强化混凝去除黄浦江水有机物的试验研究

强化混凝去除有机物的效果与水源的分子量分布特性有着密切的关系.由于黄浦江水中低分子量的溶解性有机物占多数,因此,强化混凝处理有机物效果有限.对于＜1k分子量区间的有机物.增加混凝剂投量可有效去除紫外吸光值(UV254),但去除溶解性有机碳(DOC)的效果很差.尽管增加混凝剂投量和降低pH都能有效地去除有机物,但决定强化混凝效果的主要因素是pH,去除黄浦江水有机物的最佳pH范围为6～5.     

Interfacial effects of suspended particles on biodegradation of N (2,4 dimethyl phenyl) N'' methylformamidine hydrochloride and dibutyl phthalate in waters

ＩｎｔｅｒｆａｃｉａｌｅｆｅｃｔｓｏｆｓｕｓｐｅｎｄｅｄｐａｒｔｉｃｌｅｓｏｎｂｉｏｄｅｇｒａｄａｔｉｏｎｏｆＮ（２，４ｄｉｍｅｔｈｙｌｐｈｅｎｙｌ）Ｎ’ｍｅｔｈｙｌｆｏｒｍａｍｉｄｉｎｅｈｙｄｒｏｃｈｌｏｒｉｄｅａｎｄｄｉｂｕｔｙｌｐｈｔｈ...     

城市空气质量数值预报系统对PM2.5的数值模拟研究

发展了南京大学城市空气质量数值预报模式系统(NJU-CAQPS),在模式系统中引入了气溶胶模块.运用该系统对南京地区冬夏两季PM2.5浓度的时间变化规律和空间分布特征进行了数值模拟研究,通过与实际观测资料对比,检验发展后的模式系统对于细颗粒物的模拟性能.结果表明,南京市城近郊内冬夏两季PM2.5浓度具有明显的时空变化特征,一般在半夜和清晨会出现较高浓度,午后至傍晚浓度较低.冬季浓度高于夏季,冬夏两季算例的浓度日均值之比为1.51.空间分布受到排放源位置、地面流场等因素影响.二次气溶胶在PM2.5中占相当的份额,冬夏两季算例中二次气溶胶在PM2.5中所占比例分别为12%和15%,夏季二次气溶胶对PM2.5浓度贡献较冬季大.与实际观测资料的对比验证表明,经过发展的该模式系统对于城市PM2.5等颗粒物的模拟性能良好.     

典型北方高碱度微污染水体强化混凝的示范研究

以高碱度、受有机物污染的典型北方水体为例,探索适宜的强化混凝技术.在水质调查的基础上,提出适合水质特征的强化混凝目标.研究了高碱度水体强化混凝技术方法.研究表明,可以通过3条技术途径提高水体中有机物的去除效率.其一在混凝前优化pH,促进絮凝剂水解形成中聚体,AlCl3在pH 6左右,FeCl3在pH 5左右时,有机物去除率可以提高一倍左右;其二是强化沉淀软化;其三是絮凝剂优化.结合我国实际情况,通过对传统絮凝剂进行改性,研制出了适合我国北方水质特征的高效絮凝剂,能较传统絮凝剂将有机物去除率提高30%以上.     

南京北郊冬夏季大气PM2.5中水溶性有机碳的研究

为研究南京北郊大气PM_(2.5)中水溶性有机碳(WSOC)的浓度及来源特点,在冬、夏季分别采集PM_(2.5)样品,还同步收集臭氧(O_3)浓度与相对湿度(RH)数据,分析了PM_(2.5)、有机碳(OC)、水溶性有机碳(WSOC)浓度特征,并对WSOC冬、夏季来源及其二次来源差异进行了探讨.结果显示,南京北郊冬季大气污染水平明显高于夏季且来源更复杂,与冬季静稳的天气条件及化石燃料和生物质燃烧排放较严重有关.冬季PM_(2.5)平均值为(136.7±42.4)μg·m~(-3),OC、WSOC浓度分别为(13.4±4.4)、(8.5±3.1)μg·m~(-3);夏季PM_(2.5)、OC、WSOC平均浓度分别为(61.5±14.6)、(6.7±2.1)、(4.6±1.7)μg·m~(-3).冬、夏季WSOC/OC值分别为67%±20%、69%±13%,且二次有机碳(SOC)与WSOC显著正相关,说明二次来源对WSOC有显著影响.冬季WSOC与O_3的负相关性不显著,与RH显著正相关;而夏季WSOC与O_3、RH的相关性正好与冬季相反,说明冬、夏季二次WSOC形成途径存在差异.冬季二次WSOC可能主要来自液相氧化,夏季可能主要来自光化学氧化.通过主成分因子分析法进一步确定南京北郊冬、夏季WSOC分别主要来源于二次来源和生物质燃烧、汽车尾气和扬尘.     

