US3076749A - Method of unhairing skins and hides - Google Patents
Method of unhairing skins and hides Download PDFInfo
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- US3076749A US3076749A US37062A US3706260A US3076749A US 3076749 A US3076749 A US 3076749A US 37062 A US37062 A US 37062A US 3706260 A US3706260 A US 3706260A US 3076749 A US3076749 A US 3076749A
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- 238000000034 method Methods 0.000 title claims description 23
- 102000004190 Enzymes Human genes 0.000 claims description 22
- 108090000790 Enzymes Proteins 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 22
- 239000003638 chemical reducing agent Substances 0.000 claims description 15
- 230000007935 neutral effect Effects 0.000 claims description 13
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 239000011593 sulfur Substances 0.000 claims description 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 150000004820 halides Chemical class 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 49
- 108091005804 Peptidases Proteins 0.000 description 42
- 239000004365 Protease Substances 0.000 description 34
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 32
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 28
- 210000003491 skin Anatomy 0.000 description 27
- 241000233866 Fungi Species 0.000 description 21
- 229940088598 enzyme Drugs 0.000 description 21
- 235000010265 sodium sulphite Nutrition 0.000 description 14
- 238000009950 felting Methods 0.000 description 13
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 10
- 102000035195 Peptidases Human genes 0.000 description 10
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 8
- 230000001580 bacterial effect Effects 0.000 description 8
- 239000002609 medium Substances 0.000 description 8
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000000080 wetting agent Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 150000004763 sulfides Chemical class 0.000 description 6
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 235000019270 ammonium chloride Nutrition 0.000 description 5
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 5
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 5
- 235000011130 ammonium sulphate Nutrition 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 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 4
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000002255 enzymatic effect Effects 0.000 description 4
- 239000001103 potassium chloride Substances 0.000 description 4
- 235000011164 potassium chloride Nutrition 0.000 description 4
- 230000001603 reducing effect Effects 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 4
- 235000010344 sodium nitrate Nutrition 0.000 description 4
- 239000004317 sodium nitrate Substances 0.000 description 4
- 229910052979 sodium sulfide Inorganic materials 0.000 description 4
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 4
- 150000003464 sulfur compounds Chemical class 0.000 description 4
- 235000011437 Amygdalus communis Nutrition 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 241000220304 Prunus dulcis Species 0.000 description 3
- 102000001400 Tryptase Human genes 0.000 description 3
- 108060005989 Tryptase Proteins 0.000 description 3
- 235000020224 almond Nutrition 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229940117927 ethylene oxide Drugs 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 238000004321 preservation Methods 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 102000006995 beta-Glucosidase Human genes 0.000 description 2
- 108010047754 beta-Glucosidase Proteins 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 2
- -1 sodium sulfide Chemical class 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 102000002464 Galactosidases Human genes 0.000 description 1
- 108010093031 Galactosidases Proteins 0.000 description 1
- 102000004366 Glucosidases Human genes 0.000 description 1
- 108010056771 Glucosidases Proteins 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-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
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000003190 augmentative effect Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229940079919 digestives enzyme preparation Drugs 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229940116357 potassium thiocyanate Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011833 salt mixture Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 238000005406 washing 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
- C14C1/00—Chemical treatment prior to tanning
- C14C1/06—Facilitating unhairing, e.g. by painting, by liming
- C14C1/065—Enzymatic unhairing
-
- 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
- C14C1/00—Chemical treatment prior to tanning
- C14C1/06—Facilitating unhairing, e.g. by painting, by liming
Definitions
- This invention relates to methods for unhairing skins and hides.
- Softened skins and hides have also been treated in the prior art with pulverized proteolytic enzymes or enzyme pastes whereby a very good removal of hair can be effected.
- pulverized proteolytic enzymes or enzyme pastes whereby a very good removal of hair can be effected.
- such treatment requires relatively large amounts of enzyme, and is very expensive.
- skins and hides may be unhaired without any attack of the hair by presoftening the hides by a suitable process such as washing in water, then further softening the hides with a powdered or pasty enzyme product containing a proteolytic enzyme, and then treating the hides with inorganic neutral salts of the alkali metals and of ammonium and/or sulfur compounds which are reducing agents.
- the need for expensive enzyme preparations can be reduced to a minimal amount, while nevertheless a complete removal of hair is effected.
- the hair is maintained fully integral and can be removed together with the hair roots, any adhering residue of epidermis, pigments, and sebaceous glands.
- proteases formed by microorganisms and bacteria are particularly desirable for use in the process of the invention. Pancreatic tryptase is also useful.
- the enzyme softening of the invention is conveniently effected by felting water-soaked and softened hides with from 0.05 percent to 1.5 percent, preferably with from 0.1 percent to 1 percent, of the enzyme, the percentages being by weight of the hides treated.
- the felting of the hides is carried out for from 15 minutes to 2 or 3 hours, suitably for from 30 minutes to an hour, after which the enzymes are permitted to work on the hides for an additional period of from 30- minutes to an hour, or two or three hours.
