Influence of synthesis parameters on sol-gel transition and physical properties of Nb2O5 mesoporous ambigels

被引:9
|
作者
Granados, Laura [1 ]
de Souza, Luciana V. [1 ]
Falk, Gilberto [1 ]
Hotza, Dachamir [1 ,2 ]
Escobar, Jairo A. [3 ]
Rodrigues Neto, Joao B. [1 ,4 ]
Rambo, Carlos R. [1 ,5 ]
机构
[1] Fed Univ Santa Catarina UFSC, Grad Program Mat Sci & Engn PGMAT, BR-88040900 Florianopolis, SC, Brazil
[2] Fed Univ Santa Catarina UFSC, Dept Chem & Food Engn EQA, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Los Andes UNIANDES, Dept Mech Engn, Cra 1 18A-12, Bogota, Colombia
[4] Fed Univ Santa Catarina UFSC, Dept Mech Engn EMC, BR-88040900 Florianopolis, SC, Brazil
[5] Fed Univ Santa Catarina UFSC, Dept Elect & Elect Engn EEL, BR-88040900 Florianopolis, SC, Brazil
关键词
Nb2O5 mesoporous ambigels; Nb2O5; alcogels; Sol-gel; Sol-gel transition; RHEOLOGICAL PROPERTIES; OXIDE; EVOLUTION; GELATION; HYDROLYSIS; CHEMISTRY; COATINGS; ZIRCONIA; AEROGELS; NIOBIA;
D O I
10.1007/s10971-017-4435-7
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this study, Nb2O5 alcogels and mesoporous ambigels were formed via a new acid-catalyzed polymeric synthesis pathway using NbCl5 as a precursor. The effect of hydrolysis, catalyst, and propylene oxide molar ratios on sol-gel transition, rheological properties, and physical properties of Nb2O5 ambigels were investigated. A common behavior for the sol-gel transition of Nb2O5 on the viscosity vs. time curves was identified. The molar ratios of H2O:Nb+5 and HNO3:H2O significantly influenced the gelation time, the rheological properties of alcogels, as well as the physical properties of the respective ambigels. The gels presented yield stress and shear-thinning behavior with different degrees of thixotropy. Microstructure analysis of the ambigels revealed a mesopore network formed by interconnected Nb2O5 nanoparticles. An increase in the molar ratios of HNO3:H2O (lower pH) increased the surface area and pore volume of Nb2O5, and yielded a finer nanostructure of Nb2O5 mesoporous ambigels. [GRAPHICS]
引用
收藏
页码:537 / 544
页数:8
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