Flash pyrolysis of polyethyleneglycol .2. Kinetics determined by T-jump/FTIR spectroscopy

被引:16
作者
Arisawa, H [1 ]
Brill, TB [1 ]
机构
[1] UNIV DELAWARE,DEPT CHEM,NEWARK,DE 19716
关键词
D O I
10.1016/S0010-2180(96)00123-X
中图分类号
O414.1 [热力学];
学科分类号
摘要
The rate of formation of all quantified products from flash-pyrolysis of polyethyleneglycol having Mw = 2090 (PEG-2090) was determined using T-jump/FTIR spectroscopy. In the 370-550 degrees C range and at 2 atm Ar, a discontinuity in the Arrhenius plot occurs at 460-470 degrees C. Below this temperature, E(a) = 7 +/- 8 kcal/mol and In(A/s) = 1 +/- 6. Above this temperature, E(a) = 22 +/- 4 kcal/mol and ln(A/s) = 12 +/- 3. The explanation for this discontinuity lies in the fact that pyrolysis of PEG-2090 forms both volatile products and a higher Mw residue below the transition temperature. Above the transition temperature, pyrolysis products from both the PEG-2090 and the residue are formed. In addition to global kinetics, the kinetics of formation of the individual products were analyzed separately. For both the global process kinetics and the kinetics for formation of individual species (except for 2-methoxy-1,3-dioxolane below 460 degrees C), the rate of desorption/evaporation controls the rate of release of species to the gas phase. At 11 atm, the global Arrhenius parameters for the formation of the products are E(a) = 52 +/- 0.3 kcal/mol and In(A/s) = 32 +/- 0.2 over the 400-550 degrees C range, with no discontinuity. Thus, condensed-phase reactions dominate in controlling the product evolution rate at 11 atm. (C) 1997 by The Combustion Institute.
引用
收藏
页码:105 / 112
页数:8
相关论文
共 15 条
[1]   Flash pyrolysis of hydroxl-terminated polybutadiene (HTPB) .2. Implications of the kinetics to combustion of organic polymers [J].
Arisawa, H ;
Brill, TB .
COMBUSTION AND FLAME, 1996, 106 (1-2) :144-154
[2]  
ARISAWA H, COMBUST FLAME
[3]   STUDY BY DYNAMIC THERMOGRAVIMETRY OF THERMAL DEGRADATION OF POLYMERS [J].
AUDEBERT, R ;
AUBINEAU, C .
EUROPEAN POLYMER JOURNAL, 1970, 6 (07) :965-&
[4]   AN INTRODUCTION TO MULTIVARIATE CALIBRATION AND ANALYSIS [J].
BEEBE, KR ;
KOWALSKI, BR .
ANALYTICAL CHEMISTRY, 1987, 59 (17) :A1007-+
[5]  
BLYUMENFELD AB, 1970, VYSOKOMOL SOEDIN A, V12, P633
[6]   POLYMER DEGRADATION DURING COMBUSTION [J].
BRAUMAN, SK .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1988, 26 (06) :1159-1171
[7]   T-JUMP/FT-IR SPECTROSCOPY - A NEW ENTRY INTO THE RAPID, ISOTHERMAL PYROLYSIS CHEMISTRY OF SOLIDS AND LIQUIDS [J].
BRILL, TB ;
BRUSH, PJ ;
JAMES, KJ ;
SHEPHERD, JE ;
PFEIFFER, KJ .
APPLIED SPECTROSCOPY, 1992, 46 (06) :900-911
[8]   THERMAL-DECOMPOSITION OF POLY(ETHYLENE OXIDE), POLY(METHYL METHACRYLATE), AND THEIR MIXTURES BY THERMOGRAVIMETRIC METHOD [J].
CALAHORRA, E ;
CORTAZAR, M ;
GUZMAN, GM .
JOURNAL OF POLYMER SCIENCE PART C-POLYMER LETTERS, 1985, 23 (05) :257-260
[9]   PARTIAL LEAST-SQUARES REGRESSION - A TUTORIAL [J].
GELADI, P ;
KOWALSKI, BR .
ANALYTICA CHIMICA ACTA, 1986, 185 :1-17
[10]  
GONGWER PE, IN PRESS COMBUST FLA