Reuse of sewage sludge is a general trend and land application is an essential way to reuse sludge. The outbreak of coronavirus disease has raised concerns about human pathogens and their serious threat to public health. The risk of pathogenic bacterial contamination from land application of municipal sludge has not been well assessed. The purpose of this study was to investigate the presence of pathogenic bacteria in municipal sewage sludge and to examine the survival potential of certain multidrug-resistant enteroaggregative Escherichia coli (EAEC) strain isolated from sewage sludge during heat treatment. The sewage sludge produced in the two wastewater treatment plants contained pathogenic bacteria such as pathogenic E. coli, Shigella flexneri, and Citrobacter freundii. The environmental strain of EAEC isolated from the sludge was resistant to eight types of antibiotics. It could also enter the dormant state after 4.5 h of treatment at 55 °C and regrow at 37 °C, while maintaining its antibiotic resistance. Our results indicate that the dormancy of EAEC might be why it is heat-resistant and could not be killed completely during the sludge heat treatment process. Owing to the regrowth of the dormant pathogenic bacteria, it is risky to apply the sludge to land even if the sludge is heat-treated, and there is also a risk of spreading antibiotic resistance.

Exploring effective uses of waste concrete powder (WCP), produced from recycling of construction & demolition waste is beneficial to the environment and sustainable development. In this study, WCP was first treated thermally to enhance the ability to remove Pb (II) from aqueous solutions. The experimental results revealed that the thermal treatment could enhance adsorption capacity due to modification of calcium bonding and pore structure of WCP. Preparation parameters such as temperature, particle size, and water-cement ratio were investigated to obtain the optimal operational conditions. Batch adsorption experiments were performed to explore influence factors of pH (1.00–6.00), ionic strength (0.05–2 mol/L), dosage (2–50 g/L), and temperature (25–45 °C). The pseudo-second-order kinetics model could adequately describe the adsorption process, and the Langmuir model was capable to predict the isotherm data well in the low concentration region (C₀ < 500 mg/L). The maximum uptake capacity for Pb (II) calculated by Langmuir model at 25, 35 and 45 °C were 46.02, 38.58 and 30.01 mg/g respectively, and the removal rate of Pb (II) was 92.96% at a dosage of 50 g/L (C₀ = 1000 mg/L). Precipitation, ion exchange, and surface complexation were identified to be the main mechanisms of Pb (II) adsorption through microscopic investigation by SEM-EDX, XRD, FTIR, XPS, and BET inspections. The study confirms that the WCP after thermal modification, can be selected as a promising adsorbent for the high performance and eco-friendliness.

Phytoremediation of metal(loid)s contaminated sites is widely used, while there is scarce of investigation on the metal-enriched biomass waste safely disposal which resulted in risks of causing secondary pollution to the soil and water bodies and even to human health. Thus, this study compared the effects of ashing and pyrolysis treatments on cadmium (Cd) and zinc (Zn) hyperaccumulation plant Sedum plumbizincicola. Chemical speciation, the Toxicity Characteristic Leaching Procedure (TCLP), and diethylenetriamine pentaacetic acid (DTPA) extraction were employed to characterize the bioavailability and leachability of Cd and Zn in the solid residues after pyrolysis and ashing. The risk assessment code (RAC) and potential ecological risk index (RI) were subsequently used to evaluate the risk of the solid residues to the environment. The results showed that both ashing and pyrolysis treatments could transform the bioavailable Cd and Zn in S. plumbizincicola into a more stable form, and the higher the temperature the greater the stablility. Pyrolysis converted a maximum of 80.0% of Cd and 70.3% of Zn in S. plumbizincicola to the oxidisable and residual fractions, compared with ashing which achieved only a ∼42% reduction. The pyrolysis process minimised the risk level of Cd and Zn to the environment based on the RAC and RI assessments. The results of the TCLP test, and DTPA extraction confirmed that the leaching rate and the bioavailable portion of Cd and Zn in the biochars produced by pyrolysis were invariably significantly (p < 0.05) lower than the solid residues produced by ashing, and reached the lowest at 650 °C. In other words, pyrolysis was better than ashing for thermal treatment of the metal-enriched hyperaccumulator plant, in view of minimising the bioavailability and leachability of Cd and Zn from the solid residues to the environment. This study provides fundamental data on the choice of treatments for the disposal of metal-enriched plant biomass.

