我国化学品安全技术说明书(SDS)的管理现状研究

从分析我国化学品安全技术说明书的监管现状出发,研究对比了我国和国外在SDS覆盖化学品的范围、审核监督制度以及信息保密机制等管理技术方面的不同做法;指出我国对化学品安全技术说明书的监管在这三方面存在缺陷和不足;提出加强和完善化学品安全技术说明书的监管是提高我国化学品安全监管水平的重要手段;认为借鉴欧盟、美国和加拿大等国家的先进做法拓宽需要编制SDS的化学品范围、建立化学品安全技术说明书第三方检测制度、加强监督、完善信息保密机制将对促进我国的化学品安全监管水平具有重要意义。     

《化工过程安全》双语教学课程的教材体系研究

在《化工过程安全》双语教学过程中,照搬使用国外教材不符合应用型本科院校学生的实际情况,达不到双语教学的预期效果。因此,根据笔者所在应用型本科院校安全工程专业学生的英语水平、专业知识基础及国外原版化工过程安全教材内容的广度与深度,对如何构建适合于应用型本科院校安全工程专业使用的《Chemical Process Safety》双语教材的知识体系进行了研究。形成的初步讲义在双语教学实践过程中取得了较好的效果,有望在继续修改后编印成一本适合于应用型本科院校安全工程专业学生使用的《Chemical Process Safety》英文讲义。     

危险化学品事故防控应急救援联动系统的开发与设计

通过采集和分析扬州区域所涉及化学品企业、危险化学品种类与分布、应急资源等相关信息,采用Access建立数据库,并基于Visual Basic平台开发和设计了危化品信息查询、危险源管理、地图信息查询、应急资源管理等计算机模型。在化学事故发生时,可通过该系统进行信息查询、提供可行的应急救援方案及资源配置,对化学事故进行快速有效的应急救援。江苏扬农化工在液氯泄漏应急演练时采用了该系统平台,实现了危化品信息的查询、应急救援方案的确定、应急资源的配置及应急方法等,为事故现场指挥部门的决策提供科学的和系统的依据。     

基于X3D技术的化学灾害事故处置在线培训系统

从消防部门处置化学灾害事故训练需求出发,采用基于Web的虚拟现实和智能组卷技术,设计并实现了一种化学灾害事故处置在线培训系统。按照化学危险品在储存、运输、生产环节中发生泄漏、燃烧和爆炸等事故类型进行分类,提供了危险源理化性质、事故特点及危害性分析、灭火救援行动措施等知识的在线学习和考试功能。在技术实现方面,采用互联网Web3D标准X3D技术,以三维方式模拟事故场景和表现知识内容,为用户提供了一个网络化、沉浸式的三维互动学习模式和环境。系统的设计和实现为化学灾害事故处置培训工作网络化、培训内容系统化、表现形式多样化提供了一种新的思路。     

危险化学品企业安全验收评价结论量化分析

为了使危险化学品企业安全验收评价结论更加准确、客观,根据安全验收评价结论编制的原则和相关导则,从法律法规符合性、外部安全条件、总平面布局及建筑结构、主要生产装置设施、主要储存装置设施、公用工程和辅助设施、安全管理及从业人员条件和应急救援等八个方面建立了安全验收评价结论定量评估指标体系。基于层次分析法确定各级指标权重,建立了安全验收评价结论定量评估模型。为方便对安全验收评价结论进行准确、快速地评估,利用EXCEL软件建立了安全验收评价结论定量评估系统。该评估模型和评估系统可以客观、快速、准确地对危险化学品企业安全验收评价结论进行定量评估。     

基于范例推理的灾害性地震应急物资需求预测研究

基于范例推理(CBR)理论,利用最近相邻法和粗糙集理论搜索相似度最高的主震历史范例,分析各主要物资需求量的影响因素,预测当前范例主震期应急物资需求量。通过序贯决策,采用马尔科夫预测模型预测余震类型,进而搜索余震历史范例,预测余震期应急物资需求量。以"玉树"地震为例,运用该方法估算地震发生后食物类、生活用品类、药品类、工程机械类的需求量。     

改进GM(1,1)模型在我国危险化学品事故预测中的应用

针对传统GM(1,1)模型建模方法存在偏差,当发展系数的绝对值较大时,模型偏差较大,无法用于中长期预测,甚至不能做短期预测等问题.从优化GM(1,1)背景值出发,通过提高背景值的构造精度,实现对传统GM(1,1)模型的改进,利用MATLAB软件编制高效的计算机程序,实现模型的模拟和预测,并将其应用于我国危险化学品事故起数及死亡人数预测.实例结果表明,改进GM(1,1)模型无论对变化平缓的低增长序列,还是变化急剧的高增长序列,都有较好的适应性,及更好的拟合和预测效果,为提高建模精度提供了新的途径.     

