北方湖库沉积物重金属区域特征及生态风险评价

以白洋淀、衡水湖、于桥水库、松花湖、大伙房水库和小兴凯湖沉积作为研究对象,通过对北方六湖库沉积物中Cu、Zn、Pb、Cr、Ni等重金属元素进行分析,并与国内外其他水域重金属污染情况进行多因素比较,探讨了六湖库主要重金属污染源的差异性,区域分布特征以及与国内外其他水域污染的相似性和区别.结果表明,六湖库沉积物重金属污染处于中等偏下水平.六湖库之间主要重金属污染源存在差别.沉积物重金属含量未出现明显上升的趋势.其中Zn、Pb存在富集现象,但Pb含量与历史数据相比出现下降,Zn的含量与其他地区相比整体偏高.大伙房水库沉积物重金属污染较重,Cu、Zn、Pb、Cr、Ni含量平均值分别为56.28,142.3,17.44,97.9,44.44mg/kg.小兴凯湖沉积物重金属含量最低,Cu、Zn、Pb、Cr、Ni含量平均值分别为2.41,63.90,13.37,56.36,26.09mg/kg.六湖库综合风险评价结果为大伙房水库>于桥水库>白洋淀>衡水湖>松花湖>小兴凯湖,重金属整体潜在生态风险指数为低.     

2018年春节期间京津冀地区污染过程分析

为了解2018年春节期间京津冀地区空气污染情况,利用近地面污染物浓度数据、激光雷达组网观测数据,结合WRF气象要素、颗粒物输送通量和HYSPLIT气团轨迹综合分析污染过程.结果表明,春节期间出现3次污染过程.春节前一次污染过程,各站点PM_2.5浓度均未超过200μg/m³;除夕夜,廊坊站点PM_2.5峰值浓度达到504μg/m³,是清洁天气的26倍;年初二~初五,各站点PM_2.5始终高于120μg/m³,且污染主要聚集在500m高度以下,北京地区存在高空传输,800m处最大输送通量达939μg/（m³·s）,此次重污染过程为一次典型的区域累积和传输过程.京津冀地区处于严格管控状态时,燃放烟花爆竹期间PM_2.5峰值浓度可达无燃放时PM_2.5峰值的3.2倍.为防止春节期间重污染现象的发生,需对静稳天气下燃放烟花炮竹采取预防对策.     

Revealing the changes of bacterial community from water source to consumers tap: A full-scale investigation in eastern city of China

This study profiled the bacterial community variations of water from four water treatment systems, including coagulation, sedimentation, sand filtration, ozonation-biological activated carbon filtration (O₃-BAC), disinfection, and the tap water after the distribution process in eastern China. The results showed that different water treatment processes affected the bacterial community structure in different ways. The traditional treatment processes, including coagulation, sedimentation and sand filtration, reduced the total bacterial count, while they had little effect on the bacterial community structure in the treated water (before disinfection). Compared to the traditional treatment process, O₃-BAC reduced the relative abundance of Sphingomonas in the finished water. In addition, ozonation may play a role in reducing the relative abundance of Mycobacterium. NaClO and ClO₂ had different effects on the bacterial community in the finished water. The relative abundance of some bacteria (e.g. Flavobacterium, Phreatobacter and Porphyrobacter) increased in the finished water after ClO₂ disinfection. The relative abundance of Mycobacterium and Legionella, which have been widely reported as waterborne opportunistic pathogens, increased after NaClO disinfection. In addition, some microorganisms proliferated and grew in the distribution system, which could lead to turbidity increases in the tap water. Compared to those in the finished water, the relative abundance of Sphingomonas, Hyphomicrobium, Phreatobacter, Rheinheimera, Pseudomonas and Acinetobacter increased in the tap water disinfected with NaClO, while the relative abundance of Mycobacterium increased in the tap water disinfected with ClO₂. Overall, this study provided the detailed variation in the bacterial community in the drinking water system.     

Density functional theory (DFT) studies of vanadium-titanium based selective catalytic reduction (SCR) catalysts

Based on density functional theory (DFT) and basic structure models, the chemical reactions on the surface of vanadium-titanium based selective catalytic reduction (SCR) denitrification catalysts were summarized. Reasonable structural models (non-periodic and periodic structural models) are the basis of density functional calculations. A periodic structure model was more appropriate to represent the catalyst surface, and its theoretical calculation results were more comparable with the experimental results than a non-periodic model. It is generally believed that the SCR mechanism where NH₃ and NO react to produce N₂ and H₂O follows an Eley-Rideal type mechanism. NH₂NO was found to be an important intermediate in the SCR reaction, with multiple production routes. Simultaneously, the effects of H₂O, SO₂ and metal on SCR catalysts were also summarized.     

