NZ623269B2 - Environmentally friendly tanning composition - Google Patents

Abstract

The disclosure relates to a composition suitable for leather tanning comprising zeolite contacted with monocarboxylic acid and to a method for manufacturing said composition. The method comprises providing zeolite into a reactor and keeping said zeolite in motion while introducing concentrated monocarboxylic acid thereto provided that the mean temperature of the resulting composition is 50°C or below. Furthermore, the disclosure provides use of said composition for treating leather and the resulting product and uses thereof. In one embodiment, the composition comprises zeolite having a Si to Al ration of 0.7 to 2.5 and a monocarboxylic acid selected from formic acid, acetic acid, propionic acid, glycolic acid, lactic acid, and a mixture thereof. arboxylic acid thereto provided that the mean temperature of the resulting composition is 50°C or below. Furthermore, the disclosure provides use of said composition for treating leather and the resulting product and uses thereof. In one embodiment, the composition comprises zeolite having a Si to Al ration of 0.7 to 2.5 and a monocarboxylic acid selected from formic acid, acetic acid, propionic acid, glycolic acid, lactic acid, and a mixture thereof.

Description

PCT/F12012/050933 ENVIRONMENTALLY FRIENDLY TANNING COMPOSITION The present invention relates to a ition suitable for tanning leather. In addi- tion, the present invention relates to a method for manufacturing said nd and, more specifically, to certain uses thereof. ound Tanning is one process stage in manufacturing animal skins into durable leather.

In tanning the protein structure of the skin is permanently altered. The tanning pro- cess aims at, in addition to avoiding rotting of the skin, increasing resistance to water, humidity and usage together with increasing flexibility, anti-allergenic prop- erties and visual attractiveness. Pre-treatment processes known in the art are so called beamhouse operations comprising stages following curing and preceding the actual tannage of the skin aiming at decreasing the amount of unwanted com— ponents.

There are three dominating tanning methods; aldehyde or synthan tanning, miner- al tanning predominated by chrome tanning and ble tanning. Each of these tanning agents produces leathers with different properties. However, singly environmentally friendly solutions such as chrome or de free g agents are favoured, especially within e.g. automotive industry. 2O Chrome tanning with basic chrome sulphate is used in 85 % of the world's tanned leather processing. A major advantage in this approach is the very high shrinkage temperature, 100 °C or more, provided to the finished leather by the method. The major future drawback will be the environmentat problems related to the use of chromium and depletion of the availability of the ore. The visual appearance of blu- ish hue in colour is another unwanted product feature. In chrome tanning the chromium salts crosslink en protein molecules which make the hides less susceptible to effects of heat and putrefaction. The chrome tanning s, how- ever, requires use of additional chemicals such as buffering and cation solu— tions. Prior to the uction of the basic chromium, several steps are required to produce a tannable hide including ng, liming, introduction of alkali agents such as sodium ide, deliming, restoring neutral pH, bating, or softening the skin with enzymes, pickling i.e. lowering pH of the hide with salt and sulphuric ac- id. The pH is very acidic when the chromium is introduced to ensure that the chromium complexes are small enough to fit in between the fibres and residues of PCT/F12012/050933 the collagen. Once the desired level of penetration of chrome into the hide is achieved, pH of the material is raised again i.e."basified” to tate the process.

At this stage, the chrome tanned skins obtain the bluish colour.

Vegetable tanning is an earlier process to mineral tanning the name originating from the use of tannin in the process. s bind to the collagen proteins in the hide and coat them causing them to become less water-soluble, more resistant to bacterial attack, and increasing the hide flexible. This g method is, however, quite slow and has been largely overcome by the more efficient chrome tanning which is faster, taking less than a day, and es a stretchable leather which is 1O excellent for use eg. in gs and garments. Vegetable tanning is still in use for e.g. furniture and luggage leathers.

In aldehyde tanning amino groups of collagen are reacted with des. The shrinkage temperature obtained is adequate, about 75 °C, but the colour hue of the tanned hide is ish, or sometimes even orange. The major ck is that the hide can only partly be modified. Aldehyde tanning is typically used in con- junction with other tanning agents but it is not suitable as the sole tanning agent.

The possible formaldehyde release is another concern. Specifically, this is an is- sue in the automotive and toy industry wherein strict concentration limits have been imposed.

Modern chrome—free mineral tanning comprises the use of sodium aluminium sili— cates (NAS) providing tanned leather with whitish or white colour hue. Synthetic zeolites have been tested also ing durable, resistant, readily e pro- cessable, shavable and dimensionally stable leather products. A typical drawback in these ses is the lowered shrinkage temperature, TS, of the hides com— pared to chrome tanning due to formation of less stable complexes with collagen.

Costantini et al., "Studies on the tanning reactions of zeolite” in JALCA, vol. 95, 2000, pp. 125-137 discloses a study on the reactions involved in pretanning or tanning when using zeolite based masking agents. The hydrothermal stability of sodium aluminium te is considered to be too low for use in tanning solely by a zeolite. The role of pH and acidic solutions in aluminosilicate breakdown are em- phasized and discussed in detail. Maleic acid and phtalic acid are considered the only possible carboxylic acids to elevate the age temperature to an accepta— PCT/F12012/050933 ble level. The shrinkage temperatures are determined by differential scanning spectroscopy. The hides are ned before the actual tanning. (382368346 discloses a pre-tannage system for leather comprising treating the hide with a zeolite material, such as sodium aluminium silicate in a first pre- tannage step and thereafter treating the hide with one or more modified aldehyde tanning agents. At this stage, the hide is suitable for a number of different tanning steps namely chrome tannage, vegetable tannage, synthetic e or combina- tions thereof. 1O Sodium aluminium silicate used for tanning leather must be added in the acidic phase with the result that it hydrolyses to alkaline aluminium salts and llcic acids. As the sodium aluminium silicate has not enough time to fully penetrate into the skin and become an active tanning agent prior to the decomposition, the tan— ning action will be restricted to the outer layers of the hide. 318 and US4264319 disclose a process of tanning for the tion of d fur skins. ln this process pickled fur skins are subjected to the action of an aqueous liquor containing tanning . A water-insoluble aluminosilicate con- g bound water, of the formula (Catg/nO)X‘Al203'(Si02)y wherein Cat represents a cation selected from the group consisting of alkali metals, bivalent metal ions, trivalent metal ions and mixtures thereof; n represents an integer from 1 to 3; or x is a number of from 0.5 to 1.8; and y is a number of from 0.8 to 50, is added to the pickling bath as the tanning agent. Auxiliary tanning agents such as chrome and further als such as carboxylic acids having at least two carboxyl groups maybe added into the pretanning stage and tanning.

