[0001] The invention relates to compositions of water-insoluble or very sparingly soluble
U.V. absorbers that are stable to storage under both cold and warm storage conditions.
[0002] GB Patent 2,187,746 discloses compositions suitable for applying U.V. absorbers of
the benztriazole series to a substrate in the form of a dispersion in water.
[0003] Also EP-A-0354174 describes aqueous dispersions of UV absorbers of the benztriazole
series with anionic as well as non-ionic dispersing agents but the exemplified compositions
always contain montmorrillonite as a thickener.
[0004] Improved compositions of this type have now been found according to the present invention
which surprisingly demonstrate improved stability and performance compared to those
of GB 2,187,746. The compositions of the present invention comprise a 4-part composition
comprising a mixture of a sparingly soluble U.V. absorber, water, a dispersing agent
and a surfactant, whereas those of GB 2,187,746 comprise a 3-part composition, comprising
the U.V. absorber, water and a dispersing agent. GB 2,187,746 also discloses the optional
presence of non-ionic surfactants which are addition products of C
1-12alkylphenol and alkylene oxides. A preferred surfactant is the addition product of
C
1-12alkylphenol (preferably nonylphenol) and a C
2-3 alkyleneoxide.
[0005] The present invention provides a composition (A) comprising, based on the total weight
of said composition:
a) |
20 to 45% |
of a insoluble or sparingly soluble U.V. absorber of the 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chloro-benztriazole
series having an average particle size of less than 5 µm; |
b) |
7 to 25% |
of a dispersing agent which is a condensation product of a sulphonated tolylether
and formaldehyde; |
c) |
0.5 to 10% |
of a non-ionic surfactant which is an addition product of ethylene oxide or propylene
oxide or both ethylene oxide and propylene oxide, and a mixture of fatty alcohols,
fatty acids, fatty amides or fatty esters having 7-20 carbon atoms, preferably 14-18
carbon atoms or either tristyrylphenol or distyrylphenol; |
d) |
|
and water. |
[0006] In a preferred embodiment of the present invention there is provided a composition
(B) comprising, based on the weight of the total composition:
a) |
20 to 45% |
of an insoluble or sparingly soluble U.V. absorber of the 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chloro-benztriazole
series having an average particle size of less than 5 µm; |
b) |
7 to 20% |
of a dispersing agent which is a condensation product of a sulphonated tolylether
and formaldehyde; |
c) |
1 to 6% |
of a non-ionic surfactant which is an addition product of ethylene oxide or propylene
oxide or both ethylene and propylene oxide and tristyrylphenol; |
d) |
|
and water. |
[0007] In a further preferred embodiment of the present invention there is provided a composition
(C) comprising, based on the weight of the total composition:
a) |
20 to 45% |
of an insoluble or sparingly soluble U.V. absorber of the 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chloro-benztriazole
series having an average particle size of less than 5 µm; |
b) |
7 to 25% |
of a dispersing agent which is a condensation product of sulphonated tolylether and
formaldehyde; |
c) |
0.5 to 10% |
of a non-ionic surfactant which is an addition product of 1 mole of fatty alcohols
with 14-18 carbon atoms and 10-50 moles ethylene oxide or propylene oxide, or a total
of 10-50 moles ethylene oxide and propylene oxide; |
d) |
|
and water. |
[0008] Compositions according to the invention may comprise, based on total weight of said
composition, one or more additional components selected from the group of:
e) |
up to 1.6 % |
of a solubilizing agent |
f) |
0.1 to 0.2 % |
of a buffer |
g) |
0.1 to 0.3 % |
of an antifouling agent |
h) |
0.1 to 1.0 % |
of an antifoaming agent. |
[0009] Preferred dispersing agents are those commercially available (for example BAYKANOL
SL), as described in U.S Patent 4, 386,037, especially Example 15. The disclosure
of U.S. Patent No. 4,386,037 is incorporated herein by reference. The preferred amount
of formaldehyde used per mole of sulphonated tolylether is from 0.2 to 3.0 moles.
[0010] Preferred U.V absorbers of the 2-(2'-hydroxyphenyl)-benztriazole series are those
described in Japanese Kokai 56-31084 and Swiss Patent 494,060. The Kokai and the Swiss
Patent are incorporated herein by reference.
[0011] The diameter of the U.V. absorbers used in a composition according to the invention
is generally less than 5 µm. Suitably the particles have a diameter in the range of
from 0.1 to 3 µm. Preferably the mean diameter of the U.V. absorbers is less than
1 µm. The mean particle size can be measured by placing a sample on a microscope on
which a scale has been superimposed.
