扎哈淖尔露天煤矿南帮压煤回采边坡稳定性分析

针对露天矿边帮普遍存在的压煤问题,基于极限平衡及强度折减理论,从控制边坡稳定性角度出发,结合扎哈淖尔露天煤矿南帮软岩边坡工程实际,通过定量计算与定性分析,提出横采内排压帮开采方式。采用二维刚体极限平衡与三维数值模拟相结合的方法分析了横采深部开挖角度及内排跟踪距离对边坡稳定性的影响及其程度,优化设计了扎哈哈淖尔露天矿横采南帮边坡形态。结果表明:南帮边坡滑坡模式为以IVC煤层底板弱层为底界面的切层-顺层滑动;横采内排压帮开采方式可借助边坡三维效应提高露天矿边坡角度及其自身稳定性,进而达到安全、高效地回收边帮压煤,提高露天矿煤炭资源回收率;扎哈淖尔露天煤矿横采南帮边坡稳定性随内排跟踪距离增大呈负指数降低;最终确定横采开挖位置为+908水平,内排跟踪距离为100 m,深部开挖角度为42°,可累计为扎哈淖尔露天煤矿多采出IV煤4 701.39万t,经济效益显著。     

水环境中石油类物质分析方法探讨

在详述了国内外石油类分析方法的基础上,对各方法的适用范围、优缺点及可比性进行了深入分析,阐述了各类方法存在的共性问题,指出按照石油类物质毒性大小分别定量分析的方法将是未来的发展趋势。     

太阳翼驱动机构的扰振力矩测试与分析

为了研究太阳翼驱动机构(solar array drive assembly,SADA)驱动太阳翼运行期间所产生的扰振力矩特性,设计了一套地面测试系统,包括应变式微振动测试平台、柔性负载以及模拟SADA在轨无重力工作环境的重力卸载装置。阐述了所设计测试系统的工作原理,并利用该测试系统进行了试验测试。测试结果表明:SADA驱动柔性负载运行期间所产生扰振力矩的扰振频率成分主要包含两部分,即:1)SADA驱动柔性负载耦合系统的低阶扭转固有频率;2)SADA电脉冲信号的输入频率及其高阶谐波。     

Competition for electrons between reductive dechlorination and denitrification

It is common that 2,4,6-trichlorophenol (TCP) coexists with nitrate or nitrite in industrial wastewaters. In this work, simultaneous reductive dechlorination of TCP and denitrification of nitrate or nitrite competed for electron donor, which led to their mutual inhibition. All inhibitions could be relieved to a certain degree by augmenting an organic electron donor, but the impact of the added electron donor was strongest for TCP. For simultaneous reduction of TCP together with nitrate, TCP’s removal rate value increased 75% and 150%, respectively, when added glucose was increased from 0.4 mmol?L^–1 to 0.5 mmol?L^–1 and to 0.76 mmol?L^–1. For comparison, the removal rate for nitrate increased by only 25% and 114% for the same added glucose. The relationship between their initial biodegradation rates versus their initial concentrations could be represented well with the Monod model, which quantified their half-maximum-rate concentration (K _S value), and K _S values for TCP, nitrate, and nitrite were larger with simultaneous reduction than independent reduction. The increases in K _S are further evidence that competition for the electron donor led to mutual inhibition. For bioremediation of wastewater containing TCP and oxidized nitrogen, both reduction reactions should proceed more rapidly if the oxidized nitrogen is nitrite instead of nitrate and if readily biodegradable electron acceptor is augmented.

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Urinary metabolomic profiling in rats exposed to dietary di(2-ethylhexyl) phthalate (DEHP) using ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS)

Di(2-ethylhexyl) phthalate (DEHP) is an omnipresent environmental chemical with widespread nonoccupational human exposure through multiple ways. Although considerable efforts have been invested to investigate mechanisms of DEHP toxicity, the key metabolic biomarkers of DEHP toxicity remain to be identified. The aim of this study was to assess the urinary metabonomics of dietary DEHP in rats using the technique of ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS). Fourteen female Wistar rats were divided into two groups and given increasing dietary doses of DEHP for 30 consecutive days. The urinary metabolite profile was studied using ultra-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. Principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) enabled clusters to be clearly separated. Eleven principal urinary metabolites were identified as contributing to the clusters. The clusters in the positive electrospray ionization (ESI) mode were xanthurenic acid, kynurenic acid, nonate, N6-methyladenosine, and L-isoleucyl-L-proline. The clusters in the negative ESI mode were hippuric acid, tetrahydrocortisol, citric acid, phenylpropionylglycine, cPA(18:2(9Z, 12Z)/0:0), and LysoPC(14:1(9Z)). The urinary metabonomic changes indicated that exposure to dietary DEHP can affect energy-related metabolism, liver and renal function, fatty acid metabolism, and cause DNA damage in rats. The findings of this study on the urinary metabolites and metabolic pathways of DEHP may form the basis for future studies on the mechanisms of toxicity of this commonly found environmental chemical.     

