矿井瓦斯煤尘爆炸传播数值模拟研究

基于连续相、燃烧、颗粒相数理方程建立瓦斯煤尘爆炸传播数理模型,并应用连续相、颗粒相计算方法,依据大型巷道瓦斯爆炸、瓦斯煤尘爆炸传播实验数据,借助普遍应用的流场模拟平台,成功开发瓦斯、煤尘爆炸数值模拟系统。该系统可有效地模拟煤矿瓦斯、煤尘的爆炸事故过程,对瓦斯爆炸的爆燃转爆轰、煤尘是否参与爆炸、爆炸冲击传播速度、衰减规律以及爆炸灾害的波及范围都能进行较准确的模拟。     

关于“四沿”化工安全的战略性思考与探索

以基本能浓缩中国化工概貌的江苏省沿江、沿河、沿湖、沿海化工企业为背景,依据其形成和发展及基本概况,结合重大化工事故灾难,以安全与环境相耦合,对"四沿"化工安全进行了战略性思考,试图勾画临水化工本质安全的模型,提出在"四沿"地区构建化工本质安全化科技支撑体系的宏观构架,即建设"江苏省四沿区域化工本质安全和化工事故防范及应急系统"的思路、探索与实践。还提出了立法深化研究和技术标准制定、严格区域规划设计与建设的监督、强化监管执法力度等急需关注的问题。以江苏省"四沿"区域的化工安全为背景所提出的思路与对策,应该对整个华东地区乃至全国临水性化工企业安全具有重要的现实和借鉴意义,对我国高危行业的安全生产和环境保护有重大的示范效应。     

气体二氧化氯对葡萄表面细菌杀菌规律研究

研究气体二氧化氯杀灭金黄色葡萄球菌、大肠杆菌、李斯特单增菌和腐生酵母菌4种葡萄表面的危险致病菌的杀菌规律。在实验范围内,随着气体二氧化氯浓度的增加和杀菌时间的延长,杀菌效果明显增加。当杀菌时间超过12min,杀菌量级几乎不再增加。杀菌效率随温度的增加而减小,在实验温度条件下,只有大肠杆菌的杀菌效果减少了5.38～6.09log量级,其他3种菌均减少了6log量级以上,杀菌作用温度在实验条件下对杀菌效果影响不大。研究表明,当气体二氧化氯的杀菌浓度为25mgl-1、杀菌时间12min、杀菌温度25℃的条件下,金黄色葡萄球菌、李斯特单增菌和腐生酵母菌均减少了6.4log量级以上,而大肠杆菌达到5.76log量级;同时表明二氧化氯气体的杀菌保鲜功能也是食品安全技术非热杀菌手段。     

煤矿瓦斯爆炸事故演化的突变模型

煤矿瓦斯爆炸事故,从微观上看,是在瓦斯积聚、引火源和氧气浓度3个条件同时具备的情况下发生的,从宏观上看,是在生产活动中存在人的不安全行为和物的不安全状态导致了微观3条件的同时具备。笔者介绍了突变理论的基本原理;在轨迹交叉事故致因理论基础上,分析了瓦斯爆炸事故演化的非线性特征;建立了事故演化的尖点突变模型。并指出:事故演化是一个流变-突变过程,其突变的程度反映了事故的严重度;人的不安全行为是事故发生的主要因素;物的因素决定事故的严重度;安全生产必须建立本质安全型矿井,避免人和物的运动轨迹越过分歧点集。     

城市燃气管道事故应急抢修方案的决策分析

通过对近年来的城市燃气管道事故抢险统计数据的分析与研究,管道事故抢险方案的选择存在着很大的主观性和片面性.为了克服应急抢修方案的种种局限,笔者应用模糊综合评判方法建立了城市燃气管道事故应急抢修方案评价选择模型;考虑可靠性、抢修时间、事故损失、抢险费用、社会影响及政治影响等6类影响因素来评判抢修方案的优劣,可以科学合理地选择最佳的管道事故应急抢修方案,达到经济合理、快速可靠的目的;实例验证,评判模型对城市燃气管道事故抢险具有重要的现实意义和参考价值.     

