构建城市公共安全应急决策参与机制的必要性和可行性

公共安全应急决策参与机制即是指政府以外的力量,包括媒体、非营利组织、社区、企业、市民和国际组织等多元主体有序地参与到公共安全应急决策程序之中,运用现代的信息与网络技术,为更高效、快捷地做出应急决策而形成的一个彼此依赖、共享权力的动态的自组织网络系统及其运行过程与方式.当今世界各国在应急管理中越来越多地吸纳来自政府外部的力量,因为有限政府原则要求应急管理主体的多元化,基于公开、直接参与的民主原则也要求应急管理主体的多元化;在全球化的今天,应急管理主体的多元化是不可违逆的趋势.在现代多元参与决策的主体网络系统中,虽然各个主体在空间上呈离散状态,分布在社会的各个角落,但是,他们能够通过彼此之间频繁互动而形成应急决策的整体合力,用动态的协作网络替代传统政府组织中机械、僵化的刚性组织层级.见下图:……     

海岸带含水层咸淡水界面随潮汐波动的数值模拟

在分析、研究了滨海地带含水层和不透水层的水文地质特性及含水层内的咸淡水渗流运动特征的基础上,运用数学推理的手法,建立了一种较为简单适用的模拟海岸带含水层咸淡水界面和天然地下水面变动规律的二维数学模型,通过该模型的计算值与实验值的比较,证明该模型的计算结果与实验结果有着非常好的拟合度,即该模型能较客观地揭示海水入侵引起的咸淡水界面的变化规律.其后,运用该模型系统的探讨了含水层以下为非平坦的不透水层的滨海地带天然地下水面、咸淡水界面伴随着潮汐的波动而变化的规律.即伴随着潮汐的波动,一方面天然地下水面和咸淡水界面与潮汐具有相似的振动波形,波动的幅度随离海岸距离的增加而减小.在海岸附近咸淡水界面的振幅大于天然地下水面的振幅,而在离开海岸一定距离后天然地下水面的振幅超过咸淡水界面的振幅.总体上天然地下水面的振幅呈负指数衰减,而咸淡水界面的振幅几乎呈直线衰减(其衰减直线的倾角在135～150 °之间变动),且潮汐波动对天然地下水面影响的范围远大于其对咸淡水界面的影响;另一方面天然地下水面和咸淡水界面波动的振幅及它们之间的相位差的大小还与天然地下水面的水力坡度、含水层的渗透系数、有效孔隙率、不透水层形状及其变动的幅度有关,但它们之间的相位差的大小与潮汐波动的幅度无关,其振幅与潮汐的振幅成比例增减.当不透水层的形状一定时,不论天然地下水面的水力坡度、含水层的渗透系数、有效孔隙率及潮汐波动的幅度怎么变动,天然地下水面、咸淡水界面振动的相位差的变化趋势及其峰值出现的位置几乎不变,即不透水层的形状决定着天然地下水面、咸淡水界面振动的相位差的变化趋势,而其大小与含水层的水文地质参数(水力坡度、渗透系数及有效孔隙率)密切相关.此外,当天然地下水面和咸淡水界面的振动存在相位和振幅的较大差异时,可以断定含水层以下存在非平坦的不透水层,且这种差异越大,不透水层凸凹不平的程度越高.     

三阶段温度控制堆肥接种法对有机氮变化规律的影响

利用原生生活垃圾,通过三阶段温度控制技术进行堆肥试验,探讨在堆肥过程中有机态氮组分的动态变化规律.结果表明,全氮、酸水解有机态氮、氨基酸态氮均在堆肥的前期呈明显的下降趋势,呈较好的相关性.与CK（对照组）处理相比,在堆肥的后期,三阶段温度控制堆肥酸水解有机态氮、氨基酸态氮、氨基糖态氮及酸解未知态氮含量呈不同程度的上升趋势,增加幅度依次为：10.67%、16.17%、7.17%、22.44%.表明三阶段温度控制技术能减少堆肥中氮素的损失,堆肥产品施入土壤后,可提高土壤的供氮潜力.     

Mn对超富集植物短毛蓼和水蓼生长、Mn吸收及氮素代谢的影响

采用水培的方法,研究了不同浓度Mn(0.0003、0.5、1、2、4、8 mmol · L^-1)对Mn超富集植物短毛蓼(Polygonum pubescens Blume)和水蓼(Polygonum hydropiper L.)叶片铵态氮、硝态氮、游离脯氨酸、可溶性蛋白质含量及氮素代谢关键酶:硝酸还原酶(NR)、谷氨酰胺合成酶(GS)、谷氨酸合酶(GOGAT)和谷氨酸脱氢酶(GDH)活性的影响.结果表明,随着Mn处理浓度的增加,短毛蓼和水蓼的根、茎、叶中Mn含量显著增加(p<0.05),在相同Mn处理浓度下短毛蓼中Mn含量均大于同部位水蓼中Mn含量.在Mn处理浓度小于1 mmol · L^-1时,Mn对短毛蓼的株高、株重影响不显著,但对水蓼的影响显著(p<0.05),表明短毛蓼比水蓼更耐Mn污染.Mn处理显著降低了短毛蓼硝态氮含量(p<0.05),提高了可溶性蛋白质含量,浓度为8 mmol · L^-1的Mn处理显著提高了水蓼硝态氮、铵态氮、可溶性蛋白质含量及短毛蓼、水蓼游离脯氨酸含量(p<0.05).Mn引起了短毛蓼和水蓼氮素代谢关键酶活性的变化,显著降低了水蓼叶片NR、短毛蓼叶片GS活性(p<0.05);在Mn处理浓度为1 mmol · L^-1时,短毛蓼叶片NR活性最高,为对照的1.91倍,而2、4、8 mmol · L^-1 Mn处理显著降低了短毛蓼和水蓼GOGAT活性(p<0.05).另外,Mn处理显著提高了短毛蓼和水蓼叶片GDH活性(p<0.05),在Mn处理浓度为8 mmol · L^-1时,短毛蓼、水蓼叶片GDH活性分别为对照的16.29倍和1.29倍.     

