The low-cost Ca-bentonite was rapidly converted to a mesoporous adsorbent via microwave-assisted acidification and the obtained materials were employed for the removal of contaminants from waste lubricant oil. In order to understand the role of acid combinations on activation, the agent compositions were prepared according to the mixture design algorithm. The waste oil recovery was carried out in a batch system to determine the appropriate acid composition, optimum microwave power, radiation time, and powder/acid ratio. As power increased, the contaminant removal performance of the adsorbent was effectively raised to achieve appropriate clear base oil. The rise in power behind 600 W negatively affected the performance of the adsorbent in which the color of oil was changed from yellow to brown. The appropriate recovery of waste oil was readily achieved by employment of adsorbents in which the acidification was performed in 15 min. The microwave-assisted technique could shorten the residence time to achieve the maximum efficiency in comparison with the performance of those produced through the conventional method. Although sulfuric acid can be used for acidification of bentonite by microwave heat treatment, the combination of acetic acid, < 50 mol%, with the mentioned acid was identified as an efficient agent to improve the performance of adsorbents which is valuable from an engineering point of view.

In this work, fast sequential determination and chemical speciation analysis of inorganic arsenic and antimony in airborne particulate matter collected in outdoor and indoor environments using slurry sampling and detection by hydride generation atomic absorption spectrometry (HG-AAS) is proposed. A Doehlert design was applied to optimise the hydride generation conditions of As and Sb for fast sequential determination in the same aliquot of particulate matter samples after preparation of the slurry. The limits of quantification (LoQ) obtained for As and Sb were 0.3 and 0.9 ng m⁻³, respectively. The accuracy of the analytical method was confirmed by analysis of the certified reference material of urban particulate matter (SRM NIST 1648a), presenting concordance with certified values of 92.7±7.7% for As and 91.2±9.5% for Sb. Precision was expressed as relative standard deviation (% RSD, n=3), with our results presenting values better than 3.4% and 4.2% for total inorganic As and Sb, respectively. For all analysed samples, total As concentrations and its inorganic species were below the LoQ of the analytical method (<0.3 ng m⁻³). However, the averages of total inorganic Sb concentrations in airborne particulate matter, collected as total suspended outdoor particles (TSPₒᵤₜdₒₒᵣ), inhalable particulate matter (PM₁₀), and total suspended indoor particles (TSPᵢₙdₒₒᵣ), were 3.1±0.5, 2.4±0.6, and 2.6±0.4 ng m⁻³, respectively. Trivalent Sb (Sb³⁺) was the predominant inorganic species in all samples investigated, with mean percentages of 76%, 72%, and 73% in TSPₒᵤₜdₒₒᵣ, PM₁₀, and TSPᵢₙdₒₒᵣ, respectively. The presence of Sb and its predominant inorganic form (Sb³⁺) can be attributed to vehicular traffic close to the sampled urban areas. Therefore, fast sequential determination of As and Sb and their inorganic species in particulate matter samples prepared as slurry by FS-HG-AAS is an efficient, accurate, and precise method and can be successfully applied to routine analysis.

Bioelectrochemical systems (BESs) have great potential for treating wastewater containing polycyclic aromatic hydrocarbons (PAHs); however, detailed data on cell physiological activities in PAH biodegradation pathways stimulated by BESs are still lacking. In this paper, a novel BES device was assembled to promote the growth of Pseudomonas sp. DGYH-12 in phenanthrene (PHE) degradation. The results showed that in the micro-electric field (0.2 V), cell growth rate and PHE degradation efficiency were 22% and 27.2% higher than biological control without electric stimulation (BC), respectively. The extracellular polymeric substance (EPS) concentration in BES (39.38 mg L⁻¹) was higher than control (33.36 mg L⁻¹); moreover, the membrane permeability and ATPase activities were also enhanced and there existing phthalic acid and salicylic acid metabolic pathways in the strain. The degradation genes nahAc, pcaH, and xylE expression levels were upregulated by micro-electric stimulation. This is the first study to analyze the physiological and metabolic effect of micro-electric stimulation on a PHE-degrading strain in detail and systematically.

