Process for dyeing and foaming thermoplastic polyurethane

Patent metadata

Field	Value
Publication number	US-10876252-B2
Application number	US-201716461181-A
Country	US
Kind code	B2
Filing date	Nov 14, 2017
Priority date	Nov 16, 2016
Publication date	Dec 29, 2020
Grant date	Dec 29, 2020

Abstract

A process for the preparation of coloured and expanded thermoplastic polyurethane (coloured ETPU) material which comprises the following steps:
a) providing thermoplastic polyurethane (TPU) material and at least one gaseous fluid wherein the melting temperature of the TPU material is above the supercritical temperature of the at least one gaseous fluid b) placing the TPU material in an autoclave together with a colorant and/or a fluorescent whitening agent (FWA), wherein the colorant is selected from at least one of a disperse dye, an acid dye and a pigment; c) increasing the pressure in the autoclave by introducing the at least one gaseous fluid at a temperature below the melting point of the TPU material and at least above the supercritical temperature of the at least one gaseous fluid at the applied pressure (saturation step); and d) allowing the non-expanded TPU material to saturate; and e) decreasing the pressure in the autoclave down to ambient pressure at a temperature between the melting temperature and the glass transition temperature (Tg) of the TPU material at such a rate that the TPU material expands (expansion step) to obtain coloured ETPU material f) removing the coloured ETPU material from the autoclave.

First claim

What is claimed is:

1. A process for the preparation of coloured and expanded thermoplastic polyurethane material which comprises the following steps:
a) providing thermoplastic polyurethane material and at least one gaseous fluid wherein the melting temperature of the thermoplastic polyurethane material is above the supercritical temperature of the at least one gaseous fluid;
b) placing the thermoplastic polyurethane material in an autoclave together with a colorant and/or a fluorescent whitening agent, wherein the colorant is selected from at least one of a disperse dye, an acid dye and a pigment;
c) increasing the pressure in the autoclave by introducing the at least one gaseous fluid at a temperature below the melting point of the thermoplastic polyurethane material and at least above the supercritical temperature of the at least one gaseous fluid at the applied pressure;
d) allowing the non-expanded thermoplastic polyurethane material to saturate; and
e) decreasing the pressure in the autoclave down to ambient pressure at a temperature between the melting temperature and the glass transition temperature of the thermoplastic polyurethane material at such a rate that the thermoplastic polyurethane material expands to obtain the coloured expanded thermoplastic polyurethane material; and
f) removing the coloured expanded thermoplastic polyurethane material from the autoclave;
wherein the at least one gaseous fluid is selected from CO 2 and the saturation step is performed at a pressure in the range of 73-500 bar and at a temperature below the melting point of the thermoplastic polyurethane material and at least above the supercritical temperature of supercritical CO 2 (SC CO 2 ) at the applied pressure.

2. The process according to claim 1 , wherein step (c) is performed at pressures ranging from 100 up to 300 bar.

3. The process according to claim 1 , wherein step (c) is performed at a temperature ranging from 70 up to 170° C.

4. The process according to claim 1 , wherein step (c) and step (e) are performed at a temperature between the melting temperature and the glass transition temperature of the thermoplastic polyurethane material.

5. The process according to claim 1 , wherein the decrease in pressure during step (e) is performed at a rate of at least 5 bar/sec.

6. The process according to claim 1 , wherein the coloured expanded thermoplastic polyurethane material has volume dimensions being 1.2 to 100 times the volume of the original unexpanded thermoplastic polyurethane material.

7. The process according to claim 1 , wherein the colorant or fluorescent whitening agent dye is applied via dye transfer from dyed polyester.

8. The process according to claim 1 , wherein the disperse dye of formulae (1a)-(8) is applied:

wherein R 1 is bromine, chlorine, cyano, nitro, trifluoromethyl, C 1 -C 12 alkyl or C 1 -C 12 alkoxy,
R 2 denotes hydrogen, C 1 -C 12 alkyl, C 1 -C 12 alkoxy, bromine, chlorine, cyano, nitro or trifluoromethyl,
R 3 represents bromine, chlorine, cyano, nitro or trifluoromethyl,
R 4 is hydrogen, C 1 -C 4 alkyl, halogen, CF 3 or —NHCOR 20 wherein R 20 is C 1 -C 4 alkyl,
R 5 is hydrogen, halogen, C 1 -C 4 alkyl or C 1 -C 4 alkoxy;
R 6 and R 7 are each independently of the other hydrogen, C 1 -C 6 alkyl that is unsubstituted or substituted by hydroxy, cyano, acyloxy,

