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
  • C14C3/28—Multi-step processes
• • 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
  • C14C3/04—Mineral tanning
  • C14C3/06—Mineral tanning using chromium compounds
• • 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
  • C14C3/10—Vegetable tanning
• • 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
  • C14C3/10—Vegetable tanning
  • C14C3/12—Vegetable tanning using purified or modified vegetable tanning agents
• • 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
  • C14C3/18—Chemical tanning by organic agents using polycondensation products or precursors thereof
  • C14C3/20—Chemical tanning by organic agents using polycondensation products or precursors thereof sulfonated

Definitions

• 2,997,- 364 which consist of a mixture of chromic tanning salts and synthetic tanning agents which are prepared (a) from monoor polyvalent phenols or both types of phenols, or also polynuclear phenols or phenol resins, by condensation with sulphites and/or bisulphites and with aldehydes and/or ketones, or (u) from methylol compounds of the said phenols with sulphites and/ or bisulphites, possibly in the presence of aldehydes and/ or ketones and/ or alcohols.
• the final tanning of the pretanned hides with powdered vegetable tanning agents is initiated by means of powdered synthetic tanning agents without a liquor.
• so-called exchange tanning agents are used which have a good dispersing action, are readily soluble, and have themselves a good tanning effect.
• precursory tanning agents improve the rate of tanning through and the uniform dispersion of the tanning agent.
• chromium tanning agents or known chromium complex tanning agents or mixtures or chromium tanning agents with synthetic tanning agents and/ or naphthalene-sulphonic acids and/ or condensation products of naphthalene-sulphonic acids and formaldehyde and/ or sulphite waste liquor are used in powdered form for pretanning without liquor in the drum.
• the final tanning is subsequently carried out with powdered synthetic tanning agent and/ or vegetable tannins.
• acid number there is to be understood the consumption of mg. KOH for neutralising 1 g. of dry substance of the tanning agent to be titrated, i.e., in the present case of the precursory tanning agent.
• the undesirable drawn grain is reduced or completely prevented by this process.
• the greenish tint of the leather caused by the chromium-containing precursory tanning agents is reduced and a more reddish colour of the leather is obtained if the required acid number of precursory tanning agents is adjusted by using inorganic or organic acids the dissociation constant of which is equal to or greater than 10*
• the condensation products of naphthalene-sulphonic acids and formaldehyde to be used as precursory tanning agents can, by definition, be replaced completely or, more advantageously, in part, by sulphite waste liquors.
• the naphthalene-sulphonic acid/formaldehye condensation products to be used as precursory tannins are preferably those which can be prepared by known methods from technical naphthalene-sulphonation mixtures chiefly containing fl-naphthalene-sulphonic acid.
• the molar ration of naphthalene-sulphonic acid to formaldehyde is about 1:06 to 1 mol.
• the condensation products are usually converted into their alkali metal or ammonium salts and then dried. They contain alkali metal or ammonium sulphate originating from the sulphonic acid usually employed in excess for the sulphonation of naphthalene. It is also possible to use products freed from these neutral salts.
• sulphite waste liquor is known to mean technical mixtures which contain, as the main component lignin-sulphonic acid in the form of its salts, especially the sodium salts.
• Suitable organic acids for adjusting the required acid number of the precursory tannins are chiefly aliphatic carboxylic acids, such as acetic acid, formic acid, glutaric acid or adipic acid. Liquid as well as solid acids can be admixed to the naphthalene-sulphonic acid condensation products or to the sulphite waste liquor (precursory tannins).
• the amount of acid required for adjusting the acid number of the precursory tanning agent used for the precursory tannin is adjusted before or during this treatment with such a neutral or more weakly acidic precursory tanning agent
