Carbon disulfide (CS₂) is seen an odor-toxic organic sulfur compound, which presents a major impact on global climate change. Therefore, the conversion of CS₂ into valuable chemicals is the key to reduce the concentration of CS₂ in the atmosphere. On the basis of a CS₂ fixation strategy, CS₂-storage materials (CS₂SMs) are firstly synthesized by the reaction of CS₂ with a binary ion-like liquid systems of ethylenediamine (EDA) and ethylene glycol derivatives (EGs) under mild condition. In view of the serious shortage of sulfur fertilizer and its important position in global agricultural production, it is a promising choice to use the CS₂SMs as a new type of green sulfur fertilizer to promote the growth of eggplant, tomato, sweet pepper and cucumber. In this work, the influence of CS₂SMs on the growth of plants were studied by taking plants irrigated by using various aqueous CS₂SMs solutions as experimental groups, and those irrigated by using water and NH₄HCO₃ as control groups. The experimental results showed that all CS₂SMs could promote plant height, stem diameter, root weight, flower bud number and leaf size. Especially, several CS₂SMs presented significant influence on fluorescence and fruit number. Further studies showed that the CS₂SMs as new energy resources sulfur-containing boosted leaf area, improved root development, enhanced photosynthesis and soil nutrient uptake, and promoted vegetative and reproductive growth of these four types of plants. Thus, this work provided a new strategy for the use of CS₂ as an indirect energy source for the experimental four plants.

A highly selective sample cleanup procedure combined with molecularly imprinted solid-phase extraction (MISPE) was developed for the isolation of gonyautoxins 2,3 (GTX2,3) from Alexandrium tamarense sample. The molecularly imprinted polymer microspheres (MIPMs) were prepared by suspension polymerization using caffeine as the dummy template molecule, methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as the cross-linker and polyvinyl alcohol as the dispersive reagent. The polymer microspheres were used as a selective sorbent for the solid-phase extraction of gonyautoxins 2,3. An off-line MISPE method followed by high-performance liquid chromatography (HPLC) with fluorescence detection for the analysis of gonyautoxins 2,3 was established. Finally, the extract samples from Alexandrium tamarense were analyzed. The results showed the imprinted polymer microspheres exhibited high affinity and selectivity for gonyautoxins 2,3. The interference matrix in the extract were obviously cleaned by MISPE and the extraction efficiency of gonyautoxins 2,3 in the sample ranged from 81.74% to 85.86%.

Many surface and ground waters in the continental US are contaminated with a variety of chemical pollutants, which are usually present in concentrations in the ppm and ppb range. The effects of these pollutants on coliform bacteria, which are prominent members of the aquatic flora, are poorly understood. Using a microtiter plate assay, isolates of Escherichia coli (from chicken intestine and fresh water), and an isolate of Klebsiella pneumoniae (from bovine milk) were exposed to varying concentrations of common pollutants over a 24 h period. The herbicides/pesticides simazine, atrazine, and diazinon; the VOCs trichloroethene and MTBE; the estrogens estradiol and estrone; and caffeine, all failed to inhibit bacterial growth at ppm levels. Only ethylene glycol, and the herbicide 2,4-D, significantly inhibited bacterial growth compared to controls. These results suggest that the replication of coliform bacteria in fresh waters is not adversely impacted by many common pollutants. Using a microtiter plate assay, E. coli and Klebsiella bacteria were exposed to a panel of common chemical pollutants of fresh water; only ethylene glycol and 2,4-D inhibited bacterial replication.

An effective 3-step method for the quantification of mass of polyethylene terephthalate microplastics and nanoplastics (PET MNPs) in complex environmental matrices was developed based on a simplified in-matrix depolymerization. Liquid chromatography (LC) coupled with ultraviolet (UV) detection was used for detection and quantification. Recoveries for PET-spiked sand samples were 99 ± 2% (1 mg/L) and 93 ± 7% (30 mg/L). The limit of quantification (LOQ) for PET was 0.4 μg/g for sand, 1 mg/g for indoor dust and 0.2 μg/g for wet sludge. This method was applied to seven beach sand samples, 20 indoor dust samples and one sewage sludge sample. PET MNPs levels in sand samples were all below the limit of detection (LOD) of LC-UV (0.1 μg/g). The concentrations of PET MNPs in indoor dust samples ranged from 1.2 to 305 mg/g and the PET MNPs in liquid sludge was 1.5 mg/L.

A high selective pre-treatment method for the extraction and analysis of mebendazole in environmental water samples was developed based on molecularly imprinted solid-phase extraction (MISPE). The mebendazole imprinted polymers were synthesized in acetonitrile using methacrylic acid and ethylene glycol dimethacrylate as functional monomer and cross-linker respectively. The imprinted materials showed high adsorption ability for mebendazole and were applied as special solid-phase extraction sorbents for selective separation of mebendazole. An off-line MISPE procedure was developed for the purification and enrichment of mebendazole from natural seawater samples prior to high-performance liquid chromatography analysis. The recoveries of spiked seawater on the MISPE cartridges were from 83.0% to 90.6%, and the values of the relative standard deviation were in the range of 2.78–4.13% (n=3). The satisfied results showed that this pre-treatment methodology for extracting mebendazole in seawater was simple and effective.

