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In this study, fabrication of polymer and cotton fabric exhibiting stimuli-responsive wetting and water vapor permeability features together with antibacterial activity was aimed.

Temperature and pH-responsive poly(N-isopropyl acrylamide-graft-chitosan) (PNIPAM-g-CS) copolymer were produced via the free radical addition polymerization method and fixed to the cotton fabric using butane tetracarboxylic acid (BTCA) cross-linker by double-bath impregnation method. The chemical structure of the graft copolymer was characterized by Fourier-transform infrared spectroscopy (FT-IR) spectroscopy and H-Nuclear magnetic resonance (1H NMR) analyses. Thermo-responsive behavior of the fabric was investigated by wetting time and water uptake tests, contact angle measurement and surface energy calculation. Additionally, antibacterial activity of the fabric treated with copolymer was studied against S. aureus bacterium.

PNIPAM-g-CS graft copolymer was synthesized successfully, which had lower critical solution temperature (LCST) value of 32 °C and exhibited thermo-responsive property. The treated fabrics exhibited hydrophilic character at temperatures below the LCST and hydrophobic character at temperatures above the LCST. It was found that polymer-coated fabric could have regulated the water vapor permeability by the change in its pore size and hydrophilicity depending on the temperature. Additionally, treated fabric displayed a pH-responsive water absorption behavior and strong antibacterial activity against S.aureus bacterium.

In the study, it has been shown that the cotton fabrics can be fabricated which have antibacterial activity and capable of pH and temperature responsive smart moisture/water management by application of copolymer. It is thought that the fabric structures developed in the study will be promising in the production of medical textile structures where antibacterial activity and thermophysiological comfort are important.

The purpose of this paper is to prepare microencapsulated phase change materials (PCMs) and apply them to cotton and wool fabrics for developing thermo-regulating fabrics.

Microencapsulated n-hexadecane and n-octadecane with poly(methylmethacrylate-co-2-hydroxy ethyl methacrylate) shell was prepared. Microcapsules were fabricated using oil-in-water emulsion polymerization method. Their chemical structure, microstructure, thermal energy storage properties and thermal stability were analyzed by Fourier-transform infrared spectroscopy, polarized light microscope, differential scanning calorimeter and thermogravimetric analyzer, respectively. The mean particle size was tested by a particle sized instrument. The microcapsules were applied to the wool and cotton fabrics using pad-dry-cure method. The thermo-regulating property of the fabrics was evaluated using the T-History test. The distribution and durability of the microcapsules on the fabrics was investigated with scanning electron microscopy.

Spherical microcapsules with p(MMA-co-HEMA) shell and n-alkane core have been produced successfully. n-hexadecane in microcapsule solidifies at 14.8−15.6°C with the latent heat of 65.6−129.8 J/g and melts at 16.7−16.9°C with the latent heat of 67.6−136.9 J/g. Microencapsulated n-octadecane solidifies at 25.8−26.3°C with the latent heat of 74.1−106.2 J/g and melts at 26.8−27.4°C with the latent heat of 80.3−113.4 J/g. The microcapsules have enough thermal stability to the temperature of 150°C that was applied during the fixation of microcapsules on the fabric. The thermo-regulating effect of the microcapsule-incorporated fabrics has been proved by the T-history test.

PCM microcapsules with p(MMA-co-HEMA) shell and n-hexadecane and n-octadecane core have been produced and their usage to produce thermo-regulating textiles have been proved. To determine the thermo-regulating property of the fabrics treated with these new PCM microcapsules, a T-History system has been designed.