三唑酮在水中的光化学降解及其影响因素

以太阳光和高压汞灯为光源，研究了水溶液中三唑酮光化学降解的影响因子。结果表明：在不同光源和透光介质下，三唑酮的降解能力从大到小依次为：石英试管＋高压汞灯、玻璃试管＋高压汞灯、石英试管＋太阳光、玻璃试管＋太阳光、暗室；水溶液中三唑酮初始浓度越高，其光降解率越低，呈负相关关系；丙酮对三唑酮在水中的光解有极显著的光敏作用，光敏效率与丙酮添加量有显著相关性；三唑酮的光解实质为光氧化作用，溶解氧含量对三唑酮光解有重大影响。     

Retaining natural vegetation to safeguard biodiversity and humanity

Global efforts to deliver internationally agreed goals to reduce carbon emissions, halt biodiversity loss, and retain essential ecosystem services have been poorly integrated. These goals rely in part on preserving natural (e.g., native, largely unmodified) and seminatural (e.g., low intensity or sustainable human use) forests, woodlands, and grasslands. To show how to unify these goals, we empirically derived spatially explicit, quantitative, area-based targets for the retention of natural and seminatural (e.g., native) terrestrial vegetation worldwide. We used a 250-m-resolution map of natural and seminatural vegetation cover and, from this, selected areas identified under different international agreements as being important for achieving global biodiversity, carbon, soil, and water targets. At least 67 million km² of Earth's terrestrial vegetation (∼79% of the area of vegetation remaining) required retention to contribute to biodiversity, climate, soil, and freshwater conservation objectives under 4 United Nations’ resolutions. This equates to retaining natural and seminatural vegetation across at least 50% of the total terrestrial (excluding Antarctica) surface of Earth. Retention efforts could contribute to multiple goals simultaneously, especially where natural and seminatural vegetation can be managed to achieve cobenefits for biodiversity, carbon storage, and ecosystem service provision. Such management can and should co-occur and be driven by people who live in and rely on places where natural and sustainably managed vegetation remains in situ and must be complemented by restoration and appropriate management of more human-modified environments if global goals are to be realized.     

Impacts of backwashing on micropollutant removal and associated microbial assembly processes in sand filters

● Backwashing in sand filters with 2-h and 4-h EBCTs was simulated. ● Removal efficiency of five micropollutants recovered within 2 d at 2-h EBCT. ● Active biomass of sand filters recovered within 2 d under two EBCTs. ● Microbial composition gradually recovered to pre-backwashing level at 2-h EBCT. ● Recovered microbes only accounted for 15.55 %–25.69 % in the sand filters at 4-h EBCT. Backwashing is crucial for preventing clogging of sand filters. However, few studies have investigated the effect of backwashing on micropollutant removal and the dynamic changes in the microbial community in sand filters. Here, we used a series of manganese and quartz sand filters under empty bed contact times (EBCTs) of 2 h and 4 h to explore variations in micropollutant degradation and temporal dynamics of the microbial community after backwashing. The results showed that the removal efficiencies of caffeine, sulfamethoxazole, sulfadiazine, trimethoprim, atrazine, and active biomass recovered within 2 d after backwashing in both types of sand filters at 2-h EBCT, but the recovery of sulfadiazine and trimethoprim was not observed at 4-h EBCT. Moreover, the removal efficiency of atenolol increased after backwashing in the manganese sand filters, whereas maintained almost complete removal efficiency in the quartz sand filters at both EBCTs. Pearson correlation analysis indicated that microbial community composition gradually recovered to the pre-backwashing level (R increased from 0.53 to 0.97) at 2-h EBCT, but shifted at 4-h EBCT (R < 0.25) after backwashing. Furthermore, the compositions of the recovered, depleted, and improved groups of microbes were distinguished by applying hierarchical clustering to the differentially abundant amplicon sequence variants. The cumulative relative abundance of recovered microbes at 2-h EBCT was 82.76 % ± 0.43 % and 46.82 % ± 4.34 % in the manganese and quartz sand filters, respectively. In contrast, at 4-h EBCT, the recovered microbes dropped to 15.55 %–25.69 % in both types of sand filters.     

Enhancement of extracellular Cr(VI) reduction for anammox recovery using hydrazine: performance,pathways, and mechanism

● N₂H₄ addition enhanced and recovered anammox performance under Cr(VI) stress. ● N₂H₄ accelerated electron transfer of Cr(VI) reduction for detoxification. ● N₂H₄ enhanced anammox metabolism for activity recovery from Cr(VI) inhibition. ● Extracellular Cr(VI) reduction to less toxic Cr(III) was the dominant mechanism. The hexavalent chromium (Cr(VI)) would frequently impose inhibition to anaerobic ammonium oxidation (anammox) process, hindering the efficiency of nitrogen removal in wastewater treatment. Hydrazine (N₂H₄), which is an intermediate product of anammox, participates in intracellular metabolism and extracellular Cr(VI) reduction. However, the roles of N₂H₄-induced intracellular metabolism and extracellular reduction in nitrogen removal under Cr(VI) stress remain unclear. The addition of 3.67 mg/L of N₂H₄ increased the anammox activity by 17%. As an intermediate, N₂H₄ enhanced anammox metabolism by increasing the heme c content and electron transfer system activity. As a reductant, N₂H₄ accelerated the reduction of c-Cyts-mediated extracellular Cr(VI) to the less toxic Cr(III). Extracellular Cr(III) accounts for 74% of the total Cr in a Cr(VI)-stressed anammox consortia. These findings highlight that N₂H₄-induced extracellular Cr(VI) reduction is the dominant mechanism for the survival of anammox consortia. We also found that N₂H₄ increased the production of extracellular polymeric substances to sequester excessive Cr(VI) and produced Cr(III). Taken together, the study findings suggest a potential strategy for enhancing nitrogen removal from ammonium-rich wastewater contaminated with Cr(VI).     

