Soil-resistant, stain-resistant coatings and methods of applying on textile or other flexible materials

Patent metadata

Field	Value
Publication number	US-10704191-B2
Application number	US-201515526467-A
Country	US
Kind code	B2
Filing date	Nov 12, 2015
Priority date	Nov 12, 2014
Publication date	Jul 7, 2020
Grant date	Jul 7, 2020

Abstract

A process of fabricating the composition coating may include selecting a textile material substrate, utilizing a sol-gel comprising a silane or silane derivative and metal oxide precursor to coat the substrate, and optionally coating the substrate with a hydrophobic chemical agent and/or other chemical agents to create a surface with nanoscopic or microscopic features. The process may utilize an all solution process or controlled environment for fabricating a composition coating that prevent wetting or staining of a substrate. The composition coatings for treating textile materials improve soil-resistance and stain-resistance of the textile materials. The composition coatings and their use for treating textile materials can also impart water repellency, oil repellency, ease of cleaning stains and removing particulates. In addition, the composite solution may impart additional properties such as physical strength to the textile whilst retaining the original appearance.

First claim

What is claimed is:

1. A method for treating a substrate for improved soil-resistance or stain-resistance, the method comprising:
selecting a substrate to be coated, wherein the substrate is selected from a flexible material;
preparing a composite solution, wherein the composite solution is prepared by mixing at least water, acid, first solvent, base chemical reagent, plasticizer and bonding agent, wherein the composite solution is prepared under acidic condition where pH is equal to or less than 5, and the composite solution is free of microparticles or nanoparticle additives,
wherein further the base chemical reagent is selected from an alkoxysilane, metal oxide precursor, or a combination thereof having a general formula of M(OR) 4 , where M=Si, Al, Ti, In, Sn or Zr, and R comprises hydrogen, a substituted or unsubstituted alkyl,
the plasticizer is selected from an alkoxysilane, metal oxide precursor, or a combination thereof having a general formula of M(OR) 4−x R′ x (M=Si, Al, In, Sn or Ti; x is the integer 1, 2 or 3), where R comprise hydrogen, a substituted or unsubstituted alkyl or derivatives thereof and R′ comprise a substituted or unsubstituted alkyl, a substituted or unsubstituted alkynyl, a substituted or unsubstituted aryl or derivatives thereof, and
the bonding agent is selected from an alkoxysilane, metal oxide precursor, or a combination thereof having a general formula of M(OR) x R′ y R″ z (M=Si, Al, In, Sn or Ti; x is the integer 1, 2 or 3; y is the integer 0, 1 or 2; z is the integer 1, 2 or 3, provided that the sum of x, y and z equals 4), where R comprises hydrogen, a substituted or unsubstituted alkyl or derivatives thereof; R′ comprises hydrogen, a substituted or unsubstituted alkyl or derivatives thereof and R″ comprises a substituted or unsubstituted epoxy or glycidoxy;
utilizing the composite solution to coat the substrate;
drying or curing the substrate to allow a composite coating to form on the substrate providing the improved soil-resistance or stain-resistance, wherein a degree of polymerization of the composite solution is equal to or less than 100; and
coating the substrate with a hydrophobic solution, wherein the hydrophobic solution comprises a hydrophobic chemical agent that contains flourine dissolved in a third solvent.

2. The method of claim 1 , wherein the flexible material is a textile material.

3. The method of claim 1 , wherein the composite solution comprises 3-8 vol. % of the water, 20-30 vol. % of the first solvent, 40-60 vol. % of the base chemical reagent, 15-20 vol. % of the plasticizer, and 5-10 vol. % of the bonding agent.

4. The method of claim 3 further comprising the steps of:
diluting the composite solution further with a second solvent to a final concentration equal to or between 5 to 40 vol. %.

5. The method of claim 4 , wherein the preparation step further comprises stirring the composite solution at an elevated temperature in a range of 50−100° C.

6. The method of claim 5 , wherein the stirring at the elevated temperature is performed for ½ hour to 12 hours.

7. The method of claim 5 , wherein the composite coating formed on the substrate does not change the feel and texture of the substrate before coating.

8. The method of claim 1 , wherein the first solvent is selected from water, methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, ethylene glycol, glycerol acetone, acetonitrile, dioxane, tetrahydrofuran, dimethylformamide, dimethyl sulfoxide or a mixture thereof.

