Methods for textile treatment

Patent metadata

Field	Value
Publication number	US-11560670-B2
Application number	US-202016935244-A
Country	US
Kind code	B2
Filing date	Jul 22, 2020
Priority date	Jan 22, 2018
Publication date	Jan 24, 2023
Grant date	Jan 24, 2023

Abstract

There is disclosed a method of coating textile fibers, the method comprising applying, on the external surface of textile fibers, a pre-treated oil-in-water emulsion comprising: (i) an aqueous phase containing water; and (ii) a pre-treated oil phase containing at least one reactive condensation-curable film-forming amino-silicone pre-polymer that, subsequent to condensation curing optionally in presence of additional reactants, forms an amino-silicone coat. The pre-treated reactive oil phase includes at least one pre-treated reactant or pre-treated pre-polymer. An aqueous dispersion containing particles of a hydrophilic polymeric material is then applied to the amino-silicone coat, so as to form a polymeric layer thereon. At least one of the oil-in-water emulsion forming a first coat and of the aqueous dispersion forming a second coat may further contain a plurality of sub-micronic pigment particles dispersed therein. Suitable compositions and kits including the same are also disclosed, as well as fibers coated thereby.

First claim

We claim:

1. A method of coating textile fibers, the method comprising:
(a) providing an oil phase containing at least one reactive condensation-curable film-forming amino-silicone pre-polymer, said oil phase fulfilling at least one of the following:
(i) said at least one reactive condensation-curable film-forming amino-silicone pre-polymer includes at least one reactive condensation-curable film-forming amino-silicone monomer having a molecular weight of at most 1,000 g/mole; and
(ii) said oil phase further contains a non-amino cross-linking agent adapted or selected to cure said at least one reactive condensation-curable film-forming amino-silicone pre-polymer, said non-amino cross-linking agent having a molecular weight of at most 1,000 g/mole;

wherein at least one of said reactive condensation-curable film-forming amino-silicone pre-polymer, said reactive condensation-curable film-forming amino-silicone monomer, said non-amino cross-linking agent, or any one of a silicone oil, an amino-silicone oil and a reactive hydrophobic inorganic filler optionally further comprised therein, is a water-enriched reactant;
the water-enriched reactant having a water content, so as to obtain, following a pre-treatment duration of the oil phase, a pre-treated oil phase having at least 0.01 wt. % and optionally at most 8 wt. % of water by weight of said pre-treated oil phase;
(b) emulsifying said pre-treated oil phase with an aqueous phase, so as to obtain a pre-treated oil-in-water emulsion;
(c) applying, on an external surface of the textile fibers, said pre-treated oil-in-water emulsion; and
(d) after partial condensation curing of said pre-polymer of the pre-treated oil-in-water emulsion has occurred, so as to form an at least partially cured amino-silicone coat on the external surface of the textile fibers, applying on the at least partially cured amino-silicone coat, an aqueous dispersion comprising a plurality of polymeric particles, formed of a hydrophilic polymeric material having neutralized acid moieties, said plurality of polymeric particles being dispersed within said aqueous dispersion, to produce an overlying polymeric layer adhering to an external surface of said amino-silicone coat.

2. A method according to claim 1 , wherein said water-enriched reactant is obtained by adding an aqueous pre-treatment solution to a substantially dry reactant containing less than 1 wt. % of water by weight of dry reactant, said aqueous pre-treatment solution:
a) consisting essentially of distilled water having a pH in the range of 6.5 to 7.5; or
b) further comprising an acid, said acid being optionally a volatile acid, and wherein said aqueous pre-treatment solution optionally has a pH in the range of 0.5 to 2.5.

3. A method according to claim 1 , wherein said pre-treated oil phase is obtained by adding to the oil phase an aqueous pre-treatment solution in an amount of 8 wt. % or less, and optionally 0.01 wt. % or more by weight of the oil phase, said aqueous pre-treatment solution:
a) essentially consisting of distilled water having a pH in the range of 6.5 to 7.5; or
b) further comprising an acid, said acid being optionally a volatile acid, and wherein said aqueous pre-treatment solution optionally has a pH in the range of 0.5 to 2.5.

