我国24个典型饮用水源地中14种酚类化合物浓度分布特征

研究了14种酚类化合物在我国五大流域(黄河、海河、辽河、长江、淮河)24个典型饮用水源地水源水中的浓度水平.结果显示:14种酚类化合物在我国饮用水源地中的浓度在nd～213 ng·L-1范围内,浓度均值在2.44～31.2 ng·L-1范围内,浓度中位数在nd～40.0 ng·L-1范围内.14种酚类化合物中,硝基苯酚类化合物浓度最高,浓度中位数为37.9 ng·L-1,浓度平均值为27.4 ng·L-1.其次为苯酚、五氯酚、二氯苯酚(2,4-二氯苯酚和2,6-二氯苯酚)和三氯苯酚(2,4,6-三氯苯酚和2,4,5-三氯苯酚);四氯苯酚(2,3,5,6-四氯苯酚、2,3,4,6-四氯苯酚、2,3,4,5-四氯苯酚)和烷基苯酚(邻甲基苯酚、间甲基苯酚和对甲基苯酚)浓度较低.通过商值法对14种酚类化合物进行生态风险评价后发现,14种酚类化合物的风险商均远小于1,表明其对我国饮用水源地的生态风险较低.对8种已报道健康参考剂量或致癌斜率因子的酚类化合物进行健康风险评价,结果显示,7种酚类化合物的最大非致癌风险在10-6到10-4范围内,2,4,6-三氯酚和五氯酚的致癌风险在10-6量级以下,表明其健康危害较弱.     

淠河灌区集中式饮用水源地水质健康风险等级研究

为了解淠河灌区集中式饮用水源地水质健康风险状况,选取Cr6+、As、Cd、Pb、Mn、Cu、Zn、Fe、F、NH+4-N等10项污染因子作为健康风险指标,运用三角模糊集理论和α-截集技术,确立置信度为0.8,得到各污染指标的健康风险区间值;同时建立模糊化特征的风险等级判别标准和判别方法.结果表明,该水源地水质总健康风险值为4,风险等级为Ⅳ级(一般).3种化学致癌物Cr6+、As、Cd合计风险区间值介于5.586×10-5~9.365×10-5之间,风险由高到低的顺序依次为:Cr6+AsCd,浓度在空间上变化不大,具有一定的负面效应,但均未超过美国环保署推荐的最大可接受水平1.0×10-4;Cr6+风险区间值较大,风险等级较高,应将Cr6+作为首要的健康风险管理控制指标.其余7种非致癌化学有毒物没有风险,不存在负面效应,非致癌健康风险明显低于致癌风险.     

硫黄联合装置停工密闭吹扫的实现

介绍了中国石化济南分公司硫黄回收联合装置安全环保停工的过程,在硫黄回收联合装置停工前,研究讨论各装置停工密闭吹扫的流程及方法,并确定各装置停工吹扫的顺序、注意事项和前期准备工作。在各装置停工吹扫过程中,严格按照停工方案,采取了分装置吹扫,该装置吹扫完毕后立即加盲板隔离,最后放火炬公用系统采取倒吹扫,实现了装置停工密闭吹扫,达到了各装置停工酸性气系统吹扫不放火炬的要求。     

浅析硫黄生产过程中的风险与对策

分析了硫黄生产过程的危险性,并针对生产过程中高压、有毒、易燃易爆、腐蚀的特点,提出了预防措施。     

呼和浩特城区冬季近地面挥发性有机物污染特征初步研究

挥发性有机物(VOCs)是环境空气监测的主要目标污染物。本文运用罐采样-三级冷阱预浓缩-中心切割-气相色谱(FID)/气质联用法对人群主要活动的近地面不同高度、不同时间段及不同区域的呼和浩特冬季大气环境中挥发性有机物进行定性定量分析。发现典型天气情况下,呼和浩特城区冬季近地面挥发性有机物组分中烷烃和芳香烃占比较高,城区西侧所监测点位挥发性有机物总量(TVOCs)浓度高于其他区域,且其浓度在高度和时段上存在明显差异。     

