Dissemination of antibiotic resistance genes through fecal sewage treatment facilities to the ecosystem in rural area.

Infection of antibiotic-resistant pathogens mostly occurs in rural areas. In this paper, the dissemination of antibiotic resistance genes (ARGs) through fecal sewage treatment facilities to the ecosystem in a typical rural area is investigated. Household three-chamber septic tanks (TCs), household biogas digesters (BDs), wastewater treatment plants (WWTPs), vegetable plots, water ponds, etc. Are taken into account. The relative abundance of ARGs in fecal sewage can be reduced by BDs and WWTPs by 80% and 60%, respectively. While TCs show no reduction ability for ARGs. Fast expectation-maximization microbial source tracking (FEAST) analysis revealed that TCs and BDs contribute a considerable percentage (15-22%) of ARGs to the surface water bodies (water ponds) in the rural area. Most ARGs tend to precipitate in the sediments of water bodies and stop moving downstream. Meanwhile, the immigration of microorganisms is more active than that of ARGs. The results provide scientific basic data for the management of fecal sewage and the controlling of ARGs in rural areas.

Hydrothermal treatment of polyvinyl chloride: Reactors, dechlorination chemistry, application, and challenges.

Polyvinyl chloride (PVC) plastic wastes can bring a series of problems during pyrolysis or incineration such as the emission of dioxins, corrosion, slagging in the reactors, etc. Hydrothermal treatment of PVC plastics has been intensively studied as it can efficiently remove chlorine from PVC plastics under relatively mild reaction conditions (220-300 °C) to provide value-added products. Meanwhile, the research progress, knowledge gaps, and challenges in this field have not been well addressed yet. This paper gives a comprehensive review of hydrothermal dechlorination of PVC plastics regarding reactors, process variables and fundamentals, possible applications, and challenges. The main pathways of hydrothermal dechlorination of PVC plastics are elimination and -OH nucleophilic substitution. Catalytic hydrothermal and co-hydrothermal optimize the chemical reactions and transportation, boosting the dechlorination of PVC plastics. Hydrochar derived from PVC plastics, on the one hand, is coalified close to sub-bituminous and bituminous coal and can be used as low-chlorine solid fuel. On the other hand, it is also a porous material with aromatic structure and oxygen-containing functional groups, with good potential as adsorbent or energy storage materials. Further studies are expected to focus on waste liquid treatment, revealing the energy and economic balance, reducing the dechlorination temperature and pressure, expanding the application of products, etc. for promoting the implementation of the hydrothermal treatment of PVC plastic wastes.

Microplastics in household fecal sewage treatment facilities of rural China.

Fecal sewage (FS), composed of human feces and wastewater, potentially contains microplastics (MPs) that are prone to environmental pollution. In this study, 65 FS samples, as collected from 65 villages in 27 Chinese provinces, have been employed to investigate the characteristics of MPs in three kinds of household FS treatment facilities of rural regions, and the possibility of FS irrigation as the source of MPs in farmlands. As a result, seven physicochemical properties and microbial community of FS were detected, and pertinent social statistical data were collected to determine influencing factors of MPs. The abundance of FS-based MPs ranged from 47.16 to 143.05 particles L-1, with an average 90.38 ± 20.63 particles L-1. The FS from northern China had higher MPs abundance than that from southern and northwestern China. Average MPs abundance was cesspit (101.33) > septic tank (86.54) > biogas digester (84.11). The estimated mass of FS-based MPs entering farmlands in China was 7.8 × 103-5.6 × 104 tons a year. Chemical oxygen demand and genus Phascolarctobacterium might mainly affected MPs abundance in FS, while some other factors such as suspended substance, ambient temperature, and medical care spending were also significantly correlated with FS-based MPs abundance.

One-step synthesis of thiol-functionalized metal coordination polymers: effective and superfast removal of Hg (II) in the different matrices to ppb level.

