Granted Patent B2

US 6,951,962 · App. 10/121,880 · Granted Oct 4, 2005

Abstract

Claims (71)

1. A water-dispersible oil/grease-sizing and water-sizing agent for cellulosic materials comprising repeating units that are comprised of a polyamine with at least 3 nitrogen atoms in each recurring monomer unit wherein the amino groups are partially or completely substituted by:

a. a cellulose-reactive group which is formed by reaction of the polyamine and at least one reactive chemical which is selected from the group consisting of epi halohydrin, epi organosulfonates, and oxiranes, where the cellulose reactivity is present after reaction with the polyamine or is formed by subsequent reactivation;

b. an oleophobic and hydrophobic fluorochemical group, which is substituted with an alkyl chain which has a hydrophillic group;

wherein additionally, the cellulose-reactive group cross-links the polyamino groups and the M w molecular weight of the agent is 10,000 to 35,000,000 Daltons as measured by Size Exclusion Chromatography relative to a poly(methylmethacrylate) standard.

2. The agent of claim 1 where the polyamine has the structure:

n=1-6,

m=2-1,000,

R 2 , R 3 , R 5 =H, —(CH 2 ) 1-4 H, —(CH 2 CH 2 O) 1-10 H, —CH 2 CH(OH)CH 3 , —CH(CH 3 )CH 2 OH, —CH 2 CO 2 − Met + (Met=group 1 or 2 metal),

R 4 =H, —(CH 2 ) 1-4 H, —(CH 2 CH 2 O) 1-10 H, —CH 2 CH(OH)CH 3 , —CH(CH 3 )CH 2 OH, —CH 2 CO 2 − Met + (Met=group 1 or 2 metal), —(CH 2 ) 1-6 NH 2,1,0 (R 2 ) 0,1,2 ,

where at least two of the R 2 , R 3 , R 4 , or R 5 are H, and

where any two of R 2 , R 4 , and R 5 could be the same carbon chain.

3. The agent of claim 1 where the polyamine is a straight chain, branched or alkylated polyalkyleneimine with primary, secondary, and tertiary amine groups and the molecular weight of the polyamine is from 75 to 32,000 Daltons.

4. The agent of claim 3 where the polyalkyleneimine is selected from a group consisting of diethylenetriamine, triethylenetetraamine, tetraethylenepentamine, dihexamethylenetriamine, and their branched and/or alkylated derivatives.

5. The agent of claim 1 where the reactive chemical is an epihalohydrin or epiorganosulfonate, having the structure:

6. The agent of claim 5 having a ratio of epihalohydrins or epiorganosulfonates to nitrogen atoms on the polyamine of 0.05 to 2.0.

7. The agent of claim 1 where the cellulose-reactive group is a 3-hydroxyazetidinium group.

8. The agent of claim 7 where the 3-hydroxyazetidinium is present in at least 10 mole % relative to the moles of the polyamine as measured by nuclear magnetic resonance spectroscopy.

9. The agent of claim 1 where at least one of the cellulose reactive groups is bound to the polyamine at a nitrogen which was secondary prior to reaction with the reactive chemical.

10. The agent of claim 1 where the fluorochemical portion of the fluorochemical group is further characterized as a monovalent, perfluorinated, alkyl or alkenyl, straight, branched or cyclic organic radical having three to twenty fluorinated carbon atoms, which can be interrupted by divalent oxygen or sulfur atoms.

11. The agent of claim 1 which comprises a polymeric composition having a M w molecular weight of the agent is 10,000 to 35,000,000 Daltons as measured by Size Exclusion Chromatography relative to a poly(methylmethacrylate) standard and having the structure III:

wherein

(M=group 1 or 2 metal), —(CH 2 ) 1-6 NH 2,1,0 (R 8 ) 0,1,2 , where any two of R 8 ,

