WO2006089384A2 - Product for pelt conditioning for tanning: process for pelt conditioning and following tanning - Google Patents
Product for pelt conditioning for tanning: process for pelt conditioning and following tanning Download PDFInfo
- Publication number
- WO2006089384A2 WO2006089384A2 PCT/BR2006/000033 BR2006000033W WO2006089384A2 WO 2006089384 A2 WO2006089384 A2 WO 2006089384A2 BR 2006000033 W BR2006000033 W BR 2006000033W WO 2006089384 A2 WO2006089384 A2 WO 2006089384A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- tanning
- conditioning
- pelt
- product
- following
- 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.)
- Ceased
Links
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
Definitions
- the present invention is related to the use of a new conditioning agent for treating pelts for tanning.
- This conditioning agent consists in a composition of modified aldehydes, carboxylic acids or polycarboxylic acids and aiders.
- the conditioning agent is used to replace the steps of deliming and pickeling in the pelts treatment.
- the action of the product can eliminate the step of basification when the tanning is made with chromium salts.
- the state of the art describes the process of treating animal pelts to transform into leather involving many steps. Transformation starts when the skin is removed from the animal and treated with chemicals that maintain its conservation. The following steps describe the preparation of pelts that come from slaughter houses prior of tanning. The steps are ordered after slaughter and conservation:
- Steps from 1 to 8 are described as indispensable for tanning process whatever the tanning agent to be used. After the 8 th step the pelts are ready for tanning. Tanning will bring about special characteristics to the pelt as putrefication resistance, mechanical resistance, temperature resistance and others.
- step 6 delivery
- step 8 pickling
- steps 6 and 8 deliming and pickling respectively, generate big volumes of pollutants that remain in aqueous solution as: sodium chloride, organic nitrogen, ammonia, acids, fats, sulfides and proteins.
- Toxic vapors and gases also are formed as ammonia, sulfides, formic acid vapors that contaminate the work area.
- the step 8 pickling pose risks to workers that manipulate strong acids as sulfuric and formic and to the process, due to their reactivity.
- those acids be added without correct previous dilution, or if they are added to fast, they can cause burning spots over pelt surface or cause acid hydrolysis in the proteins, damaging the leather.
- the pelt turns out to be a very complex chemical reagent due to its protein composition.
- the technique describes alkalinity and acidity conditions as well as the products used during the transformation of pelt to leather.
- the reactivity of collagen protein, constituent of the pelts, is modified along the processing with added products. This modification is detectable by change in isoelectric point value of collagen and consequently its ionic charge.
- Tanning with inorganic products occurs rather by a chemical reaction with carboxylic groups of amino-acids that constitute the protein.
- the ionic character of the pelt after tanning with inorganic products turns cationic because of the presence of positive groups (amino groups) that has not reacted.
- Tanning with organic products preferably occurs through the chemical reaction of amino-acids amino group that compound the protein. Protein ionic character turns to anionic charge due to the presence of free negative groups (carboxyl group) that has not reacted.
- the following table describes the main products during all steps of transformation of pelt into leather, the pH range that finish each step and the consequently changes in the ionic charge and in the isoelectric point drop of collagen:
- chromium salt tanning starts in a pH range of 2.5 to 3.5 and finishes in 3.8 to 4.0.
- chromium salt addition starts after pickling the pelt has an overall cationic charge. This condition allows the chromium salt dissolves in water and penetrates along all thickness of the pelt, without reacting. Reaction will take place in a second moment when alkalis are added that promote an increase in of pH value and consequently of pelt reactivity to the chromium salt.
- This step corresponds to step 9.2 in table 1, and it is called basification.
- steps from 1 to 8 are carried on when tanning is made with other tanning agents as aluminum, titanium, zirconium, iron vegetables tannins, synthetic tannins, aldehydes, resins, silicates and polyphosphates.
- Type of tanning chromium sulfate tanning
- Tanning It is started with the addition of 60 to 70 kg of chromium III salt that contains about 25 to 27% of chromium oxyde and basicity of 33%. Reaction time is approximately 2 hours and the system is heated up to 40 0 C. The system is maintained for 8 hour at this temperature. The final pH of the reaction is between 3.8 to 4.0.
- the objective of the present invention is the of a novel composition that can replace the steps of deliming, step 6, and pickling, step 8, described before for only one step called conditioning.
