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πŸ›οΈ Indexed Academic JournalImpact Factor: 3.8 (Q1 - Elsevier)Original: δΈ­ε›½εŒ–ε­¦ε·₯程学ζŠ₯ (θ‹±ζ–‡η‰ˆ)

Chinese Journal of Chemical Engineering

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Total Research Papers: 98
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Published Research PapersFiltered: Year 2024 β€’ Vol. 31 β€’ Issue 7

Showing 2 of 98 peer-reviewed papers with full Graphical Abstracts.

Original ResearchVol. 31, Issue 7 β€’ pp. 522-534DOI: 10.1016/j_cjche_144878780β€’ Jul 25, 2024

Ca2MnO4-layered perovskite modified by NaNO3 for chemical-looping oxidative dehydrogenation of ethane to ethylene

Authors: Weixiao Ding, Kun Zhao, Shican Jiang, Zhen Huang, Fang He

Chemical-looping oxidative dehydrogenation (CL-ODH) is a process designed for the conversion of alkanes into olefins through cyclic redox reactions, eliminating the need for gaseous O2. In this work, we investigated the use of Ca2MnO4-layered perovskites modified with NaNO3 dopants, serving as redox catalysts (also known as oxygen carriers), for the CL-ODH of ethane within a temperature range of 700-780 Β°C. Our findings revealed that the incorporation of NaNO3 as a modifier significantly enhanced the selectivity for ethylene generation from Ca2MnO4. At 750 Β°C and a gas hourly space velocity of 1300 hβˆ’1, we achieved an ethane conversion up to 68.17%, accompanied by a corresponding ethylene yield of 57.39%. X-ray photoelectron spectroscopy analysis unveiled that the doping NaNO3 onto Ca2MnO4 not only played a role in reducing the oxidation state of Mn ions but also increased the lattice oxygen content of the redox catalyst. Furthermore, formation of NaNO3 shell on the surface of Ca2MnO4 led to a reduction in the concentration of manganese sites and modulated the oxygen-releasing behavior in a step-wise manner. This modulation contributed significantly to the enhanced selectivity for ethylene of the NaNO3-doped Ca2MnO4 catalyst. These findings provide compelling evidence for the potential of Ca2MnO4-layered perovskites as promising redox catalysts in the context of CL-ODH reactions.

Ca2MnO4-layered perovskite modified by NaNO3 for chemical-looping oxidative dehydrogenation of ethane to ethylene
Graphical Abstract
Original ResearchVol. 31, Issue 7 β€’ pp. 754-766DOI: 10.1016/j_cjche_144878240β€’ Jul 12, 2024

Preparation of ultrafine WC-Co powder via fluidized bed

Authors: Huijun Shang, Hengli Li, Weijun Li, Feng Pan, Zhan Du

In this study, the effects of reaction parameters on the deep-reduction and carbonization process of WO2-Co to WC-Co were studied. The results indicate that the oxygen loss rate of WO2 is positively correlated with temperature and methane partial pressure. The partial pressure of methane has no significant effect on the formation rate of WC. The carbon content and particle size of the product increase with the increase of CH4 partial pressure. By synergistically regulating the reaction temperature to 950 Β°C, the CH4 partial pressure to 1.25%, and the reaction time to 60 min, ultrafine WC-Co powder without h phase can be obtained. The particle size of the composite powder is 128 nm, with total carbon content of 6.16%, free carbon content of 0.4%, and residual oxygen content of 0.05%, respectively. The growth rate relationship of tungsten carbide is as follows: d(t) = 1.21 Γ— 10^-13 exp(-12809.72/T) √t.

Preparation of ultrafine WC-Co powder via fluidized bed
Graphical Abstract
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