Blends of fluoroalkyl-containing ester oligomers with polycarbodiimide(s)

Patent metadata

Field	Value
Publication number	US-9828722-B2
Application number	US-201514638244-A
Country	US
Kind code	B2
Filing date	Mar 4, 2015
Priority date	Jun 8, 2007
Publication date	Nov 28, 2017
Grant date	Nov 28, 2017

Abstract

For imparting enhanced water-repellency and oil-repellency properties to substrates compositions comprising blends of (A) one or more ester oligomers and (B) one or more polycarbodiimides. Also methods for applying such compositions and articles treated with such compositions.

First claim

What is claimed is:

1. A composition comprising a blend comprising:
(A) 50-90 wt-% of one or more oligomers wherein each oligomer comprises (i) at least one fluorine-containing repeatable unit and (ii) at least one fluorine-containing terminal group, and wherein said oligomers comprise the condensation reaction product of:
(a) one or more fluorinated polyols selected from the group of:
R f SO 2 N(CH 2 CH 2 OH) 2 ;
R f SO 2 N(R)CH 2 CH(OH)CH 2 OH; and
R f CON(CH 2 CH 2 OH) 2 ;

wherein:
R f is a perfluoroalkyl group having 1 to 12 carbon atoms, or a perfluoroheteroalkyl group having 3 to about 50 carbon atoms with all perfluorocarbon chains present having 1 to 6 carbon atoms, or mixtures thereof; and
R′ is an alkyl of 1 to 4 carbon atoms;

(b) one or more polyacyl compounds containing a straight chain alkylene group of 14 to 18 carbon atoms; and
(c) one or more monofunctional fluorine-containing compounds comprising a functional group that is reactive with the hydroxyl group of said polyol (a) or with the acyl group of the polyacyl compounds (b); wherein the monofunctional fluorine-containing compound is a compound of the following formula (II):
R f Q′  (II)

wherein:
R f is selected from the group consisting of a perfluoroalkyl group having 1 to 12 carbon atoms, and a perfluoroheteroalkyl group having 3 to 50 carbon atoms with all perfluorocarbon chains present having 6 or fewer carbon atoms; and
Q′ is a moiety comprising a functional group that is reactive with the terminal acyl group of the polyacyl group or terminal hydroxy group of the polyol, wherein the functional group is selected from hydroxyl, oxazolinyl, oxazolonyl, acetyl, acetonyl, carboxyl, isocyanato, epoxy, aziridinyl, thio, ester, and acyl halide groups;

wherein the ratio of component (a) to (b) to (c) is 1:0.5-0.9:0.2-1; and

(B) 10-50 wt-% of one or more polycarbodiimides selected from the group of:
PCD-1: 8 MDI/2 isostearylalcohol/(8 ODA/HDA-HSCH 2 CHOHCH 2 OH);
PCD-2: 4 MDI/isostearylalcohol/(8 iBMA-HSCH 2 CH 2 OH);
PCD-3: 4 MDI/0.5 isostearyl alcohol/0.5 stearylalcohol/(8 iBMA-HSCH 2 CH 2 OH);
PCD-4: 4 MDI/0.5 isostearyl alcohol/0.5 behenyl alcohol/(8 iBMA-HSCH 2 CH 2 OH);
PCD-5: 4 MDI/isostearyl alcohol/(4 ODA-HSCH 2 CH 2 OH);
PCD-6: 5 MDI/glycerol monostearate/2 (4 MMA-HSCH 2 CH 2 OH);
PCD-7: 12 MDI/(4 ODA/HDA-HSCH 2 CH 2 OH)/2 GMS;
PCD-8: 12 MDI/(4 ODA/HDA-MeFBSEA-HSCH 2 CH 2 OH)/2 GMS;
PCD-9: 12 MDI/(2 ODA/HDA-(2 ODI-HEMA)-HSCH 2 CH 2 OH)/2 GMS;
PCD-10: 12 MDI/((4 ODI-HEMA)-HSCH 2 CH 2 OH)/2 GMS;
PCD-11: 12 MDI/isostearylalcohol/(8 ODA/HDA-HSCH 2 CH 2 OH)/2 GMS; and
PCD-12: 12 MDI/isostearylalcohol/(8 ODA/HDA-HSCH 2 CH 2 OH)/4 GMS.

