Dissolution and processing of cellulose
The invention relates to a method for dissolving the components of gel forming materials suitable for use in wound care comprising the steps of admixing said components with an ionic liquid. The ionic liquid may be selected from the group of tertiary amine N-oxides, N,N-dimethyl formamide/nitrogen tetroxide mixtures, dimethyl sulphoxide/paraformaldehyde mixtures and solutions of limium chloride in N,N-dimethyl acetamide or N-methyl pyrrolidone.
1. A method for dissolving the components of gel forming materials suitable for use in wound care wherein the components comprise carboxymethylcellulose, the method consisting essentially of the steps of admixing said components with an ionic liquid consisting essentially of a liquid ionic compound which is liquid below 150° C., the liquid ionic compound having:
(i) a cation with a structure selected from:
2. The method as claimed in claim 1 , wherein the carboxymethylcellulose is a carboxymethylcellulose powder.
3. A method for regeneration of chemically modified cellulose that comprises preparing a solution of chemically modified cellulose, wherein the chemically modified cellulose is a carboxymethylcellulose, in an ionic liquid by dissolving the chemically modified cellulose in said ionic liquid; and admixing the solution with a liquid non-solvent for the chemically modified cellulose that is miscible with said ionic liquid, said admixing causes the cellulose and ionic liquid to form solid and liquid phases, wherein the ionic liquid consists essentially of a liquid ionic compound which is liquid below 150° C. and the properties of the dissolved or regenerated carboxymethylcellulose are similar to the properties of the carboxymethylcellulose prior to dissolution, the liquid ionic compound having:
(i) a cation with a structure selected from:
wherein
R 1 and R 2 are independently C 1 -C 6 alkyl or C 1 -C 6 alkoxyalkyl; and
R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 are independently H, C 1 -C 6 alkyl, C 1 -C 6 alkoxyalkyl, or C 1 -C 6 alkoxy; and
(ii) an anion selected from halogen, pseudohalogen, or C 1 -C 6 carboxylate.
4. The method as claimed in claim 3 , wherein the carboxymethylcellulose is a carboxymethylcellulose powder.
5. The method as claimed in claim 1 , wherein the carboxymethylcellulose is processed into a fiber, a nanofiber, a film, a coating, a foam or a sponge.
6. The method as claimed in claim 1 , wherein the carboxymethylcellulose is processed into a fiber.
7. The method as claimed in claim 6 , wherein the carboxymethylcellulose fiber is sodium carboxymethyl cellulose fiber.
8. The method as claimed in claim 7 , wherein the sodium carboxymethyl cellulose fibre has a degree of substitution of at least 0.05 carboxymethyl groups per glucose unit and a tenacity of at least 10 cN/tex.
9. The method as claimed in claim 1 , wherein the carboxymethylcellulose is suitable for use in the treatment of wounds.
10. The method as claimed in claim 3 , wherein the carboxymethylcellulose is processed into a fiber, a nanofiber, a film, a coating, a foam or a sponge.
11. The method as claimed in claim 3 , wherein the carboxymethylcellulose is processed into a fiber.
12. The method as claimed in claim 11 , wherein the carboxymethyl cellulose fibre has a degree of substitution of at least 0.05 carboxymethyl groups per glucose unit and a tenacity of at least 10 cN/tex.
13. The method as claimed in claim 3 , wherein the carboxymethylcellulose is suitable for use in the treatment of wounds.