石化生产装置微量泄漏检测方法及应用

以石化装置为例介绍了生产装置微量泄漏的含义、适用的检测仪器种类以及泄漏检测的具体做法。通过实际检测数据的分析。说明了微量泄漏检测对设备管理、工艺改造的促进作用。     

浸渍液pH值对V-Mo/Ti脱硝催化剂性能的影响研究

为提升V-Mo/Ti催化剂的脱硝性能,在催化剂制备过程中调节浸渍工艺参数,制备了一系列不同浸渍液pH值的催化剂,采用XRD、N2-吸附脱附、拉曼光谱、UV-Vis、H2-TPR、NH3-TPD等手段对催化剂进行表征,考察了pH值的变化对催化剂物理化学性能的影响,采用固定床微型反应器对催化剂的脱硝性能进行评价。结果表明,降低浸渍液pH值,可以抑制催化剂上VOx物种的聚合,提升催化剂的还原性能,有利于提升催化剂的脱硝效率,降低脱硝反应过程中N2O生成量。同时,浸渍液pH值的变化,也会影响催化剂的酸性性能。当浸渍液pH值低于3.64时,催化剂酸性性能显著降低,造成催化剂脱硝性能降低;当浸渍液pH值控制在3.64时,催化剂的还原性能和酸性性能匹配较好,从而显示了较高的脱硝性能。     

取芯过程中煤芯温度分布特征模拟研究*

针对取芯过程瓦斯解吸受煤芯的温度影响不明,造成煤层瓦斯含量测不准的问题,开展对取芯过程煤芯温度分布特征研究。采用自主研制的取芯管自动测温装置在赵固二矿原生结构煤层（f=1.71）进行深度20 m的取芯试验,获得取芯管管壁温升变化规律,变化曲线分为4个阶段:缓慢上升、加速上升、减速上升、缓慢下降阶段;应用COMSOL建立含瓦斯煤传热模型,将管壁的温度变化设置为边界条件,模拟取芯过程煤芯与管壁之间的热交换。结果表明:在取芯时间30 min内,煤芯平均温度快速上升,之后上升速度趋于平稳;在煤芯内,相同时刻,等间距的轴向与径向距离,径向较轴向的温度梯度较大,径向传导快于轴向传导;取芯过程煤芯径向温度Ta与径向距离d、时间t满足指数函数关系。研究结果可为测定取芯过程煤芯的瓦斯损失量提供参考依据。     

Modeling Flow,Nutrient, and Sediment Delivery from a Large International Watershed Using a Field‐Scale SWAT Model

A large international watershed, the St. Clair‐Detroit River System, containing both extensive urban and agricultural areas, was modeled using the Soil and Water Assessment Tool (SWAT) model. The watershed, located in southeastern Michigan, United States, and southwestern Ontario, Canada, encompasses the St. Clair, Clinton, Detroit (DT), Sydenham (SY), Upper, and Lower Thames subwatersheds. The SWAT input data and model resolution (i.e., hydrologic response units, HRUs), were established to mimic farm boundaries, the first time this has been done for a watershed of this size. The model was calibrated (2007–2015) and validated (2001–2006) with a mix of manual and automatic methods at six locations for flow and water quality at various time scales. The model was evaluated using Nash–Sutcliffe efficiency and percent bias and was used to explore major water quality issues. We showed the importance of allowing key parameters to vary among subwatersheds to improve goodness of fit, and the resulting parameters were consistent with subwatershed characteristics. Agricultural sources in the Thames and SY subwatersheds and point sources from DT subwatershed were major contributors of phosphorus. Spatial distribution of phosphorus yields at HRU and subbasin levels identified locations for potential management targeting for both point and nonpoint sources and revealed that in some subwatersheds nonpoint sources are dominated by urban sources.     

大亚湾浮游细菌的变性梯度凝胶电泳分析

于2010年12月以及2011年6月采集了大亚湾9个站点的表层水样,利用PCR-变性梯度凝胶电泳(PCR-DGGE)技术对浮游细菌DNA指纹进行了分析.结果显示,大亚湾海域浮游细菌DNA指纹比较丰富,冬季和夏季样品中分别共得到32条和33条条带,每个样品得到的条带数为18~25条.DNA指纹的Shannon-Weaver多样性指数(H')和Pielou均匀度(J)的变化范围分别为2.48~2.88和0.80~0.93.DNA指纹条带数与温度和盐度明显正相关,而与p H、DO、透明度呈明显负相关关系.结果说明PCR-DGGE技术可以在一定程度上反映细菌的群落结构和多样性,但需要与其他技术相结合方能较全面反映细菌的结构与功能.     

一维碳纳米管与金属氧化物材料研究

一维纳米结构是最吸引人的功能材料而被广泛关注.一维形态可以很容易地提高纳米结构的独特性能,使它们适合各种各样的应用程序,包括气体传感器、电致变色的设备、发光二极管、场发射器、超级电容器和纳米发电机.因此,目前已合成多种一维纳米结构形式的纳米棒、纳米线、纳米管、纳米带等.本文主要介绍了一维碳纳米管与金属氧化物的性质与研究现状,探讨两种材料的优缺点以期进行互补修饰合成新型复合材料.     