Fertilization and straw return have been widely adopted to maintain soil fertility and increase crop yields, but their long-term impacts on the accumulation and availability of cadmium (Cd) in paddy soils are still unconfirmed. Therefore, this study was undertaken in central China to investigate the accumulation, availability, and subsequent uptake of Cd by rice (Oryza sativa L.) in two adjacent field trials (P1 and P2, lasting for 10 and 12 years, respectively) under long-term straw return or in combination with chemical fertilizers. Obvious Cd accumulation, probably due to the notable Cd input from irrigation and traffic exhaust in the bulk soil (0–20 cm) of P1, was observed. The bulk soil of P2 received homogeneous straw return and chemical fertilizers, as did that of P1; however, the P2 soil almost showed Cd balance. Long-term straw return increased the portion of soil DTPA-extractable Cd to the total pool for both sites, but only P1 showed significant differences when compared to the controls. However, the highest Cd concentrations and the maximum bioconcentration factors in rice straw and grain were obtained using solo application of chemical fertilizers at both sites. Continuous additional applications of crop straw, in contrast, resulted in slightly decreased Cd uptake in rice straw, but not in grain. These findings demonstrate that neither long-term straw return nor fertilization leads directly to notable Cd accumulation, but that the promotion effects of long-term chemical fertilizer applications on Cd uptake in rice need more attention.

Anaerobic digestion (AD) is one of the best technologies for producing methane from biomass wastes with limited environmental impacts. Most AD plants need a continuous and stable supply of feedstock for their sustained operation for which lignocellulosic biomass can be effectively utilized. Switchgrass (SG), also known as Panicum virgatum, is a tall-growing grass which exists throughout the year in areas with warm climate and has the potential to produce biomethane. The present work investigated anaerobic digestion performance of SG while focusing on enhancing the methane yield by employing central composite design of response surface methodology (RSM). The aim of this research was to find out the best level of factors including feed-to-inoculum (F/I) ratio, organic loading (OL), and pH for optimizing the desired output of biomethane production from 3% KOH–pretreated SG. Results revealed that the highest value of experimental methane yield was 288.4 mL/gVS at the optimal F/I ratio, pH, and OL of 1, 6.96, and 24 gVS/L, respectively. Moreover, 3% KOH pretreatment improved the biodegradability of SG significantly from 14.23 to 85.53%. This study forms the basis for future application of SG for enhanced methane production.

Fenton’s reaction-based chemical oxidation is in principle a method that can be utilized for all organic fuel residues thus making it a potential all-purpose, multi-contaminant, in situ application for cases in which storage and distribution of different types of fuels have resulted in contamination of soil or groundwater. Since peroxide breakdown reactions are also expected to lead to a physical transport of the target compound, this secondary physical removal, or rebound concentrations related to it, is prone to be affected by the chemical properties of the target compound. Also, since soil conditions are seldom optimal for Fenton’s reaction, the balance between chemical oxidation and transport may vary. In this study, it was found that, with a high enough hydrogen peroxide concentration (5 M), methyl tert-butyl ether–spiked groundwater could be treated even under suboptimal conditions for chemical mineralization. In these cases, volatilization was not only contributing to the total removal but also leading to rebound effects similar to those associated with air sparging techniques. Likewise for diesel, temporal transport from soil to the aqueous phase was found to lead to false positives that outweighed the actual remediation effect through chemical mineralization.

