热丝和射频等离子体化学气相沉积法制备定向碳纳米管薄膜

采用热丝和射频等离子体复合化学气相沉积设备(PE-HF-CVD),以CH4、H2和N2为反应气体.在较低衬底温度下(500℃),用简单的催化剂制备方法--旋涂法在硅片上涂覆Ni(NO3)2溶液,经热处理及H2还原后的Ni颗粒为催化剂,在硅衬底上制备出了垂直于硅片且定向生长的碳纳米管薄膜.扫描电子显微镜(SEM)和透射电子显微镜(TEM)结果显示,1 mol/l的硝酸镍溶液旋涂硅片所得催化剂制得的碳纳米管管径为30～50 nm,长度超过4μm,定向性好.并用拉曼光谱(Raman)对不同摩尔浓度Ni(NO3)2溶液条件下制备的碳纳米管薄膜样品进行了表征.     

氯过氧化物酶修饰电极对一氯二甲酮的催化氯化

通过将氯过氧化物酶溶液(Chloroperoxidase, CPO)与Nafion分散的单壁碳纳米管分散液混合后直接滴涂到玻碳电极表面制得修饰电极. 这个固定了氯过氧化物酶的碳纳米管修饰玻碳电极, 在pH=5.0的磷酸缓冲溶液中测得的循环伏安曲线上有一对准可逆的氧化还原电流峰, 经过与裸电极和没有固定氯过氧化物酶的碳纳米管修饰电极上测得的循环伏安行为对比后确认, 碳纳米管对氯过氧化物酶与电极之间的电子传递反应具有很好的促进作用. 利用该修饰电极能催化一氯二甲酮氯化为二氯二甲酮, 无需添加过氧化氢作为反应启动剂, 紫外光谱的测试结果表明, 每摩尔氯过氧化物酶可催化氯化4.0×105 mol 的一氯二甲酮, 表现出很高的催化效率.     

Electrical, dielectric and surface wetting properties of multi-walled carbon nanotubes/nylon-6 nanocomposites

This paper reports that the multi-walled carbon nanotubes(MWCNT)/nylon-6 (PA6) nanocomposites with different MWCNT loadingshave been prepared by a simple melt-compounding method. Theelectrical, dielectric, and surface wetting properties of theCNT/PA6 composites have been studied. The temperature dependence ofthe conductivity of the CNT/PA6 composite with 10.0 wt{\%} CNTloading ($\sigma _{\rm RT} \sim 10^{-4}$ S/cm) are measured, andafterwards a charge-energy-limited tunnelling model (ln $\sigma (T)\sim T^{-1/2})$ is found. With increasing CNT weight percentage from0.0 to 10.0 wt%, the dielectric constant of the CNT/PA6composites enhances and the dielectric loss tangent increases twoorders of magnitude. In addition, water contact angles of theCNT/PA6 composites increase and the composites with CNT loadinglarger than 2.0 wt%even become hydrophobic. The obtainedresults indicate that the electrical and surface properties of thecomposites have been significantly enhanced by the embedded carbonnanotubes.     

微细管碳纳米管悬浮液强制对流换热实验研究

测量了水平微细圆管内蒸馏水和不同质量浓度的水基多壁碳纳米管纳米流体在低雷诺数下的强制对流换热特性。实验结果表明,与蒸馏水相比,纳米流体的对流换热系数显著提高,且随质量浓度和管内雷诺数的增大而增大;并且研究了流体管内流动阻力特性,得到的泊肃叶数f·Re值随着雷诺数的变化不明显,但纳米流体的f·Re值要明显小于纯水。     

An improved planar-gate triode with CNTs field emitters by electrophoretic deposition

An improved planar-gate triode with carbon nanotubes (CNTs) field emitters has been successfully fabricated by conventional photolithography, screen printing and electrophoretic deposition (EPD). In this structure, cathode electrodes and ITO arrays linked with gate electrodes were interdigitated and paralleled on the same plane although the gate electrodes and cathode electrodes were isolated by dielectric layer, a so-called improved planar-gate triode structure. An electrophoretic process was developed to selectively deposit CNTs field emitters onto cathode electrodes in the CNTs suspension by an applied voltage between the gate electrodes and cathode electrodes. The optical microscopy and FESEM image showed that the CNTs emitters with the uniform packing density were selectively defined onto the cathode electrodes. In addition, field emission characteristics of an improved planar-gate triode with CNTs field emitters were investigated. The experiment results indicated that the turn-on voltage of this triode structure at current density of 1 μA/cm² was approximately 55 V. The anode current and gate current came to 396 μA and 325 μA, at gate voltage and anode voltage of 100 V and 4000 V, respectively and at the anode-cathode spacing of 2000 μm. The emission image became brighter and the luminous image with dot matrix on the anode plate obviously increased with the increase of the gate voltage. Moreover, the emission current fluctuation was smaller than 5% for 11 h, which indicated that the improved planar-gate triode has a good field emission performance and long lifetime.     

基于自组装膜的光纤错位型氨气传感器

演示了一种基于单壁碳纳米管（SWCNTs）-聚合物自组装复合膜的光纤错位型氨气传感器。通过层层自组装技术在高Q谐振器上涂覆薄膜,薄膜上存在大量的游离羧基以及较大的比表面积,这提供了光与薄膜之间的强相互作用,以及对氨气的高吸附性和选择性。光谱随氨气浓度影响的有效折射率而变化。在(10～37) ×10⁻⁶的低浓度范围内,光谱变化与氨气浓度差之比即灵敏度为13.25 pm/10⁻⁶,检测极限为3.77 ×10⁻⁶并且具有良好的线性。这项工作研制为低浓度和高选择性氨气传感器提供了一种有效的方法。     

Structure-Property Dependence of Copolymers Prepared by Cationic Polymerization

α-Methylstyrene/isobutene, α-methylstyrene/diisobutene, cyclopentadiene/isobutene, and cyclopentadiene/α-methylstyrene were copolymerized by cationic polymerization techniques. Several properties of the copolymers such as softening ranges and oxidation stability depend on their constitutional composition, and were controlled by variation of the conditions of their synthesis.