R 10 , R 11 , or R 12 could be the same carbon chain,

R 7 =H, —CH 2 CH(OH)CH 2 , which can be cross-linked to nitrogen on K or L or M on a different fluro(hydroxyl)alkyl, polyalkyl amino halohydrin or organo sulfonate, where at least one of R 8 , R 9 , R 10 , R 10 , R 12 must be a fluorochemical as denoted by J, and J is selected from

wherein

A=—(CH 2 ) 1-9 —, —CH 2 CHI(CH 2 ) 1-9 BCH 2 —, —CH═CH(CH 2 ) 1-9 BCH 2 —, —(CH 2 ) 1-11 BCH 2 —,—(CH 2 ) 1-2 B(CH 2 ) 1-10 BCH 2 —, where B═O, CO 2 , CO 2 [(CH 2 ) 1-2 O] 1-10 , OCH 2 CO 2 , OCH 2 CO 2 CO 2 [(CH 2 ) 1-2 O] 1-10 , S, SO 2 , SCH 2 CO 2 , C(O)S, SCH 2 C 2 O[(CH 2 ) 1-2 O] 1-10 , S[(CH 2 ) 1-2 O] 1-10 , S(O)NR′, C(S)NR′, S(O)NR′CH 2 CH 2 O, C(O)NR′, OCH 2 C(O)NR′, OPO 3 , NR′, SCH 2 C(O)NR′, —N(R)CH 2 CO 2 , where R′=H, (CH 2 ) 1-6 ;

R=H, —(CH 2 ) 1-6 H:

R F =F(CF 2 ) 4-18 , CF 3 CF(CF 3 )(CF 2 ) 3-5 , CF 3 CF 2 CF(CF 3 )(CF 2 ) 3-5 , H(CF 2 ) 4-18 ,HCF 2 CF(CF 3 )(CF 2 ) 3-5 , HCF 2 CF 2 CF(CF 3 )(CF 2 ) 3-5 , cycloperfluoroalky radicals of the formula C z F (2z-1) where z is an integer having a value of from 4-6 inclusive;

n, p, q, s, t, v, and w are integers,

p=0, 1,

n=1-6

v+q+w+s=3-1000,

q, w, s each may be zero,

t=w+s,

Q=C1 − , Br − , I − , CH 3 C 6 H 4 SO 2 —, CH 3 SO 2 − ,

and K, L and M are randomly distributed along the polyamine and T is a amine on the end of the polyamine chain.

12. The agent of claim 11 wherein the polymeric composition comprises the reaction product of a fluorocarbon substituted polyamine of Structure IV, and the epihalohydrin or epiorganosulfonate:

R 13 , R 14 , R 15 , R 16 , R 17 =J, H,—(CH 2 ) 1-6 H, —(CH 2 CH 2 O) 1-10 H, —CH 2 CH(OH)CH 3 , —CH(CH 3 )CH 2 OH, —CH 2 CO 2 — M + (M=group 1 or 2 metal), —(CH 2 ) 1-6 NH 2,1,0 (R 13 ) 0,1,2 , where any two of R 13 , R 15 , R 16 , or R 17 could be the same carbon chain, and J is selected from

Wherein

R F =F(CF 2 ) 4-18 , CF 3 CF(CF 3 )(CF 2 ) 3-5 , CF 3 CF 2 CF(CF 3 )(CF 2 ) 3-5 , H(CF 2 ) 4-18 , HCF 2 CF(CF 3 )(CF 2 ) 3-5 , HCF 2 CF 2 CF(CF 3 )(CF 2 ) 3-5 , Cycloperfluoroalky radicals of the formula C z F (2z-1) wherein z is an Integer having a value of from 4-6 inclusive;

R=H, —(CH 2 ) 1-6 H;

n, q, s, v, and w are integers,

n=1-6,

v+q+w +s=3-1000

q, w, s each may be zero,

and V, W and Y are randomly distributed along the fluorcheicals-substituted polyamine and U is an amine on the end of the polyamine chain.

where v, n, q, w, and s have the same meaning as in claim 11 .

13. The agent of claim 12 wherein the fluorocarbon substituted polyamine is a fluoroalkyl-hydroxyl-alkylpolyamine.

14. The agent of claim 11 wherein a cellulose reactive group is chemically bound to the fluorocarbon substituted polyamine.

15. The agent of claim 14 wherein the cellulose reactive group is a 3-hydroxyazetidnium and is a chemical reaction product of epihalohydrin or epiorganosulfonate and the fluorocarbon substituted polyamine.

