Groundwater is the main source of drinking water for more than half of the residents of Hanoi (HN). It also provides about one third of the total water demand for residents of Ho Chi Minh City (HCM). However, due to rapid urbanization and frequent discharges of untreated urban wastewater to surface water, freshwater is widely contaminated by man-made chemicals, which may result in groundwater pollution. As part of an ongoing campaign to collect baseline information on the occurrence of organic micro-pollutants (OMPs) in the aquatic environment in Vietnam, 43 water samples were collected from 26 groundwater wells in HN (22) and HCM (4) in September 2013 and August 2014. Samples were analyzed by gas chromatography-mass spectrometry (GC-MS) and the resulting chromatograms were screened for 940 OMPs by an automated identification and quantification system (AIQS) within a GC-MS database. A total of 74 compounds were detected, with between 4 and 43 (median 18) compounds found at each site. Overall, contamination levels were low, with over 89 % of the detected concentrations that were less than 0.5 μg L⁻¹. Results suggest that most of the sampled aquifers have been impacted by non-point source pollution. Most of the contaminants detected are either currently not regulated in drinking water or are present at low levels. A health risk assessment for detected contaminants implied that there were no risks to humans. Since this study was based on a limited number of samples, especially in HCM, further, more detailed studies on the occurrence of OMPs in groundwater in HCM and a full risk assessment of detected contaminants should be prioritized.

Chemical leasing is a new and innovative approach of selling chemicals. It aims at reducing the risks emanating from hazardous substances and ensuring long-term economic success within a global system of producing and using chemicals. This paper explores how, through chemical leasing, the consumption of chemicals, energy, resources and the generation of related wastes can be reduced. It also analyses the substitution of hazardous chemicals as a tool to protect environmental, health and safety and hence ensure compliance with sustainability criteria. For this, we are proposing an evaluation methodology that seeks to provide an answer to the following research questions: (1) Does the application of chemical leasing promote sustainability in comparison to an existing chemicals production and management system? 2. If various chemical leasing project types are envisaged, which is the most promising in terms of sustainability? The proposed methodology includes a number of basic goals and sub-goals to assess the sustainability for eight different chemical leasing case studies that have been implemented both at the local and the national levels. The assessment is limited to the relative assessment of specific case studies and allows the comparisons of different projects in terms of their relative contribution to sustainable chemistry. The findings of our assessment demonstrate that chemical leasing can be regarded as promoting sustainable chemistry in five case studies with certainty. However, on the grounds of our assessment, we cannot conclude with certainty that chemical leasing has equivalent contribution to sustainable chemistry in respect of three further case studies.

Oxygen plays an important role during the thermal treatment of soil, contaminated with polychlorinated biphenyls (PCBs), due to the potential oxidation of PCBs to form polychlorinated dibenzofurans (PCDFs). The effect of oxygen content (0, 5, 21 and 100 %) in carrier gases on PCBs and PCDD/Fs was studied both in soil and gas after thermal desorption of PCBs contaminated soil at 500 °C. All 209 congeners of PCBs and 136 congeners of PCDD/Fs (P = 4 to 8) were analysed. Oxygen content showed little effect on PCB removal and destruction. Under different carrier gases, the removal efficiency and the destruction efficiency for PCBs attained 93.8–95.5 and 83.0–85.0 %, respectively. The levels of PCDD/Fs in soil and gas were correlated positively with oxygen content. Compared with PCDDs, PCDFs in soil were not effectively removed under oxidative conditions because there was chemistry going on and PCBs were being converted to PCDFs. The total concentration of PCDFs in soil and gas was 2.6, 11.3, 15.6 and 17.5 times of the initial PCDFs concentration (21.9 ng/g) in raw soil with increasing oxygen content. Thus, substantial amounts of PCDFs were generated in the presence of oxygen during the treatment of contaminated soil.

For a typical alpine forest reservoir that does not have other obvious mercury pollution sources, mercury levels in its downstream water can reflect the characteristics of mercury inputs and risks of a remote forest. To confirm this proposal, eight sampling campaigns were carried out in 2012 and 2013 to investigate the distribution patterns of Hg species in the water column and sediment profiles at four sampling stations in an alpine forest reservoir, southwestern China. The concentrations of total Hg (THg) and methylmercury (MeHg) in water samples of DaHong Reservoir varied from 2.8 to 8.2 ng L⁻¹and 0.06 to 2.9 ng L⁻¹, respectively. The concentrations of these Hg species in the wet seasons (summer and fall) were significantly higher than those in the dry season (winter and spring). Forest field runoff and diffusion of Hg from sediments could be the reasons for elevated concentrations of these Hg species in the wet season. Elevated MeHg concentrations in water samples from the bottom water and water-sediment interface demonstrated an active net Hg methylation in the downstream of DaHong (DH) Reservoir. Dissolved MeHg levels in the pore water of surface sediments and the bottom of downstream were apparently higher than those in the upstream, which indicated that MeHg sources of sediment pore water varied in space. MeHg diffusive fluxes from sediment to overlying water were higher in the wet season than those in the dry season, demonstrating that high temperatures favor Hg methylation processes in sediment.

