沉积物中雌激素及壬基酚、辛基酚、双酚A的测定

近些年来雌激素及烷基酚类化合物由于其对水生生物的内分泌干扰作用越来越受到广泛关注.沉积物作为环境中有机污染物的重要储存库,研究目标物在其中的浓度分布对于探明此类物质在环境中的迁移转化具有重要意义.但沉积物中基质组成复杂而雌激素又痕量存在,这增加了前处理的难度.本研究从雌激素及烷基酚类化合物的理化性质入手,采用碱液提取、液液萃取和LC-MS/MS分析测定沉积物样品中的雌激素及壬基酚、辛基酚、双酚A.结果表明,经过优化的方法对7种目标物的回收率介于61.9%～93.7%之间.该方法能有效去除沉积物中那些不溶于强碱和既溶于酸又溶于碱的有机污染物,同时操作简单、成本低,但回收率高、检出限低,可广泛适用于河流沉积物样品及土壤样品的前处理.     

基于LandsatTM数据的济宁市水体识别方法研究

文章基于济宁市2009年LANDSAT TM影像,根据影像各波段间的相关性和地物在各影像上的灰度差异,分别采用单波段阈值法、多波段谱间关系法、改进的水体指数法(MNDWI)及HIS空间水体提取模型法对济宁市水体信息进行识别提取。在此基础上,结合归一化指数法和HIS空间水体提取模型,提出了一种综合性的水体信息提取方法,并对各方法提取结果进行了精度评价。结果表明,已有方法对济宁市水体识别存在一定的缺陷,而综合法集成了归一化指数法和HIS空间水体模型的优点,很好地弥补了已有方法的不足,对济宁市水体信息进行了较好的提取,尤其是细小水体,同时也很好地消除了建筑物、阴影、水生植被等的影响,提高了济宁市水体信息识别的精度,为更好地定量评价济宁市地表水体时空演变规律等提供帮助。     

2种连续提取法提取3种类型土壤中重金属研究

连续提取法作为一种重要的化学分析方法,是土壤中重金属元素形态分析的主要环节,但不同提取法对于不同的土壤类型及同类土壤中不同重金属形态的提取效果差异很大.本文采用Tessier法和Maiz法等2种不同的连续提取法对华中地区常见的3种类型土壤(红壤、黄棕壤和黄褐土)中的Pb、Cd、Cu和Zn分别进行重金属形态分析,同时对Tessier法和Maiz法获得的结果进行了对比和分析.     

石化企业危险化学品重大危险源风险评估

阐述了定量风险评价的个人风险和社会风险指标,并从前期准备、资料数据搜集、危险辨识、失效频率分析、失效后果分析、风险计算和风险评估等环节对某石化企业液化气一级重大危险源进行了定量风险评估。评估结果显示该重大危险源的个人风险和社会风险值基本符合安监总局40号令的要求。     

DNA提取方法对活性污泥微生物多样性PCR-DGGE检测的影响

评价超声波法、2种基于SDS的裂解法、改进的化学裂解法、微波法和冻融 玻璃珠 溶菌酶 SDS等6种DNA提取方法对活性污泥微生物多样性PCR-DGGE检测的影响.结果表明,2种不同的DNA纯化方式(溶液和胶纯化)及PCR扩增方式(直接和巢式PCR)对DGGE结果没有明显的影响,但不同的DNA提取方法对DGGE结果有明显的影响,其中2种基于SDS裂解法的DGGE条带较多,其提取的DNA产量(14.85μg/g湿重)和纯度(OD260:OD280＞1.80)也最高;改进的化学裂解法和微波法次之;超声波法、冻融 玻璃珠 溶菌酶 SDS法较少.研究表明,DNA提取方法是影响活性污泥微生物多样性PCR-DGGE检测结果的关键因素,基于SDS的裂解法是用于活性污泥微生物多样性PCR-DGGE研究的一种简便、可靠的总DNA提取方法.     

