US2564022A - Manufacture of syntans from vanillin and leather tanned therewith - Google Patents
Manufacture of syntans from vanillin and leather tanned therewith Download PDFInfo
- 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
- Authority
- US
- United States
- Prior art keywords
- vanillin
- syntans
- phenol
- manufacture
- tanning
- 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
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 title claims description 13
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 title claims description 13
- 235000012141 vanillin Nutrition 0.000 title claims description 13
- 239000010985 leather Substances 0.000 title description 4
- 238000004519 manufacturing process Methods 0.000 title 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 238000006277 sulfonation reaction Methods 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- -1 phenolic aldehyde Chemical class 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 241001136792 Alle Species 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 229960004275 glycolic acid Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 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
- C14C3/08—Chemical tanning by organic agents
- C14C3/18—Chemical tanning by organic agents using polycondensation products or precursors thereof
- C14C3/20—Chemical 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.
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
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.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US48322A US2564022A (en) | 1948-09-08 | 1948-09-08 | Manufacture of syntans from vanillin and leather tanned therewith |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US48322A US2564022A (en) | 1948-09-08 | 1948-09-08 | Manufacture of syntans from vanillin and leather tanned therewith |
Publications (1)
Publication Number | Publication Date |
---|---|
US2564022A true US2564022A (en) | 1951-08-14 |
Family
ID=21953938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US48322A Expired - Lifetime US2564022A (en) | 1948-09-08 | 1948-09-08 | Manufacture of syntans from vanillin and leather tanned therewith |
Country Status (1)
Country | Link |
---|---|
US (1) | US2564022A (en) |
Citations (10)
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 |
-
1948
- 1948-09-08 US US48322A patent/US2564022A/en not_active Expired - Lifetime
Patent Citations (10)
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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