Sediments are known to be the ultimate sink for most pollutants in the aquatic environment. In this study, the concentrations of both legacy polybrominated diphenyl ethers (PBDEs) and alternative halogenated flame retardants (AHFRs) were measured in sediments samples from the Vaal River catchment. The concentrations of Σ₇BDE-congeners ranged from 20 to 78 ng g⁻¹ dry weight (dw) with BDE-209, -99, and -153 as the dominant congeners. The concentrations observed ranged from 9.4–56, 4–32, and 1–10.6 ng g⁻¹ for BDE-209, -99, and -153, respectively. The concentrations of AHFRs, mainly contributed by decabromodiphenyl ethane (DBDPE) at approximately 95% of total AHFRs, ranged from 64 to 359 ng g⁻¹ dw while the concentration of polybrominated biphenyls (PBBs), mainly PBB-209, ranged from 3.3–7.1 ng g⁻¹ dw. The ratios of AHFRs to PBDEs observed in this study were 0.76, 1.17, and 7.3 for 2-ethyl-1-hexyl-2,3,4,5-tetrabromobenzoate and bis-(2-ethylhexyl)-tetrabromophthalate (EH-TBB & BEH-TEBP)/penta-BDE; 1,2-bis-(2,4,6-tribromophenoxy) ethane (BTBPE)/octa-BDE; and DBDPE/BDE209, respectively. These results indicate dominance of some AHFRs compared to PBDEs. Our results indicates that BDE-99 poses high risk (RQ > 1) while BDE-209 posed medium risk (0.1 < RQ < 1). Though the concentration of DBDPE was several orders of magnitude higher than BDE209, its ecological risk was found to be negligible (RQ < 0.01). Thus, more attention is required to regulate the input (especially the e-waste recycling sites) of brominated flame retardants into the environment.

This study aims to examine the impact of firm lean manufacturing (LM) and environmental management (EM) practices on firm performance (i.e., environmental and financial performance). Drawing upon institutional theory, we also examine the moderating effect of institutional pressures in adopting EM practices and their subsequent effects on firm performance. The data were collected from 178 textile manufacturing firms operating in Pakistan. Covariance-based structural equation modeling was used to test the hypothesized relationships. Findings support the positive direct effect of LM practices on EM practices and the indirect effect on environmental performance which ultimately increases financial performance. Institutional pressures moderate the direct effect of EM practices on environmental performance. Firms are advised to implement LM accompanied by EM practices to ensure the protection of the natural environment as well as to enhance profit-making capability, in the long run. Further, firms can also enhance environmental performance capabilities through strict synchronization of EM practices with institutional pressures. This research fills the literature gap by investigating the effects of firm's EM practices on environmental and financial performance under the contingent effect of institutional pressures. The study also provides important implications for firms and practitioners.

The removal of acetaminophen (AAP) in aqueous solution by the UV/chlorine process was evaluated. The effect of chlorine dose, the initial AAP concentration, pH value, and UV intensity on the reaction were also investigated. The degradation mechanism and the ecological risk were further discussed. The results indicated that AAP degradation fitted pseudo-first-order kinetics. Compared with UV alone or dark chlorination, the combination of UV and chlorine significantly accelerated the degradation process. The AAP degradation was positively affected by chlorine dose and UV intensity, while negatively affected by the initial AAP concentration and ammonia nitrogen concentration during the UV/chlorine process. The frontier orbital theory analysis shows that the C5 position in the benzene ring of AAP is likely to be the first site attacked by HO• and Cl• radical to form the products. Twelve intermediates were identified by Q-TOF and GC-MS. The possible degradation pathways were also proposed. Luminescent bacteria experiment and ECOSAR prediction both revealed that acute toxicity of AAP degradation could only be partially reduced. Ecological risks during the UV/chlorine process need to be further evaluated.

The purposes of this research are to quantify the concentration of heavy metals (Zn, Cu, As, Pb, Cd, and Hg) in the water and fish tissues of common carp (Cyprinus carpio) in the upper Mekong River and to thereby elucidate the potential dietary health risks from fish consumption of local residents. Surface water and fish tissues (gill, muscle, liver, and intestine) from four representative sample areas (influence by a cascade of four dams) along the river were analyzed for heavy metal concentrations. Results revealed that the levels of heavy metals in fish were tissue-dependent. The highest Cu and As levels were found in the liver; the highest Zn and Pb levels occurred in the intestine, and the highest Hg level was found in the muscle. The total target hazard quotient (THQ) value for residents is > 1 for long-term fish consumption, and local residents are, therefore, exposed to a significant health risk. Results from the current study provide an overall understanding of the spatial and tissue distribution of heavy metals in water and fish body along the upper Mekong River under the influence of cascade dams and highlight the potential health risk of As for the local residents of long-term fish consumption.