[0012] In composition (B) the non-ionic surfactant is preferably an addition product of
tristyrylphenol and 10-50 moles of ethylene oxide or an addition product of tristyrylphenol
and ethylene oxide/propylene oxide. Most preferred is an addition product of tristyrylphenol
and 16 moles of ethylene oxide, commercially available as SOPROPHOR BSU (Rhone Poulenc).
[0013] In composition (C), the non-ionic surfactant is preferably an addition product of
1 mole of a mixture of fat alcohols having 14-18 carbon atoms and 10-50 moles of ethylene
oxide. Most preferred is an addition product of 1 mole of a mixture of fat alcohols
having 14-18 carbon atoms and 25-40 moles of ethylene oxide. Different grades of primary
alcohols may be used, e.g.
60% C14 / 40% C15 |
(Dobanol 45, Shell) |
25-35% C16 / 60-67% C18 |
(Orkus) |
20-33% C16 / 60-80% C18 |
(Laurex CS)z |
[0014] The content of unsaturated alcohol (e.g. oleylalcohol) present, may be up to 25%,
but it is not mandatory that such alcohol be present. There may be small amounts of
fractions of C
≤19 and C
≥19 present, but these will each be present at less than 5%.
[0015] Preferred solubilizing agents are addition products of poly-C
1-4-alkylene glycols (preferably polypropylene or polyethylene glycol) with propylene
oxide and/or ethylene oxide. More preferably the solubilizing agents are the addition
products of polypropylene glycol and propylene oxide and ethylene oxide, most preferably
those the polyoxypropylene part thereof, having a molecular weight of 1500 to 2500
and comprising 40 to 60% polyoxyethylene units, particularly preferred being "Pluronic"
type solubilizing agents.
[0016] Preferably the buffer is either sodium hydroxide or phosphoric acid, depending on
the acidity of the components.
[0017] Preferred antifouling agents are fungicides for example Giv Gard, a commercially
available product.
[0018] Preferred antifoaming agents are compositions based on silicone oil or alkylenediamides
(e.g. of stearic acid), preferably added in amounts of 0.5 to 1.0 % by weight of the
total composition.
[0019] A preferred composition (B) according to the invention is composition (B
1) which comprises, based on the weight of the total composition:
a) |
20 to 35 % |
of 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlorobenztriazole; |
b) |
10 to 20 % |
of a dispersing agent which is a condensation product of a ditolylethersulphonate
and formaldehyde; |
c) |
2 to 6 % |
of a surfactant which is the addition product of 1 mole of tristyrylphenol and 16
moles of ethylene oxide; |
e) |
up to 1.6 % |
of a solubilizing agent which is a polymer addition product of polypropylene glycol,
propyleneoxide and ethyleneoxide, the polyoxypropylene part thereof having a molecular
weight of 1700 to 2300; and 40 to 60 % polyoxyethylene units in the polymer; |
d) |
|
and water. |
[0020] Another preferred composition (B) according to the invention is composition (B
2) which comprises:
a) |
35 to 45 % |
of 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlorobenztriazole; |
b) |
10 to 14 % |
of a dispersing agent which is a condensation product of ditolylethersulphonate and
formaldehyde; |
c) |
2 to 6 % |
of a surfactant which is the addition product of 1 mole tristyrylphenol and 16 moles
of ethylene oxide; |
e) |
up to 1.6 % |
of a solubilizing agent which is a polymer addition product of polypropylene glycol,
propyleneoxide and ethyleneoxide, the polyoxypropylene part thereof having a molecular
weight of 1700 to 2300; and 40 to 60 % polyoxyethylene units in the polymer; |
d) |
|
and water. |
[0021] A preferred composition (C) according to the invention is (C
1) which comprises, based on weight of the total composition:
a) |
20 to 35% |
of 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlorobenztriazole; |
b) |
10 to 25% |
of a condensation product of ditolylethersulphonate and formaldehyde; |
c) |
1 to 5% |
of the addition product of 1 mole of a mixture of fat alcohols having 16-18 carbon
atoms and 40 moles of ethylene oxide |
e) |
up to 1.6% |
of a solubilizing agent which is a polymer addition product of polypropylene glycol,
propyleneoxide and ethyleneoxide, the polyoxypropylene part thereof having a molecular
weight of 1700 to 2300; and 40 to 60 polyoxyethylene units in the polymer; |
d) |
|
and water. |
[0022] Another preferred composition (C) according to the invention is (C
2) which comprises, based on weight of the total composition:
a) |
35 to 45% |
of 2-(2'-hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlorobenztriazole; |
b) |
10 to 14% |
of a condensation product of ditolylethersulphonate and formaldehyde; |
c) |
1 to 5% |
of the addition product of 1 mole of a mixture of fat alcohols having 16-18 carbon
atoms and 40 moles of ethylene oxide; |
e) |
up to 1.6% |
of the addition product of polypropylene glycol, propyleneoxide and ethyleneoxide,
the polyoxypropylene part thereof having a molecular weight of 1700 to 2300; and 40
to 60% polyoxyethylene units in the polymer |
d) |
|
and water. |
[0023] Preferably the pH of a composition according to the invention is between 4.5 and
5.8, more preferably 5.0 to 5.5.
