EP0569410B1 - Procede d'auto-tannage, de pre-tannage et de co-tannage de cuirs et de peaux, et de retannage de cuirs et de peaux - Google Patents
Procede d'auto-tannage, de pre-tannage et de co-tannage de cuirs et de peaux, et de retannage de cuirs et de peaux Download PDFInfo
- Publication number
- EP0569410B1 EP0569410B1 EP92903337A EP92903337A EP0569410B1 EP 0569410 B1 EP0569410 B1 EP 0569410B1 EP 92903337 A EP92903337 A EP 92903337A EP 92903337 A EP92903337 A EP 92903337A EP 0569410 B1 EP0569410 B1 EP 0569410B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tanning
- groups
- leather
- hides
- weight
- 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 claims abstract description 27
- 238000000034 method Methods 0.000 title claims abstract description 19
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 1
- 150000001728 carbonyl compounds Chemical class 0.000 abstract description 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 3
- -1 C¿1?-C8 alkyl groups Chemical group 0.000 abstract description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 150000001241 acetals Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 125000004437 phosphorous atom Chemical group 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 17
- 229920001864 tannin Polymers 0.000 description 7
- 239000001648 tannin Substances 0.000 description 7
- 235000018553 tannin Nutrition 0.000 description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 150000001299 aldehydes Chemical class 0.000 description 5
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000002639 sodium chloride Nutrition 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QDCJIPFNVBDLRH-UHFFFAOYSA-N 5,5-dimethyl-1,3-dioxane Chemical compound CC1(C)COCOC1 QDCJIPFNVBDLRH-UHFFFAOYSA-N 0.000 description 1
- FGWHNGDOJHDLEI-UHFFFAOYSA-N 5-butyl-5-ethyl-1,3-dioxane Chemical group CCCCC1(CC)COCOC1 FGWHNGDOJHDLEI-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- BFGKITSFLPAWGI-UHFFFAOYSA-N chromium(3+) Chemical class [Cr+3] BFGKITSFLPAWGI-UHFFFAOYSA-N 0.000 description 1
- GRWVQDDAKZFPFI-UHFFFAOYSA-H chromium(III) sulfate Chemical compound [Cr+3].[Cr+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRWVQDDAKZFPFI-UHFFFAOYSA-H 0.000 description 1
- 229910000356 chromium(III) sulfate Inorganic materials 0.000 description 1
- 239000011696 chromium(III) sulphate Substances 0.000 description 1
- 235000015217 chromium(III) sulphate Nutrition 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000991 leather dye Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 150000003754 zirconium Chemical class 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
- C14C3/16—Chemical tanning by organic agents using aliphatic aldehydes
Definitions
- the present invention relates to an improved method for sole tanning, pretanning and tanning of pelts and pelts and for retanning leather and hide.
- DE-A-17 69 059 relates to a process for leather production by treating tannable material with zinc salts, water-soluble sulfates and aldehydes or aldehyde-releasing substances and aftertreatment with dulling agents.
- acetal residues the residues customary for this are usually used, for example C1-C8-alkyl groups, preferably C1-C4-alkyl groups, such as methyl, ethyl, n-propyl, n-butyl or 2-ethylhexyl.
- the two acetal residues can be different or preferably the same.
- these two radicals can form a five- or six-membered ring, for example a 1,3-dioxolane, 1,3-dioxane, 5,5-dimethyl-1,3-dioxane or 5-n-butyl-5 -ethyl-1,3-dioxane ring.
- the compound I and its acetals are known in principle; they are prepared by the relevant methods given in the literature.
- the tanning process according to the invention is outstandingly suitable for tanning alone and pretanning skins and skins in an aqueous liquor.
- the procedure here is such that the pickled pelts, for example cowhide pelts with a gap thickness of 1.5 to 4 mm, or pelts, for example sheepskin pelts, at a pH of 2 to 7, in particular 2.5 to 4, and one Temperature of 15 to 50 °, in particular 25 to 45 ° C, are treated with an aqueous solution or dispersion of the carbonyl compound I for a period of 3 to 20 hours.
- the treatment takes place, for example, by drumming in a barrel.
- the required amount of carbonyl compound I is normally 2 to 30% by weight, in particular 5 to 20% by weight, based on the pelt weight.
- the fleet length, i.e. the percentage weight ratio of the treatment liquor to the goods is usually 30 to 200% for the bare and 100 to 2000% for the bare, in each case based on the bare weight.
