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The Influence of Process Conditions on the Chemical Composition of Pine Wood Catalytic Pyrolysis Oils

DOI: 10.5402/2012/167629

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Abstract:

Pine wood samples were used as model feedstock to study the properties of catalytic fast pyrolysis oils. The influence of two commercial zeolite catalysts (BASF and SudChem) and pretreatment of the pine wood with sodium hydroxide on pyrolysis products were investigated. The pyrolysis oils were first fractionated using column chromatography and characterized using GC-MS. Long chain aliphatic hydrocarbons, levoglucosan, aldehydes and ketones, guaiacols/syringols, and benzenediols were the major compounds identified in the pyrolysis oils. The catalytic pyrolysis increased the polycyclic hydrocarbons fraction. Significant decreases in phthalate derivatives using SudChem and long chain aliphatics using BASF catalyst were observed. Significant amounts of aromatic heterocyclic hydrocarbons and benzene derivatives were formed, respectively, using BASF and SudChem catalysts. Guaiacyl/syringyl and benzenediols derivatives were partly suppressed by the zeolite catalysts, while the sodium hydroxide treatment enriched phenolic derivatives. Zeolite catalyst and sodium hydroxide were employed together; they showed different results for each catalyst. 1. Introduction Biomass is a renewable and alternative resource that can be pyrolyzed to produce fuels and chemicals. Pyrolysis oils can potentially be substituted for fuel oil or diesel in many static applications including boilers, furnaces, engines, and turbines for electricity generation. There are also a range of chemicals that can be extracted or derived from pyrolysis oils including food flavorings, resins, agrochemicals, fertilizers, and emission control agents [1]. Considering their wide range of potential applications, understanding the molecular composition of the pyrolysis oils and upgraded products is highly desirable because it allows the determination of molecular-product property relations and the molecular processes taking place that are crucial information for the upgrading of the pyrolysis oils. It is also important for determining the changes occurring in the pyrolysis oils during handling, storage, and utilization [2]. Furthermore, the environmental impacts naturally depend on the nature of the chemical constituents; for example, polyaromatic hydrocarbons (PAH) and benzenes are less environmentally friendly than anhydrosugars such as levoglucosan. Because the pyrolysis products are complex, highly oxygenated, and unstable, analysis of pyrolysis liquids is a challenge, and the direct application of standard methods known, for example, from petroleum liquid analysis is not possible. There are several

