Activation of anthracite combustion by copper acetate: mechanism, effect of particle size and introduction method
This paper addressed the effect of copper acetate on the combustion characteristics of anthracite depending on the fractional composition of fuel and additive introduction method. Anthracite was impregnated with 5 wt% of Cu(CH 3 COO) 2 by mechanical mixing and incipient wetness impregnation. Four an...
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Published in | International journal of coal science & technology Vol. 10; no. 1; pp. 13 - 18 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Nature Singapore
01.12.2023
Springer Springer Nature B.V SpringerOpen |
Subjects | |
Online Access | Get full text |
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Summary: | This paper addressed the effect of copper acetate on the combustion characteristics of anthracite depending on the fractional composition of fuel and additive introduction method. Anthracite was impregnated with 5 wt% of Cu(CH
3
COO)
2
by mechanical mixing and incipient wetness impregnation. Four anthracite samples of different fraction with
d
< 0.1 mm,
d
= 0.1–0.5 mm,
d
= 0.5–1.0 mm, and
d
= 1.0–2.0 mm were compared. According to EDX mapping, incipient wetness impregnation provides a higher dispersion of the additive and its uniform distribution in the sample. The ignition and combustion characteristics of the modified anthracite samples were studied by thermal analysis and high-speed video recording of the processes in a combustion chamber (at heating medium temperature of 800 °C). It was found that copper acetate increases anthracite reactivity, which was evidenced by decreased onset temperature of combustion (Δ
T
i
) by 35–190 °C and reduced ignition delay time (Δ
τ
i
) by 2.1–5.4 s. Copper acetate reduces fuel underburning (on average by 70%) in the ash residue of anthracite and decreases the amount of CO and NO
x
in gas-phase products (on average by 18.5% and 20.8%, respectively). The mechanism for activation of anthracite combustion by copper acetate is proposed. |
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ISSN: | 2095-8293 2198-7823 |
DOI: | 10.1007/s40789-023-00573-w |