Colloids associated with heavy metals are ubiquitous in contaminated groundwater; waste accumulation at imperfectly sealed landfills can produce large amounts of leachate with colloids and heavy metal contaminants, which can pollute the downstream groundwater. In this study, three sites in a landfill were sampled to reveal heavy metal particle size distributions and their chemical compositions. The > 220 nm particle sizes were the predominant size in the downstream groundwater, while the < 10 nm particle sizes were the predominant size in the upstream groundwater. Total Fe increased from 35.5 μg/L in the upstream groundwater to 107 μg/L in the downstream groundwater. This increase was attributed to the enhanced migration and accumulation of colloids in the aqueous phase. The elements and the colloid size distribution in the landfill indirectly reflected the composition and degradation of the waste. Colloids played a key role in distribution of both solid particles and aqueous contaminants in the landfill. The results of this study will contribute to the knowledge of the effect of different contaminants in the vicinity of landfills without appropriate sealing systems.

Chlorophyll-a (CHLA) is a key indicator to represent eutrophication status in lakes. In this study, CHLA, total phosphorus (TP), total nitrogen (TN), turbidity (TB), and Secchi depth (SD) collected by the United States Environmental Protection Agency for the National Lakes Assessment in the continental USA were analyzed. Statistical analysis showed that water quality variables in natural lakes have strong patterns of autocorrelations than man-made lakes, indicating the perturbation of anthropogenic stresses on man-made lake ecosystems. Meanwhile, adaptive neuro-fuzzy inference systems (ANFIS) with fuzzy c-mean–clustering algorithm (ANFIS_FC), ANFIS with grid partition method (ANFIS_GP), and ANFIS with subtractive clustering method (ANFIS_SC) were implemented to model CHLA in lakes, and modeling results were compared with the multilayer perceptron neural network models (MLPNN). Results showed that ANFIS_FC models outperformed other models for natural lakes, while for man-made lakes, MLPNN models performed the best. ANFIS_GP models have the lowest accuracies in general. The results indicated that ANFIS models can be screening tools for an overall estimation of CHLA levels of lakes in large scales, especially for natural lakes.

Graphene oxide (GO) was prepared, characterized, and applied for adsorption of Sr(II) in aqueous solution. The adsorption capacity was calculated to be 137.80 mg/g according to the Langmuir model. The observation by scanning electron microscope with energy dispersive X-ray detector (SEM-EDX), high-resolution transmission electron microscope (HRTEM), and X-ray diffraction (XRD) revealed the crystal structure of Sr compound on the surface of graphene sheets. The analyses by the Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) indicated the involvement of O–C=O, C–O, and C–O–C groups during the adsorption. The X-ray absorption fine structure (XAFS) analysis provided the detail information of GO-Sr composites, and the fitting results were given by Sr(HCOO)₂ and SrCO₃ model, and the coordination numbers (CN) and interatomic distances (R) of Sr–O shell and Sr–C shell were calculated. The adsorption mechanism of Sr(II) was attributed to complexation between Sr and the acidic oxygen-containing groups, which lead to the agglomeration of graphene oxide. Two types of crystals were proposed. Type 1 was formed by coordination between Sr(II) and O–C=O groups, and type 2 was formed by coordination between Sr(II) and C–O/C–O–C groups.

Various studies have illustrated that exposure to ambient air pollution has negative impacts on health. However, little evidence exists on the effects of ambient air pollution on circulatory mortality in Xi’an, China. This study aims to investigate and ascertain the association between short-term exposure to ambient air pollutants and circulatory mortality in Xi’an, China. Daily average concentrations of PM₂.₅, SO₂, and O₃, meteorological data (temperature and relative humidity) and daily counts of circulatory mortality were obtained between January 2014 and June 2016. Mortality was stratified by gender and age group (≤ 64 years and ≥ 65 years). A generalized additive model (GAM) with natural splines (NS) was constructed to analyze the relationship between ambient air pollutants and daily circulatory mortality. There were 57,570 cases of circulatory mortality, with cerebrovascular and ischemic heart diseases accounting for 48.5% and 43.5%, respectively. All ambient air pollutants displayed different seasonal patterns. In the single pollutant model, 10 μg/m³ increase in 2-day moving average concentrations of PM₂.₅, SO₂, and O₃ was associated with relative risk of 1.288(1.198, 1.388), 1.360(0.877, 2.331), and 1.324(1.059, 1.705) in circulatory mortality, respectively. After adjusting for collinearity in the multi-pollutant model, the effects remained statistically significant. The ≥ 65 years and female sub-groups were associated with a higher risk of circulatory mortality. Short-term exposure to ambient air pollutants plays a pivotal role in the genesis of circulatory mortality in Xi’an. Responses to ambient air pollutants exposure in relation to circulatory mortality are different when analyzed by sub-groups.

