US2418655A - Recovering values from vegetable tanned leather - Google Patents
Recovering values from vegetable tanned leather Download PDFInfo
- Publication number
- US2418655A US2418655A US60065245A US2418655A US 2418655 A US2418655 A US 2418655A US 60065245 A US60065245 A US 60065245A US 2418655 A US2418655 A US 2418655A
- Authority
- US
- United States
- Prior art keywords
- leather
- acids
- tannin
- hydrolysis
- amino acids
- 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
- 239000010985 leather Substances 0.000 title description 39
- 235000013311 vegetables Nutrition 0.000 title description 21
- 235000018553 tannin Nutrition 0.000 description 41
- 229920001864 tannin Chemical class 0.000 description 41
- 239000001648 tannin Chemical class 0.000 description 41
- 239000002253 acid Substances 0.000 description 27
- 150000007513 acids Chemical class 0.000 description 26
- 235000001014 amino acid Nutrition 0.000 description 24
- 230000007062 hydrolysis Effects 0.000 description 23
- 238000006460 hydrolysis reaction Methods 0.000 description 23
- 150000001413 amino acids Chemical class 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- 239000000126 substance Substances 0.000 description 18
- 239000003795 chemical substances by application Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 17
- 235000019441 ethanol Nutrition 0.000 description 16
- 159000000000 sodium salts Chemical class 0.000 description 9
- 230000003301 hydrolyzing effect Effects 0.000 description 8
- 239000003513 alkali Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 6
- 150000003388 sodium compounds Chemical class 0.000 description 6
- 102000008186 Collagen Human genes 0.000 description 5
- 108010035532 Collagen Proteins 0.000 description 5
- 239000012670 alkaline solution Substances 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 229920001436 collagen Polymers 0.000 description 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 230000007717 exclusion Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- YQUVCSBJEUQKSH-UHFFFAOYSA-N 3,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000006228 supernatant Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical class NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000012675 alcoholic extract Substances 0.000 description 2
- -1 amino acid salts Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000013930 proline Nutrition 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical class O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical class OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical class C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical class OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000002547 anomalous effect Effects 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 150000001510 aspartic acids Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Chemical class OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 239000000413 hydrolysate Substances 0.000 description 1
- 229960002591 hydroxyproline Drugs 0.000 description 1
- 235000005772 leucine Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 description 1
- 150000003148 prolines Chemical class 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 235000004400 serine Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 235000010269 sulphur dioxide Nutrition 0.000 description 1
- 239000004291 sulphur dioxide Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Chemical class ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 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
- C14C3/32—Recovering tanning agents from leather
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
Definitions
- This invention relates to a process for preparing certain amino acids, tannins and tannin acids. It is directed particularly to the recovery of these values from vegetable tanned leather scrap or waste. At the present time scrap vegetable tanned leather has very little value. On the other hand, there is no inexpensive commercial source for these amino acids. The present invention, therefore, is one for obtaining valuable materials from substantially useless by-products which are produced in quantity in the shoe and leather fabricating industries.
- Vegetable tanned leather is essentially a combination of hide substance of animal origin, and tanning agents of vegetable origin.
- the hide substance is a protein called collagen which is composed of a group of compounds known as amino acids in their simplest form.
- the tannin agents in vegetable tanned leather which are described herein as tannin and tannin acids, are composed mainly of glucosides of certain polyhydroxyphenolic acids derived largely from gallic acid and protocatechuic acid.
- amino acids are derived from the collagen or hide substance and the tannins, tannin acids or tanning agents are obtained from the tanning agents present in the leather.
- this invention is based, first, upon the concept and determination that the collagen component and the tannin component of vegetable tanned scrap leather respond differently to hydrolyzing agents such as sodium hydroxide; and,
- Sodium hydroxide is the preferred hydrolyzing agent in the practice of this invention because of its low cost and its ready solubility in water.
- other alkalies such as potassium hydroxide or the like may be employed in place of it.
- Ethyl alcohol is preferred as the selective solvent in the process because of its low boiling characteristics and the selective solubilit which it exhibits for the products of hydrolysis.
- methyl alcohol or other low boiling alcohols and similar solvents or mixtures thereof may be employed.
