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Correlation of regenerated fibres morphology and surface ... - Lenzing

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<strong>Lenzing</strong>er Berichte, 82 (2003) 83-95<br />

Sorption properties show a behaviour, which<br />

can be correlated with the differences in<br />

<strong>morphology</strong>. CV is able to adsorb the greatest<br />

amount <strong>of</strong> solvent <strong>and</strong> low molecular weight<br />

species (iodine). This is caused by a large<br />

amount <strong>of</strong> amorphous phase (crystallinity index<br />

= 0.25), <strong>and</strong> a large volume, diameter, <strong>and</strong> inner<br />

<strong>surface</strong> <strong>of</strong> voids. The polar component <strong>of</strong> SFE<br />

indicates a similar great number <strong>of</strong> accessible<br />

polar groups as in the case <strong>of</strong> CLY, which are<br />

able to interact with polar liquids.<br />

CMD adsorbs the smallest amount <strong>of</strong> solvent<br />

<strong>and</strong> low molecular weight species; has the<br />

largest contact angle, <strong>and</strong> the smallest polar<br />

component <strong>of</strong> SFE. This is caused by the rather<br />

dense structure; the smaller void volume <strong>and</strong><br />

inner <strong>surface</strong> area even if the degree <strong>of</strong><br />

crystallinity is smaller than that <strong>of</strong> CLY.<br />

CLY <strong>fibres</strong> sorption velocity is higher than<br />

CMD; they have contact angles <strong>and</strong> polar<br />

components <strong>of</strong> SFE similar to CV. The high<br />

hydrophilicity is caused by the <strong>fibres</strong> void<br />

system <strong>and</strong> not by the <strong>fibres</strong> superstructure,<br />

nevertheless the void system is less accessible<br />

for iodine adsorption.<br />

The applied conventional treatment processes<br />

influence the <strong>fibres</strong> fine structure, increasing<br />

the crystallinity index <strong>and</strong> decreasing the<br />

tenacity. The changes in fine structure are<br />

especially pronounced in CV <strong>and</strong> CMD due to<br />

the chemical changes caused by alkali<br />

treatment. Crystallinity index increases as much<br />

as 51%. Lyocell <strong>fibres</strong> have a more complicated<br />

structure <strong>and</strong> are less affected with respect to<br />

the crystallinity index. The dense fibre inner<br />

structure prevents major structural<br />

reorganization. These findings are also reflected<br />

by the iodine adsorption. The influence on the<br />

crystalline orientation differs, it increases in the<br />

case <strong>of</strong> the less oriented CV <strong>and</strong> CLY, but<br />

decreases in case <strong>of</strong> the most oriented CMD<br />

<strong>fibres</strong>.<br />

Mercerisation has the biggest influence on the<br />

sorption properties <strong>of</strong> all three types <strong>of</strong> <strong>fibres</strong>.<br />

The tensionless alkali treatment most likely<br />

causes an increase <strong>of</strong> the inner <strong>surface</strong> <strong>and</strong> the<br />

number <strong>of</strong> polar groups accessible for polar<br />

liquids. Hence an increase <strong>of</strong> the sorption<br />

94<br />

velocities (≈115%) <strong>and</strong> the total SFE <strong>of</strong> the<br />

<strong>fibres</strong> follows, mainly due to the increase <strong>of</strong> the<br />

fibre ’ s SFE polar component (≈48%).<br />

Bleaching causes less changes in <strong>fibres</strong> supramolecular<br />

structure but it increases the SFE´s<br />

polar component by 20%. This is the<br />

consequence <strong>of</strong> the increased number <strong>of</strong> polar<br />

groups created by the oxidation process [5].<br />

A good correlation between iodine adsorption<br />

<strong>and</strong> structural changes was observed. The<br />

increase in crystallinity decreases the<br />

accessibility <strong>of</strong> <strong>fibres</strong> <strong>and</strong>, thereby, the sorption<br />

<strong>of</strong> iodine becomes lower. The observed<br />

structural changes are not pronounced enough<br />

to significantly influence fibre’s mechanical<br />

properties, with the exception <strong>of</strong> alkali treated<br />

CMD <strong>and</strong> CLY <strong>fibres</strong> where a significant<br />

decrease <strong>of</strong> tenacity was observed.<br />

Viscose <strong>fibres</strong> (raw <strong>and</strong> treated) have the fastest<br />

sorption velocities, the lowest contact angle <strong>and</strong><br />

the highest polar part <strong>of</strong> the SFE, <strong>and</strong> are<br />

therefore the most hydrophilic among<br />

<strong>regenerated</strong> cellulose <strong>fibres</strong> due to their<br />

structure (the greatest volume, diameter, <strong>and</strong><br />

inner <strong>surface</strong> <strong>of</strong> voids) <strong>and</strong> above all due to the<br />

highest contribution <strong>of</strong> the accessible groups<br />

which are able to interact with polar liquids.<br />

References<br />

1. Alex<strong>and</strong>er, L.E.: X-Ray Diffraction<br />

Methods in Polymer Science, Wiley<br />

Interscience New York, 1969.<br />

2. Bodor, G.: Structural Investigation <strong>of</strong><br />

Polymers, Ellis Horwood, New York, 1991.<br />

3. Chan, C.M.: Contact Angle Measurement,<br />

in Polymer Surface Modification <strong>and</strong><br />

Characterization, Hanser/Gardner<br />

Publications, Inc., Cincinnati, 1994, pp 35-<br />

45.<br />

4. Filipič, Z., Stana-Kleinschek, K., Kreže, T.:<br />

Tekstilec, 2000, 43 (7/8), 245-250.<br />

5. Fras, L., Stana-Kleinschek, K., et.al.:Tekstil,<br />

2000, 52, 6, 263-276.<br />

6. Glatter, O., Kratky, O.: Small Angle X-ray<br />

Scattering, Academic Press, London, 1982.<br />

7. Gould R.F.: Dispersion Force Contribution<br />

to Surface <strong>and</strong> Interfacial Tensions, Contact<br />

Angles, <strong>and</strong> Heats <strong>of</strong> Immersion, in

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