[0024] Compositions according to the invention are suitable for use in dyeing, padding or
printing processes preferably in a concentration of 0.5 to 6.0 % based on the weight
of substrate to be treated. The concentration of the composition depends on the particular
components of the dyestuff utilized in the dyeing, padding or printing process and
on the desired shade.
[0025] Compositions according to the invention have excellent stability to storage, both
cold and warm storage and have excellent shear stability under dyeing conditions.
The stability to cold storage may be observed by freezing a composition according
to the present invention and thereafter allowing the frozen composition to thaw. The
compositions of the present invention do not display phase separation during thawing.
[0026] In one aspect of the present invention, the compositions are added to the dyeing,
padding or printing composition and the thus obtained dyebath, padding liquor or printing
paste is used in a conventional dyeing, padding or printing process respectively.
[0027] Compositions according to the invention are also suitable as after-treatment compositions
being applied by padding, printing or exhaustion techniques, as a 0.5 to 6.0 % (the
percentages being by weight of the substrate being dyed) dispersion in water. Accordingly,
in a further aspect of the present invention, the compositions of the present invention
are applied to the substrate after dyeing, padding or printing has been carried out
according to a conventional process, such a treatment being referred to as an after-treatment.
[0028] Further, according to the invention there is provided a process for dyeing, padding
and printing a substrate comprising applying to the substrate 0.1 to 5 % of a dye
(preferably a disperse dye) and 0.5 to 6 % of a composition according to the invention
(the percentages being by weight of the substrate being dyed) preferably in an aqueous
medium, in a liquor to goods ratio of 10:1 to 60:1.
[0029] Substrates dyed with disperse dyes and a composition of a U.V. absorber, the composition
being according to the present invention, show excellent light fastness properties.
[0030] The invention will now be illustrated by the following examples in which all parts
and percentages are by weight and all temperatures are in °C.
Examples of Compositions (B)
Example 1
[0031] The following are mixed together in a vessel:
25.00 |
parts of 2-(2'-hydroxy-3'-tert.butyl-5'-methylphenyl)-5-chlorobenztriazole; |
14.00 |
parts of a commercially available condensation product of ditolylether sulphonate
and formaldehyde (Baykanol SL); |
1.20 |
parts of commercially available Pluronic P 75 (from BASF/Wyandotte Corp.) [the addition
product of propylene glycol and propylene oxide, followed by the further reaction
with ethylene oxide; the polyoxypropylene part of the product having a molecular weight
of 2050 (approx.) and the polymer having about 50 % polyoxyethylene units]; |
4.00 |
parts of a commercially available product of 1 mole of tristyrylphenol + 16 moles
of ethylene oxide (Soprophor BSU); |
1.00 |
part of a commercially available wetting agent (Sandozin NIT fl); |
0.20 |
parts of a commercially available conservation agent (GivGard); |
0.05 |
parts of NaOH; and |
54.55 |
parts of water. |
[0032] The mixture is then milled in a bead mill with silicoquarzite beads until the average
size of the particles of the U.V. absorber is less than 1 µm. This occurs after about
30 minutes. The resulting dispersion is filtered from the silicoquarzite beads.
[0033] The resulting concentrate exhibits a good dispersion stability.
