双侧海潮作用下海岛含水层系统中地下水位波动研究

考察了海岛地区的一个横断面,在双侧海潮及弱透水层引起的越流共同作用下,含水层系统中的地下水位波动;建立了数学模型,并得到了该模型的解析解;定义了含水层长度的阈值,对含水层长度及越流等因素对地下水位波动的影响进行了讨论.     

基于ETM+图像的植被覆盖度遥感估算模型

植被覆盖度(VFC)的定量遥感是多种地表过程研究的迫切需要.文章选用南京市一幅Landsat 7 ETM 图像,经大气校正后提取了归一化植被指数(NDVI),与地面实测的植被覆盖度进行回归分析,建立了1～4次多项式关系模型.结果表明,NDVI与VFC呈极显著的正相关关系(r = 0.874, P < 0.001).在NDVI-VFC的1～4次多项式关系模型中,模型幂次越高,拟合程度越好.综合考虑模型的精度和稳定性,3次多项式模型作为最优模型推荐使用:VFC = -1.3438 NDVI 3 0.9774 NDVI 2 0.9988 NDVI 0.1507 (R2 = 0.7961, RMSE = 0.1094),该模型精度在植被中等密集区域(VFC＝0.4～0.8)最高,植被稀疏区域(VFC < 0.4)最低,植被密集区域(VFC > 0.8)居中.模型可直接用于全图像的VFC计算,并可通过植被指数的校准,进行推广使用.     

用核子微探针进行单个大气颗粒物的分析

本文对单个大气颗粒物进行了分析研究，用核子微探针对首钢地区单个大气颗粒物进行了扫描分析，用三维等高线法给出了各种元素在一群单个大气颗粒物中的二维分布。从一群单个大气颗粒物中各元素的二维分布可对首钢地区大气污染的特征及来源进行分析研究。     

同步辐射X射线荧光和吸收谱技术在环境汞污染研究中的应用进展

汞作为一种重要的全球性重金属污染物,被许多国际组织列为优先控制污染物。常规的汞分析手段,例如电感耦合等离子体质谱(ICP-MS)、原子荧光光谱(AFS)等,对汞的分析精度较高,方法比较成熟,但对样品前处理要求也较高。同步辐射技术由于其高、精、准的优势,且对样品前处理要求比较简单、可实现原位无损分析,因此被广泛应用于环境样品的分析中。随着研究的发展,同步辐射X射线荧光光谱(SRXRF)和同步辐射X射线吸收光谱(SRXAS)技术在环境汞污染分析领域得到了越来越多的应用。主要介绍了我国环境汞污染现状及污染特征,同步辐射技术对于汞分布蓄积、含量和化学形态分析方面的独特优势,重点回顾了本项目组和其他一些研究组近几年关于SRXRF和SRXAS技术在环境介质如土壤、植物体内汞的分布蓄积、相对含量和化学形态转化研究领域的应用进展,对进一步发展并提高同步辐射技术在环境及生物体汞污染水平、毒性机理和生态毒理评价方面的应用进行了展望。     

土地处理技术在干旱-半干旱过渡带生态建设中的应用

土地处理系统是在干旱 -半干旱过渡区实现污水无害化、资源化的有效技术。内蒙古霍林河矿区污水土地处理系统设计与运行结果表明 ,该区具备推广土地处理技术的良好条件 ,土地处理系统应以慢速渗滤和污水资源利用型为主 ,实现污水处理与生态环境建设的结合。污水资源的利用有助于增加镶嵌型复合生态系统的稳定性 ,加速人工林的成林郁闭 ,增加林木蓄积量 ,改善干旱、半干旱地区的生态环境     

生物与化学表面活性剂对多氯联苯的协同增溶作用

采用室内序批试验比较研究了单一的生物/非离子化学表面活性剂(SAA)与生物-非离子混合表面活性剂对商业用多氯联苯(PCBs)Aroclor1242的增溶作用.结果表明,生物表面活性剂鼠李糖脂(RL)对Aroclor1242的增溶作用要高于三种非离子SAA,三种非离子SAA对Aroclor1242的增溶作用顺序为POE(6)＞POE(10)＞Brij35,与其亲水亲油平衡值(HLB)呈负相关;鼠李糖脂与非离子SAA对Aroclor1242的增溶存在协同效应,混合表面活性剂溶液中Aroclor1242的摩尔增溶比(MSR)、胶束相/水相间的分配系数(Kmc)均大于对应的单一表面活性剂,其协同增溶作用顺序为RL-Brij35＞RL-POE(10)＞RL-POE(6),协同增溶作用的大小与其中的非离子表面活性剂的HLB值呈正相关.     

