期刊
RSC ADVANCES
卷 4, 期 31, 页码 15983-15994出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra01170h
关键词
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资金
- Ministry of Education, Science, and Culture of Japan
- Grant-in-Aid for Development Scientific Research [24550132]
- Nagoya Institute of Technology
- Grants-in-Aid for Scientific Research [24550132] Funding Source: KAKEN
We synthesized, at room temperature, aliphatic (1-4) and aromatic (5-8) poly(ester-sulfide) s, via a thiolene click polymerization of bis(pentenyl) methylsuccinate (BPMSA) and bis(pentenyl) phthalate (BPPh), respectively, with several dithiols including 1,2-ethanedithiol (EtDt), 1,3-propanedithiol (PrDt), 1,4butanedithiol (BuDt), and 1,5-pentanedithiol (PeDt) (M-n = 0.7-5.2 Chi 10(4), M-w/M-n = 1.6-2.6). Subsequent Oxone oxidation of poly(BPPh-alt-BuDt) (7), as an example, led to the corresponding poly(ester-sulfone) 7 ' (M-n = 30 000, M-w/M-n = 1.8). We then prepared a composite of 7 ' and TiO2 by using electrophoretic deposition (EPD). The TiO2/poly(ester-sulfone) 7 ' composite was selectively deposited onto a stainlesssteel anode. The electrode's morphology was confirmed by scanning electron microscopy. We characterized the relationship between the structure of the composite-coated electrode and the zeta potential of an N, N-dimethylformamide/alcohol suspension of poly(ester-sulfone) 7 '. The measured values, -(33.27-18.3) mV, indicate that the composite had indeed been selectively deposited on the anode. Notably, from the suspension with the negative potential of -33.27 mV, the thickest composite film was obtained. Furthermore, photo-catalytic activity occurred on the surface of the composite when immersed in aqueous rhodamine-B for 1 month.
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