US2564022A - Manufacture of syntans from vanillin and leather tanned therewith - Google Patents

Manufacture of syntans from vanillin and leather tanned therewith Download PDF

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Publication number
US2564022A
US2564022A US48322A US4832248A US2564022A US 2564022 A US2564022 A US 2564022A US 48322 A US48322 A US 48322A US 4832248 A US4832248 A US 4832248A US 2564022 A US2564022 A US 2564022A
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United States
Prior art keywords
vanillin
syntans
phenol
manufacture
tanning
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Expired - Lifetime
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US48322A
Inventor
Miglarese John
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UNITED STATES LEATHER Co
US LEATHER Co
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US LEATHER Co
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Priority to US48322A priority Critical patent/US2564022A/en
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Publication of US2564022A publication Critical patent/US2564022A/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
    • C14C3/08Chemical tanning by organic agents
    • C14C3/18Chemical tanning by organic agents using polycondensation products or precursors thereof
    • C14C3/20Chemical tanning by organic agents using polycondensation products or precursors thereof sulfonated

Definitions

  • CHO Vanillin may be produced as a degradation produce of lignin.
  • An object of my invention is to utilize vanillin because its unique composition consisting of a phenolic group and an aldehyde group which are available to make a syntan, rich in phenolic groups, contribute surprisingly good leathering characteristics in tanning.
  • Another object of my invention is to make a leathering material practically in one step without the use of expensive equipment, merely by dissolving the phenol and vanillin and sulfonating, causing simultaneous sulfonation and condensation of the phenolic aldehyde and phenol, to a tanning material as follows:
  • Example 1 One mol of vanillin and two mols of phenol are dissolved in each other, and 1 mols of sulfuric acid (98%) is added with stirring in the course of 1 hour. Permit the temperature to rise of its own exothermic reaction. Stir for 1 /2 hours, add its weight of 5% lactic acid and neutralize the mass to a pH of 3.5 with sodium hydroxide which is ready for use in tanning.
  • Example 2 Condense 75.2 grams of phenol with 60.8 grams of vanillin (about 2 mols of phenol to 1 of vanillin) and 5 grams of oxalic acid for 3 hours, at the end of which produces a resinous masshaving a red color.
  • 45-60 cc. of concentrated 98% H2804 is added to the mass gradually. The mass is made less viscous by a water bath to facilitate stirring. The H2804 is added in a period of /2 hour. The temperature is kept around -90 and the mixture is stirred for one hour at this temperature. The red mass is diluted with its weight of water. 20 grams of concentrated hydroxy acetic acid is added to the mass. The whole is made of pH of 3.5 with caustic soda or sodium carbonate.
  • the synthetic tanning extract is now ready to be used for tanning.
  • a piece of depickled skin is introduced into the liquor having 3% tanning content and the ratio of the liquor to the hide or skin is 5 to 1.
  • the skin or hide is permitted to stand in liquor until the tanning material has struck through.
  • the leather is oiled, dried and finished having full and excellent feel.
  • Example 3 The phenolic aldehyde, vanillin, can be used to condense 1 mol of phenol and 1 mol meta cresol in the presence of sulfuric acid performed the same way as in Example 1. The presence of cresol gives a brownish red colored tanning product and a brown leather. The skin is tanned as in Example 2.
  • the method of producing a tanning material which comprises subjecting a mixture of a phenol and vanillin, in the proportions of about 2 mols of phenol to 1 of vanillin, to condensation and to sulfonation with concentrated sulfuric acid to form a water soluble condensation and sulfonated product and reducing the acidity of the resulting product to a pH of around 3.5.
  • the following references are of record in the 211221124 A1195 June 1938 file of this patent: 32 3 g2 a e ec.

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  • 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

