Hou Jun, Zhang Mingzhi, Wang Peifang, Wang Chao, Miao Lingzhan, Xu Yi, You Guoxiang, Lv Bowen, Yang Yangyang, Liu Zhilin
Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes, Ministry of Education, Hohai University, Nanjing 210098, People's Republic of China; College of Environment, Hohai University, Nanjing 210098, People's Republic of China.
Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes, Ministry of Education, Hohai University, Nanjing 210098, People's Republic of China; College of Environment, Hohai University, Nanjing 210098, People's Republic of China.
Environ Pollut. 2017 Oct;229:49-59. doi: 10.1016/j.envpol.2017.05.059. Epub 2017 May 31.
This study investigated the transport and long-term release of stabilized silver nanoparticles (AgNPs), including polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs) and bare AgNPs (Bare-AgNPs), in the presence of natural organic matters (NOMs; both humic acids (HA) and alginate (Alg)) and an electrolyte (Ca) in a sand-packed column. Very low breakthrough rate (C/C) of AgNPs (below 0.04) occurred in the absence of NOM and the electrolyte. Increasing the concentration of NOM and decreasing the influent NOM solution's ionic strength (IS) reduced the retention of AgNPs. The reduced NP retention at high NOM and low IS was mainly attributed to the increased energy barrier between the AgNPs and the sand grain surface. Notably, the retention of PVP-AgNPs was enhanced at high Alg concentration and low IS, which mainly resulted from the improved hydrophobicity that could increase the interaction between the PVP-AgNPs and the collector. The total release amount of PVP-AgNPs (10.03%, 9.50%, 28.42%, 6.37%) and Bare-AgNPs (3.28%, 2.58%, 10.36%, 1.54%) were gained when exposed to four kinds of NOM solutions, including deionized water, an electrolyte solution (1 mM Ca), HA with an electrolyte (1 mM Ca), and a Alg (40 mg/L) solution with an electrolyte (1 mM Ca). The long-term release of retained silver nanoparticles in the quartz sand was mostly through the form of released Ag NPs. The factors that increased the mobility of AgNPs in quartz sand could improve the release of the AgNPs. The release of AgNPs had no significant change in the presence Ca but were increased in the presence of HA. The Alg slightly decreased the release of AgNPs by increasing the hydrophobicity of AgNPs. The results of the study indicated that all the tested NOM and Ca have prominent influence on the transport and long-term release behavior of silver nanoparticles in saturated quartz sand.
本研究考察了在天然有机物(NOMs,包括腐殖酸(HA)和藻酸盐(Alg))以及电解质(Ca)存在的情况下,稳定化银纳米颗粒(AgNPs),包括聚乙烯吡咯烷酮包覆的AgNPs(PVP-AgNPs)和裸AgNPs(Bare-AgNPs),在填充砂柱中的传输和长期释放情况。在不存在NOM和电解质的情况下,AgNPs的穿透率(C/C)非常低(低于0.04)。增加NOM浓度并降低进水NOM溶液的离子强度(IS)会降低AgNPs的保留率。在高NOM和低IS条件下NP保留率降低主要归因于AgNPs与砂粒表面之间能量屏障的增加。值得注意的是,在高Alg浓度和低IS条件下,PVP-AgNPs的保留率增强,这主要是由于疏水性提高,从而增加了PVP-AgNPs与收集剂之间的相互作用。当暴露于四种NOM溶液中时,获得了PVP-AgNPs(10.03%、9.50%、28.42%、6.37%)和Bare-AgNPs(3.28%、2.58%、10.36%、1.54%)的总释放量,这四种NOM溶液包括去离子水、电解质溶液(1 mM Ca)、含电解质(1 mM Ca)的HA以及含电解质(1 mM Ca)的Alg(40 mg/L)溶液。石英砂中保留的银纳米颗粒的长期释放主要通过释放的Ag NPs形式。增加AgNPs在石英砂中迁移率的因素可以促进AgNPs的释放。AgNPs的释放在存在Ca的情况下没有显著变化,但在存在HA的情况下会增加。Alg通过增加AgNPs的疏水性略微降低了AgNPs的释放。研究结果表明,所有测试的NOM和Ca对饱和石英砂中银纳米颗粒的传输和长期释放行为都有显著影响。