- the unhairing effects produced according to the invention are even more pronounced if the proteolytic enzyme is combined with oligases, particularly with the glucosidases and galactosidases found in almond emulsin (synaptase). These are enzymes which act only on oligosaccharide, but do not decompose polysaccharides. Reference is made to the book by K.
- the oligases are suitably used in combination with enzymes in amounts of between about 0.105 percent to 0.5 percent, preferably about 0.1 to 0.3 percent, by weight of hides treated.
- sulfur-containing reducing agents mentioned herein can be combined with proteases in the softening process (of. Examples 2, 5, 6, 7 infra).
- proteases in the softening process (of. Examples 2, 5, 6, 7 infra).
- Those of these compounds which contain oxygen are particularly suitable in such combinations, and are suitably used in amounts of from about 0.1 percent to 5 percent, preferably about 0.2 percent to 2 percent, based on the weight of hides treated.
- wetting agents can be used together with the enzymes.
- Cationic wetting agents known to the art for hide treating, or non-ionogenic wetting agents of the same type as ethylene oxide condensation products preferably having 6-16 polymerized ethylene-oxide oxyhydrocarbon units are particularly effective.
- the pH of the hides suitably is kept at a weakly alkaline to weakly acid pH, e.g. between about 5.5 and 8, preferably between about 6.0 and 7.5.
- weakly acid pH e.g. between about 5.5 and 8, preferably between about 6.0 and 7.5.
- the same pH range is employed when the enzymes are combined with sulfur containing reducing agents as hereinbefore described.
- the hides are next treated with inorganic neutral salts and/ or sulfur containing reducing agents.
- the salts are suitably employed in the presence of from about 30 to percent, preferably of from about 30 to 50 percent, of water, based on the weight of the skins or hides being treated.
- the use of larger amounts of water, such as in amounts of 200 to 300 percent by weight of the hides is not excluded, but requires a correspondingly greater amount of salt.
- the salt solutions can be used with the addition of a thickening agent such as kaolin and applied to the fleshy side of the enzymatically softened hides and skins.
- the inorganic neutral salts most suitable for use in the invention are the salts, with alkali metals and ammonium, of strong inorganic acids such as the inorganic oxy-acids (e.g. sulfates, nitrates, chlorates, etc.) or the hydrohalic acids (e.g. chlorides, iodides, etc.), or of other strong acids such as thiocyanic acid.
- the salts are employed, with the amounts of water mentioned above, in amounts of from about 0.1 percent to about 10 percent, preferably from about 0.2 percent to 7 percent or 0.5 percent to 5 percent, by weight of the hides treated.
- Soluble inorganic reducing sulfo-salts are particularly suitable, specifically those containing sulfur atoms having. a valence less than +6. Solublesulfites, bisulfites, thiosulfates, 'hyposulfites, sulfides, and hydrosulfides are particularly advantageous. Salts of thioacids such as thioglycolic acid can also be used to advantage.
- the metal ion'of the soluble salts is not critical, but sodium comcost;- Where sulfides'are used in the present process,-they are employed in amountsonly 'to A the amounts prc viously used in the art for complete unhairing'using sulfides alone.
- the aqueous media containing thesalts and/or sulfur compounds are suitably maintained weaklyalkaline or weakly. acid,-at values like those mentioned for the enzyme treatment.
- a strongly alkaline pH for example between about 9 and 10 to 12 or 13, is suitable. 1 i r
- the sulfur-containing reducing agents canbe used in combination with non-ionic or anionic wetting agents known to the art in hide treating. a
- Example 1 Indian goatskins were pre-softened with water for 24 hours and then enzymatically softened, without addition
- Example 2 Dried Indian goatskins were softened in water for 24 hoursand then enzymatically softened by placing in a vessel, without addition of water, with 0.6 percent of mold fungus protease in powdered form, calculated on the weight of the pre-softened skins, 0.5 percent sodium sulfate, and 0.1 percent of a preservation agent.
- the skins were felted for 1 hour. After 1 hour of standing, 50 ners nto .watena d p r ntio p t i m nitrate were, added, and the skins were felted for an additional hour,
- the hair was then removed from the hides.
- the mold fungus protease medium was at a pH between 7 and 7.5; the solution containing sodium nitrate had a pH of 7.
- Example 3 Dried Spanish goatskins were pre-softened in water for 24 hours and thereafter enzymatically softened by placing in a vessel, without addition of water, with 0.5 percent mold fungus protease, calculated on the weight of the pre-softened skins, and 0.1 percent of a preserving agent.
- the skins were felted forl hour. After 1 hours standing, 50 percent of water, 1 percent of calcined sodium pounds are usually-employed commercially because of sulfite, and 1.2 percent of potassium chloride were added.
- the skins were felted for l hourand allowed to stand for 24 hours. The hair was then removed.
- the action of the mold fungus protease and the salts took place in media with a pH of 7.
