负载型非晶态Co-B催化剂在1-辛烯氢甲酰化中的应用

引用本文: 龙俊英, 马兰, 贺德华. 负载型非晶态Co-B催化剂在1-辛烯氢甲酰化中的应用[J]. 物理化学学报, 2010, 26(10): 2719-2725. doi: 10.3866/PKU.WHXB20101022 shu

Citation: LONG Jun-Ying, MA Lan, HE De-Hua. 1-Octene Hydroformylation Using Supported Amorphous Co-B Catalysts[J]. Acta Physico-Chimica Sinica, 2010, 26(10): 2719-2725. doi: 10.3866/PKU.WHXB20101022 shu

负载型非晶态Co-B催化剂在1-辛烯氢甲酰化中的应用

基金项目:
国家自然科学基金(20921001)资助项目 (20921001)

摘要:

以醇凝胶-氮气热处理方法制备的ZrO₂、碳纳米管(CNTs) 及介孔分子筛SBA -15作为载体, 采用化学还原法制备了负载型非晶态Co-B催化剂, 利用粉末X 射线衍射(XRD) 、氮气吸附等温线、透射电子显微镜(TEM) 、电感耦合等离子体-原子发射光谱(ICP-AES) 以及X 射线光电子能谱(XPS) 等对催化剂进行了表征. 以1-辛烯的氢甲酰化为目标反应, 考察了负载型非晶态Co-B 催化剂在氢甲酰化反应中的性能及循环使用效果. 表征结果显示, 以NaBH₄ 为还原剂制备的负载型Co-B 催化剂上的Co-B 为非晶态, 负载Co-B 组分对载体的晶相结构没有影响. 反应结果表明, 在1-辛烯的氢甲酰化反应中, 负载型非晶态Co-B 催化剂都显示较高的初始活性. 随着循环次数的增加, 三种催化剂的活性下降, 但下降幅度有所不同, Co-B/CNTs 和Co-B/SBA-15 的循环使用稳定性高于Co-B/ZrO₂.

关键词:

English

1-Octene Hydroformylation Using Supported Amorphous Co-B Catalysts

1.
1. Innovative Catalysis Program, Key Laboratory of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China;
2. Institute of Chemical Defence, Beijing 102205, P. R. China
Received Date: 26 April 2010
Available Online: 27 September 2010
Fund Project:
国家自然科学基金(20921001)资助项目

Abstract:

Co-B catalysts supported on ZrO₂ (prepared by alcogel nitrogen thermo-treatment method), carbon nanotubes (CNTs), and mesoporous SBA-15 as supports were prepared by chemical reduction method and characterized by X-ray diffraction (XRD), nitrogen physisorption, transmission electron microscopy (TEM), inductively coupled plasma -atomic emission spectrometry (ICP-AES) and X-ray photoelectron spectroscopy (XPS). Hydroformylation of 1-octene was used as a probe reaction to investigate the catalytic performance and stability of the catalysts in recycles. The as-prepared Co-B catalysts showed amorphous characteristics and the support structures were unchanged. The reaction results reveal that the catalytic activities of Co-B/CNTs, Co-B/ZrO₂ and Co-B/SBA-15 in the hydroformylation of 1-octene were comparatively high. However, the catalytic activities decreased upon recycling. Nevertheless, the Co-B/ CNTs and Co-B/SBA-15 were relatively stable compared with Co-B/ZrO₂.

Key words:

1. [1]
  