火电汽轮机组热电解耦技术研究

针对供热机组受传统“以热定电”运行模式限制,单机调峰能力低(最大仅有50%),无法满足深度调峰的问题,以国电集团西北地区所辖火电供热机组的实际运行情况为出发点,结合汽轮机组节能诊断及机组改造经验,提出了高、低压旁路联合供热,低压缸切缸运行两种热电解耦技术方案,通过比选得出两种技术方案的优缺点及适用范围。     

软弱基底排土场堆载过程中稳定性数值模拟*

针对软弱基底排土场普遍存在稳定性差的问题,在分析了排土场失稳的主要影响因素以及常见的5种失稳模式的基础上,结合胜利东二露天煤矿南排土场南帮边坡工程地质实际,基于强度折减理论,运用大型岩土数值模拟软件FLAC3D对排土场逐水平堆载过程中基底与边坡岩体变形破坏规律及稳定性进行了数值模拟分析,确定了南排土场南帮边坡的破坏模式以及最终排弃高度。结果表明:胜利东二露天矿南排土场边坡变形破坏主要受排弃物料重力影响,随着排弃高度的增加,基底内部第四系弱层最大位移呈线性增加,弱层以下岩土体变形量较小,其滑坡模式为沿基底内部弱层发生的剪切圆弧滑动,可在原设计基础之上继续排弃一个排土台阶高度,提高了排土场的空间利用率,并为类似排土场边坡设计提供借鉴。     

改性壳聚糖复合凹凸棒土絮凝油漆废水

将壳聚糖、阳离子淀粉和二甲基二烯丙基氯化铵(DMDAAC)进行三元接枝共聚,制备了三元接枝改性壳聚糖(CTS-DMDAAC-CS),通过红外光谱和扫描电镜对其结构进行了表征。并且将三元接枝改性壳聚糖与凹凸棒土进行优化复配,对油漆废水进行了絮凝实验,得出了当pH=12,沉降时间为20 min,复合絮凝剂投加量为0.2 g,三元接枝共聚物∶凹凸棒土=1∶10时,该复合絮凝剂对油漆去除率最佳能够达到89.3%,并且絮凝效果好,是一种新型绿色环保的有机-无机复合絮凝剂。     

UASB-SBR-絮凝工艺处理地沟油制生物柴油废水

采用UASB-SBR-絮凝工艺处理地沟油制生物柴油废水,考察了各个阶段的废水处理效果。实验结果表明：UASB稳定运行阶段进水COD约为15000mg/L时,COD去除率约为87%,出水COD在2500mg/L以下,出水挥发性脂肪酸（VFA）浓度为4~6mmol/L,最佳容积负荷为15.0kg/（m3·d）;采用SBR处理UASB出水,当容积负荷为1.5kg/（m3·d）时,出水COD在200mg/L以下,COD去除率在83%以上,ρ（NH₃-N）在5mg/L以下,TP约为25mg/L。向SBR出水中加入质量分数为5%的聚合氯化铝进行化学除磷,加入量为5mL/L,处理后废水TP为4~6mg/L。处理后废水的COD,ρ（NH₃-N）,TP均达到CJ343-2010《污水排入城市下水道水质标准》的A类要求。     

Fe(III)–EDDS complex in Fenton and photo-Fenton processes: from the radical formation to the degradation of a target compound

The present work compares the efficiency of homogenous Fenton and photo-Fenton processes in the presence of Fe(III)–EDDS complex under different experimental conditions. 4-tert-Butylphenol (4-t-BP), which is one of the endocrine disrupting chemicals, was used as a model pollutant to investigate the Fenton and photo-Fenton application. The efficiency of homogenous photo-Fenton process was significantly much higher than homogenous Fenton process, which is due to the rapid formation of Fe²⁺ under UV irradiation of the iron complex and the photochemical formation of HO^? from the photolysis of the complex Fe(III)–EDDS. Through the degradation of 4-t-BP, the effect of Fe(III)–EDDS concentration, H₂O₂ concentration, pH, and oxygen was investigated in both processes. Such trend was also correlated with pH calculating the polychromatic Fe²⁺ quantum yield formation at pH 4.0, 6.0, and 8.6. The results showed that at high Fe(III)–EDDS and H₂O₂ concentrations, a negative effect was found. By the way, the Fenton process was found to be enhanced at basic pH. These results can be very useful for the use and optimization of such iron complex in water treatment process as function of different physico-chemical conditions.