Simultaneous determination of dissolved organic nitrogen, nitrite, nitrate and ammonia using size exclusion chromatography coupled with nitrogen detector

Accurate quantification of dissolved organic nitrogen (DON) has been a challenge due to the cumulative analytical errors in the conventional method via subtracting dissolved inorganic nitrogen species (DIN) from total dissolved nitrogen (TDN). Size exclusion chromatography coupled with an organic nitrogen detector (SEC-OND) has been developed as a direct method for quantification and characterization of DON. However, the applications of SEC-OND method still subject to poor separations between DON and DIN species and unsatisfied N recoveries of macromolecules. In this study, we packed a series of SEC columns with different lengths and resin materials for separation of different N species and designed an independent vacuum ultraviolet (VUV) oxidation device for complete oxidation converting N species to nitrate. To guarantee sufficient N recoveries, the operation conditions were optimized as oxidation time ≥ 30 min, injection mass (sample concentration × injection volume) < 1000 µL × mg-N/L for macromolecular proteins, and neutral pH mobile eluent. The dissolved O₂ concentration in SEC mobile phase determined the upper limit of VUV oxidation at a specific oxidation time. Compared to conventional HW50S column (20 × 250 mm), HW40S column (20 × 350 mm) with mobile phase comprising of 1.5 g/L Na₂HPO₄·2H₂O + 2.5 g/L KH₂PO₄ (pH = 6.85) could achieve a better separation of DON, nitrite, nitrate, and ammonia. When applied to river water, lake water, wastewater effluent, groundwater, and landfill leachate, the SEC-OND method could quantify DON as well as DIN species accurately and conveniently even the DIN/TDN ratio reached 0.98.     

Insights into reactive oxygen species formation induced by water-soluble organic compounds and transition metals using spectroscopic method

Ambient particulate matter (PM) can cause adverse health effects via their ability to produce Reactive Oxygen Species (ROS). Water-Soluble Organic Compounds (WSOCs), a complex mixture of organic compounds which usually coexist with Transition Metals (TMs) in PM, have been found to contribute to ROS formation. However, the interaction between WSOCs and TMs and its effect on ROS generation are still unknown. In this study, we examined the ROS concentrations of V, Zn, Suwannee River Fulvic Acid (SRFA), Suwannee River Humic Acid (SRHA) and the mixtures of V/Zn and SRFA/SRHA by using a cell-free 2′,7′-Dichlorodihydrofluorescein (DCFH) assay. The results showed that V or Zn synergistically promoted ROS generated by SRFA, but had an antagonistic effect on ROS generated by SRHA. Fluorescence quenching experiments indicated that V and Zn were more prone to form stable complexes with aromatic humic acid-like component (C1) and fulvic acid-like component (C3) in SRFA and SRHA. Results suggested that the underlying mechanism involving the fulvic acid-like component in SRFA more tending to complex with TMs to facilitate ROS generation through π electron transfer. Our work showed that the complexing ability and complexing stability of atmospheric PM organics with metals could significantly affect ROS generation. It is recommended that the research deploying multiple analytical methods to quantify the impact of PM components on public health and environment is needed in the future.     

呼和浩特市不同粒径空气颗粒物中汞的分布规律

采用分级采样装置 ,于冬夏两季采集呼市三个不同功能区不同粒径空气颗粒物中的汞进行分析 ,结果表明 :呼市空气颗粒物中的汞含量冬季明显高于夏季 ;冬季空气颗粒物中的汞含量为居民区 >交通区 >对照区 ,夏季为交通区 >居民区 >对照区 ;空气中汞主要富集在可吸入粒子中。     

光化学反应的环境效应

光化学反应具有良好的环境效应，本文概述了有机合成和环境化学中光化学反应对环境的影响。