but, as before stated, it is preferably previously immersed in the sodium chlorid solution. 0 the chromic acid solution made from the crystals a small amount of potassium chrome alum or sodium chrome alum may be added. The hide is preferably allowed to remain in the chromic acid solution until it is only partially impregnated, and the color shows about one-fourth through from the grain and flesh sides, leaving about one-half the thickness of the hide at the center nncolored. The hide is then removed and placed in a reducing solution such, for example, as a solution of thiosulfate of sodium, and is allowed to remain in this solution until the surface shows the dingy, greenish color. The hide is then removed before the central part is impregnated with the solution and the surplus material allowed to drain off. The hide is then placed in a tannic acid solution which may be the ordinary bark or extract solution, and of the ordinary strength of such solution, and the tanning finished the same as in any of the tanning processes Where such tannic acid solution is used.
The sole leather turned out by this prochas for its object to Specification of Letters Patent.
Application filed December 27, 1904.
Patented Jan. 31, 1911. Serial No. 238,417.
(Specimens) ess is firm and solid and does not become soft or rot on standing, and is very tough and not liable to be cracked by bending.
The time required to produce sole leather by this process is much shorter than in the processes now used, and requires only a few days. If the hide is allowed to remain in the solutions until thoroughly saturated unnecessary time is taken up, and the result secured is interior as the leather is hard and brittle. lVhen the hide is only partially impregnated with chromic acid and thiosulfate of sodium prior to inserting it in the tannic acid solution, such solution acts upon the other solutions, that is, the chromic acid and thiosulfate of sodium that have not united, and appears to drive them toward the center so that they run ahead of the tan nic solution. At the same time the tannic solution follows the other solutions into the pores of the hide, and the interval between the impregnation wit-h the other solutions and the action of the tannic solution is thus reduced to a minimum. The driving ahead of the other solutions also keeps the material porous so that the tannic solution may rapidly and easily impregnate the pores of the skin. The change of the skin from the chromic acid and thiosulfate of sodium so lution to the tannic acid solution should not be delayed too long, for if it is the resulting leather will be hard and brittle. I may also add under ordinary conditions sodium chrome alum or sodium bichromate, etc., to the chromic acid solution, as I find that the presence of these materials benefits the action and tends to open up the pores and make the hide more spongy. The proportion of these parts may be varied, depending upon the conditions. I may, for example, add one or two ounces of the material to, say, five gallons of the solution.
I have described the preferred form of using the various solutions, as this method secures the best results. It is of course evident, however, that instead of immersing the hide in the separate solution the solutions may be combined in a proper manner, the chromic acid and the thiosulfate of sodium, for example, being placed in the same tank successively, that is, one solution being placed in the tank and permitted to act and then the other solution being placed in the same tank.
It is of course evident that the depth which the various solutions are permitted to penetrate before placing the hide in the tannic acid solution may be varied, and will depend upon the result desired. 1 have found the following solution to give satisfactory results: A solution of sodium chlorid in the proportion of one pound of sodium chlorid to five gallons of water. The hide is immersed in this solution and remains there about twenty-four hours, more or less; the hide is then immersed in a chromic acid solution made from chromic acid crystals and Water in the proportion of two ounces of crystals to live gallons of water. The hide preferably remains in the solution only such a. length of time as to permit the solution to permeate part way through, leaving the central portion free from acid. The thiosulfate of sodium is then used, the proportions being two pounds of thiosulfate of sodium to ten gallons of water. The hide preferably remains in this solution until partly saturated, being removed before the central part becomes impregnated. The hide is then immersed in the tanning solution. The length of time required for the material to be impregnated in the proper degree with the solution will, of course, depend upon the material itself, and will vary as this material varies.
I claim:
1. The process of tanning hides which consists in immersing the hide in a solution containing chromic acid and permitting it to remain until it becomes partially saturated, then stopping the penetration of the chromic acid by removing the hide from such solution, then immersing the hide in a solution of thiosulfate of sodium, then removing said hide and immersing it in a tannic acid solution.
2. The process of tanning hides which consists in immersing the hide in a solution containing chromic acid, then limiting the penetration of said chromic acid so as to prevent the interior of the hide from becoming saturated, then immersing said hide in a solution containing a reducing agent. then limiting the penetration of said reducing agent before the interior becomes saturated, then removing the hide and immersing it in a tannic acid solution.
JOHN ALEXANDER TANNER.
lVitnesses JAMES EDWARD BAXTER, PETER H. GARRITY.
US23841704A 1904-12-27 1904-12-27 Process of making sole-leather. Expired - Lifetime US983005A (en)

Priority Applications (1)

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US23841704A US983005A (en) 1904-12-27 1904-12-27 Process of making sole-leather.

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US23841704A US983005A (en) 1904-12-27 1904-12-27 Process of making sole-leather.

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US983005A true US983005A (en) 1911-01-31

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0326399A2 (en) * 1988-01-29 1989-08-02 Ngk Insulators, Ltd. Oxygen sensor

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0326399A2 (en) * 1988-01-29 1989-08-02 Ngk Insulators, Ltd. Oxygen sensor
EP0326399A3 (en) * 1988-01-29 1990-11-28 Ngk Insulators, Ltd. Oxygen sensor

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