Ground air monitoring stations have been installed in Taiwan since 1993 to ensure whether the criteria air pollutants meet the ambient air quality standards. In the present study, the data from the monitoring stations were used to evaluate long-term (2005–2015) trend of NO₂ and SO₂ in three metropolitan cities (northern Taipei, central Taichung, and southern Kaohsiung), two eastern coastal cities (Hualien and Taitung), and one agricultural city in west-central plain (Douliu); those cities essentially covered the entire region of Taiwan. The results indicate that SO₂ and NO₂ concentrations of all studied six cities meet the annual average standards of 30 and 50 ppb, respectively. After deseasonalizing the original data and using 7-month moving average, the trend analysis reveals a decreasing trend ranging from 0.15 to 0.57 ppb/year (R² from 0.33 to 0.85) for NO₂ and 0.06 to 0.45 ppb/year (R² from 0.32 to 0.92) for SO₂; the corresponding reductions over the 10-year span are 4 to 42% for NO₂ and 22 to 52% for SO₂. The reduction trend, despite the growth in GDP, vehicle numbers and energy consumption, industrial output, etc., is similar to those of developed countries. Clearly, there are seasonal/monthly variation patterns for these two precursor gases with minimum levels in summer (July) and maximum in winter (December). The concentration reductions, however, were lagging behind the respective emission reductions. There are significant correlations among six cites for NO₂ (r = 0.58–0.93) and, to some extent, SO₂ (0.32–0.66). The correlation between SO₂ and NO₂ (r = 0.46–0.74) indicates same or similar emission sources. Furthermore, the correlation between observed pollutant concentrations and their emission is excellent for SO₂ in two cities (0.79–0.96). The SO₂/NO₂ ratios vary with city and time and the value is site specific. For example, in 2005, the SO₂/NO₂ ratio was 0.38 in Kaohsiung and 0.18 in both Taipei and Taichung, the latter reflecting significant contribution from mobile sources. However, they all converged to 0.18–0.28 in 2015 in the six cities evaluated. All in all, the policies/measures made by the central and local government are effective in reducing ambient SO₂ and NO₂ levels.

In this study, a magnesium oxide–rice husk biochar composite (MgO–BCR) was successfully prepared by a MgO impregnation method, and its adsorption performance was investigated in Cd(II) aqueous solution. A pseudo-second-order kinetic model described the Cd(II) adsorption behaviour on BCR and MgO–BCR well, while a Langmuir adsorption isotherm was more suitable for Cd(II) adsorption on the adsorbent. The fitting results of the monolayer model indicated that the number of ions captured by per site varied between 0.97 and 1.09. The calculated thermodynamic parameters indicated that Cd(II) adsorption onto MgO–BCR was spontaneous and endothermic. Characterisation of the adsorbent revealed that in situ precipitation, surface complexation, and electrostatic attraction contributed to the Cd(II) adsorption. The adsorption capacities of rice husk biochar (BCR) and MgO–BCR for Cd(II) reached 6.36 and 18.1 mg/g, respectively. The results demonstrated that MgO–BCR composite could be used as an effective and eco-friendly adsorbent to enhance the removal of Cd(II) from aqueous solution.

Green microalgae colonizing stone surfaces represent a major problem for the conservation of heritage monuments, since they lead to biodegradation and aesthetic issues. Previous studies in La Glacière show cave (France) have demonstrated that UV-C may have a strong effect on microalgae, thus leading to chlorophyll bleaching, which was increased when biofilms were maintained under VIS-light condition unlike to those maintained in the dark. To understand the physiological mechanisms underlying this response and in order to optimize in situ treatment, 30 kJ m⁻² UV-C exposure times were applied to Chlorophyta Chlorella sp. and chlorophyll degradation kinetics were then monitored. UV-C irradiation was enough to inhibit photosynthesis and to directly kill all algal cells. Results also showed that chlorophyll a was degraded faster than chlorophyll b and that 14 h were necessary for complete degradation of all the present chlorophyll. In addition, our results highlighted the importance of visible light exposition after UV-C treatment which leading to chlorophyll bleaching. Irradiated algae cultivated in the dark were still green 5 days after treatment while cultivated samples in the light lost their green color after 14 h. An efficient UV-C treatment applicable to show caves and other heritage monuments was proposed.