2. The composition of claim 1 wherein said oligomers are of the formula (I):
R f Q[OR 2 O] o [C(O)R 1 C(O)OR 2 O] n [C(O)R 1 C(O)] m T  (I)

wherein:
o is a number from 0 to 1 inclusive;
n is a number from 1 to 10 inclusive;
m is number from 0 to 1 inclusive;
R f is a perfluoroalkyl group having 1 to 6 carbon atoms;
Q is a divalent linking group derived from the one or more monofunctional fluorine-containing compounds of component (c);
R 1 is the same or different polyvalent organic group that is a residue of a polyacyl compound, that is a straight chain alkylene group of 14 to 18 carbon atoms;
R 2 is the same or different divalent organic group that is a residue of the fluorinated polyol (a), at least a portion of which are substituted with or contain one or more perfluoroalkyl groups, perfluoroheteroalkyl groups, or mixtures thereof; and
T is R f Q or a non-fluorine containing monofunctional group capable of reacting with a polyacyl compound or a polyol.

3. The composition of claim 1 wherein said oligomers are of the formula (IIIa):
R f Q[C(O)R 1 C(O)OR 2 O] n [C(O)R 1 C(O)] m QR f   (IIIa)

wherein:
n is a number from 1 to 10 inclusive;
m is 1;
R f is a perfluoroalkyl group having 1 to 6 carbon atoms;
Q is a divalent linking group derived from the one or more monofunctional fluorine-containing compounds of component (c);
R 1 is a straight chain alkylene of 14 to 18 carbon atoms;
R 2 is a polyvalent organic group which is a residue of the fluorinated polyol (a), that is a straight or branched chain alkylene, cycloalkylene, arylene or heteroalkylene group of 1 to 14 carbon atoms, or an arylene group of 6 to 12 carbon atoms wherein at least a portion of R 2 groups comprise one perfluoroalkyl group, perfluoroheteroalkyl group, or mixtures thereof.

4. The composition of claim 1 wherein the oligomer comprises the condensation reaction product of one or more fluorinated polyols, one or more non-fluorinated polyols, one or more polyacyl compound, and one or more monofunctional fluorine-containing compounds.

5. The composition of claim 1 wherein the oligomer comprises the condensation reaction product of one or more fluorinated polyols, an excess amount (relative to the polyol) of one or more linear alkylene diacyl compounds, and sufficient fluorinated monoalcohols to react with the terminal acyl groups.

6. The composition of claim 1 wherein the fluorine containing group of said polyol is a perfluoroalkyl group of 6 or fewer carbon atoms.

7. The composition of claim 1 wherein the fluorine containing group of said polyol is a perfluoroalkyl group of 3 to 5 carbon atoms.

8. The composition of claim 1 wherein the fluorine containing group of said polyol is a perfluorobutyl group.

9. The composition of claim 1 wherein said fluorochemical oligomer further comprises the reaction product of one or more non-fluorinated polyols.

10. The composition of claim 1 further comprising (C) one or more additives selected from the group consisting of siloxanes; acrylate and substituted acrylate polymers and copolymers; fluorinated acrylates; N-methylolacrylamide-containing acrylate polymers; urethanes; blocked isocyanate-containing polymers and oligomers; condensates or precondensates of urea or melamine with formaldehyde; glyoxal resins; condensates of fatty acids with melamine or urea derivatives; condensation of fatty acids with polyamides and their epichlorohydrin adducts; waxes; polyethylene; chlorinated polyethylene; alkyl ketene dimers, esters, and amides; and mixtures thereof.

11. The composition of claim 1 further comprising (C) a solvent.

12. The composition of claim 1 further comprising (C) a melamine-formaldehyde condensate.

13. The composition of claim 1 wherein said composition is an aqueous solution, dispersion, or suspension.

14. An article comprising a substrate having a coating of the composition of claim 1 on one or more surfaces of said substrate.

15. The article of claim 14 wherein the substrate is selected from the group consisting of hard substrates and fibrous substrates.

16. The article of claim 14 wherein the substrate is a laminate.

17. A method of imparting repellency to a substrate comprising the steps of applying the composition of claim 1 onto one or more surfaces of said substrate.

18. The method of claim 17 further comprising curing said composition at ambient or elevated temperatures.

Assignees

• 3M Innovative Properties Co

Inventors

• Jariwala Chetan P
• Elsbernd Cheryl L S
• Butler Thomas M

Classifications

• C08J7/0427

  with only one layer of a composition containing a polymer binder (with more layers C08J7/042) · CPC title

• B05D3/0254

  After-treatment · CPC title

• C09D167/02

  Polyesters derived from dicarboxylic acids and dihydroxy compounds (C09D167/06 takes precedence) · CPC title

• Y10T442/2172

  Also specified as oil repellent · CPC title

• C08G63/682

  containing halogens · CPC title