Fluorine-free fibrous treating compositions including isocyanate-derived ethylenically unsaturated monomer-containing oligomers, and treating methods

Patent metadata

Field	Value
Publication number	US-10294609-B2
Application number	US-201615548196-A
Country	US
Kind code	B2
Filing date	Feb 9, 2016
Priority date	Feb 13, 2015
Publication date	May 21, 2019
Grant date	May 21, 2019

Abstract

A fluorine-free composition includes one or more compounds derived from a reaction mixture that includes: (i) at least one isocyanate-reactive (i.e., functionalized) oligomer comprising 2 to 20 repeating units; (ii) at least one polyisocyanate; (iii) optionally at least one additional isocyanate-reactive compound; and (iv) optionally at least one isocyanate blocking agent; wherein the isocyanate-reactive oligomer is made by the radical-initiated reaction of a reaction mixture comprising at least one mercaptan and Sat least one (meth)acrylate monomer, wherein the at least one (meth)acrylate monomer comprises at least one isocyanate-derived group (e.g., a urethane group or a urea group) and at least one hydrocarbon group having at least 16 carbon atoms (and in some embodiments, up to 60 carbon atoms). Such compositions are useful for treating fibrous substrates to enhance their water-repellency.

First claim

What is claimed is:

1. A fluorine-free treating composition comprising:
one or more compounds derived from a reaction mixture comprising:
(i) at least one isocyanate-reactive oligomer comprising 2 to 20 repeating units;
(ii) at least one polyisocyanate;
(iii) optionally at least one additional isocyanate-reactive compound; and
(iv) optionally at least one isocyanate blocking agent;

wherein the isocyanate-reactive oligomer is made by the radical-initiated reaction of a reaction mixture comprising at least one mercaptan and at least one (meth)acrylate monomer, wherein the at least one (meth)acrylate monomer comprises at least one isocyanate-derived group and at least one hydrocarbon group having at least 16 carbon atoms.

2. The fluorine-free composition of claim 1 wherein the isocyanate-reactive oligomer is made from at least 70 wt-% (meth)acrylate monomers having an isocyanate-reactive group and a hydrocarbon group having at least 16 carbon atoms, based on the total weight of monomers.

3. The fluorine-free composition of claim 1 wherein the mercaptan is non-functionalized or is functionalized with at least one isocyanate-reactive group.

4. The fluorine-free composition of claim 3 wherein the mercaptan is functionalized with at least one alcohol or amine group.

5. The fluorine-free composition of claim 1 wherein the isocyanate-reactive oligomer comprises a blocked isocyanate group.

6. The fluorine-free composition of claim 1 wherein the (meth)acrylate comprising at least one isocyanate-derived group and at least one hydrocarbon group having at least 16 carbon atoms has at least one of the following formulas:
R 1 —NH—C(O)O-L 1 -OC(O)C(R 2 )═CH 2   (Formula I);

R 3 —X 1 —C(O)NH-L 2 -OC(O)C(R 4 )═CH 2   (Formula II); or

R 5 —X 2 —C(O)NH-Q-NH—C(O)O-L 3 -OC(O)C(R 6 )═CH 2   (Formula III);

wherein:
R 1 , R 3 , and R 5 are independently a hydrocarbon group having at least 16 carbon atoms;
R 2 , R 4 , and R 6 are independently H or CH 3 ;
L 1 , L 2 , and L 3 are independently a branched or straight chain alkylene group having 2 to 10 carbon atoms, an arylene group, or a combination thereof;
X 1 and X 2 are independently O, S, —NH, or —N(R 10 ), wherein R 10 is a hydrocarbon group having 1 to 20 carbon atoms; and
Q is a divalent isocyanate residue.

7. The fluorine-free composition of claim 1 wherein the oligomer comprises at least one of the following formulas:
Y 1 —[R 1 —NH—C(O)O-L 1 -OC(O)C(R 2 )—CH 2 ] m —S—R 7 -(T 1 ) p   (Formula IV);

Y 2 —[R 3 —X 1 —C(O)NH-L 2 -OC(O)C(R 4 )CH 2 ] m —S—R 8 -(T 2 ) p   (Formula V); or