The presence of cyanide ions in wastewater is dangerous to the health and life of living creatures, especially humans. Cyanide concentration should not exceed the acceptable limit in wastewaters to avoid their adverse effects to the environment. In this paper, in order to select the most appropriate method to remove cyanide from the wastewater of the Moteh gold mine, based on the experts’ opinions, the use of calcium hypochlorite, sodium hypochlorite, and hydrogen peroxide was chosen as forerunning alternative in the form of a multi-stage model. Then, seven criteria including the amount of material consumed, ease of implementation, safety, ability to remove cyanide, pH, time, and cost of the process to assess the considered methods were determined. Afterwards, seven experts conducted numerous experiments to examine the conditions of each of these criteria. Then, by employing a mathematical method called “numerical taxonomy,” the use of sodium hypochlorite was suggested as the best method to remove cyanide from the wastewater of the Moteh gold mine. Finally, the TOPSIS model was used to validate the proposed model, which led to the same results of the suggested method. Also, the results of employing taxonomic analysis and TOPSIS method suggested the use of sodium hypochlorite as the best method for cyanide removal from wastewater. In addition, according to the analysis of various experiments, conditions for complete removal of cyanide using sodium hypochlorite included concentration (8.64 g/L), pH (12.3), and temperature (12 °C).

Modified Hummer’s method has been used in this study to synthesize graphene oxide (GO) solution that was utilized for the fabrication of three-dimensional (3D) graphene sponges and their subsequent functionalization through a low-cost and facile vapor-based surface enhancement approach. The functionalized 3D-graphene sponge is an excellent absorbent, which can remove more than 3300 wt.% of crude oil (calculated with respect to the original sorbent mass). The functionalization of the obtained graphene sponges with trichloro (1H,1H,2H,2H-perfluorooctyl)silane enhanced their wettability properties due to the super-hydrophobic nature of the resulting materials characterized by the contact angles in water greater than 150°. Furthermore, their elastic compression modulus (estimated by conducting a series of compression tests) was about 22.3 kPa. The equilibrium modeling of the oil removal process, which was performed by plotting Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich isotherms, confirmed the properties of the fabricated 3D graphene sponges as exceptional absorbents for crude and diesel oil, which could be attributed to the oleophilic nature of graphene. Moreover, the obtained 3D graphene sponges could be regenerated via heat treatment, which was conducted to release the adsorbed species. After five adsorption-desorption cycles, the sorption capacity of the produced 3D graphene sponges towards crude oil reached 95% of the initial value.

Low-pressure (LP) UV treatment after chlorine disinfection was associated with enhanced formation of trichloronitromethane (TCNM), a halonitromethane disinfection by-product (DBP), due to the chlorination of tryptophan. Evidence was found that the concentration of TCNM from tryptophan increased quickly to the maximum for the first instance. Moreover, the increase of TCNM under UV exceeded 10 times than under dark. Then, it was found to have an obvious decrease in the formation of TCNM, even finally hardly disappear. In order to elucidate reasons for this phenomenon, the effects of light intensity, initial tryptophan concentration, free chlorine concentration, pH, and tert-butanol (TBA) on the formation of TCNM were investigated under UV/chlorine treatment. Finally, the effects of tryptophan on the formation of TCNM and the direct photodegradation of TCNM under LP UV irradiation were studied for analyzing the possible pathways of TCNM formation from amino acid. Since amino acids are very common in water sources, further research into chemical oxidation of these species by LP UV and chlorine is recommended. It can help us to find the precursors of TCNM formation and reduce the risk of TCNM formation for drinking water and wastewater utilities.

Triclosan is a synthetic chemical with broad antimicrobial activity that has been used extensively in consumer products, including personal care products, textiles, and plastic kitchenware, although the exposure which is widespread evidence from human studies is scarce. Our study aims to investigate the relationship between triclosan exposure and male fertility. Triclosan (TCS) urinary concentrations were measured using gas chromatography coupled with tandem mass spectrometry in 315 men recruited from a male reproductive health clinic with normal sperm concentration (≥ 15 mln/ml) (WHO 2010) under 45 years of age. Participants were interviewed and provided a semen sample. TCS was detected in 84.13% of urine samples, with a median concentration of 2.83 μg/l (2.57 μg/g creatinine). A multiple linear regression analysis showed a positive association between the urinary concentrations of triclosan 50th–75th percentile and ≥ 50 percentile and percentage of sperm with abnormal morphology (p = 0.016 and p = 0.002, respectively). The study provides evidence that exposure to triclosan is associated with poorer semen quality. Future studies are needed to confirm these findings.

