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Surface Modification of Cellulose Acetate with Cutinase and ...

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<strong>Surface</strong> <strong>Modification</strong> <strong>of</strong> Synthetic Fibres - Introduction<br />

In the laboratory, nylon 6,6 can also be made using adipoyl chloride instead <strong>of</strong> adipic. It<br />

is difficult to get the proportions exactly correct, <strong>and</strong> deviations can lead to chain<br />

termination at molecular weights less than a desirable 10,000 Daltons. To overcome this<br />

problem, a crystalline, solid "nylon salt" can be formed at room temperature, using an<br />

exact 1:1 ratio <strong>of</strong> the acid <strong>and</strong> the base to neutralize each other. Heated to 285 °C, the<br />

salt reacts to form nylon polymer. Above 20,000 daltons, it is impossible to spin the<br />

chains into yarn, so to combat this, acetic acid is added to react <strong>with</strong> a free amine end<br />

group during polymer elongation to limit the molecular weight. In practice, <strong>and</strong><br />

especially for 6,6, the monomers are <strong>of</strong>ten combined in a water solution. The water used<br />

to make the solution is evaporated under controlled conditions, <strong>and</strong> the increasing<br />

concentration <strong>of</strong> "salt" is polymerized to the final molecular weight (Kohan, 1992).<br />

3.2. Polyamide 6,6 fibres properties<br />

Despite <strong>of</strong> all the excellent properties exhibited, nylon fibers present low hydrophylicity<br />

<strong>and</strong> low reactivity <strong>with</strong> the most usual finishing <strong>and</strong> colouring agents. Coating finishing<br />

effects are difficult to obtain when hydrophobic polyamide fabrics are used. Recent<br />

studies clearly indicate that the modification <strong>of</strong> synthetic polymers <strong>with</strong> enzymes is an<br />

effective <strong>and</strong> environmentally friendly alternative to chemical methods using alkaline<br />

products (Silva et al., 2004).<br />

4. Acrylic<br />

Acrylic fibers are synthetic fibers made from a polymer (polyacrylonitrile) <strong>with</strong> an<br />

average molecular weight <strong>of</strong> approximatly 100,000 Dalton. To be called acrylic the<br />

polymer must contain at least 85% acrylonitrile monomer (Greenley, 1989). Typical<br />

comonomers are vinyl acetate or methyl acrylate. The polymer is formed by free-radical<br />

polymerization. The fiber is produced by dissolving the polymer in a solvent such as<br />

N,N-dimethylformamide or aqueous sodium thiocyanate, metering it through a multihole<br />

spinnerette <strong>and</strong> coagulating the resultant filaments in an aqueous solution <strong>of</strong> the<br />

same solvent. Washing, stretching, drying <strong>and</strong> crimping complete the processing.<br />

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