Abstract: A cellulose ether that is predominantly substituted in the C3 position of the anhydroglucose unit of the cellulose is described. In an embodiment of the present invention, the partial degree of substitution in the C3 position of the cellulose ether is ?60%, based on the total degree of substitution.

Abstract: A water-soluble, biodegradable hydroxyalkyl cellulose-2-hydroxycarboxylic acid ester is disclosed. The hydroxyalkyl cellulose-2-hydroxycarboxylic acid ester has: (i) a molecular degree of substitution of the hydroxyalkyl group of less than 1.5 (MShydroxyalkyl<1.5); and (ii) a molecular degree of substitution of the 2-hydroxycarboxylic acid group of greater than 0.4 and less than 3 (0.4<MS2-hydroxycarboxylic acid<3). Also described is a method of preparing the hydroxyalkyl cellulose-2-hydroxycarboxylic acid ester, and methods of using it, e.g., as a consistency regulator in at least one of foodstuffs, cosmetics, building materials, paints and strippers.

Abstract: Cellulose ethers with a specific substitution pattern, wherein they are substituted predominantly in the C3 position of the anhydroglucose unit of the cellulose.

Abstract: A cellulose ether that is predominantly substituted in the C3 position of the anhydroglucose unit of the cellulose is described. In an embodiment of the present invention, the partial degree of substitution in the C3 position of the cellulose ether is ≧60%, based on the total degree of substitution. Also described is a process for preparing the cellulose ether of the present invention. The process involves, reacting cellulose, dissolved in N-methylmorpholine-N-oxide monohydrate (NMMNO) and optionally other inert organic solvents, with alkylation reagents. The reaction takes place in the presence of: (i) an insoluble solid phase catalyst, e.g., solid ion exchange resins based on polystyrene having quaternary ammonium groups; (ii) stabilizers, e.g., propyl gallate; and (iii) optionally additional soluble co-catalysts, e.g., trimethylbenzylammonium hydroxide.

Abstract: Samples of commercial cellulose having high crystallinity (>80%) and a degree of polymerization of approximately 1500 were pretreated enzymatically under various conditions with commercial endoglucanases, before the chemical conversion to substituted cellulose derivatives was carried out. The enzymatically pretreated cellulose samples exhibited a significantly higher substitution, up to 222% higher, in comparison with control samples which had been treated with buffer without enzyme. The increase in substitution during the chemical reaction could be observed in the presence of various amounts of alkali, but fell as the amounts of alkali decreased. At the same degree of substitution of the cellulose derivative, the use of cellulose pretreated with endoglucanase significantly reduced the amount of alkali required by 60%, as compared with the use of cellulose pretreated only with buffer.

Abstract: The present invention relates to a process for the preparation of branched and/or crosslinked polyamino-ethers in which polyamino-ethers, which are prepared from glycol dichlorohydrins or polyglycol dichlorohydrins and diamines and still contain free chlorohydrin groups, are crosslinked in an essentially aqueous solution under alkaline conditions under the influence of heat.

Abstract: The present invention relates to water-soluble, particularly ternary, preferably ionic, cellulose mixed ethers, more particularly to anionic water-soluble cellulose mixed ethers, as additives for drilling fluid applications.

Abstract: The present invention relates to novel thermoplastic, biodegradable polysaccharide ether esters, such as for example cellulose ether esters or starch ether esters, and to the production of such graft copolymers from polysaccharides, epoxides and dicarboxylic acid anhydrides and to the use thereof, for example as moldings, films or coatings.

Abstract: Superabsorbent polymers based on partly hydrolysed homopolymers and/or copolymers of acrylonitrile which are cross-linked through the incorporation of polyfunctional monomers, wherein 30 to 80 mol-% of the nitrile groups are converted into carboxylate groups, 20 to 70 mol-% of the nitrile groups are converted into carbonamide groups and 0 mol-% to 20 mol-% of the nitrile groups are unchanged, and the said cross-linked polymers possess a swelling capacity of 700 g/g in water and of up to 60 g/g in physiological saline and a gel strength of from 20 g to 100 g, their preparation and their use.