Summary of the invention The object of the present invention is to provide a toxic free ition suitable for tanning leather and providing an adequate shrinkage temperature perfor- mance.

Another object is to provide a cost efficient and easy-to-handle composition le for tanning leather.

A further object is to provide a tanning composition able to tan throughout the hide cross section, not only the hide surface as is the case with the presently known tanning agents.

A yet further object is to provide a method for manufacturing a composition suitable for tanning r and having an adequate shrinkage temperature performance.

The foregoing objects should be read disjunctively with the object of at least providing the public with a useful choice.

In the first aspect of the present invention an environmentally friendly composition suitable for tanning leather is provided.

In the second aspect, a method is provided for manufacturing an environmentally friendly composition, and especially the composition defined herein.

In the third aspect the use of the environmentally friendly ition for treating leather is provided. in the fourth aspect a method is ed for producing tanned leather using the composition defined herein.

In the fifth aspect the uses of the leather manufactured by the method defined herein are ed. in one aspect, there is provided a method for manufacturing a composition suitable for leather tanning comprising e contacted with concentrated monocarboxylic acid, wherein said method ses providing zeolite having a Si to Al ratio from 0.7 to 2.5 into a reactor and keeping said zeolite in motion while introducing trated monocarboxylic acid selected from the group of formic acid, acetic acid, propionic acid, glycolic acid, lactic acid and es thereof, the concentration thereof being more than 84% by , thereto [f0llowed by page 4a] provided that the mean temperature of the resulting composition is maintained at a temperature of 50°C or below. in a r aspect, there is provided a composition suitable for r tanning leather, wherein said composition is in a form of a powdery solid having moisture content less than 25 % by weight sing zeolite having a Si to Al ratio from 0.7 to 2.5 treated with concentrated rboxylic acid selected from formic acid, glycolic acid or acetic acid, at a temperature of 50 °C or below, the concentration of said monocarboxylic acid being more than 84% by weight, and having the e structure intact.

In a further , there is provided a use of the composition as herein described for ng leather.

In a further aspect, there is provided a method for producing tanned leather comprising the steps of deliming, bating, optionally washing and pickling the hide, and tanning the hide using the tanning agent composition as herein described, and depickling.

In using the composition of the present invention for eg. tanning it was found that the zeolite which has been modified by eg. formic acid, and preferably with a metal salt such as an acidic aluminium salt, results in effective tanning. The hide is tanned not merely from the e thereof but the tanning agent is able to penetrate deeper into the hide. The pH increase in the hide is slow due to the buffering action of the used composition formulation.

Figures Figure 1 shows the pH of the tanning solution as a on of the amount and quality of added tanning agent according to example 8.

Figure 2 shows a scanning electron microscopic (SEM) image of the distribution of tanning agent throughout the hide according to example 11F. [followed by page 5] PCT/F12012/050933 Detailed ption of the invention which is able to replace In the first aspect of the present invention a composition of the chromium compounds in tanning is provided. in addition, the composition and/or basification present invention is able to simultaneously replace the buffering agents ed in The composition of the t e.g. chrome tanning process. invention can thus be used instead of all the three typically used chemicals; basic will streamline the tanning pro~ chromium sulphate, the buffer and the base which costs. cess considerably and reduce processing invention is A further advantage in using a composition according to the present white instead of being bluish as is the that the colour hue of the final leather will be case in chrome tanning. zeolite which is specifically The composition of the present invention comprises a acid is ably concen- treated with a monocarboxylic acid. The monocarboxylic into the trated monocarboxylic acid which is specifically impregnated or diffused zeolite structure i.e. contacted with the used zeolite. The monocarboxylic acid acid, glycolic acid, lac- preferably selected from formic acid, acetic acid, nic acid is found advan— tic acid or mixtures thereof. The use of lower monocarboxylic such as e.g. Costantini et al. as it provides tageous contrary to the prior teaching the zeolite structure and pores therein com— an enhanced ability to penetrate into pared to higher monocarboxylic acids.

In one embodiment the monocarboxylic acid is selected from formic acid, acetic the monocarboxylic acid is for— acid or glycolic acid or mixtures thereof, preferably mic acid. unit volume and as ent in order to provide as effective y as le per acidifying and g response as possible, the use of trated monocar- the monocarboxylic acid to be boxylic is favoured. Preferably, the concentration of % or more, most preferably used is 84 % by weight or more, more preferably 90 is preferred in order to provide 95 % or more, such as 99%. A concentrated acid as possible. The dry or dried zeolite as low moisture content for the end product of the powdery preferred as moisture affects, for example, handling properties t such as flowability.

WO 5764 PCT/F12012/050933 In a red embodiment the composition is a reaction product of e con- tacted with concentrated formic acid, preferably 99% by weight formic acid, and is depicted by formula 1: NaAlSiO4.xH20 + xHCOOH (1) This contacting is anticipated to lead into formation of sodium formats, NaCOOH, and an acidified zeolite, H2A|204.Si02.xH20 but in analysis of the produced com- position no sodium formate could be detected. Moreover, no teristic odour of free formic acid could be ed in the formed compound suggesting that no free formic acid is present.

Furthermore, the zeolite structure remains intact after the treatment with monocar— boxylic acid i.e. the analysis shows that no own or disintegration takes place. As the pore volume of the zeolite varies the amount of carboxylic acid readily impregnated may vary ingly.