- Example 4 Salted red cowhides were pre-softened with water, rinsed, and then put in a vessel, without addition of water, for additional softening with 0.75 percent mold fungus protease in powdered form, calculated on the weight of the pre-softened hides, and 0.1 percent of a preservation agent. The hides were then felted for 30 minutes. After standing for 1 hour, 50 percent of water and -1 percent of ammonium chloride were added. After an additional hours felting, the hideswere set aside for 24 hours and the hair was then removed. The action of the mold fungus protease and of the ammonium chloride took place in solutions at a pH of 7.
- Example 5 water, with 0.5 percent bacterial protease in powdered form, 0.2 percent of almond emulsin having a betaglucosidase value of 0.01 asd 0.5 percent calcined sodium bisulfite. water and 1 percent of ammonium chloride were added. After felting for 10 minutes, the hides were set aside for 24 hours and then unhaired. The protease medium had a pH of 6-6.5; that of the ammonium chloride was at pH 7.
- Example 7 centsodium sulfite, and 1 percent sodium chloride were After one hours standing, 50 percent of After rinsing, they were felted for Example 8 Indian goatskins previously softened by a 48 hour treatment with water were further softened by 1 hours felting in a vessel with 1.0 percent of pancreatic tryptase in powdered form, calculated on the weight of the pre-- softened hides. After 2 hours standing, 50 percent water, 1 percent ammonium sulfate, and 0.5 percent of potassium chloride were added. After an additional one hours felting, the hides were set aside for 36 hours and then unhaired. The action of the pancreatic tryptase took place in a medium at pH 7-7.5, that of the salts at pH 7. The unhairing effect can be increased by raising the pH of thesalt solution to pH 9, for example by the addition of soda.
- Example 9 Dried Indian goatskins were presoftened with water and then felted for 30 minutes with 0.5 percent of mold fungus protease, calculated on the weight of the presoftened hides, and 0.3 percent of a preservation agent. After two hours standing, 50 percent of water and 5 percent of anhydrous sodium thiosulfate were added. After another 30 minutes of felting, the hides were allowed to stand overnight. After 24 hours, they were dehaired. The action of the mold fungus protease was in a medium at pH 6.5-7; the solution of sodium thiosulfate had a pH of 7.
- Example 11 Calfskins, presoftened and rinsed with water, were felted for 30 minutes with 0.6 percent bacterial protease, 0.4 percent calcined sodium bisulfite, and 0.8 percent of ammonium sulfate. After 2 hours standing, 50 percent water and 3 percent of calcined sodium sulfite were added. After an additional 30 minutes of felting, the hides were allowed to stand, and were unhaired after 24- 36 hours. The action of the bacterial protease takes place in a medium at pH 6-6.5; the action of the sodium sulfite takes place in a medium at pH 7.5-8.
- Example 12 Red cowhides, presoftened with water and then rinsed, were felted for one-half hour with 0.6 percent bacterial protease, 0.5 percent sodium bisulfite, and 0.4 percent ammonium sulfate. After one hour's standing, 50 percent water and 4 percent of sodium sulfite were added and felted for an additional 30 minutes. The hides were then left to stand and were unhaired after about 40 hours. The action of the bacterial protease was in a medium at pH 6-6.5; that of the sodium sulfite in a medium at pH 7.5-8.
- Example 14 Water softened goatskins were felted for one-half hour with 0.5 percent mold fungus protease and 0.3 percent of a preserving agent. After 3 hours standing, 50 percent of water, 2 percent of 98 percent thioglycolic acid neutralized with ammonia were added. After an additional 30 minutes of felting, the hides were set aside and after 24 hours were dehaired. The action of the mold fungus protease and the thioglycolic acid was at pH 7.
- Example 15 A dried Indian goatskin 'was washed and soaked with water for 24 hours and divided into 4 parts. The first part was felted for 1 hour with 0.5 percent by weight of skin of a mold fungus protease without addition of water. After 24 hours, 20 to 25 percent of the hair on the skin was loosened.
- the second part of the skin was felted for one hour with 50 percent water and 1 percent of sodium nitrate. After 24 hours, no loosening of hair was observable.
- the third portion of the skin was felted for one hour with 0.5 percent by weight of the mold fungus protease and 1 percent by weight of sodium nitrate without the addition of water. After 24 hours, about 20 percent of the hair had been loosened.
- the fourth part of the skin was felted for 1 hour with 0.5 percent of mold fungus protease without the addition of water. After an additional hour, 50 percent of water and 1 percent of sodium nitrate were added and the skin was felted for 30 minutes. The treated hide was then set aside. After 24 hours from the beginning of the treatment, substantially 100 percent of the hair could be removed from the skin.
- the other neutral salts mentioned earlier herein give corresponding results when employed according to the last-mentioned methods. Potassium thiocyanate and ammonium chloride are especially effective.
- Example 16 An Indian goatskin was softened with water and divided into 4 parts. The first part was felted for 30 minutes with 3 percent of mold fungus protease, calculated on the weight of the softened hide, according to the process described in German Patent 1,026,038, without the addition of water. After 24 hours, 100 percent of the hair could be removed.