Abstract: Polysaccharides corresponding to formula (I) ##STR1## in which S is a recurrent monosaccharide unit andB is a group of formula (Ia) attached to the monosaccharide unit S by an O atom ##STR2## are prepared by reaction of polysaccharides with an alkyl halide corresponding to formula (II) ##STR3##

Abstract: A method for preparing a chloroethylglucopyranose which comprisesa) reacting glucose with from 2 to 10 times the molar amount of chloroethanol at from 100.degree. to 130.degree. C. in the absence of a catalyst, optionally removing water,b) further reacting the product of step (a) at 60.degree. to 90.degree. C. in the presence of an acidic catalyst for from 10 to 600 minutes andc) Separating therefrom the chloroethylglucopyranose.

Abstract: The invention relates to a process for the production of carbonic acid esters of polysaccharides which is characterized in that polysaccharides are reacted with carbonic acid esters.

Abstract: The present invention relates to novel thermoplastic, water-insoluble cellulose hydroxyalkyl hydroxycarboxylic acid esters of the general structureCell--O--Rwhere Cell--O is the substituted OH group of a polymeric cellulose unit and R is either a monomeric and/or polymeric hydroxyalkylether hydroxycarboxylic acid ester of the structure X:X=--A--B--in which A is a linear polyether chain:A=(--D--O--).sub.nin which D signifies a linear aliphatic branched or unbranched chain with 2 to 11 C atoms and n is a whole number equal to or greater than 1, and B is a linear polyester chain: ##STR1## in which E signifies a linear aliphatic branched or unbranched chain with 2 to 5 C atoms and m is a whole number equal to or greater than 1, or R is equal to A or B or X and a combination thereof in any ratio, or R is equal to H (hydrogen) according to the degree of substitution per anhydroglucose unit (max. 3) with A, B or X, and a process for their production and use of these cellulose derivatives as biodegradable mouldings.

Abstract: The present invention relates to carboxymethylcellulose (CMC) having a lower degree of substitution and to its use in textile printing.

Abstract: New polysaccharides have recurring units I or a salt thereof.

Abstract: The invention relates to certain highly substituted carboxymethyl sulfoethyl cellulose ethers (CMSEC), to a simplified and economic process for their production and to their use as thickeners in textile printing.

Abstract: A method for the preparation of water-soluble, cationic amine polymers by the continuous or batch-wise reaction of a polymer having primary, secondary or tertiary amine functions in its side chain or primary chain as a starting material, wherein the reaction is carried out with an epoxide, a glycidyl ether or a mixture of different epoxides and glycidyl ethers in aqueous solution without additional solvent at a temperature of 30.degree. to 90.degree. C. and at a pH of 8 to 14 within 3 to 30 minutes, the epoxides or glycidyl ethers are added as one batch or in portions, and after adjusting the pH of the aqueous solution of the cationic polymer, which is >13.5 after the reaction with epoxide or glycidyl ether, using a mineral or carboxylic acid, the product solution is obtained without additional work-up steps.

Abstract: The present invention relates to sulphoalkylcellulose derivatives, in particular sulphoethylcellulose, with a degree of substitution by sulphoethyl groups of 1.2 to 2.0 using a one- to three-step, preferably two-step process and the use of the sulphoalkyl-cellulose derivatives as thickening agents or rheology improvers in textile printing.

Abstract: The invention relates to a process for the continuous production of polyacrylonitrile hydrolyzates and to their use as dispersion and grinding aids for pigments and fillers, such as for example kaolin, CaCO.sub.3 or gypsum.

Abstract: The present invention relates to the use of anionic alkyl cellulose mixed ethers, preferably alkyl carboxy-methyl cellulose mixed ethers and, more preferably methyl carboxymethyl cellulose mixed ethers (MCMC), as auxiliaries in the textile industry and preferably as thickeners for textile printing pastes.