氮掺杂碳包覆Cu-ZrO2催化剂的制备及其催化脱氢性能研究
收稿日期: 2019-04-10
网络出版日期: 2019-06-13
基金资助
项目受国家自然科学基金(No.21576229)资助.
Study on Preparation of Cu-ZrO2 Catalyst Coated by Nitrogen-Doped Carbon and Catalytic Dehydrogenation Performance
Received date: 2019-04-10
Online published: 2019-06-13
Supported by
Project supported by the National Natural Science Foundation of China (No. 21576229).
本研究以三聚氰胺作为碳源和氮源,经高温热解制得具有核壳结构氮掺杂碳(CN)包覆的Cu-ZrO2(CZ)纳米催化剂(CZ@CN催化剂),并研究了铜与三聚氰胺不同物质的量比对催化剂的影响.采用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线衍射(XRD)、X射线光电子能谱(XPS)、N2物理吸脱附测试(BET)、H2程序升温还原(H2-TPR)等表征技术分析了催化剂的形貌结构及物化性质.考察了催化剂用于二乙醇胺脱氢的催化性能.在铜与三聚氰胺物质的量比为4:1时,制备的CZ@CN催化剂催化活性最高,亚氨基二乙酸钠收率达92.8%,与普通CZ催化剂相比,反应时间缩短了40%,催化剂重复使用8次后收率依然达到88.4%.结果表明,适度的CN层的引入使催化剂具有更多的Lewis碱性位,在脱氢反应中有利于羟基的活化及氢的转移.同时CN层还可以稳定铜纳米颗粒,提高催化剂稳定性.
王永胜 , 赵云鹭 , 赵珍珍 , 兰小林 , 徐金霞徐伟祥 , 段正康 . 氮掺杂碳包覆Cu-ZrO2催化剂的制备及其催化脱氢性能研究[J]. 化学学报, 2019 , 77(7) : 661 -668 . DOI: 10.6023/A19040124
Glyphosate is one of the most widely used herbicides in the world. Current production of glyphosate starts with iminodiacetic acid (IDA). One method of producing IDA starts with the catalytic dehydrogenation of diethanolamine (DEA) using Cu-ZrO2 (CZ), which is a fairly simple, pollution-free, and cost-effective process. The Cu-ZrO2 catalysts used in this dehydrogenation are fairly efficient and inexpensive, but they tend to agglomerate and inactivate. The development of highly efficient and stable Cu-ZrO2 catalyst is of great significance. Carbon coated nano-metal particles are a new type of nano-carbon/metal composite materials. Metal materials can be imparted in a small space due to the surface acidity and alkalinity of carbon coated materials and their unique structural characteristics, which is of great significance for the dispersion and oxidation resistance of the loaded nano-metal materials. In this study, melamine was used as a carbon source and a nitrogen source to prepare a Cu-ZrO2 nanocatalyst (CZ@CN catalyst) coated with nitrogen-doped carbon (CN) with core-shell structure. The effect of different molar ratios of copper and melamine on the catalyst was studied. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), N2 physical adsorption and desorption test (BET), H2 temperature-programmed reduction (H2-TPR) were used to investigate the morphology and structure of the catalyst. The catalytic performance of the catalyst for the dehydrogenation of diethanolamine was investigated. When the molar ratio of copper to melamine is 4:1, the prepared CZ@CN-1 catalyst has the highest catalytic activity. The yield of sodium iminodiacetic acid is 92.80%, and the reaction time is shorter than that of ordinary CZ catalyst by 40%. The yield of sodium iminodiacetic acid still reaches 88.45% after reusing 8 times. The results showed that the introduction of the CN layer makes the catalyst exhibit more Lewis basicity. Meanwhile, it is beneficial to the activation of hydroxyl groups and the transfer of hydrogen in the dehydrogenation reaction. The CN layer can also stabilize copper nanoparticles and improve the stability of the catalyst.
[1] Zhu, Y.; Kong, X.; Li, X.; Ding, G.; Zhu, Y.; Li, Y. W. ACS Catal. 2014, 4, 3612.
[2] Duan, Z. K.; Li, S.; Xie, F.; Yan, J. H.; Zhang, T. Chem. Res. Appl. 2015, 27, 417. (段正康, 李晟, 谢帆, 闫建华, 张涛, 化学研究与应用, 2015, 27, 417.)
[3] Tang, Q. L.; Liu, Z. P. J. Phys. Chem. 2010, 114, 8423.
[4] Agrell, J.; Birgersson, H.; Boutonnet, M.; Melián-Cabrera, I.; Navarro, R. M.; Fierro, J. L. G. J. Catal. 2003, 219, 389.
