基于Meta分析的全氟化合物对鱼类生态毒性效应

全氟及多氟化合物（PFAS）是难降解的有机污染物,具有普遍存在、生物蓄积和生物学毒性效应等特点.为探讨PFAS对鱼类的生物毒性效应,综述了64篇文献,通过Meta分析合并效应值探讨鱼类暴露于PFAS对其功能性状的毒性,为PFAS的毒性评估提供参考,有利于PFAS污染的优先控制管理.结果表明：①在研究的12种功能性状中,鱼类的7类功能性状易感,毒性响应顺序为畸形（lnRR=-2.5599）、发育（lnRR=-0.4103）、细胞损伤（lnRR=-0.3962）、生殖（lnRR=-0.3724）、甲状腺水平（lnRR=-0.2492）、生长（lnRR=-0.2194）和生存（lnRR=-0.2192）;②鱼类性别和所处发育阶段显著影响PFAS的水生毒性,PFAS易对雌鱼产生不良影响（lnRR=-0.1628）,且胚胎期鱼类的生理功能受PFAS影响最显著（lnRR=-0.3553）;③研究涉及的PFAS共13种,其中具有磺酸盐基团的PFAS和长链PFAS更易对鱼类的功能性状产生不良影响（P<0.05）;④现有数据揭示PFAS在中低浓度（0.01~10 mg ·L^-1）下易对鱼类产生急性毒性（P<0.05）.     

水泥注浆中六价铬总溶出量的影响因素研究

水泥注浆过程中析出液中的六价铬Cr(Ⅵ)易造成地下水的重金属污染,对生态和环境具有较大危害性,为了有效降低水泥注浆中Cr(Ⅵ)总溶出量,采用化学还原的方法,探讨了各种降铬剂及其掺量对降低Cr(Ⅵ)总溶出量的效果,研究了颗粒粒度、液固比对Cr(Ⅵ)总溶出量的影响.结果 表明,硫酸亚铁降铬剂的效果最显著,当用量在3％以内时...     

磷石膏对麦田CO2排放和小麦产量的影响及其经济环境效益分析

磷石膏是一种可以利用的磷化工废渣,本文以磷石膏为麦田温室气体减排剂,研究磷石膏对小麦生长、麦田温室气体二氧化碳(CO2)排放的影响,并分析磷石膏资源化利用的经济环境效益.结果表明,在常规施肥条件下,增施磷石膏2 100kg·hm-2能显著促进小麦生长,增产达37.71%.磷石膏对麦田CO2的减排作用在小麦生长的各个时期有所不同:施用磷石膏1 050 kg·hm-2处理,在小麦生长拔节期、抽穗期和灌浆期对麦田CO2的减排效果较为明显,相比对照分别减少8%、10%和6%;在整个小麦生长季累计减少CO2排放3%;施用磷石膏2 100 kg·hm-2处理,在小麦越冬返青期、拔节期和抽穗期,相比对照减少CO2排放11%、4%和12%,在小麦生长季累计减少CO2排放7%.磷石膏施用量较大的处理对CO2的抑制和减排效果较好.研究还表明在施用磷石膏的情况下,一定范围内,CO2的排放强度(单位鲜重CO2排放与单位产量CO2排放)与小麦穗长、鲜重和产量呈现显著负相关:即穗长越长,鲜重和产量越大,CO2的排放效率越低.在碳交易背景下,磷石膏资源化利用具有较高的经济和环境效益,主要体现在:与对照相比,投入/产出从1∶8.3变为1∶10.7,即在相同投入的情况下可提高28.92%的产出;每吨磷石膏作为麦田温室气体减排剂,可节省治理环境的费用与增产总额合计约290元.废渣磷石膏资源化利用,不仅可以减少环境污染、促进小麦生长,而且可以减少CO2排放,对发展低碳农业、生态农业以及可持续发展农业具有重要应用价值.     