- the product of this invention allows preparing the pelt for tanning by means of just one product addition.
- the proposed system neutralizes the alkalinity and hence remove solubility of Calcium from the liming operation attached in the pelt.
- the action on the amino acids is strongly directed to the amino groups via Amadori reaction:
- the pH of the pelt has high reactivity to cationic products (eg.: Al 3+ , Fe 3+ , Ti 3+ , Zr 3+ e Cr 3+ ).
- cationic products eg.: Al 3+ , Fe 3+ , Ti 3+ , Zr 3+ e Cr 3+ .
- Chromium III sulfate is enhanced due to the fact that it is the most widely used for tanning.
- This system permits to minimize or eliminate completely the bad features referred to the tanning operation described in the state of the art.
- the acidity supplied by the chromium salt dissolution is enough to low the pH value of the to the range of 3.8 - 4.0 needing no further addition of alkalis to accomplish the reaction. So, for chromium tanned pelts, the normally required addition of basification product can be cancelled in the new system.
- Another novelty of the process is the use of the system, object of present invention, to prepare pelts to alternative tanning processes, where other products can be used instead of chromium salt.
- the process described in the present invention is characterized by fact of advantages in process optimization for pelt tanning, due to the replacement of 2 or 3 steps for only one step by means of addition of only 1 product. Besides the elimination of hazardous, toxic and dangerous chemicals due to the process characteristic, the new process described in the present invention provides a lesser amount of chromium salt to be used in the tanning operation step.
- Table above shows that the new system can reduce the number of steps and chemicals normally used in the preparation of pelts for tanning.
- Example 2 application of the present invention
- Quantity 1000 Kg of limed pelts 5 mm thickness -
- Type of tanning chromium sulfate salt tanning
- Enzymatic bating reaction of the pelt with approximately 1,0 kg of a non- concentrated enzymatic solution diluted in 800 liters of water and keep it reacting for 40 - 60 minutes. At the end the pelts are washed again with 1500 liters of water for 15 minutes in a closed drum.
- composition of the system here described is obtained from functional aldehydes with the general formulation as follows:
- the system comprises functional aldehydes to which are added a combination or just one of the following chemicals: mono, di, tri and polycarboxylic acids; anydrides; fumaric, maleic, phthalic and anhydrides of dicarboxylic acids that contains at least 2 to 8 carbon atoms; esters of mono, di, tri and polycarboxylic acids; EDTA; boric acid and sodium and calcium tripolyphosphate.
- solvents to stabilize the system one or a mixture of the following compounds: water, branched or non-branched aliphatic alcohols, glycols and polyols.
- ammonium hydroxyde sodium hydroxyde
- sodium bicarbonate ammonium bicarbonate
- anionic or non-ionic surfactants As additives it is used one or a blend of the following compounds: ammonium hydroxyde, sodium hydroxyde, sodium bicarbonate, ammonium bicarbonate and anionic or non-ionic surfactants.
- the system can be obtained according to the following example:
- ammonium hydroxide sodium hydroxide
- sodium bicarbonate ammonium bicarbonate
- anionic and non-ionic surfactants As additives it is used just one or a blend of the following compounds: ammonium hydroxide, sodium hydroxide, sodium bicarbonate, ammonium bicarbonate, anionic and non-ionic surfactants.
- the product of the present invention can be obtained like this:
- the solvent of this solution can be one or a mixture of the following solvents: water, aliphatic alcohols (branched or no branched), glycols and polyols.
- This solution has a concentration that can be 25 or 85% on active materials.
- A) An amount of the solution prepared in A is weighed and to it is added a mixture of the following compounds: mono, di, tri and polycarboxylic acids or one of their derivatives in the form of anhydrides and esters. The proportion can vary from 10 to 80 % of the weight of original solution.
- As an auxiliary it can be added to the composition still 0.5 to 3.0% w/w from solution prepared in A) EDTA, sodium or calcium polyphosphates and anionic and non-ionic surfactants.
- the system produced in B) has its pH value adjusted to values between 2.0 and 7.0 with the addition of 0.5 to 5% of one of the following products: sodium, ammonium or potassium hydroxide; sodium ammonium or potassium carbonate.
