Destructable fluorinated alkoxysilane surfactants and repellent coatings derived therefrom

• US 5,274,159 A
• Filed: 02/18/1993
• Issued: 12/28/1993
• Est. Priority Date: 02/18/1993
• Status: Expired due to Term

• Current Assignee: Minnesota Mining and Manufacturing Co (3M Company)
• Original Assignee: Minnesota Mining and Manufacturing Co (3M Company)
• Inventors: Jones, Richard R. M., Pellerite, Mark J.
• Primary Examiner(s): PRESCOTT, ARTHUR
• Application Number:
  US08/019,069
• Time in Patent Office: 313 Days
• Field of Search: 556/485, 556/488, 556/400, 556/413, 556/422, 556/427, 556/428, 556/465, 556/482, 252/DIG. 1, 252/47.5, 252/48.4, 252/54, 252/58, 526/243, 526/248, 524/858, 524/860, 524/869, 428/391, 428/411.1, 428/421
• US Class Current: 556/485
• CPC Class Codes: C03C 17/30 with silicon-containing compounds
• CPC Class Codes: C04B 2103/406 non-ionic
• CPC Class Codes: C04B 2111/10 Compositions or ingredients thereof characterised by the absence or the very low content of a specific material
• CPC Class Codes: C04B 2111/203 Oil-proof or grease-repellant materials
• CPC Class Codes: C04B 2111/27 Water resistance, i.e. waterproof or water-repellent materials
• CPC Class Codes: C04B 41/455 the coating or impregnating process including a chemical conversion or reaction
• CPC Class Codes: C04B 41/4944 containing atoms other than carbon, hydrogen, oxygen, silicon, alkali metals or halogens, e.g. N-silyldisilazane: Image
• CPC Class Codes: C07F 7/0838 Compounds with one or more Si-O-Si sequences compounds with a ring containing only alternating Si and O atoms, i.e. cyclosilanes C07F7/21
• CPC Class Codes: C07F 7/1804 Compounds having Si-O-C linkages Si-O-acyl linkages C07F7/1896
• CPC Class Codes: C07F 7/188 by reactions involving the formation of Si-O linkages
• CPC Class Codes: C09K 23/54 Silicon compounds
• CPC Class Codes: D06M 13/513 with at least one carbon-silicon bond
• CPC Class Codes: D06M 15/657 containing fluorine
• CPC Class Codes: Y10S 516/01 Wetting, emulsifying, dispersing, or stabilizing agents
• CPC Class Codes: Y10T 428/31504 Composite [nonstructural laminate]

Abstract

The present invention provides liquid, destructible fluorinated nonionic surfactants that are water-soluble or dispersible, that are useful as stabilizers for emulsions, and that on curing as a layer on a substrate can provide the substrate with an oil- and water-repellent coating that is free of surfactant, the destructible surfactant comprising a fluorocarbylalkoxysilane having at least one polyfluorinated aliphatic group that is both hydrophobic and oleophobic and at least one, preferably two, polyoxyalkylene or other hydrophilic groups which can be cleaved from the hydrophobe by hydrolysis. More particularly, a fluorocarbylalkoxysilane comprises at least one polyfluorinated aliphatic group and at least one polyoxyalkylene group or other hydrophilic group, said fluorocarbylalkoxysilane being destructible by hydrolysis.

The invention further provides an aqueous composition for providing a substrate with an oil and water repellent coating comprising the fluorocarbylalkoxysilane of the invention as well as a process for providing a substrate with an oil and water repellent coating.

Claims

1. A fluorocarbylalkoxysilane surfactant comprising a hydrophilic portion and a hydrophobic portion, said surfactant comprising at least one polyfluorinated aliphatic or polyfluorinated ether group and at least one hydrophilic polyol, polyol ether, or polyoxyalkylene group, said fluorocarbylalkoxysilane being destructible by hydrolysis.

2. The fluorocarbylalkoxysilane according to claim 1 wherein said hydrophilic polyol, polyol ether, or polyoxyalkylene group can be completely or partially cleaved from said hydrophobic portion of said surfactant by hydrolysis and completely or partially condensed to a siloxane.

3. The fluorocarbylalkoxysilane according to claim 1 having a cloud point at a temperature in the range of 0 to 100°

C. when 1 weight percent of said fluorocarbylalkoxysilane is admixed with water.

9. A composition of matter comprising the fluorocarbylsilane and its partial hydrolysis and condensation products according to claim 2 and water.

10. The composition according to claim 9 further comprising at least one hydrocarbylalkoxysilane or halocarbylalkoxysilane having an alkyl or haloalkyl group of 1 to 24 carbon atoms and at least one C₁ to C₄ alkoxy group.

11. The composition according to claim 10 wherein said hydrocarbylalkoxysilane or halocarbylalkoxysilane has the formula

12. The composition according to claim 10 wherein said hydrocarbylalkoxysilane is selected from the group consisting of methyltriethoxysilane, dimethyldiethoxysilane, butyltriethoxysilane, octyltrimethoxysilane, dodecyltriethoxysilane, octadecyltriethoxysilane, phenyltriethoxysilane, the corresponding chlorosubstituted alkylalkoxysilanes, and tetraethoxysilane.

