外浮顶原油储罐VOCs排放核算参数对排放量的影响研究

依据美国环保署颁布的储罐VOCs排放量核算公式,从环境参数、原油参数和储罐结构参数3个方面对外浮顶储罐VOCs排放的影响进行了研究,其中包括了边缘密封排放挂壁排放、浮盘附件排放和浮盘着陆期间排放等几个相关排放核算数学公式。结果表明:环境风速增大,环境温度升高或太阳辐射强度提高均导致排放量增大;原油温度升高或原油周转量增加也导致排放量增加;储罐直径增加,罐漆颜色浅,或者罐壁锈蚀情况好会降低VOCs排放量。     

带支撑基坑围檩受力性状分析及数值模拟

通过对带支撑基坑围檩受力性状的分析,提出支撑与围檩正交、斜交分别对应的几种基坑围檩轴力分布形式,并以武汉市凯德广场古田项目为例,从实测数据出发,分析了基坑围檩轴力的变化规律,在对基坑内支撑平面有限元计算中设置在围檩上的边界条件的特性进行深入研究的基础上,使用数值模拟手段对基坑围檩轴力进行了计算与数值模拟验证。结果表明:与开挖工况一致,围檩轴力呈现"两阶段"增长过程,地下室主体结构施工完成后,围檩轴力趋于稳定;桩(墙)平行于围檩走向的切向约束客观存在,本例中围檩轴力呈现梯形交替递增分布形式;桩(墙)对围檩的约束方向包括切向和法向,其约束形式表现为线约束和弹性约束。     

罕见冬季降雨中人工增雨微物理过程分析研究

用Micaps实时资料、CPAS卫星反演分析资料、NCEP再分析资料、ECMWF再分析资料,多普勒雷达PUP产品资料,对2015年12月1日夜间至2日凌晨沈阳地区罕见冬季降雨过程,进行了天气学分析、及大气微物理人工增雨作业条件分析,并结合沈阳地区人工增雨作业指标,得出本次降雨过程在厄尔尼诺正在发生的背景下,为常见的高空槽转东北冷涡型,水汽、动力等微物理作业条件也适合于开展人工增雨作业,并给出了相应的作业指导参数,为沈阳地区今后在冬季降雨天气过程中开展人工增雨作业积累了宝贵经验.     

基于预应力杆的空间桁架天线固有频率调节技术

目的研究预应力杆对大型空间桁架天线固有频率影响,提出采用作动器实时对在轨空间天线低阶固有频率进行调整,主动避免共振现象发生。方法针对大型空间桁架天线结构有限元模型,采用降温法对桁架杆施加预应力,重点分析预应力大小、预应力杆位置、预应力杆数量对整体结构固有频率的影响。结果增加预应力大小、合理布置预应力杆位置、增加预应力杆数量能够增加空间桁架天线固有频率的改变率。结论合理优化空间桁架天线上预应力杆,可实现对在轨运行的空间桁架天线低阶固有频率实时调整,可为空间桁架天线避振设计提供参考。     

氯化磁性凹土树脂的制备与表征研究

利用表面负载的方法将有机化磁性凹土与苯乙烯、二乙烯苯等制备磁性凹土树脂;对磁性凹土树脂进行氯甲基化改性,制备出氯化磁性凹土树脂.表征了样品的形貌、结构以及表面积,研究了树脂对天然有机物(腐殖酸)的吸附性能.结果表明:氯化后的磁性凹土树脂的比表面积是原有的1.9倍,对附腐殖酸的饱和吸附能力也从原有的41.84 mg/g提高到了51.02 mg/g,这表明改性后的树脂增强了其对腐殖酸的去除能力.     

固载化瓜环的制备及其对磺胺间甲氧嘧啶的吸附性能研究

在微波无极灯下将烯氧基瓜环固载到巯基硅胶(MSG)上,制得固载化瓜环(ACB[6]-SG).通过红外光谱表征固载产物,并研究固载化瓜环对磺胺间甲氧嘧啶(SMM)的吸附性能.结果表明,SMM在固载化瓜环上的吸附基本在2 min内即可达到平衡;Henry方程和Freundlich方程均能较好地拟合SMM在固载化瓜环和巯基硅胶上的等温吸附曲线,但是SMM在固载化瓜环上的吸附主要是在瓜环中的分配,而SMM在巯基硅胶上的吸附则主要是多分子层的表面吸附作用;SMM在固载化瓜环上的平衡吸附量远大于在巯基硅胶上的平衡吸附量;SMM在两者上的吸附过程是一个放热过程,温度越低吸附效果越好.     

