模糊综合评价在天然水体水质评价中的应用研究

采用模糊数学方法,对河网地区面源污染影响较大的代表性河流的水质状况进行综合评价研究。根据监测断面水质污染特点,确定了8个指标作为评价因子,建立了评价因素矩阵,计算出影响因子的权重。在此基础上,提出了模糊综合评价的水质级别,证明该河网地区的污染物主要是氮、磷和有机物。     

基于时域权重矩阵的模糊综合水质评价法及其应用

水质评价作为合理开发和保护水资源的一项重要工作,越来越受到人们重视。传统的模糊综合水质评价方法因未考虑到水质指标权重的季节变化而可能影响评价结果,故对水质指标权重向量进行了改进,提出了时域权重矩阵的概念,并将实测权重向量与时域权重矩阵相结合,进行组合赋权,得到综合权重向量。应用改进的模糊综合评价方法对某引水明渠水质进行综合评价,结果相比于传统模糊综合水质评价法更符合实际。     

模糊综合评价在天然水体水质评价中的应用研究

采用模糊数学方法，对河网地区面源污染影响较大的代表性河流的水质状况进行综合评价研究。根据监测断面水质污染特点，确定了8个指标作为评价因子，建立了评价因素矩阵，计算出影响因子的权重。在此基础上，提出了模糊综合评价的水质级别，证明该河网地区的污染物主要是氮、磷和有机物。     

基于熵权法的松河矿水环境质量评价研究

根据松河矿水文条件对5个断面(W1~W5)水质进行监测,采用标准指数法对各断面水质的监测数据进行处理,并用熵权法确定各断面的指标权重,由各指标权重得出各断面的污染综合评分。结果表明,松河矿地表水水质中污染指数较高的是石油类,其次是SS、氨氮、BOD、COD,最后是硫化物。其中,影响各断面水质权重最大的是SS,其权重为0.2。综合污染指数和基于熵权法的断面评分排序一致,均为W1W2W3W4W5,表明基于熵权法的松河矿水环境质量评价结果准确可信。     

基于动态RBF神经网络的地下水质量评价

提出一种基于动态RBF神经网络的地下水质综合评价方法。该方法采用最近邻聚类算法,构建动态RBF神经网络,利用神经网络对待测水质进行分类识别,根据网络输出,实现水质等级的确定。应用结果表明,该方法具有训练速度快、评价准确度高的优点,提高了水质综合评价的精度和客观性。     

M-AHP-熵权组合赋权法在垃圾渗滤液处理技术评价中的应用

通过分析目前综合评价赋权方法存在的弊端,提出了主客观相结合对指标进行赋权的方法,即采用基于MATLAB优化工具箱的层次分析法(M-AHP)建立主观权重,采用熵权法建立客观权重,将主客观权重加以综合来确定评价指标的权重。最后将该方法应用于重庆市卫生填埋场的处理技术的评价指标,然后按照模糊积分评价模型得出综合评价值,从3种备选方案中得出了MBR(膜生物反应器)+NF(纳滤)工艺为最佳方案。     

基于模糊权物元理论的地下水水质评价模型构建及应用

在物元分析的基础上,结合模糊权重理论与层次分析方法,构建用于评价地下水水质的模糊权物元分析模型。应用此模型对徐州市的重要水源地——张集水源地的地下水水质进行了综合评价。选取数据较为完整的20个监测井的监测数据进行评价。结果表明,研究区的20个采样点水质为Ⅱ、Ⅲ级的占95%,绝大多数地下水水质较好,符合饮用水的要求。与投影寻踪法和模糊概率法的评价结果比较发现,得出的评价结果与以上2种评价结果基本一致。     

综合权重的集对分析模型在污水处理厂改造决策中的应用

针对污水处理厂升级改造的多目标决策问题,运用集对分析理论,构建了污水处理厂运行效果综合评价模型。通过引入熵权法和层次分析法确定指标权重,构造了一种新的计算指标综合权重的方法。应用该模型对上海市11座污水处理厂进行综合评价,与模糊综合法的评价结果做了比较。结果表明:基于综合权重的集对分析模型具有更高的准确性和合理性,为污水处理厂的升级改造决策提供了一种较为可靠的评价方法。     

不同模糊评价方法在水环境质量评价中的应用比较

近年来,运用模糊评价方法对水质和水体营养化程度进行评价逐渐受到重视。目前,对模糊评价方法的研究多集中在实测数据标准化、权重的确定和模糊模式识别模型研究几个方面。以滇池历年营养物质数据为实测数据,通过对几种实测数据标准化方法、权重确定方法和模糊模式识别方法的组合应用,获得水环境质量模糊评价最优组合方法。结果表明,在评价方法中,实测数据标准化方法采用线性内插法,权重的确定采用超标倍数法,模糊模式识别模型采用广义海明距离和加权海明距离法,即采用超标倍数法的广义海明距离和加权海明距离法能够更真实反映水环境质量的实际情况。     