13. The composition according to claim 12 wherein said halocarbylalkoxysilane is selected from the group consisting of chloromethyltriethoxysilane, chlorobutyltriethoxysilane, 3-(2,2,2-trifluoroethoxy)propyltriethoxysilane, 3-(N-ethylperfluorooctylsulfonamido)propyltrimethoxysilane, 3-(perfluorooctylamido)propyltrimethoxysilane, and 3-(perfluoroheptylmethoxy)propyltriethoxysilane.

14. The composition according to claim 9 further comprising an effective amount of a catalyst for hydrolysis and condensation reaction.

15. The composition according to claim 9 which is useful in oil- and water-repellent applications.

16. The cured composition according to claim 2.

17. The cured composition according to claim 9.

18. An article comprising a substrate comprising a layer of the composition according to claim 16.

19. An article comprising a substrate comprising a layer of the composition according to claim 9.

20. A method for preparing an article having oil and water repellant properties comprising the steps:

1) providing an aqueous composition of destructible nonionic surfactant according to claim 1 as described above;

2) coating the substrate with a layer of the composition of step 1 or immersing the substrate into the composition of step 1 for a time sufficient to form an adsorbed layer of the composition on at least a portion of the substrate;

3) drying the coating; and

4) curing the coating.

21. The method according to claim 20 wherein said substrate is selected from the group consisting of a textile, glass, ceramic, metal, concrete, and masonry.

22. The method according to claim 21 wherein said textile is selected from the group consisting of cotton, polyester, acrylic, nylon, polyolefin, wool, and combinations of the foregoing.

23. A method for preparing a destructible fluorinated alkoxysiloxane surfactant according to claim 1 comprising the steps of

reacting a polyoxyalkylene alcohol with a polyfluoroaliphatic halosilane, a polyfluoroaliphatic alkoxysilane, a polyfluoroaliphatic bis(alkoxysilane) or a polyfluoroaliphatic bis(halosilane), to provide a destructible surfactant.

24. The method according to claim 20 further comprising the step of hydrolyzing said destructible surfactant in the presence of a substrate so as to provide a water- and oil-repellent coating on said substrate or to provide oil- and water-repellent particles.

4. The fluorocarbylalkoxysilane according to claim I comprising at least one of the formulae:

##STR19## wherein;

each A is independently

     1) a covalent bond, or

     2) a divalent hydrophilic group (a) having the formula

space="preserve" listing-type="equation">(CHR.sup.2 --CH.sub.2 O).sub.q

in which q is a number having a value of 1 to 40, preferably 2 to 10, R² is hydrogen or methyl, and that at least 70% of R² is hydrogen, or (b) derived from a polyol or its alkyl ether or polyether derivative by removal of one OH and one hydroxyl hydrogen;

B is a divalent organic connecting group joining Si to R_f or R_f¹ that is substantially stable against hydrolysis;

R_f is a monovalent polyfluoroaliphatic group having at least 2 carbon atoms and at least 30 weight percent fluorine;

R_f¹ is a divalent polyfluoroaliphatic group having at least 6 carbon atoms and at least 30 weight percent of fluorine;

R¹ is an alkyl group having 1 to 18 carbon atoms or phenyl;

R² is hydrogen, or methyl, no more than 30% of R² being methyl;

R³ is independently hydrogen or lower alkyl group having I to 4 carbon atoms;

m independently is an integer having a value of 1, 2, or 3;

n independently is zero or an integer having a value of 1 or 2;

m+n has a sum total value of 1, 2, or 3;

with the provisos that at least one of A is a divalent hydrophilic group as previously disclosed and that the balance of R_f or R_f¹ groups to said hydrophilic groups is such that a one percent by Weight mixture of the surfactant in water has a cloud point in the range of 0°

C. to 100°

C.

5. The fluorocarbylalkoxysilane according to claim 4 wherein B comprises a divalent connecting group selected from the group consisting of an arylene group,

6. The fluorocarbylalkoxysilane according to claim 4 wherein R_f --B is selected from the group consisting of ##STR21##

7. The fluorocarbylalkoxysilane according to claim 4 wherein R_f is selected from the group consisting of (1) a monovalent straight chain or branched polyfluoroaliphatic group having 2 to 24 carbon atoms, cyclic polyfluoroaliphatic group having 4 to 24 carbon atoms, optionally containing chlorine atoms, or oxygen bonded only to carbon atoms, provided that not more than one atom of either of hydrogen or chlorine is present for every two carbon atoms, or (2) a monovalent polyfluoroalkoxy poly(fluorooxyalkylene) group having a number average molecular weight of 250 to 2,000.

8. The fluorocarbylalkoxysilane according to claim 4 wherein R_f¹ is selected from the group consisting of (1) a divalent straight chain, branched chain, or cyclic polyfluoroaliphatic group having 6 to 24 carbon atoms, optionally containing chlorine atoms, or optionally containing oxygen bonded only to carbon atoms, provided that no more than one atom of either hydrogen or chlorine is present for every two carbon atoms, or (2) a divalent poly(fluorooxyalkylene) group having a number average molecular weight of 300 to 2,000.