N-phthalimidyl or by phenoxy, x being a number from 0 to 4 and it being possible for the alkyl chain, from C 2 upwards, optionally to be interrupted by one or more oxygen atoms,
or are a radical of formula —CH 2 CH 2 —COOR 21 , —CH 2 CH 2 —O—COR 21 ,

or of formula

R 21 and R 22 each independently of the other being C 1 -C 4 alkyl and R 23 being hydrogen or C 1 -C 4 alkyl;

wherein R 1 R 2 and R 3 are as defined above and
R 8 denotes C 1 -C 12 alkyl or C 1 -C 12 alkoxyalkyl,

wherein R 1 R 2 and R 3 are as defined above and
R 9 and R 10 are each independently of the other hydrogen, C 1 -C 12 alkyl which is unsubstituted or substituted by cyano, carboxy, hydroxy, C 1 -C 6 alkoxy or C 2 -C 8 alkoxyalkoxy,
or are C 6 -C 24 aryl which is unsubstituted or substituted by cyano, carboxy, hydroxy, C 1 -C 6 alkoxy or C 2 -C 8 alkoxyalkoxy,
or are C 7 -C 25 aralkyl which is unsubstituted or substituted by cyano, carboxy, hydroxy, C 1 -C 6 alkoxy or C 2 -C 8 alkoxyalkoxy;

wherein R 4 , R 5 , R 6 and R 7 are as defined above,
R 11 is C 1 -C 12 alkyl,
R 12 denotes hydrogen, chlorine, bromine, nitro or cyano, and
R 13 represents chlorine, bromine or cyano;

wherein R 8 , R 11 , R 12 and R 13 are as defined above;

wherein R 9 , R 10 , R 11 , R 12 and R 13 are as defined above;

wherein R 4 , R 5 , R 6 and R 7 are as defined above;

wherein R 14 is hydrogen, C 1 -C 6 alkoxy, C 6 -C 24 aryloxy or —SO 2 —NH—R 24 , with R 24 being C 1 -C 12 alkyl which is unsubstituted or substituted by cyano, carboxy, hydroxyl or C 1 -C 6 alkoxy,
R 15 and R 16 are each independently of the other amino, hydroxyl, nitro, phenylamino, 4-(2-hydroxyethyl)phenylamino, benzoylamino, o-chlorobenzoylamino, m-chlorobenzoylamino, p-chlorobenzoylamino, phenylaminosulfonyl, phenylsulfonylamino, p-tolylsulfonylamino or phenylmercapto,
R 17 and R 18 are each independently of the other hydrogen, amino, hydroxyl or nitro;

wherein R 19 represents C 2 -C 12 alkoxyalkyl or C 3 -C 15 alkoxyalkoxyalkyl;

9. The process according to claim 1 , wherein the flouorescent whitening agent of formulae (2a)-(2c) is applied:

wherein R 20 and R 21 are each independently of the other C 1 -C 12 alkoxy, bis(C 1 -C 12 hydroxyalkyl)amino, C 1 -C 12 hydroxyalkoxy or N-morpholino,
R 22 and R 23 each independently of the other represent hydrogen, sulfo or 2-hydroxyethylsulfonyl;

wherein R 25 denotes hydrogen, C 1 -C 6 alkyl, C 6 -C 14 aryl or C 7 -C 24 aralkyl and
X is a bivalent radical of formula (2c1), (2c2) or (2c3)

Assignees

• Huntsman Int Llc

Inventors

• Bohmer Lars
• Burnell Ian
• Klein Rene Alexander
• Vandenbroeck Jan
• Weismann Anja

Classifications

• D06P1/0016 Primary

  Dye baths containing a dyeing agent in a special form such as for instance in melted or solid form, as a floating film or gel, spray or aerosol, or atomised dyes · CPC title

• D06L4/643

  wherein the brightener is introduced in a gaseous environment or in solid phase, e.g. by transfer, by use of powders or by use of super-critical fluids · CPC title

• C08J9/18

  by impregnating polymer particles with the blowing agent · CPC title

• C08J9/122

  Hydrogen, oxygen, CO2, nitrogen or noble gases · CPC title

• D06P3/24

  Polyamides; Polyurethanes · CPC title