Se Tylose Gmbh & Co. Kg

Arbaflame Technology As

Mike Kleinert

Thomas Heinze

Roland Stern

Rune Brusletto

Tim Liebert

Diana Wischang

Marc Kostag

Rudolf Ehrler

The invention relates to a method for producing a low-viscosity cellulose ether product, and to the use thereof.

Oxidative degradation of cellulose ethers

Reversibly crosslinked, water-soluble cellulose ethers having at least two different ether components is disclosed. At least one ether component is an alkyl, hydroxyalkyl or carboxymethyl group and at least one is an alkyl group having an aldehyde function which forms hydrolyzable hemiacetals with free OH groups of the cellulose ether. The cellulose ethers are obtainable by selective oxidation of cellulose ethers containing alkyl groups having vicinal OH groups (glycol cleavage). Preferably, water-soluble cellulose ethers are co-etherified simultaneously or subsequently with 2,3-epoxypropanol (glycidol) or 3-chloro-1,2-propanediol and the 2,3-dihydroxypropyl ether groups converted entirely or partly into 2-oxoethyl ether groups by oxidation. Suitable oxidants include periodate, periodic acid or lead tetraacetate. After washing and drying, cellulose ethers reversibly crosslinked via hemiacetals can be dispersed in water or aqueous solutions, going into solution homogeneously with a time delay. No low molecular weight dialdehydes or other problematical crosslinking reagents are liberated on dissolution.

Reversibly crosslinked cellulose ethers and process for the production thereof by selective oxidation of vicinal OH groups

Nonionic, water-soluble cellulose ethers are disclosed with hydroxyalkyl groups and &#x3c9;-alkynyl groups, each joined to the cellulose via an ether bond, the degree of molar substitution MS(alkyne) being in the range from 0.001 to 0.30. The cellulose ethers may further contain azido groups, preferably 3-azido-2-hydroxypropyl groups, likewise joined to the cellulose by an ether bond, the MS(AHP) being in the range from 0.001 to 0.3. To obtain an adhesive, cellulose ether is mixed with water or, if the cellulose ether contains no alkyne groups, is mixed additionally with a non-ionic cellulose ether containing &#x3c9;-alkyne groups and hydroxyalkyl groups, each bonded to the cellulose by ether bonds. The mixture is applied to at least one of the surfaces to be bonded and then is contacted with a copper(I) catalyst or a ruthenium catalyst. The adhesive is especially suitable for bonding wood, paper, cardboard or other cellulosic material.

Cellulose ethers substituted with hydroxyl and alkyne groups and with hydroxyalkyl, alkyne and azide groups, and use thereof as water-insoluble adhesives

The present invention provides a carbon-enriched biomass material, a method of producing the carbon-enriched biomass material, and a method for using the carbons-enriched biomass material. A lignocellulosic material is used as a starting material and is treated at elevated temperatures under partially oxidizing conditions in a reaction vessel which is isolated from the environment. The carbon enriched biomass can be used in domestic or industrial combustion processes.

Method of producing carbon-enriched biomass material

Non-ionic water-soluble cellulose ethers modified with 3-azido-2-hydroxypropyl groups bound via an ether link are provided having a molar degree of substitution MSin the range from 0.001 to 0.50. Exemplary cellulose ethers are alkyl cell doses, including methyl, hydroxyalkyl (e.g. hydroxyethyl hydroxypropyl) or alkylhydroxyalkyl cellulose (e.g. methylhydroxyethyl). Reaction products with alkyne compounds are also provided, resulting in a terminal alkyne group. The reaction of azide with the alkyne proceeds as a 1,3-dipolar cycloaddition reaction, advantageously with Cu(I) or ruthenium catalysts. A multiplicity of cellulose ethers can be obtained from the conversion reaction. Variations in the macroscopic properties can be achieved by controlled modification, ranging from increased or reduced viscosity. The reaction, taking place within a few seconds, requires only minimal catalyst. Gel formation is reversible by adjustment of the pH such that a monophasic system (high-viscous fluid) arises again from a biphasic system (gel+low-viscous water phase).

Cellulose ethers having reactive anchor group, modified cellulose ethers obtainable therefrom and methods for the preparation thereof

Non-ionic water-soluble cellulose ethers modified with 3-azido-2-hydroxypropyl groups bound via an ether link are provided having a molar degree of substitution MSin the range from 0.001 to 0.50. Exemplary cellulose ethers are alkyl celluloses, including methyl, hydroxyalkyl (e.g. hydroxyethyl or hydroxypropyl) or alkylhydroxyalkyl cellulose (e.g. methylhydroxyethyl). Reaction products with alkyne compounds are also provided, resulting in a terminal alkyne group. The reaction of azide with the alkyne proceeds as a 1,3-dipolar cycloaddition reaction, advantageously with Cu(I) or ruthenium catalysts. A multiplicity of cellulose ethers can be obtained from the conversion reaction. Variations in the macroscopic properties can be achieved by controlled modification, ranging from increased or reduced viscosity. The reaction, taking place within a few seconds, requires only minimal catalyst. Gel formation is reversible by adjustment of the pH such that a monophasic system (high-viscous fluid) arises again from a biphasic system (gel+low-viscous water phase).

Solutions of cellulose or cellulose ethers in solvent containing triethylheptylammonium chloride, triethyloctylammonium chloride, triethylhexylammonium acetate, triethylheptylammonium acetate, triethyloctylammonium acetate, triethylnonylammonium acetate and/or triethyldecylammonium acetate are provided. The solvent may further include up to 70 wt % of at least one organic solvent, with acetone being the preferred organic solvent. The solution can be formed into a paste for removing paint from wood or metal surfaces. The cellulose (ether) solution can also serve as a reaction medium in which the cellulose and/or the cellulose ether are chemically modified. Finally, the cellulose (ether) solution can be processed into cellulosic shaped articles.

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Mainz, Germany

Mike Kleinert