Attenuation effects of ZVI/PDS pretreatment on propagation of antibiotic resistance genes in bioreactors: Driven by antibiotic residues and sulfate assimilation.

Sulfate radical-based advanced oxidation processes (AOPs) combined biological system was a promising technology for treating antibiotic wastewater. However, how pretreatment influence antibiotic resistance genes (ARGs) propagation remains largely elusive, especially the produced by-products (antibiotic residues and sulfate) are often ignored. Herein, we investigated the effects of zero valent iron/persulfate pretreatment on ARGs in bioreactors treating sulfadiazine wastewater. Results showed absolute and relative abundance of ARGs reduced by 59.8%- 81.9% and 9.1%- 52.9% after pretreatments. The effect of 90-min pretreatment was better than that of the 30-min. The ARGs reduction was due to decreased antibiotic residues and stimulated sulfate assimilation. Reduced antibiotic residues was a major factor in ARGs attenuation, which could suppress oxidative stress, inhibit mobile genetic elements emergence and resistant strains proliferation. The presence of sulfate in influent supplemented microbial sulfur sources and facilitated the in-situ synthesis of antioxidant cysteine through sulfate assimilation, which drove ARGs attenuation by alleviating oxidative stress. This is the first detailed analysis about the regulatory mechanism of how sulfate radical-based AOPs mediate in ARGs attenuation, which is expected to provide theoretical basis for solving concerns about by-products and developing practical methods to hinder ARGs propagation.

Insights into removal of sulfonamides in anaerobic activated sludge system: Mechanisms, degradation pathways and stress responses.

The fate of antibiotics in activated sludge has attracted increasing interests. However, the focus needs to shift from concerning removal efficiencies to understanding mechanisms and sludge responding to antibiotic toxicity. Herein, we operated two anaerobic sequencing batch reactors (ASBRs) for 200 days with sulfadiazine (SDZ) and sulfamethoxazole (SMX) added. The removal efficiency of SMX was higher than that of SDZ. SDZ was removed via adsorption (9.91-21.18%) and biodegradation (10.20-16.00%), while biodegradation (65.44-86.26%) was dominant for SMX removal. The mechanisms involved in adsorption and biodegradation were investigated, including adsorption strength, adsorption sites and the roles of enzymes. Protein-like substance (tryptophan) functioned vitally in adsorption by forming complexes with sulfonamides. P450 enzymes may catalyze sulfonamides degradation via hydroxylation and desulfurization. Activated sludge showed distinct responses to different sulfonamides, reflected in the changes of microbial communities and functions. These responses were related to sulfonamides removal, corresponding to the stronger adsorption capacity of activated sludge in ASBR-SDZ and degradation capacity in ASBR-SMX. Furthermore, the reasons for different removal efficiencies of sulfonamides were analyzed according to steric and electronic effects. These findings propose insights into antibiotic removal and broaden the knowledge for self-protection mechanisms of activated sludge under chronic toxicities of antibiotics.

Calcium-Loaded Municipal Sludge-Biochar as an Efficient and Stable Catalyst for Biodiesel Production from Vegetable Oil.

In this contribution, biochar from municipal sludge was used as a novel matrix for the synthesis of a series of calcium-based heterogeneous catalysts toward biodiesel production. Their catalytic activity was investigated in terms of catalyst loading and calcination temperature during preparation, in addition to the transesterification parameters including the methanol/oil molar ratio, reaction time, and catalyst amount. The highest biodiesel yield up to 93.77% was achieved with the 30Ca/A-SBC-700, and it maintained as high as 84.9% even after 10 cycles of a consecutively alternating catalysis and regeneration process. It was revealed that the porous municipal sludge biochar and autologous SiO2 were accountable for the superior stability of the present catalyst. This work may provide a new path to value-added valorization of sludge waste and also a renewable and efficient catalyst for biodiesel production at a low cost.

Significant enhancement of electron transfer from Shewanella oneidensis using a porous N-doped carbon cloth in a bioelectrochemical system.