The structures and reactivity of es can be modified by confining specific mol- ecules into the small pores therein. For example, hydrogen form of zeolites typical- ly prepared by ion exchange are powerful solid state acids and can facilitate to host acid catalysed reactions. Synthetic zeolites can be tailor made to fulfil the ic uses aimed at. Presently, about 200 unique zeolite frameworks are identi— fied and over 40 naturally occurring frameworks are known. 2O The zeolites of the present invention preferably comprise essentially of Al and Si oxides. The zeolite comprised in the composition of the present invention is pref- erably a basic zeolite. More preferably, the pH of the basic e is about 10. The zeolites to be used are microporous aluminosillcate minerals with open three di- mensional ork structures built of SiO4 and AlO4 tetrahedra linked to each other by sharing all the oxygen atoms to form regular intra crystalline cavities and channels of molecular dimensions. These frameworks are typically negatively charged and attract positive cations that reside in cavities to compensate the neg- ative charge of the framework. Preferably, alkali metals or earth ne metals are included into the zeolites of the present invention. More preferably the zeolites comprise Na, K, Mg, Ca or Ba alumlnosilicates.

The ratio of Si to Al in the zeolite is preferably from 0.7 to 2.5. More preferably, the ratio is from 0.7 to 1.2, and most preferably from 0.7 to 1.1 such as from 0.9 to 1.1 or very close to unity.

PCT/F12012/050933 In another preferred embodiment the alkali or earth alkaline Si:Al ratio of the zeolite is about 1 :1 :1, the alkali metal being ably sodium.

In one embodiment the zeolite is selected from the group of faujasit, zeolite A, and mordenite, zeolite X, which have a nearly maximal aluminium content possible in the tetrahedral framework, or the mixtures thereof. Preferably the zeolite is type A.

The number of cation exchange sites is the highest in these zeolites rendering them highly selective for polar or zable molecules.

In r embodiment the zeolite is selected from zeolites defined by their CA8 numbers of 1344-00—9, 13181 and/or1318-02—1.

Preferably, the e according to the present invention has a low moisture con- tent of less than 25% by weight, more preferably less than 10%, most preferably less than 7 %, such as less than 5 %, or even 4% or less. The zeolite may be dried, preferably overdried, before subjecting it to monocarboxylic acid treatment.

According to one embodiment zeolite A 4 having a pore size of 4 A is preferred.

Especially, the combination of overdried zeolite A4 treated with concentrated for- mic acid was found to exhibit an excellent performance.

The ratio of monocarboxylic acid to zeolite is preferably from 5 to 4O % by .

The ratio is to some extent dependent on the quality of the acid used. For formic acid the more preferred ratio is from 7 to 30 °/o, most preferably from 8 to 28 °/o, such as from 10 to 25 %. The characteristic smell of formic acid becomes clearly evident when the ratio exceeds 40% by weight.

For acetic acid and glycolic acid the more preferred ratio is from 7 to 35 °/o, most preferably from 10 to 34 %, such as from 13 to 33 %. ebly, the zeolites and the impregnated zeolites used according to the pre— sent invention do not include any heavy metals or toxic metals such as chrome.

The tanning agent composition comprising the rboxylic acid d zeolite may further comprise ning . These co-tanning agents include inorgan- ic salts enhancing the required pH behaviour of the composition in aqueous tan- ning stage. These solid state salts comprise pH buffering salts, ably metal sulphates, more preferably aluminium sulphate. Aluminium sulphate forms sul- phuric acid upon dissolution in water and aids in lowering and stabilising the pH.

Furthermore, co-tanning agents may include solid carboxylic acids, preferably cit- PCT/F12012/050933 ric acid, ortophosphoric acid, salicylic acid, lactic acid, maleic acid, tartaric acid or polyaluminium silicate sulphate (PASS). Moreover, organic boosters, preferably glutaraldehyde, glyoxal, tetrakis hydroxymethyl phosphonium sulphate (THPS) or a low molecular weight resin, ably metylol resins, may be used as co-tanning in a preferred embodiment the tanning agent composition further comprises aluminium te. The sulphate salt aids in buffering the tanning solution and re— sults in ed performance in combination with the rboxylic acid, pref— erably formic acid, treated zeolite. The rise in pH during tanning is delayed and the tanning procedure is more controlled when using sulphate salt addition. The hide becomes tanned to the core and the g is more efficient. The tanning effect will be restricted to the hide surface it mere zeolite is used without the monocar- boxylic acid and/or aluminium salts and/or polycarboxylic acids, and the core will become inflexible and unyielding. Despite of the on of a sulphate salt and polycarboxylic acids monocarboxylic acid impregnation is required.

Most preferably the composition according to the present invention is formulated into a dual component system. This means that there are at least two sequential additions of tanning agent compositions comprising the zeolite contacted with con- centrated formic acid, as described above. At least one of the dual component system compounds to be added further comprises additional aluminium ) and polycarboxylic acid(s). The dual ent system preferably ses a more acidic compound and a less acidic compound.

A preferred more acidic dual component system compound comprises the follow- ing formulations based on components i, ii and iii: i. Aluminium sulfate from 40% to 70% by weight, preferably from 45% to 60%, more preferably from 50% to 55% ii. Formic acid contacted zeolite from 30% to 60% by weight, preferably from % to 50%, more preferably from 40% to 45% iii. Citric acid up to 12% by weight, preferably from 2% to 8%, more preferably from 3% to 5%.

A preferred less acidic dual component system compound comprises the following formulations based on components i, ii and iii: W0 2013/045764 PCT/F12012/050933 i. Aluminium sulfate up to 20% by weight, preferably up to 10%, more prefera- bly up to 5% ii. Formic acid ted zeolite more than 70% by weight, preferably more than 80%, more preferably more than 90% iii. Citric acid up to 12% by weight, preferably up to 8%, more ably up to Another possible less acidic dual component system compound is the basic formic acid contacted zeolite, as such.

The use of the dual component system enables a particularly thorough tanning mance throughout the hide cross section and superior final leather quality.

Furthermore, the tanning action is completely nous throughout the leather.

The composition of the present invention is preferably essentially ess. lt preferably exhibits a pH of from 3.5 to 7,5, more preferably from 3.8 to 6.8 when 1 % by weight of the composition according to the present invention is dispersed in water.

The appearance of the material is a solid powder, and it has preferable the same flowability as the zeolite used as precursor i.e. the treatment according to the in- vention does not degrade the handling properties. The solid appearance provides ng advantage compared to e.g. liquid tanning agents. The tanning agent of 2O the present invention has good solubility in acidic aqueous solutions, especially at pH of about 2.5 - 3.5 which is the l pH for g.

