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In this study, an alternative Pd activation process was developed for electroless Ni plating on polyester fabric modified with a self‐assembled monolayer (SAM) of 3‐aminopropyltrimethoxysilane (APTMS). The presence of a highly oriented amino‐terminated SAM and the formation of Pd‐activated APTMS were demonstrated by X‐ray photoelectron spectroscopy analysis. After activation, electroless Ni plating was successfully initiated, and the Ni coating was deposited onto the surface of the polyester fibers. The resulting Ni coating was examined by scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, and X‐ray diffraction. The electromagnetic interference (EMI) shielding effectiveness (SE) and adhesive strength of the Ni‐plated polyester fabric were evaluated. On the basis of the experimental results, the Ni coating produced with a Pd‐activated SAM was uniform and dense. As the Ni weight on the treated fabric was 32 g/m2, the EMI SE of the Ni‐plated polyester fabric modified with APTMS obtained was more than 30 dB at frequencies that ranged from 2 to 18 GHz. Compared with the conventional two‐step activation method, Ni coating on the Pd‐activated polyester fabric modified with APTMS improved the coating adherence stability. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013

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In this study, silver/reduced graphene oxide (Ag/RGO) coated polyester (PET) fabrics with dopamine as adhesive agent were prepared through an efficient chemical reduction method under microwave irradiation.

A novel CO2-responsive cotton as an eco-friendly adsorbent derived from poly­(4-acryloyloxybenzophenone-co-2-(dimethylamino) ethyl methacrylate) and cotton was fabricated via a facile and fast dip-coating method. As expected, upon CO2 stimulation, the protonated cotton presented CO2-induced “on–off” selective adsorption behaviors toward anionic dyes owing to electrostatic interactions. The adsorption isotherms and kinetics of the CO2-responsive cotton toward anionic dyes obeyed the Langmuir isotherm and pseudo-second-order kinetics models, respectively. It is noteworthy that the CO2-responsive cotton exhibited high adsorption capacity and ultrafast adsorption rate toward anionic dyes with the maximum adsorption capacities of 1785.71 mg g–1 for methyl orange (MO), 1108.65 mg g–1 for methyl blue (MB), and 1315.79 mg g–1 for naphthol green B (NGB), following the adsorption equilibrium times of 5 min for MO, 3 min for MB, and 4 min for NGB. Moreover, the CO2-responsive cotton also exhibited high removal efficiency toward anionic dyes in synthetic dye effluent. Additionally, the CO2-responsive cotton could be facilely regenerated via heat treatment under mild conditions and presented stable adsorption properties even after 15 cycles. Finally, the as-prepared CO2-responsive cotton exhibited outstanding antibacterial activity against E. coli and S. aureus. In summary, this novel CO2-responsive cotton can be viewed as a promising eco-friendly adsorbent material for potential scalable application in dye-contaminated wastewater remediation.