水中苯挥发引起的热力学焓变过程

利用水槽试验对苯的挥发特性进行研究,在此基础上,通过数值计算探求苯在挥发过程中热力学因素焓的变化规律.结果表明,焓变的时空变化与浓度的时空变化密切相关.随挥发时间的增加,苯浓度下降,焓变的数值也越来越小;随水流下移,苯浓度峰值下移,焓变峰值的位置也不断下移;随着铅垂高度Y的增加,苯的扩散速度增大,焓变值不断减小;而在同一时刻,在宽度Z方向,焓变的数值曲线都呈阶梯性变化.     

基于嗅觉效应的土壤二甲基二硫醚修复目标值制定

我国现行风险评估导则多采用基于土壤中污染物质量分数的Johnson-Ettinger(J&E)模型评估VOCs呼吸暴露健康风险,但对于土壤中异味污染物的特殊性考虑不足。以某农药污染地块土壤中异味污染物二甲基二硫醚为研究对象,分析了二甲基二硫醚在土壤与土壤气中的赋存状态,采用土壤气挥发通量与J&E模型分别计算室内呼吸暴露途径的健康与环境风险,探索基于异味污染物对人体嗅觉效应的土壤修复目标值制定方法。结果表明,土壤中二甲基二硫醚最高检出质量分数与土壤气挥发通量最大值检出点位一致,其余点位土壤气中二甲基二硫醚均有不同程度检出而土壤只有2个点位有检出;二甲基二硫醚作为挥发性比较强的有机物更容易赋存于土壤气相中,采用土壤气挥发通量测试结果来表征二甲基二硫醚的环境风险会更加客观可信。研究区域内二甲基二硫醚人体健康风险可接受,但室内暴露质量浓度最高值为5.28 mg·m⁻³,超过了污染物嗅阈值,存在异味引起的环境风险。基于嗅觉效应采用土壤气挥发通量制定的修复目标值为0.193 mg·kg⁻¹,相比J&E模型提高了一个数量级,修复方量减少约29.75%。基于土壤气挥发通量综合考虑健康风险和嗅觉阈值进行风险评估与土壤修复目标值的制定,既能确保异味污染地块安全利用,又在一定程度上避免了过度修复的问题。本研究结果可为异味污染地块的环境管理提供参考。     

渗滤液灌溉土壤N2O释放及氨挥发的研究

选用2种供试土壤（S1和S2）,通过培养试验研究了渗滤液投加土壤后N₂O释放、氨挥发及矿物氮的转化,并讨论了土壤理化性质对上述过程的影响.土壤pH值较大程度地决定了氨的挥发,仅投加渗滤液的碱性土S1在培养期的前5 d内测到氨挥发,通过氨挥发共损失了约3.0‰的渗滤液氮.投加同等含量的渗滤液后,不同土壤可导致N₂O释放量近20倍的差异(p<0.01).土壤含水率（WFPS）影响了土壤中硝酸盐氮的生成速率,从而制约了N₂O释放通量的高低.与WFPS为46%时相比,投加蒸馏水的土壤S1、投加渗滤液的土壤S1和土壤S2在WFPS为70%的条件下N₂O的释放通量均值分别提高了6.5 (p>0.05)、 1.8(p>0.05)和2.2倍(p<0.05).渗滤液投加土壤在10 d培养期内,土壤S1和S2因N₂O释放分别损失了41.1‰和2.3‰的渗滤液氮.为此,控制灌溉土壤的含水率(<70% WFPS),并选用酸性土壤可有效地控制渗滤液灌溉下N₂O的释放和氨挥发.     