Recent advances in catalytic decomposition of ozone

Ozone (O₃), as a harmful air pollutant, has been of wide concern. Safe, efficient, and economical O₃ removal methods urgently need to be developed. Catalytic decomposition is the most promising method for O₃ removal, especially at room temperature or even subzero temperatures. Great efforts have been made to develop high-efficiency catalysts for O₃ decomposition that can operate at low temperatures, high space velocity and high humidity. First, this review describes the general reaction mechanism of O₃ decomposition on noble metal and transition metal oxide catalysts. Then, progress on the O₃ decomposition performance of various catalysts in the past 30 years is summarized in detail. The main focus is the O₃ decomposition performance of manganese oxides, which are divided into supported manganese oxides and non-supported manganese oxides. Methods to improve the activity, stability, and humidity resistance of manganese oxide catalysts for O₃ decomposition are also summarized. The deactivation mechanisms of manganese oxides under dry and humid conditions are discussed. The O₃ decomposition performance of monolithic catalysts is also summarized from the perspective of industrial applications. Finally, the future development directions and prospects of O₃ catalytic decomposition technology are put forward.     

Effect of struvite and organic acids on immobilization of copper and zinc in contaminated bio-retention filter media

Few studies have been carried out to connect nutrient recovery as struvite from wastewater and sustainable utilization of the recovered struvite for copper and zinc immobilization in contaminated soil. This study revealed the effect of struvite on Cu and Zn immobilization in contaminated bio-retention soil in the presence of commonly exuded plant organic acids. The research hypothesis was that the presence of both struvite and organic acids may influence the immobilization of Cu and Zn in soil. The outcome of this research confirmed that more than 99% of Cu and Zn was immobilized in bio-retention filter media by struvite application. Water-soluble Cu and Zn concentrations of struvite treated soil were less than 1.83 and 0.86 mg/kg respectively, and these concentrations were significantly lower compared to the total Cu and Zn content of 747.05 mg/kg in the contaminated soil. Application of struvite to Cu- and Zn-contaminated soil resulted in formation of compounds similar to zinc phosphate tetrahydrate (Zn₃(PO₄)₂?4H₂O) and amorphous Cu and Zn phases. Struvite was effective in heavy metal remediation in acidic soil regardless of the presence of Ca impurities in struvite and the presence of plant organic acids in soil. Overall, this study revealed that struvite recovered from wastewater treatment plants has potential for use as an amendment for heavy metal remediation in contaminated bio-retention soil.     

基于边介数的省域生态廊道构建方法优化

我国城市建设和生态保护工作均对土地资源有大量需求,二者之间的矛盾在经济优先发展区表现尤为明显.为了有效地改善生态环境,管控土地利用并引导其变化发展,需要建设具备不可替代特征的省域生态廊道.最小累积阻力模型（minimum cumulative resistance,MCR）是识别生态廊道最常用、有效的模型,但在应用于省域尺度时,MCR模型识别的潜在廊道路由存在冗余的问题.因此,通过引入网络科学中的边介数指数（edge-betweenness）对MCR模型进行优化,计算潜在廊道路由的边介数指数值,选取出其中最为重要和简明的结构来连通生态源地,即提取潜在路由中的骨干路由（backbone route）和关键战略点（key strategic point）作为不可替代的结构来指导省域生态廊道建设.将优化后的MCR模型应用于广东省,构建了全长5 493 km的省域生态廊道,其中包含生态源地20处,关键战略点11个,骨干生态廊道29条.骨干路由与关键战略点构成的不可替代省域生态廊道（irreplaceable provincial corridor）能够实现"廊道数量和占地面积最少、连通性基本不变"的目标.研究显示,边介数能够对潜在路由进行优化筛选,识别出维护省域生态安全的关键结构;不可替代生态廊道能够指导省域生态规划和土地空间的发展利用,并为更高水平的生态安全环境提供了演进的基础;同时也为土地资源紧张的地区提供了建设生态廊道的参考与依据.      

