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991.
Several varieties of blue ballpoint pen inks were analyzed by high performance liquid chromatography (HPLC) and infrared spectroscopy (IR). The chromatographic data extracted at four wavelengths (254, 279, 370 and 400 nm) was analyzed individually and at a combination of these wavelengths by the soft independent modeling of class analogies (SIMCA) technique using principal components analysis (PCA) to estimate the separation between the pen samples. Linear discriminant analysis (LDA) measured the probability with which an observation could be assigned to a pen class. The best resolution was obtained by HPLC using data from all four wavelengths together, differentiating 96.4% pen pairs successfully using PCA and 97.9% pen samples by LDA. PCA separated 60.7% of the pen pairs and LDA provided a correct classification of 62.5% of the pens analyzed by IR. The results of this study indicate that HPLC coupled with chemometrics provided a better discrimination of ballpoint pen inks compared to IR. The need to develop a suitable IR method for analysing blue ballpoint pen inks has been emphasized and it is hoped that the development of such a method would indeed provide a valuable tool for the non-destructive analysis of blue ballpoint pen ink samples for forensic purposes. 相似文献
992.
以ZnO纳米柱阵列为模板, 采用溶胶-凝胶法制备出TiO2/ZnO和N掺杂TiO2/ZnO的复合纳米管阵列. 扫描电镜(SEM)、X射线光电子能谱(XPS)和紫外-可见漫反射吸收光谱(UV-Vis)的结果表明: 两种阵列的纳米管均为六角形结构, 直径约为100 nm, 壁厚约为20 nm; 在N-TiO2/ZnO复合纳米管阵列中, 掺入的N离子主要是以N-Ox、N-C和N-N的形式化学吸附在纳米管表面, 仅有少量的N离子以取代式掺杂的方式占据TiO2晶格O的位置; 表面N物种形成的表面态能级和取代式掺杂导致带隙的窄化, 增强了纳米管阵列的光吸收效率, 促进了光生载流子的分离. 光催化实验结果表明, N离子的掺杂有利于N-TiO2/ZnO复合纳米管阵列光催化活性的提高. 相似文献
993.
《Surface and interface analysis : SIA》2003,35(10):835-841
We have examined the optimal interface structure, ideal work of adhesion and bonding character of polar Ti(110)/TiN(111) interfaces by first‐principles density‐functional plane‐wave pseudopotential calculations. Both Ti‐ and N‐terminated interfaces, including six different interface structures, were calculated. The interface structure for each termination, continuing the TiN crystal structure across the interface, has the largest work of adhesion. Although both terminations yield substantial adhesion energies in the range 3–7 J m?2, the N‐terminated interface is ~4 J m?2 stronger than the Ti‐terminated interface. Analysis of the interfacial electronic structure shows that the Ti‐terminated interface is a mixed strong, metallic and weak covalent character, whereas the N‐terminated interface is a polar covalent bond similar to the Ti/TiC interface. Further study of the separation of the optimal interface shows that the cleavages will never fracture at the interface due to the strong bonding, which is consistent with the experimental results. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
994.
建立了高效毛细管电泳拆分阿苯达唑亚砜对映体的方法,考察了背景电解质pH、环糊精种类和浓度,有机改性剂种类和浓度对分离的影响,对分离条件进行了优化。实验结果表明:在含36g/L磺化β-环糊精和10%甲醇的20mmol/L Tris-H3PO4(pH2.5)缓冲体系中,阿苯达唑亚砜对映体具有良好的分离效果。 相似文献
995.
交替三线性分解算法与反相高效液相-二极管阵列检测方法相结合同时测定苯二酚的位置异构体 总被引:3,自引:0,他引:3
利用交替三线性分解算法与反相高效液相 二极管阵列检测 (RP HPLC DAD)相结合 ,在洗脱时间为1 0 86min~ 1 399min(间隔 1 / 1 50min)、紫外吸收波长为 2 68nm~ 2 98nm(间隔 1nm)时对苯二酚位置异构体的重叠及光谱体系进行了分辨研究。分辨结果与实际结果一致。同时测定了水溶液中共存的邻苯二酚、间苯二酚和对苯二酚的含量 ,回收率分别为 (1 0 0 1± 1 0 ) % ,(99 4± 1 4) % ,(1 0 0 5± 1 7) %。研究结果表明 :该方法定量快速准确 ,实验操作步骤简单 ,解决了在干扰物存在条件下三者很难同时分辨的问题。 相似文献
996.
