Enhanced carbon dioxide absorption capacity of Cu-BTC through the combination of Cu-g-C3N4 at room temperature

被引:3
|
作者
Zhu, Jiantao [1 ]
Wen, He [1 ]
Han, Wei [1 ]
Ma, Jiantai [2 ]
Zhang, Feng [1 ]
Liu, Chaowei [1 ]
机构
[1] Petrochem Res Inst, Lanzhou Petrochem Res Ctr, PetroChina, Lanzhou 730060, Gansu, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem SKLAOC, Gansu Prov Engn Lab Chem Catalysis, Lanzhou 730000, Peoples R China
关键词
Cu-BTC; Cu-g-C3N4; Nanocomposites; CO2; adsorption; Metal-organic frameworks; Environmental effects; METAL-ORGANIC FRAMEWORKS; GRAPHITE OXIDE COMPOSITES; CO2; ADSORPTION; SEPARATION;
D O I
10.1007/s11051-023-05817-z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The growing concern about the environmental consequences of anthropogenic CO2 emissions significantly stimulated the research of low-cost, efficient, and recyclable solid adsorbents of CO2 capture. Metal-organic frameworks (MOFs) are a promising porous material for CO2 adsorption. Hybrid materials consisting in copper benzene-1,3,5-tricarboxylate (Cu-BTC) and Cu doped graphitic-carbon nitride (Cu-g-C3N4) were prepared through solvothermal method as CO2 adsorbent. The size range of Cu-BTC@1.8%Cu-g-C3N4 was 9.0 similar to 19.4 mu m, which was lower than the size range of Cu-BTC (14.6 similar to 29.6 mu m). The hybrid adsorbents had lower Brunauer-Emmett-Teller (BET) surface areas and pole volume due to the combination with Cu-g-C3N4. The CO2 adsorption capacity of Cu-BTC@1.8%Cu-g-C3N4 increased by 49.5% compared with that of pure Cu-BTC because of more adsorption sites including unsaturated metal centers and N atoms. Moreover, the Cu-BTC@1.8%Cu-g-C3N4 had good stability in CO2 adsorption capacity after multiple adsorption cycles.
引用
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页数:13
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