- a second part of the skin was felted with 0.5 percent mold fungus protease for 30 minutes. After 24 hours, about 15 percent of the hair was loosened.
- the fourth part of the skin was treated with 0.5 percent of mold fungus protease for 30 minutes. After 2 hours,[
- At least one reagent selected from the group con sisting essentially of sulfur containing reducing agents and inorganic neutral salts of the alkali metals and ammonium.
- wetting agent is a polyglycol ether, the moleculesof which comprise 6 to 16 polymerized units of ethylene oxide.
- wetting agent is "(Eontac'ted'with the'hides' together with said reagent selected'frdmthe group consisting essentially of sulfur containing reducing agents and inorganic neutral salts of "the alkali metals and ammonium.
- proteolytic enzyme is the enzyme of a micro-organism.
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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)
- Cosmetics (AREA)
Description
United States Patent 3,076,749 METHOD OF UNHAIRING SKINS AND HIDES Otto Grimm, Darmstadt, Germany, assignor to Rohm & Haas G.m.b.H., Darmstadt, Germany No Drawing. Filed June 20, 1960, Ser. No. 37,062
Claims priority, application Germany June 24, 1959 Claims. (Cl. 195-6) This invention relates to methods for unhairing skins and hides.
It is known in the art that lime and sulfides, particularly sodium sulfide, are effective for the removal of hair from skins and hides. Also, sulfur compounds which are reducing agents, such as sulfites, bisulfites, and hyposulfites, show some effect as hair loosening agents. Nevertheless, methods of removing hair employing the latter compounds are of little practical value, because the hair removal is completely unsatisfactory. Thus, hair removal is not uniform. Large amounts of chemicals are used and the treatment requires strongly alkaline solutions. Also, when dry rawhides are treated, the process may take several days. In contrast, the use of sulfides, to be sure, brings about a removal of hair. However, when small amounts of sulfides are used, hair removal is scanty, and when large amounts are employed, the hair is attacked or fully i destroyed, leaving the hair roots unremoved from the hide. Thioglycolates, also used in the prior art for unhairing, show only a very weak hair loosening effect at a pH below 8. Above pH 9, hair is strongly attacked'by this reagent.
Softened skins and hides have also been treated in the prior art with pulverized proteolytic enzymes or enzyme pastes whereby a very good removal of hair can be effected. However, such treatment requires relatively large amounts of enzyme, and is very expensive.
It has now been found that skins and hides may be unhaired without any attack of the hair by presoftening the hides by a suitable process such as washing in water, then further softening the hides with a powdered or pasty enzyme product containing a proteolytic enzyme, and then treating the hides with inorganic neutral salts of the alkali metals and of ammonium and/or sulfur compounds which are reducing agents.
By this process, the need for expensive enzyme preparations can be reduced to a minimal amount, while nevertheless a complete removal of hair is effected. In the un hairing, the hair is maintained fully integral and can be removed together with the hair roots, any adhering residue of epidermis, pigments, and sebaceous glands.
-It is emphasized that neither the amount of enzyme used in the softening according to the invention, nor the amount of neutral salts and/ or reducing sulfur compounds employed in the present unhairing process is sufficient alone to bring about a removal of hair.
In view of the experiences of the prior art in unhairing with sulfur-containing reducing agents, it is a surprising result that the hair-removing efficiency of these compounds can be improved by a prior treatment of hides and skins with a 'relatively small amount of the enzyme to give a usefuh sure, and cheap method for removing hair.
As proteolytic enzymes, the proteases formed by microorganisms and bacteria are particularly desirable for use in the process of the invention. Pancreatic tryptase is also useful. As concerns the enzyme concentrates employed in the specific examples herein, reference is made to the Gerbereichemisches Taschenbuch, by A. Kiintzel, Theodor Steinkopff, publishers, Dresden and Leipzig, 1955, page 86. The enzyme softening of the invention is conveniently effected by felting water-soaked and softened hides with from 0.05 percent to 1.5 percent, preferably with from 0.1 percent to 1 percent, of the enzyme, the percentages being by weight of the hides treated. These amounts of enzyme are substantially smaller than the amounts used in the prior art to effect unhairing and alone, in the absence of the further treatment of the hides as contemplated by this invention, are insufficient to effect a satisfactory unhairing.
The felting of the hides is carried out for from 15 minutes to 2 or 3 hours, suitably for from 30 minutes to an hour, after which the enzymes are permitted to work on the hides for an additional period of from 30- minutes to an hour, or two or three hours. The unhairing effects produced according to the invention are even more pronounced if the proteolytic enzyme is combined with oligases, particularly with the glucosidases and galactosidases found in almond emulsin (synaptase). These are enzymes which act only on oligosaccharide, but do not decompose polysaccharides. Reference is made to the book by K. Myrback, Enzymatische Katalyse, Walter de Gruyder & Company, Berlin, W. 35, 1935, pages 44-45, concerning the enzymatic efficiency of these oligases. The oligases are suitably used in combination with enzymes in amounts of between about 0.105 percent to 0.5 percent, preferably about 0.1 to 0.3 percent, by weight of hides treated.
