活性碳纤维改性技术研究进展

介绍了活性碳纤维(ACF)的孔结构及表面官能团,综述了国内外ACF改性技术的研究现状.ACF的改性主要包括孔结构调控和表面化学改性,表面化学改性包括氧化还原法、表面负载法、浸渍法、热处理法、远程等离子体处理法、微波辐照法等,也可将多种方法结合来对ACF进行改性,以改善和提高ACF的吸附性能.在总结现有研究的基础上,对ACF改性技术发展趋势进行了展望.     

环境中VOCs的污染现状及处理技术研究进展

综述了近十年来大气环境中挥发性有机物(VOcs)的污染现状及其主要处理技术的研究进展.介绍了目前大气环境中VOCs的主要处理技术(包括吸附、冷凝及膜分离等回收技术和燃烧、等离子体、光催化降解和生物降解等销毁技术)的适用条件、经济性、可操作性和净化效率.提出要对VOCs的吸收和生物降解的反应动力学模型、催化机制、材料的性能及微生物活性进行深入研究的建议.     

高活性萘降解细菌Hydrogenophaga Palleronii LHJ38的研究

为了研究微生物对多环芳烃的降解和转化规律,以萘作为研究对象,从餐厨油烟污染土壤中筛选到一株萘降解活性较高的细菌菌株,经菌种鉴定,定名为帕氏氢噬胞菌(H ydrogenophaga Palleronii)LH J38。测定了该菌的生长曲线和萘降解曲线,建立了菌株对萘的降解活性的定量测定方法,并研究了其最适生长条件。结果表明,在28℃、初始pH6.6、碳氮摩尔比为4的最适培养条件下,LH J38对初始质量浓度为2 000m g/L的萘在96h内的降解率可达98%以上;处于对数生长期的LH J38对萘的降解活性可达47.3nm o l/(m g.m in)。     

不同耐性作物中几种酶活性对Cd胁迫的反应

为探讨作物对重金属毒害的耐受机理,本文采用盆栽试验及生理生化分析方法,研究了作物体内酶系统在耐受Cd胁迫中的作用。结果表明,在Cd胁迫下,耐性作物体内,SOD和PPO的活性未受明显影响或活性略增强,CAT活性明显增强;POD及硝酸还原酶活性的变化无明显规律。这说明,SOD、CAT和PPO活性的维持和提高是作物耐受Cd胁迫的物质基础之一。     

Effects of metal cations on sorption-desorption of p-nitrophenol onto wheat ash

The mutual e ects of metal cations (Cu2+, Pb2+, Zn2+, and Cd2+) and p-nitrophenol (NP) on their adsorption desorption behavior onto wheat ash were studied. Results suggested that Cu2+, Pb2+, and Zn2+ diminished the adsorption and increased the desorption of NP remarkably, while Cd2+ had no such e ect. In contrast, NP diminished the adsorption of Cu2+, Pb2+, and Zn2+ onto ash, however, this suppression e ect depended on the initial concentrations of metal cations. NP had no e ect on Cd2+ adsorption on ash. Fourier transform infrared (FT-IR) and X-ray absorption spectroscopic (XAS) studies suggested the following mechanisms responsible for the metal suppression e ect on NP adsorption: (1) large hydrated Cu2+, Pb2+, and Zn2+ shells occupied the surface of ash and prevent nonspecific adsorption of NP onto ash surface; (2) Cu2+, Pb2+, and Zn2+ may block the micropores of ash, resulting in decreased adsorption of NP; (3) complexation of Cu2+, Pb2+, and Zn2+ was likely via carboxyl, hydroxylic and phenolic groups of wheat ash and these same groups may also react with NP during adsorption. As a “soft acid”, Cd2+ is less e cient in the complexation of oxygencontaining acid groups than Cu2+, Pb2+, and Zn2+. Thus, Cd2+ had no e ect on the adsorption of NP on wheat ash.     

Ambient volatile organic compounds at a receptor site in the Pearl River Delta region: Variations, source apportionment and effects on ozone formation

We present the continuously measurements of volatile organic compounds（VOCs） at a receptor site（Wan Qing Sha, WQS） in the Pearl River Delta（PRD） region from September to November of 2017. The average mixing ratios of total VOCs（TVOCs） was 36.3 ± 27.9 ppbv with the dominant contribution from alkanes（55.5%）, followed by aromatics（33.3%）. The diurnal variation of TVOCs showed a strong photochemical consumption during daytime,resulting in the formation of ozone（O₃）. Five VOC sources were ...     

