Pyrolysis mechanism and electrical properties of 3D-hybrid organic–inorganic materials based on zirconium oxides-hydroxides, 3-butenoates and vinyltrimethoxysilane

被引:0
作者
S. Lavina
R. Campostrini
F. Girardi
P. B. Aswath
V. Di Noto
R. Di Maggio
机构
[1] University of Padova,Dipartimento di Scienze Chimiche
[2] University of Trento,Dipartimento di Ingegneria Industriale
[3] University of Trento,Dipartimento di Ingegneria Civile, Ambientale e Meccanica
[4] University of Texas at Arlington,College of Engineering
来源
Journal of Thermal Analysis and Calorimetry | 2015年 / 119卷
关键词
Dielectric hybrid materials; Pyrolysis mechanims; HRTEM; TG-MS; BES;
D O I
暂无
中图分类号
学科分类号
摘要
This report is focused on the quantitative thermogravimetric–mass spectrometric (TG–MS) analyses and the electrical response of two hybrid organic–inorganic materials (HYP and HYPC), obtained reacting together nanoclusters of zirconium oxides-hydroxides with 3-butenoates and cross-linked with vinyltrimethoxysilane. HYP was cured at 363 K, while HYPC at 403 K. Condensation of the silanol groups, producing shrinkage, alcoholation and the release of 3-butenoic acid and methyl 3-butenoate are the main processes involved in the early stages of pyrolysis from 323 to 633 K. The nominal formula for the two samples with a fair degree of approximation was obtained by elemental analysis and quantitative TG–MS measurements. Morphology of HYP and HYPC is determined by high-resolution transmission electron microscopy. In both HYP and HYPC, the electric response is characterized by a molecular dipole relaxation detected at higher frequencies and an inter-domain polarization phenomenon revealed at the lower frequencies, due to the presence of charged interfaces between nanodomains with different permittivities. HYP material showed a further dipole relaxation at intermediate frequencies, which assists the charge migration process. HYPC, containing a smaller density of 3-butenoate groups, reveals a long-range charge migration event of mobile species by hopping processes between relatively stiff sites.
引用
收藏
页码:2305 / 2319
页数:14
相关论文
共 178 条
[1]  
Schubert U(2001)Polymers reinforced by covalently bonded inorganic clusters Chem Mater 13 3487-3494
[2]  
Schubert U(2004)Organofunctional metal oxide clusters as building blocks for inorganic–organic hybrid materials J Sol–Gel Sci Technol 31 19-24
[3]  
Kickelbick G(2001)Inorganic clusters in organic polymers and the use of polyfunctional inorganic compounds as polymerization initiators Mon Chem 132 13-30
[4]  
Schubert U(2003)Concepts for the incorporation of inorganic building blocks into organic polymers on a nanoscale Prog Polym Sci 28 83-114
[5]  
Kickelbick G(2005)Advanced functional nanomaterials—from nanoscale objects to nanostructured inorganic and hybrid materials Prog Solid State Chem 33 57-3083
[6]  
Sanchez C(2001)Designed hybrid organic–inorganic nanocomposites from functional nanobuilding blocks Chem Mater 13 3061-371
[7]  
Sanchez C(1999)Organically functionalized metallic oxo-clusters: structurally well-defined nanobuilding blocks for the design of hybrid organic–inorganic materials Comments Inorg Chem 20 327-406
[8]  
de Soler-Illia GJ(2001)Swelling behavior and thermal stability of poly(methylmethacrylate) crosslinked by the oxozirconium cluster Zr Appl Organomet Chem 15 401-159
[9]  
Ribot F(2003)O J Non-Cryst Solids 322 154-366
[10]  
Lalot T(2001)(methacrylate) Macromol Symp 175 357-259