膜分离腐殖质前后晚期渗滤液可生化性的变化

晚期渗滤液由于含有大量难降解有机物腐殖质,可生化性差,较难处理。采用特定分子量的超滤膜对晚期渗滤液中的腐殖质进行有效的分离,研究了膜分离腐殖质前后渗滤液的可生化性的变化：渗滤液中腐殖质类物质去除率为90．7％,BOD5/COD值提高了6倍,可生物降解的有机物在总有机物中所占比率提高了约4倍。结果表明,分离腐殖质可提高渗滤液的可生化性。     

Interaction and combined toxicity of microplastics and per- and polyfluoroalkyl substances in aquatic environment

● Adsorption of PFASs on MPs and its mechanisms are critically reviewed. ● MPs could alter the transport and transformation of PFASs in aquatic environments. ● Combined toxicity of MPs and PFASs at organismal and molecular levels is discussed. Microplastics (MPs) are recognized as vectors for the transport of organic contaminants in aquatic environments in addition to their own adverse effects on aquatic organisms. Per- and polyfluoroalkyl substances (PFASs) are widely present in aquatic environments due to their widespread applications, and thus coexist with MPs. Therefore, we focus on the interaction of MPs and PFASs and related combined toxicity in aquatic environments in this work. The adsorption of PFASs on MPs is critically reviewed, and new mechanisms such as halogen bonding, π-π interaction, cation-π interactions, and micelle formation are proposed. Moreover, the effect of MPs on the transport and transformation of PFASs in aquatic environments is discussed. Based on four typical aquatic organisms (shellfish, Daphnia, algae, and fish), the toxicity of MPs and/or PFASs at the organismal or molecular levels is also evaluated and summarized. Finally, challenges and research perspectives are proposed, and the roles of the shapes and aging process of MPs on PFAS biogeochemical processes and toxicity, especially on PFAS substitutes, are recommended for further investigation. This review provides a better understanding of the interactions and toxic effects of coexisting MPs and PFASs in aquatic environments.     

挂膜方法对生物膜特性及生化尾水深度处理的影响

为探索低浓度生化尾水生物深度处理的快速挂膜方法,采用4种方法（投加壳聚糖法、投加铁离子法、接种排泥法和自然挂膜法）进行挂膜,考察其对生物膜主要特性（生物膜量MLSS、胞外聚合物（EPS））和废水处理效果的影响.结果表明：在挂膜期间,投加壳聚糖法有利于生物膜量、EPS迅速增加,两者平均含量达到4种方法中的最大值,分别为（9.26 ±3.30） mg/cm³和（42.51 ±33.49） mg/（gSS）,但其生物膜活性f值最低,污染物的去除效果不是最佳;投加铁离子成膜时,生物膜特性稳定,活性高,污染物去除效果最佳,COD_Cr、NH₄⁺-N、TP去除率分别较快稳定在（66.13 ±2.30）%、（92.03 ±7.72）%和（62.75 ±4.41）%;接种排泥法的生物膜量、EPS均含量、污染物去除效果比投加壳聚糖、铁离子法稍低;自然挂膜法前期对污染物去除率低,稳定时间较长,除TP外,COD_Cr、NH₄⁺-N去除率在挂膜后期与投加壳聚糖法、接种排泥法相差不大.综合地看,投加铁离子法,虽然生物膜量、EPS含量略低于投加壳聚糖法,但生物膜活性高、污染去除效果好,是低浓度尾水挂膜的最佳方法.     

Effects of alkalinity on interaction between EPS and hydroxy-aluminum with different speciation in wastewater sludge conditioning with aluminum based inorganic polymer flocculant

Extracellular polymeric substances (EPS) form a stable gel-like structure to combine with water molecules through steric hindrance, making the mechanical dewatering of wastewater sludge considerably difficult. Coagulation/flocculation has been widely applied in improving the sludge dewatering performance, while sludge properties (organic fraction and solution chemistry conditions) are highly changeable and have important effects on sludge flocculation process. In this work, the alkalinity effects on sludge conditioning with hydroxy-aluminum were comprehensively investigated, and the interaction mechanisms between EPS and hydroxy-aluminum with different speciation were unraveled. The results showed that the effectiveness of hydroxy-aluminum conditioning gradually deteriorated with increase in alkalinity. Meanwhile, the polymeric hydroxy-aluminum (Al₁₃) and highly polymerized hydroxy-aluminum (Al₃₀) were hydrolysed and converted into amorphous aluminum hydroxide (Al(OH)₃), which changed the flocculation mechanism from charge neutralization and complexing adsorption to hydrogen bond interaction. Additionally, both Al₁₃ and Al₃₀ showed higher binding capacity for proteins and polysaccharides in EPS than monomeric aluminum and Al(OH)₃. Al₁₃ and Al₃₀ coagulation changed the secondary structure of proteins in EPS, which caused a gelation reaction to increase molecular hydrophobicity of proteins and consequently sludge dewaterability. This study provided a guidance for optimizing the hydroxy-aluminum flocculation conditioning of sludge with high solution alkalinity.     

