基于矿井通风三维仿真系统软件的矿用空气幕选型方法

根据矿井风流调节的具体要求,合理选择矿用空气幕的型号是应用矿用空气幕技术的关键。在分析矿用空气幕选型依据及原理的基础上,应用矿井通风三维仿真系统软件模拟矿用空气幕运行的效果,来研究确定矿用空气幕的选型参数及影响因素。结果表明,应用矿井通风三维仿真系统软件所选择的矿用空气幕与理论推导的计算结果一致,此方法能够最大限度地反映矿山实际情况,具有直观、高效等特点。     

内排压脚与边坡稳定性的关系

为了研究边坡角及边坡形状与边坡稳定性的关系,采用有限元软件ANSYS模拟了不同边坡角对应的稳定系数,以及不同平盘宽度和压脚高度所形成的等储备强度边坡的稳定系数。模拟中假设材料符合相关联的理想弹塑性本构关系,强度准则符合Drucker-Prager准则,用计算收敛性作为边坡稳定性的准则,用强度折减法得出边坡的稳定系数。为了形成等储备强度边坡,由下到上分步骤进行压脚。先在平面边坡最下台阶压脚,这样提高了边坡稳定系数,在边坡进入临界状态时,最下两台阶的塑性状态相同,则压脚停止;再在最下两台阶同时压脚,在边坡进入临界状态时,最下3个台阶的塑性状态相同,则压脚停止;以此类推,在最下边n个台阶同时压脚,在边坡进入临界状态时,压到与第n+1个台阶的塑性状态相同为止。结果表明,边坡总是从坡脚开始形成塑性区,在重力加载过程中,塑性区以弧形条带向坡顶扩展,形成滑带。最有效的内排压脚是从最下台阶开始形成等储备强度边坡的压脚。     

基于RS&GIS的长白山地区生态安全评价研究

以遥感影像数据、专题数据、DEM数据、气象站实测数据和统计数据为数据源,采用极差法、层次分析法、综合指数法、RS&GIS等方法对长白山地区的生态安全进行了评价.结果表明:长白山地区生态安全水平呈现出明显的空间差异性,整体由中部向东西两端逐渐降低.各生态安全等级面积从大到小为临界安全等级、较安全等级、不安全等级、较不安全等级、安全等级.统计了各行政单元的平均生态安全指数和等级构成,各县市生态安全水平从高到低为长白县、抚松县、安图县、和龙市、临江市,各县市的生态安全等级构成也有所差异.长白山地区生态安全水平以临界安全等级为主,整体上生态环境质量一般,系统服务功能受到了一定程度的破坏.     

含多弱层复合边坡滑坡治理三维数值分析

白音华二号矿滑坡区边坡治理工程是针对稳定性差的南帮非工作帮和南排土场构成的复合边坡进行的。滑坡体受多层弱层控制,治理过程中易导致边坡失稳,所以治理工程采取分区开采的条采方案,充分利用边坡治理的三维效应来进行边坡的失稳破坏研究和稳定性分析。选取滑坡区的典型剖面作为研究对象,基于强度折减方法(SRM),应用有限差分FLAC3D软件,在两种开挖条件下,对含多弱层的复合边坡的稳定性规律和破坏机制进行了数值模拟分析,揭示了多弱层对复合边坡的失稳破坏及稳定性的影响。研究结果表明,治理工程中,弱层被揭露一定宽度,滑体沿煤底板弱层水平错动、竖直方向拉裂破坏;随弱层暴露宽度的增加,边坡稳定性明显降低,说明治理边坡具有三维效应;开挖至3-3煤层底板,开挖坡角20°,弱层暴露宽度为400m,边坡的稳定系数刚好达到安全储备系数1.1,建议矿方首选此方案,可以最大限度的回收煤炭资源。     

基于MDE和分形优化SVM的周期来压预测

为了解决周期来压的预测问题,首先对已知支架周期来压荷载曲线使用多重差异进化算法(MDE)进行拟合,将每重拟合形成的单一正弦曲线与上次差余曲线(Ei)再作差余曲线(Ei+1)。将这些Ei图通过分形几何的盒子法计算维度和相关系数(r)。将每条Ei的维度、r和支架相对距离(L)作为输入值,对应的Ei的周期Ti、缩放系数Si和纵移系数Di作为目标值,使用支持向量机(SVM)进行训练。通过对维度和r规律的研究得到拟设置支架处荷载各Ei的维度和r,带入训练后的SVM模拟得到Ei的Ti、Si和Di,进而得到Ei的表达式。将上述Ei求和即为所求拟设置支架处的周期来压荷载。实例分析说明,该种方法预测结果可以大体反映支架周期来压的基本形式和变化规律。     