Similarly, the sulfur-containing reducing agents mentioned herein can be combined with proteases in the softening process (of. Examples 2, 5, 6, 7 infra). Those of these compounds which contain oxygen are particularly suitable in such combinations, and are suitably used in amounts of from about 0.1 percent to 5 percent, preferably about 0.2 percent to 2 percent, based on the weight of hides treated. By such combinations, the unhairing effects of the process can be augmented.
Advantageously, wetting agents can be used together with the enzymes. Cationic wetting agents, known to the art for hide treating, or non-ionogenic wetting agents of the same type as ethylene oxide condensation products preferably having 6-16 polymerized ethylene-oxide oxyhydrocarbon units are particularly effective.
- The simultaneous use of enzymes with the inorganic neutral salts used for post-treating the enzyme-softened hides does not accomplish a satisfactory unhairing.
In the enzyme treatment, the pH of the hides suitably is kept at a weakly alkaline to weakly acid pH, e.g. between about 5.5 and 8, preferably between about 6.0 and 7.5. The same pH range is employed when the enzymes are combined with sulfur containing reducing agents as hereinbefore described.
After enzymatic softening, the hides are next treated with inorganic neutral salts and/ or sulfur containing reducing agents. The salts are suitably employed in the presence of from about 30 to percent, preferably of from about 30 to 50 percent, of water, based on the weight of the skins or hides being treated. The use of larger amounts of water, such as in amounts of 200 to 300 percent by weight of the hides is not excluded, but requires a correspondingly greater amount of salt. In case a painting process is indicated, the salt solutions can be used with the addition of a thickening agent such as kaolin and applied to the fleshy side of the enzymatically softened hides and skins.
The inorganic neutral salts most suitable for use in the invention are the salts, with alkali metals and ammonium, of strong inorganic acids such as the inorganic oxy-acids (e.g. sulfates, nitrates, chlorates, etc.) or the hydrohalic acids (e.g. chlorides, iodides, etc.), or of other strong acids such as thiocyanic acid. The salts are employed, with the amounts of water mentioned above, in amounts of from about 0.1 percent to about 10 percent, preferably from about 0.2 percent to 7 percent or 0.5 percent to 5 percent, by weight of the hides treated. Anionic, cationic,
Soluble inorganic reducing sulfo-salts are particularly suitable, specifically those containing sulfur atoms having. a valence less than +6. Solublesulfites, bisulfites, thiosulfates, 'hyposulfites, sulfides, and hydrosulfides are particularly advantageous. Salts of thioacids such as thioglycolic acid can also be used to advantage. The metal ion'of the soluble salts is not critical, but sodium comcost;- Where sulfides'are used in the present process,-they are employed in amountsonly 'to A the amounts prc viously used in the art for complete unhairing'using sulfides alone. Suchprior art processes also undesirably destroy the hair, as noted earlier." i i These reducing agents are used inamounts similar to those described for the neutral salts, in corresponding amounts of water. r a The simultaneous use of neutral salts and reducing sulfur-containing agents, particularly those which contain oxygen, has shown itself to be particularly advantageous (cf. Examples 3, 6, 7 infra). When combinations of the salts areused, the total amount of treating agents used falls within the limits mentioned herein for the substances used'separately. Y
The aqueous media containing thesalts and/or sulfur compounds are suitably maintained weaklyalkaline or weakly. acid,-at values like those mentioned for the enzyme treatment. However, whenoxygen-free sulfur containing reducing agents are employed, a strongly alkaline pH, for example between about 9 and 10 to 12 or 13, is suitable. 1 i r The sulfur-containing reducing agents canbe used in combination with non-ionic or anionic wetting agents known to the art in hide treating. a
In both the enzymatic softening step and the application of neutral salts and/or sulfur-containin'g-reducing agents, the unhairing is readilyand conveniently effected at room temperature (about 18-20 C.) andcan even be accomplished at lower temperatures such as 1015 C. The use of higher temperatures factory, and-is in no way excluded. 1 t 1 A better understanding of the-invention and of its many advantages can be had by reference to the following illustrative examples.
Example 1 Indian goatskins were pre-softened with water for 24 hours and then enzymatically softened, without addition Example 2 .Dried Indian goatskins were softened in water for 24 hoursand then enzymatically softened by placing in a vessel, without addition of water, with 0.6 percent of mold fungus protease in powdered form, calculated on the weight of the pre-softened skins, 0.5 percent sodium sulfate, and 0.1 percent of a preservation agent. The skins were felted for 1 hour. After 1 hour of standing, 50 ners nto .watena d p r ntio p t i m nitrate were, added, and the skins were felted for an additional hour,
subsequent is also satisafter which they were set aside for 24 hours. The hair was then removed from the hides. The mold fungus protease medium was at a pH between 7 and 7.5; the solution containing sodium nitrate had a pH of 7.