The addition of the composition according to the present invention into an aqueous tanning hide solution of pH from 2.5—3.5, preferably about 3, will provide self- buffering of the pH to a value of from 3.8 to 5.5, preferably from 4 to 5, more pref~ erably from 4.2 to 4.8 when dispersed into the tanning bath.

The composition according to the present ion has been found environmen- tally cial eg. in tanning solutions as it simplifies the g process while retaining an overall affordable sing. Furthermore, this composition may ab- sorb further liquids such as free formic acid, aldehyde, metyloi resins, and the like, that are known to be beneficial in tanning and leather finishing processes.

The composition of the present invention suitable for use as a tanning agent has the advantage that it can directly replace the chrome tanning agent typically used W0 2013/‘045764 PCT/F12012/050933 in the hide manufacturing process. No substantial changes into the process flow chart are required. In a typical mineral tanning process the hide is pickled with formic acid containing solution at a pH from 2.5 to 3.5 before addition of the tan— ning agent. This necessitates the use of a sodium formate buffer for buffering the solution, and a slow acting base such as ium oxide or sodium bicarbonate for basification in order to achieve the final pH higher than 4 for completing the g. The tanning agent of the present invention already contains the . it dissolves at the pH from 2.5 to 3.5into formic acid pickle and self—basifies to pH higher than 4 in about 8 h. The use of the nd of the present invention thus removes the need for a separate buffering and/or basifying, as well. in a preferred embodiment the composition of the t invention comprises ze- olite, preferably zeolite having a Si to Al ratio from 0.7 to 2.5, more preferably A4 zeolite, treated with concentrated formic acid, ably the concentration of the acid is more than 84 °/o by weight, more preferably 90 °/o or more, most preferably 95 % or more, such as 99% and having the zeolite structure still intact; an acidic salt, preferably metal sulphate salt, more preferably aluminium sulphate salt; solid additional carboxylic acid, preferably citric acid; and is in a form of a powdery solid having a moisture content less than 25 % by weight. In this composition the amount of formic acid treated zeolite is preferably from 38 to 46 % by , more ably from 39 to 45 % by weight. The amount of acidic salt is preferably from 50 to 62 % by weight, and the amount of solid additional ylic acid is from O to 8 % by weight.

In a yet red embodiment the composition of the present invention comprises zeolite having a Si to Al ratio from 0.7 to 2.5 treated with concentrated formic acid, preferably the concentration of the acid being more 95 % and having the zeolite structure still intact; aluminium sulphate salt; citric acid; and is in a form of a pow- dery solid having a moisture content less than 25 % by weight wherein the amount of zeolite is from 34 to 39 % by weight, the amount of formic acid (calculated as 99%) is from 1 to 6 %, the amount of aluminium sulphate (including crystal water) is from 51 to 61 % by weight and the amount of citric acid is from 0 to 8 % by weight. The use of this type of composition results in a final pH of the tanning pro- cess to be from 3.8 to 4.8, preferably from 3.9 to 4.7, most preferably from 4.0 to 4.6.

In a yet preferred ment the composition of the present invention comprises zeolite having a Si to Al ratio from 0.7 to 2.5 treated with concentrated formic acid, preferably the concentration of the acid being 99 % by weight and having the zeo- PCT/F12012/050933 lite structure still ; aluminium sulphate salt; citric acid; and is in a form of a powdery solid having a moisture content less than 25 % by weight wherein the amount of zeolite is from 34 to 39 % by weight, the amount of formic acid (calcu- lated as 99%) is from i to 6 %, the amount of aluminium sulphate (including crys- tal water) is from 51 to 61 % by weight and the amount of citric acid is from O to 4 % by weight, preferable from 0.1 to 4 % by weight. The use of this type of compo- sition results in a final pH of the tanning process to be from 4.0 to 4.6. The final pH in this range s the quality of the sed leather. The shrinkage tempera- ture is high, preferably above 75 9C, the resulting hide is especially soft and the physical strength of the hide was found to be excellent at the same time as the preferred colour hue remains white after the tanning treatment. This provides op— timal leather quality for demanding applications. Depending on the thickness and post tanning, the strength and softness of the r are close to those values that are normally obtained with leathers that are produced with basic chrome sul- phate.

The composition pH may further be adjusted by addition of a metal oxide, such as magnesium oxide, if necessary.

In the second aspect of the present invention a method for manufacturing a com- position suitable for eg. leather tanning is ed. In this method zeolite is first 2O introduced into a r, or another vessel suitable for withstanding the ed treatment conditions. The provided e is kept in motion while concentrated monocarboxylic acid is introduced onto the zeolite residing inside the reactor.

It is essential to introduce the acid in a spray form i.e. slowly and uniformly enough to ensure that a nous solid powdery ition is obtained and main— tained, similar to the original zeolite powder, and aneously the temperature of this mixture is controlled. The temperature of the mixture should stay low enough, at a critical value of 50 9C, preferably below 50 °C, to avoid unwanted re- actions to take place as the treatment of the monocarboxylic acid with the zeolite is exothermic. Such unwanted reactions originate from heat peaks, and additional- ly, too high temperature causes volatilization of the acid. ed reactions may comprise degradation of the zeolite structure such as decomposition, sed effect of acid loading, formation of hard particles or other undesired or detrimental side effects.

By the term spray is meant a small droplet size atomised liquid flow. A spray is generally taken to mean a dynamic collection of drops dispersed in gas. The pro- WO 45764 PCT/F12012/050933 cess of forming a spray is called atomisation. A spray nozzle is typically used to generate a spray. The main characteristic of a spray is to distribute the material over a specified cross section and to generate a liquid surface area. A man skilled in the art is able to select the most appropriate spray technology depending on the reactor configuration.

Preferably, a suitable spray is provided by a nozzle atomizer capable of injecting a ing spray with a small droplet size, ably in the range from 0.01 to 1 mm diameter. The mass transfer rate of the acid may be adjusted by measuring the temperature of the resulting zeolite-acid e and setting the mass transfer rate into a value wherein this temperature is still below the critical value. Spraying may be performed continuously or discontinuously.