Temuco is a mid-size city representative of severe wood smoke pollution in southern Chile; i.e., ambient 24-h PM2.5 concentrations have exceeded 150 μg/m3 in the winter season and the top concentration reached 372 μg/m3 in 2010. Annual mean concentrations have decreased but are still above 30 μg/m3. For the very first time, a molecular marker source apportionment of ambient organic carbon (OC) and PM2.5 was conducted in Temuco. Primary resolved sources for PM2.5 were wood smoke (37.5%), coal combustion (4.4%), diesel vehicles (3.3%), dust (2.2%) and vegetative detritus (0.7%). Secondary inorganic PM2.5 (sulfates, nitrates and ammonium) contributed 4.8% and unresolved organic aerosols (generated from volatile emissions from incomplete wood combustion), including secondary organic aerosols, contributed 47.1%. Adding the contributions of unresolved organic aerosols to those from primary wood smoke implies that wood burning is responsible for 84.6% of the ambient PM2.5 in Temuco. This predominance of wood smoke is ultimately due to widespread poverty and a lack of efficient household heating methods. The government has been implementing emission abatement policies but achieving compliance with ambient air quality standards for PM2.5 in southern Chile remains a challenge.

Tetrabromobisphenol A (TBBPA) is the most widely used brominated flame retardant worldwide. A detailed examination of the degradation products emitted during thermal decomposition of TBBPA is presented in the study. Runs were performed in a laboratory furnace at different temperatures (650 and 800 °C) and in different atmospheres (nitrogen and air). More than one hundred semivolatile compounds have been identified by GC/MS, with special interest in brominated ones. Presence of HBr and brominated light hydrocarbons increased with temperature and in the presence of oxygen. Maximum formation of PAHs is observed at pyrolytic condition at the higher temperature. High levels of 2,4-, 2,6- and 2,4,6- bromophenols were found. The levels of polybrominated dibenzo-p-dioxins and furans have been detected in the ppm range. The most abundant isomers are 2,4,6,8-TeBDF in pyrolysis and 1,2,3,7,8-PeBDF in combustion. These results should be considered in the assessment of thermal treatment of materials containing brominated flame retardants.

This study focuses primarily on the inventory of PCDD/Fs and PBDD/Fs associated with the low-temperature thermal processing of scrap printed circuit boards (PCBs). Twelve 2,3,7,8-substituted PBDD/Fs congeners were found in various sample outputs, with a total content of 60,000ng TEQ/kg at 250°C under air atmosphere. A rapid increase of PBDD/Fs was produced with 160,000ng TEQ/kg, at 275°C—about twice that under the N₂ atmosphere. At 275°C, the total contents of PCDD/Fs were only 170 and 770ng TEQ/kg under an N₂ and air atmospheres respectively. The results reveal that a large contribution of PBDD/Fs emission may be expected from the dismantling or any other thermal processing of PCB scrap. PCDD/Fs, however, are formed and released into the environment in a variety of ways. Additional research is required to look for the causal factors that affect emissions.

Advanced oxidation processes (AOPs) based on peroxymonosulfate (PMS) activation have attracted increasing attention in recent years for organic pollutants removal. Herein, we put forward a facile method to form cobalt phosphide/carbon composite for PMS activation. Combining impregnation approach with pyrolysis treatment enabled the formation of Co₂P/biochar composites using baker’s yeast and Co²⁺ as precursors. The as-synthesized products exhibited excellent catalytic activity for sulfamethoxazole (SMX) degradation over the pH range 3.0–9.0 b y activating PMS. For example, 100% of SMX (20 mg L⁻¹) removal was achieved in 20 min with catalyst dosage of 0.4 g L⁻¹ and PMS loading of 0.4 g L⁻¹. Near zero Co²⁺ leaching was observed during catalytic reaction, which remarkably lowered the toxic risk of transition metal ion in water. Meanwhile, the reusability of catalyst could be attained by thermal treatment. SMX degradation intermediates were identified by liquid chromatography-mass spectrometry (LC-MS), which facilitated the proposal of possible SMX degradation pathways. Ecological Structure Activity Relationships (ECOSAR) analysis indicated that SMX degradation intermediates may not pose ecological toxicity to the environment. Further investigation verified that Co₂P/biochar composites could set off PMS activation not only for the degradation of SMX but also for other sulfonamides. In this study, we not only developed a facile method of utilizing environmental-benign biomass for transition metal phosphide/carbon composite formation, but also achieved highly efficient antibiotic elimination by PMS-based AOP.