Example 2
[0034] Example 1 is repeated using the following components:
40.00 |
parts of 2-(2'-hydroxy-3'-tert.butyl-5-methylphenyl)-5-chlorobenztriazole; |
10.14 |
parts of a commercially available condensation product of ditolylether sulphonate
and formaldehyde; |
1.16 |
parts of commercially available Pluronic P 75; |
4.00 |
parts of a commercially available product of 1 mole of tristyrylphenol + 16 moles
of ethylene oxide (Soprophor BSU); |
1.01 |
parts of a commercially available wetting agent (Sandozin NIT fl); |
0.28 |
parts of a commercially available conservation agent (GivGard); |
0.07 |
parts of NaOH; and |
43.34 |
parts of water. |
Example 3
[0035] Example 1 is repeated omitting to add the commercially available Pluronic P 75 and
using 55.75 parts water in place of the 54.55 parts of Example 1.
Example 4
[0036] Example 1 is repeated, omitting to add the commercially available Pluronic P 75,
using 2 parts of a commercially available product of 1 mole of tristyrylphenol + 16
moles of ethylene oxide, (rather than 4 parts as in Example 1); and using 57.75 parts
water.
Example 5
[0037] Example 1 is repeated, omitting to add both the commercially available Pluronic P
75 and the wetting agent (Sandozin NIT fl); and using 56.75 parts water.
Example 6
[0038] Example 1 is repeated, omitting to add both the commercially available Pluronic P
75 and the wetting agent (Sandozin NIT fl); using 2 (rather than 4 parts) of a commercially
available product of 1 mole of tristyrylphenol + 16 moles of ethylene oxide; and using
58.75 parts water.
Example 7 (Comparative Example 1)
[0039] Example 1 is repeated, omitting to add the commercially available Pluronic P 75,
the wetting agent (Sandozin NIT fl) and the commercially available product of 1 mole
of tristyrylphenol + 16 moles of ethylene oxide; and using 60.75 parts water.
Example 8 (Comparative Example 2)
[0040] Example 1 is repeated using the following components:
25.00 |
parts of 2-(2'-hydroxy-3'-tert.butyl-5'-methylphenyl)-5-chlorobenztriazole; |
8.00 |
parts of the commercially available product of 1 mole of tristyrylphenol + 16 moles
of ethylene oxide (Soprophor BSU), which is the minimum amount necessary in order
to obtain a mean particle diameter of 1 µm; |
0.28 |
parts of a commercially available conservation agent (GivGard); |
0.07 |
parts of NaOH; and |
66.65 |
parts of water. |
Example 9 (Comparative Example 3)
[0041] Example 8 is repeated, using 12 parts of the commercially available product of 1
mole of tristyrylphenol + 16 moles of ethylene oxide and 62.65 parts water, in an
attempt to further improve the shear stability of the dispersion of Example 8.
Example 10 (Application Example)
[0042] A dyebath is prepared using the following components:
0.75% of C.I. Disperse Red 74;
0.75% of the dispersion of Example 1; and
98.50% water.
[0043] The pH is brought to 5.0 by the addition of ammonium sulphate/formic acid in a ratio
of 10:1.
[0044] The above described dyebath (1000 parts) is warmed to 60° in a dyeing autoclave and
100 parts of a polyester fabric (the quality of which is adequate for use as automobile
upholstery) is added thereto, the autoclave is closed and the circulating bath is
heated to 135°. Dyeing is carried out at 135° for 20 minutes after which the bath
is cooled to 80° and the dyed substrate is removed from the bath. It is then washed,
reductively cleaned, washed again and dried. The light-fastness of the dyed fabric
is substantially better than that dyed without the benztriazole present.
[0045] Instead of using 0.75% of the dispersion of Example 1, Application Example 10 can
be repeated using 0.75% of the dispersion of any one of the compositions of Examples
2 to 6 above.
Application Examples (Examples 11 - 18)
[0046] Using a fine polyester yarn (Dtex 167f) and a precision winder (density ca. 0.4),
a small cross-wound bobbin of 40 g is produced. This bobbin is dyed with one of the
dyestuff combinations given below, in a circulation dyeing apparatus (e.g. Colorstar
by Zeltex AG, CH). The pressure difference and flow rate are displayed by the dyeing
apparatus.
[0047] A goods-to-liquor ratio of 1:10, with water of 11 ° d (German Hardness) is employed.
[0048] Each of the dyestuff combinations of examples 11 to 18 comprises:
0.19% C. I Disperse Yellow 86
0.185% C. I Disperse Yellow 42
0.122% C. I Disperse Red 91
0.05% C. I Disperse Blue 56
0.44% C. I Disperse Blue 77
and in addition, each of these combinations comprises 3,5% of one of the dispersions
of examples 1-9 above; as is indicated in Table 1 below.
