Yanping Yang, Tongming Su, Xinling Xie, Xuan Luo, Hongbing Ji, Jin-Chung Sin, Sze-Mun Lam, Zuzeng Qin
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The characterization results revealed that slight oxidation of the Ti<sub>3</sub>C<sub>2</sub> surface generated highly dispersed TiO<sub>2</sub> nanoparticles that the doping of TiO<sub>2</sub>‒Ti<sub>3</sub>C<sub>2</sub> in the Cu‒Al<sub>2</sub>O<sub>3</sub> catalyst increased the specific surface area of the catalyst and promoted the formation and growth of Cu nanoparticles, and that strong interactions occurred between TiO<sub>2</sub>‒Ti<sub>3</sub>C<sub>2</sub> and the Cu components. The number of oxygen vacancies at the interface between TiO<sub>2</sub>‒Ti<sub>3</sub>C<sub>2</sub> and Cu increased by 17%, and the electronic kinetic energy of Cu<sup>0</sup> decreased by 0.1 eV, with the electron-rich oxygen vacancies transferring electrons to Cu<sup>2+</sup> ions and maintaining more Cu species in lower oxidation states. Reactions were carried out at 260 °C and 3.0 MPa with a gaseous hourly space velocity (GHSV) of 1500 cm<sup>3</sup>‧g<sup>−1</sup>‧h<sup>−1</sup> using Cu–Al<sub>2</sub>O<sub>3</sub>–TiO<sub>2</sub>–Ti<sub>3</sub>C<sub>2</sub>/HZSM-5 with 5.0 wt% Ti<sub>3</sub>C<sub>2</sub> as the hydrogenation catalyst, which provided a CO<sub>2</sub> conversion of 26.8% with 57.8% selectivity for DME.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":508,"journal":{"name":"Catalysis Letters","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2024-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of Cu–Al2O3–TiO2–Ti3C2/HZSM-5 Catalysts for Catalytic CO2 Hydrogenation to Dimethyl Ether\",\"authors\":\"Yanping Yang, Tongming Su, Xinling Xie, Xuan Luo, Hongbing Ji, Jin-Chung Sin, Sze-Mun Lam, Zuzeng Qin\",\"doi\":\"10.1007/s10562-024-04828-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>To develop efficient catalysts for CO<sub>2</sub> hydrogenation to dimethyl ether, Cu–Al<sub>2</sub>O<sub>3</sub>–TiO<sub>2</sub>–Ti<sub>3</sub>C<sub>2</sub>/HZSM-5 bifunctional catalysts were prepared by the surfactant PVP-assisted coprecipitation. 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引用次数: 0
摘要
为了开发二氧化碳加氢制二甲醚的高效催化剂,采用表面活性剂 PVP 辅助共沉淀法制备了 Cu-Al2O3-TiO2-Ti3C2/HZSM-5 双功能催化剂。研究了 Ti3C2 对 Cu-Al2O3 催化剂的影响。表征结果表明,Ti3C2 表面轻微氧化会产生高度分散的 TiO2 纳米颗粒,在 Cu-Al2O3 催化剂中掺杂 TiO2-Ti3C2 会增加催化剂的比表面积,促进 Cu 纳米颗粒的形成和生长,TiO2-Ti3C2 与 Cu 成分之间会产生强烈的相互作用。TiO2-Ti3C2 与 Cu 之间界面的氧空位数量增加了 17%,Cu0 的电子动能降低了 0.1 eV,富电子的氧空位将电子传递给 Cu2+ 离子,使更多的 Cu 保持在较低的氧化态。使用含 5.0 wt% Ti3C2 的 Cu-Al2O3-TiO2-Ti3C2/HZSM-5 作为加氢催化剂,在 260 °C 和 3.0 MPa 条件下以 1500 cm3‧g-1‧h-1 的气体时空速度(GHSV)进行了反应,其二氧化碳转化率为 26.8%,对二甲醚的选择性为 57.8%。
Preparation of Cu–Al2O3–TiO2–Ti3C2/HZSM-5 Catalysts for Catalytic CO2 Hydrogenation to Dimethyl Ether
To develop efficient catalysts for CO2 hydrogenation to dimethyl ether, Cu–Al2O3–TiO2–Ti3C2/HZSM-5 bifunctional catalysts were prepared by the surfactant PVP-assisted coprecipitation. The influence of Ti3C2 on Cu–Al2O3-based catalysts was investigated. The characterization results revealed that slight oxidation of the Ti3C2 surface generated highly dispersed TiO2 nanoparticles that the doping of TiO2‒Ti3C2 in the Cu‒Al2O3 catalyst increased the specific surface area of the catalyst and promoted the formation and growth of Cu nanoparticles, and that strong interactions occurred between TiO2‒Ti3C2 and the Cu components. The number of oxygen vacancies at the interface between TiO2‒Ti3C2 and Cu increased by 17%, and the electronic kinetic energy of Cu0 decreased by 0.1 eV, with the electron-rich oxygen vacancies transferring electrons to Cu2+ ions and maintaining more Cu species in lower oxidation states. Reactions were carried out at 260 °C and 3.0 MPa with a gaseous hourly space velocity (GHSV) of 1500 cm3‧g−1‧h−1 using Cu–Al2O3–TiO2–Ti3C2/HZSM-5 with 5.0 wt% Ti3C2 as the hydrogenation catalyst, which provided a CO2 conversion of 26.8% with 57.8% selectivity for DME.
期刊介绍:
Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
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