预浓缩与GC-MS联用分析垃圾填埋场恶臭气体

采用预浓缩与气相色谱-质谱联用,建立了垃圾填埋场几种恶臭气体的分析方法。该法用SUMMA罐采集垃圾填埋场臭气,经预浓缩系统冷凝浓缩后,用GC-MS分析测定。几种臭气的检出限均低于3.0×10-3mg/m3,经6次重复测定,其相对标准偏差低于10%。该法已用于西安市江村沟垃圾填埋场臭气的采样分析。该法的应用增强了西安市对臭气的监测分析能力。     

生活垃圾转运站恶臭污染指标初探

报道了广州部分垃圾转运站恶臭指标的检测结果.发现国家标准(GB14554-1993)中的单项污染物指标的测定值大多远低于标准限值,而综合指标臭气浓度普遍超标,两类指标间存在严重不符.利用SAS统计软件综合分析各指标的检测数据,结果表明,垃圾转运站臭气中恶臭指标的含量存在较大的变异,且在垃圾站内的变异程度更大;恶臭单项指标在垃圾站内和垃圾站边界点的测定均值问无显著差异;臭气浓度和恶臭单项指标整体间可能存在一定的线性关系,但和某个具体的恶臭指标的线性相关性并不显著.     

浅议《恶臭污染物排放标准》的修订

简述了国内外环境恶臭标准发展概况,针对目前国内恶臭标准在实际监测管理中存在的缺少污染种类及采样位置、测算方法等问题,提出增加《恶臭污染物排放标准》中的污染物种类,完善臭气浓度计算方法以及制定地方恶臭排放标准的建议.     

恶臭源厂界空气中恶臭物质监测技术要点及结果分析探讨——以西安市某大型垃圾填埋场为例

建立了水杨酸-次氯酸钠法分析氨的标准曲线,通过对西安市某垃圾填埋场的实地监测,探索了恶臭气体中氨气的分析方法。分析了臭气、氨气、硫化氢之间的浓度相关性,利用本次监测数据,找出了针对该垃圾处理场的高浓度氨气样品初步分析方案。恶臭产生的主要点位为垃圾场渗滤液污水处理站及下游区域,垃圾场臭气呈现出由点源污染(作业面)到面源污染扩散的态势。     

上海化学工业区污水处理厂废气中挥发性有机物主要成分的测定

建立了使用活性炭管采集臭气中的挥发性有机物,经二硫化碳解吸,用GC-MS仪Scan扫描方式确定挥发性有机物的组分后优化GC-MS条件定性定量分析上海化学工业区污水处理厂臭气中主要挥发性有机物的方法。结果表明,从臭气中检测出11种VOCs,线性相关系数R2均大于0.99,相对标准偏差为3.0%～4.7%,除了苯乙烯、α-甲基苯乙烯和4-甲基苯乙烯的解吸效率依次分别为72%、74%和66%,其他挥发性有机物的解吸效率均为91%～100%。本方法操作简便,能够有效分离和准确测定臭气中挥发性有机物,具有较低的检出限和较好的精确度,适合臭气中挥发性有机物的检测分析,可为臭气控制提供可靠的数据。     

三点比较式臭袋法测定环境中臭气浓度

就三点比较式臭袋法在测定环境空气臭气浓度时应注意的现场踏勘、采样点的选择、采样次数、配气、嗅辨过程,以及臭气浓度计算等问题进行探讨,使该方法更加完善、简便.     

恶臭国标测定方法和便携式恶臭测定仪测定结果的比对分析

比对了恶臭国标测定方法《GB/T 14675—1993》和便携式恶臭测定仪对厂界环境空气无组织排放臭气浓度的测定结果。结果显示,恶臭国标测定方法和便携式恶臭测定仪的测定值基本在同一范围内,具有一定的可比性,但2种方法在嗅辨方式、工作地点、结果计算方式、配气方法、样品原始性和测定范围上都存在差异。     

恶臭监测嗅觉测试方法的比较分析

通过恶臭污染监测技术的比较分析,阐明了各类恶臭监测技术的特点和发展方向,指出嗅觉测试法在目前技术水平下的重要作用和地位,依据古典心理物理学中最小可觉差法及平均差误法对欧洲EN13725标准方法和中国三点比较式臭袋法进行了比较分析,得到2种实验方法的特点。古典物理学是科学心理学一百多年的发展历程中已经形成的经典研究技术,主要用于外界刺激对人的感觉器官作用的测试技术。其中最小可觉差法是采用已知"标准刺激"对未知的"比较刺激"进行比较的感受阈值测定方法。平均差误法则是将"标准刺激"阈值视为零,并将接近零的平均实验结果作为感觉阈值的测定方法。在欧洲嗅辨实验所用的"标准刺激"为标准臭气样,而中国嗅辨实验暂时没有标准臭气样品,仍依据嗅觉阈值为零的概念进行恶臭样品实验。通过多年对嗅辨员的考核经验,总结了人的嗅阈值的分布特征,进而提出标准臭气样品的制备研究方法,提出培训嗅辨师以增强对环境恶臭污染识别能力的观点,借以深入理解恶臭嗅觉测定技术方法。     

