正丁醇/水混合溶剂中一步合成NO3-LDH的研究

以尿素为沉淀剂，正丁醇/水混合液为溶剂，采用水热法直接合成层状双金属氢氧化物ZnAl-NO₃-LDHs。通过X射线衍射（XRD）、傅里叶变换红外光谱（FT-IR）、扫描电镜（SEM）和元素分析（CHN）等对所得样品进行表征，证明在尿素存在条件下，NO₃^-进入LDHs层间；XRD、SEM结果和丁达尔现象显示所得NO₃-LDHs可在甲酰胺溶液中剥离。对尿素存在条件下形成NO₃-LDH而非CO₃-LDH的机理进行了探讨。以氯化盐和硫酸盐为原料，采用本文方法成功合成了Cl-LDH和SO₄-LDH，此研究结果可为制备不同阴离子插层的LDHs提供一种简单直接的方法。     

基于V-BLAST的多载波直接序列扩频CDMA系统上行链路性能分析

提出了一种应用多输入多输出（MIMO）的垂直分层空时（V-BLAST）检测算法的多载波直接序列扩频CDMA（MC-DS-CDMA）的系统结构,对系统上行链路的误码率性能进行了理论分析,推导出了接收天线数大于发射天线数条件下系统误码率的理论表达式,并通过计算机仿真进行了验证,数值结果表明,收发天线数对系统性能具有较大的影响,相对于传统MC-DS-CDMA系统,减少发射天线数或增加接收天线数均可使基于V—BLAST算法的MC-DS-CDMA系统的性能和容量有不同程度的改善．     

热处理条件对IrO2-pH电极性能的影响

在700℃炉冷、870℃空冷和炉冷三种热处理条件下,制备了氧化铱pH微电极,并对比了微电极的线性范围及响应时间.结果表明:热处理条件对Ir氧化物膜的均匀性有很大影响,进而影响其开路电位的稳定性及响应速度.700℃炉冷和870℃空冷制得的电极氧化膜表面粗糙,孔隙率不均匀并伴随有裂纹;而870℃炉冷条件下制得的电极具有表面氧化膜均匀、响应时间短以及线性好等优点.铱氧化物的形成机理是Ir丝被空气中的O2氧化,而高温Li2CO3起到一种溶剂的作用.铱氧化物电极的H+响应是由于电极表面水合氧化铱与溶液中H+发生化学反应,反应为Ir4+与Ir3+之间的转变.     

任意方向运动多层介质中电磁波的传播特征

利用Lorentz变换矩阵和运动各向同性均匀介质中电磁场量间的关系及边界条件,详细推导了,当多层介质沿任意方向运动时,入射波在运动系下,在静止参考系中其多层介质界面上电磁波场量传播特征的矩阵递关系和波矢量的变化关系.     

Serum levels of perfluorinated compounds in the general population in Shenzhen, China

Perfluorinated compounds (PFCs) have been detected in many environmental matrices, biota, and nonoccupationally exposed populations in China recently. However, little is known about the distribution and levels of various PFCs in the general population living in areas where there is PFC exposure. In the present study, the levels and prevalence of ten target PFCs were determined in 227 serum samples from a population of nonoccupationally exposed individuals in Shenzhen, China. Results indicated that human exposure to PFCs was prevalent in Shenzhen. Perfluorooctanoate (PFOA) was the dominant PFC contaminant in the serum samples, with a median concentration of 6.72 ng/mL, followed by perfluorooctane sulfonate (PFOS) with a median concentration of 2.07 ng/mL. Other PFCs were detected at much lower concentrations, with median concentrations ranging from 0.02 to 0.87 ng/mL. Statistically, no significant (P>0.05) gender differences were observed for any of the PFCs. Significant (P<0.01) positive correlations were found between age and serum concentrations of the target PFCs, except for perfluorobutane sulfonate (R = 0.16, P = 0.01), perfluorohexanoic acid (R = 0.08, P = 0.22), and perfluoroheptanoic acid (R = 0.11, P = 0.10). Based on the one-compartment pharmacokinetic model, the total daily intakes of PFOA and PFOS for the general population in Shenzhen were calculated as 0.63 and 0.20 ng/kg body weight/day, respectively.     

