Hypochlorite free method for preparation of stable carboxylated carbohydrate products
View Patent ↗A method of making a carboxylated carbohydrate is disclosed, cellulose being a preferred carbohydrate material. Carboxylated cellulose fibers can be produced whose fiber strength and degree of polymerization is not significantly sacrificed. The method involves the use of a catalytic amount of a hindered cyclic oxammonium compounds as a primary oxidant and chlorine dioxide as a secondary oxidant in an aqueous environment. The oxammonium compounds may be formed in situ from their corresponding amine, hydroxylamine, or nitroxyl compounds. The oxidized cellulose may be stabilized against D.P. loss and color reversion by further treatment with an oxidant such as sodium chlorite or a chlorine dioxide/hydrogen peroxide mixture. Alternatively it may be treated with a reducing agent such as sodium borohydride. In the case of cellulose the method results in a high percentage of carboxyl groups located at the fiber surface. The product is especially useful as a papermaking fiber where it contributes strength and has a higher attraction for cationic additives. The product is also useful as an additive to recycled fiber to increase strength. The method can be used to improve properties of either virgin or recycled fiber. It does not require high α-cellulose fiber but is suitable for regular market pulps.
1. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxide is 2,2,2′,2′,6,6,6′,6′octa-methyl-4,4′-bipiperidinyl-1,1′-dioxy di-radical, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
2. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxide is 2,2,6,6-tetramethyl-4-hydroxypiperidinyl-1-oxy free radical, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
3. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxide is 2,2,6,6-tetramethyl-4-methoxypiperidinyl-1-oxy free radical, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
4. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxide is 2,2,6,6-tetramethyl-4-benzyloxypiperidinyl-1-oxy free radical, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
5. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxides are compositions having the structure
in which R 1 -R 4 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 1 may together be included in a five or six carbon alicyclic ring structure, and R 6 is hydrogen or C 1 -C 5 alkyl, and R 7 is hydrogen, C 1 -C 5 alkyl, phenyl, carbamoyl, alkyl carbamoyl, phenyl carbamoyl, or C 1 -C 8 acyl, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
6. The method of claim 5 in which the nitroxide is 2,2,6,6-tetramethyl-4-aminopiperidinyl-1-oxy free radical.
7. The method of claim 5 in which the nitroxide is 2,2,6,6-tetramethyl-4-acetylaminopiperidinyl-1-oxy free radical.
8. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxides are compositions having the structure
in which R 1 -R 4 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 4 may together be included in a five or six carbon alicyclic ring structure, and X is oxygen, sulfur, NH, N-alkyl, NOH, or NOR 8 where R 8 is lower alkyl, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
9. The method of claim 8 in which the nitroxide is 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
10. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxides are compositions having the structure
wherein R 1 -R 1 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 4 may be linked into a five or six carbon alicyclic ring structure, X is oxygen, sulfur, -alkyl amino, or acyl amino, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
11. The method of claim 10 in which the nitroxide is 3,3,5,5-tetramethylmorpholine-1-oxy free radical.
12. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxides are compositions having the structure
wherein R 1 -R 4 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 4 may be linked into a five or six carbon alicyclic ring structure, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
13. The method of claim 12 in which the nitroxide is 3,4-dehydro-2,2,6,6,-tetramethylpiperidinyl-1-oxy free radical.
14. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxides are compositions having the structure
wherein R 1 -R 4 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 4 may together be included in a five or six carbon alicyclic ring structure, X is methylene, oxygen, sulfur, or alkylamino, and R 9 and R 10 are one to five carbon alkyl groups and may together be included in a five or six member ring structure which, in turn, may have one to four lower alkyl or hydroxy alkyl substituents, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
15. The method of claim 14 in which each X is oxygen, the oxygen atoms being linked by a two to three carbon alkyl chain to form a cyclic ketal substituent.
