US2004083553A1PendingUtilityA1
Treating textile materials with polyorganosiloxanes
Priority: Oct 5, 2000Filed: Oct 3, 2001Published: May 6, 2004
Est. expiryOct 5, 2020(expired)· nominal 20-yr term from priority
D06M 2200/50D06M 2200/00D06M 2200/25D06M 15/6436
40
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Claims
Abstract
The invention concerns a method for treating textile materials providing said textile materials with a soft feel, absence of yellowing and good hydrophily, which consists in contacting the textile materials with a composition comprising at least a linear, cyclic or three-dimensional polyorganosiloxane of formula (I), wherein: the symbols Z, identical or different, represent R1, and/or V; and the symbols V represent a group of stericallyhindered piperidinyl function(s).
Claims
exact text as granted — not AI-modified1 . A method for treating textile materials in order to provide them with a soft feel, absence of yellowing and good hydrophilicity, in which the textile materials are brought into contact with a composition comprising at least one linear, cyclic or three-dimensional polyorganosiloxane of formula (I):
in which:
(1) the symbols Z, which are identical or different, represent R 1 , and/or V;
(2) the symbols R 1 , R 2 and R 3 , which are identical and/or different, represent a monovalent hydrocarbon radical chosen from linear or branched alkyl radicals having from 1 to 4 carbon atoms, linear or branched alkoxy radicals having from 1 to 4 carbon atoms, a phenyl radical and, preferably, a hydroxyl radical, an ethoxy radical, a methoxy radical or a methyl radical;
(3) the symbols V, functional groups which are identical and/or different, represent a group containing a sterically hindered piperidinyl functional group or groups chosen from:
For the groups of formula (II):
R 4 is a divalent hydrocarbon radical chosen from:
linear or branched alkylene radicals having 2 to 18 carbon atoms;
alkylene-carbonyl radicals in which the linear or branched alkylene portion contains 2 to 20 carbon atoms;
alkylene-cyclohexylene radicals in which the linear or branched alkylene portion contains 2 to 12 carbon atoms and the cyclohexylene portion contains an OH group and optionally 1 or 2 alkyl radicals having 1 to 4 carbon atoms;
radicals of formula —R 7 —O—R 7 in which the radicals R 7 , which are identical or different, represent alkylene radicals having 1 to 12 carbon atoms;
radicals of formula —R 7 —O—R 7 in which the radicals R 7 have the meanings indicated above and one of them or both of them are substituted by one or two —OH group or groups;
radicals of formula —R 7 —COO—R 7 in which the radicals R 7 have the meanings indicated above;
radicals of formula —R 8 —O—R 9 —O—CO—R 8 in which the radicals R 8 and R 9 , which are identical or different, represent alkylene radicals having 2 to 12 carbon atoms and the radical R 9 is optionally substituted by a hydroxyl radical;
U represents —O— or —NR 10 —, R 10 being a radical chosen from a hydrogen atom, a linear or branched alkyl radical containing 1 to 6 carbon atoms and a divalent radical of formula:
in which R 4 has the meaning indicated above, R 5 and R 6 have the meanings indicated below and R 11 represents a linear or branched divalent alkylene radical having from 1 to 12 carbon atoms, one of the valency bonds (that of R 11 ) being linked to the atom of —NR 10 —, the other (that of R 4 ) being linked to a silicon atom;
the radicals R 5 , which are identical or different, are chosen from linear or branched alkyl radicals having 1 to 3 carbon atoms and the phenyl radical;
the radical R 6 represents a hydrogen radical or the radical R 5 or O.
For the groups of formula (III):
R′ 4 is chosen from a trivalent radical of formula:
where m represents a number from 2 to 20, and a trivalent radical of formula:
where p represents a number from 2 to 20;
U′ represents —O— or NR 12 —, with R 12 being a radical chosen from a hydrogen atom, a linear or branched alkyl radical containing 1 to 6 carbon atoms;
R 5 and R 6 have the same meanings as those given with respect to the formula (II); and
(4) the number of units ηSi with no group V is between 10 and 450,
the number of units ηSi with a group V is between 1 and 5,
0≦w≦10 and 8≦y≦448.
2 . The method as claimed in the preceding claim, characterized in that the number of units ηSi with no group V is between 50 and 250, and the number of units ηSi with a group V is between 1 and 3.
3 . The method as claimed in any one of the preceding claims, characterized in that the polyorganosiloxane of formula (I) is linear.
4 . The method as claimed in any one of the preceding claims, characterized in that V is chosen from the functional groups of formula (II).
5 . The method as claimed in any one of the preceding claims, characterized in that the composition containing the polyorganosiloxane is in liquid form.
6 . The method as claimed in any one of the claims, characterized in that the composition containing the polyorganosiloxane in liquid form is an aqueous emulsion.
7 . The method as claimed in any one of the preceding claims, characterized in that said method is carried out on a woven, knitted or nonwoven material, said material being at least intrinsically hydrophilic.
8 . The method as claimed in any one of the preceding claims, characterized in that the material treated is based on cotton, flax, wool, viscose, rayon, hemp, silk or a mixture of these materials.
9 . The method as claimed in any one of the preceding claims, characterized in that the quantity of polyorganosiloxane deposited on the treated textile material corresponds to a quantity of between 0.1 and 2% by weight relative to the weight of the treated dry textile material.Join the waitlist — get patent alerts
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