The e needs to be in motion inside the reactor. Preferably, this motion is vig- orous enough in order to ensure good uniformity for the acid contact and to avoid generation of local hot spots. A preferred option is to use a drum reactor or the like wherein the rotation speed may be adjusted according to the mixing needs. A skilled person is able to optimize the mixing to maintain a uniform ature be- low the critical value.

In a preferred embodiment the r is equipped with a cooling system to ensure that the temperature of the mixture is maintained below the al temperature.

More preferably, a drum reactor with a cooling casing or jacket is ed. There are several other commercially available options for cooling in a reactor set up suitable for the present use which may be applicable and within the ise of a skilled person. in a preferred embodiment the amount of the monocarboxylic acids sprayed onto the zeolite is within the ratio of from 5 to 50 "/0 by weight, more preferably from 7 to %, most preferably from 10 to 30 %. The pore size and amount of the zeolite may cause some variation on the desired outcome.

In a red embodiment the ratio of Si to Al in the zeolite is from 0.7 to 2.5.

Preferably, the ratio is from 0.7 to 1.2, and more preferably from 0.7 to 1.1 such as from 0.9 to 1.1 or very close to unity.

In a further preferred embodiment concentrated formic acid, most preferably 99% by weight formic acid, is sprayed onto zeolite, preferably a basic zeolite of type A or X. The critical temperature in this case is 50 °C, preferably 45 °C, most prefera- bly 35 °C such as 30 °C.

PCT/F12012/050933 In another preferred ment concentrated acetic acid, preferably 99% by weight acetic acid, is sprayed onto zeolite, preferably a basic zeolite of type A or X. The critical temperature in this case is 50 °C, preferably 45 °C, most preferably °C such as 30 °C.

In another preferred embodiment concentrated glycolic acid, preferably 75% by weight glycolic acid, is sprayed onto zeolite, preferably a basic zeolite of type A or X. The critical temperature in this case is 50 °C, preferably 45 °C, most preferably °C such as 30 °C.

In yet another preferred ment concentrated propionic acid, preferably 99% by weight propionic acid, is sprayed onto zeolite, preferably a basic zeolite of type A or X. The critical temperature in this case is 50 °C, preferably 45 °C, most pref- erably 35 °C such as 30 °C.

When all the monocarboxylic acid is dosed into the reactor the reaction is com- pleted. After cooling down to room temperature the product is ready. The product has a shelf life of at least l months, possibly years.

In a preferred embodiment metal sulphate, preferably aluminium sulphate, and op- tionally polycarboxylic acid, is added into the composition after providing the zeo- lite with the monocarboxyiic acid. This addition aids in preserving or even ng the final temperature of the ition which tends to increase due to the exo— thermic reaction between the e and the monocarboxylic acid.

In a preferred embodiment of the present ion the method comprises provid- ing zeolite having a Si to Al ratio from 0.7 to 2.5 into a reactor and keeping said zeolite in motion while introducing concentrated monocarboxylic acid, the concen— tration thereof being more than 95% by weight, thereto provided that the mean temperature of the resulting composition is maintained at a temperature of 45°C or below, preferably 40°C or below, more preferably 35°C or below . After the formic acid treatment of zeolite metal salt, preferably aluminium sulphate, and ally solid ylic acid, preferably citric acid, are introduced into the reactor with ad- ditional mixing. Preferably, the ratio of ium sulphate to formic acid treated zeolite if from 1.1 to 1.6. The ratio of citric acid to formic acid treated zeolite is preferably up to 0.15, preferably up to 0.12.

In the third aspect of the present invention the use of the ition for leather treatment is ed. This treatment is preferably tanning the hide.

WO 2013045764 PCT/F12012/050933 In the fourth aspect of the present invention a method for producing tanned leather using the composition according to the present invention is provided. The method comprises the steps of deliming, bating, optional washing and ng the hide.

Subsequently, the hide is subjected to g preferably at a temperature from 25 to 35 9C, more preferably from 26 to 30 9C, using the tanning agent composition according to the t invention and depickling.

In a preferred embodiment the hide is subjected to a multiple tanning sequence, preferably using the dual component system compound. The hide is first tanned with part of the tanning agent which is preferably the more acidic dual ent system compound, for a desired running time, preferably from 30 min to 180 min, and the treatment is repeated with at least one further running time, preferably us ing the less acidic dual ent system compound. This processing scheme is r illustrated in table 2.

In one embodiment when the hide has been pre-treated by deliming and bating and it has passed the pickling stage having a typical pH of about 2.5 — 3.5 it is subjected to tanning. At this stage the composition of the present ion is added into the hide tanning vessel comprising an aqueous solution which is mainly water, preferably in an amount ranging from 5 to 20 % by weight of the hide mass, ably from 4 to 15 %. The tanning compound is added and tanning is carried out. uently, the hides are removed from the solution and the solution typi— cally becomes waste. in a preferred embodiment the processing sequence comprises (a) a deliming stage; (b) washing the hide; (c) a pickling stage including additions of water, formic acid and sulphuric acid before providing the zeolite tanning agent treated with monocarboxylic acid according to the present invention to the tanning solution.

When using eg. chrome tanning agent the tanning stage further ses addi- tions of further chemicals such as pretanning agents, buffering agents such as metal formates and/or cation agents such as metal bicarbonates. in using the zeolite treated with monocarboxylic acid as the tanning agent the need for these further als becomes redundant.

In a preferred embodiment a final pH aimed at in the tanning process is from 3.8 to .5, preferably from 4.0 to 5.0, most preferably from 4.2 to 4.8. The differences in PCT/F12012/050933 the final pH arise typically from the differences in the acid/base balance of the used formulation. Furthermore, the buffering ty of the applied buffering agent has a further influence in the tanning treatment behaviour of the leather.