9. The method of claim 1 , wherein the composite solution further comprises a chelating agent, wherein the chelating agent is selected from an alkoxysilane, metal oxide precursor, or a combination thereof having a general formula of M(OR) x R′ y R″ z (M=Si, Al, In, Sn or Ti; x is the integer 1, 2 or 3; y is the integer 0, 1 or 2; z is the integer 1, 2 or 3, provided that the sum of x, y and z equals 4), where R comprises hydrogen, a substituted or unsubstituted alkyl or derivatives thereof; R′ comprises hydrogen, a substituted or unsubstituted alkyl or derivatives thereof and R″ comprises a substituted or unsubstituted alky or alkenyl group comprising from 3 to 20 carbon atoms, or
the chelating agent is selected from an alkoxysilane, metal oxide precursor, or a combination thereof having a general formula of M(OR) x R′ y R″ z (M=Si, Al, In, Sn or Ti; x is the integer 1, 2 or 3; y is the integer 0, 1 or 2; z is the integer 1, 2 or 3, provided that the sum of x, y and z equals 4), where R comprises hydrogen, a substituted or unsubstituted alkyl or derivatives thereof; R′ comprises hydrogen, a substituted or unsubstituted alkyl or derivatives thereof and R″ comprises a substituted or unsubstituted amine (including primary, secondary and tertiary) or thiol.

10. The method of claim 1 , wherein the composite solution further comprises a viscosity modifier selected from an alkylsiloxane in oligomer/co-oligomer form, polymer/co-polymer form, or a combination thereof having a general formula of

where R and R′ can be the same or different and comprise hydrogen, a substituted or unsubstituted alkyl or derivatives thereof.

11. The method of claim 1 , wherein the composite solution further comprises a functional additive that provides UV absorbing or blocking, anti-reflective, anti-abrasion, fire-retardant, conducting, anti-microbial, anti-bacterial, anti-fungal, or pigmentation properties.

12. The method of claim 1 , wherein the hydrophobic chemical agent is selected from a fluoroalkylsilane [CF 3 (CF 2 ) a (CH 2 ) b ] c SiR d X e (where X=Cl, Br, I or other organic leaving groups, R comprise a substituted or unsubstituted alkyl, a substituted or unsubstituted alkenyl, a substituted or unsubstituted alkynyl, a substituted or unsubstituted aryl or derivatives thereof, a is the integer 0, 1, 2, 3 . . . to 20, b is the integer 0, 1, 2, 3 . . . to 10, c is the integer 1, 2, 3, d is the integer 0, 1, 2, 3 and e is the integer 1, 2, 3, provided that the sum of c, d and e equals 4), or
the hydrophobic chemical agent is selected from an alkoxyfluoroalkylsilane [CF 3 (CF 2 ) a (CH 2 ) b ] c SiR d [alkoxy] e (where [alkoxy] comprise methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, or a combination thereof; R comprise a substituted or unsubstituted alkyl, a substituted or unsubstituted alkenyl, a substituted or unsubstituted alkynyl, a substituted or unsubstituted aryl or derivatives thereof, a is the integer 0, 1, 2, 3 . . . to 20, b is the integer 0, 1, 2, 3 . . . to 10, c is the integer 1, 2, 3, d is the integer 0, 1, 2, 3 and e is the integer 1, 2, 3, provided that the sum of c, d and e equals 4.

13. The method of claim 12 , wherein the third solvent is selected from toluene, benzene, xylene, trichloroethylene, 1,2-dichloroethane, dichloromethane, chloroform, carbon tetrachloride, tetrachloroethylene, n-propyl bromide, diethyl ether, acetone, diisopropyl ether, methyl-t-butyl ether, petroleum ethers or petroleum hydrocarbons.

14. The method of claim 12 , wherein the fluoroalkylsilane is selected from trichloro (3,3,3-trifluoropropyl)silane, dichloro-methyl(3,3,3-trifluoropropyl)silane, chloro-dimethyl(3,3,3-trifluoropropyl)silane, trichloro(1H,1H,2H,2H-perfluorobutyl)silane, dichloro-methyl(1H,1H,2H,2H-perfluorobutyl)silane, chloro-dimethyl(1H,1H,2H,2H-perfluorobutyl)silane, trichloro(1H,1H,2H,2H-perfluorohexyl)silane, dichloro-methyl(1H,1H,2H,2H-perfluorohexyl)silane, chloro-dimethyl(1H,1H,2H,2H-perfluorohexyl)silane, trichloro(1H,1H,2H,2H-perfluorooctyl)silane, dichloro-methyl(1H,1H,2H,2H-perfluoroo

Assignees

• Univ Houston System

Inventors

• Curran Seamus
• Liao Kang-Shyang
• Alley Nigel
• Haldar Amrita
• Wang Alexander

Classifications

• D06M2200/05

  Lotus effect · CPC title

• D06M15/657

  containing fluorine · CPC title

• D06M13/503

  without bond between a carbon atom and a metal or a boron, silicon, selenium or tellurium atom · CPC title

• D06M13/50

  with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms · CPC title

• D06M2200/11

  Oleophobic properties · CPC title