[0049] The dyestuff combination is poured over the bobbin, and thereafter a static pressure
of 2 bar is applied. At the start of dyeing, a flow rate of 0.6 l/min is set. Under
these conditions, there is initially a differential pressure (internal/external) of
ca. 0.05 - 0.1 bar. The dye liquor is heated to 130° at a rate of 2°/min, and after
dyeing for 30 minutes, cooling is effected to 80°, at a rate of 5°/min. During the
entire dyeing procedure, the flow rate, the differential pressure and the temperature
are recorded by a three-channel recording instrument.
[0050] The dispersions of the present invention are evaluated by the following parameters:
- maximum pressure difference (internal/external) (△P) bar
- minimum flow rate (F, l/min)
- levelness of the dyeing (internal/external) (E)
- presence of deposits inside the bobbin (A)
[0051] The results may be seen from the following Table 1:
Table 1.
Application Ex. No. |
Dispersion |
△Pmax |
Fmin |
E |
A |
11 |
Example 1 |
0.45 |
0.16 |
good |
no |
12 |
Example 3 |
0.18 |
0.46 |
very good |
no |
13 |
Example 4 |
0.47 |
0.13 |
very good |
no |
14 |
Example 5 |
0.10 |
0.37 |
very good |
no |
15 |
Example 6 |
0.64 |
0.30 |
very good |
no |
16 |
Example 7 |
>1.00 |
0.20 |
bad |
yes |
17 |
Example 8 |
0.95 |
0.15 |
bad |
yes |
18 |
Example 9 |
0.50 |
0.12 |
bad |
yes |
[0052] As may be seen from the table, when a dispersing agent in the form of a sulphonated
tolylether / formaldehyde condensate and a commercially available surfactant product
consisting of 1 mole of tristyryl phenol and 16 moles of ethylene oxide are both present
in the composition, there is a considerable improvement over compositions which contain
only one of these two components. This can be seen by comparing for example Application
Examples 14 and 16. Accordingly in Application Example 14 both the sulphonated tolylether
/ formaldehyde condensate and the surfactant are present, whereas in Application Example
16, there is no surfactant. The maximum pressure difference between the inside and
outside of the bobbin is much greater in the case of Example 16 than in the case of
Example 14. Such high differences in internal/external pressure in the case of Application
Example 16, is attributed to the instability of the U.V.-containing dispersion, which
agglomerates to or forms deposits on the internal surface of the bobbin, thus leading
to an increase in the internal/external pressure difference. By comparing the other
parameters measured, one also sees the clear superiority of the dispersion used in
Application Example 14 over that of Application Example 16.
[0053] A similar comparison between the results of Application Example 17 (which contains
no sulphonated tolylether / formaldehyde condensate and contains the minimum quantity
of the surfactant in order to obtain a mean particle diameter of 1 µm) and either
Application Example 14 or Application Example 15, shows again that a composition of
the present invention in which both a dispersing agent and a surfactant are present
demonstrates superior characteristics over a comparable composition which does not
contain the dispersing agent.
Examples of Composition (C)
Example 19
[0054] The following are mixed together in a vessel:
25.00 |
parts of 2-(2'-hydroxy-3'-tert.butyl-5'-methylphenyl)-5-chlorobenztriazole; |
18.00 |
parts of a commercially available condensation product of ditolylether sulphonate
and formaldehyde (Baykanol SL); |
1.20 |
parts of commercially available Pluronic P 75; |
1.5 |
parts of a commercially available addition product of 1 mole of a mixture of fat alcohols
having 14-18 carbon atoms and 40 moles of ethylene oxide; |
1.00 |
part of a commercially available wetting agent (Sandozin NIT fl); |
0.20 |
parts of a commercially available conservation agent (GivGard); |
0.05 |
parts of NaOH; and |
53.05 |
parts of water. |
[0055] The mixture is then milled in a bead mill as in Example 1.
[0056] The resulting concentrate is stable as a dispersion for 2 days at a temperature of
about 50°C.
