EP1177321A1 - Application of carbonyl compounds in the process of tanning hides - Google Patents
Application of carbonyl compounds in the process of tanning hidesInfo
- Publication number
- EP1177321A1 EP1177321A1 EP00901424A EP00901424A EP1177321A1 EP 1177321 A1 EP1177321 A1 EP 1177321A1 EP 00901424 A EP00901424 A EP 00901424A EP 00901424 A EP00901424 A EP 00901424A EP 1177321 A1 EP1177321 A1 EP 1177321A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tanning
- bath
- hides
- chrome
- add
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 34
- 230000008569 process Effects 0.000 title claims abstract description 33
- 150000001728 carbonyl compounds Chemical class 0.000 title claims abstract description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 41
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
- 239000001257 hydrogen Substances 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 4
- 239000003085 diluting agent Substances 0.000 claims abstract description 3
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 51
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims description 20
- 229920001864 tannin Polymers 0.000 claims description 13
- 239000001648 tannin Substances 0.000 claims description 13
- 235000018553 tannin Nutrition 0.000 claims description 13
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 235000021110 pickles Nutrition 0.000 claims 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 40
- 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 20
- 235000019253 formic acid Nutrition 0.000 description 20
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 19
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 19
- 235000011130 ammonium sulphate Nutrition 0.000 description 19
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 18
- HSJKGGMUJITCBW-UHFFFAOYSA-N 3-hydroxybutanal Chemical compound CC(O)CC=O HSJKGGMUJITCBW-UHFFFAOYSA-N 0.000 description 14
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 12
- 238000005554 pickling Methods 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 9
- 239000010985 leather Substances 0.000 description 8
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 8
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 8
- 238000002203 pretreatment Methods 0.000 description 7
- 102000008186 Collagen Human genes 0.000 description 6
- 108010035532 Collagen Proteins 0.000 description 6
- DSHWASKZZBZKOE-UHFFFAOYSA-K chromium(3+);hydroxide;sulfate Chemical compound [OH-].[Cr+3].[O-]S([O-])(=O)=O DSHWASKZZBZKOE-UHFFFAOYSA-K 0.000 description 6
- 229920001436 collagen Polymers 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 239000003899 bactericide agent Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000008030 elimination Effects 0.000 description 3
- 238000003379 elimination reaction Methods 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- AIJULSRZWUXGPQ-UHFFFAOYSA-N Methylglyoxal Chemical compound CC(=O)C=O AIJULSRZWUXGPQ-UHFFFAOYSA-N 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 159000000032 aromatic acids Chemical class 0.000 description 2
- -1 as for example Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 2
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 2
- 230000003467 diminishing effect Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000000835 fiber Chemical group 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- FGRBYDKOBBBPOI-UHFFFAOYSA-N 10,10-dioxo-2-[4-(N-phenylanilino)phenyl]thioxanthen-9-one Chemical compound O=C1c2ccccc2S(=O)(=O)c2ccc(cc12)-c1ccc(cc1)N(c1ccccc1)c1ccccc1 FGRBYDKOBBBPOI-UHFFFAOYSA-N 0.000 description 1
- UIKQNMXWCYQNCS-UHFFFAOYSA-N 2-hydroxybutanal Chemical compound CCC(O)C=O UIKQNMXWCYQNCS-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 239000002610 basifying agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 231100000647 material safety data sheet Toxicity 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 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
- 230000008961 swelling Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- UPUJGSUSGASQJV-UHFFFAOYSA-J tetrasodium;disulfite Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S([O-])=O.[O-]S([O-])=O UPUJGSUSGASQJV-UHFFFAOYSA-J 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003440 toxic substance 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
- C14C3/02—Chemical tanning
- C14C3/08—Chemical tanning by organic agents
Definitions
- the present invention describes the application of carbonyl compounds in the process of tanning hides.
- this invention describes the application of hydroxy ketones in the process of tanning hides.
- R may be a linear or ramified alkyl group or even aromatic group and R and R
- R may be a linear or ramified alkyl group or even aromatic group and R ;
- the referred carbonyl compounds may be used in an aqueous solution, in concentrations varying from 0.1% till its pure state, that is, 100%, or yet in mixtures with other organic compounds that act as diluents.