A hybrid polymer for deep removal of arsenic from aqueous solutions was obtained by loading of waste Fe/Mn oxides into a chitosan matrix. The process was optimized by studying the influence of selected individual factors and their reciprocal combinations on the adsorptive and physical properties of the product. The influence of chitosan solution concentration, inorganic load amount, the ratio of Fe/Mn oxides to chitosan, and polymer cross-linking degree on kinetics of As(III) and As(V) adsorption was examined. The optimal values of the parameters were chitosan polymer concentration 1.5% w/w, inorganic load to chitosan ratio 1.67, and glutaraldehyde to chitosan amine groups molar ratio 3:1. The selected products were evaluated in terms of their morphology (scanning electron microscopy (SEM) with EDS analysis), porosity (N₂ and CO₂ adsorption isotherms), surface properties (Fourier-transform infrared spectroscopy (FTIR), isoelectric point determination) and durability in an acidic environment. The proposed process makes it possible to obtain a product combining beneficial adsorptive properties toward arsenic with the physical form and durability essential in fixed-bed adsorption systems.

During the operation of a mine, waste rock is often deposited in heaps and usually left under ambient conditions allowing sulfides to oxidize. To focus on waste rock management for preventing acid rock drainage (ARD) formation rather than ARD treatment could avoid its generation and reduce lime consumption, costs, and sludge treatment. Leachates from 10 L laboratory test cells containing sulfide-rich (> 60% pyrite) waste rock with and without the addition of lime kiln dust (LKD) (5 wt.%) were compared to each other to evaluate the LKD’s ability to maintain near neutral pH and reduce the sulfide oxidation. Leaching of solely waste rock generated an acidic leachate (pH < 1.3) with high concentrations of As (21 mg/L), Cu (20 mg/L), Fe (18 g/L), Mn (45 mg/L), Pb (856 μg/L), Sb (967 μg/L), S (17 g/L), and Zn (23 mg/L). Conversely, the addition of 5 wt.% LKD generated and maintained a near neutral pH along with decreasing of metal and metalloid concentrations by more than 99.9%. Decreased concentrations were most pronounced for As, Cu, Pb, and Zn while S was relatively high (100 mg/L) but decreasing throughout the time of leaching. The results from sequential extraction combined with element release, geochemical calculations, and Raman analysis suggest that S concentrations decreased due to decreasing sulfide oxidation rate, which led to gypsum dissolution. The result from this study shows that a limited amount of LKD, corresponding to 4% of the net neutralizing potential of the waste rock, can prevent the acceleration of sulfide oxidation and subsequent release of sulfate, metals, and metalloids but the quantity and long-term stability of secondary minerals formed needs to be evaluated and understood before this method can be applied at a larger scale.

Due to its adverse impact on health, as well as its global distribution, long atmospheric lifetime and propensity for deposition in the aquatic environment and in living tissue, the US Environmental Protection Agency (US EPA) has classified mercury and its compounds as a severe air quality threat. Such widespread presence of mercury in the environment originates from both natural and anthropogenic sources. Global anthropogenic emission of mercury is evaluated at 2000 Mg year⁻¹. According to the National Centre for Emissions Management (Pol. KOBiZE) report for 2014, Polish annual mercury emissions amount to approximately 10 Mg. Over 90% of mercury emissions in Poland originate from combustion of coal.The purpose of this paper was to understand mercury behaviour during sub-bituminous coal and lignite combustion for flue gas purification in terms of reduction of emissions by active methods. The average mercury content in Polish sub-bituminous coal and lignite was 103.7 and 443.5 μg kg⁻¹. The concentration of mercury in flue gases emitted into the atmosphere was 5.3 μg m⁻³ for sub-bituminous coal and 17.5 μg m⁻³ for lignite. The study analysed six low-cost sorbents with the average achieved efficiency of mercury removal from 30.6 to 92.9% for sub-bituminous coal and 22.8 to 80.3% for lignite combustion. Also, the effect of coke dust grain size was examined for mercury sorptive properties. The fine fraction of coke dust (CD) adsorbed within 243–277 μg Hg kg⁻¹, while the largest fraction at only 95 μg Hg kg⁻¹. The CD fraction < 0.063 mm removed almost 92% of mercury during coal combustion, so the concentration of mercury in flue gas decreased from 5.3 to 0.4 μg Hg m⁻³. The same fraction of CD had removed 93% of mercury from lignite flue gas by reducing the concentration of mercury in the flow from 17.6 to 1.2 μg Hg m⁻³. The publication also presents the impact of photochemical oxidation of mercury on the effectiveness of Hg vapour removal during combustion of lignite. After physical oxidation of Hg in the flue gas, its effectiveness has increased twofold.