- the proposed system is characterized as a viscous yellow to pale liquid with concentration of 20 to 80 %, density between 0.9 e 1.4 g/cm 3 and pH between 2,0 and 7,0. It can be applied diluted or concentrated in one or more additions over the limed pelts.
- the amount of product to be applied, taking into account the active substance, is about 20 and 50 grams per kg of limed pelt.
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
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX2007007962A MX2007007962A (en) | 2005-02-22 | 2006-02-21 | Product for pelt conditioning for tanning: process for pelt conditioning and following tanning. |
| AU2006218259A AU2006218259A1 (en) | 2005-02-22 | 2006-02-21 | Product for pelt conditioning for tanning: process for pelt conditioning and following tanning |
| US11/813,355 US20080168606A1 (en) | 2005-02-22 | 2006-02-21 | Product For Pelt Conditioning For Tanning: Process For Pelt Conditioning and Following Tanning |
| EP06721593A EP1853738A2 (en) | 2005-02-22 | 2006-02-21 | Product for pelt conditioning for tanning: process for pelt conditioning and following tanning |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BRPI0500604-0 | 2005-02-22 | ||
| BRPI0500604-0A BRPI0500604A (en) | 2005-02-22 | 2005-02-22 | tanning skin conditioning product and resulting tanning skin conditioning process |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| WO2006089384A2 true WO2006089384A2 (en) | 2006-08-31 |
| WO2006089384A3 WO2006089384A3 (en) | 2006-11-09 |
| WO2006089384A8 WO2006089384A8 (en) | 2007-07-26 |
Family
ID=36927775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/BR2006/000033 Ceased WO2006089384A2 (en) | 2005-02-22 | 2006-02-21 | Product for pelt conditioning for tanning: process for pelt conditioning and following tanning |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20080168606A1 (en) |
| EP (1) | EP1853738A2 (en) |
| CN (1) | CN101103125A (en) |
| AU (1) | AU2006218259A1 (en) |
| BR (1) | BRPI0500604A (en) |
| MX (1) | MX2007007962A (en) |
| RU (1) | RU2007133667A (en) |
| WO (1) | WO2006089384A2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101376914B (en) * | 2008-07-17 | 2012-05-30 | 嘉兴学院 | Black leather tanning method |
| CN101857907B (en) * | 2010-06-03 | 2012-09-05 | 烟台大学 | Method for dying leather by adopting tannin extract mordanting method |
| CN102719571B (en) * | 2012-06-12 | 2014-10-29 | 陕西科技大学 | Method for preparing aluminum-containing tannins |
| CN116536460B (en) * | 2023-05-10 | 2024-05-24 | 四川大学 | Method for preparing transparent leather based on refractive index phase matching principle |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3516842A1 (en) * | 1985-05-10 | 1986-11-13 | Hoechst Ag, 6230 Frankfurt | METHOD FOR CHROME SAVING |
| BR9603419A (en) * | 1996-07-31 | 1998-06-09 | Set S A Extrativa Tanino De Ac | Leather tanning process |
-
2005
- 2005-02-22 BR BRPI0500604-0A patent/BRPI0500604A/en not_active IP Right Cessation
-
2006
- 2006-02-21 EP EP06721593A patent/EP1853738A2/en not_active Withdrawn
- 2006-02-21 RU RU2007133667/12A patent/RU2007133667A/en not_active Application Discontinuation
- 2006-02-21 MX MX2007007962A patent/MX2007007962A/en unknown
- 2006-02-21 AU AU2006218259A patent/AU2006218259A1/en not_active Abandoned
- 2006-02-21 WO PCT/BR2006/000033 patent/WO2006089384A2/en not_active Ceased
- 2006-02-21 US US11/813,355 patent/US20080168606A1/en not_active Abandoned
- 2006-02-21 CN CNA2006800022165A patent/CN101103125A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006089384A8 (en) | 2007-07-26 |
| CN101103125A (en) | 2008-01-09 |
| MX2007007962A (en) | 2007-08-23 |
| AU2006218259A1 (en) | 2006-08-31 |
| US20080168606A1 (en) | 2008-07-17 |
| RU2007133667A (en) | 2009-03-27 |
| BRPI0500604A (en) | 2006-10-10 |
| EP1853738A2 (en) | 2007-11-14 |
| WO2006089384A3 (en) | 2006-11-09 |
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