Patented Aug. 14,1951
MAN F CTU E OF SYNTANS; FROM VANIL:
LIN AND LEATHER TANNED THEREWITH John Miglarese, Cincinnati, Ohio, assignor to The United States Leather Company, New York, N. Y., a corporation of New Jersey No Drawing. Application September 8, 1948, Serial No. 48,322
i2 Claims. (01. 26049) My invention relates to a novel type of syntan made from vanillin and to the surprising results of the use of such syntan.
In the preparation of syntans it has been proposed to make a syntan by treating the concentrated sulphonation mixture (including unchanged sulphuric acid) of phenol sulphonic acid with formaldehyde at a temperature of 30 to 35 C. (Bureau of Standards Technological Papers,
vol. 20, No. 309, by Edward Wolensensky). Thus CHO Vanillin may be produced as a degradation produce of lignin.
An object of my invention is to utilize vanillin because its unique composition consisting of a phenolic group and an aldehyde group which are available to make a syntan, rich in phenolic groups, contribute surprisingly good leathering characteristics in tanning.
Another object of my invention is to make a leathering material practically in one step without the use of expensive equipment, merely by dissolving the phenol and vanillin and sulfonating, causing simultaneous sulfonation and condensation of the phenolic aldehyde and phenol, to a tanning material as follows:
Example 1 One mol of vanillin and two mols of phenol are dissolved in each other, and 1 mols of sulfuric acid (98%) is added with stirring in the course of 1 hour. Permit the temperature to rise of its own exothermic reaction. Stir for 1 /2 hours, add its weight of 5% lactic acid and neutralize the mass to a pH of 3.5 with sodium hydroxide which is ready for use in tanning.
Example 2 Condense 75.2 grams of phenol with 60.8 grams of vanillin (about 2 mols of phenol to 1 of vanillin) and 5 grams of oxalic acid for 3 hours, at the end of which produces a resinous masshaving a red color. 45-60 cc. of concentrated 98% H2804 is added to the mass gradually. The mass is made less viscous by a water bath to facilitate stirring. The H2804 is added in a period of /2 hour. The temperature is kept around -90 and the mixture is stirred for one hour at this temperature. The red mass is diluted with its weight of water. 20 grams of concentrated hydroxy acetic acid is added to the mass. The whole is made of pH of 3.5 with caustic soda or sodium carbonate. The synthetic tanning extract is now ready to be used for tanning. A piece of depickled skin is introduced into the liquor having 3% tanning content and the ratio of the liquor to the hide or skin is 5 to 1. The skin or hide is permitted to stand in liquor until the tanning material has struck through. The leather is oiled, dried and finished having full and excellent feel.
Example 3 The phenolic aldehyde, vanillin, can be used to condense 1 mol of phenol and 1 mol meta cresol in the presence of sulfuric acid performed the same way as in Example 1. The presence of cresol gives a brownish red colored tanning product and a brown leather. The skin is tanned as in Example 2.
Comparative tests on the skin tanned in accordance with Example No. 2 with skins tanned with other types of syntans and with vegetable tanning reagents indicate a quality of tanning heretofore unknown. There is a fullness and plumpness and soft feel which makes the skin tanned in accordance with my invention as set forth herein, stand out as different in physical properties than leathers tanned in other ways.
Having thus described my invention, what I claim as new and desire to secure by Letters Patent is:
1. The method of producing a tanning material which comprises subjecting a mixture of a phenol and vanillin, in the proportions of about 2 mols of phenol to 1 of vanillin, to condensation and to sulfonation with concentrated sulfuric acid to form a water soluble condensation and sulfonated product and reducing the acidity of the resulting product to a pH of around 3.5.
2. A synthetic tanning material produced in Number Name Date accordance with the process of claim 1. 1,539,517 Schmidt May 26, 1925 JOHN MIGLARESE. 1,679,322 McIntosh July 31, 1928 2,040,212 Orthner May '12, 1936 REFERENCES CITED 5 2,099,717 Alles NOV. 23, 1937 The following references are of record in the 211221124 A1195 June 1938 file of this patent: 32 3 g2 a e ec.
UNITED STATES PATENTS 2,186,509 Wallace Jan. 29, 1940 Number Name Date 10 2,191,737 Alles Feb. 27, 1940

Claims (1)

1. THE METHOD OF PRODUCING A TANNING MATERIAL WHICH COMPRISES SUBJECTING A MIXTURE OF A PHENOL AND VANILLIN, IN THE PROPORTIONS OF ABOUT 2 MOLS OF PHENOL TO 1 OF VANILLIN, TO CONDENSATION AND TO SULFONATION WITH CONCENTRATED SULFURIC ACID TO FORM A WATER SOLUBLE CONDENSATION AND SULFONATED PRODUCT AND REDUCING THE ACIDITY OF THE RESULTING PRODUCT TO A PH OF AROUND 3.5.
US48322A 1948-09-08 1948-09-08 Manufacture of syntans from vanillin and leather tanned therewith Expired - Lifetime US2564022A (en)

Priority Applications (1)

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Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1430477A (en) * 1920-03-25 1922-09-26 Fulcra Tan Company Tanning preparation
US1539517A (en) * 1921-08-27 1925-05-26 Basf Ag Process for tanning
US1679322A (en) * 1922-04-04 1928-07-31 Diamond State Fibre Company Synthetic resin and method of making same
US2040212A (en) * 1936-05-12 Water-soluble condensation
US2099717A (en) * 1934-11-09 1937-11-23 Ig Farbenindustrie Ag Process for the production of water-soluble condensation products
US2122124A (en) * 1936-01-31 1938-06-28 Ig Farbenindustrie Ag Water-soluble condensation products and a process of producing same
US2148893A (en) * 1936-08-22 1939-02-28 Ig Farbenindustrie Ag Process for preparing tanning agents
US2184622A (en) * 1937-05-13 1939-12-26 Ig Farbenindustrie Ag Manufacture of tanning agents
US2186509A (en) * 1938-07-12 1940-01-09 Robeson Process Company Finishing leather
US2191737A (en) * 1937-09-23 1940-02-27 Ig Farbenindustrie Ag Production of water-soluble condensation products

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2040212A (en) * 1936-05-12 Water-soluble condensation
US1430477A (en) * 1920-03-25 1922-09-26 Fulcra Tan Company Tanning preparation
US1539517A (en) * 1921-08-27 1925-05-26 Basf Ag Process for tanning
US1679322A (en) * 1922-04-04 1928-07-31 Diamond State Fibre Company Synthetic resin and method of making same
US2099717A (en) * 1934-11-09 1937-11-23 Ig Farbenindustrie Ag Process for the production of water-soluble condensation products
US2122124A (en) * 1936-01-31 1938-06-28 Ig Farbenindustrie Ag Water-soluble condensation products and a process of producing same
US2148893A (en) * 1936-08-22 1939-02-28 Ig Farbenindustrie Ag Process for preparing tanning agents
US2184622A (en) * 1937-05-13 1939-12-26 Ig Farbenindustrie Ag Manufacture of tanning agents
US2191737A (en) * 1937-09-23 1940-02-27 Ig Farbenindustrie Ag Production of water-soluble condensation products
US2186509A (en) * 1938-07-12 1940-01-09 Robeson Process Company Finishing leather

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