高效液相色谱-三重四级杆/复合线性离子阱质谱法测定饮用水中22种邻苯二甲酸酯

建立了一种同时测定饮用水中22种邻苯二甲酸酯(PAEs)的高效液相色谱-三重四级杆/复合线性离子阱质谱方法:饮用水样品经针头过滤器过滤,选用Biphenyl液相色谱柱进行分离,以含0.1%甲酸的水溶液和含0.1%甲酸的甲醇溶液为流动相,电离模式为电喷雾正离子,选用多反应监测触发增强子离子扫描模式进行检测。结果表明,22种PAEs的灵敏度良好,定量限为0.001～0.1 μg/L。配制浓度为0.1～100.0 μg/L的混标溶液进行进样分析,分析结果显示,22种PAEs在该范围内的线性关系良好,相关系数均大于0.995,方法的平均回收率为82.9%～108.9%,相对标准偏差为0.9%～11.2%。同时,使用增强子离子扫描谱图进行搜库匹配,定性准确性高。该方法适用于饮用水中PAEs的检测。     

饮用水源微生物快速检测技术的发展及应用

微生物是威胁饮用水安全的首要问题,水环境微生物快速检测技术的开发和应用是推动饮用水源微生物快速检测和水质安全预警技术发展的保障。随着对水质微生物污染快速检测和准确预警新要求的提出,水环境中微生物在线检测和预警技术得到了越来越多的开发和应用。笔者总结了水环境常见微生物检测方法和技术的发展,重点讨论了饮用水源微生物快速检测技术的发展和应用,根据各项技术的应用和推广使用程度,将其归纳为常用快速检测技术、潜在适用快速检测技术和新型快速检测技术等类别,并详细阐述了一些应用较广的技术,以期为构建水质微生物污染早期预警系统提供参考。     

Qualidex – A New Software for Generating Water Quality Indice

Water quality indice are necessary for resolving lengthy, multi-parameter, water analysis reports into single digit scores. This, in turn, is essential for comparing the water quality of different sources and in monitoring the changes in the water quality of a given source as a function of time and other influencing factors.In this paper we present the computer-automated tool QUALIDEX (water QUALIty inDEX), which has been developed by us to generate and operate water quality indice. Several popular indice – such as the Oregon Water Quality Index developed in the 1970s by Oregon Department of Environmental Quality and later updated in 1995, the Aquatic Toxicity Index developed by Wepener and coworkers for protection of aquatic life at the Olifants river, Kruger National Park, South Africa, the water quality index developed by Dinius in 1987, the Overall Index of Pollution (of surface waters) developed at the National Environmental Engineering Research Institute (NEERI), and the water quality index of the Central Pollution Control Board (CPCB) – have also been added to QUALIDEX in modular form. There is also a New water quality index sub-module which enables the user to generate his or her own index and compare its performance with these well-known indice. The package is also capable of analyzing the variations in the water quality of different sites at different times. The software has been coded in Visual C++ and has been integrated with MS Access database.     

Chlorination Byproducts in Drinking Water Produced from Thermal Desalination in United Arab Emirates

Oil activities in the Arabian Gulf can potentially affect the quality of the intake water available for coastal desalination plants. This paper addresses such situation by investigating the quality of intake water and desalinated water produced by a desalination plant located near a coastal industrial complex in United Arab Emirates (UAE). Analyses of the organic compounds on the intake seawater reported non-detected levels in most samples for the three tested organic groups; namely Polyaromatic Hydrocarbons (PAHs), Phenols, and Polychlorinated Biphenyls (PCBs). Trihalomethanes (THMs) and Haloacetic Acids (HAAs) were also tracked in the intake sea water, throughout the desalination processes, and in the final produced drinking water, to evaluate the undertaken pre- and post chlorination practices. The levels of considered Chlorination Byproducts (CBPs) were mostly found below the permissible international limits with few exceptions showing tangible levels of bromoform in the intake seawater and in the final produced drinking water as well. Lab-controlled experiments on the final produced distillate showed little contribution of its blending with small percentage of seawater upon the formation of trihalomethane and in particular, bromoform. Such results indicate that the organic precursors originated in the seawater are responsible for bromoform formation in the final distillate.     

某市给水管网中铁释放现象影响因素与控制对策分析

针对某市管网水中铁浓度的变化规律进行了系统的研究,确定了管垢向管网水中释放出的铁是管网水中铁超标的主要原因.研究中发现铸铁管和镀锌钢管中管垢的主要化学组分为铁.在给水管网中,管网水的溶解氧和余氯浓度低时,对应的管网水中铁释放现象严重,其原因是还原条件使管垢表面的致密钝化层被破坏,造成二价铁的大量释放.根据试验结果提出了给水管网中铁释放和“红水”现象的控制对策.