- the hide is composed of proteins, lipids, glycides, mineral salts, water etc.; collagen is the most important protein, from the point of view of the tanner (Reference: A. White and collaborators, "Principles of Biochemistry", 5 th Ed., pJ40). Collagen reacts with tanning agents, originating leather; therefore, the tanning process is one of the essential operations in the process of producing leather.
- Tanning through a phenomenon of reticulation, inherent to the agent used, transforms the hide into a stable and non-putrescible material.
- traditional processes use 2% to 2.5% of chrome oxide (Cr 2 O 3 ); generally, the leather will be tanned when about 3.5% of Cr 2 O 3 are incorporated into the hide.
- Chrome salts adequate for normally tanning are the chrome (III) salts, as, for example, chrome (III) sulfate or basic chrome (III) sulfate [Cr(OH)SO 4 ; 33% basicity in Schrolemmer degrees] (Reference: E.Hoinacki, "Hides and Leathers", 2 nd Edition, 1989) containing 25% to 26% of Cr 2 O 3 .
- the 20% to 30% of the unabsorbed chrome oxide leaves a chrome residue in the tanning bath that may reach 1% (10 g of Cr 2 O 3 /liter of bath).
- the chrome (III) compounds are not damaging to plants and animals, specially in neutral conditions, where they are insoluble, but international standards have imposed low limits for chrome (III) and other heavy metals in water and air. (Reference: Ullmann's Encyclopedia of Industrial Chemistry, Vol. A15, p. 269).
- the hide is tanned with a mixture of chrome (III) salt, binding acid agents, as for example, dolomite, magnesium oxide and carbonate or bicarbonate of alkaline and alkaline terrous metals and di- and tricarboxylic aromatic acids, as for example, phthalic, isophthalic, succinic and similar acids, and their salts or anhydrides.
- chrome (III) salt binding acid agents
- binding acid agents as for example, dolomite, magnesium oxide and carbonate or bicarbonate of alkaline and alkaline terrous metals and di- and tricarboxylic aromatic acids, as for example, phthalic, isophthalic, succinic and similar acids, and their salts or anhydrides.
- the pre-treatment of the hides with the described carboxylic compounds preferentially hydroxy ketones and, still better, ⁇ -hydroxy ketones, that present advantages, if compared to the carboxylic acid-aldehyde compounds and carboxylic acid-ketone compounds since, besides propitiating a higher absorption of the chrome from the bath, its also dispense the previous use of the pickling stage.
- the step of basification in the chrome tanning process can cause stains in the leather, in the case of quick additions of the basifying agent or larger doses than necessary; it is, therefore, always a problematic stage, that should be made with care and attention.
- Aldehydes in general are extremely toxic and have a small limit of exposition, as for example, 2-hydroxyl butanal (aldol), whose LD 50 is 2180 mg/kg (mice, oral) (Reference: H.E. Christensen, Toxic Substances, Edition 1974, p. 166).
- the present invention describes the application of carbonyl compounds, such as hydroxy ketones and, preferentially, ⁇ -hydroxy ketones, where the hides, before the chrome tanning process or tannin process, with or without pickling, are pre-treated with the carbonyl product, at 0.1% to 30%, preferentially 0.5% to 10% and, better still, 1% to 5% of weight, in relation to the weight of the hides.
- carbonyl compounds such as hydroxy ketones and, preferentially, ⁇ -hydroxy ketones
- the hides, pre-treated with the carbonyl compounds of general structure (I) and (II), are prepared for the process to produce the "Wet Blue” leathers, and may also be pre-treated by the process described in this invention to be used for the "Wet White” manufacturing process or for vegetal tanning with tannins, aiming he manufacture of sole leather.
- the carbonyl compounds used in this invention are preferentially ⁇ -hydroxy ketones, added into the water tanning bath itself, in their pure form or in mixture with inert compounds, preferentially pure or in a water solution.
- the subsequent chrome tanning treatment is made in the traditional manner, using the commercially available chrome (III) salts, such as basic chrome sulfate; the pre-treatment using the carbonyl compounds, described in this invention permits a larger absorption of the chrome, with a consequent diminishing of residual chrome in the bath.