This final pH is obtained preferably by using a tanning agent composition compris- ing zeolite having a Si to Al ratio from 0.7 to 2.5 treated with concentrated formic acid, preferably the concentration of the acid being more 95 % and having the zeo- lite structure still intact; ium sulphate salt; citric acid; and being in a form of a powdery solid having a moisture content less than 25 % by weight wherein the amount of zeolite is from 34 to 39 % by weight, the amount of formic acid (calcu- lated as 99%) is from 1 to 6 %, the amount of ium sulphate (including crys- tal water) is from 51 to 61 % by weight and the amount of citric acid is from O to 8 % by weight. The final pH has a clear visual and mechanical effect on the leather quality. The shrinkage temperature is increased, ably above 75 9C, the re— sulting hide is especially soft and the al strength of the hide was found to be excellent. The preferred colour hue still remains whitish after the tanning treatment to this range of final pH. Optimal leather quality is thus provided for demanding applications.

One advantage in using the composition of the present invention as the tanning agent is that the waste solution will be um-free and can be easily exposed of, or even recycled. A further advantage is that the actual hide or r product ating from the tanning process is also totally chrome-free. -free leather is provided having a high shrinkage temperature, Ts, which is higher than 65 °C, preferably higher than 70 °C, more ably higher than 72°C, such as 75 °C, and which does not have a bluish colour hue but a whitish or white one. The chrome-free leather is obtained by the above described tanning method and composition. Preferably the leather product obtained is tanned to the core and provides an especially soft touch sensation.

Moreover, the dyeability of the leather produced by using the tanning ition of the present invention s superior to application of any other presently known tanning agent system. This is evident from a visual observation and evalua- WO 45764 PCT/F12012/050933 tion of the tanned leathers using known tanning agents in direct comparison with the tanning agent of the present invention.

Besides the chromium-free advantage of the g waste water solutions of the present invention the waste water of superior COD (Chemical Oxidation Demand) value is provided. As an example, after application of the first tanning step on bo- vine hides COD values like 9300 mg/l are obtained for chromium sulphate, 32550 mg/I for glutaraldehyde and merely 3800 mg/l for the tanning agent waste solution of the present invention.

By shrinkage ature, Ts, is meant a temperature measured according to ASTIVI D6076 — 08 Standard Test which method is designed to determine the tem— perature at which a ghly wetted leather specimen experiences shrinkage.

Shrinkage occurs as a result of hydrothermal denaturation of the collagen protein molecules which make up the fiber ure of the leather. The shrinkage temper- ature of leather is influenced by many different factors, most of which appear to af~ fect the number and nature of crosslinking interactions between adjacent polypep- tide chains of the collagen protein molecules. The value of the shrinkage tempera- ture of r is commonly used as an indicator of the type of tannage or the de- gree of tannage, or both. In the present ion Ts is the temperature at which a thoroughly wetted leather experiences shrinkage. 2O In the fifth aspect of the present invention the uses of the r manufactured by the method the present invention are ed. The excellent leather quality ob- tained based on the use of the tanning composition as described above enables the use of thus treated leather for demanding application. In a preferred a— tion the produced leather is used for manufacturing shoes, upholstery, automotive and garments or accessories. In these applications it is especially advantageous to use leather which is tanned homogenously and throughout the whole hide ess.

The invention is further illustrated by the ing non-limiting examples.

Examples 2012/050933 Example 1 A powdery, overdried Zeolite A4 having Na:Si:Ai ratio of 1:121 (from Industrial Chemicals Limited) was added into a turbulent mixer (Lbdige VT(A) 300 paddle dryer) equipped with a cooling system. Concentrated formic acid, 99% by weight (Kemira Chemicals), was sprayed on the zeolite slowly and continuously while mixing the resulting composition vigorously. The contacting was completed when all formic acid was introduced into the mixture.

The following formic acid to zeolite ratios in weight °/o were tested: Sample A: 1:3 i.e. 24.5 % by weight formic acid and 75.5 % by weight e; Sample B: 2:3 i.e. 4O % by weight formic acid and 50 % by weight e; Sample C: 3:7 i.e. 30% by weight formic acid and 70 °/o by weight zeolite The formic acid d exothermally with the zeolite. Temperature of the mixture was kept below 50 °C by efficient mixing and external cooling.

Free flowing solid powder was obtained which was free from formic acid smell in test A. Analysis showed that the test sample had 75.5 % by weight of Zeolite 4A and 24.5 % by weight of formic acid. Moreover, the zeolite structure was found to be intact.

Free flowing solid powder was obtained in test C. The sample had a slight acidic smell suggesting the presence of some free formic acid.

Solid powder with some spherical agglomerates was obtained in test B. The sam— ple had a clear acidic smell suggesting the presence of free formic acid.

Example 2 A powdery, overdried Zeolite A4 having Na:Si:Ai ratio of 1:1:1 (from industrial als d) was added into a turbulent mixer (Lodige VT(A) 300 paddle dryer). Concentrated acetic acid, 99% by weight (Kemira Chemicals) was sprayed on the zeolite slowly and continuously while mixing vigorously. Reaction was com- pleted when all acetic acid was introduced into the mixture.

A sample of acetic acid to zeolite ratio of 1:2 i.e. 30 % by weight of acetic acid to 70 % by weight of e was prepared. 2012/050933 The acetic acid reacted exothermally with the zeolite. Temperature of the mixture was kept below 50 °C by efficient mixing and external cooling.

Free flowing solid powder was obtained which was free from acetic acid smell.

Analysis showed that the test sample had 70 °/o by weight of Zeolite 4A and 30 °/o by weight of acetic acid. Moreover, the zeolite structure was found intact.

Example 3 The product A of example 1 was introduced into pure water in concentration of 1 "/0 by weight. A white slurry was formed having pH of 5.86.

When this product was introduced into pure water in a concentration of 10 % by weight a clearly white slurry was formed having pH of 5.78.

Example 4 Samples D and E were ed the same way as in example 1 with the differ- ence that the ratio of formic acid to zeolite was D: 24% to 76 % by weight E: 36 % to 64 % by weight The samples were sieved to a particle size of below 125 um. Two aqueous solu- tions were prepared by adjusting the pH thereof into 2.5 by addition of concentrat- ed formic acid. uently, samples D and E were gradually introduced into these ons in increments of about 0.08 g.

PCT/F12012/050933 Table 1 shows the results obtained.