- the conditions of time, temperature and concentration of the alkali may be varied to yield a maximum hydrolysis of the hide substance and a minimum hydrolysis of the tanning agent. Hydrolysis is' accelerated with an increase in heat and also with an increase in theconcentration of the lye solution. Pressure also may be employed if desirable to accelerate the hydrolysis.
- the mixture is now permitted to cool and approximately 3000 parts of ethyl alcohol by volume per each 1000 parts of hydrolysate mixture are added thereto and the mixture is then agitated, preferably out of contact with the air, for a short period of time to insure thorough mixing.
- two layers separate, one being a supernatant liquid and the other being a viscous brownish to black residue.
- the supernatant liquor may readily be decanted from the viscous residue.
- the supernatant, liquor or alcoholic extract contains the sodium salts of the amino acids and However,
- the alcohol may be recovered for reuse by distillation, leaving the sodium salts oi the amino acids.
- These include particularly the sodium salts of glycine, alanine, proline and hydroxyproline.
- the sodium salts of other amino acids that may be present in appreciable amounts are aspartic acids, glutamic acid, leucine, serine and the like.
- arginine and lysine are hydrolytic products of collagen, the alkali hydrolysis may cause partial or complete dismutation of these. Some ammonia and amines are also liberated in the hydrolysis.
- the black residue which is left after the alcoholic extract has been removed comprises the sodium compounds of the tanning agents originally present in the leather which will be found to have suffered a minimum of decomposition.
- This black residue first may be Washed with alcohol if it is desired to free it of any amino acids which may be present. It may also be neutralized by acids such as sulphuric acid supplemented with sulphur dioxide, if desirable.
- the sodium sulphate formed in this treatment is permitted to crystallize from the residue whereupon the resulting brown liquid will be foundto possess tanning properties and may be used in the preparation of new vegetable tanned leather.
- This brown liquor containing the sodium compounds of the tannins and the tannin acids also may be heated or fused at higher temperatures with or without additional alkali to completely hydrolyze the tannins and tannin acids to gallic and protocatechuic acids from which pyrogallol and pyrocatechol, respectively, may be prepared; Accordingly, either the tanning agents or the polyhydroxyphenolic acids may be recovered which enables the process to be practiced according to which of the final products is most in demand.
- the solution of the sodium salts of the amino acids may be used as a source for the individual acids or the solution may be treated with alkaline oxidizing agents directly by methods heretofore described, whereby the prolines are converted into pyrrole,
- Vegetable tanned leather contains appreciable quantities of glucose and magnesium sulphate. These constituents are removed from finely comrninuted leather if such removal is desired, by
- a process for recovering useful values from Vegetable tanned leather which method comprises effecting hydrolysis of the hide substance to hydrolysis by an aqueous alkaline: solution,
- a process for recovering amino acids and tannins and tannin acids from vegetable tanned leather which comprises subjecting said leather in the absence of air to hydrolysis by an aqueous alkaline solution, then separatingthe amino acid salts resulting from hydrolysis of the leather hide substance from the alkali compounds of the tannine and tannin acid by means of ethyl alcohol.
- the process for the recovery of amino acids and tannins and tannin acids from vegetable tanned leather comprises subject,- ing said leather to hydrolysis by an aqueous solution of sodium hydroxide, with the exclusion of air, and separating the sodium salts of the amino acids resultingfrom hydrolyzation of the hide substance of the leather from the sodium compounds of the tannins and tannin acids by means of a low boiling alcohol.
- the process for the recovery-ofamino acids and tannins and tannin acids from vegetable tanned leather comprises subjecting said leather to hydrolysis by an aqueous solution of sodium hydroxide, with the exclusion of air, and separating the sodium salts of the amino acids resulting from hydrolyzation of the hide substance of the leather from the sodium compounds of the tannins and tannin acids by means of ethyl alcohol.
- tannins-and tannin acids from vegetable tanned leather which process comprises treating said leather with an aqueous alkaline solution, controlled as to time and temperature, and in the absence of air, toefiect hydrolysis'of the hide a low boiling alcohol in which the amino acids are soluble.