油田储油罐非甲烷总挥发实验及仿真模拟

针对油田单井拉油罐非密封生产带来的油气泄漏问题,建立小型原油储油罐挥发损耗实验模拟平台,通过气相色谱法探究各因素对其损耗的影响,利用Fluent仿真软件模拟储油罐的泄漏扩散。结果表明:储液温度和有无风环境对储油罐非甲烷总烃(NMHC)挥发影响较大,储液高度和环境温度对其影响较小;仿真模拟无风环境下,储油罐泄漏口短时间内存在油气积聚现象;有风环境下,当风速为1 m/s,油气积聚不明显;随风速增大,扩散浓度场面积不断增大,油品损耗量增大,在风速为5 m/s的环境下,扩散300 s时的浓度场面积相比扩散200 s时较小,但泄漏口处的油气积聚面积增大。     

Photodegradation and volatility of pesticides

BACKGROUND AND OBJECTIVES: Among the factors affecting the environmental fate of surface-applied pesticides several biological as well as abiotic factors, such as volatilization and photochemical transformations are of particular interest. Whereas reliable measurement methods and models for estimating direct photodegradation are already available for the compartments of water and atmosphere and individual subprocesses have already been described in detail, there is still a need for further elucidation concerning the key processes of heterogeneous photodegradation of environmental chemicals on surfaces. METHODS: In order to systematically examine the direct and indirect photodegradation of 14C-labeled pesticides on various surfaces and their volatilization behavior, a new laboratory device ('photovolatility chamber') was designed according to US EPA Guideline 161-3. Model experiments under controlled conditions were conducted investigating the impact of different surfaces, i.e. glass, soil dust and radish plants, and environmental factors, i.e. irradiation and atmospheric ozone (O3), on the photodegradation and volatilization of surface-deposited [phenyl-UL-14C]parathion-methyl (PM). RESULTS AND DISCUSSION: Depending on the experimental conditions, parathion-methyl was converted to paraoxon-methyl, 4-nitrophenol, unknown polar products and 14CO2. With respect to the direct photodegradation of PM (experiments without O3), the major products were polar compounds and 14CO2, due to the rapid photochemical mineralization of 4-nitrophenol to 14CO2. Paraoxon-methyl and 4-nitrophenol formation was mainly mediated by the combination of light, O3, and *OH radicals. In radish experiments PM photodegradation was presumably located in the cuticle compartment, which exhibited a sensitized photodegradation, as more unknown products were yielded compared to the glass and soil dust experiments. This could be explained by intensifying the inherent PM degradation in the dark with the same product spectrum. Due to photochemical product formation, which is an antagonistic process to the volatilization of parent compound, the volatilization of unaltered parathion-methyl from each surface generally decreased in the presence of light, particularly in combination with increasing O3 concentrations and *OH radical production rates. CONCLUSION: First results demonstrated that the photovolatility chamber provides a special tool for the systematic evaluation of (a) photodegradation of surface-located pesticide residues, i.e. measuring qualitative aspects of direct and indirect photodegradation together with relative photodegradation rates, and (b) volatilization of pesticides on surfaces by including and optionally varying relevant parameters such as light, atmospheric O3 concentration, surface temperature, air temperature, air flow rate. OUTLOOK: The experimental facility represents an important complement to lysimeter and field studies, in particular for experiments on the volatilization of pesticides using the wind tunnel system. With the photovolatility chamber special experiments on photodegradation, volatilization and plant uptake can be conducted to study key processes in more detail and this will lead to a better understanding of the effects of certain environmental processes on the fate of released agrochemicals contributing to an improved risk assessment.     

菜地氨挥发损失及影响因素原位研究

为获得菜地氨挥发通量和氨挥发损失率,并探讨其与环境影响因素之间的关系,于2009年1月～2009年5月,采用由风洞系统-大气气态污染物连续收集与在线分析装置和离子色谱联用组成的、时间分辨率为15min的氨挥发在线测定系统,用模拟试验方法对菜地(蔬菜上海青和生菜)施用尿素氨挥发特征进行研究.结果表明,系统氨气收集效率为(...     

