Modified Pechini synthesis of Bi2ZnB2O7 nanoparticles

被引:17
作者
Chrunik, M. [1 ]
Majchrowski, A. [1 ]
Zasada, D. [2 ]
Chlanda, A. [3 ]
Szala, M. [4 ]
Salerno, M. [5 ]
机构
[1] Mil Univ Technol, Inst Appl Phys, Kaliskiego 2, PL-00908 Warsaw, Poland
[2] Mil Univ Technol, Dept Adv Mat & Technol, Kaliskiego 2, PL-00908 Warsaw, Poland
[3] Warsaw Univ Technol, Fac Mat Sci & Engn, 141 Woloska Str, PL-02507 Warsaw, Poland
[4] Mil Univ Technol, Fac Adv Technol & Chem, Kaliskiego 2, PL-00908 Warsaw, Poland
[5] Ist Italiano Tecnol, Mat Characterizat Facil, Via Morego 30, I-16163 Genoa, Italy
关键词
Nanoparticles; Borates; Complex oxides; Pechini method; NLO materials; DTA/TG; XRD; SEM; AFM; IEP; PHOTOLUMINESCENCE PROPERTIES; OPTICAL-PROPERTIES; DOPED BI2ZNB2O7; BI2ZNOB2O6; CRYSTAL; GROWTH; COMPOSITES; PHOSPHOR; BISMUTH; FIBERS;
D O I
10.1016/j.jallcom.2017.07.172
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Synthesis of Bi2ZnB2O7 nanoparticles by means of the modified Pechini method is reported. The introduced modifications are based on a proper selection of complexing and polymeric agents, as well as on an optimization of process parameters. The purpose of this optimization was to reduce process duration and temperature. A polymeric system of ethylenediaminetetraacetic acid and mannitol was used. The thermal behavior of the applied polymeric system is discussed, based on its thermogravimetric measurements. The phase uniformity of obtained powders was studied using X-ray diffraction and crystallographic calculations were done to confirm their orthorhombic structure. The morphology of synthesized materials was investigated by means of a scanning electron microscopy and atomic force microscopy. The influence of organic part quantity on Bi2ZnB2O7 particles size and their agglomeration is discussed. The electrophoretic measurements for a Bi2ZnB2O7 powder were performed to evaluate its isoelectric point. Owing to deagglomeration process and filtration, nano-fraction of Bi2ZnB2O7 particles was separated. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:587 / 597
页数:11
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