- the affinity of the chrome salts for the protein, collagen is minimal, and so the penetration of the tanning agent occurs.
- the carbonyl compounds described in this invention react with the free amino groups of the polypeptydic chain of the collagen.
- the new bond formed in the polypeptydic chain alters the isoelectric point, pH where there is no migration of a dipolar ion when submitted to an electric field, to values lower than the isoelectric point of the collagen.
- This new isoelectric point of the polypeptydic chain permits a greater ionization of the carboxyls at a higher pH, allowing a higher reactivity and penetration of the chrome salts into the hide.
- the hides after the steps of deliming and bating can be pre- treated with the carbonyl compounds described in this invention and are prepared for tanning with chrome salts or tannin, with the complete elimination of pickling, the basification step and with a larger exhaustion of the chrome bath; the residual chrome in the process of this invention can reach levels as low as 0.02% to 0.05% of chrome.
- the elimination of the pickling step still permits a large reduction of the polluting load coming from the residues of sulfuric acid and the sodium chloride used in the pickling stage.
- the application of the carbonyl products described in this invention for the tanning hides reduces the use of chemical inputs and reduces the tanning processing time, consequently giving a gain in productivity.
- the carbonyl compounds of general structure (I) and (II) described in this invention preferentially ⁇ -hydroxy ketones and more preferentially, ⁇ -hydroxy ketones, besides of reacting with the amino groups of the collagen, as described previously, confer an additional advantage, since the hydroxyl groups are capable of bonding to determined groups of the polypeptydic chain by hydrogen bond.
- the hides divided to 3-4 mm (37 kg) are first washed at the temperature of 35°C to 37°C for 20 minutes, in a tanning drum containing 200% of water and 0.2% of ammonium sulfate, based on the weight of the hides.
- the drum is drained and the hides are delimed for 2 hours, adding 1.7% of ammonium sulfate, 0.5% of a non-swelling organic acid and 1% of sodium bissulfite.
- Add 0.15% of a commercial proteolytic enzyme for ex.: "Lipose S"
- the cross section of the hides is colorless to phenolphthalein.
- Add 0.1% of formic acid run the drum for 40 minutes, drain the bath and wash the hides 3 times for 10 minutes, with water at ambient temperature.
- the pH of the cross section of the hide is around 5.5.
- the final temperature of the bath is 40°C to 42°C and the final pH is 3.8 to 4.0.
- a tensoactive agent for ex.: "Pardon Green”
- a tensoactive agent for ex.: ' ⁇ usapon S
- the pH of the bath is around 7.0 to 7.2 and the cross section of the hide is colorless to phenolphthalein.
- the hides are prepared for the normal vegetal tanning sequence with tannins, to manufacture sole leather.
- One thousand nine hundred kg (1900 kg) of 'grupons' are placed into a tanning drum and washed for 15 minutes with 150% of water and 0.2% of ammonium sulfate. Drain the bath, add 20% of water, 2% of ammonium sulfate, 1.2% of sodium bisulfate, 0J% of "eusapon", 0.6% of "interox” and run for 2 hours.
- the pH of the bath is around 7.0 to 7.2 and the cross section of the hide is colorless to phenolphthalein.
- EXAMPLE 8 One thousand nine hundred kg (1900 kg) of 'grupons' are placed into a tanning drum and washed for 15 minutes with 150% of water and 0.2% of ammonium sulfate at a temperature of 35°C. Drain the bath, add 20% of water, 2% of ammonium sulfate, 1.2% of sodium bisulfate, 0.1% of "eusapon", 0.6% of "interox” and run for 2 hours. At the end of this time, the pH of the bath is around 7.0 to 7.2 and the cross section of the hide is colorless to phenolphthalein. Add 0.03% of a bacterial purge, run for 40 minutes and drain.
- EXAMPLE 9 One thousand eight hundred kg (1800 kg) of 'grupons' are placed into a tanning drum and washed for 20 minutes with 150% of water and 0.2% of ammonium sulfate at a temperature of 35°C. Drain the bath, add 20% of water, 2% of ammonium sulfate, 1% of sodium bisulfate, 0.1% of "eusapon", 0.6% of "interox” and run for 2 hours. At the end of this time, the pH of the bath is around 7.0 to 7.2 and the cross section of the hide is colorless to phenolphthalein. Add 0.03% of a bacterial purge, run for 40 minutes and drain.