生活污水灌溉对麦秸还田稻田氨挥发排放的影响

以养分回用为目的,在原状土柱模拟试验条件下,采用间歇密闭式抽气法研究了生活污水灌溉对麦秸还田稻田田面水铵态氮浓度、田面水pH以及稻田氨挥发损失的影响.结果表明:1麦秸还田显著增加了田面水NH_4~+-N浓度,生活污水灌溉则显著降低了田面水NH_4~+-N浓度.2正常灌溉施肥秸秆不还田稻田处理的总氨挥发量为58.29 kg·hm-2,占总施氮量的24.29%;麦秸还田显著增加了稻田的氨挥发损失,氨挥发损失量增加了近一倍,达总施氮量的45.66%;而生活污水灌溉显著降低了稻田氨挥发损失量,氨挥发损失量降至总施肥量的17.26%(秸秆不还田)和32.72%(秸秆还田).秸秆还田与生活污水处理具有显著的正交互作用.在3个肥期中,分蘖肥期氨挥发损失率最高,占总氮肥用量的7.38%~24.44%.3无论秸秆还田与否,氨挥发通量与田面水NH_4~+-N浓度之间均存在极显著的正相关关系,与田面水pH值则相关性不显著.麦秸还田增加了稻田氨挥发损失,而麦秸还田与生活污水灌溉耦合能降低稻田氨挥发损失,同时污水中的氮可替代44.41%的化肥氮,减少稻季化肥用量,具有显著的生态环境效益.     

植物叶片氨挥发研究进展

氨是大气污染的一个重要组成部分,植物叶片氨挥发是大气氨污染的来源之一。植物氨挥发的强弱与植株氮素利用效率有很好的相关性,很多研究表明,植株收获时的总氮量一般显著小于植株氮素最大累积量,植株生长后期体内含氮化合物的水解和氨的挥发可能是其重要原因。因此,研究植物体的氨挥发对于大气环境保护和提高氮肥利用率具有非常重要的意义。本文对植物叶片氨挥发的主要测定方法、机理和影响因素进行了综述,对植物叶片氨挥发研究中的一些问题进行了讨论。     

Volatilization of lindane from water in soil‐free and flooded soil systems

Abstract

Volatilization of ¹⁴C‐lindane from water in planchets and under flooded soil ecosystem was investigated. Lindane disappeared faster than parathion from planchets. More rapid loss of both insecticides occurred from water than from chloroform. Loss of lindane and parathion was related to measured losses of water by evaporation. During 5‐day incubation under flooded soil conditions, disappearance of lindane was faster from open vials than from sealed vials, whereas in nonflooded soil, no volatile loss of the insecticide was evident despite water evaporation. Over 5 day incubation under flooded conditions, greater volatile loss of lindane occurred in sandy soil than in alluvial soil apparently due to greater adsorption to the soil colloids decreasing the insecticide concentration in the standing water of the laterite soil. Under identical conditions of water evaporation, lindane loss was directly proportional to its initial concentration in the water. These results suggest that considerable loss of soil applied pesticides can occur by volatilization from the standing water in flooded rice fields, particularly under tropical conditions.     

垃圾焚烧飞灰基本性质的研究

分析了几种焚烧飞灰的基本性质,讨论了燃烧过程中可能影响飞灰中重金属分布的因素,研究表明:焚烧飞灰结构复杂性和性质多变,其主要的化学组成为Cl、Ca、K、Na、Si、Al、O等,主要的重金属为Zn、Pb、Cr、Cu等;飞灰多以不规则的无定形态和多晶聚合体的结构存在,浸出毒性一般超过危险废物鉴别标准;重金属主要以气溶胶小颗粒和富集于飞灰颗粒表面的形式存在于飞灰中.焚烧厂和焚烧时间的变化对于飞灰性质有较大影响,几种飞灰的Cl含量范围为6.93%～29.18%,SiO₂为4.48%～24.84%;浸出毒性则在0～163.10mg·L^-1(Pb)、0.049～164.90mg·L^-1(Zn)之间变化.