重大危险源事故风险排序研究

本文将风险管理领域中风险排序的概念引入重大危险源安全管理中，提出了基于事故情景发生概率和造成死亡人数的风险评估和排序模型，并给出了基于统计分析的事故发生概率、基于死亡半径的死亡人数的确定方法。对某开发区的20个重大危险源进行了风险评估和排序，结果表明提出的方法对重大危险源的事故风险产生了明显的细分作用。研究成果对有关政府部门或企业确定重大危险源重点监察和管理的优先序，优化资源配置，提高管理效率具有一定的指导意义。     

大型城市重大危险源监管与应急救援体系的研究

分析大型城市重大危险源的现状,指出重大危险源监管存在的主要问题,提出大型城市重大危险源监管与应急救援体系包括的子系统,即:重大危险源的普查与辨识系统、重大危险源的安全评估系统、重大危险源的管理与控制系统、重大危险源事故的应急救援系统,并对其子系统的概念、构成和内容进行分析和阐述,提出了大型城市重大危险源监管与应急救援的思路、模式和对策。     

对重大危险源安全预警系统的探讨

阐述了安全预警技术和重大危险源安全预警系统的建立.重大危险源安全预警系统的建立,将对实现重大危险源安全监察工作信息化、科学化、现代化起到积极的推动作用.     

重大危险源辨识与监控是企业建立事故应急体系的基础

本文简要介绍了重大工业事故预防控制体系要素和国家法律、法规与政策对企业重大危险源监控与应急体系建设的要求,论述了重大危险源辨识、监控是企业建立事故应急体系和重大事故预防控制体系的基础和前提,对企业重大危险源监控和应急预案编制要求提出了建议.     

水专项"十三五"时期辽河流域水环境管理研究思路初探

以水专项在辽河流域实施的阶段性成果及辽河流域水环境管理现状为基础,分析"十三五"时期辽河流域水环境管理的需求,提出构建成套流域水环境管理技术体系和管理大平台、全面建设并优化水生态环境监测网络、实行水环境管理的动态调节机制和建立健全流域水环境管理长效机制的水环境管理研究思路,并指出研究应密切结合地方管理,充分发挥地方环境管理的责任主体地位,为水专项第三阶段"综合调控"战略目标的实现提供有力支撑.     

青藏高原淡水湖泊水化学组成特征及其演化

青藏高原淡水湖具有高生态价值和高脆弱性并存的特点.以海拔5 080 m±10 m的打加芒错湖水为研究对象,测试及分析了湖水化学组分,探讨了其主要离子来源、控制因子和湖泊水化学演化趋势.结果表明,湖水阳离子以Ca2+和Na+为主,阴离子以HCO3-为主,为HCO3-Ca型水;TDS为71.2～199.8 mg·L-1,矿化度低;受地表径流的稀释作用和富铝贫钙的地质背景约束湖区东南部水体的EC、Ca2+和HCO3-浓度均较低.湖水的Na+/(Na++Ca2+)为0.08～0.75,Cl-/(Cl-+HCO3-)为0.11～0.35,Ca/Na值为0.58,Mg/Ca值为0.12,HCO3/Na值为1.46,据Gibbs模型和元素化学计量分析表明,其化学组成主要受硅酸盐岩风化控制.湖区流域参与风化的矿物岩石包括斜长石(钙长石、钠长石)、钾长石、云母、石膏、盐岩等,但以斜长石风化为主,湖水的K/Na值平均为0.059,表明流域钾长石风化程度较低.湖水中方解石、白云石、石英、石膏等矿物饱和指数(SI)大于0,石盐的SI则小于0,揭示了青藏高原上淡水湖泊演变成咸水湖的变化趋势.     

石化企业危险化学品重大危险源风险评估

阐述了定量风险评价的个人风险和社会风险指标,并从前期准备、资料数据搜集、危险辨识、失效频率分析、失效后果分析、风险计算和风险评估等环节对某石化企业液化气一级重大危险源进行了定量风险评估。评估结果显示该重大危险源的个人风险和社会风险值基本符合安监总局40号令的要求。     

Leaching of styrene and other aromatic compounds in drinking water from PS bottles

Bottled water may not be safer, or healthier, than tap water. The present studies have proved that styrene and some other aromatic compounds leach continuously from polystyrene （PS） bottles used locally for packaging. Water sapmles in contact with PS were extracted by a preconcentration technique called as ＂purge and trap＂ and analysed by gas chromatograph-mass spectrometer （GC/MS）. Eleven aromatic compounds were identified in these studies. Maximum concentration of styrene in PS bottles was 29.5 μg/L. Apart from styrene, ethyl benzene, toluene and benzene were also quantified but their concentrations were much less than WHO guide line values. All other compounds were in traces. Quality of plastic and storage time were the major factor in leaching of styrene. Concentration of styrene was increased to 69.53 μg/L after one-year storage. In Styrofoam and PS cups studies, hot water was found to be contaminated with styrene and other aromatic compounds. It was observed that temperature played a major role in the leaching of styrene monomer from Styrofoam cups. Paper cups were found to be safe for hot drinks.     

Impacts of converting from leaded to unleaded gasoline on ambient lead concentrations in Jakarta metropolitan area

Total suspended particulate mater （TSP） concentrations were monitored for one year from July 2000 and for one year from April 2003 in Jakarta City. Thirteen elemental TSP components, aluminum （Al）, sodium （Na）, iron （Fe）, lead （Pb）, potassium （K）, zinc （Zn）, titanium （Ti）, manganese （Mn）, bromine （Br）, copper （Cu）, chromium （Cr）, nickel （Ni）, and vanadium （V） were analyzed by a sequential X-ray fluorescence spectrometer. Al, Na, Fe, K, and Pb were major components at most of the sampling locations in 2000. However, only Pb in 2003 dramatically decreased to one tenth. The phase-out of leaded gasoline began on July 1, 2001 in Jakarta City and lead content in gasoline decreased to one tenth, too. The decrease in Pb concentration was a result of the phase-out of leaded gasoline, as lead emissions mainly are exhaust gas from vehicles.     

Effects of metal cations on sorption-desorption of p-nitrophenol onto wheat ash

The mutual e ects of metal cations (Cu2+, Pb2+, Zn2+, and Cd2+) and p-nitrophenol (NP) on their adsorption desorption behavior onto wheat ash were studied. Results suggested that Cu2+, Pb2+, and Zn2+ diminished the adsorption and increased the desorption of NP remarkably, while Cd2+ had no such e ect. In contrast, NP diminished the adsorption of Cu2+, Pb2+, and Zn2+ onto ash, however, this suppression e ect depended on the initial concentrations of metal cations. NP had no e ect on Cd2+ adsorption on ash. Fourier transform infrared (FT-IR) and X-ray absorption spectroscopic (XAS) studies suggested the following mechanisms responsible for the metal suppression e ect on NP adsorption: (1) large hydrated Cu2+, Pb2+, and Zn2+ shells occupied the surface of ash and prevent nonspecific adsorption of NP onto ash surface; (2) Cu2+, Pb2+, and Zn2+ may block the micropores of ash, resulting in decreased adsorption of NP; (3) complexation of Cu2+, Pb2+, and Zn2+ was likely via carboxyl, hydroxylic and phenolic groups of wheat ash and these same groups may also react with NP during adsorption. As a “soft acid”, Cd2+ is less e cient in the complexation of oxygencontaining acid groups than Cu2+, Pb2+, and Zn2+. Thus, Cd2+ had no e ect on the adsorption of NP on wheat ash.