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811.
饱和带有机污染物的厌氧反硝化微生物降解 总被引:4,自引:0,他引:4
以卤代烃和芳香烃为代表,通过室内实验模拟饱和带厌氧反硝化环境,对地下饱和带中有机污染物的厌氧反硝化可生物降解性,降解机理,降解动力学方程等进行了研究。实验结果表明,芳香烃较卤代烃易被微生物降解,在有低学葡萄糖存在时有 机物的最大生物降解速率C6H6:Lmax=17mg/(m^2.d),C7H8:Lmax=46mg/(m^2.d),CCl4;Lmax=7mg/(m^2.d),CHCl3:Lmax=6 相似文献
812.
813.
814.
多环芳烃(PAHs)化合物中的苯并[a]芘和PAHs暴露检测标志物1-羟基芘与心脏功能障碍有关,但其生物学机制尚不清楚。为研究苯并[a]芘和1-羟基芘对心脏的毒性作用,基于人胚胎干细胞分化心肌细胞(hESC-CM)研究了苯并[a]芘和1-羟基芘对心肌细胞活性氧(ROS)生成、CYP基因表达和DNA损伤等的影响。结果表明,苯并[a]芘和1-羟基芘对h ESC-CM活性无影响,但能显著增强细胞ROS水平,诱导DNA损伤。此外,苯并[a]芘还能诱导细胞线粒体促凋亡基因的表达。研究表明,苯并[a]芘和1-羟基芘能通过诱导氧化应激和DNA损伤事件导致h ESC-CM损伤,在一定程度上解释了多环芳烃暴露导致心脏疾病的分子机制。 相似文献
815.
Hongqi Wang Ruhan Jiang Dekang Kong Zili Liu Xiaoxiong Wu Jie Xu Yi Li 《Frontiers of Environmental Science & Engineering》2020,14(1):9
816.
817.
综述了用于大气颗粒物中多环芳烃(PAHs)源解析的主要定性、定量方法、并对其优缺点作了总结。比值法多用于定性解析,化学质量平衡法(CMB)要求源的成分谱较全面,而多元统计法则要求输入的数据较多。由于缺乏各污染源较完整的PAHs成分谱,且PAHs易发生化学反应,所以CMB法难以广泛推广,而多元统计法对源成分谱,且PAHs易发生化学反应,所以CMB法难以广泛推广,而多元统计不对源成分谱要求低,且不需要考虑PAHs的降解,因而具有推广价值。 相似文献
818.
利用活性炭固定床吸附分离表面活性剂和多环芳烃(PAH)的混合溶液,选取了具代表性的表面活性剂(TX100)和PAH(菲(PHE)等)。实验结果表明,流量越低、活性炭填充量越多、表面活性剂浓度越高、PAH浓度越低,越有利于表面活性剂的回收和PAH的去除。定义了有效回收时间,该时间是指PAH穿透10%的时间与表面活性剂穿透90%的时间之差,该时间越长,越有利于表面活性剂的回收。采用BDST和Thomas模型对TX100和PHE进行了吸附模拟,效果均较好;BDST模型拟合结果表明,当活性炭对TX100的吸附接近饱和时仍对PHE有较强的吸附能力。活性炭固定床吸附分离法可节约运行成本0.06元/L。 相似文献
819.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants entering into the environment through natural and anthropogenic activities. Owing to their toxicity to various life forms including humans, detoxification of PAHs is crucial to reduce their effects on cells. In this study, we have isolated two bacteria capable of degrading two common PAHs, anthracene and phenanthrene, from contaminated soil samples by using selective enrichment culture supplemented with test PAHs as the sole source of carbon and energy. The isolated bacteria were identified and affiliated as Pseudomonas aeruginosa strain KD and Stenotrophomonas maltophilia strain RC based on their 16s rRNA gene sequences. The degradation of anthracene and phenanthrene was estimated indirectly by measuring the decolourisation extent of a redox indicator, 2, 6-dichlorophenolindophenol, incorporated into PAH-supplemented mineral salt media. In the case of anthracene, ≥90% decolourisation was recorded at 20 and 48 days for P. aeruginosa and S. Maltophilia, respectively. On the other hand, ≥94% decolourisation was recorded at 56 and 52 days for P. aeruginosa and S. maltophilia, respectively during the utilisation of phenanthrene. 相似文献
820.
Kim KH Baek SO Choi YJ Sunwoo Y Jeon EC Hong JH 《Environmental monitoring and assessment》2006,118(1-3):407-422
In this study, concentrations of major aromatic VOCs were determined from landfill gas (LFG) at a total of five municipal
landfill sites in Korea including Nan Ji (NJ), Woon Jung (WJ), Sam Poong (SP), Hoei Chun (HC), and No Hyung (NH). The concentration
levels of those VOC were found to be significantly different, mainly as a function of such a parameter as landfill aging.
The VOC concentrations measured from the unclosed landfill sites (e.g., WJ) were characterized by exceedingly high values
above a few tens of ppm. However, the results of the abandoned site (e.g., SP) were about three orders of magnitude lower
than the others so as to merely exceed the typical ambient concentration levels. It was most striking to find a systematic
dominance of toluene over other aromatic VOC under most circumstances. The LFG flux values of all aromatic VOC and the four
specific major ones (termed as BTEX: benzene, toluene, ethylbenzene, and xylene) were also computed for each vent pipe from
all study sites using their concentrations and the concurrently determined environmental parameters. The results, if calculated
in terms of the average BTEX quantity emitted per vent pipe, showed that the magnitude of their emissions can vary substantially,
with the values ranging from 0.05 (SP) to 49.2 kg yr−1 (WJ in wintertime). The LFG flux values of aromatic VOC, when compared to the contribution of non-methane hydrocarbons (NMHC),
were able to explain a constant, but minor, proportion of the LFG carbon budget. 相似文献