Process for making an aminosiloxane polymer nanoemulsion

Patent metadata

Field	Value
Publication number	US-10329387-B2
Application number	US-201515500282-A
Country	US
Kind code	B2
Filing date	Jul 24, 2015
Priority date	Jul 28, 2014
Publication date	Jun 25, 2019
Grant date	Jun 25, 2019

Abstract

Nanoemulsions are prepared by:
a) solubilizing a silicone resin in an organic solvent system to yield a silicone resin solution concentration of about 80% or less, wherein the organic solvent system comprises a single solvent selected from the group consisting of monoalcohols, polyalcohols, ethers of monoalcohols, ethers of polyalcohols, fatty esters, Guerbet alcohols, isoparaffins, naphthols, glycol ethers, provided that the solvent is not diethyleneglycol monobutyl ether; b) mixing the silicone resin solution with an aminosiloxane polymer to obtain an aminosiloxane polymer:silicone resin mixture having ratio of about 20:1; c) allowing the resin mixture to age for at least about 6 hours at ambient temperature; d) adding the resin mixture to a vessel; e) optionally adding with agitation, an additional organic solvent to the resin mixture; f) mixing until homogenous; g) adding a protonating agent; h) additionally adding an aqueous carrier in an amount to produce the desired concentration of emulsion.

First claim

The invention claimed is:

1. A method of making an aqueous nanoemulsion, comprising the steps of, in the order given for steps c) through h):
a) solubilizing a silicone resin in an organic solvent system to yield a silicone resin solution concentration of 80% or less, wherein the organic solvent system comprises a single solvent selected from the group consisting of monoalcohols, polyalcohols, ethers of monoalcohols, ethers of polyalcohols, fatty esters, Guerbet alcohols, isoparaffins, naphthols, glycol ethers, provided that if the solvent is a glycol ether it is not diethyleneglycol monobutyl ether;
b) mixing the silicone resin solution from a) with an aminoalkyl-containing polyorganosiloxane (P) comprising at least 80 mol % of units of the formulae 7, 8, 9 and 10
R 1 2 SiO (4-a-b)/2   (7),

R 1 a R 2 b SiO (4-a-b)/2   (8),

R 3 3 SiO (1/2)   (9),

R 3 2 R 4 SiO (1/2)   (10),

where
a is 0 or 1,
b is 1 or 2,
a+b is 2,
R 1 are monovalent hydrocarbyl radicals having 1-40 carbon atoms, optionally substituted with halogens,
R 2 are either
a) aminoalkyl radicals of the formula 11
—R 5 —NR 6 R 7   (11)

where
R 5 are divalent hydrocarbyl radicals having 1-40 carbon atoms,
R 6 are monovalent hydrocarbyl radicals having 1-40 carbon atoms, H, hydroxymethyl or alkanoyl radicals, and
R 7 are radicals of the formula 12
—(R 8 —NR 6 ) x R 6   (12)

where
x is 0 or an integer from 1 to 40, and
R 8 is a divalent radical of the formula 13
—(CR 9 2 -) y   (13)

where
y is an integer from 1 to 6, and
R 9 are H or a hydrocarbyl radical having 1-40 carbon atoms, or
b) in the formula 11, R 6 and R 7 combine with nitrogen to form a cyclic organic radical having 3 to 8 —CH 2 — units, wherein nonadjacent —CH 2 — units are optionally replaced by —C(═O)—, —NH—, —O— or —S—, units
R 3 are hydrocarbyl radicals having 1-40 carbon atoms, and optionally substituted with halogens,
R 4 are —OR or —OH radicals, and
wherein, in the polyorganosiloxanes (P),
the average ratio of the sum of units of the formulae 7 and 8 to the sum of units of the formulae 9 and 10 is in the range from 0.5 to 500, the average ratio of units 9 to 10 is in the range from 1.86 to 100, and the polyorganosiloxanes (P) have an average amine number of at least 0.01 mequiv/g, to obtain an aminosiloxane polymer:silicone resin mixture having ratio of 20:1;
c) allowing the aminosiloxane polymer:silicone resin mixture to age for at least 6 hours at ambient temperature;
d) introducing or maintaining the aminosiloxane polymer:silicone resin mixture to a vessel;
e) optionally adding with agitation, an additional organic solvent to the aminosiloxane polymer:silicone resin mixture;
f) mixing until homogenous;
g) adding a protonating agent; and
h) adding an aqueous carrier in an amount to produce the aqueous nanoemulsion.