Efficacy of forming biofilms by <Emphasis Type="Italic">Pseudomonas migulae</Emphasis> AN-1 toward in situ bioremediation of aniline-contaminated aquifer by groundwater circulation wells

The formation and activity of aniline-degrading biofilms developed by the psychrotrophic Pseudomonas migulae AN-1 were studied for the in situ remediation of contaminated aquifer using in-well bioreactor of groundwater circulating wells (GCWs). Biofilms grown in mineral salt medium with aniline exhibited tolerance to high concentrations of aniline. In aniline degradation rate, AN-1 biofilms exhibited slight differences compared with planktonic cells. The effectiveness and bio-implication of AN-1 biofilms in GCWs were investigated to treat aniline-contaminated aquifer. The results demonstrate that AN-1 biofilms survived the GCWs treatment process with high aniline-degrading efficiency. This system provides a novel environmentally friendly technology for the in situ bioremediation of low-volatile contaminants.     

含油浮渣制备含碳吸附剂并用于含油污水的处理

以含油浮渣为原料制备含碳吸附剂,并用于含油污水的处理。用比表面分析仪和SEM技术对吸附剂进行表征。通过正交实验和单因素实验考察吸附剂加入量、吸附时间及温度、污水pH对污水处理效果的影响。表征结果显示,含碳吸附剂碳元素含量高达90%(w)以上,表面粗糙,孔径分布以中孔为主,比表面积477.5 m2/g,碘吸附值376.48 mg/g。实验结果表明:在吸附温度30℃及时间60 min、含碳吸附剂加入量20 g/L、污水pH为7的最佳实验条件下,处理初始COD为502.12 mg/L、石油类质量浓度45.31 mg/L.的含油污水,COD和石油类的去除率分别为91.51%和87.1%,处理后的COD和石油类质量浓度分别为42.62 mg/L和5.83 mg/1,达到GB 8978—1996《污水综合排放标准》中的二级排放标准;含碳吸附剂的污水处理效果优于术质活性炭。     

Melting characteristics during the vitrification of MSW incinerator fly ash by swirling melting treatment

Journal of Material Cycles and Waste Management - Pilot tests of fly ash were investigated in a 0.2&nbsp;MW swirling melting furnace at 1250–1400&nbsp;°C. The properties of raw...     

36种典型除草剂对绿藻的毒性研究

近年来,农药对生态系统的初级生产者——藻类的毒性及其生态毒理学研究引起了国内外学者的广泛关注。除草剂在生产中广泛应用,对藻类的毒性作用最强,其毒性效应远高于杀虫剂和杀菌剂。论文选择市场上具有典型代表性的36种除草剂原药,分析解读除草剂在国内的登记情况,以及在作物、旱田和水田的使用情况;明晰对藻类生长抑制急性毒性效应。结果表明:1)除草剂的作用方式和化学类别对绿藻毒性影响显著;对于抑制植物细胞分裂和作用于植物叶绿体的除草剂对绿藻毒性均较高,以人工合成植物生长素为代表的除草剂对绿藻毒性均较低;2)相同作用方式,不同化学类别的除草剂,对单一绿藻的毒性差异明显。在水稻上获得登记的除草剂对藻类毒性整体低于在旱田获得登记的除草剂对藻类的毒性。开展多种农药对水生生态毒性的研究,为农药的合理安全使用、农药在淡水环境中的生态效应评价以及保护淡水生态系统提供科学依据。     

组合指数在环境混合物联合毒性研究中的初步应用

化学品在实际环境中总是以组分繁杂多变的混合物形式存在,其混合物的毒性评估与预测一直是环境毒理学研究重点。在环境毒理学领域,浓度加和(concentration addition,CA)及独立作用(independent action,IA)是评估与预测化学混合物联合毒性的经典模型,一般认为CA适用于作用模式相似的混合物体系而IA适用于作用模式相异的混合物体系,但如何使用CA与IA一直存在争议。组合指数(combination index,CI)是在半数效应方程基础上发展起来的不依赖于作用模式的用于混合物联合毒性评估的混合物毒性指数,具有坚实的理论基础,不仅能定性地评估毒理学相互作用,也能定量地评估相互作用的大小,已在药物组合研究中得以广泛应用,近年来已引起环境毒理学研究者兴趣。本文就组合指数及药物组合应用、进入环境毒理学领域、与CA及IA的关系、存在的问题等几个方面进行评述,以期推进CI在化学混合物毒性评估与预测领域中的应用。     

Promotional effect of rare earth-doped manganese oxides supported on activated semi-coke for selective catalytic reduction of NO with NH3

Environmental Science and Pollution Research - A composite catalyst for the selective catalytic reduction (SCR) of NOx with NH3 is investigated, in which the rare earth (RE, including La, Ce, Pr,...