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 Apr. 8, 1947 RECOVERING VALUES FROM VEGETABLE TANNED LEATHER Joseph Michelman, Portsmouth, Ohio No Drawing. Application June 20, 1945, Serial No. 600,652
8 Claims. 1
This invention relates to a process for preparing certain amino acids, tannins and tannin acids. It is directed particularly to the recovery of these values from vegetable tanned leather scrap or waste. At the present time scrap vegetable tanned leather has very little value. On the other hand, there is no inexpensive commercial source for these amino acids. The present invention, therefore, is one for obtaining valuable materials from substantially useless by-products which are produced in quantity in the shoe and leather fabricating industries.
Vegetable tanned leather is essentially a combination of hide substance of animal origin, and tanning agents of vegetable origin. The hide substance is a protein called collagen which is composed of a group of compounds known as amino acids in their simplest form. The tannin agents in vegetable tanned leather, which are described herein as tannin and tannin acids, are composed mainly of glucosides of certain polyhydroxyphenolic acids derived largely from gallic acid and protocatechuic acid. In accordance with the present invention amino acids are derived from the collagen or hide substance and the tannins, tannin acids or tanning agents are obtained from the tanning agents present in the leather.
Briefly, this invention is based, first, upon the concept and determination that the collagen component and the tannin component of vegetable tanned scrap leather respond differently to hydrolyzing agents such as sodium hydroxide; and,
second, that the products resulting from hydrolyzation of vegetable tanned scrap leather possess different solubilities in certain solvents whereby the readily may be separated one from another by extraction methods. Although collagen and tannin are both known to be hydrolyzable it has now been found that a difference exists in the ease with which the hide substance is hydrolyzed by alkalies in comparison with the tanning agents; the hide substance is resolved into simple amino acids-more readily than the tanning agents are decomposed into simple polyhydroxyphenolic acids. In accordance with this invention hydrolysis of the scrap leather is conducted whereby the hide substance is substantially completely resolved into its amino acid component with a minimum efiect upon or modification of the vegetable tanning agents that are present in the leather.
As a result of this differential hydrolysis, it has been determined that whatever hydrolytic products of the tannins that are formed, as well as the undecomposed tannins, are combined with the hydrolyzing agent to render them insoluble in certain organic solvents in which the amino acids, combined with the same hydrolyzing agent, are substantially soluble. For instance, in the employment of sodium hydroxide as the hydrolyzing agent, the sodium compounds of the tannins and tannin acids are insoluble in the alcohol as a selective solvent, while the sodium compounds of the amino acids dissolve readily in the alcohol. This solubilit behavior is anomalous in view of the fact that the tannins and their polyhydroxyphenolic acids are normally alcohol soluble. Moreover, the solubility behavoir of the sodium salts of the amino acids from vegetable tanned leather also is unexpected inasmuch as the amino acids are not appreciably soluble in alcohol.
Sodium hydroxide is the preferred hydrolyzing agent in the practice of this invention because of its low cost and its ready solubility in water. However, other alkalies such as potassium hydroxide or the like may be employed in place of it. Ethyl alcohol is preferred as the selective solvent in the process because of its low boiling characteristics and the selective solubilit which it exhibits for the products of hydrolysis. methyl alcohol or other low boiling alcohols and similar solvents or mixtures thereof may be employed.
A typical example of the process is as follows:
400 parts by weight of vegetable tanned leather, preferably shredded or finely comminuted, and 1000 parts by weight of aqueous sodium hydroxide solution of 15% to 25% concentration by weight are placed in a container which is equipped with a lid so that it may be tightly closed. During hydrolysis air should be excluded as the tannins and tannin acids oxidize readily in alkaline solution. The leather and the lye solution are heated to a temperature of approximately C. to C. from four to ten hours. During this treatment the leather is dissolved upon hydrolysis of the hide substance and a brownish-black liquor results which may form a soft gel upon cooling. The conditions of time, temperature and concentration of the alkali may be varied to yield a maximum hydrolysis of the hide substance and a minimum hydrolysis of the tanning agent. Hydrolysis is' accelerated with an increase in heat and also with an increase in theconcentration of the lye solution. Pressure also may be employed if desirable to accelerate the hydrolysis.
