Dyes and Pigments 74 (2007) 371e379

www.elsevier.com/locate/dyepig

Synthesis of polyurethane acrylate oligomers as aqueous UV-curable

binder for inks of ink jet in textile printing and pigment dyeing
M.M. El-Molla*
Textile Research Division, National Research Centre, Dyeing and Printing, Tahrir Street, Dokki, Cairo 12622, Egypt
Received 12 October 2005; received in revised form 11 December 2005; accepted 17 February 2006
Available online 24 April 2006

Abstract

Polyurethane acrylate oligomers were prepared from isophorone diisocyanate, mixture of polyethylene glycol 1000 and 2000 and hydroxy
ethyl acrylate using dibutyl tin dilaurate as a catalyst. The rheological properties and its utilization as a UV-curable binder for inks of ink jet
printing and pigment dyeing of cotton, viscose, wool, polyester and nylon 66 fabrics using pigment dyes were thoroughly investigated. It was
found that the prepared binder is characterized by low viscosity (0.0042 Pa S ¼ 4.2 cP) at a rate of shear of 10.0007 S1. Furthermore, the results
obtained indicate that the aqueous UV-curable binder of polyurethane acrylate oligomer based on the mixture of PEG1000 and PEG2000 can be
used safely for inks of ink jet printing and also in pigment dyeing to give coloured goods characterized by soft handling and from good to ex-
cellent color fastness properties. Infra-red spectra of the mixture of PEG1000 and PEG2000 before and after the preparation of polyurethane
acrylate oligomer indicate some physicochemical changes in the structure.
Ó 2006 Elsevier Ltd. All rights reserved.

Keywords: Synthesis; Polyurethane acrylate; Oligomers; Aqueous UV-curable; Binder; Inks; Ink jet; Textile printing pigment dyeing

1. Introduction when cured, and the curing equipment occupies much less
space than the conventional thermal drying convegors. The
Ink jet printing and UV-curing technologies have developed US Environmental Protection Agency views UV-curable inks
in parallel. Manufacturers have integrated ink jet print heads, as a green technology that it deems preferable to conventional
printing mechanisms, UV-curable inks and UV-curing systems solvent-based ink systems [1].
to address a number of industrial printing needs [1]. The use of Currently, pigment printing is perhaps the most commonly
UV-curable ink with analog printing methods, including flex- and extensively used technique for printing textile, due to its
ography, gravure, offset and screen process, is growing at easy application to a variety of fabrics and relatively clean
a rate that exceeds the growth rates for the use of these pro- and environmentally friendly aspects [3,4]. On a global basis,
cesses. For example, the total flexographic ink market for la- about 50% of printed textiles are processed by pigment printing.
bels is projected to grow at 3% per annum, while UV-curing In the United States, the share reaches nearly 88%, in England
ink is growing at 17% [2]. The printing industry adopted 50%, and in China 60e80% [5]. However, pigment printing has
UV-curing inks and coatings because they emit little to no vol- a few problems such as relatively high temperature cure, stiff
atile organic compound (VOC) solvents, do not dry during hand, and poor crock fastness of printed goods. Formaldehyde
print process before curing, but will dry almost instantly emissions and clogging on the screens during the actual printing
process must also be taken into account [6e8]. These disadvan-
tages are related to the binders used. Thus, to improve the qual-
* Tel.: þ20 123825747; fax: þ20 23370931. ity of the pigment printed goods, the overall properties of the
E-mail address: [email protected] binder need to be improved.

0143-7208/$ - see front matter Ó 2006 Elsevier Ltd. All rights reserved.
doi:10.1016/j.dyepig.2006.02.021
372 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379

Fig. 1. IR spectra of mixed polyethylene glycol 1000 þ 2000 before and after the preparation of polyurethane acrylate based on PEG1000þ2000.