Volatile organic compounds (VOCs) are of public concern due to their adverse health effects. Botanical air filtration is a promising technology for reducing indoor air contaminants, but the underlying mechanisms are not fully understood. This study assessed active botanical biofilters for their single-pass removal efficiency (SPRE) for benzene, ethyl acetate and ambient total volatile organic compounds (TVOCs), at concentrations of in situ relevance. Biofilters containing four plant species (Chlorophytum orchidastrum, Nematanthus glabra, Nephrolepis cordifolia ‘duffii’ and Schefflera arboricola) were compared to discern whether plant selection influenced VOC SPRE. Amongst all tested plant species, benzene SPREs were between 45.54 and 59.50%, with N. glabra the most efficient. The botanical biofilters removed 32.36–91.19% of ethyl acetate, with C. orchidastrum and S. arboricola recording significantly higher ethyl acetate SPREs than N. glabra and N. cordifolia. These findings thus indicate that plant type influences botanical biofilter VOC removal. It is proposed that ethyl acetate SPREs were dependent on hydrophilic adsorbent sites, with increasing root surface area, root diameter and root mass all associated with increasing ethyl acetate SPRE. The high benzene SPRE of N. glabra is likely due to the high wax content in its leaf cuticles. The SPREs for the relatively low levels of ambient TVOCs were consistent amongst plant species, providing no evidence to suggest that in situ TVOC removal is influenced by plant choice. Nonetheless, as inter-species differences do exist for some VOCs, botanical biofilters using a mixture of plants is proposed.

Previous studies revealed that superphosphate fertilizer (SSP) as an additive in compost can reduce the nitrogen loss and improve the effectiveness of phosphorus during composting. However, few studies have explored the influence of adding SSP with high levels on ammonia and greenhouse gas emission and the suitable amount for SSP addition according to a combined assessment of the composting process and product. The present study aimed to evaluate the impact of SSP with high additive amounts on NH₃, CO₂, CH₄, and N₂O emission and organic carbon loss. All piles were mixtures of pig manure and cornstalks with different levels of SSP addition including 10%, 14%, 18%, 22%, 26%, and 30% dry weight basis of raw materials. Compared with the control without SSP, the amount of NH₃ cumulative emissions was decreased by 23.8–48.1% for the treatments with 10–30% SSP addition, and the emission of greenhouse gas including CO₂, CH₄, and N₂O by 20.9–35.5% (CO₂ equivalent) was reduced by 20.9–35.5%. Adding SSP with the amount exceeding 14% to compost could reduce CO₂ emissions by 32.0–38.4% and more than 30% carbon loss at the end of composting but exceeding 26% had an adverse impact on maturity of the composts. Therefore, considering the maturity and safety of compost and gas emission reduction, 14–26% SSP was the optimum amount for composting addition, which is an effective and economical way to increase the nutrient level of carbon, nitrogen, and phosphorus in compost and reduce environmental risks.

Organochlorine pesticides (OCPs) are a more persistent and lipophilic group of insecticides. The present study aims to evaluate the residues of OCPs in meat, liver, and kidney of the cattle and sheep. A total of 54 samples were obtained from butcheries and local markets in Birjand, east of Iran. The residual contents of aldrin; dieldrin; dichlorodiphenyltrichloroethane; and its metabolites (DDTs), endosulfan isomers, endrin, hexachlorocyclohexane isomers (HCHs), heptachlor, heptachlor epoxide, chlordans, methoxychlor, and hexachlorobenzene (HCB), were analyzed in all samples. OCP residues were extracted by using the QuEChERS technique and quantified by gas chromatography-mass spectrometry (GC-MS). All of the analyzed OCPs were lower than the detection limit. The findings showed that meat and edible organs marketed in this region enjoyed a good status in terms of the residues of OCP. Monitoring of pesticide residues in meat and edible organs is necessary from the public health point of view.