The mixture is now permitted to cool and approximately 3000 parts of ethyl alcohol by volume per each 1000 parts of hydrolysate mixture are added thereto and the mixture is then agitated, preferably out of contact with the air, for a short period of time to insure thorough mixing. Upon standing twelve to twenty-four hours two layers separate, one being a supernatant liquid and the other being a viscous brownish to black residue. The supernatant liquor may readily be decanted from the viscous residue.
The supernatant, liquor or alcoholic extract contains the sodium salts of the amino acids and However,
is substantially free from the sodium salts of tannin and tannin acids. From this extract the alcohol may be recovered for reuse by distillation, leaving the sodium salts oi the amino acids. These include particularly the sodium salts of glycine, alanine, proline and hydroxyproline. The sodium salts of other amino acids that may be present in appreciable amounts are aspartic acids, glutamic acid, leucine, serine and the like. Although arginine and lysine are hydrolytic products of collagen, the alkali hydrolysis may cause partial or complete dismutation of these. Some ammonia and amines are also liberated in the hydrolysis.
The black residue which is left after the alcoholic extract has been removed comprises the sodium compounds of the tanning agents originally present in the leather which will be found to have suffered a minimum of decomposition. This black residue first may be Washed with alcohol if it is desired to free it of any amino acids which may be present. It may also be neutralized by acids such as sulphuric acid supplemented with sulphur dioxide, if desirable.
The sodium sulphate formed in this treatment is permitted to crystallize from the residue whereupon the resulting brown liquid will be foundto possess tanning properties and may be used in the preparation of new vegetable tanned leather. This brown liquor containing the sodium compounds of the tannins and the tannin acids also may be heated or fused at higher temperatures with or without additional alkali to completely hydrolyze the tannins and tannin acids to gallic and protocatechuic acids from which pyrogallol and pyrocatechol, respectively, may be prepared; Accordingly, either the tanning agents or the polyhydroxyphenolic acids may be recovered which enables the process to be practiced according to which of the final products is most in demand. Moreover, the solution of the sodium salts of the amino acids may be used as a source for the individual acids or the solution may be treated with alkaline oxidizing agents directly by methods heretofore described, whereby the prolines are converted into pyrrole,
Vegetable tanned leather contains appreciable quantities of glucose and magnesium sulphate. These constituents are removed from finely comrninuted leather if such removal is desired, by
preliminary washing of the scrap with Water. If thetannins and tannin acids are intended to be used as tanning agents then preliminary removal of the magnesium sulphate and the glucose enables a more concentrated tanning extract to be prepared, I 1
Having described my invention, 1' claim:
-1 The method ofobtaining useful values from vegetable tanned'leather, which method com prises subjecting said-leather when it is in a comminuted form to differential hydrolysis in alkaline solution with exclusion of air to substantiallycompletely hydrolyze the hide substance of the leather with a minimum efiecton the tanning agents in the leather, and then, bymeans of a lower alcohol selectively. extracting the products resulting from hydrolysis of the hide substance from the tanning matter and itsderivatives.
2. .A process for the preparation of amino acids. and tanninsand tannin acids from vegetable tanned leather, which process comprises subjecting the leather todifierential hydrolysis in alkaline solution with exclusion of air and thereby substantially hydrolyzing the hide substance of theleather with minimum hydrolyzation of the tannins and tannin acids, and then separating the amino acids resulting from hydrolysis of the hide substance from thetannins and tannin acids by selective solvent extraction with a lower alcohol.
3. A process for recovering useful values from Vegetable tanned leather, which method comprises effecting hydrolysis of the hide substance to hydrolysis by an aqueous alkaline: solution,
in the absence of air then separating the amino acid salts resulting from hydrolysis of the leather hide substance from the alkali compounds of the tannins and tannin acids by means of a low boiling alcohol.
5. A process for recovering amino acids and tannins and tannin acids from vegetable tanned leather, which comprises subjecting said leather in the absence of air to hydrolysis by an aqueous alkaline solution, then separatingthe amino acid salts resulting from hydrolysis of the leather hide substance from the alkali compounds of the tannine and tannin acid by means of ethyl alcohol.
6. The process for the recovery of amino acids and tannins and tannin acids from vegetable tanned leather, which process comprises subject,- ing said leather to hydrolysis by an aqueous solution of sodium hydroxide, with the exclusion of air, and separating the sodium salts of the amino acids resultingfrom hydrolyzation of the hide substance of the leather from the sodium compounds of the tannins and tannin acids by means of a low boiling alcohol.
