EP0583697A2 - Verfahren zur Chromspar- und Chromfüllgerbung - Google Patents

Verfahren zur Chromspar- und Chromfüllgerbung Download PDF

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Publication number
EP0583697A2
EP0583697A2 EP93112579A EP93112579A EP0583697A2 EP 0583697 A2 EP0583697 A2 EP 0583697A2 EP 93112579 A EP93112579 A EP 93112579A EP 93112579 A EP93112579 A EP 93112579A EP 0583697 A2 EP0583697 A2 EP 0583697A2
Authority
EP
European Patent Office
Prior art keywords
chrome
weight
tanning
chromium
pelts
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Withdrawn
Application number
EP93112579A
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German (de)
English (en)
French (fr)
Other versions
EP0583697A3 (pt
Inventor
Karlheinz Fuchs
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG
Original Assignee
Hoechst AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hoechst AG filed Critical Hoechst AG
Publication of EP0583697A2 publication Critical patent/EP0583697A2/de
Publication of EP0583697A3 publication Critical patent/EP0583697A3/xx
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C1/00Chemical treatment prior to tanning
    • C14C1/08Deliming; Bating; Pickling; Degreasing
    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C3/00Tanning; Compositions for tanning
    • C14C3/02Chemical tanning
    • C14C3/04Mineral tanning
    • C14C3/06Mineral tanning using chromium compounds

