Preparation of AgCl/TNTs nanocomposites for organic dyes and inorganic heavy metal removal

In this study, TiO 2 nanotubes (TNTs) and AgCl-modified TNTs nanocomposites with multiple crystal phases were synthesized through a hydrothermal method without calcination. The resultant samples had a large Brunauer-Emmett-Teller surface area. Additionally, the Ag modification process reduced the re...

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Veröffentlicht in:Environmental science and pollution research international 2019-07, Vol.26 (21), p.22082-22096
Hauptverfasser: Tsai, Cheng-Yen, Liu, Chen-Wuing, Hsi, Hsing-Cheng, Lin, Kuen-Song, Lin, Yi-Wen, Lai, Li-Chi, Weng, Tsung-Nan
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Sprache:eng
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Zusammenfassung:In this study, TiO 2 nanotubes (TNTs) and AgCl-modified TNTs nanocomposites with multiple crystal phases were synthesized through a hydrothermal method without calcination. The resultant samples had a large Brunauer-Emmett-Teller surface area. Additionally, the Ag modification process reduced the recombination rate of electron-hole pairs in the synthesized sample and possessed more oxygen vacancy sites. The surface area of the AgCl-modified TNTs was smaller than that of non-modified TNTs sample; however, the nanocomposites exhibited outstanding photocatalytic performance and adsorption properties. AgCl compounds present on the TNTs surface effectively interacted with Hg 0 , improving the dye photodegradation efficiency. The Hg 0 removal efficiencies of the TNTs and AgCl-modified TNTs samples were about 63% and 86%, respectively. The crystal violet (CV) and malachite green (MG) removal efficiencies of the AgCl-modified TNTs sample were around 57% and 72%, respectively. Both dyes photodecomposition efficiencies for AgCl-modified TNTs sample are higher than those of TNTs sample. The oxygen vacancy on the AgCl-modified TNTs surface was determined to be advantageous for OH − and arsenate adsorption through ligand exchange. The maximum adsorption quantity of As 5+ calculated by Langmuir equation was 15.38 mg g −1 (TNTs) and 21.10 mg g −1 (AgCl-modified TNTs).
ISSN:0944-1344
1614-7499
DOI:10.1007/s11356-019-05570-8