16. The method of claim 15 in which the nitroxide composition is the 1,2-ethanediol cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
17. The method of claim 15 in which the nitroxide composition is the 1,3-propanediol cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
18. The method of claim 15 in which the nitroxide composition is the 2,2-dimethyl-1,3-propanediol cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
19. The method of claim 15 in which the nitroxide is the glyceryl cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
20. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting cof hindered heterocyclic oxammonium salts in which the carbon atoms adjacent the oxammonium nitrogen lack .alpha.-hydrogen substitution, the corresponding amines, hydroxylamines, and nitroxides of these oxammonium salts, and mixtures thereof, in which the nitroxides have a five atom ring structure with 2,2,5,5 lower alkyl substitution, and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
21. The method of claim 20 in which the nitroxides are compositions having the structure
in which R 1 -R 4 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 4 may together be included in a five or six carbon alicyclic ring structure, and X may be methylene, sulfur, oxygen, —NH, or NR 11 , in which R 11 is a lower alkyl.
22. The method of claim 21 in which the nitroxide composition is 2,2,5,5-tetramethylpyrrolidinyl-1-oxy free radical.
23. A method of making a carboxylated carbohydrate product which comprises: oxidizing a carbohydrate compound by reacting the carbohydrate in an aqueous system with a sufficient amount of a primary oxidant selected from the group consisting of hindered cyclic nitroxides having the composition
wherein R 1 -R 4 are one to four carbon alkyl groups but R 1 with R 2 and R 3 with R 4 may together be included in a five or six carbon alicyclic ring structure, X is methylene, oxygen, sulfur, or alkylamino, and R 9 and R 10 are one to five carbon alkyl groups and may together be included in a five or six member ring structure which, in turn, may have one to four lower alkyl or hydroxy alkyl substituents; and a secondary oxidant selected from chlorine dioxide and latent sources of chlorine dioxide in a sufficient amount to induce an increase in carboxyl substitution in the carbohydrate of at least 2 meq/100 g.
24. The method of claim 23 in which each X is oxygen, the oxygen atoms being linked by a two to three carbon alkyl chair to form a cyclic ketal substituent.
25. The method of claim 24 in which the nitroxide is the glyceryl cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
26. The method of claim 24 in which the cyclic ketal is selected from the group consisting of the 1,2-ethanediol, 1,3-propanediol, 2,2-dimethyl-1,3-propanediol, and glyceryl ketals of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radicals and mixtures thereof.
27. The method of claim 26 in which the nitroxide composition is the 1,2-ethanediol cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
28. The method of claim 26 in which the nitroxide composition is the 1,3-propanediol cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
29. The method of claim 26 in which the nitroxide composition is the 2,2-dimethyl-1,3-propanediol cyclic ketal of 2,2,6,6-tetramethyl-4-piperidone-1-oxy free radical.
30. The method of claim 23 in which the carbohydrate is a polymeric compound and which further comprises protecting the carbohydrate against degree of polymerization (D.P.) loss by further treating it in aqueous suspension with a stabilizing agent selected from the group consisting of oxidizing agents and reducing agents in order to remove any substituents which tend to cause molecular chain breakage.
31. The method of claim 30 in which the carbohydrate compound is cellulose.
32. The method of claim 31 in which the cellulose is fibrous and is selected from the group consisting of bleached and unbleached kraft wood pulps, prehydrolyzed kraft wood pulps, sulfite wood pups and mixtures thereof.
33. The method of claim 32 in which the cellulose fiber is recycled secondary fiber.
34. The method of claim 31 which further comprises treating the carboxylated cellulose fibers with a tertiary oxidizing agent to stabilize the product by substantially converting any aldehyde substituents to additional carboxyl groups.
35. The method of claim 34 in which the tertiary oxidant is selected from the group consisting of alkali metal chlorites, a chlorine dioxide/hydrogen peroxide mixture, and peracids.
36. The method of claim 35 in which the tertiary oxidant is a mixture of chlorine dioxide and hydrogen peroxide.
37. The method of claim 35 in which the tertiary oxidant is sodium chlorite.