Dispersing agent

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Reexamination Certificate

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C536S004100, C536S124000, C536S119000, C536S018600, C536S018500

Reexamination Certificate

active

06559301

ABSTRACT:

The invention relates to the use of specific fructan derivatives as a dispersing agent.
Dispersed solid particles usually have the tendency to flocculate and/or to precipitate. A dispersing agent prevents this flocculation and as a result stabilises the dispersion. In addition, a dispersing agent lowers the viscosity of the dispersion. As a result the dispersions can be pumped or processed more easily at higher concentrations of solid particles. This is important both from the technical and from the economic standpoint.
Phosphates and polyphosphates, such as sodium hexametaphosphate, are widely used as inorganic dispersing agents. These inorganic agents have a good dispersing action but have the disadvantage that they are not stable to hydrolysis. As a result, the viscosity of the dispersion will increase in the course of time.
Organic dispersing agents used are polymers and copolymers of acrylic acid and methacrylic acid having a molecular weight of 5,000 to 100,000. For instance, dispersions of more than 50% by weight of solid particles (such as clay particles) with a polyacrylate as dispersing agent are described in WO 95/25146. DE-A 2 700 444 describes the use of copolymers of maleic acid, JP-A-56-115630 that of unsaturated sulphonic acids and EP-A 705 893 that of phosphonocarboxylic acids as dispersing agents or as deflocculants.
The disadvantage of the organic dispersing agents used to date is that they are all based on petrochemical, and thus non-renewable, raw materials. Furthermore, these substances are poorly degradable and/or toxic to surface water or soil. There is therefore a need for organic dispersing agents which score better than the known petrochemical products with regard to these aspects.
It has been found that carboxyl-containing fructans and salts thereof meet this need. These derivatives have a dispersing action for solid substances, in particular pigments, are biodegradable and are non-toxic. The invention therefore relates to a method for the preparation of dispersions and to dispersions obtainable in this way, as described in the appended claims.
In this context fructans are understood to include all oligosaccharides and poly-saccharides which have a majority of anhydrofructose units. The fructans can have a poly-disperse chain length distribution and can be straight-chain or branched. The fructan can contain mainly &bgr;-2,6 bonds, as in levan. Preferably the fructan contains mainly &bgr;-2,1 bonds, as in inulin.
In this context carboxyl-containing fructans are understood to be a derivative of inulin or another fructan that contains 0.3-3 carboxyl groups per anhydrofructose unit. In particular the derivative contains at least 0.8 carboxyl groups per anhydrofructose unit. The carboxyl groups can be present in the form of carboxyalkyl groups, such as carboxymethyl, carboxyethyl, dicarboxymethyl or carboxyethoxycarbonyl groups. These can be obtained by etherification of the fructan in a known manner. The carboxyl groups can also be present in the form of oxidised hydroxymethylene or hydroxymethyl groups. Mixed carboxyfructans can also be used. Preferably, the number of carboxymethyl groups is greater than the number of other carboxyl groups. Carboxymethylinulin (CMI) is the most preferred.
Carboxymethylinulin (CMI) with a DS (degree of substitution) of 0.15-2.5 is disclosed in WO 95/15984 and in the article by Verraest et al. in
JAOCS,
73 (1996) pp. 55-62. It is prepared by reaction of a concentrated solution of inulin with sodium chloroacetate at elevated temperature. Carboxylethylinulin (CEI) is disclosed in WO 96/34017. The oxidation of inulin is, for example, disclosed in WO 91/17189 and WO 95/12619 (C3-C4 oxidation, leading to dicarboxyinulin, DCI) and WO 95/07303 (C6 oxidation). In the case of mixed carboxyl derivatives the inulin can have been first carboxymethylated and then oxidised or (preferably) the other way round.
The carboxyl-containing fructan has an average chain length (=degree of polymerisation, DP) of at least 3, rising to about 1000. Preferably, the average chain length is 6-60 monosaccharide units. The fructan can optionally have been subjected to a reduction treatment beforehand in order to remove reducing groups.
Modified fructan derivatives which according to the invention can be converted to carboxyalkylfructan are, for example, fructans in which the chain length has been enzymatically extended, and fructan hydrolysis products, that is to say fructan derivatives having a shortened chain, and fractionated products having a modified chain length. Fractionation of fructans such as inulin can be effected by, for example, low temperature crystallisation (see WO 94/01849), column chromatography (see WO 94/12541), membrane filtration (see EP-A 440 074 and EP-A 627 490) or selective precipitation with alcohol. Prior hydrolysis to produce shorter fructans can, for example, be effected enzymatically (endo-inulinase), chemically (water and acid) or by heterogeneous catalysis (acid column). Hydroxyalkylated and/or cross-linked fructans also come into consideration for use in the method according to the invention after carboxyalkylation and, if appropriate, oxidation.
The carboxymethylfructan can be used in the form of the purified substance, but use can also be made of the technical grade product obtained directly by carboxymethylation. Specifically, it has been found that any impurities, such as glycolic acid and diglycolic acid, have no adverse effects on the action of the CMI. It is possible to make use of the free acid, but also of a salt, such as the sodium, potassium or ammonium salts.
The solid to be dispersed or suspended can be any solid which is sufficiently chemically inert to be able to be dispersed or suspended in water. The particles are usually inorganic and insoluble in water. Examples are talc, barite, calcium carbonate, mica, kaolin, bentonite and other types of clay, zinc oxide, calcium sulphate, zeolite, carbon, haematite and the like. The carboxyfructans can be used as dispersing agents for soluble or semi-soluble solids.
Dispersions of calcium carbonate and titanium dioxide can be used in paints and other coating compositions. Other widely used pigments which can be dispersed using the carboxyfructans according to the invention are, for example, iron oxide, carbon black and aluminium stearate. The pigment can also be a corrosion-inhibiting pigment, such as red lead, zinc oxide, zinc powder or aluminium powder, citrates and the like. It is also possible to prepare bentonite dispersions, which can be used as softeners in, for example, detergents and weighting materials in drilling muds; Furthermore, the carboxyfructans can be used for a wide variety of dispersions of low viscosity, for coating paper. Pigments which can be used for this purpose are, for example, kaolin, satin white, calcium carbonate and talc. Other uses are e.g. in dispersing mining products.
For rapid dispersion the particle size of the solids is preferably as small as possible, preferably less than 1 mm and in particular between 1 and 50 &mgr;m. The solids concentration is 1-90% by wt based on the total weight of the dispersion. From the economic standpoint, the concentration is at least 30% by wt rising to, for example, 80% by wt.
The carboxyl-containing fructan can first be mixed with the pigment (or other substance to be dispersed or to be suspended) and then added to the water, or it can first be added to the water before the pigment is added with vigorous stirring.
The quantity of carboxyl-containing fructan, in particular CMI, is in general between 0.05 and 10% by wt, in particular between 0.2 and 2% by wt. It is also possible to use mixtures of the carboxyl-containing fructan and other dispersing agents, such as polyacrylates or phosphonates, preferably in a ratio of at least I part carboxyl-containing fructan to one part other agent. The pH of the dispersion system is usually neutral to slightly. alkaline (pH 6-12); the pH is often above 7. If necessary, other solvents, such as alcohols, can be added to the water; however water usual

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