Abstract: The invention relates to a method for the production of at least alkylated, non-ionic cellulose ethers, whereby at least 10% of all hydroxy groups contained therein are alkylated and which may flocculate in water, within a temperature range of 45 to 95° C. The invention is characterized in that at least one surfactant in solid, liquid, or solution form is added to the cellulose for production of the cellulose ether.

Abstract: The present invention relates to water-soluble ionic cellulose ethers from the group of the hydroxyalkylcelluloses which are substituted by on average from 0.001 to 1.0 alkyl group per anhydroglucose unit and which carry from 0.01 to 0.1 sulfoalkyl group per anhydroglucose unit, to processes for preparing them and to the use of water-soluble ionic cellulose ethers from the group of the hydroxyalkylcelluloses which are substituted by on average from 0.001 to 1.0 alkyl group per anhydroglucose unit and which carry from 0.01 to 0.4 sulfoalkyl group per anhydroglucose unit as protective colloids in polymerizations.

Abstract: Water-soluble sulfoalkyl-containing hydrophobically modified cellulose ethers, processes for preparing them, and their use in emulsion paints

Abstract: The present invention relates to water-soluble ionic cellulose ethers from the group of the hydroxyalkylcelluloses which are substituted by on average from 0.001 to 1.0 alkyl group per anhydroglucose unit and which carry from 0.01 to 0.1 sulfoalkyl group per anhydroglucose unit, to processes for preparing them and to the use of water-soluble ionic cellulose ethers from the group of the hydroxyalkylcelluloses which are substituted by on average from 0.001 to 1.0 alkyl group per anhydroglucose unit and which carry from 0.01 to 0.4 sulfoalkyl group per anhydroglucose unit as protective colloids in polymerizations.

Abstract: Water-soluble sulfoalkyl-containing hydrophobically modified cellulose ethers, processes for preparing them, and their use as protective colloids in polymerizations

Abstract: Water-soluble sulfoalkyl-containing hydrophobically modified cellulose ethers, processes for preparing them, and their use in emulsion paints The present invention relates to water-soluble ionic cellulose ethers from the group of the hydroxyalkylcelluloses which are substituted by on average from 0.001 to 1.0 alkyl group per anhydroglucose unit and which carry from 0.01 to 0.1 sulfoalkyl group per anhydroglucose unit, to processes for preparing them and to the use of water-soluble ionic cellulose ethers from the group of the hydroxyalkylcelluloses which are substituted by on average from 0.001 to 1.0 alkyl group per anhydroglucose unit and which carry from 0.01 to 0.4 sulfoalkyl group per anhydroglucose unit in emulsion paints.

Abstract: The present invention relates to water-soluble, organosilylated cellulose ethers in which the organosilyl groups are attached hydrolysis-stably to the cellulose ethers and the remaining substituents on the silicon atoms of the organosilyl groups are likewise stable to hydrolysis. The cellulose ethers of the invention exhibit a strongly thickening action in aqueous solution, even at very low degrees of silylation, and are suitable as thickeners, for example, in paints, adhesives, and cosmetics. They are further suitable as protective colloids in the preparation of polymer dispersions.

Abstract: Water-soluble, nonionic cellulose ethers selected from the group consisting of alkylcelluloses and hydroxyalkylcelluloses which are additionally substituted by butenyl groups are used as protective colloids in the preparation of aqueous polymer dispersions.

Abstract: In the process and the apparatus, a gas stream is divided into three partial gas streams. The first partial gas stream transports the material to be ground into the grinding and friction space of a mill (26), while the second partial gas stream runs around the friction space in the mill. The third partial gas stream is connected to the output side of the mill and takes up the reduced and dried ground material, transported out of the mill by the first and second partial gas streams, in order to transport it to a separator (30).

Abstract: Water-soluble, nonionic cellulose ethers selected from the group consisting of alkylcelluloses and hydroxyalkylcelluloses having an average degree of polymerization of less than 900 which is substituted by, on average, from 0.01 to 0.04 2-propenyl groups per anhydroglucose unit are used as protective colloids in the preparation of aqueous polymer dispersions.

Abstract: Low molecular weight cellulose ethers which are suitable as a coating material for solid metered units and as an additive in ceramic compositions or cosmetics formulations or as a polymerization auxiliary are obtained by irradiation of a mixture of a higher molecular weight cellulose ether and a base with electrons.

Abstract: In the process and the apparatus, a gas stream is divided into three partial gas streams. The first partial gas stream transports the material to be ground into the grinding and friction space of a mill (26), while the second partial gas stream runs around the friction space in the mill. The third partial gas stream is connected to the output side of the mill and takes up the reduced and dried ground material, transported out of the mill by the first and second partial gas streams, in order to transport it to a separator (30).

Abstract: Cellulose ethers which contain hydroxyalkyl groups are prepared, with the recovery of sodium hydroxide, by cellulose being etherified with alkylene oxide in a water-containing organic suspension medium in the presence of at least 1.0 mol of sodium hydroxide per mole of anhydroglucose units, the water-containing organic suspension medium being separated off after the etherification reaction is complete, the crude cellulose ether being extracted with a suitable solvent mixture, the lower-boiling organic components being distilled off from the solvent mixture after the extraction, the water-containing organic suspension medium separated off being added to the distillation residue of the solvent mixture to form a multiphase mixture, the bottom phase of the multiphase mixture being separated and the sodium hydroxide present in the bottom phase being reused.

Abstract: Water-soluble polysaccharides which containa) substituents selected from the group consisting of alkyl, hydroxyalkyl, carboxyalkyl and sulfoalkyl,b) N,N-disubstituted aminoalkyl groups,are prepared by alkylation of a polysaccharide in the presence of a base with one or more alkylation reagents, selected from the group consisting of compounds transferring alkyl groups, compounds transferring hydroxyalkyl groups, compounds transferring carboxyalkyl groups and compounds transferring sulfoalkyl groups, and also with an N,N-disubstituted amino-alkylsulfuric acid ester. The modified polysaccharides are used in paper production and waste-water purification and also in cosmetics.

Abstract: Low molecular weight cellulose ethers which are suitable as a coating material for solid metered units and as an additive in ceramic compositions or cosmetics formulations or as a polymerization auxiliary are obtained by irradiation of a mixture of a higher molecular weight cellulose ether and a base with electrons.

Abstract: Process for the preparation of low molecular weight polysaccharide ethers which can be employed in binders for improving adhesive power and film-forming properties, by oxidative degradation of relatively high molecular weight polysaccharide ethers, which comprises initially introducing a relatively high molecular weight polysaccharide ether in suspension (e.g. in a slurry), adding a perborate or a mixture of perborate and perborate activator, and carrying out the oxidative degradation at a temperature of between 25.degree. and 90.degree. C.

Abstract: Disclosed is a compound of the general formula ##STR1## wherein L=H or CO--(R.sup.1).sub.n (CX.sub.3).sub.m, M=alkylene, alkenylene, Q=S, Se, O, dialkylmethylene, alken-1,2-ylene, 1,2-phenylene or N-R, with M+Q together forming 3 or 4 ring members, R=alkyl, aralkyl or alkoxyalkyl, R.sup.1 is an aromatic group and X=Cl, Br or I, with n=O and m=1 or n=1 and m=1 or 2. The compounds, on exposure, eliminate HX and form free radicals and are therefore highly effective as acid donors and free radical initiators for photochemical processes.