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    Co-combustion of Zn/Cd-hyperaccumulator and textile dyeing sludge: Heavy metal immobilizations, gas-to-ash behaviors, and their temperature and atmosphere dependencies
    (Elsevier, 2023) Wu, Xieyuan; Chen, Zhiliang; Liu, Jingyong; Wei, Zebin; Chen, Zihong; Evrendilek, Fatih; Sun, Shuiyu; Chen, Zhibin
    This study quantified and revealed the temperature and atmosphere dependencies of the enrichment rates and speciation distributions of Zn and Cd and the behaviors of Cl and S for the co-combustion of a hyperaccumulator (SAH) of Zn and Cd and textile dyeing sludge (TDS) at a blend ratio of 3:1 (ST31). The addition of Al-rich TDS to SAH provided the chemisorption sites for Zn and Cd and generated stable Al/Si structures for their stabilization in the ST31 ash. The rising temperature and the atmosphere change from N-2/O-2 to CO2/O-2 transformed Zn and Cd into their oxidizable and residual fractions. Cl promoted the volatilizations of the heavy metals, with its content in the ST31 ash falling from 86.28% at 650 ? to 17.98% at 950 ?. The S content (31.08-33.86%) of the ST31 ash existed mainly as CaSO4 and was slightly higher in the CO2/O-2 than N-2/O-2 atmosphere (29.45%) since the high CO2 concentration adversely influenced the decomposition of CaCO3, while S indirectly affected the migrations of Zn and Cd. The combined results of the experiments, thermodynamic simulations, and multi-objective optimization pointed to 850 ? in the oxy-fuel atmosphere with 30% O-2 concentration as the optimal settings in order to stabilize Zn and Cd with an acceptable risk. The possible reaction pathways and immobilization mechanisms were also derived considering the interactions among minerals, Zn, Cd, Cl, and S.
  • Küçük Resim Yok
    Öğe
    Co-combustion of Zn/Cd-hyperaccumulator and textile dyeing sludge: Heavy metal immobilizations, gas-to-ash behaviors, and their temperature and atmosphere dependencies
    (Elsevier Science Sa, 2023) Wu, Xieyuan; Chen, Zhiliang; Liu, Jingyong; Wei, Zebin; Chen, Zihong; Evrendilek, Fatih; Sun, Shuiyu
    This study quantified and revealed the temperature and atmosphere dependencies of the enrichment rates and speciation distributions of Zn and Cd and the behaviors of Cl and S for the co-combustion of a hyperaccumulator (SAH) of Zn and Cd and textile dyeing sludge (TDS) at a blend ratio of 3:1 (ST31). The addition of Al-rich TDS to SAH provided the chemisorption sites for Zn and Cd and generated stable Al/Si structures for their stabilization in the ST31 ash. The rising temperature and the atmosphere change from N-2/O-2 to CO2/O-2 transformed Zn and Cd into their oxidizable and residual fractions. Cl promoted the volatilizations of the heavy metals, with its content in the ST31 ash falling from 86.28% at 650 ? to 17.98% at 950 ?. The S content (31.08-33.86%) of the ST31 ash existed mainly as CaSO4 and was slightly higher in the CO2/O-2 than N-2/O-2 atmosphere (29.45%) since the high CO2 concentration adversely influenced the decomposition of CaCO3, while S indirectly affected the migrations of Zn and Cd. The combined results of the experiments, thermodynamic simulations, and multi-objective optimization pointed to 850 ? in the oxy-fuel atmosphere with 30% O-2 concentration as the optimal settings in order to stabilize Zn and Cd with an acceptable risk. The possible reaction pathways and immobilization mechanisms were also derived considering the interactions among minerals, Zn, Cd, Cl, and S.
  • Küçük Resim
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    Oxy-fuel and air combustion performances and gas-to-ash products of aboveground and belowground biomass of Sedum alfredii Hance
    (ELSEVIER SCIENCE SA, 2021) Wu, Xieyuan; Wei, Zebin; Liu, Jingyong; Chen, Zihong; Evrendilek, Fatih
    The eco-friendly disposal choices of phytoremediation biomass still remain to be explored. This study characterized the combustions of Sedum alfredii Hance (SAH) in response to its aboveground (SAH-A) and belowground (SAH-B) parts, the oxy-fuel (CO2/O2) and air (N2/O2) atmospheres, temperature, and heating rate. The decomposition behaviors, gas-to-ash characteristics, thermo-kinetic parameters, and mineral transformations were quantified. In both atmospheres, the combustion performances were better for SAH-A than SAH-B at the same heating rate. In the range of 400.0-598.8 degrees C, the maximum mass loss rate of both samples obviously decreased and delayed with CO2 replacing N2 at the same oxygen concentration. The SAH-A and SAH-B combustions in both atmospheres emitted C- (CO2, CO, CH4, and small molecular organic substances) and N-containing (HCN and NH3) gases. In both atmospheres, the temperature dependency of the gas emissions remained the same. Both empirical indices and ternary phase diagrams indicated that both samples had a high deposition risk. Thermochemical equilibrium simulations were used to predict the slagging risk in response to ash mineral transformations. Our findings can provide new insights into the combustion dynamics of phytoremediation biomass and its effect on CO2 capture, utilization, and storage in mitigating climate change.
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    Oxy-fuel co-combustion dynamics of phytoremediation biomass and textile dyeing sludge: Gas-to-ash pollution abatement
    (Elsevier, 2022) Wu, Xieyuan; Liu, Jingyong; Wei, Zebin; Chen, Zihong; Evrendilek, Fatih; Huang, Wenxiao
    The environmental pressures of major wastes in the circular economies can be abated leveraging the complementarity and optimal conditions of their co-combustion. The oxy-fuel co-combustion of phytoremediation biomass of Sedum alfredii Hance (SAH) and textile dyeing sludge (TDS) may be a promising choice for sustainable CO2 capture and a waste-to-energy conversion. This study characterized and quantified their co-combustion performances, kinetics, and interactions as a function of blend ratio, atmosphere type, and temperature. With a focus on the characteristic el-ements of SAH (Ca, K, Zn, and Cd) and TDS (Al and S), changes in the mineral phases and ash melting and slagging trends of K2O-Al2O3-SiO2 and CaO-Al2O3-SiO2 systems were quantified. The Zn and Cd residual rates of the co-combustion of 75% SAH and 25% TDS rose by 58.52% and 5.93%, respectively, in the oxy-fuel atmosphere at the 30% oxygen concentration, relative to the mono-combustion of SAH in the air atmosphere. The co-combustion in the oxy-fuel atmosphere at the 20% oxygen concentration delayed the release peaks of SO2, C2S, and H2S, while the Ca-rich SAH captured S in TDS through the formation of CaSO4. Our findings provide new and practical insights into the oxy-fuel co-combustion toward the enhanced co-circularity.