  1. Cornils, B.; Rasch, M.; Otto, R. Angew. Chem. Int. Edit., 1994, 33: 2144
  1. Cornils, B.; Rasch, M.; Otto, R. Angew. Chem. Int. Edit., 1994, 33: 2144
2. [2]
  2. Chapuis, C.; Jacoby, D. Appl. Catal. A, 2001, 221: 932. Chapuis, C.; Jacoby, D. Appl. Catal. A, 2001, 221: 93
3. [3]
  3. Botteghi, C.; Paganelli, S.; Moratti, F. J. Mol. Catal. A-Chem., 2003, 200: 1473. Botteghi, C.; Paganelli, S.; Moratti, F. J. Mol. Catal. A-Chem., 2003, 200: 147
4. [4]
  4. Russell, M. J. H. PlatinumMet. Rev., 1988, 32(4): 1794. Russell, M. J. H. PlatinumMet. Rev., 1988, 32(4): 179
5. [5]
  5. Ungvary, F. C. Chem. Rev., 1997, 167: 2335. Ungvary, F. C. Chem. Rev., 1997, 167: 233
6. [6]
  6. Klingler, R. J.; Chen, M. J.; Rathke, J. W.; Kramarz, K. W. Organometallics, 2007, 26(2): 3526. Klingler, R. J.; Chen, M. J.; Rathke, J. W.; Kramarz, K. W. Organometallics, 2007, 26(2): 352
7. [7]
  7. Dieguez, M.; Pamies, O.; Claver, C. Tetrahedron: Asymmetry, 2004, 15(14): 21137. Dieguez, M.; Pamies, O.; Claver, C. Tetrahedron: Asymmetry, 2004, 15(14): 2113
8. [8]
  8. Lin, Q.; Jiang, W. D.; Fu, H. Y.; Chen, H.; Li, X. J. Appl. Catal. A, 2007, 328(1): 838. Lin, Q.; Jiang, W. D.; Fu, H. Y.; Chen, H.; Li, X. J. Appl. Catal. A, 2007, 328(1): 83
9. [9]
  9. Fu, H. Y.; Li, M.; Chen, H.; Ji, X. J. Mol. Catal. A-Chem., 2006, 259(1-2): 1569. Fu, H. Y.; Li, M.; Chen, H.; Ji, X. J. Mol. Catal. A-Chem., 2006, 259(1-2): 156
10. [10]
  10. Zhou,W.; He, D. H. Green Chem., 2009, 11: 114610. Zhou,W.; He, D. H. Green Chem., 2009, 11: 1146
11. [11]
  11. Zhou,W.; He, D. H. Catal. Lett., 2009, 127: 43711. Zhou,W.; He, D. H. Catal. Lett., 2009, 127: 437
12. [12]
  12. Fierro, J. L. G.; Merchan, M. D.; Rojas, S.; Terreros, P. J. Mol. Catal. A-Chem., 2001, 166(2): 25512. Fierro, J. L. G.; Merchan, M. D.; Rojas, S.; Terreros, P. J. Mol. Catal. A-Chem., 2001, 166(2): 255
13. [13]
  13. Kainulainen, T. A.; Nieme, M. K.; Krause, A. O. I. J. Mol. Catal. A-Chem., 1997, 122: 3913. Kainulainen, T. A.; Nieme, M. K.; Krause, A. O. I. J. Mol. Catal. A-Chem., 1997, 122: 39
14. [14]
  14. Kainulainen, T. A.; Niemela, M. K.; Krause, A. O. I. J. Mol. Catal. A-Chem., 1999, 140: 17314. Kainulainen, T. A.; Niemela, M. K.; Krause, A. O. I. J. Mol. Catal. A-Chem., 1999, 140: 173
15. [15]
  15. Zhang, H.; Qiu, J.; Liang, C.; Li, Z.; Wang, X.; Wang, Y.; Feng, Z.; Lin, C. Catal. Lett., 2005, 101: 21115. Zhang, H.; Qiu, J.; Liang, C.; Li, Z.; Wang, X.; Wang, Y.; Feng, Z.; Lin, C. Catal. Lett., 2005, 101: 211
16. [16]
  16. Wang, M. H.; Li, H. X.; Deng, J. F. Chin. J. Catal., 1999, 20: 548 [王明辉,李和兴, 邓景发. 催化学报, 1999, 20: 548]16. Wang, M. H.; Li, H. X.; Deng, J. F. Chin. J. Catal., 1999, 20: 548 [王明辉,李和兴, 邓景发. 催化学报, 1999, 20: 548]
17. [17]
  17. Li, H.; Xu, Y.; Yang, H. X.; Zhang, F.; Li, H. X. J. Mol. Catal. A- Chem., 2009, 307: 10517. Li, H.; Xu, Y.; Yang, H. X.; Zhang, F.; Li, H. X. J. Mol. Catal. A- Chem., 2009, 307: 105
18. [18]
  18. Li, H.; Zhao, Q. F.; Li, H. X. J. Mol. Catal. A-Chem., 2008, 285: 2918. Li, H.; Zhao, Q. F.; Li, H. X. J. Mol. Catal. A-Chem., 2008, 285: 29
19. [19]
  19. Lü, Z. G.; Guo, Z. M. Chem. Ind. Eng. Prog., 1998, 21(8): 552 [吕志果,郭振美. 化工进展, 1998, 21(8): 552]19. Lü, Z. G.; Guo, Z. M. Chem. Ind. Eng. Prog., 1998, 21(8): 552 [吕志果,郭振美. 化工进展, 1998, 21(8): 552]