Photochemical alteration of the molecular weight of dissolved organic matter

Molecular weight (MW) is a key control on the physical, chemical, and biological characteristics of dissolved organic mater (DOM). This study investigated the effect of photooxidation on the average MW of DOM by exposing DOM of diverse origins to simulated solar radiation at varying levels of dissolved oxygen and under different incident light wavelength regimes. During irradiation, high-molecular-weight fractions were destroyed and low-molecular-weight constituents were formed. The average MW decreased with irradiation time in all treatments in a manner that can be described by a quasi-exponential function, which suggests that solar radiation is incapable of completely mineralizing DOM even after prolonged exposure. Increasing the oxygen concentration accelerated the MW reduction while the removal of oxygen strongly suppressed this process. The fractional contributions from UV-B, UV-A, and visible radiations to full-spectrum photoinduced MW reduction varied considerably among the DOM samples examined, ranging from 19% to 60%, 17% to 36%, and 15% to 46%, respectively. The MW changes in time-series irradiations were inversely correlated with the ratio of the absorbance at 250 nm to that at 365 nm (i.e., the E₂/E₃ quotient). Photoinduced MW reduction was accompanied by a decrease of polydispersity, which is indicative of a reduced DOM heterogeneity.     

The origin of stable halogenated compounds in volcanic gases

BACKGROUND: Halogenated compounds in the atmosphere are of great environmental concern due to their demonstrated negative effect on atmospheric chemistry and climate. Detailed knowledge of the emission budgets of halogenated compounds has to be gained to understand better their specific impact on ozone chemistry and the climate. Such data are also highly relevant to guide policy decisions in connexion with international agreements about protection of the ozone layer. In selected cases, the relevance of specific emission sources for certain compounds were unclear. In this study we present new and comprehensive evidence regarding the existence and relevance of a volcanic contribution of chlorofluorocarbons (CFCs), hydrofluorocarbons (HFCs), hydrochlorofluorocarbons (HCFCs), halons (bromine containing halo(hydro)carbons), and fully fluorinated compounds (e.g. CF4 and SF6) to the atmospheric budget. METHODS: In order to obtain new evidence of a volcanic origin of these compounds, we collected repeatedly, during four field campaigns covering a period of two years, gases from fumaroles discharging over a wide range of temperatures at the Nicaraguan subduction zone volcanoes Momotombo, Cerro Negro and Mombacho, and analysed them with very sensitive GC/MS systems. RESULTS AND DISCUSSION: In most fumarolic samples certain CFCs, HFCs, HCFCs, halons, and the fully fluorinated compounds CF4 and SF6 were present above detection limits. However, these compounds occur in the fumarole gases in relative proportions characteristic for ambient air. CONCLUSION: This atmospheric fingerprint can be explained by variable amounts of air entering the porous volcanic edifices and successively being incorporated into the fumarolic gas discharges. Recommendation and Outlook. Our results suggest that the investigated volcanoes do not constitute a significant natural source for CFCs, HFCs, HCFCs, halons, CF4, SF6 and NF3.     

丁烯氟虫腈光降解反应过程及机理

考察了乙腈/水混合溶液中丁烯氟虫腈的光解速率及水体中主要溶解性物质对其光解的影响,通过产物鉴定及模拟计算判定了丁烯氟虫腈光降解反应机理.结果表明,模拟日光下丁烯氟虫腈快速发生光降解,纯水中反应半衰期为17.34 min.腐殖酸通过竞争光吸收来抑制丁烯氟虫腈的光解,NO3-和Cl-对其光解无影响.丁烯氟虫腈光解反应位点位为亚砜基团上的硫原子,主要产物为脱硫化物(MW 442.0),砜化物(MW 506.0)及2种硫化物(MW 473.9和405.8).键级和键长分析也证实丁烯氟虫腈硫原子连接的化学键不稳定,易发生断裂重排反应,生成上述转化产物.