Khanh An Huynh

Heteroaggregation of graphene oxide (GO) with nanometer- and micrometer-sized hematite colloids, which are naturally present in aquatic systems, is investigated in this study. The heteroaggregation rates between GO and hematite nanoparticles (HemNPs) were quantified by dynamic light scattering, while the heteroaggregation between GO and micrometer-sized hematite particles (HemMPs) was examined through batch adsorption and sedimentation experiments. The heteroaggregation rates of GO with HemNPs first increased and then decreased with increasing GO/HemNP mass concentration ratios. The conformation of GO–HemNP heteroaggregates at different GO/HemNP mass concentration ratios was observed through transmission electron microscopy imaging. Initially, GO underwent heteroaggregation with HemNPs through electrostatic attraction to form primary heteroaggregates, which were further bridged by GO to form bigger clusters. At high GO/HemNP mass concentration ratios where GO outnumbered HemNPs, heteroaggregation resulted in the formation of stable GO–HemNP nanohybrids that have a critical coagulation concentration of 308 mM NaCl at pH 5.2. In the case of HemMPs, GO adsorbed readily on the microparticles and, at an optimal GO/HemMP ratio of ∼0.002, the sedimentation of HemMPs was the fastest, most likely because of the formation of “electrostatic patches” leading to favorable aggregation of the microparticles.

The presence of silver nanoparticles (AgNPs) in aquatic environments could potentially cause adverse impacts on ecosystems and human health. However, current understanding of the environmental fate and transport of AgNPs is still limited because their properties in complex environmental samples cannot be accurately determined. In this study, the feasibility of using asymmetric flow field-flow fractionation (AF4) connected online with single particle inductively coupled plasma mass spectrometry (spICPMS) to detect and quantify AgNPs at environmentally relevant concentrations was investigated. The AF4 channel had a thickness of 350 µm and its accumulation wall was a 10 kDa regenerated cellulose membrane. A 0.02 % FL-70 surfactant solution was used as an AF4 carrier. With 1.2 mL/min AF4 cross flow rate, 1.5 mL/min AF4 channel flow rate, and 5 ms spICPMS dwell time, the AF4–spICPMS can detect and quantify 40 – 80 nm AgNPs, as well as Ag-SiO₂ nanoparticles (51.0 nm diameter Ag core and 21.6 nm SiO₂ shell), with good recovery within 30 min. This system was not only effective in differentiating and quantifying different types of AgNPs with similar hydrodynamic diameters, such as in mixtures containing Ag-SiO₂ core-shell nanoparticles and 40 – 80 nm AgNPs, but also suitable for differentiating between 40 nm AgNPs and elevated dissolved Ag content. The study results indicate that AF4–spICPMS is capable of detecting and quantifying AgNPs and other engineered metal- nanomaterials in environmental samples. Nevertheless, further studies are needed before AF4–spICPMS can become a routine analytical technique.