4. A method according to claim 1 , wherein the pre-treatment duration of the oil phase is of 24 hours or less.

5. A method according to claim 1 , wherein said at least one reactive condensation-curable film-forming amino-silicone pre-polymer has at least one of the following structural features:
a) at least 3 silanol and/or hydrolysable groups (3+SiOH), so as to form a 3-dimensional network;
b) a solubility in water of less than 1% by weight, at 23° C.; and
c) includes reactive groups selected from the group consisting of alkoxy-silane reactive groups, silanol reactive groups and combinations thereof.

6. A method according to claim 1 , wherein said oil phase or said pre-treated oil phase, exclusive of all inorganic content and of any pigment, is devoid of a glass transition temperature.

7. A method according to claim 1 , wherein said partial condensation curing is effected at a temperature of at most 75° C., and optionally, at least 15° C.

8. A method according to claim 1 , wherein said oil-in-water emulsion or pre-treated oil-in-water emulsion has a surface zeta potential greater than zero, or at least +1 mV; and optionally, at most +100 mV, said surface zeta potential being further optionally measured at a native pH of said oil-in-water emulsion.

9. A method according to claim 1 , wherein at a pH of said aqueous dispersion, said oil-in-water emulsion or pre-treated oil-in-water emulsion has a first surface zeta potential (ζ1), and said aqueous dispersion has a second zeta potential (ζ2), wherein a zeta potential differential (Δζ) at said pH is defined as Δζ=ζ1−ζ2, and wherein Δζ, in millivolts (mV), fulfills at least one of the following:
(i) Δζ is at least 10;
(ii) Δζ is within a range of 10 to 80; and
(iii) for said pH being within a range of 4 to 11, said first surface zeta potential (ζ1), is greater than zero (ζ1>0).

10. A method according to claim 1 , further comprising sufficiently converting said hydrophilic polymeric material into a conjugate acid thereof, so as to obtain a hydrophobic polymeric layer.

11. A method according to claim 1 , wherein:
i) at least one of said oil phase or said pre-treated oil phase of the pre-treated oil-in-water emulsion further contains a first pigment, optionally as a plurality of sub-micronic first pigment particles and further optionally contains a first dispersant, said sub-micronic first pigment particles being dispersed within said first dispersant, said first dispersant optionally being in an amount within a range of 25% to 400% by weight of the first pigment; and/or
ii) said plurality of polymeric particles of the aqueous dispersion further contains a second pigment, optionally as a plurality of sub-micronic second pigment particles and further optionally contains a second dispersant, said sub-micronic second pigment particles being dispersed within said second dispersant, said second dispersant optionally being in an amount within a range of 25% to 400% by weight of the second pigment;
the first and second pigment and/or the first and second dispersant being same or different.

12. A method according to claim 1 , wherein the textile fibers are selected from: natural keratinous fibers, natural non-keratinous fibers and synthetic fibers.

Assignees

• Landa Labs 2012 Ltd

Inventors

• Landa Benzion
• Abramovich Sagi

Classifications

• D06P1/54 Primary

  Substances with reactive groups together with crosslinking agents · CPC title

• D06P1/008

  Preparing dyes in situ (D06P1/12, D06P1/145 take precedence) · CPC title

• D06P1/445

  Use of auxiliary substances before, during or after dyeing or printing · CPC title

• D06P5/22

  Effecting variation of dye affinity on textile material by chemical means that react with the fibre {(documents concerning material modified in the mass by compounding with modifying agents affecting the dye affinity after spinning, are not classified here: see the relevant groups C08, D01F, D06P3/00; grafting of monomers on textile materials C08F, D06M11/00)} · CPC title

• D06P1/5292

  containing Si-atoms · CPC title