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951.
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Omar El Tall Nicole Jaffrezic‐Renault Monique Sigaud Olivier Vittori 《Electroanalysis》2007,19(11):1152-1159
Boron‐doped Diamond (BDD) electrode has become one of the important tools for heavy metal detection. By studying some analytical parameters of DPASV method, like deposition time and potential in different electrolyte concentrations (acetate buffer), the conditions for detecting very low metal ion levels (Zn, Cd, Pb, and Cu) could be chosen. Diluted electrolyte (0.01 M buffer) was one of the factors favoring low detection and quantification limits, but its quantification range is short in comparison to more concentrated media. For ?1.7 V deposition potential, the detection of single metal at ppb levels was reached in 60 s deposition time. Understanding different metal‐metal interactions shows the limits to the simultaneous determination of heavy metals at BDD. Quantification was possible for the simultaneous determination of Zn, Cd and Pb despite the overlapping of Zn and Cd peaks. The performance of the BDD was compared with that of another C‐based solid electrode: the glassy carbon electrode (without mercury plating). A lower base line current, wider potential range, higher sensitivity (3 to 5 times higher than GC) and longevity of the material were noticed for the BDD. 相似文献
954.
水溶性含C_(60)聚电解质的制备及其与重氮树脂自组装膜AFMFFM的初步研究 总被引:4,自引:0,他引:4
通过BPO引发的溶液聚合 ,合成了水溶性的星状C6 0 苯乙烯 苯乙烯磺酸钠的三元共聚物 [Star shapedC6 0 poly(St SS) ],运用自组装技术 ,在水溶液中 ,含C6 0 的三元共聚物与重氮树脂 (Diazoresin)通过正负离子间的吸附力在云母基片上交替一层一层有序地组装成固体膜 .自组装膜经紫外光幅照反应 ,通过重氮基的分解 ,层间连接的离子键转变成共价键 ,从而增加薄膜的稳定性和堆砌密度 .用原子力显微镜 摩擦力显微镜(AFM FFM)考察了C6 0 在膜中的承载作用及比较不同链结构、不同链长、不同层数自组装膜的表面形貌和微摩擦性能 .初步的研究结果显示了聚合物薄膜的微摩擦性能与聚合物的化学结构、链长和膜的层数有密切关系 相似文献
955.
《Chemphyschem》2002,3(12):1024-1030
N,N,N‐butylethylpentylpropylammonium iodide 4 and related molecules have been selectively synthesised from commercially available aldehydes, amines and alkyl iodides using a reductive alkylation procedure. The crystalline texture of 4 obtained on cooling is optically isotropic between crossed polarisers, indicating a cubic structure. Differential scanning calorimetry (DSC, +10 K min?1) reveals a glass phase transition at ?59 °C and a melting point at 192 °C. The melting entropy (23.9 J mol?1 K?1) indicates a first‐order transition between a highly disordered mesophase and the isotropic liquid. Powder X‐ray diffraction patterns were indexed in the cubic system (a=14.08Å; Pm n space group). In this cell, the molecular packing with Z=6 corresponds to a rather low compactness of 65 %. Iodine and tetraalkylammonium ions occupy positions with a m2 site symmetry. These highly symmetrical states may be generated by stepwise rotation of the ammonium cation. The same structural model for orientationally disordered crystal (ODIC) phases can be applied to a series of tetraalkylammonium bromides and iodides. 相似文献
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957.
室温下SO2 -4/ZrO2 催化剂 (SZ)上13 C标记的正丁烷异构化反应的原位13 CMASNMR谱研究结果表明 :其反应动力学符合Langmuir Hinshelwood一级可逆表面反应动力学公式 ,由该动力学公式计算得到的反应速率常数可以用于衡量固体催化剂的表面超强酸性 .这种新的表征方法显示采用一步 -醇热 -超临界干燥综合技术合成的SZ催化剂不仅比表面和硫酸根含量高 ,而且其超强酸性和异构化反应活性均明显优于常规法合成的催化剂 ,具有良好的应用前景 . 相似文献
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Horn M Ihringer J Glink PT Stoddart JF 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(17):4046-4054
A template-directed dynamic clipping procedure has generated a library of nine [2]rotaxanes that have been formed from three dialkylammonium salts-acting as the dumbbell-shaped components-and three dynamic, imino bond-containing, [24]crown-8-like macrocycles-acting as the ring-shaped components-which are themselves assembled from three dialdehydes and one diamine. The rates of formation of these [2]rotaxanes differ dramatically, from minutes to days depending on the choice of dialkylammonium ion and dialdehyde, as do their thermodynamic stabilities. Generally, [2]rotaxanes formed by using 2,6-diformylpyridine as the dialdehyde component, or bis(3,5-bis(trifluoromethyl)benzyl)ammonium hexafluorophosphate as the dumbbell-shaped component, assembled the most rapidly. Those rotaxanes containing this particular electron-deficient dumbbell-shaped unit, or 2,5-diformylfuran units in the macroring, were the most stable thermodynamically. The relative thermodynamic stabilities of all nine of the [2]rotaxanes were determined by competition experiments that were monitored by (1)H NMR spectroscopy. 相似文献