Definitions

  • Chrome tanning is an essential step in leather production.
  • chromium salts are offered in a concentration which corresponds to an equivalent of 2 to 2.5% by weight of Cr 2 O 3, based on nakedness, in order to achieve a cookable leather. Of these, however, only 70 to 80% are actually permanently fixed in the skin, so that 20 to 30% of the chromium tannin offered ends up in the wastewater.
  • the degree of exhaustion of the chrome tanning agents can be improved beyond the usual level.
  • the increased astringency of the chrome tanning agents leads to scarring i.e. lower quality leathers. In most cases, a loss of space also has to be accepted.
  • aromatic di- and tricarboxylic acids such as phthalic acid and / or their salts
  • aromatic di- and tricarboxylic acids are used in the pimple or in the chrome tanning in order to achieve better fixation of the chromium in the skin. If they are used in the pimple, however, this leads to a significant reduction in the penetration rate of the subsequent chrome tanning agents, an uneven chrome distribution and, in the case of stronger, unsplit nakedness, even insufficient tanning in some cases.
  • tanning must usually be carried out in two stages in order to reduce these deficiencies by using mild organic tanning which is carried out with mostly organically masked chromium (III) sulfate tanning agent and then adding the aromatic di- and tricarboxylic acids follow alone or in the presence of further chrome tanning agent and / or a base agent.
  • mild organic tanning which is carried out with mostly organically masked chromium (III) sulfate tanning agent and then adding the aromatic di- and tricarboxylic acids follow alone or in the presence of further chrome tanning agent and / or a base agent.
  • chrome-saving tanning process US Pat. No. 4,715,861 in which 0.1 to 2% by weight of an aldehyde or keto carboxylic acid, preferably glyoxylic acid, is used as a replacement or partial substitute for the sulfuric acid or formic acid usually used before tanning in the pimple bath will.
  • the chrome tanning is carried out in the same bath. This process results in very soft leather with tightly fitting scars and improved physical properties. The consumption of the chrome tanning liquor is improved significantly, but without meeting the increased demands in all cases.
  • chromium tanning process with high exhaustion uses chromium (III) salts which are tanned with 0.5 to 12% by weight, preferably 3 to 6% by weight, based on the pelt weight Peel, a combination of basifying agents such as magnesium oxide and aldehyde and / or ketocarboxylic acids and subsequent addition of sodium aluminum silicates.
  • the pelts are tanned with 0.5 to 2.0% by weight of an aldehyde or keto carboxylic acid, preferably glyoxylic acid and 0.5 to 1.0% by weight of one, before tanning Mixture of chromium (III) salts, acid-binding agents and aromatic di- and tricarboxylic acids pretreated. Thereafter, tanning is carried out in the same bath in the customary manner and then tanned with 1 to 3% by weight of a mixture of chromium (III) salts, acid-binding agents and aromatic di- or tricarboxylic acids or their salts.
  • the object of the invention is to provide a chrome tanning process which does not have the aforementioned disadvantages and which, in addition to improved chromium exhaustion of the tanning liquor, guarantees greater abundance, better softness and grain resistance of the leather.
  • the invention relates to a process for chrome tanning and chrome fill tanning, in which the pelts in the pimple bath are mixed with an aldehyde and / or ketocarboxylic acid and then tanned, characterized in that before the addition of the aldehyde and / or ketocarboxylic acid and optionally other organic and / or inorganic acids, the decalcified and pickled pelts are pretreated with an anionic, colloidal silicate solution.
  • Anionic colloidal silicate solutions are usually aqueous dispersions of colloidally distributed, anionically charged silicon dioxide particles, preferably so-called silica sols.
  • the aqueous dispersions are usually prepared by "in situ" growth of silicon dioxide micro-nuclei and not by redispersion of particles which have already formed.
  • the silicon dioxide particles produced in this way are non-porous and amorphous.
  • dispersions of different particle size or different specific surface can be produced.
  • the dispersions are stabilized with organic or inorganic bases, such as ammonia, amines, for example ethanolamines, and sodium, potassium or lithium hydroxide.
  • the silicon dioxide particles usually have a particle size between 5 and 135 nm, preferably 5 to 25 nm and a specific surface area between 50 and 500 m2 / g, preferably between 100 and 150 m2 / g.
  • the pH of the dispersion is generally between 5 and 10.
  • the aqueous dispersions of colloidally distributed, anionically charged silicon dioxide particles preferably include so-called silica sols, as are known from Ralph K. Iler, The Chemistry of Silicium, John Wiley and Sons, New York 1979. The manufacture and properties of these silica sols are discussed in Chapter 4, pages 312 to 461.
  • silica sols are available under the name ®Klebosol (trademark of governing civile Hoechst) and are described in the brochure of cioslaube Hoechst "Klebosol, sols de silice-silicasols-Kieselsole".
  • Anionic colloidal silicate solutions are generally 5 to 65% by weight, preferably 20 to 40% by weight, aqueous dispersions of colloidally distributed, anionically charged silicon dioxide particles.
  • the decalcified and pickled pelts are preferably 0.3 to 5.0% by weight, particularly preferably 0.3 to 0.6% by weight, of an anionic, colloidal silicate solution, based on the weight of the Bare, pretreated.
  • the pH is then adjusted to a pH of less than 6, preferably 2.8 to 4.3, by adding an aldehyde and / or ketocarboxylic acid, preferably glyoxylic acid or pyruvic acid and optionally other organic and / or inorganic acids.
  • an aldehyde and / or ketocarboxylic acid preferably glyoxylic acid or pyruvic acid and optionally other organic and / or inorganic acids.
  • the addition of 0.25 to 2.5% by weight of the aldehyde and / or keto carboxylic acid, based on the pimple weight of the pimple, is usually sufficient for this.
  • Glyoxylic acid is preferably used alone or in combination with other organic and / or inorganic acids, such as formic acid and sulfuric acid.
  • the tanning is then carried out in the same bath with the customary commercially available chromium (III) tannins, whereby the modern, self-dulling chromium (III) tannins can also be used without any problems.
  • colloidal silicate solutions with a particle size of 5 to 25 nm are combined with those between 26 and 135 nm and glyoxylic acid in the pimple, a "wet white” is obtained which is easily subjected to the mechanical processes of splitting or folding (splitting waste and folding waste are Aldehyde, chrome and aluminum free; they can be recycled or disposed of in an environmentally friendly manner and then tanned with chrome tanning agents (or other tanning agents).
  • chrome tanning agents or other tanning agents.
  • the character of the chrome leather is not affected by the pretreatment.
  • the residual chromium content of the exhausted tanning liquors is less than 100 mg Cr2O3 per liter.
  • the process according to the invention is distinguished by the very high degree of exhaustion of the chrome tanning agents.
  • the residual chromium content of the exhausted tanning liquors is less than 200 mg Cr2O3 per liter.
  • the wet blue produced is particularly full, soft and strikingly bright.
  • the bright wet blue color does not have a negative effect on the color build-up in the subsequent dyeing. Due to the fullness and softness already achieved in the tanning process, the retanning and fat supply in the wet finish can be significantly reduced.

