As silica nanoparticles (SiNPs) pervade the global economy, however, the followed emissions during the manufacturing, use, and disposal stages inevitably bring an environmental release, potentially result in harmful impacts. Endothelial dysfunction precedes cardiovascular disease, and is often accompanied by mitochondrial impairment and dysfunction. We had reported endothelial dysfunction induced by SiNPs, however, the related mechanisms by which SiNPs interact with mitochondria are not well understood. In the present study, we examined SiNPs-induced mitochondrial dysfunction, and further demonstrated their adverse effects on mitochondrial dynamics and biogenesis in endothelial cells (HUVECs). Consequently, SiNPs entered mitochondria, caused mitochondrial swelling, cristae disruption and even disappearance. Further analyses revealed SiNPs increased the intracellular level of mitochondrial reactive oxygen species, eventually resulting in the collapse of mitochondrial membrane potential, impairments in ATP synthesis, cellular respiration and the activities of three ATP-dependent enzymes (including Na+/K+-ATPase, Ca2+-ATPase and Ca2+/Mg2+-ATPase), as well as an elevated intracellular calcium level. Furthermore, mitochondria in SiNPs-treated HUVECs displayed a fission phenotype. Accordingly, dysregulation of the key gene expressions (FIS1, DRP1, OPA1, Mfn1 and Mfn2) involved in fission/fusion event further certified the SiNPs-induced perturbation of mitochondrial dynamics. Meanwhile, SiNPs-treated HUVECs displayed declined levels of mitochondrial DNA copy number, PGC-1α, NRF1 and also TFAM, indicating an inhibition of mitochondrial biogenesis triggered by SiNPs via PGC-1α-NRF1-TFAM signaling. Overall, SiNPs triggered endothelial toxicity through mitochondria as target, including the induction of mitochondrial dysfunction, as well as the perturbations of their dynamics and biogenesis.

Increasing interests in carbon dots (CDs) research resulted in the increased production of CDs and the risk to be released into the environment, including surface water and groundwater. To assess the environmental behavior of CDs, the stability of CDs in aqueous solutions were first examined by different environmental conditions, followed by the systematic investigation of the adsorption behaviors of CDs onto Al2O3 surface. Electrostatic interactions were considered as the dominant forces in CDs adsorption onto Al2O3 process, which were further confirmed by controlling experiments as compared with other minerals or oxides, such as montmorillonite, kaolinite and SiO2. Theoretical calculations and characterization of Al2O3/CDs revealed chemisorptions exist in the adsorption process. Our investigation results provided fundamental understanding towards the interaction of CDs with Al2O3 surface, and potential fate of CDs under natural conditions in aquatic environment, as well as in soils and sediments.

In this study, solid acid amorphous Fe3O4/SiO2 ceramic coating decorated with sulfur on Q235 carbon steel as Fenton-like catalyst for phenol degradation was successfully prepared by plasma electrolytic oxidation (PEO) in silicate electrolyte containing Na2S2O8 as sulfur source. The surface morphology and phase composition were characterized by SEM, EDS, XRD and XPS analyses. NH3-TPD was used to evaluate surface acidity of PEO coating. The results indicated that sulfur decorated amorphous Fe3O4/SiO2 ceramic coatings with porous structure and higher acid strength had the similar pore size and the surface became more and more uneven with the increase of Na2S2O8 in the silicate electrolyte. The Fenton-like catalytic activity of sulfur decorated PEO coatings was also evaluated. In contrast to negligible catalytic activity of sulfur undecorated PEO coating, catalytic activity of sulfur decorated PEO coating was excellent and PEO coating prepared with 3.0 g Na2S2O8 had the highest catalytic activity which could degrade 99% of phenol within 8 min under circumneutral pH. The outstanding performance of sulfur decorated PEO coating was attributed to strong acidic microenvironment and more Fe²⁺ on the surface. The strong acid sites played a key factor in determining catalytic activity of catalyst. In conclusion, rapid phenol removal under circumneutral pH and easier separation endowed it potential application in wastewater treatment. In addition, this strategy of preparing immobilized solid acid coating could provide guidance for designing Fenton-like catalyst with excellent catalytic activity and easier separation.

