我国南方冰雪灾害的特征与城市救灾对策研究

在对2008年初中国南方所发生的冰雪灾害的损失、影响和成因进行分析的基础上,指出该次灾害具有受灾范围的全面性、灾害过程的发展性和救灾行动的艰难性等特征,阐明冰雪灾害在城市会造成停电停水、交通瘫痪和通讯中断等严重灾情,进而引发断油断粮、物价飞涨和人心恐慌等综合性灾害。通过冰雪灾害对城市救灾行动的总结,指出冰雪灾害给城市政府的深刻启示在于城市规模的急速扩张必须同时加强防灾救灾的软硬件建设,并提出城市必须采取持久开展防灾救灾知识宜传教育、大力加强防灾救灾基础设施建设、科学制订各类灾害的专业性应急预案和努力构建协同联动救灾机制等对策,有效提升城市应对灾害的能力,减少灾害造成的损失。     

细水雾中雾滴和高温环境的热质交换研究

由雾滴的表面的组分方程和能量方程入手,探讨雾滴在静止的高温环境中的热质交换及生存时间。应用折算薄膜理论,通过特征时间的比较,提出雾滴与高温环境主要通过沸腾机制实现热质交换;考虑滴径与速度变化的耦合作用,应用数值方法研究雾滴在强迫对流环境中与高温环境的热质交换情况。结果表明:对于滴径较小的雾滴不可能达到火焰区或可燃物表面实施火焰冷却和表面冷却,其灭火作用主要依赖于汽化吸热。     

省域高速公路交通应急救援联动机制探讨

在系统分析省域高速公路应急救援组织体系存在问题的基础上,通过广泛调研和系统研究,结合我国国情,提出省域高速公路交通应急救援的组织指挥体系、可靠联动模式、运行机制、联动保障、技术路线等方案与措施。建立了基于领导机构、办事机构、工作机构、专家组4个层次的救援组织指挥体系,构建了高速公路交通应急救援的协调管理的基本机制,设计了对应协调管理基本机制的联动处置流程,并提出建设先进的高速公路交通应急救援调度信息中心的具体内容,为建立高效、稳健的高速公路交通应急救援组织体系与联动机制提供科学依据。该方案与措施有助于统一协调指挥多个救援部门之间的工作,实现救援部门之间的信息共享,确保交通应急救援调度和协调管理工作的顺利实施。     

日本工伤事故瞒报问题的原因及对策分析

从经济全球化引发的雇用形态的变化入手,分析日本工伤事故瞒报问题的原因;针对已有的事故瞒报手法及危害,介绍对其防范、发现和处治的主要措施;通过对比分析中日两国事故瞒报防范工作的特点,提出更有利于事故控制预防、更有效地解决我国工伤事故瞒报问题的重要思路,即:在加大对事故瞒报单位的惩治力度、提高其违法成本的同时,还应建立针对依法报告事故单位的不惩罚机制或制定降低依法报告事故后的被处罚成本方面的规定;在行政责任追究和领导绩效考核时,不仅仅以事故后果或事故多少而是以其在强化安全管理方面"作为"与否为更重要的根据来进行。     

臭氧生物活性炭有机物吸附与生物降解量化分析

以西安北石桥污水净化中心出水为研究对象,通过对臭氧-生物陶粒与臭氧-生物活性炭处理工艺的对比研究,分析比较了两种生物过滤系统的生物活性及有机物去除特性,建立了臭氧-生物活性炭工艺在有机物降解过程中吸附和生物降解作用的量化计算方法,探讨了臭氧-生物活性炭工艺有机物降解过程及去除机理.研究表明:臭氧-生物活性炭工艺对有机物的去除是活性炭吸附和生物降解的协同作用,其中生物降解占主导作用,约占有机物总去除量的65%,生物降解作用去除的有机物几乎全部是易于降解的溶解性有机物;而吸附作用去除的有机物约占有机物总去除量的35%,去除的有机物中难降解和易于降解的有机物的量基本相当.     

锚喷粉尘受力及产尘机理分析

通过对锚喷粉尘的受力分析,基于粉尘颗粒的基本性质,运用牛顿运动规律、流体力学的紊流射流、两相流等相关理论,对锚喷产尘原因及运动规律研究,认为锚喷尘源产生的4种方式: 粉尘颗粒自身的特性及二次风流的影响,高速喷射气流带动周围的空气运动所产生的剪切作用,锚喷高速射流内部中团粒间的相互作用以及物料与受喷面的碰撞是影响锚喷产生粉尘的主要原因.     

