Coupled systems for selective oxidation of aromatic alcohols to aldehydes and reduction of nitrobenzene into aniline using CdS/g-C3N4 photocatalyst under visible light irradiation

Applied Catalysis B: Environmental

Volumn 158-159, Issue , 2014, Pages 382-390

  Dai, Xia ^a,b   Xie, Mengli ^b   Meng, Sugang ^b   Fu, Xianliang ^b   Chen, Shifu ^a,b  

^a ANHUI SCIENCE AND TECHNOLOGY UNIVERSITY   (China)

^b HUAIBEI NORMAL UNIVERSITY   (China)

Author keywords

Coupled system; Photocatalysis; Reduction; Selective oxidation

Indexed keywords

ALDEHYDES; ANILINE; AROMATIC COMPOUNDS; AROMATIZATION; CADMIUM SULFIDE; COMPLEXATION; NITROBENZENE; OXIDATION; PHOTOCATALYSIS; REDUCTION; SCANNING ELECTRON MICROSCOPY; TRANSMISSION ELECTRON MICROSCOPY; X RAY POWDER DIFFRACTION;

BRUNAUER EMMETT TELLERS; CDS; COMPOSITE PHOTOCATALYSTS; COUPLED SYSTEMS; DIFFUSE REFLECTION SPECTROSCOPY; PHOTOCATALYTIC ACTIVITIES; SELECTIVE OXIDATION; VISIBLE-LIGHT IRRADIATION;

PHOTOCATALYSTS;

EID: 84901029972     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcatb.2014.04.035     Document Type: Article

References (62)