The aim of the present work is to prepare aqueous UV-cur- - Photoinitiator, Esacure DP 250 was supplied by Iamberti
able binder of polyurethane acrylate oligomers based on the SPa, Italy.
mixture of PEG1000 and PEG2000. These compounds having
low viscosity measurement can be used either in inks of ink
2.2. Methods
jet printing or for pigment dyeing for all types of fabrics using
pigment dyes.
2.2.1. Synthesis of polyurethane acrylate oligomers
The reaction of mixture of PEG1000 and PEG2000 with IPDI
2. Experimental was conducted according to a procedure described elsewhere
[9,10] which was modified and carried out as follows: mixture
2.1. Materials of PEG1000 and PEG2000 was added as a 70% acetone mixture
into a three-necked flask equipped with stirrer, thermometer,
- Polyethylene glycol (PEG, Mn 1000 and 2000) was sup- and reflux condenser under nitrogen atmosphere. IPDI contain-
plied by Merck, Germany. PEG1000 was dried and ing 0.05% (w/w) DBTDL was slowly dropped into the reactor
degassed at 90  C/1e2 mm Hg until no bubbling was at 40  C for over an hour and the reaction mixture was stirred
observed.
- Isophorone diisocyanate (IPDI) supplied by Lyondell
Chemical Co., Germany, dibutyl tin dilaurate (DBTDL) 300
as a catalyst supplied by Fluka Chemical Co., Switzerland
and hydroxy ethyl acrylate supplied by Degussa, Germany 250
Rate of shear ( sec.-1 )

were used without further purification.

200
- Mill scoured, bleached and mercerized plain weave cotton
fabric (135 g/m2), wool fabric [100% wool] of 145 g/m2, 150
polyamide fabric [100% nylon 66] of 110 g/m2, polyester
Ebecryl 2002
fabric [100% PES, satin] of 85 g/m2 and viscose fabric 100 PUA based on PEG1000 +
[100% viscose] of 140 g/m2 were supplied by private sec- PEG2000
Ebecryl 2002 after storing
50
tor co. PUA based on PEG1000 +
- Pigment dispersions for ink jet printing have narrow parti- PEG2000 after storing
0
cle distribution and mean particle size around 165 nm, 0 100 200 300 400 500 600
which is pigment Blue 153-16 (10% PiG) supplied by Shearing stress ( dyne/cm2 )
Minerva miner print, Italy. Fig. 2. Rheological properties of aqueous UV-curable binder of polyurethane
- Commercial binder, Ebecryl 2002 was supplied by surface acrylate based on the mixture of PEG1000þ2000 and/or Ebecryl 2002 (10%)
specialties (UCb Chemicals), Belgium. before and after storing for 10 days.
 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379 373

300 10% (w/w) were measured using fluids spectrometer RFS II

(Rheometrics Co 1483), Germany, at 25  C and at different
Rate of shear ( sec.-1 )

250
shear rates.
200
2.3.2. Infra-red analysis
150
The infra-red of the mixture of polyethylene glycol
Ebecryl 2002
100 PUA based on PEG1000 + (1000 and 2000) before and after the preparation of the
PEG2000
Ebecryl 2002 containing the dye
polyurethane acrylate based on polyethylene glycol (1000
50
PUA based on PEG1000 + and 2000) was measured using Infra-red spectrometer,
PEG2000 containing the dye Perkin Elmer, system 2000 FT-IR (Fourier transform IR
0
0 100 200 300 400 500 600 spectrometer).
Shearing stress ( dyne/cm2 )

