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.     

A strategy for aromatic hydrocarbon bioremediation under anaerobic conditions and the impacts of ethanol: a microcosm study

Increased use of ethanol-blended gasoline (gasohol) and its potential release into the subsurface have spurred interest in studying the biodegradation of and interactions between ethanol and gasoline components such as benzene, toluene, ethylbenzene and xylene isomers (BTEX) in groundwater plumes. The preferred substrate status and the high biological oxygen demand (BOD) posed by ethanol and its biodegradation products suggests that anaerobic electron acceptors (EAs) will be required to support in situ bioremediation of BTEX. To develop a strategy for aromatic hydrocarbon bioremediation and to understand the impacts of ethanol on BTEX biodegradation under strictly anaerobic conditions, a microcosm experiment was conducted using pristine aquifer sand and groundwater obtained from Canadian Forces Base Borden, Canada. The initial electron accepter pool included nitrate, sulfate and/or ferric iron. The microcosms typically contained 400 g of sediment, 600 approximately 800 ml of groundwater, and with differing EAs added, and were run under anaerobic conditions. Ethanol was added to some at concentrations of 500 and 5000 mg/L. Trends for biodegradation of aromatic hydrocarbons for the Borden aquifer material were first developed in the absence of ethanol, The results showed that indigenous microorganisms could degrade all aromatic hydrocarbons (BTEX and trimethylbenzene isomers-TMB) under nitrate- and ferric iron-combined conditions, but not under sulfate-reducing conditions. Toluene, ethylbenzene and m/p-xylene were biodegraded under denitrifying conditions. However, the persistence of benzene indicated that enhancing denitrification alone was insufficient. Both benzene and o-xylene biodegraded significantly under iron-reducing conditions, but only after denitrification had removed other aromatics. For the trimethylbenzene isomers, 1,3,5-TMB biodegradation was found under denitrifying and then iron-reducing conditions. Biodegradation of 1,2,3-TMB or 1,2,4-TMB was slower under iron-reducing conditions. This study suggests that addition of excess ferric iron combined with limited nitrate has promise for in situ bioremediation of BTEX and TMB in the Borden aquifer and possibly for other sites contaminated by hydrocarbons. This study is the first to report 1,2,3-TMB biodegradation under strictly anaerobic condition. With the addition of 500 mg/L ethanol but without EA addition, ethanol and its main intermediate, acetate, were quickly biodegraded within 41 d with methane as a major product. Ethanol initially present at 5000 mg/L without EA addition declined slowly with the persistence of unidentified volatile fatty acids, likely propionate and butyrate, but less methane. In contrast, all ethanol disappeared with repeated additions of either nitrate or ferric iron, but acetate and unidentified intermediates persisted under iron-enhanced conditions. With the addition of 500 mg/L ethanol and nitrate, only minor toluene biodegradation was observed under denitrifying conditions and only after ethanol and acetate were utilized. The higher ethanol concentration (5000 mg/L) essentially shut down BTEX biodegradation likely due to high EA demand provided by ethanol and its intermediates. The negative findings for anaerobic BTEX biodegradation in the presence of ethanol and/or its biodegradation products are in contrast to recent research reported by Da Silva et al. [Da Silva, M.L.B., Ruiz-Aguilar, G.M.L., Alvarez, P.J.J., 2005. Enhanced anaerobic biodegradation of BTEX-ethanol mixtures in aquifer columns amended with sulfate, chelated ferric iron or nitrate. Biodegradation. 16, 105-114]. Our results suggest that the apparent conservation of high residual labile carbon as biodegradation products such as acetate makes natural attenuation of aromatics less effective, and makes subsequent addition of EAs to promote in situ BTEX biodegradation problematic.     

石化企业事故应急预案中的安全防护距离探讨

对石化企业在事故应急预案中安全防护距离的确定给出了各种可以参考的计算方法及参考数据,为企业在事故应急中合理确定安全防护距离提供了决策参考。     

城市综合防灾与公共安全规划编制

本文介绍了城市综合防灾与公共安全规划编制的指导思想与原则,对城市面临灾害及研究对象层次进行了分类,对城市综合防灾与公共安全规划框架体系进行了探讨,对影响城市的主要灾害提出了防御标准和目标,对城市综合防灾与公共安全防灾保障体系进行了讨论。     

煤矿作业人员防护服装的设计研究

煤矿井下作业人员的防护服装对生产的安全、高效有一定的保障作用.本文在调查和分析了井下作业的环境条件、主要工作内容和动作的基础上,对煤矿井下作业人员的防护服装面料的性能要求和设计要点进行了系统的分析.提出了具体的设计方案.本研究的结果可以为此类功能服装的设计与生产提供参考和借鉴.     

警用头盔的人机工程学分析

警用头盔是武警部队使用最为频繁的单兵防护用具,本文基于人机工程学的理论,用人机工程学的观点对武警部队现装备的警用头盔进行分析和探讨,提出解决途径的设想,展望警用头盔的发展前景。     

Variations of metal distribution in sewage sludge composting

In the study, the variations of heavy metal distributions (of Cu, Mn, Pb, and Zn) during the sewage sludge composting process were investigated by sequential extraction procedures. The total content of Cu and Zn in the composted mixture increased after the composting process. Mn and Zn were mainly found in mobile fractions (exchangeable fraction (F1), carbonate fraction (F2), and Fe/Mn oxide fraction (F3)). Cu and Pb were strongly associated with the stable fractions (organic matter/sulfides fraction (F4) and residual fraction (F5)). These five metal fractions were used to calculate the metal mobility (bioavailability) in the sewage sludge and composted mixture. The mobility (bioavailability) of Mn, Pb, and Zn (but not Cu) increased during the composting process. The metal mobility in the composted mixture ranked in the following order: Mn>Zn>Pb>Cu.     

中美新化学物质管理制度的比较

简要叙述了中美两国新化学物质管理的基本情况,分别从管理原则、管理范围、管理具体要求、申报种类、评审程序、监督管理等方面重点论述了中美新化学物质管理制度的特点。通过借鉴美国新化学物质管理的优点及经验,提出了强化和完善中国新化学物质管理制度的对策。     

Enhancement of solubilization and acidification of waste activated sludge by pretreatment

The effects of various pretreatment methods, including thermo-acid, thermo-alkaline, ultrasonic-alkaline and ultrasonic-acid, on solubilization and subsequent acidification efficiency of waste activated sludge (WAS) were investigated. The results showed that both thermo-alkaline and ultrasonic-alkaline significantly improved the solubilization of WAS at a high concentration (7.4% of total solids). Solubilization of volatile solids (VS) and crude protein was 60.2-61.6% and 66.8-67.5%, respectively. Thermo-alkaline or ultrasonic-alkaline pretreatment also enhanced the efficiency of subsequent WAS acidification. Experimental results showed that they had similar effects on the acidification of WAS. The conversion ratio from VS to total volatile fatty acids (TVFAs) was 0.230 in the case of the ultrasonic-alkaline pretreatment. Through this pretreatment, the level of TVFAs was 68% more than the untreated WAS after 252 h of fermentation. The mechanism of TVFAs production under different pretreatment methods was further investigated and the results indicated that soluble protein was the main substrate for TVFAs production from the WAS after the thermo-alkaline or ultrasonic-alkaline pretreatment.