Cotransport of Graphene Oxide Nanoparticles and Kaolinite Colloids in Porous Media

被引:93
作者
Chrysikopoulos, Constantinos V. [1 ]
Sotirelis, Nikolaos P. [1 ]
Kallithrakas-Kontos, Nikolaos G. [2 ]
机构
[1] Tech Univ Crete, Sch Environm Engn, Khania 73100, Greece
[2] Tech Univ Crete, Sch Mineral Resources Engn, Khania 73100, Greece
关键词
Graphene oxide; Kaolinite; Cotransport; Glass beads; Quartz sand; Porous media; DEEP-BED FILTRATION; QUARTZ SAND; ENGINEERED NANOPARTICLES; AGGREGATION KINETICS; VIRUS COTRANSPORT; SATURATED COLUMNS; ANALYTICAL-MODELS; IONIC-STRENGTH; CLAY-MINERALS; HUMIC-ACID;
D O I
10.1007/s11242-017-0879-z
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This study examines the influence of pH and ionic strength () on the cotransport of graphene oxide (GO) nanoparticles and kaolinite (KGa-1b) colloids. Several flowthrough experiments were conducted in water-saturated columns, packed with either glass beads or quartz sand, in order to determine the transport behavior of GO and KGa-1b independently, as well as the cotransport behavior of GO together with KGa-1b. Various water chemistry conditions ( and ) were considered. Collision efficiencies were calculated using the classical colloid filtration theory. Interaction energy profiles between GO nanoparticles or KGa-1b colloids and glass beads or quartz sand were constructed for the various experimental conditions, by using measured zeta potentials and applying the classical Derjaguin-Landau-Verwey-Overbeek theory. The cotransport experimental breakthrough data suggested that by lowering the pH, the retention of GO nanoparticles is enhanced, due to a possible increase in heteroaggregation between GO nanoparticles and KGa-1b colloids. Also, by increasing the values, the retention of GO nanoparticles was slightly increased. The mass recovery of GO nanoparticles was reduced, and the transport of GO nanoparticles was retarded in the presence of KGa-1b colloids. Furthermore, the retention of GO nanoparticles was greater for columns packed with quartz sand than glass beads.
引用
收藏
页码:181 / 204
页数:24
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