提高节理面c和Ψ对岩坡开挖变形的影响

为了反映岩质边坡在节理面注浆后的变形效应,首先,通过室内试验,分析注浆前后岩体变形和破坏的全过程,以探讨其抗剪性能(粘结力c和内摩擦角Ψ)的变化;然后,基于理想弹塑性本构模型的Mohr-Coulomb准则,运用拉格朗日元数值方法(FLAC3D),对岩坡注浆前后变形效应(水平位移、垂直位移、剪应变增量)进行模拟.结果表明:注浆加固后,岩体的位移场变得均匀和连续,节理面处的较大位移受到抑制,边坡的整体性得到提高,有利于边坡的稳定性.     

ERT技术在无机酸污染场地调查中的应用

利用高密度电阻率法对硫酸废液污染的场地进行污染调查,由于硫酸废液侵入土壤,使其介质的溶质浓度发生了改变,导致SO₄2-与地表潜水作用,电传导性提高,被污染土壤含盐量增加,但是电阻率降低与未被硫酸废液侵入的土层形成了一定的电性差异. 通过二维和三维电阻率层析成像(ERT)技术,圈定硫酸废液侵入土壤中的分布范围、侵蚀深度以及扩散羽流等,并对ERT结果进行土工试验异常验证. 结果表明:硫酸废液污染土壤的视电阻率小于6.0 Ω·m,污染区域长度达25.0 m,深度约4.0 m;地表土污染长度为12.0 m,表面宽度约4.0 m,污染土壤的总体积约为222.0 m3.      

Occurrence of organic pollutants in recovered soil fines from construction and demolition waste

The objective of this study was to characterize recovered soil fines from construction and demolition (C&D) waste recycling facilities for trace organic pollutants. Over a period of 18 months, five sampling trips were made to 14 C&D waste recycling facilities in Florida. Screened soil fines were collected from older stockpiles and newly generated piles at the sites. The samples were analyzed for the total concentration (mg/kg) of a series of volatile organic compound (VOCs) and semi-volatile organic compounds (semi-VOCs). The synthetic precipitation leaching procedure (SPLP) test was also performed to evaluate the leachability of the trace organic chemicals. During the total analysis only a few volatile organic compounds were commonly found in the samples (trichlorofluoromethane, toluene, 4-isopropyltoluene, trimethylbenzene, xylenes, and methylene chloride). A total of nine VOCs were detected in the leaching test. Toluene showed the highest leachability among the compounds (61.3-92.0%), while trichlorofluoromethane, the most commonly detected compound from both the total and leaching tests, resulted in the lowest leachability (1.4-39.9%). For the semi-VOC analysis, three base-neutral semi-VOC compounds (bis(2-ethylhexyl)phthalate, butyl benzyl phthalate, and di-n-butyl phthalate) and several PAHs (acenaphthene, pyrene, fluoranthene, and phenanthrene) were commonly detected in C&D fines samples. These compounds also leached during the SPLP leaching test (0.1-25%). No acid extractable compounds, pesticides, or PCBs were detected. The results of this study were further investigated to assess risk from land applied recovered soil fines by comparing total and leaching concentrations of recovered soil fines samples to risk-based standards. The results of this indicate that the organic chemicals in recovered soil fines from C&D debris recycling facilities were not of a major concern in terms of human risk and leaching risk to groundwater under reuse and contact scenarios.     

Growth responses of Picea mongolica seedlings to defoliation rate

Picea mongolica W. D. Xu. is an endemic species in China. The spruce forest is only found in semi-arid habitat in Inner Mongolia Autonomous Region of China. Based on the simulative defoliation experiment, it was proved that Picea mongolica seedlings had the compensatory and overcompensatory effects under the certain defoliation rate. The results of variance analysis on growth indexes showed that in PM I (natural regeneration seedlings under Picea mongolica forest), the differences of H1 (height in June 23 ) and H2 (height in September 3) were extremely significant, and the difference of D(diameter at the breast height) were not significant. In PM Ⅱ (artificial regeneration seedlings under Betula platyphylla Suk. forest), the difference of H1 was significant, the difference of H2 was not significant, and the difference of D was extremely significant. The regression equations were established and the compensatory and overcompensatory points were obtained. In PM I, the compensatory points of H1, H2, and D were 0.7628, 0.7436, 0.5725, and the overcompensatory points were 0.6056, 0.5802 and 0.2909 respectively. In PM Ⅱ, the compensatory points of H1, H2, and D are 0.5012, 0.3421, 0.2488, and the overcompensatory points are 0.4137, 0.2633 and 0.0747 respectively. These results suggested that the induction of compensatory growth mechanisms in spruce seedlings required a threshold level of defoliation, and the insects in Picea mongolica forest could be controlled in a certain de clree.     

