Silica-based composite and mixed-oxide nanoparticles from atmospheric pressure flame synthesis

被引:14
作者
Akurati, Kranthi K.
Dittmann, Rainer
Vital, Andri [1 ]
Klotz, Ulrich
Hug, Paul
Graule, Thomas
Winterer, Markus
机构
[1] Swiss Fed Labs Mat Testing & Res, Lab High Performance Ceram, CH-8600 Dubendorf, Switzerland
[2] Univ Duisburg Essen, Inst Combust & Gas Dynam, D-47057 Duisburg, Germany
关键词
flame aerosol process; atmospheric pressure; mixed oxide; composite; SiO2; SnO2; TiO2;
D O I
10.1007/s11051-005-9024-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Binary TiO2/SiO2 and SnO2/SiO2 nanoparticles have been synthesized by feeding evaporated precursor mixtures into an atmospheric pressure diffusion flame. Particles with controlled Si:Ti and Si:Sn ratios were produced at various flow rates of oxygen and the resulting powders were characterized by BET (Brunauer-Emmett-Teller) surface area analysis, XRD, TEM and Raman spectroscopy. In the Si-O-Ti system, mixed oxide composite particles exhibiting anatase segregation formed when the Si:Ti ratio exceeded 9.8:1, while at lower concentrations only mixed oxide single phase particles were found. Arrangement of the species and phases within the particles correspond to an intermediate equilibrium state at elevated temperature. This can be explained by rapid quenching of the particles in the flame and is in accordance with liquid phase solubility data of Ti in SiO2. In contrast, only composite particles formed in the Sn-O-Si system, with SnO2 nanoparticles predominantly found adhering to the surface of SiO2 substrate nanoparticles. Differences in the arrangement of phases and constituents within the particles were observed at constant precursor mixture concentration and the size of the resultant segregated phase was influenced by varying the flow rate of the oxidant. The above effect is due to the variation of the residence time and quenching rate experienced by the binary oxide nanoparticles when varying the oxygen flow rate and shows the flexibility of diffusion flame aerosol reactors.
引用
收藏
页码:379 / 393
页数:15
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