journal article·2016-02

Self-template synthesis of CuO@Cu 3 (BTC) 2 composite and its application in cumene oxidation

Feifei Wang, Shaoyi Jia, Danlin Li, Bo Yu, Liwei Zhang, Yong Liu, Xu Han, Ran Zhang, Songhai Wu

Materials Letters· Volume 164
Publisher page

Abstract

Abstract CuO@Cu 3 (BTC) 2 composite (BTC=benzene-1,3,5-tricarboxylate) was synthesized via a facile self-template method using CuO as the precursor. Cu 3 (BTC) 2 is a representative MOF (metal-organic framework), which is a class of crystalline inorganic–organic hybrid materials. By controlling synthesis time, CuO@Cu 3 (BTC) 2 with different content of Cu 3 (BTC) 2 was obtained. The products were characterized by X-ray diffraction (XRD), thermogravimetric (TG) analysis, transmission electron microscopy (TEM) and N 2 sorption measurement. It suggested that when controlling longer synthesis time, CuO@Cu 3 (BTC) 2 contained more Cu 3 (BTC) 2 and showed larger surface area and total pore volume. CuO@Cu 3 (BTC) 2 can effectively catalyze oxidation of cumene to cumene hydroperoxide (CHP) and the yield of CHP reached 18.1%, which was better than 13.6% by CuO or 8.7% by Cu 3 (BTC) 2 . When the ratio of CuO:Cu 3 (BTC) 2 in CuO@Cu 3 (BTC) 2 was 1:0.073 and 1:0.115, CHP yield was 18.1% and 14.2%, respectively. This study provides an approach for the oxidation of alkyl benzene using metal-oxide@MOF composite as catalyst.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Catalytic Processes in Materials Science · Advanced Nanomaterials in Catalysis

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References (16)

Show source-provided references
1. Zhan · J. Am. Chem. Soc. · 2013 · 135 · 192610.1021/ja311085e ↗
2. Zhu · Chem. Soc. Rev. · 2014 · 43 · 546810.1039/C3CS60472A ↗
3. Wang · Catal. Commun. · 2011 · 12 · 87510.1016/j.catcom.2011.02.001 ↗
4. Lu · Nat. Chem. · 2012 · 4 · 31010.1038/nchem.1272 ↗
5. Ke · J. Mater. Chem. · 2012 · 22 · 949710.1039/c2jm31167d ↗
6. Esken · J. Mater. Chem. · 2011 · 21 · 590710.1039/c1jm10091b ↗
7. Müller · Chem. Mater. · 2008 · 20 · 457610.1021/cm703339h ↗
8. Wang · Catal. Commun. · 2011 · 12 · 87510.1016/j.catcom.2011.02.001 ↗
9. Chui · Science · 1999 · 283 · 114810.1126/science.283.5405.1148 ↗
10. Marx · J. Catal. · 2011 · 281 · 7610.1016/j.jcat.2011.04.004 ↗
11. Zhang · J. Am. Chem. Soc. · 2012 · 134 · 92810.1021/ja208256u ↗
12. Zhang · Chem. Mater. · 2006 · 18 · 86710.1021/cm052256f ↗
13. Nurullina · Pet. Chem. · 2009 · 49 · 38510.1134/S0965544109050089 ↗
14. Liu · Chem. Commun. · 2012 · 48 · 881410.1039/c2cc34192a ↗
15. Sachse · Chem. Commun. · 2012 · 48 · 474910.1039/c2cc17190b ↗
16. Liao · Appl. Catal. A: Gen. · 2014 · 478 · 110.1016/j.apcata.2014.03.024 ↗