College of Environmental Science and Engineering, Zhongkai University of Agriculture and Engineering, Guangzhou, 510025, China.
College of Chemistry and Environmental Sciences, Guangdong Ocean University, Zhanjiang, 524088, People's Republic of China.
Environ Sci Pollut Res Int. 2020 Apr;27(11):12746-12754. doi: 10.1007/s11356-020-07682-y. Epub 2020 Feb 1.
The present study investigated the impacts of humic acid (HA) and surfactants (SDBS and CTAB), which were ubiquitously found in the aquatic environments, on the removal of Cr(VI) by the hydroxylated MWCNTs-OH. The results showed that MWCNTs-OH could remove Cr(VI) from aqueous solution via adsorption coupled with reduction, and the kinetics followed the pseudo-first-order model with the rate of 3.5 × 10 h. In the presence of anionic SDBS, the removal percentage of Cr(VI) was greatly inhibited because the hydrophobic interaction and π-π interaction between SDBS and MWCNTs-OH surfaces not only decreased the adsorption sites for Cr(VI) but also made the surfaces more negatively charged. On the contrary, the existence of cationic CTAB could lead to the surfaces more positively charged, which consequently enhance the electrostatic attraction between Cr(VI) and the surfaces as well as the removal of Cr(VI). Noticeably, the presence of HA could promote the removal of Cr(VI), which was attributed to the reduction of Cr(VI) by the adsorbed HA. The ESR spectra indicated the existence of π-type radicals in HA structure and conduction electrons in MWCNTs-OH, and then the π-π interaction between MWCNTs-OH and adsorbed HA possibly increase the electron-donating ability of HA. Moreover, the promotive effect of HA could be enhanced with the addition of Ca. This study was helpful for us to understand the role of MWCNTs-OH in controlling the fate of Cr(VI) when HA and surfactants were present.
本研究考察了腐殖酸(HA)和表面活性剂(SDBS 和 CTAB)在水环境中普遍存在的情况下对羟化多壁碳纳米管(MWCNTs-OH)去除 Cr(VI)的影响。结果表明,MWCNTs-OH 可以通过吸附和还原的方式去除水溶液中的 Cr(VI),动力学遵循拟一级模型,速率常数为 3.5×10^-1 h。在阴离子 SDBS 的存在下,Cr(VI)的去除率大大受到抑制,因为 SDBS 和 MWCNTs-OH 表面之间的疏水相互作用和 π-π 相互作用不仅减少了 Cr(VI)的吸附位点,而且使表面带更多负电荷。相反,阳离子 CTAB 的存在会导致表面带更多正电荷,从而增强 Cr(VI)与表面之间的静电吸引以及 Cr(VI)的去除。值得注意的是,HA 的存在可以促进 Cr(VI)的去除,这归因于吸附的 HA 还原 Cr(VI)。ESR 谱表明 HA 结构中存在 π 型自由基和 MWCNTs-OH 中的传导电子,然后 MWCNTs-OH 和吸附的 HA 之间的 π-π 相互作用可能增加 HA 的供电子能力。此外,随着 Ca 的添加,HA 的促进作用可以增强。本研究有助于我们了解当 HA 和表面活性剂存在时,MWCNTs-OH 在控制 Cr(VI)命运中的作用。