多参数指示南极普里兹湾浮游植物的时空变化

以南极普里兹湾沉积物为研究对象,运用气相色谱技术,研究了生物标志物菜子甾醇、甲藻甾醇、长链烯酮对应指示的硅藻、甲藻、颗石藻等浮游植物的生产量和种群结构的历史变化,结合2001—2011年实测和遥感水体ρ(Chla)(Chla为叶绿素a)及SST(海水表层温度)数据,探讨了该湾浮游植物生产量时空变化特征及其影响因素. 结果表明:过去100多年间南极普里兹湾浮游植物总生产量(212.04~759.10 ng/g)〔以w(菜子甾醇)+w(甲藻甾醇)+w(长链烯酮)计〕和w(硅藻)所占比例(62.28%~87.13%)〔以w(菜子甾醇)所占比例计〕均呈上升趋势,而w(甲藻)所占比例(10.09%~27.98%)〔以w(甲藻甾醇)所占比例计〕和w(颗石藻)所占比例(1.97%~9.74%)〔以w(长链烯酮)所占比例计〕则呈下降趋势. 全球变暖背景下浮游植物种群变动通过改变南大洋对CO₂的吸收进而影响全球碳循环. 水体ρ(Chla)与沉积生物标志物指示的浮游植物总生产量均具有湾内高、湾外低的空间分布特征. 湾内ρ(Chla)与SST的年际变化趋势相似,二者以2002—2003年和2009—2010年相对较高,SST分别为-0.30和0.01 ℃,ρ(Chla)分别为1.69和2.31 mg/m3;以2001—2002年和2010—2011年相对较低,SST分别为-1.19和-0.95 ℃,ρ(Chla)分别为1.08和0.79 mg/m3,表明该湾SST变化可较明显地影响浮游植物的生长.      

Uncertainties in a risk management context in early phases of offshore petroleum field development

The current risk management approach for the Norwegian offshore petroleum industry came into effect in 2001 and has been stable with minor changes for 15 years. Relatively few new installations were slated for development until quite recently, and several new projects have been started in the last few years. The paper considers the risk management approach in the pre-FEED phase and builds on two case studies selected from the most recent cases. These case studies have been evaluated with respect to how uncertainties are considered in the early phase, based on the submission of the Plan for Development and Operation, their evaluations by authorities and the supporting documents. Both case studies involve new concepts for which there is no experience from similar environments and/or water depths. In spite of what could have been expected, the case studies conclude that uncertainties have not been in focus at all during concept development. This appears to be definitely the case for the licensees, but also to be the case for the authorities. Some suggestions are presented for what could have been considered by the licensees and authorities.     

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%.     

污水处理厂低温等离子体恶臭治理技术

利用低温等离子体技术处理污水厂恶臭气体,是一种新的技术。介绍了该技术处理恶臭的机理和相关工程的工艺流程以及处理效果,实际应用表明该技术对污水处理厂恶臭气体的治理是十分有效的。     

Y形通风采空区自燃与有害气体排放的数值模拟

基于非均质多孔介质漏风渗流方程、多相气体渗流-扩散方程和多孔介质渗流综合传热方程,建立了采空区瓦斯与自燃发火耦合数值模型,开发了用迎风格式有限元方法联立求解的计算机程序(简称G3).计算以图形方式给出各量的区域分布解,从理论上描绘了Y形通风采空区的漏风流态,动态描绘了瓦斯、氧和CO的体积分数以及温度分布状态及其变化过程,并证明了Y形通风形式能避免采空区瓦斯向工作面涌出.计算中采空区按冒落非均质介质处理,考虑了瓦斯涌出对自燃的耦合作用,给出了这种耦合作用关系和解决办法.Y形通风采煤的自燃,两者存在着顾此失彼的关系.     

轧钢污泥综合利用的技术研究

阐述了一种轧钢污泥的回收处理技术,该技术可把轧钢污泥有效地分离成氧化铁粉和混合油,实现综合利用,减少铁素资源浪费,有良好的经济效益和环境效益.     