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)
EP93112579A 1992-08-14 1993-08-05 Verfahren zur Chromspar- und Chromfüllgerbung Withdrawn EP0583697A2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4226983 1992-08-14
DE4226983 1992-08-14

Publications (2)

Publication Number Publication Date
EP0583697A2 true EP0583697A2 (de) 1994-02-23
EP0583697A3 EP0583697A3 (pt) 1994-04-27

Family

ID=6465587

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93112579A Withdrawn EP0583697A2 (de) 1992-08-14 1993-08-05 Verfahren zur Chromspar- und Chromfüllgerbung

Country Status (9)

Country Link
US (1) US5501709A (pt)
EP (1) EP0583697A2 (pt)
JP (1) JPH06166900A (pt)
KR (1) KR940004061A (pt)
CN (1) CN1082613A (pt)
AU (1) AU4459093A (pt)
BR (1) BR9303380A (pt)
TW (1) TW248571B (pt)
ZA (1) ZA935923B (pt)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100415999B1 (ko) * 2001-05-24 2004-01-24 삼성전자주식회사 컴퓨터
CN101307368B (zh) * 2008-07-01 2012-03-21 中国科学院昆明动物研究所 用于制作亚洲象姿态标本的象皮处理方法
CN101550459B (zh) * 2009-05-14 2013-04-03 四川大学 利用环氧化油脂制造油鞣革的方法
CN104450995B (zh) * 2014-11-11 2016-02-10 陕西科技大学 SiO2气凝胶/乙烯基聚合物复合高吸收铬鞣助剂及其制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0349892A2 (de) * 1988-07-06 1990-01-10 Henkel Kommanditgesellschaft auf Aktien Gerbverfahren mit hoher Chromauszehrung der Gerbflotten
EP0437997A1 (fr) * 1989-12-27 1991-07-24 Societe Francaise Hoechst Procédé autorisant la refente aisÀ©e des peaux à l'état de tripe ou de stain
EP0551785A1 (fr) * 1992-01-14 1993-07-21 SOCIETE FRANCAISE HOECHST Société anonyme dite: Application de sols de silice à l'obtention d'une peau dite blanc picklé stabilisé ou blanc stabilisé

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2276315A (en) * 1941-06-04 1942-03-17 Du Pont Tanning
AR208085A1 (es) * 1974-05-18 1976-11-30 Bayer Ag Procedimiento de curtido al cromo
DE3516842A1 (de) * 1985-05-10 1986-11-13 Hoechst Ag, 6230 Frankfurt Verfahren zur chromspargerbung
DE3814220A1 (de) * 1988-04-27 1989-11-09 Hoechst Ag Verfahren zur chromspargerbung
FR2666097B1 (fr) * 1990-08-21 1992-12-11 Hoechst France Procede d'echarnage des peaux.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0349892A2 (de) * 1988-07-06 1990-01-10 Henkel Kommanditgesellschaft auf Aktien Gerbverfahren mit hoher Chromauszehrung der Gerbflotten
EP0437997A1 (fr) * 1989-12-27 1991-07-24 Societe Francaise Hoechst Procédé autorisant la refente aisÀ©e des peaux à l'état de tripe ou de stain
EP0551785A1 (fr) * 1992-01-14 1993-07-21 SOCIETE FRANCAISE HOECHST Société anonyme dite: Application de sols de silice à l'obtention d'une peau dite blanc picklé stabilisé ou blanc stabilisé

Also Published As

Publication number Publication date
CN1082613A (zh) 1994-02-23
US5501709A (en) 1996-03-26
TW248571B (pt) 1995-06-01
ZA935923B (en) 1994-03-11
KR940004061A (ko) 1994-03-14
AU4459093A (en) 1994-02-17
BR9303380A (pt) 1994-03-15
EP0583697A3 (pt) 1994-04-27
JPH06166900A (ja) 1994-06-14

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