Quantitation of Hydroxyl Radicals from Photolysis of Fe(III)-Citrate Complexes in Aerobic Water (5 pp)

Background For their high photoreactivity, Fe(III)-carboxylate complexes are important sources of H2O2 for some atmospheric and surface waters. Citrate is one kind of carboxylate, which can form complexes with Fe(III). In our previous study, we have applied Fe(III)-citrate complexes to degrade and decolorize dyes in aqueous solutions both under UV light and sunlight. Results have shown that carboxylic acids can promote the photodegradation efficiency. It is indicated that the photolysis of Fe(III)-citrate complexes may cause the formation of some reactive species (e. g. H2O2 and ·OH). This work is attempted to quantify hydroxyl radicals generated in the aqueous solution containing Fe(III)-citrate complexes and to interpret the photoreactivity of Fe(III)-citrate complexes for degrading organic compounds. Methods By using benzene as the scavenger to produce phenol, the photogeneration of ·OH in the aqueous solution containing Fe (III)-citrate complexes was determined by HPLC. Results and Discussion In the aqueous solution containing 60.0/30.0 mM Fe(III)/citrate and 7.0 mM benzene at pH 3.0, 96.66 mM ·OH was produced after irradiation by a 250W metal halide light (l ≥ 313 nm) for 160 minutes. Effects of initial pH value and concentrations of Fe(III) and citrate on ·OH radical generation were all examined. The results show that the greatest photoproduction of ·OH in the aqueous solution (pH ranged from 3.0 to 7.0) was at pH 3.0. The photoproduction of ·OH increased with increasing Fe(III) or citrate concentrations. Conclusion In the aqueous solutions containing Fe(III)-citrate complexes, ·OH radicals were produced after irradiation by a 250W metal halide light. It can be concluded that Fe(III)-citrate complexes are important sources of ·OH radicals for some atmospheric and surface waters. Recommendations and Outlook It is believed that the photolysis of Fe(III)-citrate complexes in the presence of oxygen play an important role in producing ·OH both in atmospheric waters and surface water where high concentrations of ferric ions and citrate ions exist. The photoproduction of ·OH has a high oxidizing potential for the degradation of a wide variety of natural and anthropogenic organic and inorganic substances. We can use this method for toxic organic pollutants such as organic dyes and pesticides.     

Determination and impact of volatile organics emitted during rush hours in the ambient air around gasoline stations

This study analyzes the volatile organic compounds (VOCs) in the ambient air around gasoline stations during rush hours and assesses their impact on human health. Results from this study clearly indicate that methyl tertiary butyl ether (MTBE), toluene, and isobutane are the major VOCs emitted from gasoline stations. Moreover, the concentrations of MTBE and toluene in the ambient air near gasoline stations are remarkably higher than those sampled on surrounding roads, revealing that these compounds are mainly released from gasoline stations. The concentration of VOCs near the gasoline stations without vapor recovery systems are approximately 7.3 times higher than those around the gasoline stations having the recovery systems. An impact on individual health and air quality because of gasoline station emissions was done using Integrated Risk Information System and Industrial Source Complex Short Term model.     

Distribution and dissipation pathways of nonylphenol polyethoxylates in the Yellow River: Site investigation and lab-scale studies

Spatial distribution of nonylphenol polyethoxylates (NPEOs) and nonylphenol (NP) was investigated in a field study in Lanzhou Reach of the Yellow River. NPEOs and their metabolites were found in the river, with the maximum dissolved concentrations of 6.38 nmol/L for NPEOs, 0.19 nmol/L for nonylphenol ethoxy acetic acids (NPECs) and 0.79 nmol/L for NP, respectively. The maximum concentrations in the sediment and suspended particle samples were 1.50 and 5.09 nmol/g for NPEOs and NP, respectively. The effects of particles, light and microorganism on the dissipation of NPEOs in the river water were investigated based on lab-scale experiments. When natural particles were removed, 72% and 22% degradation of NPEOs were achieved at 120 h in non-sterile and sterile conditions with light, respectively. Different concentrations of NPECs were also observed in these experiments. When suspended particle matters (SPMs) were present, about 38-50% of NPEOs were sorbed to the particulate phase in only 1 h. As a result, the degradation of NPEOs and production of NPECs were inhibited. However, the combined sorption and degradation in the presence of SPMs resulted in lower dissolved NPEO concentrations than those in the absence of SPMs. Biodegradation was the most important pathway for NPEOs degradation in the river water, while NPECs seemed to be produced through both biological and abiological pathways.     

振动加载下转换型密封电磁继电器的性能退化行为研究

目的研究航空用继电器的失效机理。方法通过对电磁继电器进行振动与工作载荷单独施加以及二者综合加载情况下的试验方法及性能退化行为研究,实时监测继电器内部触点间接触电阻等性能参数的变化趋势,并对不同条件下触点表面的微观形貌进行对比分析。结果发现相比较工作载荷单独施加而言,振动应力的加入使得继电器的寿命大幅度降低,并使得触点表面呈现"雪花"一般的形貌。结论振动环境导致了触点之间电弧的变化,以及触点表面接触压力、接触面积和接触超程等,并通过燃弧时间和超程时间的变化趋势对其进行了验证。     

