Enhanced humification of full-scale apple wood and cow manure by promoting lignocellulose degradation via biomass pretreatments.

Agroforestry waste and cow manure pollute the environment, of which, agroforestry waste is difficult to degrade. Compost is an effective way to dispose agroforestry waste; however, the low degradation efficiency of lignocellulose in agroforestry waste affects the process of composting humification. This study investigated lignocellulose degradation and composting humification in full-size apple wood and cow manure composting processes by applying different pretreatments (acidic, alkaline, and high-temperature) to apple wood. Simultaneously, physicochemical characterization and metagenome sequencing were combined to analyze the function of carbohydrate-active enzymes database (CAZy). Therefore, microbial communities and functions were linked during the composting process and the lignocellulose degradation mechanism was elaborated. The results showed that the addition of apple wood increased the compost humus (HS) yield, and pretreatment of apple wood enhanced the lignocellulose degradation during composting processes. In addition, pretreatment improved the physicochemical properties, such as temperature, pH, electric conductivity (EC), ammonium nitrogen (NH4+), and nitrate nitrogen (NO3-) in the compost, of which, acid treated apple wood compost (AcAWC) achieved the highest temperature of 58.4 °C, effectively promoting nitrification with NO3- ultimately reaching 0.127 g/kg. In all composts, microbial networks constructed a high proportion of positively correlated connections, and microorganisms promoted the composting process through cooperation. The proportions of glycosyltransferase (GT) and glycoside hydrolase (GH) promoted the separation and degradation of lignocellulose during composting to form HS. Notably, the adverse effects of the alkali-treated apple wood compost on bacteria were greater. AcAWC showed significant correlations between bacterial and fungal communities and both lignin and hemicellulose, and had more biomarkers associated with lignocellulose degradation and humification. The lignin degradation rate was 24.57 % and the HS yield increased by 27.49 %. Therefore, AcAWC has been confirmed to enhance lignocellulose degradation and promote compost humification by altering the properties of the apple wood and establishing a richer microbial community.

Biochar-goethite composites inhibited/enhanced degradation of triphenyl phosphate by activating persulfate: Insights on the mechanism.

In this study, the biochar-goethite composites (MBC@FH) were synthesized through co-ball milling and the degradation of triphenyl phosphate (TPhP) was compared in persulfate (PDS) alone system and MBC@FH&PDS systems. The results showed that TPhP can be effectively degraded in PDS alone system and degradation efficiency reached up to 90 % within reaction of 8 h, at a PDS concentration of 10 mM, a reaction temperature of 30 °C and a system pH of 6.12. The obvious degradation can be ascribed to the reactive oxygen species (ROS) generated by self-decompose of PDS, among which 1O2, ∙OH and O2∙- play a major role in the degradation process. Although 350 °C biochar-goethite composites (MBC35@FH) and 800 °C biochar-goethite composites (MBC80@FH) facilitated PDS activation to produce more ROS, the catalytic degradation of TPhP was different in their systems. The degradation of TPhP was inhibited by MBC35@FH due to its stronger adsorption for TPhP, while MBC80@FH promoted TPhP degradation and degradation efficiency was up to 100 % within 6 h. 1O2 and SO4∙- played a stronger degradation role than ∙OH and O2∙- in above systems. The transformation of Fe species, functional groups (oxygen-containing functional groups, pyrrolic nitrogen) and persistent free radicals (PFRs) on the MBC@FH were involved in the PDS activation to produce ROS. Furthermore, MBC80@FH was more capable of activating PDS than MBC35@FH due to its abundant defect sites, larger specific surface area, more PFRs, higher Fe content and stronger electron transfer capability. In addition, seven possible TPhP intermediates were identified and possible degradation pathways of TPhP were proposed accordingly. This study illustrated that not all metallic carbon catalysts are necessarily beneficial for organic contaminants degradation.

Enhanced removal of tetrabromobisphenol A by Burkholderia cepacian Y17 immobilized on biochar.