Example 20
[0057] Example 19 is repeated using:
40.00 |
parts of 2-(2'-hydroxy-3'-tert.butyl-5-methylphenyl)-5-chlorobenztriazole; |
10.14 |
parts of a commercially available condensation product of ditolylether sulphonate
and formaldehyde; |
1.16 |
parts of commercially available Pluronic P 75; |
2.4 |
parts of a commercially available product of 1 mole of a mixture of fat alcohols having
14-18 carbon atoms and 40 moles of ethylene oxide; |
1.01 |
parts of a commercially available wetting agent (Sandozin NIT fl); |
0.28 |
parts of a commercially available conservation agent (GivGard); |
0.07 |
parts of NaOH; and |
44.94 |
parts of water. |
Example 21
[0058] Example 19 is repeated, omitting to add the commercially available addition product
of 1 mole of a mixture of fatty alcohols having 14 to 18 carbon atoms and 40 moles
of ethylene oxide, and using 54.55 parts water.
Example 22
[0059] Example 20 is repeated omitting to add the commercially available addition product
of 1 mole of a mixture of fatty alcohols having 14 to 18 carbon atoms and 40 moles
of ethylene oxide, and using 47.34 parts water.
Application Examples (Examples 23-28)
Application Example (Example 23)
[0060] A dyebath is prepared using the following components:
0.75% |
C.I. Disperse Red 74; |
0.75% |
of the dispersion of Example 19; and |
98.5% |
water. |
[0061] The pH is brought to 5.0 by the addition of ammonium sulphate/formic acid in a ratio
of 10:1. The dyebath is then warmed as in Example 10 above and the dyeing procedure
according to Example 10 is followed.
[0062] The light fastness of the dyed fabric is substantially better than that dyed without
the benztriazole present.
[0063] Instead of using 0.75% of the dispersion of Example 19, Example 23 can be repeated
using 0.50% of the dispersion of Example 20.
Example 24
[0064] Using a fine polyester yarn (Dtex 167fl), a small cross-wound bobbin of 40 g is produced
as in Example 11 above. This bobbin is dyed according to the dyeing conditions of
Example 11.
[0065] A goods-to-liquor ratio of 1:10, with water of 11° d (German Hardness) is employed.
[0066] Each of the dyestuff combinations comprises:
0.19 % C. I Disperse Yellow 86
0.185 % C. I Disperse Yellow 42
0.122 % C. I Disperse Red 91
0.49 % C. I Disperse Blue 77
and 3.5% of the dispersion of example 19.
[0067] The dispersions are evaluated as in Examples 11-18 above.
Application Example 25
[0068] Application Example 24 is repeated using 2.18% of the dispersion of example 21, instead
of 3.5% of the dispersion of example 19.
Application Example 26
[0069] Application Example 24 is repeated using 2.18% of the dispersion of example 20, instead
of 3.5% of the dispersion of example 19.
Application Example 27
[0070] Application Example 24 is repeated using 2.18% of the dispersion of example 22, instead
of 3.5% of the dispersion of example 19.
[0071] The results obtained from application examples 24-27 may be seen from the following
Table 2.
Table 2
Application Ex. No. |
Dispersion |
△Pmax |
Fmin |
E |
A |
24 |
Example 19 |
0.1 |
0.6 |
very good |
no |
25 |
Example 21 |
0.8 |
0.05 |
bad |
yes |
26 |
Example 20 |
0.1 |
0.6 |
very good |
no |
27 |
Example 22 |
0.75 |
0.05 |
bad |
yes |
[0072] As can be seen from the table, the presence in the dispersion of a sulphonated tolylether/
formaldehyde condensate and a commercially available product consisting of an addition
product of 1 mole of a mixture of fat alcohols with 14-18 carbon atoms and 40 moles
of ethylene oxide (Application Examples 24 and 26), causes a considerable improvement
over dispersions which contain only the sulphonated tolylether/formaldehyde condensate
(Application Examples 25 and 27), that is no addition product.
