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101.
M. Ebihara Y. S. Chung W. Chueinta B.-F. Ni T. Otoshi Y. Oura F. L. Santos F. Sasajima Sutisna A. K. B. H. Wood 《Journal of Radioanalytical and Nuclear Chemistry》2006,269(2):259-266
Summary Seven Asian countries have been collaborating in collecting airborne particulate matter (APM) in their individual countries
and analyzing them by neutron activation analysis as a common analytical tool. APM samples were collected into two fractions
of fine and coarse grains (PM2 and PM2-10, respectively). Analytical data were compared from several viewpoints such as particulate
sizes, locality of sampling sites (either urban or rural) and geographical location of participating countries. Chemical composition
and their monthly variations as well as mass concentrations appear to be highly characteristic for individual sampling sites,
suggesting that NAA data are suitable for evaluating the air quality in each site. 相似文献
102.
Huang M Jin Y Jiang H Sun X Chen H Liu B Wang E Dong S 《The journal of physical chemistry. B》2005,109(32):15264-15271
Multiple-deposited Pt overlayer modified Pt nanoparticle (MD-Pt overlayer/PtNPs) films were deliberately constructed on glassy carbon electrodes through alternately multiple underpotential deposition (UPD) of Ag followed redox replacement reaction by Pt (II) cations. The linear and regular growth of the films characterized by cyclic voltammetry was observed. Atomic force spectroscopy (AFM) provides the surface morphology of the nanostructured Pt films. Rotating disk electrode (RDE) voltammetry and rotating ring-disk electrode (RRDE) voltammetry demonstrate that the MD-Pt overlayer/PtNPs films can catalyze an almost four-electron reduction of O(2) to H(2)O in air-saturated 0.1 M H(2)SO(4). Thus-prepared Pt films behave as novel nanostructured electrocatalysts for dioxygen reduction and hydrogen evolution reaction (HER) with enhanced electrocatalytic activities, in terms of both reduction peak potential and peak current, when compared to that of the bulk polycrystalline Pt electrode. Additionally, it is noted that after multiple replacement cycles, the electrocatalytic activities improved remarkably, although the increased amount of Pt is very low in comparison to that of pre-modified PtNPs due to the intrinsic feature of the UPD-redox replacement technique. In other words, the electrocatalytic activities could be improved markedly without using very much Pt by the technique of tailoring the catalytic surface. These features may provide an interesting way to produce Pt catalysts with a reliable catalytic performance as well as a reduction in cost. 相似文献
103.
104.
105.
Xiong JY Narayanan J Liu XY Chong TK Chen SB Chung TS 《The journal of physical chemistry. B》2005,109(12):5638-5643
Kinetics as well as the evolution of the agarose gel topology is discussed, and the agarose gelation mechanism is identified. Aqueous high melting (HM) agarose solution (0.5% w/v) is used as the model system. It is found that the gelation process can be clearly divided into three stages: induction stage, gelation stage, and pseudoequilibrium stage. The induction stage of the gelation mechanism is identified using an advanced rheological expansion system (ARES, Rheometric Scientific). When a quench rate as large as 30 deg C/min is applied, gelation seems to occur through a nucleation and growth mechanism with a well-defined induction time (time required for the formation of the critical nuclei which enable further growth). The relationship between the induction time and the driving force which is determined by the final setting temperature follows the 3D nucleation model. A schematic representation of the three stages of the gelation mechanism is given based on turbidity and rheological measurements. Aggregation of agarose chains is promoted in the polymer-rich phase and this effect is evident from the increasing mass/length ratio of the fiber bundles upon gelation. Continuously increasing pore size during gelation may be attributed to the coagulation of the local polymer-rich phase in order to achieve the global minimum of the free energy of the gelling system. The gel pore size determined using turbidity measurements has been verified by electrophoretic mobility measurements. 相似文献
106.
The reduction of C = C double bonds is one of the most fundamental synthetic transformations and plays a key role in the manufacturing of a wide variety of bulk and fine chemicals. Hydrogenation of olefinic substrates can be achieved readily with molecular hydrogen in many cases, but transfer hydrogenation methods using suitable donor molecules such as formic acid or alcohols are receiving increasing attention as possible synthetic alternatives because it requires no special equipment and avoids the handling of potentially hazardous gaseous hydrogen. 相似文献
107.
以十四酸根阴离子柱撑Zn-Al水滑石Zn0.77Al0.22(OH)2.0.22C13H27COO.0.81 H2O(记为ZnAl-14A)为预撑前体,在水溶液中用离子交换法将以2∶17缺位杂多酸根离子(P2Mo16VO61)11-记为(P Mo V)为配体的稀土杂多配阴离子Ce(P2Mo16VO61)219-(记为Ce(PMoV)2)插层组装到水滑石层板间,合成了一种具有大的层间距(3.37 nm)的超分子插层材料Zn0.77Al0.23(OH)2.0.0105[Ce(P1.9Mo15.7V1.1O61)2].0.011C13H27COO.0.83H2O(记为ZnAl-Ce(PMoV)2)。用ICP,IR,XRD和DTA对产物的组成和结构进行了表征。结果表明,该产物中Ce(PMoV)2配阴离子沿其长轴垂直于层板的方向分布于水滑石层间;产物具有规整的层状结构和热稳定性;产物对乙酸与正丁醇的酯化反应,二甘醇的脱水-环化反应和H2O2氧化环己烷的反应有良好的催化性能,且易于回收重复使用。 相似文献
108.
提出了用PVC功能膜固相透射吸光光度法测定钯的方法。研究发现 ,在pH 3~ 4HOAc NaOAc介质中 ,钯与均匀分布在PVC功能膜上的硫代米氏酮形成疏水性的配合物 ,在自制的固相透射分光光度附件上测定。在 5 2 0nm波长处具有最大吸收 ,钯浓度在 0~ 7.5 μg 10ml范围内 ,A与C有良好的线性关系 ,检出限为 0 .0 15 μg·ml-1,标准偏差为 0 .78%。方法简便、快速、试剂用量少 ,可直接用于矿样中钯的测定 相似文献
109.
H. Sh. Bai H. X. Jin H. Q. Fan J. Du F. Wang D. M. Chen Zh. Cheng 《Journal of Radioanalytical and Nuclear Chemistry》1998,236(1-2):87-95
The behavior of153Sm-EDTMP in vitro and vivo is analyzed by the size exclusion HPLC. The experimental results show that EDTMP amounts have an
obvious effect on the stability in vitro and uptake of153Sm-EDTMP in the liver. HPLC analysis of urine sample indicates that153Sm-EDTMP es excreted in the original form. The behavior in vivo of153Sm-EDTMP containing 4 μg is similar to that of153Sm-EDTMP containing 50 μg EDTMP at 1 h post-injection. 相似文献
110.
Jin Yan Dong Ye Gao Chen Hong Chuan Song Yan Ping He Lei Li Yong Ping Zhong Yan Hui Zhu Jie Cao Luo Wang Ke Qin Zhang Laboratory for Conservation Utilization of Bioresources Yunnan University Kunming China Department of Chemistry Yunnan Normal University Kunming China Provincial Key Lab of Rural Energy Engineering Yunnan Normal University Kunming China 《中国化学快报》2007,18(2):165-167
Microbial transformation of nigranoic acid by Caryospora carllicarpa YMF1.01026 afforded the new derivative 6β-hydro-xynigranoic acid. Its structure was elucidated by spectroscopic methods. 相似文献