污水处理厂还原硫化物和臭气浓度的电子鼻监测技术探究

用电子鼻监测技术探究污水处理厂还原硫化物质量浓度和臭气质量浓度预测方法。结果表明,使用响应面分析法(RSM)建立还原硫化物质量浓度与电子鼻响应值关系,构建还原硫化物质量浓度预测模型,准确率可达95%。使用偏最小二乘法(PLS)建立不同质量浓度还原硫化物的传感器响应值与对应臭气质量浓度之间的关系,构建臭气浓度预测模型,并用实际样品验证。     

生物滤床处理酒精生产企业恶臭废气技术探讨

对酒精生产企业在生产过程中产生的恶臭废气的来源和气量进行了较详细的分析,在对此类恶臭废气理化特性进行分析的基础上,通过对沉砂池、污水处理站等设施产生的气体进行加盖封闭、抽风、碱液喷淋、生物滤床除臭等措施,完成了对上述臭气的收集和处理,其中硫化氢、氨、甲硫醇去除率达到95%以上,可实现达标排放,区域环境空气质量和群众对环境的满意率得到显著提高。     

气相色谱-质谱法测定环境空气中恶臭硫化物成分

摘要：采用苏玛罐采样、冷阱顶浓缩处理样品、气相色谱质谱联用法测定环境空气中的甲硫醇、乙硫醇、甲硫醚、乙硫醚、甲乙硫醚、二甲二硫、二硫化碳等7种恶臭硫化物。结果表明，该方法的线性较好，7种硫化物的检出限为8．0×10-4～1．4×10-3mg／m3，混合标准气体平行测定时RSD范围在3．32％～6．17％，加标回收率为100％～117％。该方法对于环境空气恶臭硫化物的测定准确可靠，能够用于常规环境空气中恶臭硫化物的分析检测。     

石油炼制项目竣工环保验收监测检查常见问题

根据建设项目竣工环境保护验收监测相关标准规范要求和实践经验,总结了石油炼制项目竣工环境保护验收监测实践工作中的若干常见问题。根据石油炼制项目污染物来源和特点,分析了加热炉废气监测、恶臭VOCs治理、含油污水监测、防渗措施和地下水监测以及污水处理"三泥"(含油污泥、气浮浮渣、剩余的废活性污泥)和碱渣处置等常见重点难点问题,在此基础上提出了一些对策和建议,为今后开展验收监测检查工作提供借鉴。     

工业城市有机化工异味应急监测快速溯源

结合淄博化工园区有机化工异味的应急监测,研究了工业城市有机化工异味的快速溯源。针对多种异味混杂,现场利用便携式GC-MS对空气中引起异味的有机化合物进行定性和定量,结合三点比较式臭袋法测定厂界臭气浓度值,根据风向,对照企业污染物名单快速溯源,并根据测定结果和厂界臭气浓度限值对排污企业进行行政处理。     

淄博化工园区大气有机污染应急监测与管理对策

针对工业聚集区内多种恶臭混杂的情况，以淄博化工园区为例，研究了大气有机污染突发事件中有机物的应急监测方法，并提出了治理对策。利用便携式气相色谱-质谱联用仪，对重点企业事先监测，掌握各企业特征污染物，作为应急监测查找污染源头的依据；现场分析受污染空气中的化合物组成及浓度，通过查询、比对各企业特征污染物，确认责任排污企业。提出了末端监测处罚治理与对重点污染企业推行清洁生产相结合，应急监测与有机污染物在线监测相结合，建立企业污染源特征组分数据库，加强企业无组织排放监测与监管等治理大气有机污染的建议。     

Adsorption of Cotton Fabric Dyestuff Waste Water on Nigeria Agricultural Semi-Activated Carbon

The Kaduna river in Nigeria is in such great environmental stress that the self-purifying capacity of the river has been exceeded as a result of industrial discharges. The river water is blue-green and pollution build-up is evident on the river banks. Techniques were designed to rid the river of visible signs of pollution by incorporating the principles of adsorption and incineration.Semi-activated carbon from agricultural wastes were used to treat the waste water. Residual colors, amber, yellow and orange, were obtained and the solute removed ranged from 96-99.8% and the volatile residue removed by carbon treatment ranged from 3-3.8%. Incineration of 1 kg waste water yielded 40 g solid residue.Adsorption of dyestuff present in the waste water was linear and increased with concentrations of waste water per unit mass of guinea corn carbon. Replicate results yielded: y = 2.5 + 0.130x y = 2.306 + 0.017x where x =log10% concentration of dyestuff waste water (independent variable); y = log10 adsorption of dyestuff waste-weight gramme-1 carbon. Unit of weight = milligramme (dependent variable).For maize carbon, adsorption was linear but decreased with increasing concentrations. Replicate results were: y = 1.583 - 0.21x y = 0.52 - 0.32x x and y here are the same as above; with cane sugar carbon, adsorption was independent of concentrations. Student t-test showed no statistical difference between the replicates at the 99.5% level.     