Modifying the surface of an anode can improve electron transfer, thus enhancing the performance of the associated bioelectrochemical system. In this study, a porous N-doped carbon cloth electrode was obtained via a simple thermal reduction and etching treatment, and then used as the anode in a bioelectrochemical system. The electrode has a high nitrogen-to­carbon (N/C) ratio (~3.9%) and a large electrochemically active surface area (145.4 cm2, about 4.4 times higher than that of the original carbon cloth), which increases the bacterial attachment and provides more active sites for extracellular electron transfer. Electrochemical characterization reveals that the peak anodic current (0.71 mA) of the porous N-doped carbon cloth electrode in riboflavin is 18 times higher than that of the original carbon cloth electrode (0.04 mA), confirming the presence of more electroactive sites for the redox reaction. We also obtained a maximum current density of 0.29 mA/cm2 during operation of a bioelectrochemical system featuring the porous N-doped carbon cloth electrode, which is 14.5 times higher than that of the original carbon cloth electrode. This result demonstrates that the adoption of our new electrode is a viable strategy for boosting the performance of bioelectrochemical systems.

Steamed cake-derived 3D carbon foam with surface anchored carbon nanoparticles as freestanding anodes for high-performance microbial fuel cells.

Anode design is highly significant for microbial fuel cells, since it simultaneously serves as the scaffold for electroactive microorganisms and as a medium for electron migration. In this study, a stiff 3D carbon foam with surface anchored nitrogen-containing carbon nanoparticles was facilely constructed via in-situ polyaniline coating of carbonized steamed cake prior to the carbonization process. The resultant product was determined to be an excellent freestanding anode that enabled the microbial fuel cell to deliver a maximum power density of up to 1307 mW/m2, which significantly outperformed its non-coated counterpart, the widely used commercial carbon felt. Further investigations revealed that the overall performance enhancement was associated with the open porosity, enlarged electroactive surface, increased biocompatibility, and decreased electric resistance of the anode scaffold. This promising anode material would offer a green and economical option for fabricating high-performance microbial fuel cell-based devices towards various ends.

Comparison of sodium hydroxide and calcium hydroxide pretreatments on the enzymatic hydrolysis and lignin recovery of sugarcane bagasse.

Sodium hydroxide (NaOH) and calcium hydroxide (Ca(OH)2) respectively dissolved in water and 70% glycerol were applied to treat sugarcane bagasse (SCB) under the condition of 80°C for 2h. NaOH solutions could remove more lignin and obtain higher enzymatic hydrolysis efficiency of SCB than Ca(OH)2 solutions. Compared with the alkali-water solutions, the enzymatic hydrolysis of SCB treated in NaOH-glycerol solution decreased, while that in Ca(OH)2-glycerol solution increased. The lignin in NaOH-water pretreatment liquor could be easily recovered by calcium chloride (CaCl2) at room temperature, but that in Ca(OH)2-water pretreatment liquor couldn't. NaOH pretreatment is more suitable for facilitating enzymatic hydrolysis and lignin recovery of SCB than Ca(OH)2 pretreatment.

Nitrogen-doped carbon dots from plant cytoplasm as selective and sensitive fluorescent probes for detecting p-nitroaniline in both aqueous and soil systems.

Nitrogen-doped carbon dots with excellent water- and ethanol-solubility were facilely prepared from plant cytoplasm via a one-step hydrothermal route and revealed as low-cost, label-free and highly sensitive and selective probes for detecting p-nitroaniline in both aqueous and soils owing to a proposed hydrogen-bonding effect.

Fluxible nanoclusters of Fe3O4 nanocrystal-embedded polyaniline by macromolecule-induced self-assembly.

We have prepared Fe3O4 nanocrystal-embedded polyaniline hybrids with well-defined cluster-like morphology through macromolecule-induced self-assembly. These magnetic and electrically conductive composite nanoclusters show flowability at room temperature in the absence of any solvent, which offers great potential in applications such as microwave absorbents and electromagnetic shielding coatings. This macromolecule-induced self-assembly strategy can be readily applied on the fabrication of other ion oxide/conjugated polymer composites to achieve robust multifunctional materials.