The mercury in water bodies has posed a great threat to the environment and humans, and removing mercury and purifying wastewater has become a global environmental issue. Adopting Zn(II) coordination polymers (Zn-CPs) emerged as a new approach, however, the kind of Zn-CPs, which solely consisted of amino groups, exhibited unsatisfactory performance in capturing Hg(II) at a low level and causing the subsequent leaching of Zn(II) after adsorption. In this study, we fabricated the thiol-modified Zn-based coordination polymers (Zn-CPs-SH) through a one-step solvothermal reaction to efficiently capture Hg(II) from wastewater. Its preeminent adsorption performance could be maintained across a broad range of pH (2-7), ion strength (Cl-, SO42-, and NO3- at 0-10,000 mg/L), and dissolved organic matter (0-100 mg/L). The impressive properties, including fast kinetics (k2∼1.01 × 10-4 L/min), outstanding adsorption capacity (1278.72 mg/g, 298 K), superior selectivity (Kd∼2.3 × 104 mL/g), and excellent regeneration capability (Re = 93.54% after 5 cycles), were attributed to the ultra-abundance of adsorption sites donating from thiol groups, which was revealed by XPS analysis, DFT calculations, and molecular orbital theory. Noteworthy, the high practical application potential of Zn-CPs-SH was demonstrated by its outstanding Hg(II) removal efficiency (Re ≥ 99.10%) in various Hg(II)-spiked water matrices, e.g., tap water, river water, and industrial wastewater. Importantly, the residual Hg(II) in the treated water declined to the ppb level without any Zn(II) leaching. Overall, it is highly anticipated that the incorporation of Zn-CPs-SH would facilitate the practical implementation of highly efficient Hg(II) removal in wastewater treatment owing to its exhibiting high selective affinity, superior adsorption capacity, and enhanced efficiency.

Restricted-magnesium-vapor-reduction of amorphous SiO/C precursors to polycrystalline Si/SiOx/C hybrid anodes.

Considering the electrochemical activity/stability and preparation feasibility of silicon (Si) nanomaterials, we designed a restricted-magnesium-vapor-reduction to fabricate sustainable Si/SiOx/C porous anodes with nanopores and polycrystalline structures.

Fabrication of durable self-cleaning photocatalytic coating with long-term effective natural light photocatalytic degradation performance.

The practical application of photocatalytic coating has been greatly challenged in terms of its long-term effective natural light photocatalytic degradation due to its vulnerability and easy contamination caused by poor self-cleaning properties. In this work, photocatalytic coating with self-cleaning properties was prepared by spraying fluorinated dual-scale TiO2 on the inorganic lithium silicate adhesive, enabling excellent durability and long-term effective photocatalytic degradation performance under natural light. The coating exhibits superhydrophobic properties even after abrasion testing, acid and alkali immersion testing, and UV aging, laying a foundation for the practical use. Moreover, the coating can be applied to various substrates and its excellent self-cleaning properties make it resistant to particulate and liquid contamination that may occur in the environment. Besides, we evaluated the photocatalytic stability of the coating by subjecting it to acidic and alkaline environments and high pollution concentrations. Furthermore, benefiting from the synergistic effect of photocatalytic and self-cleaning properties, the coating achieves long-term effective photocatalytic degradation of dye wastewater under natural light, which still has a high removal rate of 95.8% for methylene blue even after 30 cycles of use. Meanwhile, due to the coating's excellent durability, the long-term quality loss rate of the coating still remained below 0.3%, which avoids the risk of secondary environmental pollution caused by nanoparticle leakage. Therefore, these excellent properties enable the coating to have a broad range of application prospects for the treatment of pollutants in water.

Biomass porous carbon as the active site to enhance photodegradation of oxytetracycline on mesoporous g-C3N4.