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
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BR9901948 | 1999-04-30 | ||
BRPI9901948-5A BR9901948B1 (en) | 1999-04-30 | 1999-04-30 | leather tanning process with carbonic compounds. |
PCT/BR2000/000006 WO2000066793A1 (en) | 1999-04-30 | 2000-02-02 | Application of carbonyl compounds in the process of tanning hides |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1177321A1 true EP1177321A1 (en) | 2002-02-06 |
Family
ID=4072497
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00901424A Withdrawn EP1177321A1 (en) | 1999-04-30 | 2000-02-02 | Application of carbonyl compounds in the process of tanning hides |
Country Status (9)
Country | Link |
---|---|
US (1) | US20020046426A1 (en) |
EP (1) | EP1177321A1 (en) |
CN (2) | CN1495276A (en) |
AR (1) | AR022465A1 (en) |
AU (1) | AU2271800A (en) |
BR (1) | BR9901948B1 (en) |
CO (1) | CO5221129A1 (en) |
WO (1) | WO2000066793A1 (en) |
ZA (1) | ZA200001356B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104531915A (en) * | 2014-12-17 | 2015-04-22 | 广东菲安妮皮具股份有限公司 | Method for processing cowhide leather |
CN106191335A (en) * | 2016-08-12 | 2016-12-07 | 桐乡市鑫诺皮草有限公司 | A kind of standard mink skin process for tanning |
CN113399445A (en) * | 2021-07-14 | 2021-09-17 | 河北科技大学 | Method for efficiently leaching and repairing chromium-contaminated soil |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU1666542A1 (en) * | 1989-04-11 | 1991-07-30 | Центральный научно-исследовательский институт кожевенно-обувной промышленности | Penetrator for leather dressing |
DE4102545A1 (en) * | 1991-01-29 | 1992-07-30 | Basf Ag | METHOD FOR GELING, PRELIMINATING AND GIVING BARE AND FUR BLOSSES AND FOR LEAVING LEATHER AND FUR |
DE4430290A1 (en) * | 1994-08-26 | 1996-02-29 | Basf Ag | Leather mfr. with reduced chemical consumption and amt. of waste liquor |
BR9604733A (en) * | 1996-12-20 | 1998-09-08 | Khalil Ibrahim Chahine | Tanning process for animal skins free of sodium chloride and autobasically using acetaldol as a conditioning agent |
-
1999
- 1999-04-30 BR BRPI9901948-5A patent/BR9901948B1/en not_active IP Right Cessation
-
2000
- 2000-01-31 AR ARP000100417A patent/AR022465A1/en unknown
- 2000-02-02 AU AU22718/00A patent/AU2271800A/en not_active Abandoned
- 2000-02-02 CN CNA031484247A patent/CN1495276A/en active Pending
- 2000-02-02 WO PCT/BR2000/000006 patent/WO2000066793A1/en not_active Application Discontinuation
- 2000-02-02 EP EP00901424A patent/EP1177321A1/en not_active Withdrawn
- 2000-02-02 CN CN00806974.3A patent/CN1349564A/en active Pending
- 2000-03-16 ZA ZA200001356A patent/ZA200001356B/en unknown
- 2000-03-30 CO CO00022813A patent/CO5221129A1/en not_active Application Discontinuation
-
2001
- 2001-10-26 US US10/016,781 patent/US20020046426A1/en not_active Abandoned
Non-Patent Citations (1)
Title |
---|
See references of WO0066793A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2000066793A1 (en) | 2000-11-09 |
US20020046426A1 (en) | 2002-04-25 |
BR9901948B1 (en) | 2008-11-18 |
ZA200001356B (en) | 2000-10-17 |
CO5221129A1 (en) | 2002-11-28 |
AR022465A1 (en) | 2002-09-04 |
CN1349564A (en) | 2002-05-15 |
BR9901948A (en) | 2000-10-31 |
AU2271800A (en) | 2000-11-17 |
CN1495276A (en) | 2004-05-12 |
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