过一硫酸盐的活化及其降解水中有机污染物机理的研究进展

基于活化过一硫酸盐（PMS）产生SO₄^-·的新型高级氧化技术,在芬顿和类芬顿催化降解水中有机污染物的研究中占有重要地位。本文从活化PMS方法的特点和用途出发,对目前活化PMS的主要方法进行了论述,并对活化PMS降解水中有机污染物的机理进行了探讨,最后对该领域研究中存在的问题进行了分析。指出,开发高效的协同活化PMS的方法将成为该领域研究的必然趋势。     

Bioavailability of bound residue derived from 14C-labeled chlorsulfuron in soil and its mechanism of phytotoxicity

The bioavailability of bound residue(BR) derived from ^14C-labeled chlorsulfuron in soil and effect of the main components of the BR on growth of rape( brassica napus) and rice( Oryza sativa L. ) were investigated. The results showed that the BR with the concentration of 0.28 and 0.56 nmol/g air-dried soil, which was calculated by special radioactivity of ^14C-labeled chlorsulfuron parent compound, resulted in significant depression effect on growth of rape seedling. It was assured that the main components(2-amino-4-methoxyl-6-methyl-1,3,5-triazine, 2-amino-4-hydroxyl-6-methyl-1,3,5-triazine, and 2-chloro-benzenesul-fonamide) of the BR did not inhibit the growth of rape and rice. LC-MS analysis demonstrated that the parent compound previously bound to the soil matrix could be again released and transformed into methanol-extractable residue during the course of rape growth. It was concluded that the molecular leading to the phytotoxicity to rape and rice in the BR is still the parent compound.     

Photodegradation mechanism of two dyes: the influence of adsorption behavior on the novel TiO2 particles

The relationship between adsorption behavior and photocatalytic mechanism of the two dyes was investigated. Adsorption isotherms showed that the adsorption of cationic pink FG was Langmuir type behavior, while the reactive brilliant red k-2G was Freundlich type behavior. The increasing pH favored the adsorption of FG but have little effect on the photodegradation. The increasing pH favored the adsorption and the photodegradation of k-2G. The presence of scavenger of hvb^ and OH. radical potassium iodide inhibited the degradation of k-2G, free radicals scavenger tetranitromethane inhibited the photodegradation of FG. These results indicated that the photodegradation of FG mainly via free radicals in solution, and the photodegradation of k-2G was mainly on the catalysts surface or near the interface of solid and solution by react with hvb^ and surface-bound OH.. The different effect of SO4^2- , HCO3^- on the adsorption and photodegradation of two dyes confirmed these results.     

A review of gas-phase chemical mechanisms commonly used in atmospheric chemistry modelling

The atmospheric chemical mechanism is an essential component of airshed models used for investigating the chemical behaviors and impacts of species. Since the first tropospheric chemical mechanism was proposed in the 1960s, various mechanisms including Master Chemical Mechanism (MCM), Carbon Bond Mechanism (CBM), Statewide Air Pollution Research Center (SAPRC) and Regional Atmospheric Chemistry Mechanism (RACM) have been developed for different research purposes. This work summarizes the development and applications of these mechanisms, introduces their compositions and lumping methods, and compares the ways the mechanisms treat radicals with box model simulations. CBM can reproduce urban pollution events with relatively low cost compared to SAPRC and RACM, whereas the chemical behaviors of radicals and the photochemical production of ozone are described in detail in RACM. The photolysis rates of some oxygenated compounds are low in SAPRC07, which may result in underestimation of radical levels. As an explicit chemical mechanism, MCM describes the chemical processes of primary pollutants and their oxidation products in detail. MCM can be used to investigate certain chemical processes; however, due to its large size, it is rarely used in regional model simulations. A box model case study showed that the chemical behavior of OH and HO₂ radicals and the production of ozone were well described by all mechanisms. CBM and SAPRC underestimated the radical levels for different chemical treatments, leading to low ozone production values in both cases. MCM and RACM are widely used in box model studies, while CBM and SAPRC are often selected in regional simulations.