石英砂负载氧化铁吸附除磷的热动力学研究

通过吸附动力学实验及等温吸附实验,考察了在10～40℃的温度条件下石英砂负载氧化铁(IOCS)吸附磷的热动力学性质.结果表明:准二级反应动力学模型及Langmuir等温吸附模型可分别较好地描述IOCS对磷的吸附动力学及吸附等温线实验结果(R2≥0.98);吸附速率及吸附容量随温度的增加而增加.吸附速率k从0.0095增加到0.0173,吸附容量从0.06 mg/g增加到0.08 mg/g.根据标准吉布斯自由能变(△G0＜0)和标准反应焓变(△H0＞0)值判断,IOCS对磷的吸附是自发的、吸热的化学吸附反应.     

Discovery of emerging organic pollutants in the atmosphere through an omics approach

● We review the framework of discovering emerging pollutants through an omics approach. ● High-resolution MS can digitalize atmospheric samples to full-component data. ● Chemical features and databases can help to translate untargeted data to compounds. ● Biological effect-directed untargeted analyses consider both existence and toxicity. Ambient air pollution, containing numerous known and hitherto unknown compounds, is a major risk factor for public health. The discovery of harmful components is the prerequisite for pollution control; however, this raises a great challenge on recognizing previously unknown species. Here we systematically review the analytical techniques on air pollution in the framework of an omics approach, with a brief introduction on sample preparation and analysis, and in more detail, compounds prioritization and identification. Through high-resolution mass spectrometry (HRMS, typically coupled with chromatography), the complicated environmental matrix can be digitalized into “full-component” data. A key step to discover emerging compounds is the prioritization of compounds from massive data. Chemical fingerprints, suspect lists and biological effects are the most vital untargeted strategies for comprehensively screening critical and hazardous substances. Afterward, compressed data of compounds can be identified at various confidence levels according to exact mass and the derived molecular formula, MS libraries, and authentic standards. Such an omics approach on full-component data provides a paradigm for discovering emerging air pollutants; nonetheless, new technological advancements of instruments and databases are warranted for further tracking the environmental behaviors, hence to evaluate the health risk of key pollutants.     

改性氧化铝微波诱导催化氧化处理高浓度苯酚废水的研究

采用微波诱导催化氧化技术,以改性氧化铝为催化剂,对高浓度模拟苯酚废水进行氧化处理。考察了微波功率、催化剂投加量、H202投加量、废水pH值和微波反应时间等因素对苯酚去除效果的影响。实验结果表明,处理30mL质量浓度为1 100mg/L的苯酚模拟废水,在微波功率500W,催化剂加入量1 g(液固比30∶1),30％双氧水...     

Perfluorinated compounds in the Pearl River and Yangtze River of China

A total of 14 perfluorinated compounds (PFCs) were quantified in river water samples collected from tributaries of the Pearl River (Guangzhou Province, south China) and the Yangtze River (central China). Among the PFCs analyzed, perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) were the two compounds with the highest concentrations. PFOS concentrations ranged from 0.90 to 99 ng/l and <0.01–14 ng/l in samples from the Pearl River and Yangtze River, respectively; whereas those for PFOA ranged from 0.85 to 13 ng/l and 2.0–260 ng/l. Lower concentrations were measured for perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), perfluorooctanesulfoamide (PFOSA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorononaoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA). Concentrations of several perfluorocarboxylic acids, including perfluorododecanoic acid (PFDoDA), perfluorotetradecanoic acid (PFTeDA), perfluorohexadecanoic acid (PFHxDA) and perfluorooctadecanoic acid (PFOcDA) were lower than the limits of quantification in all the samples analyzed. The highest concentrations of most PFCs were observed in water samples from the Yangtze River near Shanghai, the major industrial and financial centre in China. In addition, sampling locations in the lower reaches of the Yangtze River with a reduced flow rate might serve as a final sink for contaminants from the upstream river runoffs. Generally, PFOS was the dominant PFC found in samples from the Pearl River, while PFOA was the predominant PFC in water from the Yangtze River. Specifically, a considerable amount of PFBS (22.9–26.1% of total PFC analyzed) was measured in water collected near Nanjing, which indicates the presence of potential sources of PFBS in this part of China. Completely different PFC composition profiles were observed for samples from the Pearl River and the Yangtze River. This indicates the presence of dissimilar sources in these two regions.