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71.
72.
矿物超细颗粒在自然环境中普遍存在,具有独特的环境行为和效应,对元素地球化学循环、污染物迁移转化和生态环境演变等有重要影响.矿物超细颗粒的环境行为和效应与其形成过程和结构特征密切相关.综述了物理、化学和生物过程驱动的矿物超细颗粒的形成机制,介绍了用于表征矿物超细颗粒结构特征的显微镜、光谱、质谱和同步辐射技术,分析了矿物超细颗粒在环境中的迁移转化及其与污染物的吸附、氧化还原和催化转化作用,总结了矿物超细颗粒的食物链积累、生物和生态毒性等环境效应,并对颗粒结晶路径、风险管控和微纳界面调控等重要研究方向进行了展望.超细颗粒是连接微观物质与宏观矿物晶体之间的桥梁,全面认识复杂基质中矿物颗粒的环境属性及其与污染物的微观作用机制,有助于指导矿物超细颗粒在环境污染修复中的应用,从而优化功能材料的设计,促进绿色低碳纳米技术的发展. 相似文献
73.
Jun Hu Fengkui Duan Kebin He Yongliang Ma Shuping Dong Xiande Liu 《Frontiers of Environmental Science & Engineering》2016,10(5):12
Direct individual analysis using Scanning Electron Microscopy combined with online observation was conducted to examine the S-rich particles in PM2.5 of two typical polluted haze episodes in summer and winter from 2014 to 2015 in Beijing. Four major types of S-rich particles, including secondary CaSO4 particles (mainly observed in summer), S-rich mineral particles (SRM), S-rich water droplets (SRW) and (C, O, S)-rich particles (COS) were identified.We found the different typical morphologies and element distributions of S-rich particles and considered that (C, O, S)-rich particles had two major mixing states in different seasons. On the basis of the S-rich particles’ relative abundances, S concentrations and their relationships with PM2.5 as well as the seasonal comparison, we revealed that the S-participated formation degrees of SRM and SRW would enhance with increasing PM2.5 concentration. Moreover, C-rich matter and sulfate had seasonally different but significant impacts on the formation of COS.
相似文献
74.
基于PMF模式的南京市大气细颗粒物源解析 总被引:3,自引:0,他引:3
为研究南京市大气细颗粒物(PM2.5)污染来源,分别在3个点位、4个季节开展了PM2.5环境样品的采集,共获得170个有效样本.对样本进行了化学成分分析,包括Al、Fe、Na、Mg、K、Ba、Li、Tl、Mn、Co、Ni、Cu、Zn、Sb、Pb、Cr、Ce、Na+、NH4+、Mg2+、Ca2+、SO42-、NO3-、Cl-、以及OC、EC,共计26种.首先采用OC/EC最小比值法估算出二次有机气溶胶(SOA)的含量;然后利用正矩阵因子分解法(PMF)对PM2.5的非SOA部分进行来源解析,共解析出6类因子:二次无机气溶胶(SIA)、燃煤、机动车排放、地面扬尘、冶金和其它源,贡献率分别25.0%、23.5%、20.4%、17.1%、3.0%和11.0%;最后基于南京市SO2、NOx、VOCs三种主要前体污染物的排放量,分别对SIA和SOA在一次来源中进行再分配.最终结果表明,南京市PM2.5主要来源为燃煤、机动车、扬尘、工业和其它源,其贡献率分别为29.6%、22.4%、14.6%、18.7%和14.7%. 相似文献
75.
黄山大气气溶胶新粒子生长特性观测分析 总被引:1,自引:0,他引:1
利用2012年9月22日~10月28日黄山地区大气气溶胶、二氧化硫和臭氧观测数据,结合气象数据,分析气溶胶新粒子的生成-增长特征.分析发现,在33个有效观测日中,有新粒子生成-增长的观测日占总数的18.2%,其中晴天的发生频率为37.5%,新粒子生成-增长都开始于晴天上午,与无新粒子观测日相比,太阳辐射量、风速、SO2及O3浓度较高,环境温度和相对湿度较低.气溶胶新粒子的增长具有由小及大的特点,核模态气溶胶粒子(10~20nm)数浓度最先增加,爱根核模态粒子(20~50nm)数浓度随着时间推移逐渐增大,但浓度峰值依次下降,平均增长率为3.58nm/h. SO2浓度先于核模态气溶胶数浓度到达峰值,其氧化后的产物H2SO4为新粒子的核化提供前体物,并且参与新粒子的增长过程,当SO2浓度较低时,不会发生新粒子生长事件. 相似文献
76.