SRV菌去除电镀废水中铜的研究

为探索新的铜废水处理方法,更有效地治理铜废水造成的环境污染,用微生物及电镜法对SRV菌去除电镀废水中铜进行了研究。研究了菌量、铜离子浓度、溶液的pH值、作用的温度和时间等因素对SRV菌去除溶液中铜离子的影响。在菌废比1:1的情况下,对铜浓度为246.8mg/L的废水去除率达99.12％。观察了SRV菌处理铜废水前、后的扫描电镜、超薄切片透射电镜,推测其去除机制为铜与SRV菌代谢产物反应生成沉淀或直接被吸附于菌体表面而去除。     

苄·丁可湿性粉剂中丁草胺在稻田土壤和田水中残留动态

采用气相色谱法研究了35%苄·丁可湿性粉剂中丁草胺在2006年和2007年湖北省、广东省2年两地水稻田土壤和水中的残留降解动态和最终残留量.研究结果表明丁草胺在土壤和田水添加回收率分别为82.78%～93.20%和90.31%～93.51%.丁草胺在稻田土壤和田水中降解动态符合一级动力学指数模型,在湖北省和广东省水稻田土壤中的半衰期分别为3.21～3.83 d、2.49～3.66 d,水稻田水中的半衰期分别为1.20～1.66 d、1.13～1.48 d.861 g(a.i.)·hm-2和高剂量1 292 g(a.i.)·hm-2两个剂量施药后丁草胺在稻田土壤中的最终残留量为0.001 0～0.002 9 mg·kg-1.     

胚胎期和哺乳期全氟辛烷磺酸(PFOS)暴露致大鼠学习记忆能力下降

为了探讨全氟辛烷磺酸(PFOS)的发育神经毒性,寻找PFOS发育神经毒性作用的敏感期,利用水迷宫和组织病理切片技术,研究了胚胎期和哺乳期暴露于PFOS后新生大鼠发育情况、学习记忆能力、抓力以及海马组织病理学改变。结果显示：PFOS导致仔鼠发育迟缓,睁眼期延迟。仔鼠出生后体重与对照组相比出现显著性降低。同一PFOS暴露浓度下,胚胎期暴露组体重低于哺乳期暴露组,抓力差异不显著。水迷宫实验结果显示,TT15(胚胎期和哺乳期均暴露于15 mg·L^-1 PFOS)和TC15(仅胚胎期暴露于15 mg·L^-1 PFOS)暴露组仔鼠逃避潜伏期显著高于对照组,且TC15暴露组仔鼠逃避潜伏期显著性高于CT15(仅哺乳期暴露于15 mg·L^-1 PFOS)暴露组。空间探索实验中,TT15暴露组仔鼠在目标象限的游泳时间显著性低于对照组,其他组无显著性差异。组织病理切片结果显示暴露组海马组织细胞数量减少,出现细胞凋亡现象。结果表明,PFOS造成仔鼠的发育延迟以及学习记忆能力下降的关键作用时期可能是胚胎期。     

A review of atmospheric mercury emissions,pollution and control in China

Mercury, as a global pollutant, has significant impacts on the environment and human health. The current state of atmospheric mercury emissions, pollution and control in China is comprehensively reviewed in this paper. With about 500-800 t of anthropogenic mercury emissions, China contributes 25%-40% to the global mercury emissions. The dominant mercury emission sources in China are coal combustion, non-ferrous metal smelting, cement production and iron and steel production. The mercury emissions from natural sources in China are equivalent to the anthropogenic mercury emissions. The atmospheric mercury concentration in China is about 2-10 times the background level of North Hemisphere. The mercury deposition fluxes in remote areas in China are usually in the range of 10-50μg·m^-2·yr^-1. To reduce mercury emissions, legislations have been enacted for power plants, non-ferrous metal smelters and waste incinerators. Currently mercury contented in the flue gas is mainly removed through existing air pollution control devices for sulfur dioxide, nitrogen oxides, and particles. Dedicated mercury control technologies are required in the future to further mitigate the mercury emissions in China.