In this paper, a highly selective sample cleanup procedure combining molecular imprinting technique (MIT) and solid-phase extraction (SPE) was developed for the isolation of malachite green in seawater and seafood samples. The molecularly imprinted polymer (MIP) was prepared using malachite green as the template molecule, methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as the cross-linking monomer. The imprinted polymer and non-imprinted polymer were characterized by scanning electron microscope and static adsorption experiments. The MIP showed a high adsorption capacity and was used as selective sorbent for the SPE of malachite green. An off-line molecularly imprinted solid-phase extraction (MISPE) method followed by high-performance liquid chromatography with diodearray detection for the analysis of malachite green in seawater and seafood samples was also established. Finally, five samples were determined. The results showed that malachite green concentration in one seawater sample was at 1.30μgL⁻¹ and the RSD (n=3) was 4.15%.

An aerobic denitrification system, initially bioaugmented with Pseudomonas strain T13, was established to treat coal-based ethylene glycol industry wastewater, which contained 3219 ± 86 mg/L total nitrogen (TN) and 1978 ± 14 mg/L NO₃ ⁻-N. In the current study, a stable denitrification efficiency of 53.7 ± 4.7% and nitrite removal efficiency of 40.1 ± 2.7% were achieved at different diluted influent concentrations. Toxicity evaluation showed that a lower toxicity of effluent was achieved when industry wastewater was treated by stuffing biofilm communities compared to suspended communities. Relatively high TN removal (~50%) and chemical oxygen demand removal percentages (>65%) were obtained when the influent concentration was controlled at below 50% of the raw industry wastewater. However, a further increased concentration led to a 20–30% decrease in nitrate and nitrite removal. Microbial network evaluation showed that a reduction in Pseudomonas abundance was induced during the succession of the microbial community. The napA gene analysis indicated that the decrease in nitrate and nitrite removal happened when abundance of Pseudomonas was reduced to less than 10% of the overall stuffing biofilm communities. Meanwhile, other denitrifying bacteria, such as Paracoccus, Brevundimonas, and Brucella, were subsequently enriched through symbiosis in the whole microbial network.

Wastewater samples originating from an explosives production plant (3,000 mg N l−1 nitrate, 4.8 mg l−1 nitroglycerin, 1.9 mg l−1 nitroglycol and 1,200 mg l−1 chemical oxygen demand) were subjected to biological purification. An attempt to completely remove nitrate and to decrease the chemical oxygen demand was carried out under anaerobic conditions. A soil isolated microbial consortium capable of biodegrading various organic compounds and reduce nitrate to atmospheric nitrogen under anaerobic conditions was used. Complete removal of nitrates with simultaneous elimination of nitroglycerin and ethylene glycol dinitrate (nitroglycol) was achieved as a result of the conducted research. Specific nitrate reduction rate was estimated at 12.3 mg N g−1 VSS h−1. Toxicity of wastewater samples during the denitrification process was studied by measuring the activity of dehydrogenases in the activated sludge. Mutagenicity was determined by employing the Ames test. The maximum mutagenic activity did not exceed 0.5. The obtained results suggest that the studied wastewater samples did not exhibit mutagenic properties.

To provide the progressive global demand for energy, the use of renewable energies is being rapidly developed. Since solar radiation is available in most parts of the earth, the photovoltaic (PV) power plant is one of the worthwhile solutions. As a deficiency, temperature rise in photovoltaic cells leads to a drop in their electrical output power. In this experimental study, the circulation of carbon black nanofluid was investigated as a coolant of PV modules. Both water and ethylene glycol (EG) were used as the base fluids. It is found that all modified cases generate more output power than the conventional one. For instance, water + carbon nanofluid yields 54% more output power compared with the conventional one. To make a real assessment of using nanofluid as a coolant, the electrical consumption by pump and fan must be counted. Therefore, in this study, the net output power is calculated. In the cases of EG and EG + carbon, the net output powers get lower than the conventional module. So, they are not justifiable. In this paper, a modified formula is proposed to calculate the exergy efficiency, in order to achieve more accurate results. Accordingly, from an exergy viewpoint, 16.3% and 4.5% in electrical and thermal exergy efficiencies are achieved, when water + carbon nanofluid was used. Moreover, the values of entropy generation and lost exergy were reported for all considered cases.

In this study, nanoporous anodic film was produced by anodization of niobium, Nb in a fluoride ethylene glycol electrolyte. The effect of anodization voltage and electrolyte temperature was studied to find an optimum condition for circular, ordered, and uniform pore formation. The diameter of the pores was found to be larger when the applied voltage was increased from 20 to 80 V. The as-anodized porous film was also observed to comprise of nanocrystallites which formed due to high field-induced crystallization. The nanocrystallites grew into orthorhombic Nb₂O₅ after post-annealing treatment. The Cr(VI) photoreduction property of both the as-anodized and annealed Nb₂O₅ samples obtained using an optimized condition (anodization voltage: 60 V, electrolyte temperature: 70 °C) was compared. Interestingly, the as-anodized Nb₂O₅ film was found to display better photoreduction of Cr(VI) than annealed Nb₂O₅. However, in terms of stability, the annealed Nb₂O₅ presented high photocatalytic efficiency for each cycle whereas the as-anodized Nb₂O₅ showed degradation in photocatalytic performance when used continually.