含信号控制人行横道的街道峡谷污染物扩散三维数值模拟

耦合微观交通仿真和机动车尾气排放模型,分别对含信号控制人行横道和不含信号控制人行横道的街道峡谷污染物排放进行计算,并以此为排放源,采用k-ε两方程模型与组分输运方程对风向与街道垂直时的污染扩散情况进行了三维数值模拟.结果表明,k-ε两方程模型与组分输运方程可以较好地模拟风向与街道垂直时三维街道峡谷内的污染物扩散情况.峡...     

Effect of platinum on the photocatalytic degradation of chlorinated organic compound

TiO2 nanoparticles, doped with di erent Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO2, H2PtCl6 6H2O and methanol as the solvents. The physicochemical properties of Pt/TiO2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray di raction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO2 and Pt/TiO2 were evaluated. The average diameter and BET surface area of the TiO2 catalyst particles were 300 nm and 50 m2/g, respectively. The degradation e ciency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation e ciency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO2 process was capable of e ciently decomposing gaseous DCM in air.     

Competition of bloom-forming marine phytoplankton at low nutrient concentrations

Competition of three bloom-forming marine phytoplankton (diatom Skeletonema costatum, and dinoflagellates Prorocentrum minimum and Alexandrium tamarense) was studied through a series of multispecies cultures with di erent nitrate (NaNO3) and phosphate (NaH2PO4) levels and excess silicate to interpret red tide algae succession. S. costatum outgrew the other two dinoflagellates in nitrate and phosphate replete cultures with 10 mol/L Na2SiO3. Under nitrate limited (8.82 mol/L NaNO3) conditions, the growth of S. costatum was also dominant when phosphate concentrations were from 3.6 to 108 mol/L. Cell density of the two dinoflagellates only increased slightly, to less than 400 and 600 cells/mL, respectively. Cell density of S. costatum decreased with time before day 12, and then increased to 4000 cells/mL (1.5 mg/L dry biomass) at NaNO3 concentrations between 88.2 and 882 mol/L with limited phosphate (0.36 mol/L NaH2PO4) levels. In addition, P. minimum grew well with a maximal cell density of 1690–2100 cells/mL (0.5–0.6 mg/L dry biomass). Although S. costatum initially grew fast, its cell density decreased quickly with time later in the growth phase and the two dinoflagellates were dominant under the nitrate-limited and high nitrate conditions with limited phosphate. These results indicated that the diatom was a poor competitor compared to the two dinoflagellates under limited phosphate; however, it grew well under limited nitrate when growth of the dinoflagellates was near detection limits.     

Resistance and biosorption mechanism of silver ions by Bacillus cereus biomass

Biosorption of silver ions onto Bacillus cereus biomass was investigated. Overall kinetic experiments were performed for the determination of the necessary contact time for the attainment of equilibrium. It was found that the overall biosorption process was best described by pseudo second-order kinetic model. The crystals detected by scanning electron microscope and X-ray photoelectron spectroscopy suggested the precipitation was a possible mechanism of biosorption. The molecular genetics of silver resistance of B. cereus biomass was also detected and illustrated by a whole cell sensor tool.     

Adsorptive property of Cu^2＋-loaded montmorillonite clays for Escherichia coli K_（88） in vitro

The Cu²⁺-loaded montmorillonite clays (MMT-Cu) may be a good material for the adsorbed and eliminated pathogenic bacteria from aqueous solution.     

Reversibly enhanced aqueous solubilization of volatile organic compounds using a redox-reversible surfactant

Surfactant-enhanced remediation (SER) is an effective method for the removal of volatile organic compounds (VOCs) from contaminated soils and groundwater. To reuse the surfactant the VOCs must be separated from the surfactant solutions. The water solubility of VOCs can be enhanced using reversible surfactants with a redox-acive group, (ferrocenylmethyl)dodecyldimethylammonium bromide (Fcl2) and (ferrocenylmethyl)tetradecanedimethylammonium bromide (Fcl4), above and below their critical micelle concentrations (CMC) under reducing (I⁺) and oxidative (I²⁺) conditions. The CMC values of Fcl2 and Fcl4 in I⁺ are 0.94 and 0.56 mmol/L and the solubilization of toluene by Fcl2 and Fcl4 in I⁺ for toluene is higher than the solubilization achieved with sodium dodecyl sulfate, cetyltrimethylammonium bromide and Trition X-114. The solubilization capacity of the ferrocenyl surfactants for each tested VOCs ranked as follows: ethylbenzene > toluene > benzene. The solubilities of VOCs by reversible surfactant in I⁺ were 30% higher than those in I²⁺ at comparable surfactant concentrations. The effects of Fcl4 concentrations on VOCs removal efficiency were as follows: benzene > toluene > ethylbenzene. However, an improved removal efficiency was achieved at low ferrocenyl surfactant concentrations. Furthermore, the reversible surfactant could be recycled through chemical approaches to remove organic pollutants, which could significantly reduce the operating costs of SER technology.