Body odorants typically transfer to clothing fabrics by way of liquid sweat, yet investigations of odor retention in textiles often neglect this route of exposure in their test procedures. This paper describes a novel method for transferring selected odorous volatile organic compounds to six types of textile fibers in yarn bundle form by an aqueous sweat solution. Headspace volatile organic compounds varying by chemical class (ketones, aldehydes, carboxylic acids) were monitored at discrete time intervals (30 min, 3 h, 24 h) using proton transfer reaction mass spectrometry. Lower intensities of ketones and aldehydes were detected in the headspace above cellulosic fibers (cotton, mercerized cotton, viscose) than above wool, nylon, and polyester fibers at 30 min. A rapid decrease in ketones occurred for all fibers, but lower intensities of ketones were released after 3 h for cellulosic and wool fibers. Nylon fibers typically released the highest amounts of ketones and aldehydes at 30 min, but by 24 h higher intensities of these compounds were released from polyester. Carboxylic acids exhibited minimal differences in intensities between 30 min and 3 h, with few differences evident among fiber types. Understanding the preferential sorption of odorants when clothing is exposed to volatile organic compounds in aqueous solutions such as sweat is enhanced from the results of this investigation.

The release of fragmented fibers (FFs), including microplastics from textiles, during their service life is considered an established source of environmental pollution. The yarn structure is identified to affect the amount and length distribution profile of shed FFs from textiles. In the present work, the impact of yarn structures spun from 100% polyester staple fibers, using commercially relevant spun yarn technologies in the textile industry, on the release of FFs from textiles is studied. The bespoke woven fabric samples produced from three types of spun yarns, which include ring, airjet (air vortex) and rotor yarns, were subjected to an accelerated washing process, for up to five washes, to quantify shed FFs and their length distribution profile. The morphological shapes of FF ends associated with the nature of fiber damage were also investigated. The results demonstrated that airjet and rotor yarn structures had released 28% and 33% less mass of FFs, respectively, as compared to the ring yarn structure during the whole washing process. The length distribution profile identified that the ring yarn structure shed longer length FFs as compared to both airjet and rotor ones. The damaged ends highlight the importance of textile manufacturing processes on the generation of FFs. The results of this study give a better understanding of the yarn structural effect of commercially relevant technologies on shedding of FFs, which are released as a pollutant to the environment.