References

[1]  S. Czernik and A. V. Bridgwater, “Overview of applications of biomass fast pyrolysis oil,” Energy and Fuels, vol. 18, no. 2, pp. 590–598, 2004.
[2]  A. V. Bridgwater, D. Meier, and D. Radlein, “An overview of fast pyrolysis of biomass,” Organic Geochemistry, vol. 30, no. 12, pp. 1479–1493, 1999.
[3]  V. A. Huffman and A. V. Bridgwater, The Characterization of Fast Pyrolysis Bio-Oils, Advances in Thermochemical Biomass Conversion, vol. 2, Blackie, London, UK, 1st edition, 1994.
[4]  R. Maggi and B. Delmon, Characterization of Bio-Oils Produced By Pyrolysis, Advances in Thermochemical Biomass Conversion, vol. 2, Blackie, London, UK, 1st edition, 1994.
[5]  T. Milne, F. Agblevor, M. Davis, S. Deutch, and D. Johnson, A Review of the Chemical Composition of Fast-Pyrolysis Oils From Biomass, Blackie, London, UK, 1997.
[6]  L. Ingram, D. Mohan, M. Bricka et al., “Pyrolysis of wood and bark in an auger reactor: physical properties and chemical analysis of the produced bio-oils,” Energy and Fuels, vol. 22, no. 1, pp. 614–625, 2008.
[7]  J. H. Marsman, J. Wildschut, F. Mahfud, and H. J. Heeres, “Identification of components in fast pyrolysis oil and upgraded products by comprehensive two-dimensional gas chromatography and flame ionisation detection,” Journal of Chromatography A, vol. 1150, no. 1-2, pp. 21–27, 2007.
[8]  B. Scholze and D. Meier, “Characterization of the water-insoluble fraction from pyrolysis oil (pyrolytic lignin). Part I. PY-GC/MS, FTIR, and functional groups,” Journal of Analytical and Applied Pyrolysis, vol. 60, no. 1, pp. 41–54, 2001.
[9]  E. Mészáros, E. Jakab, and G. Várhegyi, “TG/MS, Py-GC/MS and THM-GC/MS study of the composition and thermal behavior of extractive components of Robinia pseudoacacia,” Journal of Analytical and Applied Pyrolysis, vol. 79, no. 1-2, pp. 61–70, 2007.
[10]  L. Fagernas, Chemical and Physical Characterization of Biomass-Based Pyrolysis Oils. Literature Review, Technical Research Centre of Finland, Espoo, Finland, 1995.
[11]  M. Garcia-Perez, A. Chaala, H. Pakdel, D. Kretschmer, and C. Roy, “Characterization of bio-oils in chemical families,” Biomass and Bioenergy, vol. 31, no. 4, pp. 222–242, 2007.
[12]  K. Sipil?, E. Kuoppala, L. Fagern?s, and A. Oasmaa, “Characterization of biomass-based flash pyrolysis oils,” Biomass and Bioenergy, vol. 14, no. 2, pp. 103–113, 1998.
[13]  K. L. Sobeih, M. Baron, and J. Gonzalez-Rodriguez, “Recent trends and developments in pyrolysis-gas chromatography,” Journal of Chromatography A, vol. 1186, no. 1-2, pp. 51–66, 2008.
[14]  S. Yaman, “Pyrolysis of biomass to produce fuels and chemical feedstocks,” Energy Conversion and Management, vol. 45, no. 5, pp. 651–671, 2004.
[15]  A. V. Bridgwater, “Catalysis in thermal biomass conversion,” Applied Catalysis A, vol. 116, no. 1-2, pp. 5–47, 1994.
[16]  J. Adam, M. Blazsó, E. Mészáros et al., “Pyrolysis of biomass in the presence of Al-MCM-41 type catalysts,” Fuel, vol. 84, no. 12-13, pp. 1494–1502, 2005.
[17]  J. F. Li, R. Yan, B. Xiao, X. L. Wang, and H. Yang, “Influence of temperature on the formation of oil from pyrolyzing palm oil wastes in a fixed bed reactor,” Energy and Fuels, vol. 21, no. 4, pp. 2398–2407, 2007.
[18]  M. Garcia-Perez, S. Wang, J. Shen, M. Rhodes, W. J. Lee, and C. Z. Li, “Effects of temperature on the formation of lignin-derived oligomers during the fast pyrolysis of Mallee woody biomass,” Energy and Fuels, vol. 22, no. 3, pp. 2022–2032, 2008.
[19]  D. Mohan, C. U. Pittman, and P. H. Steele, “Pyrolysis of wood/biomass for bio-oil: a critical review,” Energy and Fuels, vol. 20, no. 3, pp. 848–889, 2006.
[20]  F. A. Agblevor, A. Murden, and B. R. Hames, “Improved method of analysis of biomass sugars using high-performance liquid chromatography,” Biotechnology Letters, vol. 26, no. 15, pp. 1207–1210, 2004.
[21]  F. A. Agblevor, S. Beis, N. O. Mante, and N. Abdoulmoumine, “Fractional catalytic pyrolysis of hybrid poplar wood,” Industrial and Engineering Chemistry Research, vol. 49, no. 8, pp. 3533–3538, 2010.
[22]  C. N. Satterfield, Heterogeneous Catalysis in Industrial Practice, McGraw-Hill, New York, NY, USA, 1981.
[23]  J. álvarez, S. Ordó?ez, R. Rosal, H. Sastre, and F. V. Díez, “A new method for enhancing the performance of red mud as a hydrogenation catalyst,” Applied Catalysis A, vol. 180, no. 1-2, pp. 399–409, 1999.
[24]  S. Julien, E. Chornet, P. K. Tiwari, and R. P. Overend, “Vacuum pyrolysis of cellulose: fourier transform infrared characterization of solid residues, product distribution and correlations,” Journal of Analytical and Applied Pyrolysis, vol. 19, pp. 81–104, 1991.
[25]  J. Piskorz, D. Radlein, D. S. Scott, and S. Czernik, “Pretreatment of wood and cellulose for production of sugars by fast pyrolysis,” Journal of Analytical and Applied Pyrolysis, vol. 16, no. 2, pp. 127–142, 1989.
[26]  S. Julien, E. Chornet, and R. P. Overend, “Influence of acid pretreatment (H2SO4, HCl, HNO3) on reaction selectivity in the vacuum pyrolysis of cellulose,” Journal of Analytical and Applied Pyrolysis, vol. 27, no. 1, pp. 25–43, 1993.
[27]  F. W. Atadana, Catalaytic pyrolysis of cellulose, hemicellulose and lignin model compounds [M.S. thesis], Virginia Polytechnic Institute and State University, 2010.
[28]  D. Fengel and G. Wegener, Wood Chemistry, Ultrastructure, Reaction, Walter De Gruyter, New York, NY, USA, 1989.
[29]  P. A. Horne and P. T. Williams, “The effect of zeolite ZSM-5 catalyst deactivation during the upgrading of biomass-derived pyrolysis vapours,” Journal of Analytical and Applied Pyrolysis, vol. 34, no. 1, pp. 65–85, 1995.

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