Low-temperature CO oxidation over Au-doped 13X-type zeolite catalysts: preparation and catalytic activity

Au-supported 13X-type zeolite (Au/13X) was synthesized using a common deposition–precipitation (DP) method with a solution of sodium carbonate as a precipitate agent. Further testing was conducted to test for catalytic oxidation of CO. A study was conducted on the effects of different preparation conditions (i.e., chloroauric acid concentration, solution temperature, pH of solution, and calcinations temperature) on Au/13X for CO oxidation. In respect to the catalytic activity, the relationship between different the preparation conditions and gold particles in 13X zeolite was analyzed using X-ray diffraction, TEM and XPS. The activity of Au/13X catalysts in CO oxidation was dependent on the chloroauric acid concentration. From XRD results, a higher chloroauric acid concentration induced larger gold nanoparticles, which resulted in lower catalytic activity. Results revealed that higher temperatures induced higher Au loading, homogeneous deposit, and smaller gold clusters on the support of 13X, resulting in higher CO activity. Furthermore, a pH of 5 or 6 generated greater amounts of Au loading and smaller Au particles on 13X than at a pH of 8 or 9. This may be a result of an effective exchange between Au(OH)2Cl2- and Au(OH)₃Cl^- on specific surface sites of zeolite under the pH’s 5 and 6. The sample calcined at 300°C showed the highest activity, which may be due to the sample’s calcined at 200°C inability to decompose completely to metallic gold while the sample calcined at 400°C had larger particles of gold deposited on the support. It can be concluded from this study that Au/13X prepared from a gold solution with an initial chloroauric acid solution concentration of 1.5 × 10^-3 mol·L^-1 gold solution pH of 6, solution temperature of around 90°C, and a calcination temperature of 300°C provides optimum catalytic activity for CO oxidation.     

Removal of selenite using ‘waste’ Fe(III)/Cr(III) hydroxide: Adsorption kinetics and isotherms

Removal of selenite [Se (IV)] from aqueous solution on to industrial solid ‘waste’ Fe(III)/Cr(III) hydroxide as adsorbent was investigated in the present article. Maximum adsorption was found to be at pH 4.0. Pretreated Fe(III)/Cr(III) hydroxide was found to be more efficient for the removal of selenite compared to untreated adsorbent. Langmuir and Freundlich isotherms have been studied. The Langmuir adsorption capacity (Q ₀) of the pretreated and untreated adsorbents was found to be 15.63 and 6.04?mg?g^?1, respectively. The adsorption process fit into the second-order kinetics. Thermodynamic parameters show that the adsorption process is spontaneous and endothermic in the temperature range 32 to 60°C. Coexisting anions vanadate and phosphate significantly affect the adsorption of selenite for both the pretreated and untreated adsorbents. Molybdate, thiocyanate, sulphate, nitrate and chloride do not significantly affect the removal of selenite for pretreated adsorbent.     

Influence of temperature and pH on the effects of zinc and copper on proteolytic activities of the intestinal mucosa of planktivorous and benthophagous fishes and their potential preys

Influences of temperature (0 and 20°C) and pH (3.0, 5.0, and 7.4) on the effect of zinc (Zn) and copper (Cu) on proteolytic activities of intestinal mucosa in planktivorous (blue bream, bleak), bentophagous (bream, roach) fishes and their potential preys (pond snail Limnaea stagnalis, planorbid Planorbarius purpura, dreissena Dreissena polymorpha, midge larvae Chironomus sp., water flea Daphnia longispina and total zooplankton) are revealed in this article. Cu decreases the caseinolytic and hemoglobinolytic activities in both fish and their preys more than Zn at temperature 20°C and pH 7.4. Low temperature intensifies the negative effect of the metals on the protease activity in fish (in the case of Zn 5–10 times, in the case of Cu 5–30 times). In fish prey species, the negative effect of the metals on the proteinase activity may be more significant. The influence of pH on Zn and Cu effects is less pronounced than that of low temperature. Maximum reduction of enzyme activities is observed for the combined action of low temperature and pH as well as of the studied metals.     

水体中磺胺甲恶唑和甲氧苄氨嘧啶的自然光降解

实验研究了磺胺甲恶唑和甲氧苄氨嘧啶连续暴露于自然光下72 h,在pH值为4.0、7.0、9.0水体中的光降解行为,同时考察了黑暗条件下对照样品在不同pH条件下的稳定性.实验表明,光强、光照时间、水体pH都直接影响到磺胺甲恶唑的去除率.在自然光照环境下,不同pH溶液中的磺胺甲恶唑均易发生光降解,而黑暗对照样品去除率较小.甲氧苄氨嘧啶则比较稳定,几乎未发生降解,但黑暗对照样品在pH值为4.0和7.0的溶液中,与起始浓度相比,去除率大于10%,这可能主要与该药物在不同pH溶液中的离子形态及光照过程中的温度波动有关.