原生动物与BOD_5相关性的研究

本文着重研究了原生动物平衡期及密度与ＢＯＤ５浓度的相关性。研究结果表明，原生动物平衡期与ＢＯＤ５的浓度有着ｙ＝１５６２７·ｅ０２４０·ｘ的指数关系，相关性为显著相关；原生动物密度与ＢＯＤ５浓度有着ｙ＝１１３４＋００３６·ｘ的线性关系，相关性为高度相关     

Mercury in rivers in NW England: from rural headwaters to the heartlands of the historic industrial base

Total mercury (T-Hg) concentrations in rivers are described across a rural to urban/industrial and agricultural landscape gradient in NW England. T-Hg ranges between 0.2 and 230 ng L(-1). The regional median was 3.6 ng L(-1) with individual river medians ranging between 1.9 and 8.3 ng L(-1). Median T-Hg concentrations were sometimes moderately higher for the lowland areas and at higher flows. Our estimates suggest that the Ribble estuary receives 9.2 kg y(-1) and the Wyre estuary 0.7 kg y(-1). In order to examine regional inputs from urban/industrial components, regression analysis was undertaken by comparing three types of hydrochemical signature: suspended sediments (SS), which provide a measure of the particulate component, dissolved organic carbon (DOC) that provides an indication of humic/fulvic acids that are part of the organic colloids and strong chelating agents, and boron a marker of sewage effluents and population density. The results show high positive relationships of T-Hg with both SS and DOC, but no relationship with the urban/industrial signal. The regression analysis with T-Hg indicated on average a gradient of 0.33 ng mg(-1) for DOC and 0.2 ng mg(-1) for SS. They indicate the primary importance of a diffuse source of T-Hg. For the upland areas and cleaner river systems, the linkages between T-Hg and DOC were particularly strong, while for the lowland areas, the linkage with SS proved stronger. Analysis of a latter subset of data that partition the SS into organic and inorganic fractions indicated that the T-Hg was primarily linked with the organic fraction. Indeed, multiple regression of T-Hg with DOC and POM reveals gradients similar to other parts of the World.     

遥感法与高怠速法尾气排放状况对照检测试验研究

募集100辆点燃式发动机在用汽车进行遥感法和高怠速法尾气排放对照检测试验。结果表明,多数车辆CO遥测值比高怠速值大,HC则相反。通过对高怠速值(y)与遥测值(x)进行回归分析,得到CO的回归方程为y=0.81x+453.03,t检验显示方程具有线性(α=0.10)。如果将两种方法配合使用,可以有效提高机动车尾气排放日常管理的效果。     

不同地质条件下土壤重金属质量评价比较

对黎塘研究区不同地质条件下土壤重金属含量进行了分析和评价。结果表明,不同地层土壤以Mn含量最高,其次为Cr,石炭系下统岩关阶和泥盆系中统东岗岭阶土壤重金属含量较高,而白垩系下统小店组和第四系全新统土壤重金属含量较低。泥盆系中统东岗岭阶土壤重金属污染因子为Ni、As、Cr,综合质量级别为中等;石炭系下统岩关阶土壤重金属污染因子为Ni、As、Cr、Cu,综合质量级别为很坏;白垩系下统土壤污染因子为Cr,综合质量级别为警戒级;第四系全新统土壤重金属质量级别均为好,综合质量级别为好。     

Two high-speed, portable GC systems designed for the measurement of non-methane hydrocarbons and PAN: results from the Jungfraujoch High Altitude Observatory

Near real-time measurements of light non-methane hydrocarbons (NMHCs) and peroxyacetyl nitrate (PAN) have been performed in the free troposphere using two fast gas chromatography (GC) instruments designed for use on aircraft. A GC-helium ionisation detector (HID) system measured 15 C(2)-C(5) hydrocarbons with 5 min time resolution and a dual channel GC-Electron Capture Detector (ECD) measured PAN with 90 s resolution. Both instruments had low parts per trillion by volume (pptV) detection limits and ran continuously at the remote Jungfraujoch (JFJ) research station in the Swiss Alps (46.55[degree]N, 7.98[degree]E), 3580 m above mean sea level (AMSL), during February/March 2003. Carbon monoxide, ozone, nitrogen oxide and nitrogen dioxide and all odd nitrogen species (NO(y)) were also measured continuously. Hydrocarbons and CO were strongly correlated in all air-masses whilst PAN exhibited both positive and negative correlations with respect to O(3), dependent on age and origin of the air-mass sampled. PAN was found to contribute [similar]20% to the NO(y) sampled on average. The experiment, as well as providing interesting datasets from this remote location, also demonstrated that when optimised, GC techniques have the potential to measure at a time resolution significantly greater than is traditionally considered, with high sensitivity and low uncertainty.