
4
UNITEX nr. 1 - 2014
Eco-efficient hybrid coatings for
durable textile applications by UV curing -
Hybritex
F. Goethals
a
, K. Eunger
a
, S. De Vrieze
a
, M. Vanneste
a
, A. Schumann
b
, A. Wypkema
c
Introduction
UV curing is a photochemical process that can be
applied to cure inks, adhesives and coatings.
1
Similar
to thermal curing the resins are cross-linked, resulting
in a xed and polymerized lm (gure 1). However,
UV curing offers some major advantages over thermal
curing. For one, UV curing is very fast and will therefore
signicantly reduce the production time. Secondly, UV
formulations are either solvent-free or water-based,
resulting in a very low VOC emission. UV curing
systems also require less energy and space compared
to large and high energy consuming thermal ovens.
This makes UV curing a sustainable and eco-friendly
curing technology.
Figure 1: cross-linking of oligomers by UV radiation
To be UV curable, the formulations must contain
suitable resins and a photo-initiator to initiate the
polymerization reaction. Monomers, viscosity modiers
and functional additives can be added, allowing to
modify and tailor the coatings.
By adding functional additives, properties like ame
retardancy, hydrophobicity, abrasion resistance or UV
stability can be obtained.
Sol-gel systems are interesting additives to give added
value to UV coatings, especially towards abrasion
resistance. Traditional sol-gel systems are metal oxide
based (mostly silicon or titanium).
2
The main advantages of sol-gel systems are the ease
to functionalise them. This means that they could
also possess antibacterial, ame retardant, water,
oil and soil repellent properties. The combination of
functionalized inorganic sol-gel systems with organic
UV curable resins results into so-called hybrid systems.
Applications for UV curing in the textile industry
UV curing is already well-known and frequently applied
in many industrial branches such as the graphic sector
and the wood sector. However in textile industry, this
technology is not widely adapted yet. One of the
reasons is that UV coatings were initially developed
as hard, protective coatings which were as such not
suitable for application as exible textile coatings.
As UV resin manufacturers are also looking for new
markets, they are developing UV curable resins for
exible substrates. As a result, resins are available on
the market offering interesting opportunities for the
textile industry. Using viscosity modiers and diluting
agents (like monomers) formulations for both coating
and nishing can be developed.
In this paper, we present results of a study aimed
at developing UV formulations containing sol-gel
additives for textile substrates. High- and low-viscosity
formulations were prepared and these were applied on
polyester fabrics by knife-over-roll coating and pad-
bath nishing. After UV curing the inuence of the
coatings and nishes on the abrasion resistance was
tested and evaluated.
High-viscosity formulations – textile coatings
Figure 2: set-up for knife-over-roll coating of fabric samples
High-viscosity formulations, suitable for fabric coating
by knife-over-roll (gure 2), can be either 100% or
water-based systems. 100% systems are solvent-free
and usually need to be diluted with reactive monomers
to obtain the right viscosity. Water-based formulations
are often too low in viscosity and a thickening agent
needs to be added. After application, water-based
coatings need to be dried before UV curing to remove
the water (e.g. by thermal heating or IR radiation).
It was found that the product Ebecryl 210 (urethane
acrylate, Allnex) is a good 100% binder for coating
polyester fabrics. To this formulation, two different
sol-gel systems (provided by Devan Chemicals) were
added in different concentrations. After coating, full
curing was achieved by illuminating the fabrics for 4s
under a Hg UV lamp (gure 3).
Figure 3: set-up for UV curing of fabric samples
The abrasion resistance was tested by a modied EN
530-2 test. The coatings were sandpapered with type
F02 paper stopping after 500 cycles. The reduction
in weight was determined for the different coatings
(gure 4).
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