1. Eine Zusammensetzung, welche bezogen auf das Gesamtgewicht der Zusammensetzung, enthält:
a) |
20 bis 45% |
des unlöslichen oder schwer löslichen UV-Absorbers 2-(2'-Hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlor-benztriazol,
welcher eine durchschnittliche Teilchengrösse von weniger als 5 µm besitzt; |
b) |
7 bis 25% |
eines Dispersionsmittels, welches ein Kondensationsprodukt eines sulfonierten Tolylethers
und Formaldehyd ist; |
c) |
0,5 bis 10% |
eines nicht-ionischen Tensids, welches ein Additionsprodukt von Ethylenoxid oder Propylenoxid
oder von sowohl Ethylenoxid als auch Propylenoxid und einer Mischung von Fettalkoholen,
Fettsäuren, Fettsäureamiden oder Fettsäureestern mit 7 bis 20 Kohlenstoffatomen, vorzugsweise
14 bis 18 Kohlenstoffatomen oder entweder Tristyrylphenol oder Distyrylphenol ist; |
d) |
|
und Wasser. |
2. Eine Zusammensetzung wie im Patentanspruch 1 beansprucht, welche enthält:
a) |
20 bis 45% |
des unlöslichen oder schwer löslichen UV-Absorbers 2-(2'-Hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlor-benztriazol,
welcher eine durchschnittliche Teilchengrösse von weniger als 5 µm besitzt; |
b) |
7 bis 20% |
eines Dispersionsmittels, welches ein Kondensationsprodukt eines sulfonierten Tolylethers
und Formaldehyd ist; |
c) |
1 bis 6 % |
eines nicht-ionischen Tensids, welches ein Additionsprodukt von Ethylenoxid oder Propylenoxid
oder sowohl von Ethylenoxid als auch von Propylenoxid und Tristyrylphenol ist; |
d) |
|
und Wasser. |
|
3. Eine Zusammensetzung wie im Patentanspruch 1 beansprucht, welche enthält:
a) |
20 bis 45% |
des unlöslichen oder schwer löslichen UV-Absorbers 2-(2'-Hydroxy-3'-tert.butyl-5'-methyl-phenyl)-5-chlor-benztriazol,
welcher eine durchschnittliche Teilchengrösse von weniger als 5 µm besitzt; |
b) |
7 bis 25% |
eines Dispersionsmittels, welches ein Kondensationsprodukt eines sulfonierten Tolylethers
und Formaldehyd ist; |
c) |
0,5 bis 10% |
eines nicht-ionischen Tensids, welches ein Additionsprodukt von 1 Mol Fettalkoholen
mit 14-18 Kohlenstoffatomen und 10-50 Molen Ethylenoxid oder Propylenoxid oder total
10-50 Molen Ethylenoxid und Propylenoxid ist; |
d) |
|
und Wasser. |
4. Eine Zusammensetzung wie im Patentanspruch 3 beansprucht, worin das nichtionische
Tensid ein Additionsprodukt von 1 Mol einer Mischung von Fettalkoholen mit 14-18 Kohlenstoffatomen
und 10-50 Molen Ethylenoxid ist.
5. Eine Zusammensetzung wie in einem der Patentansprüche 1 bis 4 beansprucht, enthaltend
einen oder mehrere der folgenden Bestandteile:
e) |
bis zu 1,6% |
eines Lösungshilfsmittels |
f) |
0,1 bis 0,2% |
eines Puffers |
g) |
0,1 bis 0,3% |
eines fäulnisverhütenden Mittels |
h) |
0,1 bis 1,0% |
eines Antischaummittels |
6. Eine Zusammensetzung wie in einem der Patentansprüche 1 bis 5 beansprucht, worin der
mittlere Durchmesser des U.V.-Absorbers weniger als 1 µm beträgt.
7. Ein Verfahren zum Färben, Appretieren oder Bedrucken eines Substrats, welches das
Anbringen von
0,1 bis 5% eines Farbstoffes und
0,5 bis 6% einer Zusammensetzung gemäss einem der Patentansprüche 1 bis 6
auf das Substrat umfasst, wobei die Prozentanteile auf das Gewicht des zu färbenden,
zu appretierenden oder zu bedruckenden Substrats bezogen sind.
8. Ein Verfahren zur Behandlung eines Substrats, welches gemäss üblichem Färbe-, Appretier-
oder Druckverfahren gefärbt, appretiert oder bedruckt wurde, wobei nachfolgend auf
dieses Färbe-, Appretier- oder Druckverfahren das Substrat mit einer, in einem der
Patentansprüche 1 bis 6 beanspruchten, Zusammensetzung behandelt wird.
9. Verwendung einer, in einem der Patentansprüche 1 bis 6 beanspruchten, Zusammensetzung
zum Färben, Appretieren oder Bedrucken eines Substrats oder zur Behandlung eines Substrats,
welches unter Verwendung von üblichen Färbe-, Appretier- oder Druckverfahren gefärbt,
appretiert oder bedruckt wurde.