Fig. 3. Rheological properties of aqueous UV-curable binder of polyurethane 2.3.3. Surface tension measurement
acrylate based on the mixture of PEG1000þ2000 and/or Ebecryl 2002 (10%) be- The surface tension of the inks was measured with a cali-
fore and after preparing ink using 20% Blue pigment 153-16 (10% piG). brated Kruss K12 surface tensiometer (Kruss, Hamburg, Ger-
many). It determines the force required to detach a platinum
ring from the surface of the ink. The measurement procedure
for an additional 1 h at 50  C to ensure an acceptable reaction
was repeated six times to obtain an average value of the
rate without gelation. A calculated amount of hydroxy ethyl
force. Before each sample measurement the ring was thor-
acrylate was gradually added to the reaction mixture for over
oughly rinsed in distilled water and flamed by a Bunsen
an hour at 60  C and the reaction mixture was stirred for another
burner to remove any residue. This preparation is needed
2 h continuously at 60  C to cap all of the terminal NCO group.
because the condition of the ring is crucial for the measure-
The resulting product was a clear solution of polyurethane acry-
ment accuracy [11].
late oligomers. Deionized water was added into the kettle to form
an aqueous solution of polyurethane acrylate binder with 40%
(w/w) solids content. The reaction yield was evaluated. 2.3.4. Conductivity measurement
The conductivity was measured by a conductivity meter
LF318 standard conductivity cell Tetra cons, Germany.
2.2.2. Ink preparation
Aqueous pigmented inks are composed of Blue 153-16 2.3.5. Color strength
(10% PiG), Esacure DP 250, and Ebecryl 2002 as a binder The relative color strength of the prints expressed as K/S
and/or the prepared binder of polyurethane acrylate based on value [12] of the coloured samples was determined by reflec-
the mixture of PEG1000 and PEG2000 and deionized water. tion measurements using data color international model SF
500, USA.
2.2.3. Coloration of the textile and dye fixation
The printing of textile using Drop-on Demand ink jet print- 2.3.6. Fastness properties
ing engine is the piezo head (Mimaki JV2-130, Japan) or dye- Fastness to washing [13], rubbing [14] and perspiration [15]
ing using a padding machine (Foulard), Switzerland. The dried was assessed according to the standard methods.
textile fabric was padded through the prepared ink at 100%
wet pickup. The padded fabrics were only air dried (or oven 3. Results and discussion
dried at 80  C for 30 s) and then the fabrics were subjected
to UV light source (Fusion UV-curing systems model 3.1. Synthesis of polyurethane acrylate oligomer
K52312, USA) for 20 s (5 passes at 4 s per pass) to fix the
color, through polymerization process. Most acrylated oligomers are based on polyether, polyester,
and epoxy resins. This is because the functionality of these
2.3. Testing and measurements condensation resins can be precisely controlled to 2 or 3 to
prevent gelling and to keep viscosity at low, diisocyanate
2.3.1. Rheological properties could react with polyethylene glycol to form isocyanato-termi-
The rheological properties and apparent viscosity of the nated polyurethane prepolymer. The reaction can be repre-
prepared binder of aqueous polyurethane acrylate solution of sented as follows:

O O
catalyst
HO-R-OH + OCN-D-NCO OCN-D-NH-C-O-R-O-C-NH-D-NO
Polyethylene glycol Diisocyanate Urethane prepolymer

where R = -CH2 -CH2 ( O-CH2-CH2) n O-CH2-CH2- and D = Isophorone

374 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379

After that the urethane prepolymer reacted with hydroxy after storage, and the rheogram curves are nearest to axis of
ethyl acrylate to give polyurethane acrylate oligomer based the rate of shear, indicating a decrease in the apparent
on polyethylene glycol as follows: viscosity.

O O O
-
OCN-D-NH-C-O-R-O-C-NH-D-NCO + HO-R-O-C-CH=CH2
Urethane prepolymer HEA

O O O O O O
- -
CH2=CH-C-O-R-O-C-NH-D-NH-C-O-R-O-C-NH-D-NH-C-O-R-O-C-CH=CH2
Polyurethane acrylate oligomer based on polyethylene glycol

-
Where R = -CH2-CH2-

The apparent viscosity decreased with increasing rate of

The formation of the polyurethane acrylate oligomer was shear. At constant rate of shear, the apparent viscosity of
evidenced by the emergence of the strong absorption at Ebecryl 2002 is higher than that of PUA based on
1245 cm1 (CeO), 1466 cm1 (CeNeC), 1538 cm1 (NeCO), PEG1000þ2000 and it decreased by storage e.g. at a rate of shear
1620 cm1 (NeH), 1637 cm1 (C]C), 1720 cm1 (C]O) of 10.0007 s1, the viscosity of freshly prepared Ebecryl 2002
and the sharpening of the absorption band at 3330 cm1 as is 285 cP but the viscosity of PUA based on PEG1000þ2000 is
shown in Fig. 1, which is the infra-red spectra of the mixture 4.85 cP, after storage for 10 days the viscosity of Ebecryl
of PEG1000 with PEG2000 (1:1) before and after the preparation 2002 is 88.5 cP and the viscosity of PUA based on
of the polyurethane acrylate based on the mixed PEG. It is also PEG1000þ2000 is 4.32 cP.
clear from the infra-red spectra that there is no absorption band Fig. 3 shows the rheological behavior of PUA based on
at approximately 2274 cm1 [16] which corresponds to NCO PEG1000þ2000 and Ebecryl 2002 before and after the prepara-
group, and this indicates that the entire amount of isophorone tion of ink using 20% Blue pigment 153-16 (10% PiG).
diisocyanate enters into the reaction and the end product is It is seen that the rheogram curve of Ebecryl 2002 without
free from isocyanate. All this confirm the occurrence of the dye was shifted far from the axis of the rate of shear indicating
addition reaction to obtain the aqueous UV-curable binder of an increase in the apparent viscosity but after using prepared
polyurethane acrylate oligomer based on the mixture of ink using the Blue pigment 153-16, the rheogram curve was
PEG1000 and PEG2000. shifted nearest to the axis of the rate of shear indicating a
decrease in the apparent viscosity but the inverse happened in
3.2. Rheological properties case of PUA based on PEG1000þ2000 e.g. at a rate of shear of
10.0007 s1 the viscosity of Ebecryl 2002 without dye is
The rheological properties and viscosity of polyurethane 285 cP and when we added the dye it decreased to 2.6 cP but
acrylate based on the mixture of PEG1000 and PEG2000 in case of PUA based on PEG1000þ2000 it increased from 4.85
and/or Ebecryl 2002 (10%) before and after storing for 10 to 6.99 cP and this may be due to the dispersant medium of
days were measured using Rheometrics CO 1483. The rhe- the Blue pigment containing some groups which result in cross-
ological properties were measured at 25  C. The rheograms linking or hydrogen bonding with PUA oligomer based on
are given in Fig. 2. It is clear from these rheograms that all
samples are characterized by non-Newtonian pseudoplastic
behavior where, the up and down flow curves are coinci- Table 1
dent. It is also clear from the same figure that the location Apparent viscosity, surface tension, conductivity and pH measurements of the
prepared water-based ink using UV-curable binder of polyurethane acrylate
of the rheogram and its slope seems to be not only depen- based on the mixture of PEG1000 and PEG2000 and/or Ebecryl 2002 using
dent on the type of binder used but also on the time of stor- 20% Blue pigment 153-16 (10% piG)
age. When commercial binder used, which is Ebecryl 2002, Binder used Binder Viscosity at Surface Conductivity pH
the rheogram curve shifted far from the axis of the rate of concentration rate 10.0007 S1 tension (mS/cm)
shear indicating an increase in the apparent viscosity, but (%) (Pa S) (mN/m)
storage has a significant effect on its apparent viscosity as Ebecryl 2002 5 0.00133 34.163 715 7.95
the rheogram curve after storing for 10 days was shifted 10 0.00257 35.675 813 6.83
nearest to the axis of the rate of shear, indicating a decrease 20 0.00905 38.404 970 6
in its apparent viscosity. While the rheogram curves of pre- PUA based on 5 0.00312 33.527 837 7.89
pared binder which is polyurethane acrylate oligomer before PEG1000þ2000 10 0.00699 35.401 749 7.75
and after storing for 10 days are nearly the same and are 20 0.0373 36.274 533 7.62
coincident indicating that there is no change in the viscosity 1 Pa S ¼ 1000 cP.
 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379 375

PEG1000þ2000 which leads to an increase in the molecular weight fabrics using prepared PUA based on PEG1000þ2000 by concen-
and this leads to an increase in the viscosity but the inverse hap- tration 5% and Ebecryl 2002 by concentration 10% as UV-cur-
pened in case of Ebecryl 2002, where as this groups make dilu- able binders using Blue pigment 153-16. It is clear from the data
tion in the oligomer chains and this is due to the different in the in Table 2 that in spite of the lower concentration of PUA based
first component of polyol of the two binder used. on PEG1000þ2000 (5%) used in prepared ink for ink jet printing
but give higher color strength in case of viscose, nylon 66 and
3.3. Ink property measurements prepared using aqueous
polyester fabric and slightly lower values in case of cotton com-
UV-curable binder
pared with the Ebecryl 2002 which is used by (10%) and this
may be due to the difference in the first component of the two
The evaluation of the ink stability requires a constant mon-
binders, used may be in case of used mixture of PEG1000þ2000
itoring of various ink properties. The quantitative ink data are
the average of hydroxyl values is higher than the first compo-
obtained through the following measurements such as, viscos-
nent of polyol which is used for prepared Ebecryl 2002 and
ity, surface tension, conductivity and pH measurements.
this is lead to not only increase in the urethane groups in the pre-
The viscosities of water-based inks are relatively low, usually
pared binder but also increase in the number of unsaturation site
less than 10 cP. Table 1 shows the viscosity, surface tension,
of vinyl group which is responsible for fixed of the dispersed
conductivity and pH measurements of prepared water-based
pigment using UV light through the polymerization process.
ink using prepared UV-curable binder of polyurethane acrylate
All the printed goods were characterized by soft handle. Also
based on the mixture of PEG1000þ2000 and/or Ebecryl 2002
it is clear from the data in Table 2 that the color fastness to rub-
using Blue pigment 153-16. It is clear from the data in Table 1
bing in case of cotton, viscose and nylon 66 ranged from good
that the viscosity of ink on using Ebecryl 2002 by 10% is
to very good but in case of polyester ranged from moderate to
lower than the viscosity of ink on using PUA based on
good and in case of wool from poor to moderate. Furthermore
PEG1000þ2000 by 5% which is equal 2.57 cP compared with
the color fastness to washing in case of cotton, viscose ranged
3.12 cP, but in the case of used ink containing 10% of PUA
from good to very good but in case of wool, nylon 66 and poly-
based on PEG1000þ2000 the viscosity is equal 6.99 cP. The
ester ranged from poor to moderate. The color fastness to per-
surface tension increases with increase in the concentration
spiration in case of cotton and viscose ranged from very good
of binder, but the pH decrease and the conductivity in case
to excellent and in the other fabrics it is very good. This was
of used Ebecryl 2002 as a binder in the ink preparation its
true irrespective of the nature of the binder used for prepared
increase by increase the concentration of Ebecryl 2002
ink for ink jet printing.
but the inverse is true in case of used PUA based on
PEG1000þ2000 and this may be due to increase the concentra-
tion lead to high increase in the viscosity on compared with 3.5. Using the prepared ink in dyeing of textile fabric
Ebecryl 2002 which leads to decrease in the conductivity. through padding process

3.4. Using the prepared ink in ink jet printing 3.5.1. Effect of the type and concentration of
of textile fabric UV-curable binder
The effect of the type and concentration of binder used on
Table 2 shows the color strength and fastness properties of the color strength of the coloured cotton, viscose, wool, nylon
ink jet printed cotton, viscose, wool, nylon 66 and polyester 66 and polyester fabric upon using polyurethane acrylate

Table 2
Colour strength and overall fastness properties of ink jet printed fabrics using prepared polyurethane acrylate based on the mixture of PEG1000 and PEG2000 and/or
Ebecryl 2002 as UV-curable binders for ink preparation using 20% Blue pigment 153-16 (10% piG)
Binder used Type of fabric Colour strength Rubbing fastness Washing fastness Perspiration fastness
Acidic Alkaline
Dry Wet Staining Alteration Staining Alteration Staining Alteration
Ebecryl 2002 (10%) Cotton 3.49 3e4 3 3 4 4 5 5 5
PUA based on PEG1000þ2000 (5%) 3.33 3 3e4 3 4 4 5 5 5
Ebecryl 2002 (10%) Viscose 3.66 3 3 2e3 3 4 5 4 4
PUA based on PEG1000þ2000 (5%) 4.01 3 3 2e3 3 5 5 4 5
Ebecryl 2002 (10%) Wool 2.48 1e2 1e2 3 2 4 4 4 4
PUA based on PEG1000þ2000 (5%) 1.97 1e2 1e2 2 1 4 4 5 4
Ebecryl 2002 (10%) Nylon 66 2.61 3e4 3 2e3 2 3 4 2 4
PUA based on PEG1000þ2000 (5%) 3.01 3e4 2e3 2 2 4 4 4 4
Ebecryl 2002 (10%) Polyester 2.54 2e3 2e3 2 1 4 4 3e4 4
PUA based on PEG1000þ2000 (5%) 2.63 2e3 2 2 1 4 4 4 4
The washing fastness in case of cotton and viscose is at 60  C, but in case of wool, nylon 66, and polyester it is at 40  C.
All samples showed soft handling.
376 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379

9 10
8 9

Colour strength ( K / S )
Colour strength ( K / S )

8
7
7
6
6
5
5
4
4
3 3
2 2 Ebecryl 2002
Ebecryl 2002
1 1 PUA based on PEG 1000 + PEG2000
PUA based on PEG1000 + PEG2000
0 0
10% 15% 20% 25% 0% 5% 10% 15% 20% 25%
0% 5%
Binder concentration Binder concentration

Fig. 4. Effect of the concentration of the aqueous UV-curable binder used in Fig. 6. Effect of the concentration of the aqueous UV-curable binder used in
the prepared ink on the K/S of the coloured cotton fabric using 20% Blue pig- the prepared ink on the K/S of the coloured wool fabric using 20% Blue pig-
ment 153-16 (10% piG). ment 153-16 (10% piG).

oligomer based on the mixture of PEG1000 and PEG2000 and/or 9

Ebecryl 2002 as UV-curable binders in the prepared ink using 8

20% Blue pigment 153-16 (10% PiG) is represented by Figs. Colour strength ( K / S ) 7
4e8. It is clear from Figs. 4e8 that in case of using Ebecryl 6
2002, as the concentration increases a slower rate of increase 5
in the color strength or may be fixed, this was true irrespective
4
of the type of coloured fabric. But in case of using polyure-
3
thane acrylate based on the mixture of PEG1000 and
PEG2000, as the concentration increases the color strength of 2 Ebecryl 2002
the coloured fabrics increases. Furthermore, on using polyure- 1 PUA based on PEG1000 + PEG2000
thane acrylate based on the mixture of PEG1000 and PEG2000 0
as a UV-curable binder in ink preparation, the color strength 0% 5% 10% 15% 20% 25%

results are higher than the color strength results on using Binder concentration
Ebecryl 2002. For example the K/S values were 8.05, 10.17, Fig. 7. Effect of the concentration of the aqueous UV-curable binder used in
9.05, 8.31 and 7.95 for cotton, viscose, wool, nylon 66, and the prepared ink on the K/S of the coloured nylon 66 fabric using 20% Blue
polyester, respectively, on using 20% of polyurethane acrylate pigment 153-16 (10% piG).
based on the mixture of PEG1000 and PEG2000 as a UV-curable
binder in ink preparation, while it was 6.61, 7.42, 5.86, 7.4 and 9
6.55 for cotton, viscose, wool, nylon 66 and polyester, respec-
8
tively, on using 20% of Ebecryl 2002, this may be due to the
Colour strength ( K / S )

7
difference in the structure and the amount of unsaturation
groups of the two binders. 6

5
4
12
3
Colour strength ( K / S )

10 2 Ebecryl 2002
1 PUA based on PEG1000 + PEG2000
8
0
0% 5% 10% 15% 20% 25%
6
Binder concentration
4 Fig. 8. Effect of the concentration of the aqueous UV-curable binder used in
the prepared ink on the K/S of the coloured polyester fabric using 20% Blue
Ebecryl 2002
2 pigment 153-16 (10% piG).
PUA based on PEG 1000 + PEG2000
0
0% 5% 10% 15% 20% 25% 3.5.2. Fastness properties
Binder concentration Tables 3e7 show the color strength and fastness properties
Fig. 5. Effect of the concentration of the aqueous UV-curable binder used in
of coloured cotton, viscose, wool, nylon 66 and polyester fab-
the prepared ink on the K/S of the coloured viscose fabric using 20% Blue pig- rics using prepared polyurethane acrylate based on the mixture
ment 153-16 (10% piG). of PEG1000 and PEG2000 and/or Ebecryl 2002 as aqueous
 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379 377