20. [20]
  20. Nitta, Y.; Imanaka, T.; Teranishi, S. Bull. Chem. Soc. Jpn., 1980, 53: 315420. Nitta, Y.; Imanaka, T.; Teranishi, S. Bull. Chem. Soc. Jpn., 1980, 53: 3154
21. [21]
  21. Chen, Y. Z.;Wu, K. J. Appl. Catal., 1991, 78: 18521. Chen, Y. Z.;Wu, K. J. Appl. Catal., 1991, 78: 185
22. [22]
  22. Pei, Y.; Guo, P. J.; Qiao, M. H.; Li, H. X.; Wei, S. Q.; He, H. Y.; Fan, K. N. J. Catal., 2007, 248: 30322. Pei, Y.; Guo, P. J.; Qiao, M. H.; Li, H. X.; Wei, S. Q.; He, H. Y.; Fan, K. N. J. Catal., 2007, 248: 303
23. [23]
  23. Ma, L.; Peng, Q. R.; He, D. H. Catal. Lett., 2009, 130: 13723. Ma, L.; Peng, Q. R.; He, D. H. Catal. Lett., 2009, 130: 137
24. [24]
  24. Li, H. X.; Wang, W. J.; Li, H.; Deng, J. F. J. Catal., 2000, 194: 21124. Li, H. X.; Wang, W. J.; Li, H.; Deng, J. F. J. Catal., 2000, 194: 211
25. [25]
  25. Chen, X. Y.; Wang, S.; Zhuang, J. H.; Qiao, M. H.; Fan, K. N.; He, H. Y. J. Catal., 2004, 227: 41925. Chen, X. Y.; Wang, S.; Zhuang, J. H.; Qiao, M. H.; Fan, K. N.; He, H. Y. J. Catal., 2004, 227: 419
26. [26]
  26. Zhang, Q.; Zhao, M. Q.; Liu, Y.; Cao, A. Y.; Qian, W. Z.; Lu, Y. F.;Wei, F. Chinese Science Bulletin, 2009, 54: 1794 [张强, 赵梦强,刘毅, 曹安源,骞伟中,卢云峰,魏飞. 科学通报, 2009, 54: 1794]26. Zhang, Q.; Zhao, M. Q.; Liu, Y.; Cao, A. Y.; Qian, W. Z.; Lu, Y. F.;Wei, F. Chinese Science Bulletin, 2009, 54: 1794 [张强, 赵梦强,刘毅, 曹安源,骞伟中,卢云峰,魏飞. 科学通报, 2009, 54: 1794]
27. [27]
  27. Xu, B. Q.; Wei, J. M.; Yu, Y. J. Phys. Chem. B, 2003, 107: 520327. Xu, B. Q.; Wei, J. M.; Yu, Y. J. Phys. Chem. B, 2003, 107: 5203
28. [28]
  28. Zhao, D. Y.; Feng, J. L.; Huo, Q. S.; Melosh, N.; Fredrickson, G. H.; Chmelka, B. F.; Stucky, G. D. Science, 1998, 279: 54828. Zhao, D. Y.; Feng, J. L.; Huo, Q. S.; Melosh, N.; Fredrickson, G. H.; Chmelka, B. F.; Stucky, G. D. Science, 1998, 279: 548
29. [29]
  29. Ocampo, A. L.; Miranda, H. M.; Morgado, J.; Montoya, J. A.; Sebastian, P. J. J. Power Sources, 2006, 160(2): 91529. Ocampo, A. L.; Miranda, H. M.; Morgado, J.; Montoya, J. A.; Sebastian, P. J. J. Power Sources, 2006, 160(2): 915
30. [30]
  30. Wang, Y.; Noguchi, M.; Takahashi, Y.; Ohtsuka, Y. Catal. Today, 2001, 68: 330. Wang, Y.; Noguchi, M.; Takahashi, Y.; Ohtsuka, Y. Catal. Today, 2001, 68: 3
31. [31]
  31. Wonterghem, J. V.; Morup, S. C.; Koch, J. W.; Charles, S.W.; Wells, S. Nature, 1986, 322: 62231. Wonterghem, J. V.; Morup, S. C.; Koch, J. W.; Charles, S.W.; Wells, S. Nature, 1986, 322: 622
32. [32]
  32. Dillon, A. C.; Jones, K. M.; Bekkedahl, T. A. Nature, 1997, 386: 37732. Dillon, A. C.; Jones, K. M.; Bekkedahl, T. A. Nature, 1997, 386: 377
33. [33]
  33. Manuela, V.; Fabrizio, C. Chem. Phys. Lett., 2003, 371: 476
  33. Manuela, V.; Fabrizio, C. Chem. Phys. Lett., 2003, 371: 476

扫一扫看文章

计量

PDF下载量: 1050
文章访问数: 3067
HTML全文浏览量: 63

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

负载型非晶态Co-B催化剂在1-辛烯氢甲酰化中的应用

English

1-Octene Hydroformylation Using Supported Amorphous Co-B Catalysts

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

负载型非晶态Co-B催化剂在1-辛烯氢甲酰化中的应用

English

1-Octene Hydroformylation Using Supported Amorphous Co-B Catalysts

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南： 你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

文章相关

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs