Characteristics and origin of char and coke from fast and slow, catalytic and thermal pyrolysis of biomass and relevant model compounds
Literature Information
Shoucheng Du, Julia A. Valla, George M. Bollas
Char and coke from biomass catalytic pyrolysis have different origins. They cannot be lumped as one since they occupy different locations on the catalyst surface and, thus, contribute differently to catalyst deactivation. In this study, catalyst (ZSM-5) deactivation in the perspective of comparison of char and coke from pyrolysis of different biomass types is investigated. Pine sawdust, glucose, and cellulose are used as feedstocks in the pyrolysis experiments. Biomass char and coke samples produced via slow and fast, thermal and catalytic pyrolysis are characterized with respect to their overall content, oxidation reactivity, catalyst surface area, pore size distribution changes, bonding groups and their effect on catalyst performance. In particular, it is shown that char forms as an external layer on the catalyst surface and in its macropores, whereas coke forms inside the zeolite micropores via hydrogen transfer and addition reactions. The catalyst effect on glucose and pine slow catalytic pyrolysis is minor compared with that on cellulose slow catalytic pyrolysis, due to macropore blocking by char formation. In fast catalytic pyrolysis, catalyst deactivation is mainly attributed to micropore blocking by coke formation. Char and coke are shown to coexist on the catalyst surface after fast catalytic experiments, with the char content after glucose fast catalytic pyrolysis being 30 wt% of the total solid residue. The origins of char and coke in the cellulose, hemicellulose and lignin components of pine are identified and mechanisms for their formation are proposed.
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Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.











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