Use of Cellulose Ethers Having 3-Azido-Hydroxyalkyl Groups in Insoluble Adhesives
AssigneeSE Tylose GmbH & Co. KG
InventorMike KLEINERT
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AssigneeSE Tylose GmbH & Co. KG
InventorMike KLEINERT
Estimating the term…
The invention relates to the use of non-ionic, insoluble cellulose ethers having 3-azido-2-hydroxypropyl (AHP) groups, which are linked to the cellulose via an ether link, wherein the molar substitution degree MSAHP is in the region of 0.001 to 0.30, for the production of insoluble, solid adhesives. The cellulose ethers substituted by AHP groups are reacted in the presence of a copper or ruthenium catalyst with alkine compounds, such as phenylacetylene, propargyl alcohol, propiolic acid or heterocyclic compounds, which have a substituent with a terminal alkine group. The reaction of the azide with the alkine occurs as a 1,3-dipolar cyclcoaddition reaction at room temperature within a few seconds, and an insoluble, solid adhesive is obtained. The adhesive is suitable in particular for adhering paper, cardboard or wood.
Water-insoluble, solid adhesives for adhesively bonding paper, paperboard, wood or other materials based on cellulose or comprising cellulose, said adhesives comprising, nonionic, water-soluble cellulose ethers with 3-azido-2-hydroxypropyl groups, joined to the cellulose via an ether bond, the cellulose having a degree of molar substitution MSAHP being in the range from 0.001 to 0.30, the cellulose ethers being reacted with an alkyne, and catalyzed by a copper compound and/or ruthenium compound.
Dependencies are inferred from the claim text.