Non-isothermal kinetic studies on co-processing of vacuum residue, plastics, coal and petrocrop

被引:45
作者
Ahmaruzzaman, M [1 ]
Sharma, DK [1 ]
机构
[1] Indian Inst Technol, Ctr Energy Studies, New Delhi 110016, India
关键词
co-processing; non-isothermal; kinetic; basra vacuum residue; polypropylene; bakelite; samla coal; Calotropis procera; bagasse;
D O I
10.1016/j.jaap.2004.11.035
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
Co-processing of petroleum vacuum residue (BVR) with plastics (polypropylene, bakelite), coal (Samla coal), and biomass (bagasse, Calotropis procera) was carried out in a thermogravimetric analyzer (TGA) reaction system in nitrogen atmosphere with a view to comparing the process of the mixture with those of the individual components. Experiments were conducted at heating rate of 40 degrees C/min, in the temperature range of 30-900 degrees C. Based on the results obtained, three temperature regimes were selected for studying the non-isothermal kinetics of TGA of individual BVR, plastics, coal, biomass as well as of the co-processing of these with BVR, i.e., below 400 degrees C, between 400 and 500 degrees C and above 500 degrees C. The kinetic studies were performed using Coats and Redfern kinetic-modeling equations. The overall activation energies were 60.83 kJ/mole for petroleum residue, 99.41 kJ/mole for polypropylene, 21.08 kJ/mole for coal, 22.68 kJ/mole for C procera and 31.9 kJ/mole for the mixture of these four materials. Thus, it has been found that there exists an overall synergy, when four materials were co-processed together. The overall orders and activation energies change during co-processing of two, three or four different macromolecules including petroleum residue as observed presently. The results obtained are being reported. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:263 / 275
页数:13
相关论文
共 28 条
[1]
Transformation of several plastic wastes into fuels by catalytic cracking [J].
Arandes, JM ;
Abajo, I ;
LopezValerio, D ;
Fernandez, I ;
Azkoiti, MJ ;
Olazar, M ;
Bilbao, J .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1997, 36 (11) :4523-4529
[2]
COMPETITIVE REACTIONS IN THERMAL DECOMPOSITION OF CELLULOSE [J].
ARSENEAU, DF .
CANADIAN JOURNAL OF CHEMISTRY, 1971, 49 (04) :632-&
[3]
COPROCESSING OF PETROLEUM RESIDUE AND COAL [J].
AUDEH, CA ;
YAN, TY .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1987, 26 (12) :2419-2423
[4]
KINETICS OF THERMAL DECOMPOSITION OF PULVERIZED COAL PARTICLES [J].
BADZIOCH, S ;
HAWKSLEY, PG .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1970, 9 (04) :521-&
[5]
BIANCO AD, 1993, FUEL, V72, P75
[6]
CHART J, 1997, POLYM DEGRADATION ST, V57, P135
[7]
COMPENSATION EFFECT IN THE THERMAL-DECOMPOSITION OF CELLULOSIC MATERIALS [J].
CHORNET, E ;
ROY, C .
THERMOCHIMICA ACTA, 1980, 35 (03) :389-393
[8]
Co-pyrolysis and co-gasification of coal and biomass in bench-scale fixed-bed and fluidised bed reactors [J].
Collot, AG ;
Zhuo, Y ;
Dugwell, DR ;
Kandiyoti, R .
FUEL, 1999, 78 (06) :667-679
[9]
DEGRADATION OF CONTAMINATED PLASTICS - A KINETIC-STUDY [J].
DAY, M ;
COONEY, JD ;
MACKINNON, M .
POLYMER DEGRADATION AND STABILITY, 1995, 48 (03) :341-349
[10]
FRITSKY KJ, 1994, J AIR WASTE MANAGE, V44, P1116