The application of nanotechnology in agriculture, pesticide delivery and other related fields increases the occurrence of engineered nanoparticles (ENPs) in soil. Since ENPs have larger surface areas and normally a high adsorption capacity for organic pollutants, they are thought to influence the transport of pesticides in soils and thereafter influence the uptake and transformation of pesticides. The adsorption pattern of racemic-metalaxyl on agricultural soils including kinetics and isotherms changed in the presence of nano-SiO2. The adsorption of racemic-metalaxyl on agricultural soil was not enantioselective, in either the presence or the absence of SiO2. The adsorption of racemic-metalaxyl on SiO2 decreased to some extent in soil-SiO2 mixture, and the absolute decrease was dependent on soil properties. The decreased adsorption of metalaxyl on SiO2 in soil-SiO2 mixture arose from the competitive adsorption of soil-dissolved organic matter and the different dispersion and aggregation behaviors of SiO2 in the presence of soil. Interactions between SiO2 and soil particles also contributed to the decreased adsorption of metalaxyl on SiO2, and the interactions were analyzed by extended Derjaguin–Landau–Verwey–Overbeek theory. The results showed that the presence of nano-particles in soils could decrease the mobility of pesticides in soils and that this effect varied with different soil compositions.

Chromium-contaminated water is regarded as one of the biggest threats to human health. In this study, a novel magnetic mesoporous MnFe2O4@SiO2−CTAB composite was prepared by a facile one-step modification method and applied to remove Cr(VI). X-ray diffraction, scanning electron microscopy, transmission electron microscopy, specific surface area, and vibrating sample magnetometer were used to characterize MnFe2O4@SiO2−CTAB composites. The morphology analysis showed that the composites displayed a core-shell structure. The outer shell was mesoporous silica with CTAB and the core was MnFe2O4 nanoparticles, which ensured the easy separation by an external magnetic field. The performance of MnFe2O4@SiO2−CTAB composites in Cr(VI) removal was far better than that of bare MnFe2O4 nanoparticles. There were two reasons for the effective removal of Cr(VI) by MnFe2O4@SiO2−CTAB composites: (1) mesoporous silica shell with abundant CTA+ significantly enhanced the Cr(VI) adsorption capacity of the composites; (2) a portion of Cr(VI) was reduced to less toxic Cr(III) by MnFe2O4, followed by Cr(III) immobilized on MnFe2O4@SiO2−CTAB composites, which had been demonstrated by X-ray photoelectron spectroscopy results. The adsorption of Cr(VI) onto MnFe2O4@SiO2−CTAB followed the Freundlich isotherm model and pseudo-second-order model. Tests on the regeneration and reuse of the composites were performed. The removal efficiency of Cr(VI) still retained 92.4% in the sixth cycle. MnFe2O4@SiO2−CTAB composites exhibited a great potential for the removal of Cr(VI) from water.

Exposure to crystalline silica (quartz) has been implicated as a potential cause of the high lung cancer rates in the neighbouring counties of Xuanwei and Fuyuan, China, where the domestic combustion of locally sourced “smoky” coal (a bituminous coal) is responsible for some of the highest lung cancer rates in the nation, irrespective of gender or smoking status. Previous studies have shown that smoky coal contains approximately twice as much quartz when compared to alternative fuels in the area, although it is unclear how the quartz in coal relates to household air pollution.Samples of ash and fine particulate matter (PM2.5) were collected from 163 households and analysed for quartz content by Fourier transformed infrared spectroscopy (FT-IR). Additionally, air samples from 12 further households, were analysed by scanning electron microscopy (SEM) to evaluate particle structure and silica content.The majority (89%) of household air samples had undetectable quartz levels (<0.2 μg/m3) with no clear differences by fuel-type. SEM analyses indicated that there were higher amounts of silica in the smoke of smoky coal than smokeless coal (0.27 μg/m3 vs. 0.03 μg/m3). We also identified fibre-like particles in a higher concentration within the smoke of smoky coal than smokeless coal (5800 fibres/m3 vs. 550 fibres/m3). Ash analysis suggested that the bulk of the quartz in smoky coal went on to form part of the ash.These findings indicate that the quartz within smoky coal does not become adequately airborne during the combustion process to cause significant lung cancer risk, instead going on to form part of the ash. The identification of fibre-like particles in air samples is an interesting finding, although the clinical relevance of this finding remains unclear.

