Abstract

Polymers with aggregation-induced emission (AIE) characteristics have attracted much attention because of their potential applications in luminescent self-assembling, anti-counterfeiting, decoration, and photoelectric devices. To date, most technologies to prepare fluorescent polymers lack versatility; moreover, the resultant material exhibits intrinsic defects of poor fluorescence intensity and durability. Herein, we covalently anchored units of tetraphenylethylene (TPE), an archetypal AIE luminogen, on the surface of conventional polymer fibers such as polyethylene/polypropylene nonwoven fabric (PE/PP NWF) via radiation-induced graft polymerization (RIGP) and subsequent chemical modification for the first time. The physicochemical properties of the original and modified fabrics were characterized in detail by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), wide-angle X-ray diffraction (WAXD), and thermogravimetric analysis (TGA). The results indicated that the TPE units were covalently and uniformly anchored on the surface of PE/PP NWF with a disordered architecture and that the as-prepared fluorescent fabric had a high thermal stability. Additionally, the fluorescent properties of the as-prepared fluorescent fabric were measured. It emitted a strong green emission and showed superior fluorescence durability after 20 cycles of accelerated laundering or in 12 M concentrated HCl and NaOH solutions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.