Solid phase extraction of trace metals from environmental samples using Amberlite XAD-7 loaded with 2-hydroxy-propiophenone-4-phenyl-3-thiosemicarbazone and determination by inductively coupled plasma–atomic emission spectrometry

A method for the solid phase extraction of trace metals, namely Co, Cu, Pb, Ni and Zn, from environmental and biological samples using column Amberlite XAD-7 loaded with 2-hydroxy-propiophenone-4-phenyl-3-thiosemicarbazone (HPPPTSC) and determination by inductively coupled spectrometry (ICP–AES) has been developed. The reagent has the capacity to form chelate complexes with the metals because of three binding sites in the reagent molecule. The optimum experimental conditions for the quantitative sorption of five metals, pH, effect of flow rate, concentration of eluent, sorption capacity and the effect of diverse ions on the preconcentration of analytes have been investigated. The sorption capacity of the resin has 83, 127, 35, 88 and 85?µmol?g^?1 for Co²⁺, Cu²⁺, Pb²⁺, Ni²⁺ and Zn²⁺, respectively. The preconcentration factors for Co²⁺, Cu²⁺, Pb²⁺, Ni²⁺ and Zn²⁺ were 100, 110, 120, 140 and 150, respectively. The accuracy of the proposed procedure was evaluated by standard reference materials. The achieved results were in good agreement with certified values. The proposed method was applied for the determination of trace metals in river water and plant leaves.     

Determination of Cd,Cr, Cu,Pb and Zn from various water samples with use of FAAS techniques after the solid phase extraction on rice bran

A facile and novel method has been developed for the determination of cadmium, chromium, copper, lead, and zinc from various water samples using FAAS. In the present investigation, a syringe was loaded with sorbent (rice bran) for the separation and enrichment of cadmium, chromium, copper, lead, and zinc, prior to their analysis by flame atomic absorption spectrometry which was described to substitute the batch and column techniques. The syringe was loaded with 2.0 g of sorbent in order to retain the analyte elements. Six milliliter of sample solution (pH 8.0 ± 0.2) was drawn into the syringe in 15 s and discharged over a period of 15 s. Then, 2.0 M HCl eluent was drawn into the syringe and ejected back to desorb the analyte elements. At the optimum conditions, the percentage recoveries of Cd, Cr, Cu, Pb, and Zn was in the range of 95.5–99.4% with SD of 0.10%. The elements could be concentrated by drawing and discharging several portions of sample successively. The detailed study of various interferences made the confirmation of the method highly selective. The risk of contamination is less than that with the column technique. The method was successfully applied for the determination of Cd, Cr, Cu, Pb, and Zn in spiked and natural water samples. The results obtained are in good agreement with the reported methods at the 95% confidence level.     

Genotoxic potential of organic extracts from municipal reclaimed water in Tianjin,China

Despite increasing pressure to make more efficient use of water resources, the widespread use of reclaimed water still remains a contentious issue, primarily because of risks to human health arising from water pollution by organic compounds. Therefore, safety evaluation of reclaimed water is an urgent need. The aim of this study was to determine the genotoxic potential of reclaimed water during low and high water periods. Reverse phase C-18 solid-phase extraction (RP-C18SPE) was used for the extraction of organic compounds from water samples. The tests, namely, Ames, micronucleus and chromosome aberrations were used to determine the damage caused by water samples on genetic material. Ames tests showed that both influent and effluent reclaimed water, except influent after metabolism by S9 in high water period, induced mutation of TA98 and TA100 strains of Salmonella typhimurium in a concentration-response manner. There were no significant differences in micronucleus and chromosome aberration tests. Even after treatment, reclaimed water in Tianjin still showed mutational effects and new strategies for reduction of genotoxins need to be considered.