城市天然气管道风险特征与肯特法的改进

根据城市高压天然气管道特点,将适合于城市天然气管道风险分析的肯特评分法加以改进,包括调整评分项目和事故因素权重,使其成为适于城市天然气管道的风险分析法。将改进后的肯特评分法应用于常州21km高压天然气管道的风险评价,得出8个相对高风险管段,其分析结果可作为安全管理人员合理分配维护资源的理论依据。工程应用实例证明:改进后的肯特法具有较强的可行性,是城市高压天然气管道风险评估的有效工具。     

煤与瓦斯突出的物理模拟和数值模拟研究

利用自行设计的实验装置,通过现场采集具有突出倾向的煤样,分别向实验装置煤样中充入吸附能力较大的CO2和吸附能力较小的N2来模拟不同级别的煤与瓦斯突出现象,物理试验结果表明:瓦斯压力越大,突出强度越大;当瓦斯压力相近时,吸附和解吸能力大的瓦斯突出强度大。通过数值模拟对煤与瓦斯突出进行研究,数值模拟再现了煤矿开采过程中诱发的煤与瓦斯突出全过程,同时验证了煤与瓦斯突出是瓦斯压力、地应力及煤岩体的力学性质综合作用的结果,该验证对进一步深入理解认识煤与瓦斯突出的机理具有重要的理论和实践意义。     

烟气脱硝技术及在我国的应用

氮氧化物气体是危害最大、最难处理的大气污染物之一。随着经济的发展,有效控制燃煤造成的大气污染已经刻不容缓,特别是控制燃煤过程中的氮氧化物,烟气脱硝技术显得相当重要。本文分析了几种常用的烟气脱硝技术（选择性催化还原脱硝技术、选择性非催化还原脱硝技术、碱性溶液吸收法和等离子体活化法等）的原理、技术特点以及在我国的应用情况。     

Sorption of polar and nonpolar organic contaminants by oil-contaminated soil

Sorption of nonpolar (phenanthrene and butylate) and polar (atrazine and diuron) organic chemicals to oil-contaminated soil was examined to investigate oil effects on sorption of organic chemicals and to derive oil–water distribution coefficients (K_oil). The resulting oil-contaminated soil–water distribution coefficients (K_d) for phenanthrene demonstrated sorption-enhancing effects at both lower and higher oil concentrations (C_oil) but sorption-reducing (competitive) effects at intermediate C_oil (approximately 1 g kg⁻¹). Rationalization of the different dominant effects was attempted in terms of the relative aliphatic carbon content which determines the accessibility of the aromatic cores to phenanthrene. Little or no competitive effect occurred for butylate because its sorption was dominated by partitioning. For atrazine and diuron, the changes in K_d at C_oil above approximately 1 g kg⁻¹ were negligible, indicating that the presently investigated oil has little or no effect on the two tested compounds even though the polarity of the oil is much less than soil organic matter (SOM). Therefore, specific interactions with the active groups (aromatic and polar domains) are dominantly responsible for the sorption of polar sorbates, and thus their sorption is controlled by available sorption sites. This study showed that the oil has the potential to be a dominant sorptive phase for nonpolar pollutants when compared to SOM, but hardly so for polar compounds. The results may aid in a better understanding of the role of the aliphatic and aromatic domains in sorption of nonpolar and polar organic pollutants.     

Evaluation of the temporal variations of air quality in Taipei City, Taiwan, from 1994 to 2003

Data collected from the five air-quality monitoring stations established by the Taiwan Environmental Protection Administration in Taipei City from 1994 to 2003 are analyzed to assess the temporal variations of air quality. Principal component analysis (PCA) is adopted to convert the original measuring pollutants into fewer independent components through linear combinations while still retaining the majority of the variance of the original data set. Two principal components (PCs) are retained together explaining 82.73% of the total variance. PC1, which represents primary pollutants such as CO, NO(x), and SO(2), shows an obvious decrease over the last 10 years. PC2, which represents secondary pollutants such as ozone, displays a yearly increase over the time period when a reduction of primary pollutants is obvious. In order to track down the control measures put forth by the authorities, 47 days of high PM(10) concentrations caused by transboundary transport have been eliminated in analyzing the long-term trend of PM(10) in Taipei City. The temporal variations over the past 10 years show that the moderate peak in O(3) demonstrates a significant upward trend even when the local primary pollutants have been well under control. Monthly variations of PC scores demonstrate that primary pollution is significant from January to April, while ozone increases from April to August. The results of the yearly variations of PC scores show that PM(10) has gradually shifted from a strong correlation with PC1 during the early years to become more related to PC2 in recent years. This implies that after a reduction of primary pollutants, the proportion of secondary aerosols in PM(10) may increase. Thus, reducing the precursor concentrations of secondary aerosols will be an effective way to lower PM(10) concentrations.