纳米Al_2O_3和Cd联合暴露对铜锈环棱螺体内Cd的生物积累和抗氧化酶活性的影响

金属氧化物纳米颗粒的广泛应用导致它们大量地释放到水环境中,其独特的理化性质有可能改变水环境中其他共存污染物(如重金属)的生态毒性。为评价沉积物中纳米氧化铝(Al2O3-NPs)对重金属Cd生态毒性的影响,采用底栖生物慢性暴露研究了Al2O3-NPs存在条件下Cd在底栖动物铜锈环棱螺体内生物积累的变化和Cd对肝胰脏抗氧化防御系统关键成分超氧化物歧化酶(SOD)与脂质过氧化指标丙二醛(MDA)以及Ⅱ相反应的关键酶谷胱甘肽-S-转移酶(GST)的影响。结果表明,低Cd浓度(5μg·g-1)时,Al2O3-NPs对Cd生物积累没有影响;中、高Cd浓度(25、100μg·g-1)时,Al2O3-NPs显著促进Cd的生物积累,Al2O3-NPs对Cd的生物转运具有明显的携带效应。低Cd浓度时,无Al2O3-NPs处理组和Al2O3-NPs处理组的SOD活性与对照组相比均没有显著差异;中Cd浓度时,SOD活性显著升高,而高Cd浓度时,SOD活性显著下降,而且Al2O3-NPs处理组的SOD活性显著低于无Al2O3-NPs处理组,Al2O3-NPs的存在加重了Cd对肝胰脏细胞的氧化胁迫或损伤。高Cd浓度时,无Al2O3-NPs处理组和Al2O3-NPs处理组的MDA水平均显著升高,但Al2O3-NPs处理组的MDA水平显著低于无Al2O3-NPs处理组,进一步证明Al2O3-NPs对Cd氧化损伤的增强作用。中、高Cd浓度时,无Al2O3-NPs处理组和Al2O3-NPs处理组的GST活性均显著下降,但Al2O3-NPs处理组的GST活性均显著低于无Al2O3-NPs处理组,同样说明了Al2O3-NPs对Cd毒性的增强作用。本研究提供了在沉积物-底栖动物体系中Al2O3-NPs促进重金属生物积累的证据,而且Cd毒性的变化与肝胰脏中Cd的生物积累水平的变化基本一致,在中、高Cd浓度下,由于Al2O3-NPs的存在显著促进了Cd的生物积累,因而增强了Cd对铜锈环棱螺的生态毒性。     

五十年的辉煌--西部防震减灾学术研讨会暨兰州观象台建台50周年纪念大会侧记

繁忙中蕴含着秩序,开拓中孕育着希望。金风送爽之际,一个地震系统的盛会——西部防震减灾学术研讨会暨兰州观象台建台50周年纪念大会吸引了众多国内外地学界领导,著名专家学者,联合国禁核组织及媒体的关注。     

基于控制网络的输送机运行故障智能诊断

对煤矿井下胶带输送机运行过程中容易出现的故障,在计算机监控系统的基础上,研究了智能化的检测和判断方法。与传统的胶带机综合保护系统相比,减少了误报和漏报现象,既提高了故障诊断的可信度,又提高了胶带机运行的效率和可靠性。     

循环流化床烟气悬浮脱硫技术中试及机理分析

设计了新的循环流化床烟气悬浮脱硫中试装置,其烟气处理量达3500m³/h.首先进行了进料钙硫比(Ca/S)、过饱和温度对装置脱硫效率影响实验,进一步研究了脱硫塔内固体颗粒物循环和烟气流速等因素对脱硫装置性能的影响.对比实验研究表明:在Ca/S=1.2时,固体颗粒物的循环使系统脱硫效率提高15% 左右;脱硫塔内烟气设计流速可以偏高一些.本文同时对系统脱硫过程进行了机理分析,指出了延长脱硫剂有效停留时间的途径.     

生态系统健康与环境管理

环境管理和生态系统健康是密不可分的,生态系统健康是环境管理的目的,生态系统健康为环境管理提供了新的思路、新的方法,健康的生态系统为实现区域可持续发展提供技术支撑和发展基础.生态系统健康的发展演替过程是优化环境管理的步骤.优化的环境管理为生态系统健康发展提供宏观决策和社会经济保障.本文从学科发展的角度论述了生态系统健康产生的背景、理论基础和应用途径;从学科交叉的角度论述了生态系统健康的评价和与环境管理的关系.提出了环境管理的目标:健康的生态系统→健康的环境→健康的食品→健康的人类生态系统→健康的社会发展.     

乙虫腈悬浮剂对新出房意大利蜜蜂的毒性研究

乙虫腈是在我国登记并广泛使用的氟虫腈替代药剂,其商品化制剂为拜尔公司研发的100 g·L~(-1)悬浮剂,目前关于乙虫腈制剂对非靶标生物的毒性研究少有报道。为探究乙虫腈制剂对蜜蜂的毒性作用,采用人工饲喂法分别测定了100 g·L~(-1)乙虫腈悬浮剂对新出房意大利蜜蜂的48 h急性和14 d慢性毒性作用。结果显示:乙虫腈悬浮剂对新出房意大利蜜蜂的48 hLC_(50)值为0.21 mg·L~(-1)(95%置信限0.16～0.26 mg·L~(-1)),相应的48 h-LD50为5.0×10~(-3)μg a.i.·蜂~(-1)(95%置信限1.0×10~(-3)～1.0×10~(-2)μg a.i.·蜂~(-1));在亚致死剂量下,蜜蜂死亡数量随暴露时间的延长而增多,且100 g·L~(-1)乙虫腈悬浮剂会引起蜜蜂显著的氧化应激反应,诱导抗氧化酶SOD和CAT活力、脂质过氧化产物MDA含量、解毒酶GST活力和底物GSH含量的显著变化。研究表明,乙虫腈悬浮剂对意大利蜜蜂毒性较高,即使在亚致死剂量下亦存在显著的影响。田间施用应防止药剂的漂移污染,并避免在作物花期施用;新出房意大利蜜蜂对药剂敏感,未来可探索其作为风险指示生物应用的可能。