Adsorption of chlorophenols from aqueous solutions by pristine and surface functionalized single-walled carbon nanotubes

The adsorption of six kinds of chlorophenols on pristine, hydroxylated and carboxylated single-walled carbon nanotubes(SWCNTs) has been investigated. Pseudo-first order and pseudo-second order models were used to describe the kinetic data. All adsorption isotherms were well fitted with Langmuir, Freundlich and Polanyi–Manes models, due to surface adsorption dominating the adsorption process. The close linear relationship between log Kowand log Kdsuggested that hydrophobicity played an important role in the adsorption. The SWCNTs' adsorption capacity for chlorophenols was weakened by addition of oxygen-containing functional groups on the surface, due to the loss of specific surface area, the increase of hydrophilicity and the reduction of π–π interaction. The best adsorption capacity of pristine SWCNTs, SWCNT-OH and SWCNT-COOH for six chlorophenols varied from 19 to 84 mg/g, from 19 to 65 mg/g and from 17 to 65 mg/g,respectively. The effect of pH on the adsorption of 2,6-dichlorophenol(2,6-DCP), was also studied. When p H is over the pK aof 2,6-dichlorophenol(2,6-DCP), its removal dropped sharply. When ionic strength increased(Na Cl or KCl concentration from 0 to 0.02 mmol/L),the adsorption capacity of 2,6-DCP on pristine SWCNTs decreased slightly. The comparison of chlorophenols adsorption by SWCNTs, MWCNTs and PAC was made, indicating that the adsorption rate of CNTs was much faster than that of PAC. The results provide useful information about the feasibility of SWCNTs as an adsorbent to remove chlorophenols from aqueous solutions.     

优化热脱附技术对十溴联苯醚污染土壤的适用性及修复效果

为了探索绿色、高效、环保的修复PBDEs污染土壤的技术,在热脱附技术基础上将木炭同时作为尾气吸附剂和燃烧热源,处理不同十溴联苯醚污染水平的PBDEs(多溴联苯醚)污染土壤,通过14种不同溴代PBDEs同系物分析十溴联苯醚的降解产物组分并计算其去除率. 结果表明:在热脱附技术处理后,十溴联苯醚初始污染水平分别为500、800和1 000 μg/kg,污染土壤中PBDEs的去除率分别为63%、81%、94%. 14种不同溴代PBDEs同系物在热脱附反应后的残留产物中均有检出,其中热脱附处理后的土壤中以三溴和四溴PBDEs产物占优势,而尾气中则以四溴和五溴PBDEs产物为主. 根据热脱附试验前后土壤中PBDEs的结构组成对比及分析可知,降解和脱溴反应在整个热脱附反应过程中发挥了重要作用. 另外,XAD树脂吸附柱中虽有少量的氯代和溴代二英类物质(PCDD/Fs和PBDD/Fs)被检出,但其毒性当量浓度均小于0.1 ng/m3,符合欧盟、日本及我国所规定的二英物质排放标准. 研究显示,在利用优化的热脱附技术修复十溴联苯醚污染土壤过程中,PBDEs的去除率与污染土壤中其污染水平相关,并且热脱附过程以降解及逐级脱溴反应为主.      

有机肥施用对盐渍土富里酸荧光特性的影响

为探讨有机肥长期培肥盐渍土后土壤富里酸(FA)结构组成及土壤环境的变化特征,对黑龙江西北部盐渍土壤连续5 a采取不同施肥处理,设置CK(对照)和TR1(处理1,施用有机肥8 000 kg/hm2)、TR2(处理2,施用有机肥4 000 kg/hm2及化肥N 80 kg/hm2、P₂O₅ 50 kg/hm2、K₂O 35 kg/hm2)、TR3(处理3,施用化肥N 160 kg/hm2、P₂O₅ 100 kg/hm2、K₂O 70 kg/hm2) 4个处理组,分析土壤中富里酸荧光光谱特征的变化情况. 结果表明:与CK比较,TR1、TR2处理可明显增加土壤中ρ(富里酸),增幅分别为98.24%、72.16%;二维荧光参数分析显示,各处理下富里酸腐殖化程度均表现为TR1>TR2>TR3>CK;三维荧光光谱区域积分比值分析结果进一步证实,TR1、TR2处理通过增加可见区类富里酸的荧光响应比值和减少紫外区类富里酸的荧光响应比值来提高富里酸的腐殖化程度. 根据三维荧光光谱结合平行因子分析结果,可将富里酸分为C1组分(生物可利用富里酸组分)、C2组分(陆生来源富里酸组分)及C3组分(类蛋白组分);施用有机肥主要增加C1组分的比例,其次为增加C2组分的比例,说明施用有机肥可提高盐渍土供肥能力,对盐渍土生态环境改善具有积极作用. 传统荧光图谱解析手段结合统计分析结果显示,施用有机肥可明显提高盐渍土富里酸含量并增加其腐殖化程度.      

流域水生态安全评估方法

为建立合理的流域水生态安全评估指标体系,以流域为对象,对水生态安全内涵进行了阐释,并对流域水生态安全评估指标进行了系统分析.基于“压力、状态、功能、风险”四要素,构建了“目标层-方案层-要素层-指标层”的评估体系,其中方案层包括水生态压力、水生态状况、水生态功能和水生态风险4个方面,涵盖土地利用、水资源利用、污染物排放、栖息地状态、水生态质量、水产品供给、休闲娱乐、水环境净化、重金属风险等9个评估要素18个评估指标,并详尽表述了各评估指标的内涵及其计算方法.采用综合指数法计算ESI(生态安全指数),并根据ESI得分将水生态系统的安全评级分为安全(3.5≤ESI≤4.0)、较安全(2.5≤ESI<3.5)、一般(1.5≤ESI<2.5)、不安全(0.5≤ESI<1.5)和很不安全(0≤ESI<0.5)5个级别,构建了多指标的流域水生态安全评估方法.