Example 3 Dried Spanish goatskins were pre-softened in water for 24 hours and thereafter enzymatically softened by placing in a vessel, without addition of water, with 0.5 percent mold fungus protease, calculated on the weight of the pre-softened skins, and 0.1 percent of a preserving agent. The skins were felted forl hour. After 1 hours standing, 50 percent of water, 1 percent of calcined sodium pounds are usually-employed commercially because of sulfite, and 1.2 percent of potassium chloride were added. The skins were felted for l hourand allowed to stand for 24 hours. The hair was then removed. The action of the mold fungus protease and the salts took place in media with a pH of 7.
Example 4 Salted red cowhides were pre-softened with water, rinsed, and then put in a vessel, without addition of water, for additional softening with 0.75 percent mold fungus protease in powdered form, calculated on the weight of the pre-softened hides, and 0.1 percent of a preservation agent. The hides were then felted for 30 minutes. After standing for 1 hour, 50 percent of water and -1 percent of ammonium chloride were added. After an additional hours felting, the hideswere set aside for 24 hours and the hair was then removed. The action of the mold fungus protease and of the ammonium chloride took place in solutions at a pH of 7.
Example 5 water, with 0.5 percent bacterial protease in powdered form, 0.2 percent of almond emulsin having a betaglucosidase value of 0.01 asd 0.5 percent calcined sodium bisulfite. water and 1 percent of ammonium chloride were added. After felting for 10 minutes, the hides were set aside for 24 hours and then unhaired. The protease medium had a pH of 6-6.5; that of the ammonium chloride was at pH 7.
H l 7 Example 6 Dn'ed Chinese goatskins were presoftened for 48 hours with water and after rinsing were further treated, during thecourse of an hours felting, in a vessel with 0.8 bacterial protease in powdered form, calculated on the weight of the presoftened hides, 0.2 percent of almond emulsin. having a beta-glucosidase value of 0.01, 0.8 percent of sodium bisulfite, and 0.8 percent of ammonium sulfate. After 2 hours standing, 50 percent of water, 3 percent of calcined sodium sulfite, and 1 percent of potassium chloride were added. After an additional hours felting, the hides were set aside for 24 to 36 hours and then unhaired. For Indian goatskins, half the quantity of enzyme/salt mixture is sufficient in the softening treatment. The action of the enzyme took place at pH 6-6.5. The solution of sodium sulfite and potassium chloride was at pH 7.
Example 7 centsodium sulfite, and 1 percent sodium chloride were After one hours standing, 50 percent of After rinsing, they were felted for Example 8 Indian goatskins previously softened by a 48 hour treatment with water were further softened by 1 hours felting in a vessel with 1.0 percent of pancreatic tryptase in powdered form, calculated on the weight of the pre-- softened hides. After 2 hours standing, 50 percent water, 1 percent ammonium sulfate, and 0.5 percent of potassium chloride were added. After an additional one hours felting, the hides were set aside for 36 hours and then unhaired. The action of the pancreatic tryptase took place in a medium at pH 7-7.5, that of the salts at pH 7. The unhairing effect can be increased by raising the pH of thesalt solution to pH 9, for example by the addition of soda.
Example 9 Dried Indian goatskins were presoftened with water and then felted for 30 minutes with 0.5 percent of mold fungus protease, calculated on the weight of the presoftened hides, and 0.3 percent of a preservation agent. After two hours standing, 50 percent of water and 5 percent of anhydrous sodium thiosulfate were added. After another 30 minutes of felting, the hides were allowed to stand overnight. After 24 hours, they were dehaired. The action of the mold fungus protease was in a medium at pH 6.5-7; the solution of sodium thiosulfate had a pH of 7.
Example 10 Kid hides were presoftened with water and then felted for 30 minutes with 0.4 percent bacterial protease, 0.3 percent of a preserving agent, 0.2 percent of calcined sodium sulfite, =and 0.4 percent ammonium sulfate. After 2 hours standing, 50 percent of water and 2 percent of sodium sulfite (or 1.75 percent sodium sulfite with 0.25 percent sodium hyposulfite-which is even more efficacious) were added. After another 30 minute long felting period, the hides were left to stand overnight. After about 24 hours, the hides were unhaired. The action of the bacterial protease occurred at pH 6.5-7; the action of the sodium sulfite at pH 7.5. The use of 50 to 250 percent of water together with between 2 and 10 percent of calcined sodium sulfitealone, without the prior protease treatment, gives no loosening of hair from the hides.
Example 11 Calfskins, presoftened and rinsed with water, were felted for 30 minutes with 0.6 percent bacterial protease, 0.4 percent calcined sodium bisulfite, and 0.8 percent of ammonium sulfate. After 2 hours standing, 50 percent water and 3 percent of calcined sodium sulfite were added. After an additional 30 minutes of felting, the hides were allowed to stand, and were unhaired after 24- 36 hours. The action of the bacterial protease takes place in a medium at pH 6-6.5; the action of the sodium sulfite takes place in a medium at pH 7.5-8.
If, in place of 50 percent water and 3 percent sodium sulfite, 250 percent water, 3 percent sodium sulfite, and 1 percent of mold fungus protease are used, a somewhat longer period is required for unhairing.