张弦网壳结构索张拉模拟计算及试验研究

施工张拉控制是张弦网壳结构的关键技术之一,提出采用控制索原长的反分析方法追踪结构施工整个过程。首先,通过控制索在预应力状态下的张拉力求出零状态和索原长,并同时获得预应力态下所有单元的内力。在此基础上,通过控制每一级张拉索的原长,进行非线性有限元迭代计算,可求出索在分级分批施工时的控制力,并用VC＋＋6.0编制相应的计算程序。这一方法有效地避免了通用有限元需要反复试算,计算繁琐的缺点。最后,以张弦网壳结构模型为试验对象,按分级分批张拉的方式模拟结构的现场施工,并跟踪施工过程中杆件单元的应力状态。结果表明,数值模拟计算与试验值吻合较好,计算结果可靠,该方法能精确模拟结构的施工成形过程,且在整个过程中,每根索只需张拉一次,简化了施工工艺。     

太湖沉积物酸可挥发性硫化物分布特征及重金属生物有效性评价

对太湖4个湖区沉积物的酸可挥发性硫化物（AVS）和同步可提取重金属（SEM）的水平和垂直分布特征进行了研究,并对沉积物重金属的潜在生态风险进行初步评价.结果表明,氧化还原电位（Eh）与AVS和SEM含量均无显著相关性;表层沉积物中AVS含量分布在研究区差异较大,变异系数达134.28%;∑SEM含量波动较小,变异系数为...     

磷在水和沉积物中的形态

文章介绍了生物可利用态的磷(总磷、有机磷、无机磷)在土耳其奥龙特斯河河水和表层沉积物中的分配结果.通过连续提取方法可获得无机态的磷,每次获得的无机磷有4种形态:松散吸附态的磷、铝绑定态磷、铁绑定态磷     

Mobilities and leachabilities of heavy metals in sludge with humus soil

Chemical forms of Zn, Ni, Cu, and Pb in municipal sewage sludge were investigated by adding humus soil to sludge and by performing sequential extraction procedures. In the final sludge mixtures, Zn and Ni were mainly found in Fe/Mn oxide-bound (F3) and organic matter/sulfide-bound (F4) forms. For Zn, exchangeable (F1), carbonate-bound (F2), and F3 forms were transformed to F4 and residual forms (F5). For Ni, F1 and F2 forms were transformed to F1, F2, and F3 forms. Both Cu and Pb were strongly associated with the stable forms F4 and F5. For Cu, F2 and F3 forms were major contributors, while for Pb, F3 and F4 forms were major contributors to F5. Humus soil dosage and pH conditions in the sludge were strongly correlated with the forms of heavy metals. Five forms were used to evaluate metal mobilities in the initial and final sludge mixtures. The mobilities of the four heavy metals studied decreased after 28 days. The metal mobilities in the final sludge mixtures were ranked in the following order: Ni > Zn > Cu = Pb. Leaching tests showed that the mobilities of Zn and Ni in lower pH conditions (pH 4) were higher than those in higher pH conditions (pH 8).     

TiO2 nanotubes as solid-phase extraction adsorbent for the determination of polycyclic aromatic hydrocarbons in environmental water samples

An analytical method based on TiO2 nanotubes solid-phase extraction (SPE) combined with gas chromatography (GC) was established for the analysis of seven polycyclic aromatic hydrocarbons (PAHs): acenaphtylene, acenaphthene, anthracene, fluorene, phenanthrene, fluoranthene and pyrene. Factors a ecting the extraction e ciency including the eluent type and its volume, adsorbent amount, sample volume, sample pH and sample flow rate were optimized. The characteristic data of analytical performance were determined to investigate the sensitivity and precision of the method. Under the optimized extraction conditions, the method showed good linearity in the range of 0.01–0.8 g/mL, repeatability of the extraction (RSD were between 6.7% and 13.5%, n = 5) and satisfactory detection limits (0.017–0.059 ng/mL). The developed method was successfully applied to the analysis of surface water (tap, river and dam) samples. The recoveries of PAHs spiked in environmental water samples ranged from 90% to 100%. All the results indicated the potential application of titanate nanotubes as solid-phase extraction adsorbents to pre-treat water samples.