• Suitable acids with a dissociation constant of 10- are, for example, sodium bisulphate, naphthalene-sulphonic acid, sulphuric acid or oxalic acid. It is also possible to use the naphthalene-sulphonic acid/formaldehyde condensation products to be employed as precursory tannins, in a partially neutralised form. This means that, after completion of the reaction, the reaction products are neutralised only to such an extent that they are still present in the form of free sulphonic acids in a quantity corresponding to the desired acid number. 7
• water-soluble inorganic neutral salts are, inter alia, sodium sulphate, sodium chloride, potassium sulphate, potassium chloride, ammonium sulphate, ammonium chloride, and other known water-soluble inorganic salts of neutral reaction.
• tanning without liquor in the meaning of the present invention comprises tanning processes in which the tanning agents are used without water or without substantial amounts of water.
• the precursory tannins are usually employed in a powdered form, but the use of solid products, e.g., in the form of blocks, or of highly concentrated syrups, is also possible.
• the tanning process itself is mainly carried out by milling the pelt or leather with the tanning agents in a rotating drum.
• the precursory tannins to be used according to the present process are employed in amounts of about 20%, preferably 812%, referred to the pelt weight.
• chromic tanning salts vegetable tannins, synthetic tannins and exchange tanning agents there are used the agents known in leather technology, which need not be explained in greater detail, since they are known to the man skilled in the art and can be seen from the literature. Some of the suitable compounds are mentioned in the patent specifications given above.
• the new process is particularly suitable for the production of sole leather, sole leather splits, inside sole leather, welting leather, vachettes or upper leather tanned in combination.
• EXAMPLE 1 (a) After the lime-house processing customary for sole leather, 500 kg. unsplit cow pelts are pretanned in the pit with a chromium complex tanning agent according to Example 1 of US. Pat. No. 3,253,879.
• the pretanned pelts are milled in the usual manner without a liquor in a drum preheated to about 30 C., with 10% (referred to the pelt weight) of a powdered precursory tanning agent as described below. After the treatment for about 3 to 4 hours, the pelts are evenly tanned through. 15% pure tannin of a sulphited quebracho are then added in powdered form. It is expedient to add about 0.5% of a sulphonated castor oil together with about 1% water simultaneously With the tannin, in order to avoid chafe marks.
• precursory tanning agent there is used a condensation product obtained by condensation of a technical naphthalene-sulphonation mixture substantially containing fl-naphthalene-sulphonic acid with 0.65 mol formaldehyde per mol naphthalene-sulphonic acid, which is present in the form of the soduim salt and has been adjusted to an acid number of 120 by the addition of glutaric acid.
• the leather (a) tanned with the precursory tanning agent according to the invention is noticeably smoother and exhibits substantially less drawn grain or none at all. This difference is still visible on the finished leather.
• EXAMPLE 2 500 kilograms unsplit cow pelts are pretanned in the same manner as described in Example 1 and milled without a liquor in the drum with 13% (referred to the pelt weight) of one of the powdered precursory tannins described below. After tanning for 3 to 4 hours, two portions of 25% pure tannin (referred to the pelt weight) of a sulphited quebracho extract in powdered form are added. After a total milling time in the drum of about 20 to 30 hours, the tanning is completed.
• precursory tanning agent there is used a condensation product of fi-naphthalene-sulphonic acid and formaldehyde (molar ratio 1:1) which has been neutralised with ammonia and then adjusted to an acid number of by the addition of oxalic acid.
• the leather obtained after finshing in the usual manner has a reddish tint and little or no drawn grain.
• EXAMPLE 3 After the usual preparation in the lime house, 500 kg. unsplit cow pelts which is suitable for the production of bag leather, are pickled in the usual manner and pretanned in the drum without a liquor with 4% (referred to the pelt weight) of the following powdered chromium complex tanning agent.