A gas chromatography/mass spectrometry method for the simultaneous analysis of 50 phenols in wastewater using deconvolution technology

Phenolic compounds exist widely in the influents and effluents of sewage treatment plants (STPs) and most are un-regulated. In this study, a gas chromatography-mass spectrometry (GC-MS) method for the simultaneous analysis of 50 phenolic compounds in wastewater was developed. Deconvolution technology was used to identify contaminants that are covered by co-extracted materials. A mass spectral library containing all 50 silylated phenolic compounds was first established and used for deconvolution. Twelve typical phenolic compounds were selected to optimize the sample preparation procedures. Solid-phase extraction using a C18 cartridge coupled with an HLB cartridge was used for pre-concentration and dichloromethane was used for elution. The solutes were derivatized and analyzed by GC-MS. The blank and matrix spike recoveries ranged from 57.46% to 136.4% and 47.87% to 114.8%, respectively. Method detection limits ranged from 3.64 to 97.64 ng L⁻¹. The relative standard deviations of all the recovery experiments were lower than 13.6%. The instrument limits of quantification ranged from 0.7 to 87.7 pg. The method has been applied to analyze the influents and effluents of 5 Chinese STPs. Except for regulated phenolic compounds (phenol and 2,4,6-trichlorophenol), three un-regulated phenolic compounds, including 2-chlorophenol, 2,5-dichlorophenol and 2,4-dichloro-3-ethyl-6-nitrophenol were identified in the effluent wastewater. The detected concentrations of un-regulated phenolic compounds could possibly cause environmental effects, indicating that immediate attention is required to prevent complications.     

成层地基中静压单桩挤土效应试验

采用室内模型试验研究了成层地基中静压桩沉桩过程,对模型桩整个沉桩过程中的挤土效应进行了分析研究。通过模型试验对在均质不同软硬地基中静力压入单桩过程产生的位移场进行了比较分析,获得了浅层土体、桩身周围、桩端处土体不同的位移变化模式,并揭示了桩周不同位置特别是软硬土层交界处土体位移随水平和深度方向的变化规律。试验结果表明,均质地基挤土位移的最大值与压桩深度存在滞后效应;对于成层地基,最大径向、竖向位移均出现在软硬土层交界面处,由于软硬土层力学性质的差异,土体位移主要表现为,软层处位移变大,硬层处位移变小。试验获得的结果便于进一步明确静压桩沉桩过程中挤土效应的内在机理,对预估沉桩的施工影响和指导沉桩设计都具有现实意义。     

贮藏温度对蓝莓活性成分及抗氧化活性的影响

研究不同贮藏温度下,蓝莓果实的活性成分及抗氧化活性的变化,确定蓝莓鲜果适宜的贮藏温度,并为研究蓝莓果实中主要的抗氧化成分提供参考.在贮藏温度为20~25,10~15,0~5℃下,于不同贮藏期取样测定蓝莓果实中花青素、总酚和总黄酮的质量分数;测定蓝莓对DPPH自由基（DPPH.）和羟自由基（OH.）的清除率,并分析3种活性成分与蓝莓抗氧化活性的相关性.结果表明,在不同的贮藏温度下,蓝莓果实中花青素、总酚和总黄酮的质量分数及抗氧化活性均呈现先上升后下降的趋势,在贮藏初期,较高的贮藏温度能明显促进蓝莓果实活性成分含量和抗氧化活性的增加,但在贮藏后期,较高的温度加速了蓝莓果实活性成分含量和抗氧化活性的下降速度,并缩短了蓝莓贮藏期;低温（0~5℃）能使蓝莓果实的活性成分含量和抗氧化活性始终维持在一个相对较高的水平,且能显著增加果实的贮藏期,是蓝莓较适宜的贮藏温度;蓝莓果实中花青素、总酚和总黄酮质量分数与其清除自由基的能力之间均呈显著正相关（P〈0.05）.     

分层饱和土中横向受荷桩动力响应分析

考虑饱和土的成层性和孔隙流体与土骨架变形的相互作用,用积分变换方法构建盘面和柱面荷载作用下土体与结构动力相互作用影响函数,用边界元方法建立相应的考虑饱和土成层性的地基与桩基础动力相互作用分析方法.以层状饱和土中横向受荷桩动力阻抗分析表明分析方法的可行性.算例分析孔隙流体对分层饱和土中横向受荷桩动力响应影响.     

新型偶氮香豆素化合物的合成及光谱特性

为对比6-偶氮香豆素和7-偶氮香豆素的光物理特性,设计、合成并测定了一系列偶氮香豆素化合物的最大紫外吸收波长和最大荧光发射波长的数据,并求得了S tock位移值。