Applying a new method for direct collection, volume quantification and determination of N2 emission from water

The emission of N₂ is important to remove excess N from lakes, ponds, and wetlands. To investigate the gas emission from water, Gao et al. (2013) developed a new method using a bubble trap device to collect gas samples from waters. However, the determination accuracy of sampling volume and gas component concentration was still debatable. In this study, the method was optimized for in situ sampling, accurate volume measurement and direct injection to a gas chromatograph for the analysis of N₂ and other gases. By the optimized new method, the recovery rate for N₂ was 100.28% on average; the mean coefficient of determination (R²) was 0.9997; the limit of detection was 0.02%. We further assessed the effects of the new method, bottle full of water, vs. vacuum bag and vacuum vial methods, on variations of N₂ concentration as influenced by sample storage times of 1, 2, 3, 5, and 7 days at constant temperature of 15°C, using indices of averaged relative peak area (%) in comparison with the averaged relative peak area of each method at 0 day. The indices of the bottle full of water method were the lowest (99.5%-108.5%) compared to the indices of vacuum bag and vacuum vial methods (119%-217%). Meanwhile, the gas chromatograph determination of other gas components (O₂, CH₄, and N₂O) was also accurate. The new method was an alternative way to investigate N₂ released from various kinds of aquatic ecosystems.     

Enhanced catalytic complete oxidation of 1,2-dichloroethane over mesoporous transition metal-doped γ-Al2O3

High-surface-area mesoprous powders of γ-Al₂O₃ doped with Cu^2 +, Cr^3 +, and V^3 + ions were prepared via a modified sol–gel method and were investigated as catalysts for the oxidation of chlorinated organic compounds. The composites retained high surface areas and pore volumes comparable with those of undoped γ-Al₂O₃ and the presence of the transition metal ions enhanced their surface acidic properties. The catalytic activity of the prepared catalysts in the oxidation of 1,2-dichloroethane (DCE) was studied in the temperature range of 250–400°C. The catalytic activity and product selectivity were strongly dependent on the presence and the type of dopant ion. While Cu^2 +- and Cr^3 +-containing catalysts showed 100% conversion at 300°C and 350°C, V^3 +-containing catalyst showed considerably lower conversion. Furthermore, while the major products of the reactions over γ-alumina were vinyl chloride (C₂H₃Cl) and hydrogen chloride (HCl) at all temperatures, Cu- and Cr-doped catalysts showed significantly stronger capability for deep oxidation to CO₂.     

Rapid and simple spectrophotometric determination of persulfate in water by microwave assisted decolorization of Methylene Blue

A rapid and simple method for determination of persulfate in aqueous solution was developed. The method is based on the rapid reaction of persulfate with Methylene Blue(MB) via domestic microwave activation, which can promote the activation of persulfate and decolorize MB quickly. The depletion of MB at 644 nm(the maximum absorption wavelength of MB) is in proportion to the increasing concentration of persulfate in aqueous solution. Linear calibration curve was obtained in the range 0–1.5 mmol/L, with a limit of detection of 0.0028 mmol/L. The reaction time is rapid(within 60 sec), which is much shorter than that used for conventional methods. Compared with existing analytical methods, it need not any additives, especially colorful Fe2+, and need not any pretreatment for samples, such as p H adjustment.     

建筑安全风险因素分级排序的风险矩阵法

为减少风险分级排序时产生的风险结,在引入施工安全事故频率的基础上,采用单元格细化和Borda序值法改进原有的风险矩阵法。改进后的方法使得风险等级数量增加,风险结数量减少。将该方法应用于脚手架工程的风险因素的分级与排序,风险等级分为6级,且实现了12个因素的明确排序。     

对氯气校正法测定高氯废水化学需氧量的方法研究

氯气校正法(HJ/T70-2001)是测定高氯废水化学需氧量的国标方法,为了减少样品测定过程带来的环境污染,研究在不改变HJ/T70-2001氧化体系及测试条件的情况下,将取样体积由20 mL减半为10 mL,试剂的使用量相应减半,对方法的检出限、相对误差、相对标准偏差等指标进行验证。结果表明,该方法的检出限符合要求,准确度较高,精密度较好,可用于高氯废水化学需氧量的测定。