With extensive application of diverse engineered nanoparticles (NPs), multiple NPs would inevitably be released into the environment. However, much emphasis in most previous studies on the interactions of pollutants with NPs has been placed on only one type of NPs at a time. This study investigated the impact of inorganic NPs (I-NPs) on the adsorption of 17β-estradiol (E2) and 17α-ethynylestradiol (EE2) by multi-walled carbon nanotubes (CNTs). The presence of I-NPs inhibited the adsorption and increased the equilibrium time of E2 and EE2 by CNTs. Moreover, the effect of Al2O3 was stronger than that of SiO2, because electrostatic attraction enhanced the interaction between oppositely charged Al2O3 and CNTs. The addition sequence of I-NPs and pollutant also influences adsorption. This is among the first studies investigating the effect of I-NPs on pollutants adsorption by CNTs, which is useful for understanding the transport and fate of CNTs and contaminants in natural aquatic systems.

The significance of biofilm on the transport and deposition behaviors of ZnO nanoparticles were examined under a series of environmentally relevant ionic strength at two fluid velocities of 4 m-d−1 and 8 m-d−1. Biofilm enhanced nanoparticles retention in porous media under all examined conditions. The greater deposition was also observed in extracellular polymeric substances (EPS) coated surfaces by employment of quartz microbalance with dissipation (QCM-D) system. Derjaguin–Landau–Verwey–Overbeek (DLVO) failed to interpret more ZnO nanoparticles deposition on biofilm (EPS) coated silica surfaces. Chemical interaction and physical morphology of biofilm contributed to this greater deposition (retention). Biofilm affected the spacial distribution of retained ZnO nanoparticles as well. Relatively steeper slope of retained profiles were observed in the presence of biofilm, corresponding to the greater deviation from colloid filtration theory (CFT). Pore space constriction via biofilm induced more nanoparticle trapped in the column inlet, leading to greater deviations (σln kf) from the CFT.

Arsenic mobility may increase in liquid phase due to association with colloidal Fe oxides. We studied the association of As with Fe oxide colloids in the effluent from water-saturated soil columns run under anoxic conditions. Upon exfiltration, the solutions, which contained Fe²⁺, were re-aerated and ferrihydrite colloids precipitated. The entire amount of effluent As was associated with the ferrihydrite colloids, although PO₄ ³⁻, SiO₄ ⁴⁻, CO₃ ²⁻ and dissolved organic matter were present in the effluent during ferrihydrite colloid formation. Furthermore, no subsequent release of As from the ferrihydrite colloids was observed despite the presence of these (in)organic species known to compete with As for adsorption on Fe oxides. Arsenic was bound via inner-sphere complexation on the ferrihydrite surface. FTIR spectroscopy also revealed adsorption of PO₄ ³⁻ and polymerized silica. However, these species could not impede the quantitative association of As with colloidal ferrihydrite in the soil effluents.

Membrane separations are powerful tools for various applications, including wastewater treatment and the removal of contaminants from drinking water. The performance of membranes is mainly limited by material properties. Recently, successful attempts have been made to add nanoparticles or nanotubes to polymers in membrane synthesis, with particle sizes ranging from 4 nm up to 100 nm. Ceramic membranes have been fabricated with catalytic nanoparticles for synergistic effects on the membrane performance. Breakthrough effects that have been reported in the field of water and wastewater treatment include fouling mitigation, improvement of permeate quality and flux enhancement. Nanomaterials that have been used include titania, alumina, silica, silver and many others. This paper reviews the role of engineered nanomaterials in (pressure driven) membrane technology for water treatment, to be applied in drinking water production and wastewater recycling. Benefits and drawbacks are described, which should be taken into account in further studies on potential risks related to release of nanoparticles into the environment.