• 225 parts by weight of the condensation product prepared according to the instructions of Example 1 of US. Pat. No. 3,065,039 are mixed with a solution of 225 parts by weight of purified sulphite waste liquor and a solution of 300 parts by weight 0 (nought)-basic chromic sulphate in 300 parts by weight hot water, and subsequently spray-dried.
• synthetic precursory tanning agent there is used a mixture of 90 parts by weight of the sodium salt of a condensation product obtained from a technical naphthalene-sulphonation mixture substantially containing ,6- naphthalene-sulphonic acid, and 1 mol formaldehyde per mol naphthalene-sulphonic acid, and parts by weight sodium sulphate.
• 7% pure tannin (referred to the weight of the pretanned leather) of a sulphited quebracho extract in powdered form and 7% pure tannin of a mimosa extract in block form.
• the tanning is completed after a further milling time of about 4 hours.
• piling the leather is sammed, set out and finished in the usual manner. A smooth leather is obtained, which has only negligible drawn grain or none at all.
• EXAMPLE 4 To produce a waterproof leather, 500 kg. of North German cow pelts are tanned, after the usual lime house processing, with a 33% basic chromic sulphate tanning agent in an amount corresponding to 1.5% CR O (referred to the pelt weight). After shaving to 2.5 mm, the leather is washed and neutralised in the usual manner so that the cut exhibits a level yellow-green coloration with the 'bromocresol green indicator.
• the leather is treated without a liquor in the drum with 8% (referred to the weight of the shaved leather) of a mixture of 70 parts by weight of the precursory tanning agent described in Example 1 and 30 parts by weight of a delimed sulphite waste liquor which is present in the form of its sodium salt.
• 8% referred to the weight of the shaved leather
• a milling time of about one hour there are added 7% pure tannin of a sulphited quebracho extract in powdered form, 7% pure tannin of a mimosa extract in powdered form and 2% of pure tannin of a conventional soft-tanning synthetic exchange tanning agent in powdered form (the percentages are referred to the weight of the shaved leather).
• the tanning is completed.
• the leather is seasoned, greased and finished in the usual manner.
• the leather or pelt material is treated with the pretanning agent, the precursory tanning agent or the other tanning agents used for final tanning, in the wet state but without a liquor.
• the wet or dripping wet state of the material presupposes, strictly speaking, a certain amount of liquor, but this is generally less than 20%, referred to the weight of the leather or pelt, and is not regarded as a tanning liquor in the technical sense.
• without liquor as used in the present application is therefore to be understood to mean that the liquor originating, for example, from deliming or pretanning (with liquor), which normally amounts to many times the volume stated above, is completely drained, pumped off or removed in any other way, whereby, obviously small residual amounts of liquor remain between the pelts; the definition of the term without liquor also excludes the addition of larger amounts of liquor to the pelt or leather before pretanning or final tanning than are taken up by the pelt or leather until the wet or dripping wet state is reached.
• EXAMPLE 5 For the manufacture of split hide cattle pelts are pickled and pretanned in the drum. without liquor with 5% (referred to the pelt weight) of the following pretanning agent:
• the pretanning agent consists of 50 parts by weight of a powdered 33% 'basic chromium sulfate tanning agent having a chromium oxide content of 25%, and 50 parts by weight of a powdered sodium salt of the condensation product of fl-naphthalene sulphonic acid and formaldehyde (condensation ratio 1:0.65).
• the pelts are evenly tanned through.
• the pretanned leathers are rinsed for a short time, the rinsing liquor completely discharged and the leathers then milled with 10% of the following precursory tanning agent:
• the precursory tanning agent is a delimed 50% sulphite waste liquor used in form of its sodium salt and containing as much acetic acid as the liquid product has an acid number of 50 referred to its content of dry substance.