Adsorption of lead on multi-walled carbon nanotubes with different outer diameters and oxygen contents: Kinetics, isotherms and thermodynamics

The effects of different outer diameters and surface oxygen contents on the adsorption of heavy metals onto six types of multi-walled carbon nanotubes (MWCNTs) were investigated in an aqueous solution and lead was chosen as a model metal ion. The results indicated that the percentage removal and adsorption capacity of lead remarkably increased with decreasing outer diameter due to larger specific surface area (SSA). The SSA-normalized maximum adsorption capacity (qm /SSA) and SSA-normalized adsorption coefficient (Kd /SSA) were strongly positively correlated with surface oxygen content, implying that lead adsorption onto MWCNTs significantly increases with the rise of oxygen content and decreases with decreasing SSA. The calculated thermodynamic parameters indicated that adsorption of lead on MWCNTs was endothermic and spontaneous. When the oxygen content of MWCNTs increased from 2.0% to 5.9%, the standard free energy (△ G0 ) became more negative, which implied that the oxygenated functional groups increased the adsorption affinity of MWCNTs for lead. Through calculation of enthalpy (△ H0 ), G0 and free energy of adsorption (Ea ), lead adsorption onto MWCNTs was recognized as a chemisorption process. The chemical interaction between lead and the phenolic groups of MWCNTs could be one of the main adsorption mechanisms due to highly positive correlations between the phenolic groups and K d /SSA or q m /SSA.     

不同材质对催化裂化装置催化剂粉尘粘附性能的试验研究

在三座DN150 mmX1600 mm有机玻璃塔试验装置上,考察了DN15的塑料拉西环、陶瓷拉西环和不锈钢拉西环三种材质填料对催化剂的粘附能力。在催化剂浓度5‰,液相负荷40 L/h,气相负荷80 m3/h的条件下,经过408h的连续运转,结果表明不同材质填料对催化剂的粘附能力均存在饱和状态,粘附在填料上的催化剂不随时间的持续增加而增多。其中,塑料填料对催化剂的粘附能力最强,增重0.125kg;不锈钢填料次之,增重为0.115kg;陶瓷填料最弱,增重为0.055kg。可为相关领域的工业应用提供借鉴和数据支撑。     

Simultaneous preconcentration of cadmium and lead in water samples with silica gel and determination by flame atomic absorption spectrometry

A new method that utilizes pretreated silica gel as an adsorbent has been developed for simultaneous preconcentration of trace Cd(II) and Pb(II) prior to the measurement by flame atomic absorption spectrometry. The effects of pH, the shaking time, the elution condition and the coexisting ions on the separation/preconcentration conditions of analytes were investigated. Under optimized conditions, the static adsorption capacity of Cd(II) and Pb(II) were 45.5 and 27.1mg/g, the relative standard deviations were 3.2% and 1.7% (for n = 11), and the limits of detection obtained were 4.25 and 0.60 ng/mL, respectively. The method was validated by analyzing the certified reference materials GBW 07304a (stream sediment) and successfully applied to the analysis of various treated wastewater samples with satisfactory results.     

Identification of key factors governing chemistry in groundwater near the water course recharged by reclaimed water at Miyun County, Northern China

Reclaimed water was successfully used to recover the dry Chaobai River in Northern China, but groundwater may be polluted. To ensure groundwater protection, it is therefore critical to identify the governing factors of groundwater chemistry. Samples of reclaimed water, river and groundwater were collected monthly at Chaobai River from January to September in 2010. Fifteen water parameters were analyzed. Two kinds of reclaimed water were different in type (Na-Ca-Mg-Cl-HCO3 or Na-Ca-Cl-HCO3 ) and concentration of nitrogen. The ionic concentration and type in river were similar to reclaimed water. Some shallow wells near the river bed had the same type (Na-Ca-Mg-Cl-HCO3 ) and high concentration as reclaimed water, but others were consistent with the deep wells (Ca-Mg-HCO3 ). Using cluster analysis, the 9 months were divided into two periods (dry and wet seasons), and all samples were grouped into several spatial clusters, indicating different controlling mechanisms. Principal component analysis and conventional ionic plots showed that calcium, magnesium and bicarbonate were controlled by water-rock interaction in all deep and some shallow wells. This included the dissolution of calcite and carbonate weathering. Sodium, potassium, chloride and sulfate in river and some shallow wells recharged by river were governed by evaporation crystallization and mixing of reclaimed water. But groundwater chemistry was not controlled by precipitation. During the infiltration of reclaimed water, cation exchange took place between (sodium, potassium) and (calcium, magnesium). Nitrification and denitrification both happened in most shallow groundwater, but only denitrification in deep groundwater.