Graphitic carbon nitride (g-C3N4) is widely used in photocatalytic adsorption and degradation of pollutants, but there are still some problems such as low adsorption performance and high electron-hole recombination efficiency. Herein, we propose a new molten salt assisted thermal polycondensation strategy to synthesize biomass porous carbon (BPC) loaded on g-C3N4 composites (designated as BPC/g-C3N4) with a hollow tubular structure, which had a high surface area and low electron-hole recombination rate. The study shows that the morphology of g-C3N4 changes dramatically from massive to hollow tubular by molten salt assisted thermal polycondensation, which provides a base for the loading of BPC, to construct a highly effective composite photocatalyst. BPC loaded on g-C3N4 could be used as the active site to enhance Oxytetracycline (OTC) removal efficiency by adsorption and with higher electron-hole separation efficiency. As a result, the BPC(5%)/g-C3N4 sample presented the highest photocatalytic degradation efficiency (84%) for OTC degradation under visible light irradiation. The adsorption capacity and photocatalytic reaction rate were 3.67 and 5.63 times higher than that of the g-C3N4, respectively. This work provided a new insight for the design of novel composite photocatalysts with high adsorption and photocatalytic performance for the removal of antibiotic pollutants from wastewater.

Food waste composting based on patented compost bins: Carbon dioxide and nitrous oxide emissions and the denitrifying community analysis.

Mature compost and rice bran were used as bulking agents to perform Food Waste Rapid Composting (FWRC) in a patented composting bin. The characteristics of CO2 and N2O emission and the denitrifying community were investigated. The release of CO2 and N2O concentrated in the early composting stage and reduced greatly after 28 h, and the N2O emission peak of the treatment with mature compost was 8.5 times higher than that of rice bran. The high N2O generation resulted from massive denitrifying bacteria and NOx--N in the composting material. The relative abundances of denitrifiers, correspondingly genes of narG and nirK were much higher in the treatment with mature compost, which contributed to the N2O emission. Moreover, the correlation matrices revealed that N2O fluxes correlated well with moisture, pH, temperature, and the abundances of nirK and nosZ genes during FWRC.

Development and validation of the DGT technique using the novel cryogel for measuring dissolved Hg(II) in the estuary.

The complex seawater matrix has significantly influenced the determination of estuarine dissolved Hg(II), hindering its monitoring and risk assessment in maricultural areas. In this work, SiO2-SH-DGT assembled by the sulfhydryl-modified silica cryogel (SiO2-SH cryogel) as the novel binding phase was developed to tackle this problem. The uniform dispersion of the cryogel into binding gel was advantageous for achieving remarkable and comparable capacity, which endowed the estimated diffusion coefficient (D) to be 1.39-3.08 times of the existing research. The SiO2-SH-DGT performance was independent of pH (3-9), ionic strength (10-800 mM), fulvic acid at low content, and seawater matrix (Na+, K+, Ca2+, Cl-), but the high content of Mg2+ did interfere with the Hg(II) accumulation, which manifested as competitive adsorption and diffusion. Therefore, the calibrated model was established by calibrating accumulated mass (M') and diffusion coefficient (D') based on the Mg2+ concentration, its high accuracy was further verified in the lab. Finally, SiO2-SH-DGT was deployed in the three typical aquaculture areas in Beibu Gulf, field trials achieved the actual Hg(II) level to be 1.52-5.38 ng/L with consideration of the diffusion boundary layer. The finding could provide new thought and technical support for metal pollution monitoring in estuary maricultural areas.

Biodegradation and potential effect of ranitidine during aerobic composting of human feces.

Ranitidine is widely concerned due to it is mainly related to the transformation into highly toxic carcinogenic products and non-readily biodegradable characteristics in aquatic environment. In this study, biodegradation of ranitidine during rural human feces (HF) aerobic composting was investigated. Results show that both levels of ranitidine are quickly removed in the first-3-day composting. The microorganisms play a vital role in the ranitidine degradation, especially for Firmicutes at the thermophilic period. The effect of ranitidine on the aerobic composting was further analyzed under the normal content (10 mg/kg) and high content (100 mg/kg). The 10 mg/kg ranitidine quickens temperature rise and organic matter degradation of the composting, while the 100 mg/kg ranitidine produces inhibiting effects. However, the effects only occur in the early stage of composting, and then tend to disappear with the removal of ranitidine. Fluorescence spectra confirm that humification and aromatization of dissolved organic matters (DOMs) in the substrates are fastened in 10 mg/kg group, while delayed in 100 mg/kg group. Metagenomic analysis reveals that relative abundances of Firmicutes and sequences related to carbohydrates metabolism increase in the groups mixed with the ranitidine at the early period. The findings provide the first new and systematical insights into degradation characteristics and potential effect of ranitidine during the rural HF composting.