湖泊水质的模糊识别评价研究

将评价参数的代表值与水质标准相比较,确定其应归属的水质级别,这就是最基本的单项评价.包含了多个参数的水质综合评价,其最通常的做法是,或用单项评价的最差级别代表综合评价结果,或用综合指数或评分迭加值来表征水质状况.这里,分级的界限是明确的,水质不是属于“清洁”,便是已受“污染”.若以综合指数值0.5作为起始污染的阈值,那么,0.49仍属于“清洁”,而0.51已属于“污染”.这种“非此即彼”的判断与推理属于和现代数学密切相关的普通集合论的范畴. 但是,绝对的突变是不存在的.在自然     

An analytical method to determine Henry's law constant for selected volatile organic compounds at concentrations and temperatures corresponding to tap water use

Henry's law constants (H) are needed to model human exposure to Volatile Organic Compounds (VOCs) in indoor air resulting from the use of tap water. This paper presents an experimental method to determine Hs for several common tap water pollutants at concentrations and temperatures used in household water. For 5 VOCs Henry's law constants were obtained simultaneously over the 25 degrees C to 45 degrees C temperature range, providing data on H beyond the currently available data (up to 35 degrees C). Henry's law constants were obtained as the ratio of equilibrium concentrations of VOCs in air and water, using simultaneous sampling from sealed bottles kept at constant temperatures. Air and water samples were concentrated by a purge-and-trap method, thermally desorbed from a Tenax trap, and analyzed with a gas chromatograph with an electron capture detector (GC-ECD). Experimental results agreed well with available literature data.     

An Analytical Method to Determine Henry’s Law Constant For Selected Volatile Organic Compounds At Concentrations And Temperatures Corresponding To Tap Water Use

Henry’s law constants (H) are needed to model human exposure to Volatile Organic Compounds (VOCs) in Indoor air resulting from the use of tap water. This paper presents an experimental method to determine Hs for several common tap water pollutants at concentrations and temperatures used in household water. For 5 VOCs Henry’s law constants were obtained simultaneously over the 25° C to 45° C temperature range, providing data on H beyond the currently available data (up to 35° C). Henry’s law constants were obtained as the ratio of equilibrium concentrations of VOCs in air and water, using simultaneous sampling from sealed bottles kept at constant temperatures. Air and water samples were concentrated by a purge-and-trap method, thermally desorbed from a Tenax trap, and analyzed with a gas chromatograph with an electron capture detector (GC-ECD). Experimental results agreed well with available literature data.     

基于三波长透射率的水体色度检测标准

为了推动有关分光光度法测量水体色度的国家标准的建立,对美国和台湾地区的水体色度标准检测方法进行了研究,提出了新的基于三波长透射率测量水体色度的方法。根据现行国家标准中的色度学相关数据,选择在595、555和445 nm 3个波长处的光谱透射率计算水样的三刺激值,依照国标推荐的色差公式建立了测量水样色度的标准检量线。利用所提出的新的水体色度测量方法对5个水样的色度值进行了实际测量,结果表明,新的测量方法所得到的水体色度值与铂钴比色法一致。     

里杜湖富营养化综合评价及预测

根据里杜湖水库的水质监测及水文资料，选择评分法结合生物优势种评价法以及“源－效应”预测模型对里杜湖水库水质的营养状态进行综合评价及预测。结果表明：里杜湖水库水质已轻度富营养化，并有逐年加重的趋势。旨在正确评价和预测里杜湖水库营养状态，并为同类水库的营养状态评价及预测提供参考和借鉴，从而为水库水质管理及富营养化的控制提供科学依据。     

基于智能优化算法的河流水质模型参数的优化

为探索河流水质模型参数新的求解方法,根据有限的实测数据,分别应用免疫进化优化算法和免疫进化优选的捕食搜索算法,对河流水质模型计算公式中的多参数进行优化。将优化得到的计算公式用于国内外若干河流的河段中DO浓度值的拟合,并与实测结果进行了比较。结果表明,将免疫进化优化算法或免疫进化优选的捕食搜索算法优化得到的水质模型参数精度不仅较高,而且相对稳定,从而为河流水质模型参数的优化提供了一种新方法。     

基于智能优化算法的河流水质模型参数的优化简

为探索河流水质模型参数新的求解方法,根据有限的实测数据,分别应用免疫进化优化算法和免疫进化优选的捕食搜索算法,对河流水质模型计算公式中的多参数进行优化。将优化得到的计算公式用于国内外若干河流的河段中DO浓度值的拟合,并与实测结果进行了比较。结果表明,将免疫进化优化算法或免疫进化优选的捕食搜索算法优化得到的水质模型参数精度不仅较高,而且相对稳定,从而为河流水质模型参数的优化提供了一种新方法。     