城市突发环境事件的三维矩阵管理模式研究

针对我国环境事件频繁发生和应急管理法制建设缺位、体制不健全之间的矛盾,结合矩阵管理与应急管理理念,创建了基于事件分级、事件生命周期和事件运行管理为三维的矩阵管理模式,并以此模式分析结果为基础,提出城市应急管理能力建设的阶段性建议。     

近10年流域江湖关系变化作用下鄱阳湖水动力及水质特征模拟

鄱阳湖水文情势受流域来水及长江共同影响,近10年流域、长江和鄱阳湖间关系发生了较大变化,导致了新的水文节律调整,进一步使得湖区水质环境发生变化.对近10年序列(2003—2012年)和1956—2002年序列的多年平均的日水文过程进行对比,分析了鄱阳湖的流域入流、湖口出流及湖区水位的年内变化过程;近10年鄱阳湖最高水位降低,湖相时间变短,河相时间增长;通过构建鄱阳湖的二维水动力水质模型,并采用实测2010年湖区水动力及水质数据对模型进行率定验证,在此基础上着重研究流域、江湖水文情势变化条件下,湖区的水动力和水质发生的变化.模拟结果显示,由于4—6月间湖区丰水期滞后13 d,8—10月间枯水期提前21 d,导致TN浓度在两个时间段内分别上升10.6%和12.4%,TP浓度在两期间内分别升高11.7%和13.6%.在8—10月期间,湖区水位下降速率增加,南部与西部的碟型湖提前与主湖区分离,形成相对静水的水塘,加剧了碟型湖的富营养化风险.     

海洋平台圆柱体坠落运动轨迹及落点分析

传统的角度偏差经验值方法导致落物风险评价过程中的落点和危险区预测存在较大误差,科学化、立体化、完整化、多因素概化的落物轨迹和落点分析方法及工具缺位。为此,以海洋平台圆柱体落物为研究对象开展先导研究,在2D运动理论模型基础上,考虑3维、6度受力与运动参数,引入粘性拖曳力系数经验公式、海流运动、旋转升力和力矩项,建立了具有普适性的落物水下3D运动轨迹预测模型,并以现场实验数据校验表明模型方法可行、结果更可信;据此以Matlab 2016为程序设计平台编制了海洋平台圆柱体坠落运动预测分析工具（MREDP）,分析了坠落运动落点分布规律。研究结果表明:随着初始倾斜角度的增大,落点偏移距离呈现先增后降的趋势,于62°时达到最大值,运动轨迹整体呈现螺线曲率减小、向轨迹曲线外开口侧偏移趋势;落点分布变化可分为Y轴偏移稳定主导阶段、X轴偏移实力型快速主导阶段和X轴偏移机会型主导阶段3个阶段;相对MREDP预测结果,DNVGL-RP-F107经验性角度偏差推荐结果较为保守,MREDP可为DNVGL-RP-F107提供更加准确、可信的轨迹曲线和落点取值。基于分析结果,提出了采用Monte Carlo方法表征实际工程中起始运动参数随机性和入水撞击产生的不确定性等建议。     

污染场地地下水中汞污染反应运移模拟

汞（Hg）是人们持续关注的全球环境污染物之一,其对地下水的污染严重威胁着与地下水相关的生态环境系统.汞在地下水系统中的物理与地球化学反应过程的准确刻画是研究汞迁移转化规律的重点和难点.基于某工业场地汞污染数据,首先采用PHREEQC研究地下水中无机二价汞的存在形态,然后利用PHT3D程序建立汞污染物反应性溶质运移二维剖面模型.该模型考虑了汞污染物在地下水系统中的对流、弥散过程及地球化学反应过程（包括水相络合作用、表面络合吸附作用及受动力学控制的氧化还原作用）.结果表明,无机二价汞的存在形态以HgCl₂和Hg（OH）Cl占主导地位,氧化还原作用是影响地下水中汞污染反应性运移的主要控制因素;另一方面,水合氧化铁HFO对汞迁移的阻滞影响较小,而溶解性有机质对汞较强的络合作用不能忽视.本文研究成果可为预测与评估特定污染场地地下水汞污染的变化趋势及制定相应的修复策略提供科学依据.     

过氧化氢存在下HCFC－22光解特性

模拟大气条件研究了ＨＣＦＣ－２２＋Ｈ２Ｏ２在有氧或无氧存在下用低压汞灯进行辐照，在２０ｍ的长光程池中用富里叶红外光仪测量其化学产物，结果表明在没有氧情况下产物为ＣＯＦ２、ＣＯ２、ＨＦ和ＨＣｌ；有氧存在时产物为ＣＯ２、Ｈ２Ｏ、ＨＦ和ＨＣｌ．从这些产物推出其可能的光解机理．     

苯并(a)芘在黄河水体不同粒径颗粒物上的表面吸附和分配作用特征

模拟实验研究了苯并(a)芘在黄河水体不同粒径颗粒物上的吸附作用,重点探讨了颗粒物粒径对苯并(a)芘的表面吸附和分配作用的影响.结果表明:(1)苯并(a)芘在黄河水体颗粒物上的吸附符合表面吸附-分配作用复合模式(2)苯并(a)芘在粒径d≥0.025 mm颗粒物上的吸附以表面吸附为主,表面吸附对吸附的贡献在68.7%至82.4%之间;当苯并(a)芘液相平衡浓度为0～8.87μg·L-1时,其在粒径0 007 mm≤d＜0.025 mm颗粒物上的吸附以表吸附作用为主,当液相平衡浓度大于8.87μg·L-1时,吸附以分配作用为主;苯并(a)芘在粒径d＜0.007 mm颗粒物上的吸附以分配作用为主;(3)苯并(a)芘在不同粒径颗粒物上的表面吸附对总吸附的贡献大小顺序为:(d≥0.025 mm)＞(0.007 mm≤d＜0 025 mm)＞(d＜0.007 mm);(4)苯并(a)芘在不同粒径颗粒物中的分配系数与有机质含量呈线性相关,其标化分配系数Koc约为1.26×105L·kg-1.