journal article·2015-11

A Convenient Surfactant‐Mediated Hydrothermal Approach to Control Supported Copper Oxide Species for Catalytic Upgrading of Glucose to Lactic Acid

Hemant Choudhary, Kohki Ebitani

ChemNanoMat· Volume 1· Issue 7
Publisher page

Abstract

Abstract Herein, we discuss a convenient surfactant‐mediated hydrothermal approach to control supported copper oxide species in a highly reproducible way and investigate their effect on the catalytic upgrading of glucose to lactic acid. Careful characterization using XRD, Raman spectroscopy, and temperature programmed reduction (TPR) studies revealed paramelaconite (Cu4O3) loaded on MgO as the catalytically active species. It was also found that the cuprite (Cu2O) phase can be prepared in the presence of N,N‐dimethyldodecylamine N‐oxide (DDAO) while the tenorite (CuO) phase was obtained in the absence of surfactant. The use of cetyltrimethylammonium bromide (CTAB) selectively gave the Cu4O3 phase as the supported species. The above‐mentioned systematic approach demonstrates that substantial improvement in the catalytic activity (or other properties) can be achieved by careful selection of the synthetic conditions for generation of desired Cu species through a simple and inexpensive preparation route.
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Research context

OpenAlex topics: Copper-based nanomaterials and applications · Mesoporous Materials and Catalysis · Catalytic Processes in Materials Science

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science Japan Advanced Institute of Science and Technology 1-1 Asahidai, Nomi Ishikawa 923 1292 Japan

Funding

Japan Society for the Promotion of Science (JSPS) · Grant-in-Aid for JSPS Fellows · Grant-in-Aid for Scientific Research (C) · Ministry of Education, Culture, Sports, Science and Technology (MEXT)

References (38)

Show source-provided references
1. 10.1038/440295a10.1038/440295a ↗
2. 10.1126/science.106720810.1126/science.1067208 ↗
3. 10.1021/ar990059e10.1021/ar990059e ↗
4. 10.1016/S0038-1098(98)00209-910.1016/S0038-1098(98)00209-9 ↗
5. 10.1002/(SICI)1521-4095(199907)11:10<840::AID-ADMA840>3.0.CO;2-210.1002/(SICI)1521-4095(199907)11:10<840::AID-ADMA840>3.0.CO;2-2 ↗
6. 10.1038/nmat81710.1038/nmat817 ↗
7. 10.1021/ja00305510.1021/ja003055 ↗
8. 10.1021/cr00016a00210.1021/cr00016a002 ↗
9. 10.1002/047122062010.1002/0471220620 ↗
10. 10.1063/1.164676010.1063/1.1646760 ↗
11. 10.1016/S0169-4332(98)00369-910.1016/S0169-4332(98)00369-9 ↗
12. 10.1016/j.ijhydene.2009.08.06210.1016/j.ijhydene.2009.08.062 ↗
13. 10.1016/j.ijhydene.2009.07.03510.1016/j.ijhydene.2009.07.035 ↗
14. 10.1016/j.catcom.2008.07.01610.1016/j.catcom.2008.07.016 ↗
15. PDF #41-0254 JCPDS Powder Diffraction File; Int. Center for Diffraction Data: Swarthmore PA 1989.
16. PDF #05-0667 JCPDS Powder Diffraction File; Int. Center for Diffraction Data: Swarthmore PA 1989.
17. PDF #083-1665 JCPDS Powder Diffraction File; Int. Center for Diffraction Data: Swarthmore PA 2004.
18. O'Keeffe M. · Am. Mineral. · 1978 · 63 · 180
19. Frondel C. · Am. Mineral. · 1941 · 26 · 657
20. 10.1107/S056774087800223X10.1107/S056774087800223X ↗
21. 10.1063/1.173241810.1063/1.1732418 ↗
22. 10.1023/A:102349522373810.1023/A:1023495223738 ↗
23. 10.1002/cctc.20100037810.1002/cctc.201000378 ↗
24. 10.1021/nl103454510.1021/nl1034545 ↗
25. 10.1021/ja106788x10.1021/ja106788x ↗
26. 10.1039/C4TA06804A10.1039/C4TA06804A ↗
27. 10.1016/j.apcatb.2014.05.01210.1016/j.apcatb.2014.05.012 ↗
28. 10.1002/cctc.20150016110.1002/cctc.201500161 ↗
29. 10.1002/aic.1219310.1002/aic.12193 ↗
30. 10.1002/cssc.20130009210.1002/cssc.201300092 ↗
31. 10.1016/j.catcom.2007.10.00510.1016/j.catcom.2007.10.005 ↗
32. 10.1002/aic.1396010.1002/aic.13960 ↗
33. 10.1021/jp303096m10.1021/jp303096m ↗
34. 10.1021/ja030167310.1021/ja0301673 ↗
35. 10.1021/jp040366o10.1021/jp040366o ↗
36. 10.1021/jp403339r10.1021/jp403339r ↗
37. 10.1006/jssc.1996.000510.1006/jssc.1996.0005 ↗
38. 10.1016/S0926-860X(98)00056-810.1016/S0926-860X(98)00056-8 ↗