对苯二甲酸对鱼类毒性的研究

通过实验室内短期毒实验，评价了对苯二甲酸对鱼草的毒性，给出了对苯二甲酸对草鱼仔鱼及幼鱼的９６ｈＬＣ５０值及其安全浓度。     

Bioaccumulation, depuration and biotransformation of 4,4'-dibromodiphenyl ether in crucian carp (Carassius auratus)

Polybrominated diphenyl ethers (PBDEs) are extensively used as a class of flame retardants and have become ubiquitous environmental pollutants. Significant biotransformation of some PBDEs via reductive debromination has been observed. However, little is known about the fate of lower brominated BDEs in fish. In this study, the tissue distribution, excretion, depuration and biotransformation of 4,4′-dibromodiphenyl ether (BDE 15) were investigated in crucian carp (Carassius auratus) which were exposed to spiked water solution at different concentrations for 50 d, followed by a 14-d depuration period. Bioaccumulation parameters were calculated and the results showed that BDE 15 was mainly concentrated in the gill and liver. In particular, five biotransformation products of BDE 15 in carp were identified using GC-MS/MS. Besides two debrominated metabolites, three of the metabolites were mono-OH-BDE 15, diOH-BDE 15 and bromophenol. Our results unequivocally suggested that BDE 15 oxidation did occur via the formation of hydroxylated (OH-) metabolites in crucian carp exposed in vivo. These findings will be useful for determination of the metabolic pathways of PBDEs in freshwater fish, especially about their oxidation metabolism.     

Ozonation of azo dye Acid Red 14 in a microporous tube-in-tube microchannel reactor: decolorization and mechanism

Despite the great success of time-weighted average passive sampling of hydrophobic contaminants, such as PCBs and PAHs, the sampling of polar organic compounds still presents a challenge because the equilibrium between water and most sampling phases is attained in a relatively short time. In this study, we proposed a new time-integrative sampler using in situ solvent extraction (TISIS) for polar organic chemicals. The sampler was composed of a 15 cm poly(dimethylsiloxane) (PDMS) tubing, with an internal diameter of 0.5 mm and wall thickness of 0.5 mm, through which an extraction solvent (acetonitrile) was passed. Four polar organic contaminants, caffeine, atrazine, diuron and 17α-ethynylestradiol, were chosen for the evaluation of the performance of the sampler. Without the use of in situ solvent extraction, the PDMS tubing when exposed to a constant aqueous concentration of the four model compounds was able to linearly accumulate those compounds for less than 12 h and equilibrium between the PDMS tubing and water was attained in 2 d under our laboratory conditions. However, TISIS when exposed to a constant aqueous concentration was able to linearly accumulate all the model compounds without any exposure time limitation. The measured sampling rates at three different extraction flow rates (0.2, 0.5, 1.5 mL min⁻¹) were similar, regardless of the chemicals, indicating that the overall mass transfer from aqueous solution to the extraction solvent was most likely dominated by partitioning to the PDMS tubing and the internal diffusion within PDMS. In addition, a pulsed exposure experiment confirmed that TISIS operated in a time-integrative mode when the environmental concentration was highly fluctuated.     

Effects of excited-state structures and properties on photochemical degradation of polybrominated diphenyl ethers: a TDDFT study

This study presents new insight into the photochemical degradation of polybrominated diphenyl ethers (PBDEs), and it provides details about the structures and properties of 27 PBDE congeners in the electronically excited state using the time-dependent density functional theory method. Each PBDE congener exhibited remarkably different geometries in the ground state and the excited state. The significant lengthening of C-Br bond in each PBDE congener was observed in the excited state for the first time by theoretical calculation, which is directly involved in the photochemistry reductive debromination of n-BDE to (n−1)-BDE. Generally, the lengthening of C-Br bonds cannot occur at the para position. Furthermore, the calculated results demonstrated that the photoreactivity of PBDEs increased with an increase of bromination degree. It was also found that the pattern of Br substituents had an effect upon the photoreactivity of PBDEs. These findings suggest that the information obtained in the excited state is crucial to the mechanism explanation of the photochemical degradation of PBDEs.     

个旧锡矿成矿热液活动的微量元素地球化学指示

通过对不同地质体中微量元素含量对比及因子分析 ,明确成矿热液活动元素 ,区分不同地球化学类型的元素集群。研究表明 ,成矿热液活动源于花岗岩岩浆侵位 ,花岗岩浆期后热液及地下水在岩体热力驱动下构成了一个系统的矿化热液活动体系 ,对区内地层产生广泛的蚀变影响 ,形成矿体、热液活动脉体及矿化热液活动元素对围岩地层的改造。成矿热液活动体系为开放系统 ,运动方式以构造断裂导流为主 ,孔隙渗透为次。     

SBR法处理化粪池出水的工艺研究

采用经实验运行得到SBR工艺处理化粪池出水的合理的操作模式,能获得90%以上稳定的COD_(cr)去除率及更好的BOD_5去除效果,NH_3-N去除率大于75%,TN去除率大于45%.并考察了污泥浓度、泥龄、污泥负荷与处理效果的关系,以及闲置期对反应周期的影响.实验结果表明,SBR工艺对处理水质、水量负荷变化很大的化粪池出水,是一种理想的工艺选择.     

土壤非饱和带柴油迁移的模拟实验

通过土柱模拟实验研究了0#柴油及其饱和水溶液在不同含水率的砂土及壤土中的入渗迁移及残留特征.结果表明,柴油在壤土中的入渗速率小于砂土,且随含水率的增加逐渐减小,而柴油在砂土中的入渗速率则随含水率的增加先增大后减小.入渗结束后,相同深度的土柱中柴油残留量随含水率的增加明显降低,沿土层深度呈先增后降的弓形趋势.随着再分布时间的延长,砂土柱中柴油残留量随土层深度逐渐增大,壤土柱中柴油含量变化较小.柴油饱和水溶液在壤土中的入渗速率明显小于砂土,穿透曲线的峰值滞后于砂土,入渗过程中,壤土中渗出液的柴油浓度小于砂土.入渗结束后,深度小于10 cm的壤土柱中集中了绝大部分柴油,而砂土中柴油残留量则略低于壤土.     

危险废物填埋过程中的防渗层设计以及渗滤液的处置方法

危险废物具有毒性、易燃性、腐蚀性、反应性和感染性,如果长期暴露于环境之中会对生态环境和人类健康造成巨大危害,所以安全而有效地处理处置危险废物意义极为重大。安全填埋是危险废物集中处置必不可少的重要手段之一,但是在填埋的过程中,危险废物容易产生渗滤液等有毒有害液体,对填埋场周围地下水又造成了污染,所以填埋场的防渗层设计建造和渗滤液的处理尤为重要。通过分析与研究,着重论述了在对危险废物的填埋过程中防渗层的设计和渗滤液处置方法。     

线性拟合在工程地震勘察技术中的应用

本文介绍利用最小二乘法建立线性拟合模型的过程,并给出一个利用一元线性拟合,实现用相遇观测时距曲线求V2的实际应用。同时给出Mathematica程序,实现此类数据处理的自动化,克服了人工处理工作量大、速度慢、繁琐之不足,更重要的是避免了人工处理时出错情况的发生。     

露天煤矿的土地复垦

本文论术字露天煤矿土地复垦的现状，着重了矿区土地地复垦规划，提出了一个土地复垦规划的模型，并且对复垦方向的选择和复垦控制进行了初步的探讨。