Identifying the European Fossil Fuel Plumes in the Atmosphere Over the Northeast Atlantic Region Through Isotopic Observations and Numerical Modelling

As part of the Danish NEAREX project the origin and variability of anthropogenic atmospheric CO₂ over the Northeast Atlantic Region (NEAR) has been studied. The project consisted of a combination of experimental and modelling activities. Local volunteers operated CO₂ sampling stations, built at University of Copenhagen, for ¹⁴C analysis at four locations (East Denmark, Shetland Isles, Faroe Isles and Iceland). The samples were only collected during winter periods of south-easterly winds in an attempt to trace air enriched in fossil-fuel derived CO₂ due to combustion of fossil fuels within European countries. In order to study the transport and concentration fields over the region in detail, a three-dimensional Eulerian hemispheric air pollution model has been extended to include the main anthropogenic sources for atmospheric CO₂. During the project period (1998–2001) only a few episodes of transport from Central Europe towards NEAR arose, which makes the data set for the evaluation of the method sparse. The analysed samples indicate that the signal for fossil CO₂, as expected, is largest (up to 3.7±0.4% fossil CO₂) at the Danish location closest to the European emissions areas and much weaker (up to ∼1.5±0.6% fossil CO₂) at the most remote location. As the anthropogenic signal is weak in the clean atmosphere over NEAR these numbers will, however, be very sensitive to the assumed background ¹⁴CO₂ activity and the precision of the measurements. The model simulations include the interplay between the driving processes from the emission into the boundary layer and the following horizontal/vertical mixing and atmospheric transport and are used to analyse the meteorological conditions leading to the observed events of high fossil CO₂ over NEAR. This information about the history of the air masses is essential if an observed signal is to be utilised for identifying and quantifying sources for fossil CO₂.     

燃料燃烧排放系数的研究

鉴于目前仍未有一套完整的燃料燃烧排放系数 ,文章主要以广州市为对象 ,通过大量的调查和深入的研究 ,使用五种不同的方法 ,得到一套适用于各种燃料及不同燃烧方式的排放系数 ,使通过燃料消耗量推算大气污染物排放量更方便准确     

液液萃取-气质联用法测定饮用水源地水中SVOCs

采用乙酸乙酯-正己烷混合溶剂（体积比为2∶1）对饮用水源地水中阿特拉津、林丹、邻苯二甲酸二正丁酯（DBP）、邻苯二甲酸二（2-乙基己基）酯（DEHP）和滴滴涕（含4种）等8种半挥发性有机物进行1次水样萃取,用气质联用法同时测定。试验表明,方法在25．0μg/L～500μg/L范围内线性良好;检出限在0．006μg/L ～0．028μg/L 之间;空白水样3个质量浓度水平的加标回收率为87．6％～109％,平行测定6次的 RSD＜5．1％;测定集中式生活饮用水源地的实际水样,未检出目标化合物,加标回收率为98．6％～109％。     

水中有机磷农药分析前处理方法探讨

分别采用液-液萃取、固相萃取前处理方法,提取水中10种常见的有机磷农药,对比了这两种提取方法的测定结果、经济成本、花费时间及对环境的影响,建议逐步用固相萃取法取代液？液萃取法提取水中有机磷农药。     

衍生化-液液萃取-气相色谱法测定水中苦味酸的技术关键

测定水中苦味酸的国标方法——衍生化-液液萃取-气相色谱法采用的提取溶剂苯毒性较大,杂质较多,苦味酸在衍生过程中有部分损失。在国标方法的基础上,改用环己烷为提取溶剂,以溶剂液封加盖的方式,降低了衍生化产物损耗。选用中口径毛细管色谱柱,优化了色谱条件,有效地将衍生化产物与杂质分离。方法在0.500μg/L～40.0μg/L范围内线性良好,检出限为0.083μg/L,标准溶液平行测定6次的RSD≤5.3%,实际样品加标回收率为93.9%～104%。     