Chemical characteristics of road dust PM2.5 fraction in oasis cities at the margin of Tarim Basin

In order to understand the compositions characteristics of particulate matter with aerodynamic diameter less than 2.5 μm (PM_2.5) fraction in road dust (RD_2.5) of oasis cities on the edge of Tarim Basin, 30 road dust (RD) samples were collected in Kashi, Cele, and Yutian in the spring, 2018, and RD_2.5 was collected using the resuspension approach. Eight water-soluble ions, 39 trace elements and 8 fractions of carbon-containing species in PM_2.5 were analyzed. Ca²⁺ and Ca were the most abundant ions and elements in RD_2.5 (7.1% and 9.5%). Cl^- in RD_2.5 was affected not only by attributed to saline-alkali soils in oasis cities of the Tarim Basin and dust from Taklimakan Desert but also by human activities. Moreover, the organic carbon/elemental carbon (OC/EC) ratio indicated that carbon components in RD_2.5 in Cele town mainly come from fossil fuel combustion, while those in Yutian and Kashi mainly come from biomass combustion. It is noteworthy that high Ca in RD_2.5 was seriously affected by anthropogenic emissions, and high Na and K contents in RD_2.5 could be derived from soil and desert dust. It was estimated that Cd, Tl, Sn and Cr were emitted from anthropogenic emissions using the enrichment factor. The coefficients of divergence (COD) result indicated that the influence of local emission on road dust emission is greater than that of long-distance transmission. This study is the first time to comprehensively analyze the chemical characteristics of road dust in oasis cities, and the results provides the sources of road dust at the margin of Tarim Basin.     

外加氮源影响下铁铝氧化物在土壤氮素转化中的作用

土壤中铁铝氧化物在团聚体稳定性和有机碳吸附方面具有重要作用,而氮添加对土壤氮循环影响的变化也可能与其有关,但是目前尚缺乏在氮循环方面的研究.为了探究铁铝氧化物在土壤氮素转化中的作用,选择福建省建瓯罗浮栲森林土壤为研究对象,采用选择性溶提技术准备不同的土壤——未经处理（T1）的土壤和去除游离态铁铝氧化物（T2）土壤、去除非晶质铁铝氧化物（T3）土壤、去除络合态铁铝氧化物（T4）土壤,在这些土壤中添加不同形态氮（40 mg/kg）——丙氨酸（氨基酸态氮,AA）、硫酸铵（铵态氮,AN）、硝酸钠（硝态氮,NAN）和亚硝酸钠（亚硝态氮,NIN）,进行室内培养试验,分析氮含量变化和氮素转化情况.结果表明:①与CK处理相比,AA和AN处理均增加了T1土壤中w（NH₄+-N）,NAN处理增加了w（NO₃--N）,但低于添加量,表明添加氨基酸和铵态氮均会促进氮矿化,添加硝态氮会增加NO₃--N的固定且抑制其硝化.②在CK处理下,与T1土壤相比,T2和T4土壤中w（NH₄+-N）、w（NO₃--N）和w（氨基酸）均降低,但T3土壤中w（NH₄+-N）和w（氨基酸）增加、w（NO₃--N）降低,表明土壤中游离态氧化铁铝和络合态氧化铁铝的存在有助于氮素矿化,非晶质氧化铁铝有助于硝化.③在不同氮处理下,各土壤的氮含量及其转化速率与CK处理规律相似.与CK处理相比,各氮处理均未显著增加T2和T4土壤中w（NH₄+-N）,且AA和AN处理均未影响T2、T3和T4土壤中w（NO₃--N）和w（氨基酸）.结果显示,氮添加并没有改变铁铝氧化物的作用,其中,矿化和氨化作用均表现为游离氧化铁铝>络合氧化铁铝>非晶质氧化铁铝,硝化作用表现为非晶质氧化铁铝>游离氧化铁铝>络合态氧化铁铝.因此,土壤铁铝氧化物的不同存在状态应该是调节氮素转化的重要土壤条件.      

国内外饮用水余氯限值及监测方法的研究进展

新型冠状病毒肺炎疫情期间大规模使用含氯消毒剂,其残留可能对水环境及人体健康造成影响.我国饮用水水源地质量标准并未设置余氯项目及其浓度限值,且缺乏统一的余氯现场快速分析方法标准.为公共卫生事件发生期间的水质余氯监测与评价提供参考,对国内外饮用水标准余氯限值、实验室标准分析方法、现场快速分析方法等进行汇总分析,结果表明:①不同国家和地区以及WHO（World Health Organization,世界卫生组织）在饮用水标准中分别设置了出厂水中余氯限值（范围为0.1~2.0 mg/L）、管网末梢水中余氯限值（范围为0.1~1.8 mg/L）及饮用水中余氯最大允许浓度（范围为4~5 mg/L）.②比色法、容量法因其具有反应迅速且稳定、准确度及精密度较高等优点而成为国内外实验室主要标准或推荐分析方法,高效液相色谱法检出限最低,灵敏度最高,可用于余氯痕量分析.③余氯现场快速分析方法多以比色法为主,在线监测方法多为电化学方法,但缺乏统一的标准方法.研究显示,国外饮用水标准中余氯最大允许浓度为5 mg/L,WHO推荐高风险环境下的管网末梢余氯浓度最低为0.5 mg/L,建议尽快开展水质余氯现场监测方法标准化研究.