Table 3
Colour strength and overall fastness properties of coloured cotton fabrics using prepared polyurethane acrylate based on the mixture of PEG1000 and PEG2000 and/
or Ebecryl 2002 as UV-curable binders for ink preparation using 20% Blue pigment 153-16 (10% piG)
Binder used Binder concentration (%) Colour strength Rubbing fastness Washing fastness Perspiration fastness
Acidic Alkaline
Dry Wet Staining on Alt. Staining on Alt. Staining on Alt.
Cotton Wool Cotton Wool Cotton Wool
Ebecryl 2002 5 5.95 3 2e3 3 3 5 4 2e3 5 4 3 5
10 6.59 3 3 3 4 5 4 4 5 4 4 5
20 6.61 3 3e4 3e4 4e5 5 5 4 5 5 4 5
PUA based 5 5.93 3 2e3 3 4 5 4 3 5 4 3 5
on the mixture 10 7.8 3 3 3 4 5 4e5 4 5 4e5 4 5
of PEG1000 and PEG2000 20 8.05 3e4 3 3e4 4e5 5 4e5 4 5 4e5 4 5
The washing fastness is at 60  C; Alt. ¼ alteration.
All samples showed soft handling.

Table 4
Colour strength and overall fastness properties of coloured viscose fabrics using prepared polyurethane acrylate based on the mixture of PEG1000 and PEG2000 and/
or Ebecryl 2002 as UV-curable binders for ink preparation using 20% Blue pigment 153-16 (10% piG)
Binder used Binder concentration (%) Colour strength Rubbing fastness Washing fastness Perspiration fastness
Acidic Alkaline
Dry Wet Staining on Alt. Staining on Alt. Staining on Alt.
Cotton Wool Cotton Wool Cotton Wool
Ebecryl 2002 5 7.08 3 2e3 2 3 4 4 3 5 4 3 5
10 7.31 3 2e3 3 3 4 4 3e4 5 4 3e4 5
20 7.42 3e4 3 3 3e4 4 4 4 5 4 4 5
PUA based 5 5.77 3 2e3 2 2 3 4 3 5 4 4 5
on the mixture 10 7.04 3e4 3 2 3 3 4 4 5 4 4 5
of PEG1000 and PEG2000 20 10.17 4 3 2e3 4 3 4 4 5 4 4 5
The washing fastness is at 60  C; Alt. ¼ alteration.
All samples showed soft handling.

Table 5
Colour strength and overall fastness properties of coloured wool fabrics using prepared polyurethane acrylate based on the mixture of PEG1000 and PEG2000 and/or
Ebecryl 2002 as UV-curable binders for ink preparation using 20% Blue pigment 153-16 (10% piG)
Binder used Binder concentration (%) Colour strength Rubbing fastness Washing fastness Perspiration fastness
Acidic Alkaline
Dry Wet Staining on Alt. Staining on Alt. Staining on Alt.
Cotton Wool Cotton Wool Cotton Wool
Ebecryl 2002 5 5.33 2 2e3 3 3 1 5 3 4 4 3 4
10 6.2 2 2e3 3e4 3e4 1 5 4 4 5 4 4
20 5.89 2 3 4 4 1 5 4 5 5 4 5
PUA based 5 5.88 3 2e3 2 3 1 4 3 4 4 3 4
on the mixture 10 6.92 3 2e3 2e3 3 2 4 4 5 4e5 4 5
of PEG1000 and PEG2000 20 9.05 3 2e3 2e3 4 2e3 4 4 5 4e5 4 5
The washing fastness is at 40  C; Alt. ¼ alteration.
All samples showed soft handling.
378 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379

