The regression of isothermal thermogravimetric data to evaluate degradation Ea values of polymers: A comparison with literature methods and an evaluation of lifetime prediction reliability

被引:39
作者
Blanco, Ignazio [1 ]
Abate, Lorenzo [2 ]
Antonelli, Marta Letizia [3 ]
机构
[1] Univ Catania, Dept Ind & Mech Engn, I-95125 Catania, Italy
[2] Univ Catania, Dept Phys & Chem Methodol Engn, I-95125 Catania, Italy
[3] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
关键词
Degradation activation energy; Kinetics of polymer degradation; Thermogravimetry; Lifetime prediction; THERMAL-DEGRADATION; POLY(METHYL METHACRYLATE); KINETIC-PARAMETERS; THERMOOXIDATIVE DEGRADATION; DECOMPOSITION; POLYETHYLENE; ACTIVATION; STABILITY; ENERGY;
D O I
10.1016/j.polymdegradstab.2011.08.005
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The thermooxidative degradation of four well known polymers, polyethylene (PE), polystyrene (PS), polycarbonate (PC) and poly(methyl methacrylate) (PMMA), was carried out in a thermogravimetric (TG) analyser, at various temperatures (in the 473-533 K range), in isothermal heating conditions. The resulting set of experimental TG data was used to determine the apparent activation energy (Ea) of degradation through two isothermal literature methods, as well as through a very simple method we set up, based on the direct regression of the experimental mass loss data, in order to verify the general applicability of our method to various polymers. The results from different methods were in good agreement. Degradation experiments in dynamic heating conditions, which were also performed, gave Ea values in good agreement with those in isothermal heating conditions for PS, PC and PMMA, while for PE a large discrepancy was observed, which was discussed and interpreted. The results suggested the general applicability of our method to all polymers, independently on their structure and degradation mechanism. A long-term (about 13 months) isothermal degradation experiment was also carried out with the same polymers at relatively low temperature (423 K). Only PE and PS evidenced appreciable mass loss in the investigated period, but the experimental data were not in agreement with those from the short-term degradations at higher temperatures, thus suggesting different degradation kinetics, and a low reliability of the lifetime predictions for polymers in service based on experiments at higher temperatures. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1947 / 1954
页数:8
相关论文
共 42 条
[1]   Kinetics of the isothermal degradation of model polymers containing ether, ketone and sulfone groups [J].
Abate, L ;
Blanco, I ;
Orestano, A ;
Pollicino, A ;
Recca, A .
POLYMER DEGRADATION AND STABILITY, 2005, 87 (02) :271-278
[2]   Determination of degradation apparent activation energy values of polymers - Regression of kinetic parameters derived from TG data [J].
Abate, L ;
Blanco, I ;
Pollicino, A ;
Recca, A .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2002, 70 (01) :63-73
[3]   The isothermal degradation of some polyetherketones: a comparative kinetic study between long-term and short-term experiments [J].
Abate, L ;
Blanco, I ;
Motta, O ;
Pollicino, A ;
Recca, A .
POLYMER DEGRADATION AND STABILITY, 2002, 75 (03) :465-471
[4]   Thermodegradative and morphological behavior of composites of HDPE with surface-treated hydroxyapatite [J].
Albano, Carmen ;
Catano, L. ;
Perera, R. ;
Karam, A. ;
Gonzalez, G. .
POLYMER BULLETIN, 2010, 64 (01) :67-79
[5]  
[Anonymous], 1967, J POLYM SCI MACROMOL
[6]  
[Anonymous], US MAN TA 3000 SYST
[7]  
[Anonymous], THERMAL METHODS ANAL
[8]  
[Anonymous], ASPECTS DEGRADATION
[9]  
[Anonymous], THERMAL DEGRADATION
[10]  
[Anonymous], KINETICS MECH