Cumulative pH in pH in E- remarks amount of D D- solution or E in g solution 0 2.49 2.46 no remarks 0.07 2.97 2.94 white at start but s clear 0.13 3.33 3.22 white at start but becomes clear 0.24 3.77 3.52 white at start but becomes quite clear (little haze) 0.32 4.01 3.66 white at start but becomes clear (little haze) af- ter a longer waiting period 0,41 4.11 3.81 white at start but becomes clear e haze) af— ter a long waiting period Example 5 Bovine hides were tanned in the conventional chrome tanning way using 1) chrome tanning agent (808) as a reference process, and 2) zeolite treated with formic acid prepared according to example 1 with the ra- tio of formic acid to zeolite 13 % by weight formic acid and 87 % by weight In the first chrome process a shrinkage temperature of 95 °C was obtained for the finished leather and in the second process with formic acid treated zeolite a tem- perature of 75 °C. The colour of the leather from the first chrome process was clearly bluish in comparison to the white colour of the r from in the second process.

WO 2013045764 PCT/F12012/050933 Example 6 Three samples F, G and H were made according to example 1 with the exceptions of using 25 kg of zeolite and Sample F: 13 % by weight formic acid (3.8 kg) and 87 % e Sample G: 25 % by weight formic acid (7.9 kg) and 75 % zeolite Sample H: 7.8 % by weight formic acid (3.8 kg) and 40 % aluminium sulphate (19.1 kg, below 280 um particle size) and 52.2% zeolite.

Zeolite was first cooled to 20 °C and formic acid was d into the mixer whereby the temperature inside the mixer was kept below 45 °C. Aluminum sul- phate was added after the formic acid feed. The formed mixtures were mixed fur— ther for half an hour.

It was found that adding aluminium sulphate resulted in decreasing the pH when the obtained solid powder was dispersed in water. A 1% by weight solution in wa- ter of sample H gave pH of 4.31 and for a 10 % by weight solution the pH was 4.39 whereas sample and G provided pHs of 5,13 and 4,77, respectively.

A comparison between three Cr-free tanning agents and the tanning agent - ing to the t invention was made. The s sequence depicted in table 2 was used. 2O The used tanning agent samples in the tanning step (X1 and X2) for preparation of tanned hides, were a reference 1, AF-ZS: aluminium mate and zeolite a reference 2, PAF-Z4: basic aluminium formate and zeolite - reference 3, PASS—ZO: basic aluminium sulphate with a silicate stabilizer with zeolite 0 sample according to the present invention similar to example 1: zeolite A4 + 99% formic acid in a weight ratio of 75,5:24,5 zeolite to formic acid.

PCT/F12012/050933 The s scheme for the nce samples 1-3 included ons of the buff— ering agent, Na-bicarbonate, in stage Y1 and Y2 whereas the process scheme for the samples according to the present invention did not include the additions of the buffering agent.

After processing according to the scheme in table 2 the end pHs of all the test solutions were measured to be the same, pH 4. The shrinkage temperatures for the finalized leathers were measured after 2 days of storage.

The shrinkage temperatures for reference 1, reference 2, reference 3 and the sample according to the invention were found to be 64, 58, 62 and 73°C, respec- tively.

These s clearly show the better tanning effect of the formic acid treated zeolite compared to the other chrome-free tanning agents. in on to the higher shrinkage temperature the feel of the leather product was softer than the feel of the reference leather samples.

PCT/F12012/050933 Table 2. --_-- _——- ——--— ——--— ----— -0,5 Nat—bicarbonate 30 0,5 arbonate - 120 pH=7,Tc=42 _ DrainNVash - -Wash 40 Water 3R/MIN - slow rotating drum Water 0)O Drain/Wash - ———-- —m-—-- -——_-- _—--- g/I Additive 1-. remark pickling 100 Water Formic acid (DQ Formic acid 03 C) 0,2 sulphuric acid 180 pH=3 tanning Tanning agent, part X2 Tanning agent, part 180 depickling 1,5 Na-Formate Y1 I'mNa—bicarbonate 00O Y2 Naabicarbonate 240 WO 45764 PCT/F12012/050933 A set of five samples i, J, K, L and M were prepared according to example 1 with the exception of using in Sample l (TT-25): Zeolite and formic acid ratio of 75% to 25 % with the maximum spraying temperature of 45 °C Sample J (TT-36): Zeolite and formic acid ratio of 64% to 36 % with the maximum spraying temperature of 45 °C Sample K (TTA—30): Zeolite and acetic acid ratio of 70% to 30 % with the maxi- mum spraying temperature of 45 °C Sample L (TT—25G): e and formic acid ratio of 75% to 25 % with the maxi- mum spraying temperature of 45 °C and grinding the resulting compound before dispersion.

Sample M (TT-25 AlSulph : Zeolite and formic acid ratio of 75% to 25 % with the maximum spraying temperature of 45 °C and adding further aluminium sul- phate to the composition at a weight ratio of 70 to 30 formic acid treated zeolite to aluminium sulphate.

The pH performance was studied by introducing the samples gradually in 0.08 g intervals into 100 ml of water made acidic (pH 2.5) by formic acid. The pH change resulting from the additions of these s is shown in figure 1.

Example 9 Various tanning agent ition were tested according to the processing scheme of table 2. The processing parameters and the results measured from leather samples are shown in tables 3-5. Tests were made for probing the influ- ence of the tanning agent composition modifications to shrinkage temperatures.

The reference samples include chrome tanning agent (BCS=basic chrome sul- , ammonium ts and aluminium sulphate products. The samples ac- cording to the present invention include formic acid and acetic acid d zeolite A4 with no or further additions of orthophosphoric acid, citric acid and TH PS (Fen- nocide). The treated leather was bovine hides (ZlG).

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PCT/F12012/050933 The s from tables 3-5 show that aluminium based tanning agent chemicals have clearly a lower shrinkage temperatures compared to the compositions ac- cording to the present invention. Furthermore, in using the tanning agents accord- ing to the present invention there was no need to use buffering and/or basifying chemicals such as sodium formate and sodium bicarbonate. The um refer- ence, M has a higher shrinkage temperature compared to the sample according to the present invention but the colour hue of the sample was clearly bluish compared to whitish colour of the other samples.

