Two stages catalytic pyrolysis of olive oil waste

被引:17
作者
Encinar, J. M. [1 ]
Gonzalez, J. F. [2 ]
Martinez, G. [1 ]
Gonzalez, J. M. [1 ]
机构
[1] UEX, Dpto Ingn Quim & Quim Fis, Badajoz 06071, Spain
[2] UEX, Dpto Fis Aplicada, Badajoz 06071, Spain
关键词
Pyrolysis; Olive oil waste; Dolomite;
D O I
10.1016/j.fuproc.2008.07.005
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A study of the pyrolysis of a waste from the extraction of olive oil has been carried out. The work objective was to characterize the char, tar and gaseous phases generated in the process for their possible utilization in energy generation. On the other hand, the influence of a set of variables has been studied, including the efficacy of the dolomite as catalyst. Finally, as previous step to the design of industrial installations, a kinetic study of the process (catalyzed and uncatalyzed), based in the generation of the principal gases, has been carried out. In the uncatalyzed process only the influence of temperature (400-900 degrees C) was studied. In the catalytic process, the influence of temperature (500,800 degrees C) and mass of catalyst (0-100 g) was studied. Also, the dolomite effectiveness as catalyst was evaluated. For this motive, consecutive experiments, without reactivating dolomite, were carried out (0-6 runs), and the yields of solids, liquids and gases were determined. An increase in reaction temperature leads to a decrease in char and tar yield and to an increase in the gas phase yield. When the catalyst is present and when the mass of the same is increased, an important decrease in the tar yield and a high increase in the gas phase yield are produced. This increment in the yield of gases is very significant in the case of hydrogen. In addition, the catalyst is very stable. Your activity remains constant during six consecutive pyrolysis experiments, without need to carry out the reactivation of the same. In the kinetic study carried out, it has been considered that the gases are formed through parallel independent first-order reactions, with different activation energy. For uncatalyzed experiments, the experimental data, once adjusted to the model, provided activation energies of 77.8, 38.6, 70.5 and 16.9 kJ mol(-1) and the Arrhenius pre-exponential factors of 210.1, 9.9, 775.3 and 0.43 min(-1) for H(2), CO, CH(4), and CO(2), respectively. For catalyzed experiments (following the same sequence) the activation energies were 15.6, 16.5, 12.7 and 23.3 kJ mol(-1) and the Arrhenius pre-exponential factors 3.8, 1.4, 4.3 and 3.5 min(-1). 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1448 / 1455
页数:8
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