1. Une composition comprenant, par rapport au poids total de ladite composition :
a) |
de 20 à 45% |
de l'absorbeur UV insoluble ou faiblement soluble le 2-(2'-hydroxy-3'-tert.-butyl-5'-méthylphényl)-5-chloro-benzotriazole
ayant une dimension moyenne des particules qui est inférieure à 5 µm; |
b) |
de 7 à 25% |
d'un agent dispersant qui est un produit de condensation d'un éther tolylique sulfoné
et de formaldéhyde; |
c) |
de 0,5 à 10% |
d'un agent de surface non ionique qui est un produit d'addition de l'oxyde d'éthylène
ou de l'oxyde de propylène ou à la fois de l'oxyde d'éthylène et de l'oxyde de propylène
sur un mélange d'alcools gras, d'acides gras, d'amides gras ou d'esters gras contenant
de 7 à 20 atomes de carbone, de préférence de 14 à 18 atomes de carbone, ou sur le
tristyrylphénol ou le distyrylphénol; |
d) |
et de l'eau. |
|
2. Une composition telle que revendiquée à la revendication 1, comprenant :
a) |
de 20 à 45% |
de l'absorbeur UV insoluble ou faiblement soluble le 2-(2'-hydroxy-3'-tert.-butyl-5'-méthylphényl)-5-chloro-benzotriazole
ayant une dimension moyenne des particules qui est inférieure à 5 µm; |
b) |
de 7 à 20% |
d'un agent dispersant qui est un produit de condensation d'un éther tolylique sulfoné
et de formaldéhyde; |
c) |
de 1 à 6% |
d'un agent de surface non ionique qui est un produit d'addition de l'oxyde d'éthylène
ou de l'oxyde de propylène ou à la fois de l'oxyde d'éthylène et de l'oxyde de propylène
sur le tristyrylphénol; |
d) |
et de l'eau. |
|
3. Une composition telle que revendiquée à la revendication 1, comprenant :
a) |
de 20 à 45% |
de l'absorbeur UV insoluble ou faiblement soluble le 2-(2'-hydroxy-3'-tert.-butyl-5'-méthylphényl)-5-chloro-benzotriazole
ayant une dimension moyenne des particules qui est inférieure à 5 µm; |
b) |
de 7 à 25% |
d'un agent dispersant qui est un produit de condensation d'éther tolylique sulfoné
et de formaldéhyde; |
c) |
de 0,5 à 10% |
d'un agent de surface qui est un produit d'addition de 1 mole d'alcools gras contenant
de 14 à 18 atomes de carbone et de 10 à 50 moles d'oxyde d'éthylène ou d'oxyde de
propylène, ou d'un total de 10 à 50 moles d'oxyde d'éthylène et d'oxyde de propylène; |
d) |
et de l'eau. |
|
4. Une composition telle que revendiquée à la revendication 3, dans laquelle l'agent
de surface non ionique est un produit d'addition de 1 mole d'un mélange d'alcools
gras contenant de 14 à 18 atomes de carbone et de 10 à 50 moles d'oxyde d'éthylène.
5. Une composition telle que revendiquée à l'une quelconque des revendications 1 à 4,
comprenant un ou plusieurs des composés suivants :
e) |
jusqu'à 1,6% |
d'un agent solubilisant |
f) |
de 0,1 à 0,2% |
d'un tampon |
g) |
de 0,1 à 0,3% |
d'un agent antipourrissement |
h) |
de 0,1 à 1,0% |
d'un agent antimousse. |
6. Une composition telle que revendiquée à l'une quelconque des revendications 1 à 5,
dans laquelle le diamètre moyen des particules de l'absorbeur UV est inférieur à 1
µm.
7. Un procédé de teinture, de foulardage ou d'impression d'un substrat, comprenant l'application
au substrat
- de 0,1 à 5% d'un colorant et
- de 0,5 à 6% d'une composition selon l'une quelconque des revendications 1 à 6,
les pourcentages étant par rapport au poids du substrat à teindre, à foularder ou
à imprimer.
8. Un procédé de traitement d'un substrat qui a été teint, foulardé ou imprimé selon
un procédé classique de teinture, de foulardage ou d'impression, dans lequel, après
ledit procédé de teinture, de foulardage ou d'impression, le substrat est traité avec
une composition telle que revendiquée à l'une quelconque des revendications 1 à 6.
9. L'utilisation d'une composition telle que revendiquée à l'une quelconque des revendications
1 à 6, pour la teinture, le foulardage ou l'impression d'un substrat ou pour le traitement
d'un substrat qui a été teint, foulardé ou imprimé selon un procédé classique de teinture,
de foulardage ou d'impression.