洪泽湖水域的环境演变遥感分析

针对传统水质监测的定点、定剖面采样分析时间及空间的局限性,为对湖泊水质进行全面系统的分析,在前人研究工作的基础上,建立了一种水域水质状况图像识别的主成分监督分类方法,通过对洪泽湖湖区的1991年12月15日和2000年1月7日,两个时相TM遥感图像数据,分别进行主成分变换,并依据不同类型水体的光学特性,分析各主成分图像的构成及其环境意义。研究表明：洪泽湖湖区的水质分布,具有从西向东,从北向南由清洁水（优）向一般水依次递减、逐年下降的特征。其清洁水体主要分布于洪泽湖西部的溧河洼、临淮头、西北部的安河洼和成子湖的北部。从1991--2000年,洪泽湖入湖的工业废水及生活污水量有所减少,湖水受污染程度明显减轻,相对“八五”期间水质污染日益加重的现象,“九五”以后水质逐渐改善。将其分类结果与所收集的洪泽湖历年水质资料对比分析表明：主成分监督分类结果与环境要素吻合较好,且基本反映了其水质环境的变化趋势。     

Determination of the temperature dependence of water solubilities of polycyclic aromatic hydrocarbons by a generator column-on-line solid-phase extraction-liquid chromatographic method

An improved dynamic coupled column liquid chromatographic (DCCLC) technique for determining water solubility data of hydrophobic compounds is presented. The technique is based on pumping water through a thermostated generator column in order to generate emulsion-free, saturated aqueous solutions of the compound under study. Through a switching valve system the solute in the aqueous solution is extracted and concentrated by an on-line solid-phase extraction process and subsequently eluted and analyzed by high performance liquid chromatography (fluorescence detection coupled to photodiode array detection). The improvements carried out to the original DCCLC technique have given rise to savings in time for the experimental work and increased sensitivity during the detection and quantification stage. Applicability of the method for studying highly hydrophobic substances is demonstrated by determining water solubility of anthracene and pyrene in the temperature range of 8.9-49.9 and 8.5-32.2 degrees C, respectively. The measured water solubilities are in good agreement with the best available literature data. The method has also been applied to the determination of water solubility of m-terphenyl, 9, 10-dihydrophenanthrene and guaiazulene, in the temperature range of 4.8-49.9, 4.8-25.0, and 4.5-29.9 degrees C, respectively. The uncertainty in the Sw values determined in this work ranged from 0.7% to 4.6%. The experimental water solubility data, as a function of temperature, are fitted to the equation In Sw = A + B/T; where Sw and T are given in mole fraction and Kelvin, respectively.     

Evaluation of the procedures for the measurement of water solubility and n-octanol/water partition coefficient of chemicals results of a ring test in Japan

A ring test by 19 labolatories in Japan was carried out in 1984 for the evaluation of the experimental manuals for the measurements of water solubility and partition coefficient (n-octanol/water). The experimental data obtained by the procedures in the manuals were collected by Environmental Agency, Japan. In the measurement of water solubility, this manual applies a modified batch method (the glass beads technique), whereas the OECD Test Guidelines suggests the use of the column elution method for chemicals having water solubility lower than 10 mg/L. Anthracene and flouranthene were used as test chemicals for the measurement of water solubility, and γ -hexachlorocyclohexane (γ -HCH) and 1,2,3-trichlorobenzene were used for partition coefficient. Good agreements were observed at a practical basis between the OECD methods and our methods for the results of mesurements of water solubility and partition coefficient. We concluded that the present ring test showed an advantage of the use of the glass beads method which requires only simple apparatus in water solubility measurement, and the HPLC method is very useful to measure partition coefficient because of the simplicity of procedure and the wide range of measurement, especially at higher values of partition coefficient.     

N-nitrosodimethylamine in drinking water using a rapid,solid-phase extraction method

A simple, rapid method for the extraction of N-nitrosodimethylamine (NDMA) from drinking and surface waters was developed using Ambersorb 572. Development of an alternative method to classical liquid-liquid extraction techniques was necessary to handle the workload presented by implementation of a provincial guideline of 9 ppt for drinking water and a regulatory level of 200 ppt for effluents. A granular adsorbent, Ambersorb 572, was used to extract the NDMA from the water in the sample bottle. The NDMA was extracted from the Ambersorb 572 with dichloromethane in the autosampler vial. Method characteristics include a precision of 4 % for replicate analyses, an accuracy of 6 % at 10 ppt and a detection limit of 1.0 ppt NDMA in water. Comparative data between the Ambersorb 572 method and liquid-liquid extraction showed excellent agreement (average difference of 12 %). With the Ambersorb 572 method, dichloromethane use has been reduced by a factor of 1,000 and productivity has been increased by a factor of 3–4. Monitoring of a drinking water supply showed rapidly changing concentrations of NDMA from day to day.