• EXAMPLE 6 The process described in Example 5 can be varied in that instead of the precursory agent there is used the same amount of a powdered mixture of 45 parts by weight of the powdered ammonium salt of the condensation product of fi-naphthalene sulphonic acid and formaldehyde (molar ratio 1:08), 30 parts by weight of a powdered delimed sulphite waste liquor in form of its sodium salt and 5 parts by weight of sodium chloride as well as 20 parts by weight of adipic acid. After completion of the tannage the leather is finished in the customary manner; smooth leather having a full handle is obtained and having little or no drawn grain.
• the precursory agent there is used the same amount of a powdered mixture of 45 parts by weight of the powdered ammonium salt of the condensation product of fi-naphthalene sulphonic acid and formaldehyde (molar ratio 1:08), 30 parts by weight of a powdered delimed sulphite waste liquor in form of its sodium salt
• EXAMPLE 7 For manufacture of waterproof leather, North Ger man cow butts are treated in the lime house in customary manner and then tanned with a chrome tanning agent which was prepared by reduction of bichromate with glucose in the presence of sulphuric acid and which is 35% basic and corresponds to 2% chromic oxide referred to the weight of the pelts.
• the chrome-tanned and shaved leather is rinsed with water and after complete discharge of the rinsing liquor pretanned with 5% (referred to the weight of the shaved leather) of the following precursory tanning agent:
• the precursory tanning agent consists of 50% of a powdered sodium salt of a condensation product of a technical naphthalene sulphonation mixture which essentially contains aand ,B-naphthalene sulphonic acids (molar ratio between naphthalene and sulphuric acid 1:1, 2), 0.62 mol formaldehyde per mol naphthalene sulphonic acid, 30% (referred to parts of the mixture) of anhydrous sodiumbisulphate and 20% (referred to 100 parts of the mixture) of anhydrous potassium or ammonium sulphate.
• a technical naphthalene sulphonation mixture which essentially contains aand ,B-naphthalene sulphonic acids (molar ratio between naphthalene and sulphuric acid 1:1, 2), 0.62 mol formaldehyde per mol naphthalene sulphonic acid, 30% (referred to parts of the mixture) of anhydrous sodiumbisulphate and 20% (referred to
• the pretanned leather is briefly rinsed, neutralised in the customary manner so that the cut exhibits a level yel low-green coloration with the bromo cresol green indicator.
• the leather is tanned without liquor with 8% pure tanning of a sulphited quebracho extract in powdered form and 8% pure tannin of a mimosa extract in powdered form.
• a tanning time of further 1 to 2 hours the tannage is completed.
• the leather is then finished in usual manner. One obtains smooth full and even leathers.
• EXAMPLE 8 Leathers of similar properties are obtained if instead of the precursory agent of Example 7, 20% (referred to the weight of the pelts) of the following about 50% product are used:
• a condensation product of a technical naphthalene sulphonation which essentially cotains EB-naphthalene sulphonic acid and 0.63 mol formaldehyde per mol naphthalene sulphonic acid is neutralised with as much ammonia as the mixture shows an acid number of 90 referred to the content of dry substance of the mixture. If necessary, water is added up to a dry substance content of 50%.
• the final tanning is initiated by applying to the pretanned leather a material which is selected from the group consisting of (a) a condensation product of naphthalene-sulfonic acids and formaldehyde, and (b) a sulfite waste liquor, said material having an acid number of less than 30, and thereafter adjusting the acid number to about -120.
• DONALD LEVY Primary Examiner US. Cl. X.R. 894.24, 94.31.

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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)

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Citations (7)

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• 1965
  • 1965-01-02 DE DEF44869A patent/DE1288233B/de active Pending
  • 1965-12-13 CH CH1711965A patent/CH465125A/de unknown
  • 1965-12-20 US US515236A patent/US3519378A/en not_active Expired - Lifetime
  • 1965-12-31 BE BE674586D patent/BE674586A/xx unknown
  • 1965-12-31 NL NL6517270A patent/NL6517270A/xx unknown
• 1966
  • 1966-01-03 GB GB76/66A patent/GB1110091A/en not_active Expired
  • 1966-01-03 FR FR44664A patent/FR1464309A/fr not_active Expired

Patent Citations (7)

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