7. The process for the recovery-ofamino acids and tannins and tannin acids from vegetable tanned leather, which process comprises subjecting said leather to hydrolysis by an aqueous solution of sodium hydroxide, with the exclusion of air, and separating the sodium salts of the amino acids resulting from hydrolyzation of the hide substance of the leather from the sodium compounds of the tannins and tannin acids by means of ethyl alcohol.
8. A process for recovering amino acids and.
tannins-and tannin acids from vegetable tanned leather, which process comprises treating said leather with an aqueous alkaline solution, controlled as to time and temperature, and in the absence of air, toefiect hydrolysis'of the hide a low boiling alcohol in which the amino acids are soluble.
JOSEPH MICHELE/IAN.
REFERENCES CITED The following references are of record in the file of this patent:
Chemical Abstracts, vol. 26, pages 1823-5
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60065245 US2418655A (en) | 1945-06-20 | 1945-06-20 | Recovering values from vegetable tanned leather |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60065245 US2418655A (en) | 1945-06-20 | 1945-06-20 | Recovering values from vegetable tanned leather |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2418655A true US2418655A (en) | 1947-04-08 |
Family
ID=24404511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US60065245 Expired - Lifetime US2418655A (en) | 1945-06-20 | 1945-06-20 | Recovering values from vegetable tanned leather |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2418655A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2935444A (en) * | 1957-02-27 | 1960-05-03 | Pfizer & Co C | Parasiticidal agent and process for producing same |
| US20080113897A1 (en) * | 2004-12-30 | 2008-05-15 | Alberto Pons Raga | Patent Of Invention P200001758,Method For The Transformation Of Chrome-Free Tanning Waste And Products Thus Obtained |
-
1945
- 1945-06-20 US US60065245 patent/US2418655A/en not_active Expired - Lifetime
Non-Patent Citations (1)
| Title |
|---|
| None * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2935444A (en) * | 1957-02-27 | 1960-05-03 | Pfizer & Co C | Parasiticidal agent and process for producing same |
| US20080113897A1 (en) * | 2004-12-30 | 2008-05-15 | Alberto Pons Raga | Patent Of Invention P200001758,Method For The Transformation Of Chrome-Free Tanning Waste And Products Thus Obtained |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4100154A (en) | Process for recovery and separation of nutritious protein hydrolysate and chromium from chrome leather scrap | |
| US2418655A (en) | Recovering values from vegetable tanned leather | |
| US1974554A (en) | Process for the production of amino acids from substances containing keratin | |
| US2928822A (en) | Proteinaceous food adjunct and method of preparing same | |
| US2504425A (en) | Separation of pure methionine from methionine nitrile hydrolyzates | |
| GB737279A (en) | Preparation of phytic acid | |
| US2009868A (en) | Method of preparing leucine | |
| US5602002A (en) | Process for the production of low-chromium protein hydrolyzates | |
| US1340721A (en) | Process for detanning chrome-leather | |
| US2559305A (en) | Manufacture of tanning substances | |
| US1860469A (en) | Process for obtaining active substances from hypophysis glands | |
| US2147542A (en) | Treating skins, hides, and pelts | |
| US1488815A (en) | Vitamin body and method of preparing the same | |
| US2362540A (en) | Hide treatment | |
| US722944A (en) | Process of devulcanizing gums. | |
| US2460809A (en) | Method of preparing gelatin | |
| ES282992A1 (en) | PROCEDURE TO RECOVER MELAMINE | |
| GB618174A (en) | Process for recovering proteolytic enzymes from the pancreas of mammals | |
| GB746413A (en) | Method of recovering para-nitrochlorobenzene | |
| US2442055A (en) | Hydrolysis of proteins | |
| US2590517A (en) | Method for the preparation of peptone and amino acid containing extracts from press water | |
| US2410776A (en) | Manufacture of hydracrylic acid | |
| US1633262A (en) | Vegetable sea-gbowth derivative and a method fob the preparation | |
| US2285193A (en) | Reaction product of water-soluble degraded proteins with phenols and aldehydes | |
| US2136771A (en) | Rubber composition and method of compounding rubber |