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941.
942.
Nonaqueous capillary electrophoretic (NACE) method for the separation of nine structurally similar chiral anticholinergic drugs was developed. The eight drug enantiomers were separated on baseline within 18 min using 20mM phosphoric acid and 10 mM NaOH, containing 10 mM heptakis(2,3-dimethyl-6-sulfato)-4beta-cyclodextrin (HDMS-beta-CD) in methanol. The results were compared with those obtained in the high performance liquid chromatography system. 相似文献
943.
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
944.
Suyun Jie Tianzhu Zhang Jiutong Chen Dongbing Liu Wei Chen 《Journal of organometallic chemistry》2005,690(7):1739-1749
A series of bridged bis(pyridinylimino) ligands were efficiently synthesized through the condensation reaction of 4,4′-methylene-bis(2,6-disubstituted aniline) with 2-pyridinecarboxaldehyde or 2-benzoylpyridine. They reacted with (DME)NiBr2 to form dinuclear Ni(II) complexes. All resultant compounds were characterized by elemental analysis, IR spectra as well as the single-crystal X-ray diffraction to confirm the structures of ligands and complexes. Activated with methylaluminoxane (MAO), these nickel complexes showed considerably good activities for ethylene oligomerization and polymerization. Their catalytic activities and the properties of PEs obtained were depended on the arched environment of ligand and reaction conditions. 相似文献
945.
946.
A single phase solid solution of Ce-Zr-O can be made by using NH4HCO3 solution as precipitating agent. The influence of preparation conditions, such as pH, Zr4+/(CO3
2-+HCO3
-) and Ce3+/Zr4+ ratio on the formation of the solid solution were investigated. The results show that a single phase Ce-Zr-O solid solution
can be formed only under a narrow window of preparation conditions, indicating that some compounds are formed in the precipitating
process. The compound may contain Ce3+, Zr4+, CO3
2-, HCO3-, and OH-. The solid solution so prepared can be described as Ce0.37Zr0.63O2.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
947.
Ying Wang Pu Xiao Gang Qiang Wu Su Qing Shi Jun Nie 《中国化学快报》2007,18(8):977-980
A benzophenone derivative photoinitiator, HBP-TDI-HQ-TDI-HBP (HTCTH), was synthesized based on 4-hydroxy benzophenone (HBP), toluene-2,4-diisocyanate (TDI) and hydroquinone (HQ). HTCTH was a more effective photoinitiator which had longer wavelength absorption in the UV-vis absorption spectra than the low molecular counterpart benzophenone (BP). It showed that both rate of polymerization (Rp) and final conversion (P) increased with increase of amine and HTCTH concentration in photopolymerization. 相似文献
948.
A series of pyrazolo[3,4‐b]pyridines was synthesized by the reaction of 5‐aminopyrazole with benzylidenemalononitrile in aqueous media. The structures were characterized by IR, 1H NMR, and elemental analysis and were further confirmed by X‐ray diffraction analysis. 相似文献
949.
Slow pyrolysis of walnut shell which is a cheap and abundantly available solid waste was carried out using thermogravimetric
analysis. The effects of raw material heating rate on the pyrolysis properties and kinetic parameters were investigated. A
two-step consecutive reaction model were used to simulate the pyrolysis process. The kinetic parameters were established by
using the pattern search method. Comparison between experimental data and the model prediction indicated that the two-step
consecutive reaction model can better describe the slow pyrolysis of walnut shell as the formation of an intermediate during
the pyrolysis process was taken into account. 相似文献
950.
Ning Li Chunhui Deng Ning Yao Xizhong Shen Xiangmin Zhang 《Analytica chimica acta》2005,540(2):317-323
In the study, we developed a simple, rapid, sensitive, and inexpensive method for determination of the disease biomarkers of acetone, hexanal and heptanal in human blood. For the first time, derivatization of carbonyls with O-2,3,4,5,6-(pentafluorobenzyl)hydroxylamine (PFBHA) was combined with headspace single-drop microextractin (HS-SDME) and gas chromatography-mass spectrometry (GC–MS) and applied to the analysis of acetone, hexanal, and heptanal in human blood. At first, acetone, hexanal and heptanal in blood were derivatized with PFBHA and formed oximes in several seconds. Sequentially, the oximes were headspace extracted and concentrated by a microdrop solvent. Finally, the extracted oximes were analyzed by GC–MS. HS-SDME conditions and method validations were studied. Due to needing of only 2 μl organic solvent, short extraction time of 8 min, and simple operation, derivatization-HS-SDME was shown to be a rapid, simple, and inexpensive technique for analysis of acetone, hexanal, and heptanal in human blood. Moreover, it had low detection limit values from 0.24 to 0.62 nM, and good reproducibility (R.S.D. less than 12%). 相似文献