陡河水库鱼体汞的生物积累初探

为了解陡河燃煤电厂大气汞释放对毗邻的陡河水库水生生态系统中鱼体汞含量、生物积累和放大等的影响,本研究采集陡河水库野生鱼、虾和螺蛳,分别测定了鱼样等生物样品中的总汞和甲基汞,并对部分代表性样品测定稳定碳氮同位素比值。鱼汞分布特征和δ13C‰和δ15N‰同位素比值分布特征显示:鱼体(鲜样)中总汞和甲基汞平均含量分别为56.4±26.7和15.5±8.4 ng·g-1,总汞含量最高的是杂食性的白条鱼为133 ng·g-1。不同食性的鱼体δ13C和δ15N稳定同位素值变化范围分别为-28.1‰~-24.4‰和12.0‰~16.1‰,Log10[Hg]与δ15N的线性相关斜率值为负值。以上结果表明:陡河水库鱼体汞总体偏低,没有发现高生物积累和生物放大,其主要原因在于陡河水库水环境中汞含量较低,且陡河水库靠近市区,过度捕捞使可以捕获的鱼样种类和数量偏少,且鱼龄较低。     

Limiting explosible concentration of hydrogen–oxygen–helium mixtures related to the practical operational case

This paper presents data on the limiting (minimum) concentrations of hydrogen in oxygen, in the presence of added helium, at elevated temperature and pressure related to the practical operational case. A 5 L explosion vessel, an ignition sub-system and a transient pressure measurement sub-system were used. Through a series of experiments carried out using this system, the limiting concentrations of hydrogen in oxygen and helium at different initial pressures and temperatures for the practical operational case were studied, and the influence of ignition energy and initial temperature on the limiting concentration of hydrogen in oxygen and helium was analyzed and discussed. The variation of ignition energy within the studied range is found to have a significant effect on the limiting concentration of hydrogen in oxygen and helium at lower initial temperature. However, when the ignition energy is higher than 32 mJ, the limiting hydrogen concentration remains almost changeless as the initial temperature increases from 21 °C to 90 °C. The limiting explosible concentration of hydrogen–oxygen–helium mixture decreases as the ignition energy increases when the initial temperature is lower. When the initial temperature is higher, the ignition energy has little effect on the limiting hydrogen concentration of hydrogen–oxygen–helium mixtures. When the initial temperature reaches 90 °C, the limiting hydrogen concentration remains almost changeless with an increase in ignition energy. The limiting explosible concentration of hydrogen in the mixtures, at the initial temperature of 21 °C and the ignition energy of 0.5 mJ, is 8.5% and that of oxygen is 11.25%.     

液氧储罐爆炸事故树分析

采用安全系数工程的方法,对液氧储罐爆炸进行丁事故树分析,通过求事故树最小割集,进行结构重要度分析,从而对液氧储罐爆炸的事故原因进行分析、预测,并提出了相应的预防控制措施。     

基于苔藓氮含量及d15N分析探讨农村大气氮沉降状况

2009~2010年在江西抚州市崇仁县10个乡镇采集了85个细叶小羽藓样品,通过对苔藓氮含量及氮同位素(d15N)的测定,估算了该地区大气氮沉降水平,并探讨了大气氮输入的主要来源.结果表明,研究区苔藓平均氮含量变化范围为2.24%~3.43%,其中农业覆盖率较大郭圩乡和礼陂镇苔藓氮含量均超过3%(平均值分别为3.07%、3.43%).研究区大气氮沉降的变化范围为29.62~54.39kg/(hm2·a),反映了大气氮沉降成为农村生态系统氮输入的重要补充.苔藓平均d15N值为-3.11‰~0.078‰,指示研究区主要受农业氨源的影响.崇仁县城区苔藓d15N为-1.7‰,低于其它农业乡镇(d15N为0‰±1‰),表明该地区还受到城市污水和人畜排泄物所释放的氨影响;孙坊镇苔藓d15N 变化范围为-5.89‰~0.61‰,提示大气氮沉降除受到农业排放的氨作用以外,还存在露天垃圾填埋场挥发氨的贡献.     

Research on polyhydroxyalkanoates and glycogen transformations: Key aspects to biologic nitrogen and phosphorus removal in low dissolved oxygen systems