As水质毒性发光细菌及微生物燃料电池在线监测技术的比选研究

针对实际应用需要,对比研究了发光细菌和微生物燃料电池两种不同毒性预警技术对典型类金属砷离子的响应差异,并考察了丰水期、枯水期河水水质背景干扰对响应信号的影响。结果表明,发光细菌法对砷离子响应较为灵敏,微生物燃料电池法对砷离子的响应非常灵敏。发光细菌法受水体水质背景干扰大,且不同生产厂家的仪器差异显著,推测可能是由于菌株来源不同、仪器响应灵敏度差异所造成。微生物燃料电池法对背景干扰的抗性较强,稳定性较高,河水加标与纯水加标样本的剂量-效应曲线差别不大。基于上述研究结果,分析了两种技术监测类金属砷的优缺点并提出实际在线运行的相关建议。     

基于铁阳极的生物阴极自养反硝化效能影响因素探究

利用微生物燃料电池(Microbial fuel cell,MFC)装置耦合零价铁脱氮和生物阴极,研发基于铁阳极的新型生物脱氮技术,可有效避免脱氮过程中外源有机物的添加,降低污水处理成本,减少二次污染.本文以MFC装置为平台,零价铁为阳极,附着生物膜的碳刷为阴极,组成零价铁自养反硝化装置.在控制变量的条件下,采用单因素试验法探究不同起始pH(5～9)、不同外接电阻(50～2000Ω)、不同阴极电导率(0～232g·L^-1)和不同起始基质浓度(42～800 mg·L^-1)对零价铁自养反硝化效能和MFC产电性能的影响.结果表明,以脱氮作为首要目标,产电作为次要目标时,零价铁生物自养反硝化体系最佳起始pH为7,最佳起始硝氮浓度为200 mg·L^-1,最佳阴极电导率为添加116 g·L^-1,最佳外接电阻为1000Ω.对自养反硝化效能影响因素的探究将有助于优化反应条件,探明碳阴极生物脱氮过程的主要干扰因素,提升生物自养反硝化技术效能.     

漂浮阴极SMFC传感器产电信号对不同重金属污染的响应特征及机制研究

我国十分重视对突发性水污染事件的监测和处置.本研究设计了一种实时在线监测重金属污染事件的漂浮阴极沉积物-微生物燃料电池传感器(漂浮阴极SMFC传感器).该传感器阳极埋设在淹水土壤中,阴极漂浮在水面作为污染响应元件,并向阴极分别加入Zn²⁺、Cd²⁺、Co²⁺、Ni²⁺、Pb²⁺、Cu²⁺、Cr⁶⁺溶液以模拟水体重金属污染事件,以探究该传感器电信号对不同重金属污染的响应特征及机制.结果显示,Cu²⁺和Cr⁶⁺污染引起传感器出现明显的电压峰,而其他5种重金属污染则未引起明显的电信号响应.该传感器电压信号对Cu²⁺污染的最低检测限为5 mg·L^-1,灵敏度为1.06 mV·L·mg^-1,线性范围为5～40 mg·L^-1;Cr⁶⁺污染的最低检测限为40 mg·L^-1,灵...     

Detection of fullerenes (C60 and C70) in commercial cosmetics

Detection methods are necessary to quantify fullerenes in commercial applications to provide potential exposure levels for future risk assessments of fullerene technologies. The fullerene concentrations of five cosmetic products were evaluated using liquid chromatography with mass spectrometry to separate and specifically detect C₆₀ and C₇₀ from interfering cosmetic substances (e.g., castor oil). A cosmetic formulation was characterized with transmission electron microscopy, which confirmed that polyvinylpyrrolidone encapsulated C₆₀. Liquid-liquid extraction of fullerenes from control samples approached 100% while solid-phase and sonication in toluene extractions yielded recoveries of 27-42%. C₆₀ was detected in four commercial cosmetics ranging from 0.04 to 1.1 μg/g, and C₇₀ was qualitatively detected in two samples. A single-use quantity of cosmetic (0.5 g) may contain up to 0.6 μg of C₆₀, demonstrating a pathway for human exposure. Steady-state modeling of fullerene adsorption to biosolids is used to discuss potential environmental releases from wastewater treatment systems.     

燃料电池发展现状及在石油行业的应用可行性

一次能源利用效率低和分散能源回收难是石油天然气行业一直面临的技术难题。为提高一次能源利用和回收转换效率、解决能源与环境的矛盾,在石油行业内应用先进的节能环保新型技术——燃料电池技术是十分必要的。文章介绍了燃料电池的主要类型、特点及国内外应用现状,分析了其在石油行业的应用前景。