- the leather or fur is usually adjusted to a pH of 4 to 8, in particular 5 to 7, for which purpose magnesium oxide, sodium carbonate or sodium hydrogen carbonate is used, optionally treated with further tanning agents and, if desired, dyed after the tanning process has ended and greased.
- the tanning process according to the invention is also outstandingly suitable for tanning bare and pelted skin together with the tanning agents of the main tanning process, which can be, for example, chrome or aluminum tanning.
- the working conditions regarding pH, temperature and duration of the treatment are adjusted to the requirements of the main components of the tanning, the same applies to the Treatment equipment and the length of the liquor as well as for post-treatment.
- the amount of carbonyl compound I required is normally 0.1 to 20% by weight, in particular 0.5 to 15% by weight, based on the pelt weight.
- the tanning process according to the invention is also outstandingly suitable for retanning leather and fur which has already been tanned, for example chrome leather, in an aqueous liquor. It is usually carried out in such a way that the pickled pelts and skins, for example cowhide pelts with a gap thickness of 1.5 to 4 mm, are used, for example, with a customary chromium-containing tanning agent such as a chromium (III) salt, e.g.
- a customary chromium-containing tanning agent such as a chromium (III) salt, e.g.
- Chromium (III) sulfate tanned in a manner known per se, the pretanned skins obtained in this way (in the case of chrome tanning "wet blues") deacidified and at a pH of 2 to 7, in particular 2.5 to 4, and at temperatures of 15 to 50 ° C, in particular 25 to 45 ° C, treated with an aqueous solution or dispersion of the carbonyl compound I for a period of 1 to 12 hours.
- This treatment takes place, for example, by drumming in a barrel.
- the amount of carbonyl compound I required, based on the shaved weight of the leather, is normally 2 to 30% by weight, in particular 5 to 20% by weight.
- the liquor length is usually 30 to 200% for bare and 100 to 2000% for bare, each based on the fold weight of the leather.
- the leather or fur is usually adjusted to a pH of 3 to 5, for which purpose magnesium oxide or an organic acid such as formic acid or its salts are used, and, if desired, dyed and greased after the treatment.
- the leather or fur retanned according to the invention may also have been treated with other tanning agents, such as polymer tanning agents or syntans, before retanning with the carbonyl compound I.
- the carbonyl compound I can also be used simultaneously with such additional tanning agents, for example in main tanning.
- tanning agents As additional or simultaneously used tanning agents, all usual agents with tanning effects on bare or fur bare are considered. A comprehensive treatment of such tannins can be found, for example, in Ullmann's Encyclopedia of Industrial Chemistry, 3rd edition, 11th volume, pages 585 to 612 (1960). Tannin classes to be mentioned individually are the mineral tannins, for example chromium, aluminum, zinc and zirconium salts, the synthetic tannins such as the polymer tannins and syntans already mentioned above, and the vegetable (vegetable) tannins.
- mineral tannins for example chromium, aluminum, zinc and zirconium salts
- synthetic tannins such as the polymer tannins and syntans already mentioned above
- vegetable (vegetable) tannins the vegetable (vegetable) tannins.
- leather and furs are produced which, in comparison to the products obtained with previously known aldehyde tannins such as glutardialdehyde, have not only a full and very soft feel and, in addition to high shrinking temperatures, but also a significantly improved tear and tensile strength.
- the leather and skins tanned according to the invention no longer have a disturbing yellow color.
- Another advantage of the tanning process according to the invention is the low volatility of the carbonyl compound I used, which has an effect, for example, on the amount of these tanning agents used, which need only be relatively low. Furthermore, the carbonyl compound I is, in a sense, a universal tanning agent since it can be combined with all other customary tanning agents and can be used both for the sole, the pre, the co-tanning and for the retanning.
- a white leather with a shrinking temperature of approx. 85 ° C. was obtained, which was very soft and easy to grip.
- a soft and non-slip leather with a shrinking temperature of approx. 90 ° C. was obtained.
- Usual sheepskin pelt was mixed with 60% by weight of table salt, 12% by weight of common fatliquor and 18% by weight of 3-oxaglutardialdehyde, based in each case on the dry weight of the pelts, at a liquor length of 1500% and 4 hours at 35 ° C. and a pH of 3.2 in the barrel. Then a pH of 5.5 was set with sodium carbonate.