Although bisphenol A (BPA), a representative endocrine-disrupting compound, has been detected frequently in landfill leachate, effective technologies for BPA removal from landfill leachates are limited. We used high silica Y-type zeolite (HSZ-385) for the selective adsorption of BPA from landfill leachate, and factors affecting this adsorption are discussed. Higher removal efficiencies at pH 5.0–9.0 imply that neutral BPA is adsorbed more easily onto HSZ-385 than monomeric or divalent BPA anions. An increase in ionic strength and sodium acetate concentration did not affect BPA adsorption significantly, while the removal efficiency decreased slightly when more than 50 mgC/L of humic acid was added. HSZ-385 was applied to synthetic leachates that simulate the composition of landfill leachate at various degradation stages. In young acidic leachates that contain sodium acetate, the use of HSZ-385 for the adsorptive removal of BPA appears to be more effective than in old alkaline leachates, which contain large amounts of humic acid. In addition, 82 % BPA removal was achieved from young raw leachates using HSZ-385, which demonstrates that selective BPA removal from actual landfill leachate has been achieved.

Effects of exogenous reduced glutathione (GSH) and cysteine (Cys) on growth, lead (Pb) accumulation, and nonprotein thiol (NPT) contents of Iris lactea var. chinensis under 100 and 500 mg L⁻¹Pb stress were studied. Our results showed that 500 mg L⁻¹Pb stress caused a dramatical decline in fresh weights, while the reduction of aboveground biomass was alleviated by exogenous GSH and Cys even though keeping higher Pb contents in roots and shoots. Exogenous GSH and Cys could enhance Pb accumulation in the shoots and roots compared with single Pb treatment. The promoting effect of GSH to Pb accumulation was larger than the effect of Cys, and the Pb contents in the shoots and roots treated with 500 mg L⁻¹Pb + GSH reached 1,712 and 14,603 mg kg⁻¹, about 4.19 and 2.78 times of single 500 mg L⁻¹Pb treatment, respectively. Microscopic imaging of Pb in roots and leaves showed that higher intensive fluorescence was observed in cell wall of root epidermis, stele, vascular tissues of the roots, and sclerenchyma cells of leaves treated with 500 mg L⁻¹Pb + GSH and treated with 500 mg L⁻¹Pb + Cys. Exogenous GSH had an apparent promoting effect on root and shoot GSH synthesis, while exogenous Cys reduced the synthesis of cellular GSH in shoot and increased Cys contents. Pb only induced the synthesis of phytochelatin (PC)₂in roots, and the PC₂content declined in GSH- and Cys-treated plant roots. These results suggested that GSH synthesis was a more effective approach to improve Pb accumulation and translocation of I. lactea var. chinensis. Further analysis of protein expression in plants by exogenous GSH and buthionine sulfoximine (BSO) application showed that the proteins regulated by GSH and BSO may constitute various enzymes involved in GSH biosynthesis and play certain roles in Pb accumulation and tolerance of I. lactea var. chinensis.

In the present study, the polycyclic aromatic hydrocarbons (PAHs) in indoor dust and outdoor dust including road and window dust around the traffic road in Hunan Province, China, were sampled and detected. The ∑PAHs in indoor dust ranged from 5007–24,236 ng g⁻¹, with a median of 14,049 ng g⁻¹. The ∑PAHs in road dust ranged from 3644–12,875 ng g⁻¹, with a median of 10,559 ng g⁻¹. The ∑PAHs in window dust ranged from 803–12,590 ng g⁻¹, with a median of 5459 ng g⁻¹. Similar pattern of PAHs was observed in road and window dust except in H3W and H4W samples, which was dominated by naphthalene (Nap), benzo(b+k)fluoranthene (B(b+k)F), phenanthrene (Phe), and fluorine (Fle). Indoor dust showed slightly different PAHs profiles, which was dominated by Nap, fluoranthene (Fla) and Phe. Risk assessment indicated that dermal contact and dust ingestion exposure pathways were more important than the inhalation pathway. Cancer risk of PAHs via dust varied from 2.73 × 10⁻⁸–8.04 × 10⁻⁶, with a median of 2.06 × 10⁻⁶for children, and from 2 × 10⁻⁸–5.89 × 10⁻⁶, with a median of 1.52 × 10⁻⁶for adult. Probit model showed that 76 and 71 % of samples in the sampling area would result in the risk of children and adult exposure to PAHs via dust higher than the acceptable level (1 × 10⁻⁶), respectively.

Ambient levels of formaldehyde (HCHO) were measured in the tropical urban mega city of Kolkata from July 2012 to April 2014, based on USEPA Compendium Method TO-11A using 2,4-dinitrophenylhydrazine (2,4-DNPH). The samples were analyzed by isocratic reverse-phase high-performance liquid chromatography (HPLC) with an ultraviolet detector at a wavelength of 360 nm. High values of HCHO were recorded at our site. The highest and average HCHO mixing ratio measured for the entire study period was 803 and 217 ppbv respectively. Seasonal wind regimes have been found to influence the seasonal pattern of HCHO mixing ratio at this site resulting in relatively higher mixing ratio of HCHO during the pre-monsoon periods as compared to the others. Apart from these, sampling-based measurements of CH₄ and continuous measurements of ozone (O₃) and CO were also performed with the objective to study the interrelationship of HCHO with these species. The results suggest the presence of highly complex chemistry among them.