Melt crystallization kinetics of polyhedral oligomeric silsesquioxane under non-isothermal conditions

被引:12
作者
Bianchi, O. [1 ]
Martins, J. N. [2 ,4 ]
Luvison, C. [1 ]
Echeverrigaray, S. G. [1 ,2 ]
Dal Castel, C. [3 ]
Oliveira, R. V. B. [2 ]
机构
[1] Univ Caxias Sul, Mat Sci Grad Program PGMAT, Ceram Mat Inst IMC, Born Principio, Brazil
[2] Fed Univ Rio Grande do Sul UFRGS, Grad Program Mat Sci PGCIMAT, Porto Alegre, RS, Brazil
[3] Univ Waterloo, Waterloo, ON N2L 3G1, Canada
[4] Feevale Univ Feevale, Novo Hamburgo, Brazil
关键词
FOSS; Nanopartide; Kinetics of crystallization; Activation energy; ASSEMBLED PACKING MORPHOLOGY; EVA CROSS-LINKING; POSS NANOCOMPOSITES; ACTIVATION-ENERGY; PHASE-CHANGE; COPOLYMERS; BLENDS; MICROSTRUCTURE; PARAMETERS; POLYMERS;
D O I
10.1016/j.jnoncrysol.2014.04.008
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
Melt crystallization of polyhedral oligomeric silsesquioxane (FOSS) was studied by differential scanning calorimeter (DSC), X-ray diffraction (XRD), Fourier transformed infra-red spectroscopy (FTIR) and scanning electron microscopy (SEM). The SEM analysis showed that PUSS samples are aggregated in micrometric size. Additionally, FTIR spectra confirmed intermolecular interactions among carbonyl groups. All samples showed that the Ozawa exponent ranged from 1 to 2.6 and the Ozawa crystallization rate constant was found to decrease with increasing temperature and reduction of average X(T). This suggests that these PUSS crystallized slower as the temperature increased. The Delta E-X(T) values for isobutyl PUSS increased monotonically until X(T) = 0.4, and for the methacryl isobutyl PUSS the Delta E-X(T) values decreased. After this point Delta E-X(T) showed similar values for both PUSS samples. The presence of the methacryl radical in PUSS cages interfered in the crystallization process due to the hysteric hindrance among PUSS-PUSS cages. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 35
页数:7
相关论文
共 52 条
[1]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[2]   Kinetics of phase change I - General theory [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (12) :1103-1112
[3]  
Avrami M., 1940, J CHEM PHYS, V8, P212, DOI DOI 10.1063/1.1750631
[4]   Assessment of Avrami, Ozawa and Avrami-Ozawa equations for determination of EVA crosslinking kinetics from DSC measurements [J].
Bianchi, O. ;
Oliveira, R. V. B. ;
Fiorio, R. ;
Martins, J. De N. ;
Zattera, A. J. ;
Canto, L. B. .
POLYMER TESTING, 2008, 27 (06) :722-729
[5]   Reactive Melt Blending of PS-POSS Hybrid Nanocomposites [J].
Bianchi, O. ;
Barbosa, L. G. ;
Machado, G. ;
Canto, L. B. ;
Mauler, R. S. ;
Oliveira, R. V. B. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2013, 128 (01) :811-827
[6]   Changes in activation energy and kinetic mechanism during EVA crosslinking [J].
Bianchi, O. ;
Martins, J. De N. ;
Florio, R. ;
Oliveira, R. V. B. ;
Canto, L. B. .
POLYMER TESTING, 2011, 30 (06) :616-624
[7]   Viscometric Characterization of PS/POSS Hybrid Nanocomposites [J].
Bianchi, Otavio ;
Repenning, Gustavo B. ;
Mauler, Raquel S. ;
Oliveira, Ricardo V. B. ;
Canto, Leonardo B. .
POLIMEROS-CIENCIA E TECNOLOGIA, 2012, 22 (02) :125-133
[8]   Nonisothermal Degradation of Wood Using Thermogravimetric Measurements [J].
Bianchi, Otavio ;
Dal Castel, Charles ;
de Oliveira, Ricardo V. B. ;
Bertuoli, Paula T. ;
Hillig, Everton .
POLIMEROS-CIENCIA E TECNOLOGIA, 2010, 20 :395-400
[9]   Non-isothermal crystallization of polymers [J].
Di Lorenzo, ML ;
Silvestre, C .
PROGRESS IN POLYMER SCIENCE, 1999, 24 (06) :917-950
[10]  
Echeverrigaray S., 2013, POLYM B