Polycyclic aromatic hydrocarbons (PAHs) are a large group of well-known toxicants with carcinogenic potential and other health effects including on the immune system. The high health risks of non-communicable diseases and relevant comorbidities in Africa, particularly in contaminated areas like e-waste and crude oil and gas exploration areas and for high consumers of food commodity groupings which are most critical for PAH exposure, are exacerbated by dietary exposure due to unsafe practices in commonly consumed foods, like those street vended.In February 2016, 20 commonly consumed street foods were purchased directly from vendors at major bus stops in Benin City and Umunede in Nigeria. The concentration of 16 priority PAHs was determined. The dietary intake of B[a]P, ∑PAH, PAH4, PAH8, and ∑B(a)Pₑq was estimated for children, peripubertal children/adolescent, and adult using the total diet study (TDS) method. Among the analyzed PAHs, there was a predominance of chrysene (17.42 μg/kg). Roasted yam (14.15 μg/kg) and fried fish (1.40 μg/kg) had the highest levels of ∑PAH and B[a]P, respectively. The mean concentration of B[a]P, ∑PAH, PAH4, PAH8, and ∑B(a)Pₑq ranged from 0.65–1.40 μg/kg, 0.20–14.15 μg/kg, 0.43–5.22 μg/kg, 0.13–7.88 μg/kg, and 0.002–2.123 μg/kg, respectively. The mean concentration of B[a]P and PAH4 reported in this study was below the maximum allowable levels of 5 and 12 μg/kg for adults and above the maximum levels for young children set at 1.0 μg/kg for both B[a]P and PAH4 in food. The estimated dietary intake of B[a]P, ∑PAH, PAH4, PAH8, and ∑B(a)Pₑq for adult, adolescent, and children was 0.56, 0.37, and 0.31 μg/day; 17.6, 10.7, and 8.81 μg/day; 5.78, 4.01, and 3.26 μg/day; 9.22, 6.19, and 5.09 μg/day; and 1.72, 0.97, and 0.82 μg/day, respectively.Street foods represent one important source of PAHs. The exposure occurring through street food compounds with that from home-made foods, environmental pollution, and lifestyle (tobacco smoke) is making up an aggregate daily exposure in the general population.The incremental lifetime cancer risk for adults and children from the consumption of street food was 7.6 × 10⁻⁸ and 2.1 × 10⁻⁸, respectively. Along with initiatives to manage environmental contamination and promote healthier lifestyle, people should be empowered on healthy cooking practices and safe food cookery environments.

Composite surface soil samples were collected at 0, 25, and 50 cm from the base of 12 utility poles on the Kenai National Wildlife Refuge in Alaska, to assess the extent to which pentachlorophenol, polychlorinated dibenzo-p-dioxins and polychlorinated dibenzo furans may have leached from pentachlorophenol-treated poles. Six pairs of utility poles were included, consisting of an “old” pole manufactured in 1959 or 1963, a “new” pole manufactured within the past 20 years, and a suitable background soil sample from the same vicinity. Old poles had greater concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) equivalents (TEQs) near the pole base and at 25 cm than “new” poles did. For all 12 poles combined, the mean pentachlorophenol levels in soil were 1810, 157, and 17.8 ppm dry weight (d.w.) near the pole bases, at 25 and 50 cm from the poles, respectively, while the mean total TEQ levels in soil were 15,200, 5170, and 1510 parts per trillion d.w. at those distances. Surface soil levels of pentachlorophenol and TCDD-TEQs exceeded both human health and ecological risk-based screening levels. The design and results of this study were similar to another project in Montreal, Quebec in Canada. Together the results are cause for concern, indicating that millions of similarly treated utility poles in North America may be point sources of pentachlorophenol and dioxins/furans to soil.