Aiqin Zhang

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Organization: Zhengzhou University of Light Industry
Department: State Laboratory of Surface and Interface Science and Technology, Henan Collaborative Innovation Center of Environmental Pollution Control and Ecological Restoration
Title:
Co-reporter:Aiqin Zhang, Yakun Tian, Yuanhua Xiao, Yuan Sun, Feng Li
Materials Science and Engineering: B 2015 Volume 197() pp:5-9
Publication Date(Web):July 2015
DOI:10.1016/j.mseb.2015.03.002
•AgNPs were prepared by solid state reaction at ambient temperature.•Only silver nitrate and ascorbic acid were needed in this reaction.•The size of the AgNPs can be tuned conveniently.•Formation mechanism of the AgNPs was investigated.A one-step strategy for preparing Ag nanoparticles (AgNPs) on large scale is demonstrated successfully, based on solid-state reactions at ambient temperature. The environmentally friendly synthesis can be achieved by simply grinding AgNO3 and ascorbic acid (AA) for about 30 min without adding any solvent and organic protectors. The size of AgNPs can be readily controlled by adjusting the reaction parameters such as AgNO3/AA molar ratio and reaction time. The nanostructures of AgNPs and their formation mechanism have been also investigated with XRD, FTIR, FESEM, HRTEM and HPLC–MS. It was found that AA can reduce Ag+ into Ag0 to form AgNPs directly in accompanying with its first oxidation into 2,3-diketogulonic acid (2,3-DKG) and then a series of fragmentary species of 2,3-DKG.
Co-reporter:Ai-Qin Zhang;Yong Zhang;Li-Zhen Wang ;Xiao-Feng Li
Polymer Composites 2011 Volume 32( Issue 1) pp:1-5
Publication Date(Web):
DOI:10.1002/pc.20983

Abstract

The composite of polyaniline and polypyrrole (PPY-PANI) was prepared by two-step electrochemical polymerization method. Techniques of scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), and thermal gravity analysis (TG/DTG) measurements were used to characterize the morphology and structure of the composite. The electrochemical properties of the composite were investigated by cyclic voltammetry (CV), galvanostatic charge-discharge, and electrochemical impedance spectroscopy (EIS). The results indicated that the polyaniline–polypyrrole composite showed better electrochemical capacitive performance than polypyrrole (PPY) and polyaniline (PANI). The specific capacitance of the composite electrode was 523 F/g at a current of 6 mA/cm2 in 0.5 M H2SO4 electrolyte. POLYM. COMPOS., 2011. © 2010 Society of Plastics Engineers

Co-reporter:Ai-Qin Zhang;Li-Zhen Wang;Lin-Sen Zhang ;Yong Zhang
Journal of Applied Polymer Science 2010 Volume 115( Issue 3) pp:1881-1885
Publication Date(Web):
DOI:10.1002/app.31345

Abstract

The copolymer of pyrrole and aniline, poly(pyrrole-co-aniline), has been prepared by chemical oxidation of corresponding monomer mixtures with ammonium peroxysulfate. Techniques of FTIR, SEM-EDS, and BET surface area measurement were used to characterize the structure and morphology of the copolymer. The electrochemical properties of the copolymer were investigated by cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. The results indicated that poly(pyrrole-co-aniline) was about 100–300 nm in diameter and showed better electrochemical capacitive performance than polypyrrole and polyaniline. The specific capacitance of the copolymer electrode was 827 F/g at a current of 8 mA/cm2 in 1 mol/L Na2SO4 electrolyte. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010

Butanal, 3,4-dihydroxy-2-oxo-, (3S)-
threo-Pentos-2-ulose(9CI)
2,3-Diketo-L-gulonic acid
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