2. A method of making a nanoemulsion of claim 1 , wherein the emulsion contains at most 1 weight percent of surfactant based on the total weight of the nanoemulsion.

3. A method of making an emulsion of claim 1 , wherein the silicone resin comprises at least 80 mol % of units of the formulas 3, 4, 5, 6:
i) R 3 SiO 1/2   (3),

ii) R 2 SiO 2/2   (4),

iii) RSiO 3/2   (5),

iv) SiO 4/2   (6),

in which R is selected from H, —OR 10 , or —OH residues or monovalent hydrocarbon residues with 1 to 40 carbon atoms, optionally substituted with halogens, where at least 20 mol % of the units are units of the formulas 5 and 6, where R 10 is a monovalent hydrocarbon residue with 1 to 10 carbon atoms, and a maximum of 10 wt % of the R residues are —OR and —OH residues.

4. The method of making a nanoemulsion of claim 1 , wherein the protonating agent is a monoprotic or multiprotic, water-soluble or water-insoluble, organic or inorganic acid.

5. The method of making a nanoemulsion of claim 1 , wherein at least one Guerbet alcohol is employed, and the Guerbet alcohol comprises at least one of 2-ethylhexanol, 2-butyl octanol, or 2-hexyl decanol.

6. The method of making a nanoemulsion according to claim 1 , wherein at least one fatty ester is employed, and fatty ester comprises at least one of isopropyl laurate, isopropyl palmitate, isopropyl myristate, isopropyl stearate, isopropyl oleate, or isopropyl linoleate.

7. The method of making a nanoemulsion of claim 1 , wherein at least one glycol ether is a mono-, di-, or triethyleneglycol alkyl ether having ether moieties containing up to 8 carbon atoms, or is a mono-, di-, or tripropyleneglycol alkyl ether having ether moieties containing up to 8 carbon atoms.

8. The method of making a nanoemulsion of claim 1 , wherein at least one silicone resin is an MQ silicone resin, having a ratio of M units to Q units of 0.67:1.

9. The method of making an aqueous nanoemulsion of claim 1 , wherein at least one protonating agent is formic acid, acetic acid, sulphuric acid, phosphoric acid, hydrochloric acid, or citric acid.

10. An aqueous nanoemulsion prepared by the method of claim 1 .

11. The method of claim 1 , wherein no surfactant is present.

12. The method of claim 1 , wherein less than 0.1 wt. % of surfactant is present based on the total weight of the nanoemulsion.

13. The method of claim 1 , wherein emulsified particles of the nanoemulsion have a mean particle size within the range of 20 nm to 750 nm.

14. The method of claim 1 , wherein emulsified particles of the nanoemulsion have a mean particle size within the range of 20 nm to 500 nm.

15. The method of claim 1 , wherein emulsified particles of the nanoemulsion have a mean particle size within the range of 50 nm to 350 nm.

16. The method of claim 1 , wherein the single solvent is selected from the group consisting of monoalcohols, polyalcohols, ethers of monoalcohols, propylene glycol monoethers, dipropylene glycol monoethers, tripropylene glycol monoethers, fatty esters, Guerbet alcohols, isoparaffins, naphthols, and mixtures thereof.

Assignees

• Wacker Chemie Ag

Inventors

• Becker Richard
• Broening Harry William
• Fliter Kristi Lynn
• Merget Markus
• Schuster Stefanie
• Selbertinger Ernst
• Sivik Mark Robert
• Vetter Nicholas David
• Whiting Patrick Brian
• Wimmer Franz

Classifications

• C08J3/07 Primary

  from polymer solutions · CPC title

• C08J2383/08

  containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen · CPC title

• C08J3/03 Primary

  in aqueous media · CPC title

• C08L2201/52

  Aqueous emulsion or latex, e.g. containing polymers of a glass transition temperature (Tg) below 20°C · CPC title

• C08J2483/04

  Polysiloxanes · CPC title