Effects of PCE on the Dispersion of Cement Particles and Initial Hydration.

The effects of polycarboxylate superplasticizers (PCEs) on the dispersing properties and initial hydration of cement particles with various water-to-cement (w/c) ratios was investigated, including the water film thickness (WFT), rheology, fluidity, adsorption of PCEs, zeta potential, degree of hydration, hydration products. The experimental results demonstrate that the initial rheological and fluidity parameters were more sensitive to the PCE dosage at a lower w/c because the WFT and the zeta potential on cement particles change more significantly. Moreover, the higher adsorption amounts of the PCEs at a lower w/c lead to a stronger inhibition of the initial hydration, whilst, at the same PCE dosage, the cement pastes have a more rapid fluidity loss and quicker hydration reactions at a higher w/c due to a lower adsorption amount of the PCE on cement particles.

Influence of Sand-Cement Ratio and Polycarboxylate Superplasticizer on the Basic Properties of Mortar Based on Water Film Thickness.

Previous studies demonstrated that water film thickness (WFT) is a key factor that affects the fluidity of mortar. Changes in the sand-cement (S/C) ratio and polycarboxylate superplasticizer (PCE) dosage will affect the WFT. In this study, several mortar samples with different S/C ratios and different PCE dosages were prepared, and the basic properties of the mortar were measured. The results show that as the S/C ratio increases, the packing density of the mortar will decrease, the WFT will decrease, and the cohesiveness will increase, resulting in a decrease in the flow spread and strength of the mortar. When the PCE dosage is increased, the packing density of the mortar will increase, the WFT will increase, and the cohesiveness will decrease, which increases the flow spread of the mortar. When the water-cement (W/C) ratio is low, the S/C ratio has a significant effect on the strength, and the strength will increase with the increasing of the PCE dosage. When the W/C ratio is high, the strength of the mortar will be reduced once the PCE dosage exceeds the saturation value. In the case of different S/C ratios or different PCE dosages, the WFT can be used as a measure of mortar cohesiveness and flow spread.

Stable Fe3O4 submicrospheres with SiO2 coating for heterogeneous Fenton-like reaction at alkaline condition.

In the traditional Fenton process, the efficient generation of hydroxyl radical (HO) strongly relies on an acidic circumstance and the iron ions would precipitate and form large amounts of hazardous iron-containing sludge at alkaline pH. To realize stable heterogeneous Fenton-like catalytic degradation at alkaline condition, Fe3O4 submicrospheres with SiO2 coating were successfully synthesized by using water glass as the silica sources via a facile ultrasound assisted method. The as-obtained Fe3O4@SiO2 spheres were further used as catalysts for the Fenton-like degradation of tetracycline hydrochloride (TC). The Fe3O4@SiO2 submicrospheres exhibited superior catalytic activity in higher pH environment (pH value = 11), and the degradation efficiency toward TC was ca. 80% after ten successive runs. The kinetics for the catalytic degradation of TC were agreed well with the second-order kinetic model. The reaction rate constant (k) over the Fe3O4@SiO2 submicrospheres at a pH value of 11 was 7.69 times greater than that at a pH value of 3. Reactive species scavenging experiments revealed that HO and superoxide radical (O2- / HO2-) played a dominant role during the Fenton-like degradation of TC at pH 3 and pH 11, respectively. Possible Fenton-like degradation pathways of TC were proposed through the identification of intermediates using the high performance liquid chromatography coupled with mass spectrometry (HPLC-MS), which involved cleavage of methyl groups, N-dimethyl group, and hydroxy groups, ring-opening reaction, etc. The degradation efficiency of TC was close to 91.5% and total organic carbon (TOC) in solution was eliminated by about 41.4% at the optimized conditions. In a word, with the unique acidic surface properties and abundant Si-OH bonds, the Fe3O4@SiO2 submicrospheres exhibited well dispersion, good catalytic activity, strong alkali resistance and excellent recyclability in an ultrasonic-Fenton-like system.