16. The agent of claim 15 where the 3-hydroxyazetidinium is present in at least 10 mole % relative to the moles of the polyamine as measured by nuclear magnetic resonance spectroscopy.

17. The agent of claim 11 where the epihalohydrin is epichlorohydrin.

18. The agent of claim 11 where the M w molecular weight of the agent is from 20,000 to 25,000,000 Daltons as measured by Size Exclusion Chromatography relative to a poly(methylmethacrylate) standard.

19. The agent of claim 11 , wherein A=—CH 2 —,—CH 2 CHI(CH 2 ) 1-9 OCH 2 —, —CH═CH(CH 2 ) 1-9 OCH 2 —, —CH 2 CHI(CH 2 ) 1-8 CO 2 CH 2 —, —CH═CH(CH 2 ) 1-8 CO 2 CH 2 —, —(CH 2 ) 1-11 OCH 2 —, —(CH 2 ) 1-11 SCH 2 —, p=0 or 1, R F =a mixture predominantly consisting of —(CF 2 ) 4-18 F, the number of J groups on a repeating unit-to-nitrogen-atoms on the polyamine has a molar ratio=0.05-0.75, R═CH 3 , H, n=2, 3, 4, or 6, the sum of v, q, w, and s is 3 to 100, R 8-12 ═H or a mix of H and CH 3 , and the ratio of epihalohydrins or epiorganosulfonates to nitrogen atoms on the polyamine of 0.05-2.0.

20. The agent of claim 11 wherein A=—CH 2 -p=1, R F =mixture of consisting predominantly of (CF 2 ) 6-12 F, the number of J groups on a repeating unit-to-nitrogen-atoms on the polyamine has a molar ratio=0.3-0.55, R═H, n=2, the sum of v, q, w, and s is 3 to 6, R 8-12 ═H, with the ratio of epihalohydrins or epiorganosulfonates-nitrogen atoms on the polyamine of 0.33-0.75.

21. A method of preparing the agent of claim 11 comprising reacting a polyamine with one or more fluorinated epoxides or fluorinated halohydrins and one or more epihalohydrins or epiorganosulfonates.

22. The method of claim 21 which comprises reacting sequentially the polyamine with one or more fluorinated epoxides or fluorinated halohydrins resulting in an intermediate product, the fluoroalkyl-hydroxyl alkylpolyamine compound, followed by reacting in a solvent the intermediate product with one or more of epihalohydrin or epiorganosuifonate.

23. The method of claim 22 where the solvent is selected from the group C 1-6 alcohols and diols, acetonitrile, C 3-6 ketones, water and mixtures thereof.

24. The method of claim 22 wherein the solvent has a concentration of solids of from 2 to 75% by weight.

25. The method of claim 22 where the fluoroalkyl-hydroxyl alkylpolyamine compound is dispersed in the solvent prior to reaction.

26. The method of claim 22 where the fluoroalkyl-hydroxyl alkylpolyamine compound is dispersed in the solvent at 40 to 110° C.

27. The method of claim 22 comprising reacting the fluoroalkyl-hydroxyl-alkylpolyamine with the epihalohydrins or epioroanosulfonates in a two stage process, where stage one is at less than 70 C for greater than 30 minutes and stage two is greater than 70 C for more than 30 minutes.

28. The method of claim 22 comprising reacting the fluoroalkyl-hydroxyl-alkylpolyamine with the epihalohydrins or epiorganosulfonates at a pH of 2.5 to 10.5.

29. An oil/grease- and water-sized paper containing agent of claim 1 .

30. An oil/grease- and water-sized paper containing agent of claim 11 .

31. A method of making paper which comprises treating paper with the agent of claim 1 .

32. A method of making paper which comprises treating paper with the agent of claim 11 .

33. A method of making paper which comprises treating paper furnish with the agent of claim 1 .

34. A method of making paper which comprises treating paper furnish with the agent of claim 11 .

35. A aqueous dispersion comprising the agent of claim 1 in water.

36. A aqueous dispersion comprising the agent of claim 11 in water.

Assignments (14)