College of Water Conservancy and Hydropower Engineering, Hohai University, Nanjing 210098, China; Department of Agricultural and Biological Engineering, University of Florida, Gainesville, FL 32611, USA.
Department of Agricultural and Biological Engineering, University of Florida, Gainesville, FL 32611, USA.
Environ Pollut. 2018 Apr;235:350-357. doi: 10.1016/j.envpol.2017.12.063. Epub 2018 Jan 4.
Simultaneous aggregation and retention of nanoparticles can occur during their transport in porous media. In this work, the concurrent aggregation and transport of GO in saturated porous media were investigated under the conditions of different combinations of temperature, cation type (valence), and electrolyte concentration. Increasing temperature (6-24 °C) at a relatively high electrolyte concentration (i.e., 50 mM for Na, 1 mM for Ca, 1.75 mM for Mg, and 0.03 and 0.05 mM for Al) resulted in enhanced GO retention in the porous media. For instance, when the temperature increased from 6 to 24 °C, GO recovery rate decreased from 31.08% to 6.53% for 0.03 mM Al and from 27.11% to 0 for 0.05 mM Al. At the same temperature, increasing cation valence and electrolyte concentration also promoted GO retention. Although GO aggregation occurred in the electrolytes during the transport, the deposition mechanisms of GO retention in the media depended on cation type (valence). For 50 mM Na, surface deposition via secondary minima was the dominant GO retention mechanism. For multivalent cation electrolytes, GO aggregation was rapid and thus other mechanisms such as physical straining and sedimentation also played important roles in controlling GO retention in the media. After passing through the columns, the GO particles in the effluents showed better stability with lower initial aggregation rates. This was probably because less stable GO particles with lower surface charge densities in the porewater were filtered by the porous media, resulting in more stable GO particle with higher surface charge densities in the effluents. An advection-dispersion-reaction model was applied to simulate GO breakthrough curves and the simulations matched all the experimental data well.
纳米颗粒在多孔介质中传输时会发生同时聚集和滞留。在这项工作中,研究了在不同温度、阳离子类型(价态)和电解质浓度组合条件下,GO 在饱和多孔介质中的同时聚集和传输。在相对高的电解质浓度(即 50mM 的 Na、1mM 的 Ca、1.75mM 的 Mg 以及 0.03 和 0.05mM 的 Al)下升高温度(6-24°C)会导致 GO 在多孔介质中的滞留增强。例如,当温度从 6°C 升高到 24°C 时,0.03mM Al 的 GO 回收率从 31.08%下降到 6.53%,而 0.05mM Al 的 GO 回收率从 27.11%下降到 0。在相同温度下,增加阳离子价态和电解质浓度也会促进 GO 的滞留。尽管在运输过程中电解质中发生了 GO 聚集,但 GO 在介质中滞留的沉积机制取决于阳离子类型(价态)。对于 50mM 的 Na,通过次级最小值的表面沉积是 GO 主要的滞留机制。对于多价阳离子电解质,GO 聚集迅速,因此物理应变和沉淀等其他机制也在控制 GO 在介质中的滞留方面发挥了重要作用。穿过柱子后,流出物中的 GO 颗粒表现出更好的稳定性,初始聚集率更低。这可能是因为孔隙水中表面电荷密度较低、稳定性较差的 GO 颗粒被多孔介质过滤掉了,从而导致流出物中具有更高表面电荷密度、更稳定的 GO 颗粒。运用了一个对流-弥散-反应模型来模拟 GO 的穿透曲线,模拟结果与所有实验数据吻合良好。