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Thermal analyses of flame‐retardant twills containing cotton, polyester and wool
Author(s) -
Trask Brenda J.,
Beninate John V.
Publication year - 1986
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1986.070320517
Subject(s) - thermogravimetric analysis , fire retardant , materials science , polyester , wool , composite material , differential scanning calorimetry , char , endothermic process , thermal decomposition , polymer chemistry , combustion , chemical engineering , chemistry , organic chemistry , physics , adsorption , engineering , thermodynamics
Medium weight twill fabrics constructed from cotton and cotton blended with polyester and/or wool were analyzed under nitrogen by three thermoanalytical techniques. Fabrics were tested both before and after treatment with [tetrakis(hydroxymethyl)phosphonium] sulfate (THPS), urea, and trimethylolmelamine. The presence of all fibers was distinguishable in differential scanning calorimetric analysis (DSC) of untreated fabrics; the relative positions of the endothermic, decomposition peak temperatures were only slightly changed. After flame‐retardant (FR) treatment, the blended cotton and wool fibers were altered. Both fibers decomposed as exotherms during DSC analysis. These data supported earlier microscopical, X‐ray evidence that wool fibers were actually reacting with the FR treatment. The two DSC peaks for polyester polymer melting and decomposing remained unaffected by either blending with other fibers or the presence of the FR finish on the fabric. There was excellent agreement between DSC peak temperatures and the temperature of maximum rate of weight loss obtained from thermogravimetric analysis (TGA). Blending cotton with either of these fibers increased the residue measured after TGA. The increased residue correlated with increased flame resistance as measured by the 45° angle, edge‐ignition burning rate test.

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