4.7 Article

Flue gas-to-ash desulfurization of combustion of textile dyeing sludge: Its dependency on temperature, lignocellulosic residue, and CaO

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 417, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.127906

Keywords

Textile dyeing sludge; Co-combustion; Spent mushroom substrate; Sulfur; Equilibrium simulations; Pollution control

Funding

  1. National Natural Science Foundation of China [51978175]
  2. Science and Technology Planning Project of Yunfu, Guangdong Province, China [2020040401]
  3. Research Fund Program of Guangdong Key Laboratory of Radioactive and Rare Resource Utilization [2019-LRRRU04, 2018B030322009]
  4. Science and Technology Planning Project of Guangdong Province, China [2019B020208017]

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In the combustion of textile dyeing sludge, controlling sulfur (S) species through flue gas-to-ash processes is crucial for achieving circular economies. The experimental study found that temperature and blend ratios play significant roles in transforming S in TDS, with the addition of spent mushroom substrate (SMS) and calcium oxide (CaO) enhancing desulfurization efficiency. The results suggest that a combination of SMS and CaO can improve the retention of S and enhance the decomposition of calcium sulfate (CaSO4).
Flue gas-to-ash controls on sulfur (S) species of the combustion of textile dyeing sludge (TDS) are pivotal in the achievement of circular and cleaner economies. This experimental study aimed to characterize S transformations in TDS as a function of temperature (600-1000 degrees C) and blend ratios of spent mushroom substrate (SMS) and calcium oxide (CaO) through thermodynamic equilibrium simulations. The conversion ratio of S to flue gas from the mono-combustion of TDS rose by 29.7% between 600 and 1000 degrees C and was 92.9% at 1000 degrees C. The increasing sulfur dioxide (SO2) emission with the high temperature occurred from the decomposition of sulfates. The conversion of S to SO2 decreased significantly with an increase in SMS from 10 to 50% and enhanced the S distribution in fly ash. Potassium and phosphorous in SMS appeared to play a significant role in the conversion of S. The addition of CaO exhibited a good desulfurization performance, with the S content of ash peaking at 5.2% at 800 degrees C with 7% CaO. The desulfurization efficiency of CaO highly depended on the temperature and blend ratios. The addition of SMS facilitated the agglomeration to form large particles at 1000 degrees C and formed more micro pores on their surfaces. Our equilibrium simulations pointed to the important role of CaO-assisted co-combustion versus mono-combustion of TDS in the S retention as well as to the enhanced decomposition of calcium sulfate (CaSO4) by SMS. Chlorine had a better affinity toward potassium to promote the release of gaseous potassium chloride (KCl) which in turn appeared to react with SO2 in flue gas and formed sulfates through sulfation reaction.

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