Yanlai HAN Michael D. Y. YANG Weixian ZHANG Weile YAN 《Frontiers of Environmental Science & Engineering》2015,9(5):813
Nanoscale iron particles (nZVI) is one of the most important engineered nanomaterials applied to environmental pollution control and abatement. Although a multitude of synthesis approaches have been proposed, a facile method to screen the reactivity of candidate nZVI materials produced using different methods or under varying synthesis conditions has yet been established. In this study, four reaction parameters were adjusted in the preparation of borohydride-reduced nZVI. The reductive properties of the resultant nanoparticles were assayed independently using two model aqueous contaminants, Cu(II) and nitrate. The results confirm that the reductive reactivity of nZVI is most sensitive to the initial concentration of iron precursor, borohydride feed rate, and the loading ratio of borohydride to ferric ion during particle synthesis. Solution mixing speed, in contrast, carries a relative small weight on the reactivity of nZVI. The two probing reactions (i.e., Cu(II) and nitrate reduction) are able to generate consistent and quantitative inference about the mass-normalized surface activity of nZVI. However, the nitrate assay is valid in dilute aqueous solutions only (50 mg·L−1 or lower) due to accelerated deactivation of iron surface at elevated nitrate concentrations. Additional insights including the structural and chemical makeup of nZVI can be garnered from Cu(II) reduction assessments. The reactivity assays investigated in this study can facilitate screening of candidate materials or optimization of nZVI production parameters, which complement some of the more sophisticated but less chemically specific material characterization methods used in the nZVI research. 相似文献
77.
为利用蒸汽相变原理促进氨法脱硫系统排放细颗粒物(PM2.5)的脱除,建立多分散颗粒的凝结增长动力学模型,利用数值模拟方法研究了可溶硫酸铵颗粒的凝结增长规律,并将典型粒径可溶与不可溶颗粒的凝结增长过程进行对比分析.结果表明:不同粒径硫酸铵颗粒的增长速率相近,等温系统的凝结增长效果优于绝热系统;对于同一初始粒径分布下的可溶和不可溶颗粒,微米尺度可溶颗粒的增长速率始终大于不可溶颗粒,亚微米尺度可溶颗粒的增长速率先大于而后小于不可溶颗粒,使得二者的增长曲线存在一个交叉点;蒸汽饱和度增大能显著促进硫酸铵颗粒的增长;等温系统中温度对硫酸铵颗粒的增长影响显著,绝热系统中温度的影响较弱. 相似文献
78.
Aiming to investigate the impacts of n-octanol addition on the oxidation reactivity, morphology and graphitization of diesel exhaust particles, soot samples were collected from a four-cylinder turbocharged diesel engine fueled with D100(neat diesel fuel), DO15(85% diesel and 15% n-octanol, V/V) and DO30(70% diesel and 30% n-octanol, V/V). All tests were conducted at two engine speeds of 1370 and 2150 r/min under a fixed torque of 125 N ·m. The soot properties were characterized by thermogravimet... 相似文献
79.
大气颗粒物吸湿性研究 总被引:6,自引:2,他引:4
大气颗粒物吸湿性是反映颗粒物理化性质的重要指标,吸湿性研究对深入了解颗粒物的环境和健康效应具有重要意义. 总结了国外近年来大气颗粒物吸湿性研究进展:①典型的大气颗粒物吸湿性分析方法为H-TDMA(吸湿性串联差分电迁移率粒径分析仪)系统及其优化方法. ②大气颗粒物吸湿性呈单峰、双峰甚至多峰分布;根据Gf(吸湿性生长因子)随粒径变化的模式,可将大气颗粒物分为强吸湿性和弱吸湿性2类,也可分为纯不溶性、混合不溶性、混合可溶性和纯可溶性4类. ③城市背景点颗粒物的Gf比城市观测点高;城市观测点的颗粒物Gf分布呈夏季高、冬季低,白天高、晚上低的特征. ④颗粒物吸湿性与其化学组成和形态密切相关,纯可溶性盐颗粒物的Gf通常较高. ⑤柴油燃烧源新排放的颗粒物属于弱吸湿性颗粒物,Gf非常小,但在其表面老化后或随燃料中硫含量的增加Gf会明显变大. ⑥生物质燃烧排放颗粒物的Gf相对较高,但存在区域差异性. 针对国内大气颗粒物吸湿性研究现状,提出了未来重点研究方向. 相似文献
80.
J. S. Bonner A. N. Ernest D. S. Hernandez R. L. Autenrieth 《Chemistry and Ecology》2013,29(1-4):139-159
Abstract Sewage sludge from four publicly-owned treatment works was sampled and characterized in terms of parameters affecting transport at the 106-mile deep ocean disposal site as part of the US Environmental Protection Agency's site monitoring programme. Samples from treatment plants in Passaic Valley, Rahway, and Elizabeth, New Jersey and New York City were characterized in terms of dynamic size distribution, suspended solids and density. the transport characteristics of sludge particles were measured using a 2 metre computer-interfaced laboratory settling column. Experiments were conducted at constant salinity (35 ppt) while varying hydrodynamic mixing, sludge type and concentration using a modified factorial experimental design. Hydrodynamic power dissipation was varied so that the vertical dispersion and rms fluid shear rate ranged between 0-6 cm2S?1 and 0-30s?1 respectively. Results indicate that at least 80% of suspended sludge particles will eventually settle under mixed conditions. the average settling velocities ranged between 0.05-4.05 × 10-3 cm s-1. Shear rates above 15 s?1 inhibited sludge settling due to aggregate breakup and boundary effects, but at a lower shear rate, differential settling and fluid shear were the dominant transport mechanisms. Sludge dilution (1/500-1/5000) had a limited effect on the settling rate. Results from this study can be used to calibrate particle transport models to determine the fate of sludge disposed at an ocean disposal site. 相似文献