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本文通过对目前锂离子电池市场及锂离子电池隔膜制备现状的研究,提出采用重离子辐照技术制备锂离子电池隔膜的新方法。拓展了重离子辐照技术的应用,为锂离子电池隔膜的国产化另辟蹊径。实验中,用能量25 MeV/u 的Kr86及11.4 MeV/u的197Au离子,以1×108 cm-2-5×109 cm-2剂量辐照聚丙烯薄膜,通过电导测量法监测蚀刻液的参数,包括温度、硫酸浓度、重铬酸钾浓度对径迹蚀刻速率的影响,得到适合的蚀刻条件;并用场发射扫描电镜对孔的形状及孔径大小进行表征;成功制备出孔径均匀、具有密度和大小可控的重离子径迹聚丙烯孔膜;对孔洞锥角的形成进行分析,给出锥角的计算公式,为利用重离子辐照技术制备锂离子电池隔膜提供了实验数据

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利用室内模拟方法,研究了重金属Hg对不同土样脲酶、转化酶和中性磷酸酶活性的影响.结果表明,Hg可显著地抑制土壤脲酶和转化酶的活性,但不同土样Hg对两种酶活性的抑制程度有很大差别.HgCl2浓度与两种酶活性之间的关系均可用对数方程很好地描述(P<0.05).4个土样的脲酶ED50(生态剂量)分别为87.99、5.47、24.05和19.88mg.kg-1;转化酶的ED50分别为76.68、727.49、236.52和316.59mg.kg-1.脲酶对Hg污染比转化酶敏感;有机质对土壤酶活性有一定的保护作用.除连续2年施用大量有机肥的草甸棕壤土样中Hg对中性磷酸酶有显著的激活作用外(P<0.05),其它土样无显著变化,表明中性磷酸酶活性对Hg污染反应不敏感.

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通过模拟方法研究了豆磺隆,呋喃丹2种农药与重金属汞(Hg)单一及复合污染对草甸棕壤和黑土4个土壤转化酶活性的影响.结果显示,在试验浓度范围内,土壤添加豆磺隆和呋喃丹后,转化酶变化幅度分别为-12%~7%和-6%~7%,表明2种农药对土壤转化酶的毒性较小;Hg对转化酶最大抑制率为22%~35%,二者之间呈显著的对数负相关关系,表明Hg对转化酶的毒性较大,转化酶在一定程度上可作为Hg污染的监测指标,通过对数方程计算出4个土样的生态剂量(ED50)分别为76.68,727.49,236.52,316.59mg/kg;Hg和2种农药之间普遍存在交互作用,豆磺隆与Hg复合污染引起土壤转化酶最大净变化量(?I)为对照的-12%~15%,呋喃丹和Hg为-25%~-6%,有机质对复合污染产生的毒性有明显的缓冲作用.

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采用TWINSPAN分类法对黄土丘陵沟壑区吴起县双树沟流域30个自然恢复草地植被进行分类,并对分类后各植被群落特征和地上生物量进行统计分析。结果表明:在自然恢复条件下,随着退耕年限的不断增加,退耕地植被自然恢复依次经历了猪毛蒿群落—赖草+长芒草群落—赖草+铁杆蒿群落—铁杆蒿群落—铁杆蒿+茭蒿群落5个发展阶段,地带性植被类型铁杆蒿+茭蒿群落在研究区内开始出现,并且已经占有一定优势;随着退耕地植被自然恢复的不断进行,Margalef等丰富度指数以及Shannon-wiener等多样性指数、Pielou等物种均匀度指数和地上生物量都呈现出先减小后增大的发展趋势;在植被自然恢复的稳定阶段,虽然物种丰富度指数和物种多样性指数有一定的增加,但是相对恢复初期来讲还是有所下降,并且有达到与初期相当水平的趋势;物种丰富度指数均在第1恢复阶段最大,而均匀度指数Jsw以及Shannon-wiener指数在第5恢复阶段最高。随着退耕地植被自然恢复的不断进行,植被群落总盖度随着退耕年限的延长而不断增大。

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IrO2/SnO2 (10%:90%, molar ratio) electrodes (ITEs) were prepared by the sol-gel method as an alternative to the electrode-position and thermal decomposition process. The electrodes were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), atomic force microscope (AFM), cyclic voltammetry (CV) and electrochemical impedance spectra (EIS). From the results of XRD, oxide films prepared at low temperature were in amorphous state, while hydrous IrO2 crystal and cassiterite phase SnO2 were formed at 300 degreesC or even to 500 degreesC. The highly porous structure was confirmed by AFM. The electrochemical experiments demonstrated that the sol-gel method made the ITEs having a fast electron transfer process with good stability and the optimal preparation temperature was 400 degreesC for the highest electroactivity. Furthermore, the electrocatalysis of pyrocatechol on the electrodes was investigated. A quasi-reversible process occurred and a linear range over three orders magnitude (1 x 10(-2) - 10 mM) was obtained by differential pulse voltammetry (DPV). Meanwhile the detection limit of pyrocatechol was 5 x 10(-3) mM. This study indicated that the sol-gel method was an appropriate route to prepare the IrO2/SnO2 electrodes for the electrocatalytic of pyrocatechol.

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A new amperometric biosensor for hydrogen peroxide was developed based on cross-linking horseradish peroxidase (HRP) by glutaraldehyde with multiwall carbon nanotubes/chitosan (MWNTs/chitosan) composite film coated on a glassy carbon electrode. MWNTs were firstly dissolved in a chitosan solution. Then the morphology of MWNTs/chitosan composite film was characterized by field-emission scanning electron microscopy. The results showed that MWNTs were well soluble in chitosan and robust films could be formed on the surface. HRP was cross-linked by glutaraldehyde with MWNTs/chitosan film to prepare a hydrogen peroxide biosensor. The enzyme electrode exhibited excellent electrocatalytic activity and rapid response for H2O2 in the absence of a mediator. The linear range of detection towards H2O2 (applied potential: -0.2 V) was from 1.67 x 10(-5) to 7.40 x 10(-4) M with correction coefficient of 0.998. The biosensor had good repeatability and stability for the determination of H2O2. There were no interferences from ascorbic acid, glucose, citrate acid and lactic acid.

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本文系统介绍了几种适用于生物大分子分析的软电离技术及其应用,井综述了以多肽、蛋白质为代表的生物活性大分子的分子量测定及序列分析.

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Studies using transmission electron microscopy, differential scanning calorimetry, and X-ray diffraction showed correlations between the crystallization behavior of the polydimethylsiloxane (PDMS) block and the morphology of the block copolymer poly (butadiene-b-dimethylsiloxane) (PB-PDMS). When the PDMS component existed as spheres dispersed in a PB matrix, the crystallization rate of the PDMS block was lower than when the PDMS phase existed in rod or cylinder form.