Biochar-immobilized bacteria have been widely used to remove organic pollutants; however, the enhanced effect of biochar-immobilized bacteria on tetrabromobisphenol A (TBBPA) removal has not been fully investigated and the removal mechanism remains unclear. In this study, a bacterial strain with high TBBPA degradation ability, Burkholderia cepacian Y17, was isolated from an e-waste disassembly area, immobilized with biochar, and used for the removal of TBBPA. Comparisons were performed of the factors affecting the immobilization and TBBPA removal efficiency, including the biochar preparation temperature, immobilization temperature, and pH. The highest 7-day TBBPA removal efficiency by immobilized bacteria was observed with the most suitable biochar preparation temperature (BC500) and an immobilization pH and temperature of 7 and 35 °C, respectively. The TBBPA removal efficiency reached 59.37%, which was increased by 30.23% and 15.88% compared to that of free and inactivated immobilized Y17, respectively. The suitable biochar preparation temperature BC500, immobilization temperature of 35 °C, and neutral pH of 7 increased the bacterial population and extracellular polymer concentration, which facilitated bacterial immobilization on biochar and promoted TBBPA removal. In this case, the high immobilized bacteria concentration (4.62 × 108 cfu∙g-1) and protein and polysaccharide contents (28.43 and 16.16 mg·g-1) contributed to the removal of TBBPA by facilitating TBBPA degradation. The main TBBPA degradation processes by BC500-immobilized Y17 involved debromination, ß-scission, demethylation, O-methylation, hydroxylation, and hydroxyl oxidation. This study proposes a method for preparing immobilized bacteria for TBBPA removal and enriches the microbial degradation technology for TBBPA.

Fe3O4 loaded on ball milling biochar enhanced bisphenol a removal by activating persulfate: Performance and activating mechanism.

In this study, pristine biochar (BC), ball milling biochar (MBC), Fe3O4 modified BC (Fe3O4@BC), and Fe3O4 modified MBC (Fe3O4@MBC) were prepared to compare the Bisphenol A (BPA) removal efficiency by activating persulfate (PDS). All catalysts exhibited excellent degradation rather than adsorption in the PDS system, and Fe3O4@MBC800 had the best BPA removal efficiency, with 96.73% degradation and negligible 1.43% adsorption due to the synergistic effect between MBC800 and Fe3O4 particles. Radical quenching experiments and electron paramagnetic resonance analysis indicated radical pathways, namely, SO4∙- and ∙OH, O2∙-, and non-radical pathway (1O2) involving BPA degradation. The abundant oxygen-containing groups, increased graphitization and mesopores of MBC800, and Fe3+/Fe2+ conversion of Fe3O4 particles facilitated PDS activation to produce reactive oxygen species. In addition, the superior electrochemical performance accelerated the electron transfer between the catalyst and PDS, promoting BPA degradation in the Fe3O4@MBC800/PDS system. More importantly, Fe3O4@MBC800 is resistant to environmental interference, including pH, anions, cations, and humic acid, and has good catalytic reusability and stability, which fulfills the requirements of engineering applications. Therefore, Fe3O4 loaded on ball-milled biochar provides a convenient strategy for preparing environmentally friendly, economical, and efficient carbon-based catalysts to remove organic contaminants.

Urinary heavy metals in residents from a typical city in South China: human exposure and health risks.

Although heavy metal pollution has developed into a major global environmental problem, most research has focused on specific elements, especially arsenic (As) and selenium (Se), and on the health risks to people in polluted areas or by occupation. This study investigated the urine of 480 participants from Guangzhou with a population of 18 million and targeted nine heavy metals: As, Se, chromium (Cr), manganese (Mn), nickel (Ni), cadmium (Cd), lead (Pb), antimony (Sb), and mercury (Hg). The heavy metals were widely detected, of which As, Se, Cd, and Pb all exceed 98%. Among the toxicants, As showed the highest concentration, followed by Se with 40.5 and 35.4 µg/L, respectively. The heavy metal levels from suburban subjects were generally higher than those in urban subjects (except for Sb), and the Cd level of males was lower than that of females. Concentrations were related to age, body mass index, alcohol consumption, and smoking. According to the health risk assessment, most subjects experienced potential non-carcinogenic risk from As, Cd, Se, and Hg, which accounted for 38.2%, 8.83%, 8.31%, and 3.38%, respectively. The carcinogenic risk of As and Cd surpassed the risk level of 10-6, and 90.1% and 35.4% of the subjects, respectively, exceeded 10-4, an unacceptable risk level. More attention to the high carcinogenic risk from heavy metals and the high detected levels of As and Cd is required.