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)
Abstract
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4102545 | 1991-01-29 | ||
DE4102545A DE4102545A1 (de) | 1991-01-29 | 1991-01-29 | Verfahren zum alleingerben, vorgerben und mitgerben von bloessen und fellbloessen und zum nachgerben von leder und fell |
PCT/EP1992/000116 WO1992013105A1 (fr) | 1991-01-29 | 1992-01-21 | Procede d'auto-tannage, de pre-tannage et de co-tannage de cuirs et de peaux, et de retannage de cuirs et de peaux |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0569410A1 EP0569410A1 (fr) | 1993-11-18 |
EP0569410B1 true EP0569410B1 (fr) | 1995-03-29 |
Family
ID=6423909
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92903337A Expired - Lifetime EP0569410B1 (fr) | 1991-01-29 | 1992-01-21 | Procede d'auto-tannage, de pre-tannage et de co-tannage de cuirs et de peaux, et de retannage de cuirs et de peaux |
Country Status (6)
Country | Link |
---|---|
US (1) | US5372609A (fr) |
EP (1) | EP0569410B1 (fr) |
JP (1) | JPH06504800A (fr) |
DE (2) | DE4102545A1 (fr) |
ES (1) | ES2070632T3 (fr) |
WO (1) | WO1992013105A1 (fr) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0554216T3 (da) * | 1992-01-28 | 1996-08-19 | Ciba Geigy Ag | Fremgangsmåde til pickling og forgarvning af ugarvede læderhuder |
DE19906190A1 (de) * | 1999-02-15 | 2000-08-17 | Boehme Chem Fab Kg | Gerbverfahren |
BR9901948B1 (pt) * | 1999-04-30 | 2008-11-18 | processo de curtimento de couros com compostos carbonÍlicos. | |
EP2055481B1 (fr) * | 2007-10-18 | 2017-08-16 | Bobst Italia S.P.A. | Ensemble racloir et un procédé pour permettre l'utilisation d'encres différentes |
ITUB20152180A1 (it) * | 2015-07-14 | 2017-01-14 | Db Patents Ltd | Metodo migliorato per conciare una pelle animale. |
DE102016004191A1 (de) * | 2016-04-06 | 2017-10-12 | Tfl Ledertechnik Gmbh | Zusammensetzung und Verfahren zur Gerbung basierend auf einem Acetal eines aldehydischen Gerbstoffes |
DE102016004192A1 (de) * | 2016-04-06 | 2017-10-12 | Tfl Ledertechnik Gmbh | Zusammensetzung und Verfahren zur Gerbung basierend auf einem Acetal eines aldehydischen Gerbstoffes |
EP3529382B1 (fr) * | 2016-10-18 | 2020-06-10 | Stahl International B.V. | Procédé de préparation de cuir |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2351338A (en) * | 1943-08-02 | 1944-06-13 | American Cyanamid Co | Tanning with d'-methoxy-d-hydroxymethyl diglycollic aldehyde |
US2516283A (en) * | 1947-03-20 | 1950-07-25 | Adolph H Winheim | Resin impregnation of a dialdehyde tanned hide |
BE593301A (fr) * | 1959-07-24 | |||
DE1769059A1 (de) * | 1968-03-28 | 1971-08-19 | Basf Ag | Verfahren zur Herstellung von Leder |
DE2137603A1 (de) * | 1971-07-27 | 1973-02-08 | Diamalt Ag | Mittel zum gerben von haeuten und fellen |
DE2549527C3 (de) * | 1975-11-05 | 1980-03-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Leder |
BR8605597A (pt) * | 1985-11-13 | 1987-08-18 | Cassella Farbwerke Mainkur Ag | Tanino e processo para a sua obtencao e sua utilizacao |
-
1991
- 1991-01-29 DE DE4102545A patent/DE4102545A1/de not_active Withdrawn
-
1992
- 1992-01-21 ES ES92903337T patent/ES2070632T3/es not_active Expired - Lifetime
- 1992-01-21 EP EP92903337A patent/EP0569410B1/fr not_active Expired - Lifetime
- 1992-01-21 DE DE59201788T patent/DE59201788D1/de not_active Expired - Lifetime
- 1992-01-21 US US08/094,026 patent/US5372609A/en not_active Expired - Fee Related
- 1992-01-21 JP JP4503478A patent/JPH06504800A/ja active Pending
- 1992-01-21 WO PCT/EP1992/000116 patent/WO1992013105A1/fr active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
JPH06504800A (ja) | 1994-06-02 |
US5372609A (en) | 1994-12-13 |
EP0569410A1 (fr) | 1993-11-18 |
WO1992013105A1 (fr) | 1992-08-06 |
ES2070632T3 (es) | 1995-06-01 |
DE59201788D1 (de) | 1995-05-04 |
DE4102545A1 (de) | 1992-07-30 |
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