4.7 Article

Co-pyrolysis of torrefied biomass and coal: Effect of pressure on synergistic reactions

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出版社

ELSEVIER
DOI: 10.1016/j.jaap.2021.105363

关键词

Co-pyrolysis; Biomass; Torrefaction; Pressure; Secondary reactions; Synergistic reactions

资金

  1. National Research Foundation (NRF) [86880]
  2. Sasol

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The co-utilization of torrefied biomass and coal in thermochemical conversion technologies results in the production of high quality oil products through synergistic reactions, which are controlled by pressure to indirectly influence reaction rates. The removal of hemicellulose during torrefaction enhances hydrogen transfer potential and suppresses dehydration and condensation reactions during co-pyrolysis, leading to substantial changes in product distribution.
The co-utilization of torrefied biomass and coal in thermochemical conversion technologies is an attractive process for the transition to green energy and chemicals. The main advantage of this process is the production of high quality oil products (closer resembling crude-oil) via synergistic interaction of primary products from the two feedstocks. These synergistic reactions often involve secondary reactions, which are promoted at high pressures. This paper reports quantitative results on the extent of synergistic reactions and the role of pressure on these reactions during co-pyrolysis of torrefied biomass and coal. Torrefied biomass was produced at 280 degrees C in a pilot rotary kiln and subsequently both pyrolysis and co-pyrolysis of torrefied biomass and coal was investigated in a fixed bed reactor (heating rate 7 degrees C/min) at temperatures of 400-600 degrees C and pressures of 1, 15 and 30 bar. The results show that the prior removal of hemicellulose during torrefaction maximized the potential of hydrogen transfer from cellulose/lignin-derived products to depolymerized coal fragments. Furthermore, the dehydration and condensation reactions of depolymerized fragments were suppressed during co-pyrolysis in favour of synergistic reactions between the fragments. These reactions occurred predominantly in the molten/ liquid phase and their rates could be indirectly controlled by pressure (through changing the evaporation rate), resulting in substantial changes in product distribution. In the presence of coal and its released vapours, the methoxyphenols (guaiacols) and furanics yields were significantly enhanced (positive deviation >54% and >40%, respectively, compared to additive predictions), whereas the phenol yields were inhibited (negative deviation >20%); suggesting the inhibition of demethoxylation reactions in the presence of coal depolymerized fragments. To date no studies have reported the molten phase synergistic reaction pathways occurring during copyrolysis of torrefied biomass and coal. Based on the findings in this paper, reaction pathways were proposed for these molten phase synergistic reactions.

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