介质阻挡放电
催化作用
能量转换效率
填充床
材料科学
X射线光电子能谱
分析化学(期刊)
多孔性
等离子体
同轴
化学工程
化学
电介质
复合材料
色谱法
有机化学
工程类
物理
电气工程
量子力学
光电子学
作者
Na Lu,Ning Liu,Chuke Zhang,Yan Su,Kefeng Shang,Nan Jiang,Jie Li,Yan Wu
标识
DOI:10.1016/j.cej.2021.129283
摘要
• CO 2 conversion can be promoted by K intercalated g-C 3 N 4 catalyst in DBD plasma system. • Decreasing reactor temperature can inhibit the reverse reaction of CO 2 conversion. • 20.6% of energy efficiency was obtained in KuCN/AO filled DBD plasma system. • Rich surface structure of KuCN/AO facilitated the adsorption and decomposition of CO 2 . • K intercalation adjusted the band structure of g-C 3 N 4 and improved CO 2 conversion. The direct conversion of CO 2 to CO and O 2 has attracted extensive attention as CO is a key C1 feedstock for chemical synthesis. The CO 2 conversion promoted by γ-Al 2 O 3 supported potassium intercalated g-C 3 N 4 (KuCN/AO) catalyst in a packed-bed dielectric barrier discharge (DBD) plasma system was investigated. A coaxial cylinder DBD plasma reactor was used with Cu powder as the high voltage electrode. Reactor temperature showed converse effect on CO 2 conversion. As the reactor temperature decreased from 120 ℃ to 50 ℃, CO 2 conversion rate and energy efficiency both increased by ca. 50%. After the catalyst was filled into the discharge area, the discharge mode changed from filamentary discharge to the combination of filamentary-surface discharge. The morphology and structure of KuCN was characterized by SEM, XRD, FTIR and XPS. KuCN kept a porous structure and K element distributed uniformly between CN interlayer spacing. In KuCN/AO assisted DBD plasma system, the highest CO 2 conversion rate, CO yield and energy efficiency were increased from 11.1%, 10.0% and 9.41% to 19.3%, 18.1% and 20.6% compared with pure DBD/γ-Al 2 O 3 system, respectively. The main mechanism of KuCN assisted enhancing CO 2 conversion in packed-bed DBD reactor was analyzed. The larger specific surface area, layers bridging and charge redistribution enabled KuCN/AO to obtain good plasma-catalytic CO 2 conversion performance.
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