TY - JOUR
T1 - Influence of coal co-firing on the particulate matter formation during pulverized biomass combustion
AU - Wang, Xuebin
AU - Hu, Zhongfa
AU - Wang, Guogang
AU - Luo, Xiaotao
AU - Ruan, Renhui
AU - Jin, Qiming
AU - Tan, Houzhan
N1 - Publisher Copyright:
© 2018 Energy Institute
PY - 2019/6
Y1 - 2019/6
N2 - Biomass is regarded as CO 2 -neutral, while the high contents of potassium and chlorine in biomass induce severe particulate matter emission, ash deposition, and corrosion in combustion facilities. Co-firing biomass with coal in pulverized-combustion (PC) furnaces is able to solve these problems, as well as achieve a much higher generating efficiency than grate furnaces. In this work, the particulate matter (PM) emission from biomass co-firing with coal was studied in an entrained flow reactor at a temperature of 1623 K simulating PC furnace condition. PMs were sampled through a 13-stage impactor, and their morphology and elemental composition were characterized by scanning electron microscopy and electron dispersive X-ray spectroscopy. SO 2 emissions were measured to interpret the possibility of potassium sulfation during co-firing. Results show that PMs from the separated combustion of both biomass and coal present a bimodal particle size distribution (PSD). The concentration and size of fine-mode submicron particles (PM 1.0 ) from biomass combustion are much higher than those from coal combustion because of the high potassium content in biomass. For the co-firing cases, with the coal ratio increasing from 0% to 50%, the PM 1.0 yield is reduced by more than half and the PM 1.0 size becomes smaller, in contrast, the concentration of coarse-mode particles with the size of 1.0–10 μm (PM 1.0-10 ) increases. The measured PM 1.0 yields of co-firing are lower than the theoretically weight-averaged ones, which proves that during the biomass and coal co-firing in PC furnaces, the vaporized potassium from biomass can be efficiently captured by these silicon-aluminate oxides in coal ash. In the studied range of coal co-firing ratio (≤50 wt.%), the chlorides and sulfates of alkali metals from biomass burning are the dominating components in PM 1.0 , and a certain amount of silicon is observed in PM 0.1-1 . The analysis of chemical composition in PM 1.0 , together with that of SO 2 emission, indicates a marginal sulfation of alkali metal chloride occurring at high temperatures in PC furnaces.
AB - Biomass is regarded as CO 2 -neutral, while the high contents of potassium and chlorine in biomass induce severe particulate matter emission, ash deposition, and corrosion in combustion facilities. Co-firing biomass with coal in pulverized-combustion (PC) furnaces is able to solve these problems, as well as achieve a much higher generating efficiency than grate furnaces. In this work, the particulate matter (PM) emission from biomass co-firing with coal was studied in an entrained flow reactor at a temperature of 1623 K simulating PC furnace condition. PMs were sampled through a 13-stage impactor, and their morphology and elemental composition were characterized by scanning electron microscopy and electron dispersive X-ray spectroscopy. SO 2 emissions were measured to interpret the possibility of potassium sulfation during co-firing. Results show that PMs from the separated combustion of both biomass and coal present a bimodal particle size distribution (PSD). The concentration and size of fine-mode submicron particles (PM 1.0 ) from biomass combustion are much higher than those from coal combustion because of the high potassium content in biomass. For the co-firing cases, with the coal ratio increasing from 0% to 50%, the PM 1.0 yield is reduced by more than half and the PM 1.0 size becomes smaller, in contrast, the concentration of coarse-mode particles with the size of 1.0–10 μm (PM 1.0-10 ) increases. The measured PM 1.0 yields of co-firing are lower than the theoretically weight-averaged ones, which proves that during the biomass and coal co-firing in PC furnaces, the vaporized potassium from biomass can be efficiently captured by these silicon-aluminate oxides in coal ash. In the studied range of coal co-firing ratio (≤50 wt.%), the chlorides and sulfates of alkali metals from biomass burning are the dominating components in PM 1.0 , and a certain amount of silicon is observed in PM 0.1-1 . The analysis of chemical composition in PM 1.0 , together with that of SO 2 emission, indicates a marginal sulfation of alkali metal chloride occurring at high temperatures in PC furnaces.
KW - Biomass co-firing
KW - Coal
KW - Fine particle
KW - High temperature
KW - Sulfation
UR - https://www.scopus.com/pages/publications/85049028977
U2 - 10.1016/j.joei.2018.05.003
DO - 10.1016/j.joei.2018.05.003
M3 - 文章
AN - SCOPUS:85049028977
SN - 1743-9671
VL - 92
SP - 450
EP - 458
JO - Journal of the Energy Institute
JF - Journal of the Energy Institute
IS - 3
ER -