Chemical Separation
Elastomeric polyurethane fibers must be separated from primary yarn components to verify composition claims in stretch fabrics. For these blends, elastane dissolution employs warm dimethylacetamide or dimethylformamide to selectively liquefy the stretch component while preserving cotton, wool, or polyamide. This method yields a clear gravimetric measure of the elastic content, which frequently dictates the correct import classification for stretch garments.
Extraction Procedure
Execution of the separation requires a controlled laboratory hotplate equipped with a reflux condenser to maintain solvent volume and concentration. During elastane dissolution, the dry specimen is agitated in the organic solvent for a specified duration, typically between thirty and sixty minutes. After the polymer has fully entered the solution, the remaining yarn structure is isolated through a sintered glass filter.
The recovered fibers are then washed with clean solvent, followed by water, to remove any remaining dissolved polymer.
Fiber Safeguard
Protection of the non-soluble fiber relies on maintaining the solvent temperature within strict limits. If the temperature is too high, the solvent may swell or partially dissolve polyamide or acetate fibers in the yarn. This unwanted secondary action compromises the accuracy of the final gravimetric analysis.
Material Limit
Moisture and finishes on the yarn can impede the penetration of the organic solvent. Sizing agents or silicone lubricants must be removed prior to the chemical extraction to ensure complete contact. Any residual elastane that escapes the solvent action will be weighed as part of the insoluble residue, leading to an underestimation of the elastomeric content.
Routine chemical pre-treatment prevents this source of error.