Example 12 Red cowhides, presoftened with water and then rinsed, were felted for one-half hour with 0.6 percent bacterial protease, 0.5 percent sodium bisulfite, and 0.4 percent ammonium sulfate. After one hour's standing, 50 percent water and 4 percent of sodium sulfite were added and felted for an additional 30 minutes. The hides were then left to stand and were unhaired after about 40 hours. The action of the bacterial protease was in a medium at pH 6-6.5; that of the sodium sulfite in a medium at pH 7.5-8.
Example 13 Goatskins were presoftened with water, rinsed, and
' then felted for one hour with 0.5 percent mold fungus protease, calculated on the weight of the presoftened skins. After two hours standing, 50 percent water and 0.5 percent of 60-62 percent sodium sulfide were added. Felting continued for an additional hour, and then the hides were set aside. After 24 hours, they were unhaired. The action of the mold fungus protease was at pH 7; that of the sodium sulfide at pH 12-13. If the presoftened hides or hides fully softenedwith water are treated only with 50 percent of water and 0.5 percent of sodium sulfide (60-62 percent), no loosening of the hair is observed.
Example 14 Water softened goatskins were felted for one-half hour with 0.5 percent mold fungus protease and 0.3 percent of a preserving agent. After 3 hours standing, 50 percent of water, 2 percent of 98 percent thioglycolic acid neutralized with ammonia were added. After an additional 30 minutes of felting, the hides were set aside and after 24 hours were dehaired. The action of the mold fungus protease and the thioglycolic acid was at pH 7. If water presoftened or fully softened goatskins are felted for one-half hour with 50 percent of water and with 2 percent of ammonia-neutralized 98 percent thioglycolic acid-without protease treatment-and are then set aside for 24 hours, a hair loosening of only 30 to 40 percent is observed, whereas skins treated with mold fungus protease according to the example can be dehaired 100 percent after 24 hours.
The criticality of the two-step process of the invention Example 15 A dried Indian goatskin 'was washed and soaked with water for 24 hours and divided into 4 parts. The first part was felted for 1 hour with 0.5 percent by weight of skin of a mold fungus protease without addition of water. After 24 hours, 20 to 25 percent of the hair on the skin was loosened.
The second part of the skin was felted for one hour with 50 percent water and 1 percent of sodium nitrate. After 24 hours, no loosening of hair was observable.
The third portion of the skin was felted for one hour with 0.5 percent by weight of the mold fungus protease and 1 percent by weight of sodium nitrate without the addition of water. After 24 hours, about 20 percent of the hair had been loosened.
The fourth part of the skin was felted for 1 hour with 0.5 percent of mold fungus protease without the addition of water. After an additional hour, 50 percent of water and 1 percent of sodium nitrate were added and the skin was felted for 30 minutes. The treated hide was then set aside. After 24 hours from the beginning of the treatment, substantially 100 percent of the hair could be removed from the skin. The other neutral salts mentioned earlier herein give corresponding results when employed according to the last-mentioned methods. Potassium thiocyanate and ammonium chloride are especially effective.
Example 16 An Indian goatskin was softened with water and divided into 4 parts. The first part was felted for 30 minutes with 3 percent of mold fungus protease, calculated on the weight of the softened hide, according to the process described in German Patent 1,026,038, without the addition of water. After 24 hours, 100 percent of the hair could be removed.
A second part of the skin was felted with 0.5 percent mold fungus protease for 30 minutes. After 24 hours, about 15 percent of the hair was loosened.
A third portion of the skin was feltedfor 30 minutes with 50 percent of waterand 2 percent of calcined sodium sulfite, both calculated on the'weight of the softened skin. After 24 hours, there was practically no loosening of the hair. a I
. The fourth part of the skin was treated with 0.5 percent of mold fungus protease for 30 minutes. After 2 hours,[
50 percentflof water and 2 percent .of calcined sodium sulfite were-added and the skin felted foran additional 30 minutes; After 24 hours, calculated from the begin ning of the enzymatic treatment, substantially 100' percentv of the hair'was easily removable. The mold fungus protease used had an, enzyme value above 5000.
Although specific embodiments have been shown and described, it is understood that they'are illustrative, and
the group consisting essentially ofsulfur containing reducing agents and inorganic neutral salts of the alkali metals and ammonium.
' 2 The method of unhairing hides which consists es-' sentially of softening water-soaked hides bycontacting. them with an amount of a powdered proteolytic enzyme insufficient to cause substantial loosening of hair, and
then contacting the softened hides, ata pH between about 5.5 and 8 and in the presence of from'about 30 percent to 250 percentof water .by weight of the softened hides,
with at least one reagent selected from the group con sisting essentially of sulfur containing reducing agents and inorganic neutral salts of the alkali metals and ammonium.
3.The method of claim 1 wherein 'said sulfur conta'inin'g 'reduc ing'age'nt is acompound containing oxygen.
