Biennial Report 2016/2017
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Selected Results<br />
Near-Infrared Chemical Imaging of Functional Finishes on Textiles<br />
O. Daikos, G. Mirschel, T. Scherzer<br />
The permanently increasing demands on product<br />
quality and homogeneity pose a continuous<br />
challenge to measuring and process control<br />
technologies that are indispensable to meet these<br />
requirements. In case of the production or processing<br />
of web-like or planar materials such as<br />
paper, polymer films, textiles, plates, sheets etc.,<br />
the homogeneity of the material and the spatial<br />
distribution of quantitative values of parameters<br />
resulting from finishing steps such as coating,<br />
impregnation, varnishing, lamination, etc. become<br />
more and more important. The advent of large<br />
hyperspectral cameras working in the NIR range<br />
broadened the potential of analytical methods for<br />
process control considerably. In the framework of<br />
this research area, new approaches for<br />
monitoring of technical processes are developed<br />
[1]. This contribution is focused on applications of<br />
NIR chemical imaging in textile surface finishing<br />
technology.<br />
Agents applied as finishes provide the textile<br />
fabric with special functional features. For<br />
example, such formulations include stiffening<br />
agents, optical brighteners, flame retardants,<br />
hydrophilic or hydrophobic agents, anti-static, and<br />
anti-microbial finishes etc. Depending on the<br />
specific substrate, agent, and intended application<br />
they may be applied with application weights in<br />
the range from less than 1 g/m² to several tens of<br />
g/m². The rather low application weight of some<br />
finishes makes very high demands on the<br />
sensitivity of the detection method.<br />
Figure 1: Chemical image of a polyester fabric provided with<br />
different amounts of a flame retardant. Gravimetric<br />
application weights: 15.5 g/m² (left) and 26 g/m² (right).<br />
Figure 2: Chemical image of the distribution of a PVAc stiffening<br />
agent on cotton fabric (gravimetric application weight:<br />
12.4 g/m²).<br />
Generally, all NIR methods require previous calibration<br />
with reference data by means of powerful<br />
chemometric techniques such as the partial least<br />
squares (PLS) algorithm for quantitative<br />
evaluation of the spectral data. The application of<br />
such approaches finally results in quantitative distribution<br />
patterns of the parameter of interest<br />
such as application weight, thickness, moisture<br />
content etc. in the context of this project. It has<br />
been shown that the application weight of finishes<br />
can be determined with typical prediction errors<br />
(RMSEP) in the order of 1 to 2 g/m² under in-line<br />
conditions, whereas more sophisticated<br />
calibration models developed for very thin layers<br />
of sizes allow the recording of chemical images<br />
with RMSEP values lower than 0.5 g/m².<br />
Figures 1 and 2 show some examples of chemical<br />
images of finished textiles. Both the flame<br />
retardant and the stiffening agent show significant<br />
inhomogeneities of the application weight<br />
resulting from the specific preparation and drying<br />
processes. Nevertheless, the textiles appear<br />
completely homogeneous in the visible range of<br />
the spectrum since both finishing agents form<br />
colourless layers.<br />
The precision of the predictions was crosschecked<br />
by integration of the individual data<br />
across the surface of each finished fabric (~10 4<br />
…10 5 ) and comparison of the resulting average<br />
value with gravimetric reference data. Typically,<br />
the deviation correlated quite well with the<br />
prediction error of the calibration model (i.e. 1…2<br />
g/m²).<br />
Further investigations by hyperspectral imaging<br />
were directed towards the in-line analysis of UVcured<br />
acrylate coatings (degree of cure,<br />
thickness), thin printed layers (homogeneity), release<br />
coatings (detection of surface<br />
discontinuities), adhesive layers inside textile<br />
laminates (lamination defects) etc.<br />
Literature<br />
[1] G. Mirschel, O. Daikos, T. Scherzer, C. Steckert, Anal.<br />
Chim. Acta 932 (<strong>2016</strong>) 69-79 (doi 10.1016/j.aca.<strong>2016</strong>.<br />
05.015).<br />
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