Y 3 —[R 5 —X 2 —C(O)NH-Q-NH—C(O)O-L 3 -OC(O)C(R 6 )CH 2 ] m —S—R 9 -(T 3 ) p   (Formula VI);

wherein:
Y 1 , Y 2 , and Y 3 are independently H or an initiator residue;
R 1 , R 3 , and R 5 are independently a hydrocarbon group having at least 16 carbon atoms;
R 2 , R 4 , and R 6 are independently H or CH 3 ;
L 1 , L 2 , and L 3 are independently a branched or straight chain alkylene group having 2 to 10 carbon atoms, an arylene group, or a combination thereof;
X 1 and X 2 are independently O, S, —NH, or —N(R 10 ), wherein R 10 is a hydrocarbon group of 1 to 20 carbon atoms;
Q is a divalent isocyanate residue;
each m is independently an integer of 2 to 20;
R 7 , R 8 , and R 9 are independently a divalent or trivalent linking group having 1 to 10 carbon atoms;
T 1 , T 2 , and T 3 are is independently —OH, —NH 2 , or —NH(R 11 ), wherein R 11 is H a hydrocarbon group having 1 to 10 carbon atoms;
each p is independently 1 or 2; and
S is sulfur.

8. The fluorine-free composition of claim 1 wherein the polyisocyanate is an aliphatic diisocyanate, an aromatic diisocyanate, an aromatic triisocyanate, an aromatic polymeric isocyanate, an aliphatic polymeric isocyanate, or a mixture thereof.

9. The fluorine-free composition of claim 1 further comprising at least one additional isocyanate-reactive monofunctional, difunctional, or polyfunctional compound.

10. The fluorine-free composition of claim 1 wherein the reaction mixture for making the one or more compounds further comprises at least one isocyanate-reactive difunctional compound having the following formula:
H—X 3 —(CH 2 ) r —(Z 1 ) o —(CH 2 ) s —X 4 —H  (Formula VII)

wherein:
X 3 and X 4 are independently O, S, —NH, or —N(R 10 ), wherein R 10 is a hydrocarbon group having 1 to 20 carbon atoms;
r and s are independently integers from 1 to 12;
o is 0 or 1; and
Z 1 is selected from:
a straight chain or branched alkylene group having 1 to 20 carbon atoms;
a divalent polydimethylsiloxane group comprising 2 to 100 dimethylsiloxane repeating units;
a divalent polyoxyalkylene group comprising 2 to 100 alkylene oxide repeating units, wherein each alkyleneoxide repeating unit independently has 2 to 10 carbon atoms; and
a combination thereof.

11. The fluorine-free composition of claim 1 wherein the oligomer is made by the oligomerization of at least one mercaptan with at least one (meth)acrylate monomer comprising at least one isocyanate-derived group and at least one hydrocarbon group having at least 16 carbon atoms, wherein the molar ratio of the mercaptan with the (meth)acrylate is 1:4 to 1:20.

12. The fluorine-free composition of claim 1 wherein the oligomer is made by the oligomerization of at least one mercaptan with at least one (meth)acrylate monomer comprising a urethane group and a hydrocarbon group having at least 16 carbon atoms, wherein the molar ratio of the mercaptan with the (meth)acrylate is 1:4 to 1:20.

13. The fluorine-free composition of claim 1 wherein the oligomer is made by the oligomerization of at least one mercaptan with at least one (meth)acrylate monomer comprising a urea group and a hydrocarbon group having at least 16 carbon atoms, wherein the molar ratio of the mercaptan with the (meth)acrylate is 1:4 to 1:20.

14. The fluorine-free composition of claim 1 wherein the composition is an aqueous dispersion optionally comprising one or more additives selected from a surfactant, a coalescing solvent, an anti-freeze solvent, an emulsifier, and a stabilizer against one or more microorganisms.

15. A method of treating a fibrous substrate comprising applying to the fibrous substrate a composition of claim 1 in an amount sufficient to make the fibrous substrate water repellent.

16. A fibrous substrate treated by the method of claim 15 .

Assignees

• 3M Innovative Properties Co

Inventors

• Dams Rudolf J
• Coppens Dirk M
• Jariwala Chetan P
• Chen Lin

Classifications

• C09D133/00

  Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers · CPC title

• D06M2200/12

  Hydrophobic properties · CPC title

• C08G18/7671

  containing only one alkylene bisphenyl group · CPC title

• C08G18/7621

  being toluene diisocyanate including isomer mixtures · CPC title

• C08G18/8077

  Oximes · CPC title