[5] Huo, J. P.; Song, H. H.; Chen, X. H.; Zhao, S. Q.; Xu, C. M. Carbon Techniques. 2006, 25, 22. (霍俊平, 宋怀河, 陈晓红, 赵锁奇, 徐春明, 炭素技术, 2006, 25, 22.)
[6] Liu, J. Y.; Yang, P. J.; Zhang, J. F.; Ma, S. J. Petrochem. Technol. 2004, 33, 330. (刘金河, 杨普江, 张景峰, 马淑杰, 石油化工, 2004, 33, 330.)
[7] Li, H. T.; Chen, H. R.; Zhang, Y.; Gao, C. G.; Zhao, Y. X. Chinese J. Catal. 2011, 32, 111. (李海涛, 陈昊然, 张因, 高春光, 赵永祥, 催化学报, 2011, 32, 111.)
[8] Roy, R. K.; Lee, K. J. Biomed. Mater. Res. B 2010, 83B, 72.
[9] Zhang, Z. Q.; Ge, C. X.; Chen, Y. G.; Wu, Q.; Yang, L. J.; Wang, X. Z.; Hu, Z. Acta Chim. Sinica 2019, 77, 60. (张志琦, 葛承宣, 陈玉刚, 吴强, 杨立军, 王喜章, 胡征, 化学学报, 2019, 77, 60.)
[10] Su, D. S.; Zhang, J.; Frank, B.; Thomas, A.; Wang, X.; Parak-nowitsch, J.; Schlögl, R. ChemSusChem 2010, 3, 169.
[11] Mabena, L. F.; Sinha Ray, S.; Mhlanga, S. D.; Coville, N. J. Appl. Nanosci. 2011, 1, 67.
[12] Dai, X. Q.; Zhu, Y. B.; Xu, X. L.; Wen, J. Q. Chin. J. Org. Chem. 2017, 37, 577. (戴小强, 朱亚波, 许孝良, 翁建全, 有机化学, 2017, 37, 577.)
[13] Watanabe, H.; Asano, S.; Fujita, S.; Yoshida, H.; Arai, M. ACS Catal. 2015, 5, 2886.
[14] Zhang, P.; Wang, Q. N.; Yang, X.; Wang, D.; Li, W. C.; Zheng, Y. P.; Chen, M. S.; Lu, A. H. ChemCatChem 2017, 9, 505.
[15] Shi, R. N.; Zhao, J. X.; Liu, S. S.; Sun, W.; Li, H. X.; Hao, P. P.; Li, Z.; Ren, J. Carbon 2018, 130, 185.
[16] Wen, Z.; Liu, J.; Li, J. Adv. Mater. 2008, 20, 743.
[17] Unnikrishnan, P.; Srinivas, D. Ind. Eng. Chem. Res. 2012, 51, 6356.
[18] Hu, Q.; Yang, L.; Fan, G. L.; Li, F. Chem. Nano. Mat. 2016, 2, 888.
[19] Wang, J.; Lei, Z.; Qin, H.; Zhang, L.; Li, F. Ind. Eng. Chem. Res. 2011, 50, 7120.
[20] Hu, Q.; Fan, G.; Yang, L.; Cao, X.; Zhang, P.; Wang, B.; Li, F. Green Chem. 2016, 18, 2317.
[21] Xu, J.; Shen, K.; Xue, B. J. Mol. Cayal. A 2013, 372, 105.
[22] ABUDUHEIREMU, Awati; Zhang, D. D.; HALIDAN, Maimaiti Chem. J. Chin. Univ. 2019, 40, 306. (阿卜杜黑热木·阿瓦提, 张得栋, 哈丽丹·买买提, 高等学校化学学报, 2019, 40, 306.)
[23] Chen, S.; Bi, J.; Zhao, L.; Yang, C.; Ma, Y.; Wu, Q.; Wang, X.; Hu, Z. Adv. Mater. 2012, 24, 5593.
[24] Sharitfi, T.; Hu, G.; Jia, X.; Wagberg, T. ACS Nano 2012, 6, 8904.
[25] Wang, X. X.; Zhang, L. H.; Lin, H. J.; Nong, Q. Y.; Wu, Y.; Wu, T. H.; He, Y. M. RSC Adv. 2014, 4, 40029.
[26] Yang, Y.; Duan, Z.; Liu, W. Chem. Reac. Eng. Technol. 2001, 17, 210.
[27] Balaraman, E.; Khaskin, E.; Leitus, G.; Milstein, D. Nat. Chem. 2013, 5, 122.
[28] Neurock, M.; Tao, Z.; Chemburkar, A.; Hibbitts, D. D.; Lglesia, E. Faraday Discuss. 2017, 197, 181.
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