硫酸介质中Ti/SnO2/PbO2析氧阳极的研究 总被引:13,自引:0,他引:13
由于硫酸溶液具有高的电导、一般条件下性质稳定、价格相对低廉等优点,所以电化学合成大多在硫酸溶液中进行.阳极析氧是电化学合成不可避免的阳极过程.但因硫酸的强腐蚀性,以及从阳极析出的氧的强氧化性,使得能满足工业生产的阳极材料很缺乏.自1950年荷兰Hen... 相似文献
997.
Steam-reforming reactions of methanol over NiO/Al2O3 and CuO/ZnO have been investigated. Over the nickel catalyst, the reaction rate is of zero kinetic order with respect to either methanol or steam, and the activation energy is 12.4 kJmol?1, whereas with copper catalyst, the rate is expressed according to the literature as kPa/(1 + KaPa + Kb+Pb) in which “a” and “b” are methanol and steam, respectively. The rate-controlling step of the reaction is assigned to the dissociation of O-H bond with dehydrogenation of C-H bond proceed rapidly to form carbon oxides. With copper catalyst the intrinsic participation of a water molecule during the dehydrogenation of C-H bond leads to the formation of carbon dioxide. With nickel catalyst, the dehydrogenation proceed more rapidly than the migration of a water molecule from an alumina site to a nickel site and causes almost exclusively the formation of carbon monoxide and hydrogen at a lower reaction temperature. 相似文献
998.
以ZnO纳米柱阵列为模板, 采用溶胶-凝胶法制备出TiO2/ZnO和N掺杂TiO2/ZnO的复合纳米管阵列. 扫描电镜(SEM)、X射线光电子能谱(XPS)和紫外-可见漫反射吸收光谱(UV-Vis)的结果表明: 两种阵列的纳米管均为六角形结构, 直径约为100 nm, 壁厚约为20 nm; 在N-TiO2/ZnO复合纳米管阵列中, 掺入的N离子主要是以N-Ox、N-C和N-N的形式化学吸附在纳米管表面, 仅有少量的N离子以取代式掺杂的方式占据TiO2晶格O的位置; 表面N物种形成的表面态能级和取代式掺杂导致带隙的窄化, 增强了纳米管阵列的光吸收效率, 促进了光生载流子的分离. 光催化实验结果表明, N离子的掺杂有利于N-TiO2/ZnO复合纳米管阵列光催化活性的提高. 相似文献
999.
以原位穆斯堡尔谱研究了活性炭担载的费-托合成铁-钼双金属催化剂的还原和碳化行为。在H_2中不同温度下还原催化剂,其中的Fe~(3+)还原为Fe~(2+),进而还原为Fe~0。但在400—450℃间发生了还原铁物类的再氧化现象,可归因于磷钼酸根Keggin结构的热分解。在500℃H_2中,铁和钼都还原为金属并形成合金,其穆斯堡尔谱为一单峰,同质异能移为-0.16mm/s。再在300℃合成气(2H_2/CO)中碳化,可生成Fe-Mo碳化物(Fe_(1-y)Mo_y)_xC,穆斯堡尔谱为δ~0.17mm/s,△~0.64mm/s的双峰。 相似文献
1000.
Three novel perylene polyimides (PPIs) containing p‐n diblock units were designed and synthesized for use in dye‐sensitized mesoporous TiO2 solar cells. They all dissolve in m‐cresol and N‐methyl‐2‐pyrrolidone (NMP). Their visible light absorption, electrochemical and photoelectrochemical properties were systematically studied. The polyimides have band gap energies of 2.16, 2.19 and 2.25 eV deduced from ultraviolet–visible absorption spectra, and electron affinity (Ea) and ionization potential (IP) of ?3.93 and 6.10 eV for PPI1, ?3.94 and 6.13 eV for PPI2, ?3.93 and 6.59 eV for PPI3, respectively, deduced from cyclic voltammogram. Experimental data show that introduction of 4,4′‐bisaminetriphenylamine cannot only greatly enhance optic‐electro conversion efficiency, but also enhance the dissolubility which in favorable for making the devices. The relationship of structure and properties of PPI is discussed and the mechanism of photocurrent generation is explained. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献