Table 6
Colour strength and overall fastness properties of coloured nylon 66 fabrics using prepared polyurethane acrylate based on the mixture of PEG1000 and PEG2000
and/or Ebecryl 2002 as UV-curable binders for ink preparation using 20% Blue pigment 153-16 (10% piG)
Binder used Binder concentration (%) Colour strength Rubbing fastness Washing fastness Perspiration fastness
Acidic Alkaline
Dry Wet Staining on Alt. Staining on Alt. Staining on Alt.
Cotton Wool Nylon 66 Wool Nylon 66 Wool
Ebecryl 2002 5 6.96 3 1e2 2e3 3 2 2e3 2e3 4 3 3 4
10 7.47 3e4 2e3 2e3 3 2 4 2e3 5 4 3 5
20 7.4 3e4 2e3 3 4 2 4 2 5 4 4 5
PUA based 5 6.79 2e3 2 1e2 3 1 2e3 2e3 4 3 3 4
on the mixture 10 8.07 3e4 2e3 1e2 3 1e2 3 3 4 4 4 4
of PEG1000 and PEG2000 20 8.31 3e4 3 2 4 2 4 4e5 4 4 4e5 5
The washing fastness is at 40  C; Alt. ¼ alteration.
All samples showed soft handling.

UV-curable binders in the prepared ink using (20%) Blue pig- polyester fabric using 5 and 10% concentration of the binder for
ment 153-16 (10% PiG). All coloured goods were character- ink preparation and this may be due to either the type of dye
ized by soft handle, on the other hand, the color strength used or these types of fabrics need some chemical treatment
depended on both the nature of the binder used and on its con- to improve this defect before coloring by using this type of
centration. The highest color strength was obtained using binders. Also from Tables 5e7 we noticed that the increase in
higher concentration of the binder, also it is clear from the the concentration of binder used improved this defect.
data in Tables 3e7 that the rubbing, washing and perspiration
fastness improve by increase in the concentration of the binder
used. This was true irrespective of the nature of the binder 4. Conclusion
used and/or the type of coloured fabrics. This may be due to
the increase in the concentration of the binder that leads to - Aqueous UV-curable inks were formulated with zero vol-
an increase in the amount of the unsaturation site of vinyl atile organic compounds and less than 10 cP viscosity us-
group which is responsible for the fixation of the dispersed ing prepared polyurethane acrylate oligomer based on the
pigment using UV light through the polymerization process. mixture of PEG1000 and PEG2000 as a binder for ink
Also it is clear from the data in Tables 3e7 that the fastness preparation.
properties’ values upon using prepared polyurethane acrylate - The highest color strength is obtained by increasing the
based on the mixture of PEG1000 and PEG2000 and/or commer- concentration of binder used and also the all fastness prop-
cial Ebecryl 2002 as UV-curable binders are comparable. The erties are improved.
washing, rubbing and perspiration fastness results range be- - The polyurethane acrylate based on the mixture of
tween good to very good for rubbing and washing fastness PEG1000 and PEG2000 can be used safely as a UV-curable
and range between very good to excellent for perspiration fast- binder for ink preparation to be used either in ink jet print-
ness. The defect was found in case of wet rubbing fastness and ing or for dyeing by padding process of all type of fabric
change in color after washing for coloured wool, nylon 66 and using pigment dyes.

Table 7
Colour strength and overall fastness properties of coloured polyester fabrics using prepared polyurethane acrylate based on the mixture of PEG1000 and PEG2000
and/or Ebecryl 2002 as UV-curable binders for ink preparation using 20% Blue pigment 153-16 (10% piG)
Binder used Binder concentration (%) Colour strength Rubbing fastness Washing fastness Perspiration fastness
Acidic Alkaline
Dry Wet Staining on Alt. Staining on Alt. Staining on Alt.
Cotton Wool Polyester Wool Polyester Wool
Ebecryl 2002 5 6.08 3 1e2 1e2 2e3 1 4 4 4 4 3 4
10 6.8 3e4 2 2 3 1e2 4 3e4 4 4 4 4
20 6.55 3e4 2 3 3e4 2 4 3e4 4 4 4 4
PUA based 5 4.75 3 2 1e2 3 1 3e4 4 4 4 3 4
on the mixture 10 5.2 3e4 2 1e2 3 1e2 4 3e4 4 4 4 4
of PEG1000 and PEG2000 20 7.95 4e5 2e3 2e3 4 2 4 3e4 4 4 4 4
The washing fastness is at 40  C; Alt. ¼ alteration. All samples showed soft handling.
 M.M. El-Molla / Dyes and Pigments 74 (2007) 371e379 379

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