Example 10 A powdery, overdried Zeolite A4 having Na:Si:Al ratio of 1:1:1 (from industrial Chemicals Limited) was added into a turbulent mixer (Lodige VT(A) 300 paddle dryer) equipped with a g system. trated formic acid, 99% by weight (Kemira Chemicals), was sprayed on the zeolite slowly and continuously while mixing the resulting ition vigorously. The reaction was completed when all formic acid was introduced into the mixture. Aluminium sulphate with 14H20 a) and citric acid (Sigma Aldrich) were introduced into the reactor with fur- ther mixing for half an hour.

The following ratios in weight °/o were tested: Sample A: 8 % citric acid, 52 % aluminium te, 35 % zeolite, 5 % formic acid; Sample B: 4 % citric acid, 52 % ium sulphate, 38 % zeolite, 2 % formic acid; Sample C: O % citric acid, 60 % aluminium sulphate, 35 % zeolite, 5 % formic acid; The formic acid reacted exothermally with the zeolite. Temperature of the mixture was kept below 45 °C by ent mixing and external cooling. Free flowing solid powder was obtained which was free from formic acid smell. The zeolite structure was found to be intact.

Tanning treatment according to table 2 sequence was performed using 4 % of samples A, B and C and additional 4 % of mere formic acid treated zeolite (87 % zeolite and 13 % formic acid). The final pH in the tanning process was for sample A:3.8; sample B: 4.2; and sample C: 4.4. A further test was made by increasing the pH with addition of MgO into 5.2 (sample D) Samples B and C provided leather with high shrinkage temperature. The feel of the leather was especially soft and the physical strength was found to be excellent.

W0 2013I045764 PCT/F12012/050933 The colour hue was whitish. The leather quality of samples A and D were still good but clearly inferior to samples B and C.

Example 11 The bovine hides were first d, bated, washed and pickled as described in example 7, table 2. The hides were washed and tanned at a ature of about 28 QC using the dual tanning agent composition system (X1 and X2). The tanning agent compositions were prepared according to example 10 and they were dual component formulations A and B containing the following components: A: 4 % citric acid, 52 % aluminium sulphate, 44 % zeolite contacted with concen- trated formic acid, and B: 0.1 % citric acid, 0.5 % aluminium sulphate, 99.4 % zeolite contacted with con- centrated formic acid.

After tanning and depickling the hides were washed and dried and subjected to SEM measurements for obtaining the aluminium and silicon contents and distribu- tions from both the flesh side and the grain side ie. the inner part and the outer surface of the hide. The results are provided by the SEM images shown in figure Sample I represents treatment of the hide with 2 % by weight solution of formula— tion A for 90 min g time.

Sample ll represents ent of the hide with 2 "/0 by weight solution of a— tion A for 90 min running time continued by another 90 min treatment with further 2 % by weight solution of formulation A.

Sample I” represents treatment of the hide with 2 °/o by weight solution of formula- tion B for 90 min running time ued by another 90 min treatment with further 2 % by weight solution of formulation B.

The aluminum and silicon are evenly spread in these samples across the whole bovine hide thickness. The amount of Al and Si observed is sed in hides tanned with ation B compared to formulation A.

Example 12 PCT/F12012/050933 The tanning according to e 11 was performed with the exception of using the following dual component system compound formulations: A: 4 % citric acid, 52 % aluminium sulphate, 44 % zeolite contacted with concen- trated formic acid, and B: 100 % zeolite contacted with concentrated formic acid.

The results showed y uniform tanning throughout the hide thickness to ex— ample 10 with a slightly increased amount of Al and Si remaining inside the hide.

Claims (17)

Claims

1. A method for manufacturing a composition suitable for leather tanning comprising zeolite contacted with concentrated rboxyiic acid, wherein said method ses providing zeolite having a Si to Al ratio from 0.7 to 2.5 into a reactor and keeping said zeolite in motion while introducing concentrated monocarboxyiic acid selected from the group of formic acid, acetic acid, propionic acid, glycolic acid, lactic acid and mixtures thereof, the tration thereof being more than 84% by weight, thereto provided that the mean temperature of the resulting composition is maintained at a temperature of 50°C or below.

2. The method ing to claim 1, wherein said uction of concentrated monocarboxyiic acid is by spraying.

3. The method according to claim 1 or 2, wherein the reactor is equipped with a g system.

4. A composition suitable for leather tanning leather, n said composition is in a form of a powdery solid having moisture t less than 25 % by weight comprising zeolite having a Si to Al ratio from 0.7 to 2.5 treated with concentrated monocarboxyiic acid selected from formic acid, glycolic acid or acetic acid, at a temperature of 50 °C or below, the concentration of said monocarboxyiic acid being more than 84% by weight, and having the zeolite structure intact.

5. The composition of claim 4, wherein said monocarboxyiic acid is formic acid.

6. The composition according to claim 4 or 5, wherein the ratio of monocarboxyiic acid to zeolite is from 5 to 40 % by .

7. The composition according to any one of claims 4 to 6, wherein said zeolite is a basic e.

8. The composition according to any one of claims 4 to 7, wherein said composition is a powdery solid having flowability equal to the zeolite before said monocarboxyiic acid treatment.

9. The composition according to any one of claims 4 to 8, wherein the composition further comprises metal sulphate.

10. The composition according to claim 9, wherein the composition further comprises aluminium sulphate.

11. The composition ing to any one of claims 4 to 10, wherein the composition further comprises a rboxylic acid.

12. Use of the composition of any one of claims 4 to 11 for treating leather.

13. The use according to claim 12, n the leather, which is a delimed and bated hide and which has been pickled at pH of 2.5 -— 3.5, is treated by tanning in s solution.

14. Use of the composition of any one of claims 4 to 11 for cturing a chromium-free leather having a shrinkage temperature, Ts, more than 65 °C and wherein the colour of said leather is white.

15. A method for producing tanned leather sing the steps of deliming, bating, optionally washing and pickling the hide, and tanning the hide using the tanning agent composition of claim 4, and depickling.

16. Use of the r produced by the method of claim 15 for manufacturing shoes, upholstery, automotive and garments or accessories.

17. The method of claim 1, substantially as herein described with reference to any one of the Examples and/or