In this paper, a study was conducted on the effect of polyhydroxyalkanoates (PHA) and glycogen transformations on biologic nitrogen and phosphorus removal in low dissolved oxygen (DO) systems. Two laboratory-scale sequencing batch reactors (SBR1 and SBR2) were operating with anaerobic/aerobic (low DO, 0.15–0.45 mg·L^-1) configurations, which cultured a propionic to acetic acid ratio (molar carbon ratio) of 1.0 and 2.0, respectively. Fewer poly-3-hydroxybutyrate (PHB), total PHA, and glycogen transformations were observed with the increase of propionic/acetic acid, along with more poly-3-hydroxyvalerate (PHV) and poly-3-hydroxy-2-methyvalerate (PH2MV) shifts. The total nitrogen (TN) removal efficiency was 68% and 82% in SBR1 and SBR2, respectively. In the two SBRs, the soluble ortho-phosphate (SOP) removal efficiency was 94% and 99%, and the average sludge polyphosphate (poly-P) content (g·g-MLVSS^-1) was 8.3% and 10.2%, respectively. Thus, the propionic to acetic acid ratio of the influent greatly influenced the PHA form and quantity, glycogen transformation, and poly-P contained in activated sludge and further determined TN and SOP removal efficiency. Moreover, significant correlations between the SOP removal rate and the (PHV+ PH2MV)/PHA ratio were observed (R²>0.99). Accordingly, PHA and glycogen transformations should be taken into account as key components for optimizing anaerobic/aerobic (low DO) biologic nitrogen and phosphorus removal systems.     

国内电炉钢发展现状与应用前景

通过电炉铜与转炉铜能耗对比,突显了电炉钢的节能与环保优势,同时介绍了国内外电炉钢应用现状。随着社会工业化的发展所带来的钢铁积蓄量的增加,以及电炉钢技术的不断完善和发展,加之迎合国家低碳经济政策的实施,国内电炉钢发展具有广阔前景。     

Electrochemical degradation of Acid Red I dye and its treatment by UV light

Degradation of Acid Red I (ARI) dye by electrochemical treatment and UV light irradiation was studied in this work. The effect of the current density and the concentration of NaCl and dye on the decoloration and degradation efficiency were studied and optimized. The UV irradiation was monitored by UV-Vis spectrophotometry and chemical oxygen demand. The kinetic constants for decoloration and degradation were calculated. Degradation of 86% was achieved in 160?min and the first-order kinetic constant was 0.013?min^?1. Degradation products were identified by gas chromatography/mass spectrometry. The mechanism for the degradation of ARI was proposed.     

采矿对山西水资源破坏过程的同位素示踪研究

综合应用水文地质勘察、同位素示踪、水化学信号等研究方法,揭示采矿活动对山西水资源的破坏过程机理.结果表明:山西矿区矿坑水为Na-Ca-SO4型水,δ18O和δD为-9.34×10-3~-9.78×10-3,-66.14×10-3~-68.91×10-3,矿区矿坑水、孔隙水、河水和浅层岩溶水聚集,存在显著的补给排泄关系,矿坑水主要由浅层岩溶水、孔隙裂隙水和河水混合补给形成.采矿活动对浅层岩溶水、孔隙裂隙水以及河水的破坏甚为严重,而对深层岩溶水与水库水影响甚微,以上示踪得出结论与实际情况及物探结论基本吻合,研究可为类似矿区水资源安全利用等提供参考.     

太原市工、商业区PM10中PAHs碳同位素组成及来源

利用中流量大气综合采样仪采集太原市工业区和商业区PM₁₀样品,使用GC/IRMS技术分析了PAHs的δ13C值(碳同位素组成),并根据碳同位素质量平衡计算了煤烟尘和机动车尾气对2类功能区的贡献率. 结果表明:工业区PM₁₀中PAHs的δ13C值在-26.0‰~-24.5‰之间,随环数增加呈贫13C趋势,与煤烟尘δ13C值的变化趋势一致,表明煤烟尘是工业区的一个主要污染源;商业区PAHs的δ13C值在-26.6‰~-26.2‰之间,较工业区显著贫13C,商业区与工业区的污染源有明显差异;除机动车尾气和煤烟尘外,工业区和商业区还有其他污染源输入,其中工业区有生物质燃烧排放输入,商业区有机动车曲轴箱润滑油残渣输入;煤烟尘和生物质燃烧对工业区的贡献率分别为59.3%~70.8%和29.2%~40.7%,表明工业区煤烟污染严重;机动车对商业区PAHs的贡献率在86.1%~95.8%之间,是商业区PM₁₀中PAHs的主要排放源,其中润滑油残渣的贡献率(在40.9%~85.3%之间)最大,机动车尾气的贡献率在8.3%~54.9%范围内,而煤烟尘的贡献率(在4.2%~13.9%之间)最小.      

四氨基钴酞菁催化产生活性氧的性能

四氨基钴酞菁作为一种有前途的可见光催化剂,可光敏化为三线态,与溶液中的O2反应产生活性氧.实验考察了反应过程中的光照时间、光敏剂质量、光照强度和pH等4个因素对活性氧产生的影响,同时确定了一种简单可行的检测方法:活性氧与卡巴肼(DPCI)反应,生成卡巴腙(DPCO),以苯-四氯化碳萃取,在563 nm处测其吸光度,从而表示出活性氧的相对产量.实验优化了四氨基钴酞菁催化产生活性氧的条件:于50 mL的溶液中,光照时间为25 min,光敏剂质量为5 mg,光照强度为60 W,pH值为4.同时证明了在反应体系中生成了自由基和单线态氧等活性氧,并且对光催化产生活性氧的机理进行了探讨.