Sawdust wastes were used as precursors to prepare adsorbents by combustion and pyrolysis for experimental and mechanism studies and determine the potential of biomass extracted from agro-industrial residues for Pb-polluted soil remediation. Pot experiments were conducted on contaminated soils near Pb–Zn mining with sawdust ash (SA) and sawdust biochar (SB) in different proportions and dosage ratios. Studies have indicated that the application of biomass materials can enhance the adsorption, complexation and precipitation of Pb cations in soil and reduce the mobility of Pb. The concentrations of SPLP-Pb and DTPA-extractable Pb in amended soils were the lowest under 1% 1:2 and 5% 1:1 treatment, respectively. Results of fraction extraction and XANES analysis showed that the materials change the main forms of Pb in soil. Moreover, the binding behavior of Pb with organic matter increases the proportion of Pb (Ac)₂, leading to the transformation of high toxicity Pb-compounds into precipitates and complexes. The remediation methods of 2% 1:2 and 5% 1:2 were better than those of other methods in stabilizing Pb in soil. This study indicated that heat-treated sawdust can be used for Pb-polluted soil remediation, which is a type of environmental remediation measure with considerable ecological potential.

Exhaust emissions from diesel vehicles are significant sources of air pollution. In this study, particle number emissions and size distributions of a modern Euro 5b -compliant diesel passenger car exhaust were measured under the NEDC and US06 standard cycles as well as during different transient driving cycles. The measurements were conducted on a chassis dynamometer; in addition, the transient cycles were repeated on-road by a chase method. Since the diesel particulate filter (DPF) removed practically all particles from the engine exhaust, it was by-passed during most of the measurements in order to determine effects of lubricant on the engine-out exhaust aerosol. Driving conditions and lubricant properties strongly affected exhaust emissions, especially the number emissions and volatility properties of particles. During acceleration and steady speeds particle emissions consisted of non-volatile soot particles mainly larger than ∼50 nm independently of the lubricant used. Instead, during engine motoring particle number size distribution was bimodal with the modes peaking at 10–20 nm and 100 nm. Thermal treatment indicated that the larger mode consisted of non-volatile particles, whereas the nanoparticles had a non-volatile core with volatile material condensed on the surfaces; approximately, 59–64% of the emitted nanoparticles evaporated. Since during engine braking the engine was not fueled, the origin of these particles is lubricant oil. The particle number emission factors over the different cycles varied from 1.0 × 10¹⁴ to 1.3 × 10¹⁵ #/km, and engine motoring related particle emissions contributed 12–65% of the total particle emissions. The results from the laboratory and on-road transient tests agreed well. According to authors’ knowledge, high particle formation during engine braking under real-world driving conditions has not been reported from diesel passenger cars.

Intentional or incidental thermal changes inevitably occur during the lifecycle of plastics. High temperatures accelerate the aging of plastics and promote their fragmentation to microplastics (MPs). However, there is little information available on the release of MPs after fires. In this study, an atomic force microscope combined with nanoscale infrared analysis was used to demonstrate the physicochemical properties of polypropylene (PP) plastics under simulated fire scenarios. Results showed that the chemical composition and relative stiffness of heat-treated plastic surfaces changed, significantly enhancing the generation of MPs under external forces; over (2.1 ± 0.2) × 10⁵ items/kg abundance of MPs released from PP which were burned at 250 °C in air and trampled by a person. The leaching of antimony (Sb) from MPs in different solutions first increased and then decreased with increasing temperature, reaching a maximum at 250 °C. Higher concentrations of humic acid (10 vs 1 mg/L) caused a greater release of Sb. Furthermore, the tap water leachates of PP burned at 250 °C had the greatest effect on the growth and photosynthetic activity of Microcystis aeruginosa. Our results suggest fires as a potential source of MPs and calls for increased focus on burning plastics in future research.