*4. Thejmethodlof claim 1 wherein said sulfur containing reducing agent is a oxygen-free compound. a
5. The method of claim 1 wherein soaked hides are contacted with a proteolytic enzyme in the presence of oligases. v
,6.- The method of claim 1 wherein the hides, during the course :of treatment, are additionally contacted with a'wetting agent.
' 7. The m'ethod of claim 6 wherein said wetting agent is a polyglycol ether, the moleculesof which comprise 6 to 16 polymerized units of ethylene oxide.
58. Themethod of claim-6 wherein said wetting agent is "(Eontac'ted'with the'hides' together with said reagent selected'frdmthe group consisting essentially of sulfur containing reducing agents and inorganic neutral salts of "the alkali metals and ammonium.
9. Themethod'of claim- 1 wherein said proteolytic enzyme is the enzyme of a micro-organism.
10. The method of claim '1 wherein said hides and proteolytic enzyme are contacted at a pH between about 5.5 and 8. V v
I References Cited in the file of this patent I UNITED STATES PATENTS 2,132,579 Rohnf Oct. 11, 1938 2,169,148? Jaeger Aug. 8, 1939 2,179,899 Rohm i Nov. 14, 1939 2,229,420, Neugebauer Jan. 21, 1941 2,857,316" Grimm Oct. 21, 1958 FOREIGN PATENTS 102,091 Australia Sept. 20, 1937 r 4 -OTHER REFERENCES smwniepn; .Sur face Active Agents, Inte'rscience Pub. Inc New York(1949), pp. 477 and 478.
Claims (1)
1. THE METHOD OF UNHAIRING HALIDES WHICH CONSISTS ESSENTIALLY OF SOFTENING WATER-SOAKED HIDES BY CONTACTING THEM AS AN AMOUNT OF A POWDERED PROTELYTIC ENZYME INSUFFICIENT TO CAUSE SUBSTANTIAL LOOSENING OF HAIR, AND THEN CONTACTING THE SOFTENED HIDES, AT A PH BETWEEN ABOUT 5.5 AND 8, WITH AT LEAST ONE REAGENT SELECTED FROM THE GROUP CONSISTING ESSENTIALLY OF SULFUR CONTAINING REDUCING AGENTS AND INORGANIC NEUTRAL SALTS OF THE ALKALI METALS AND AMMONIUM.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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DER0025792 | 1959-06-24 |
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Publication Number | Publication Date |
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US3076749A true US3076749A (en) | 1963-02-05 |
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ID=7402012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US37062A Expired - Lifetime US3076749A (en) | 1959-06-24 | 1960-06-20 | Method of unhairing skins and hides |
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US (1) | US3076749A (en) |
FR (1) | FR1265471A (en) |
GB (1) | GB922272A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4019956A (en) * | 1974-07-30 | 1977-04-26 | Omnium De Prospective Industrielle, S.A. | Process for recovering hair by dissolving the skin or hide |
US4968621A (en) * | 1983-04-09 | 1990-11-06 | Rohm Gmbh | Method for the wet degreasing of hide and skin stock |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2132579A (en) * | 1935-04-02 | 1938-10-11 | Rohm Otto | Method for producing unhaired hides with the aid of mold tryptases |
US2169148A (en) * | 1938-06-01 | 1939-08-08 | American Cyanamid & Chem Corp | Unhairing of hides and skins |
US2179899A (en) * | 1936-12-29 | 1939-11-14 | Rohm Otto | Process for preparing hides |
US2229420A (en) * | 1937-06-29 | 1941-01-21 | Kalle & Co Ag | Unhairing process |
US2857316A (en) * | 1955-03-30 | 1958-10-21 | Roehm & Haas Gmbh | Enzymatic unhairing and dewooling process |
-
1960
- 1960-06-20 US US37062A patent/US3076749A/en not_active Expired - Lifetime
- 1960-06-23 FR FR830872A patent/FR1265471A/en not_active Expired
- 1960-06-23 GB GB22003/60A patent/GB922272A/en not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2132579A (en) * | 1935-04-02 | 1938-10-11 | Rohm Otto | Method for producing unhaired hides with the aid of mold tryptases |
US2179899A (en) * | 1936-12-29 | 1939-11-14 | Rohm Otto | Process for preparing hides |
US2229420A (en) * | 1937-06-29 | 1941-01-21 | Kalle & Co Ag | Unhairing process |
US2169148A (en) * | 1938-06-01 | 1939-08-08 | American Cyanamid & Chem Corp | Unhairing of hides and skins |
US2857316A (en) * | 1955-03-30 | 1958-10-21 | Roehm & Haas Gmbh | Enzymatic unhairing and dewooling process |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4019956A (en) * | 1974-07-30 | 1977-04-26 | Omnium De Prospective Industrielle, S.A. | Process for recovering hair by dissolving the skin or hide |
US4968621A (en) * | 1983-04-09 | 1990-11-06 | Rohm Gmbh | Method for the wet degreasing of hide and skin stock |
Also Published As
Publication number | Publication date |
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FR1265471A (en) | 1961-06-30 |
GB922272A (en) | 1963-03-27 |
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