Effect of the Electric Field on the Distribution Law of Chloride Ions and Microstructure in Concrete with the Addition of Mineral Admixtures.

Migration testing of chloride under an electric field is a fast and effective method to determine the corrosion resistance of reinforced concrete against chloride. In this study, a series of admixture-involved (fly ash and slag) concrete specimens were produced for an accelerating chloride diffusion test in 3% NaCl solution under an electric field and natural chloride diffusion in 165 g/L NaCl solution under immersion conditions. Then, the chloride profile and pore structure of concretes aged 56 and 91 days were compared to investigate the effect of the electric field on chloride diffusion as well as the microstructure of the concrete. The results showed that, under accelerating electric field conditions, the degree to which chloride refined the internal pore structure of the concrete was weaker than that under natural immersion conditions. The applied electric field changed the pore structure inside the concrete, but it had little effect on the distribution of total, free, and bound chlorides and their mutual relationship. In addition, it is necessary to consider that the electric field effect on chloride migration varies with the concrete mix proportions.

Insight into chlorine evolution during hydrothermal carbonization of medical waste model.

In order to reveal the chlorine behavior during hydrothermal carbonization (HTC) of medical waste, polyvinyl chloride and medical waste model (MW) were respectively treated by HTC at temperature ranging from 220 °C to 300 °C for 30 min. HTC products were characterized by Fourier Transform Infrared Spectrometer, X-ray Photoelectron Spectroscopy, etc. It is found that HTC can efficiently remove chlorine from both polyvinyl chloride and MW. The most dramatical dechlorination can be induced by HTC at around 240 °C. With HTC temperature increased, organic chlorine in HT-MW and solid product from polyvinyl chloride HTC (HT-PVC) is decreased. Interestingly, with 240 °C HTC, the organic chlorine of HT-MW was 15.30%, much lower than that of HT-PVC of 86.84%, indicating the cellulosic materials in MW can significantly boost the conversion of organic chlorine into inorganic form in HTC at 240 °C. While spherical particles assigned to HTC of cellulosic materials aggregate at the pores of polyvinyl chloride particle, trapping the release of chlorine into the liquid, consequently to lower dechlorination efficiency compared to that of polyvinyl chloride. Since the chlorine retain in the solid product was mainly in form of inorganic, further dechlorination is potential for MW by combining HTC with leaching/extracting.

Adsorption of lead and mercury by rice husk ash.

An attempt at the use of rice husk ash, an agricultural waste, as an adsorbent for the adsorption of lead and mercury from aqueous water is studied. Studies are carried out as a function of contact times, ionic strength, particle size, and pH. Rice husk ash is found to be a suitable adsorbent for the adsorption of lead and mercury ions. The Bangham equation can be used to express the mechanism for adsorption of lead and mercury ions by rice husk ash. Its adsorption capability and adsorption rate are considerably higher and faster for lead ions than for mercury ions. The finer the rice husk ash particles used, the higher the pH of the solution and the lower the concentration of the supporting electrolyte, potassium nitrate solution, the more lead and mercury ions absorbed on rice husk ash. Equilibrium data obtained have been found to fit both the Langmuir and Freundlich adsorption isotherms.

Facile synthesis of SrCO3 nanostructures in methanol/water solution without additives.

Highly dispersive strontium carbonate (SrCO3) nanostructures with uniform dumbbell, ellipsoid, and rod-like morphologies were synthesized in methanol solution without any additives. These SrCO3 were characterized by X-ray diffraction, field emission scanning electron microscopy, and N2 adsorption-desorption. The results showed that the reaction temperature and the methanol/water ratio had important effects on the morphologies of SrCO3 particles. The dumbbell-like SrCO3 exhibited a Broader-Emmett-Teller surface area of 14.9 m2 g-1 and an average pore size of about 32 nm with narrow pore size distribution. The formation mechanism of the SrCO3 crystal was preliminary presented.