1. Fujishima A., Honda K. Nature 1972, 238:37-38.
2. Xu Y.J., Zhuang Y.B., Fu X.Z. J. Phys. Chem. C 2010, 114:2669-2676.
3. Fu X.L., Long J.L., Wang X.X., Leung D.Y.C., Ding Z.X., Wu L., Zhang Z.Z., Li Z.H., Fu X.Z. Int. J. Hydrogen Energ. 2008, 22:6484-6491.
4. Zhuang Y.B., Song H.Y., Li G., Xu Y.J. Mater. Lett. 2010, 64:2491-2493.
5. Xiang Q.J., Yu J.G., Jaroniec M. J. Am. Chem. Soc. 2012, 134:6575-6578.
6. Hou Y.D., Wu L., Wang X.C., Ding Z.X., Li Z.H., Fu X.Z. J. Catal. 2007, 250:12-18.
7. Gu Q., Fu X.L., Wang X.X., Chen S.F. Appl. Catal. B: Environ. 2011, 106:689-696.
8. Meng S.G., Li D.Z., Zheng X.Z., Wang J.X., Chen J., Fang J.L., Shao Y., Fu X.Z. J. Mater. Chem. A 2013, 1:2744-2747.
9. Fu X.L., Hu Y.F., Yang Y.G., Liu W., Chen S.F. J. Hazard. Mater. 2013, 244-245:102-110.
10. Wang X.W., Liu G., Chen Z.G., Li F., Wang L.Z., Lu G.Q., Cheng H.M. Chem. Commun. 2009, 3452-3454.
11. Yurdakal S., Palmisano G., Loddo V., Augugliaro V., Palmisano L. J. Am. Chem. Soc. 2008, 130:1568-1569.
12. Tanaka A., Hashimoto K., Kominami H. J. Am. Chem. Soc. 2012, 134:14526-14533.
13. Kamegawa T., Seto H., Matsuura S., Yamashita H. Appl. Mater. Interfac. 2012, 4:6635-6639.
14. Wu W.M., Liu G.D., Liang S.J., Chen Y., Shen L.J., Zheng H.R., Yuan R.S., Hou Y.D., Wu L. J. Catal. 2012, 290:13-17.
15. Enache D.I., Edwards J.K., Landon P., Espriu B.S., Carley A.F., Herzing A.A., Watanabe M., Kiely C.J., Knight D.W., Hutchings G.J. Science 2012, 311:362-365.
16. Zhai W.Y., Xue S.J., Zhu A.W., Luo Y.P., Tian Y. ChemCatChem 2011, 3:127-130.
17. Zhang N., Liu S.Q., Fu X.Z., Xu Y.J. J. Phys. Chem. C 2011, 115:22901-22909.
18. Zhang M., Chen C.C., Ma W.H., Zhao J.C. Angew. Chem. Int. Ed. 2008, 120:9876-9879.
19. Su F.Z., Mathew S.C., Lipner G., Fu X.Z., Antonietti M., Blechert S., Wang X.C. J. Am. Chem. Soc. 2010, 132:16299-16301.
20. Zhang P.F., Gong Y.T., Li H.R., Chen Z.R., Wang Y. RSC Adv. 2013, 3:5121-5126.
21. Zhang N., Zhang Y.H., Pan X.Y., Fu X.Z., Liu S.Q., Xu Y.J. J. Phys. Chem. C 2011, 115:23501-23511.
22. Zhang N., Liu S.Q., Fu X.Z., Xu Y.J. J. Mater. Chem. 2012, 22:5042-5052.
23. Zhang Y.H., Zhang N., Tang Z.R., Xu Y.J. Chem. Sci. 2012, 3:2812-2822.
24. Hoffman A.J., Mills G., Yee H., Hoffmann M.R. J. Phys. Chem. 1992, 96:5546-5552.
25. Entezari M.H., Ghows N. Ultrason. Sonochem. 2011, 18:127-134.
26. Chen W.T., Yang T.T., Hsu Y.J. Chem. Mater. 2008, 20:7204-7206.
27. Yang T.T., Chen W.T., Hsu Y.J., Wei K.H., Lin T.Y., Lin T.W. J. Phys. Chem. C 2010, 114:11414-11420.
28. Sheeney-Haj-Ichia L., Pogorelova S., Gofer Y., Willner I. Adv. Funct. Mater. 2004, 14:416-424.
29. Kamat P.V., Shanghavi B. J. Phys. Chem. B 1997, 101:7675-7679.
30. Habas S.E., Yang P.D., Mokari T. J. Am. Chem. Soc. 2008, 130:3294-3295.
31. Yan H.J., Yang J.H., Ma G.J., Wu G.P., Zong X., Lei Z.B., Shi J.Y., Li C. J. Catal. 2009, 266:165-168.
32. Baker D.R., Kamat P.V. Adv. Funct. Mater. 2009, 19:805-811.
33. Lee Y.L., Lo Y.S. Adv. Funct. Mater. 2009, 19:604-609.
34. Tada H., Mitsui T., Kiyonaga T., Akita T., Tanaka K. Nat. Mater. 2006, 5:782-786.
35. Kim H., Kim J., Kim W., Choi W. J. Phys. Chem. C 2011, 115:9797-9805.
36. Kobayashi J., Kitaguchi K., Tanaka H., Tsuiki H., Ueno A. J. Chem. Soc. Faraday Trans. 1987, 83:1395-1404.
37. Jia L., Wang D.H., Huang Y.X., Xu A.W., Yu H.Q. J. Phys. Chem. C 2011, 115:11466-11473.
38. Sheeney-Haj-Ichia L., Basnar B., Willner I. Angew. Chem. Int. Ed. 2005, 44:78-83.
39. Wu J.L., Bai S., Shen X.P., Jiang L. Appl. Surf. Sci. 2010, 257:747-751.
40. Cao A.N., Liu Z., Chu S.S., Wu M.H., Ye Z.M., Cai Z.W., Chang Y.L., Wang S.F., Gong Q.H., Liu Y.F. Adv. Mater. 2010, 22:103-106.
41. Gelder E.A., Jackson S.D., Lok C.M. Chem. Commun. 2005, 522-524.
42. Burge H.D., Collins D.J., Davis B.H. Ind. Eng. Chem. Prod. Res. Dev. 1980, 19:389-391.
43. Diao S.G., Qian W.Z., Luo G.H., Wei F., Wang Y. Appl. Catal. A: Gen. 2005, 286:30-35.
44. Wisniak J., Klein M. Ind. Eng. Chem. Prod. Res. Dev. 1984, 23:44-50.
45. Balasubramanian S. Luminescence behavior of tetraaza macrocylic nickel (II) complexes and non-linear Stern-Volmer quenching. J. Lumin. 2004, 106:69-76.
46. Füldner S., Pohla P., Bartling H., Dankesreiter S., Stadler R., Gruber M., Pfitzner A., König B. Green Chem. 2011, 13:640-643.
47. Imamura K., Yoshikawa T., Hashimoto K., Kominami H. Appl. Catal. B: Environ. 2013, 134-135:193-197.
48. Ge L., Han C.C., Liu J. Appl. Catal. B: Environ. 2011, 108:100-107.
49. Sobczynski A., Bard A.J., Campion A., Fox M.A., Mallouk T., Webber S.E., White J.M. J. Phys. Chem. 1987, 91:3316-3320.
50. Zhang J.Y., Wang Y.H., Jin J., Zhang J., Lin Z., Huang F., Yu J.G. Appl. Mater. Interfac. 2013, 5:10317-10324.
51. Fu J., Chang B.B., Tian Y.L., Xi F.N., Dong X.P. J. Mater. Chem. A 2013, 1:3083-3090.
52. Cao S.W., Yuan Y.P., Fang J., Shahjamali M.M., Boey F.Y.C., Barber J., Loo S.C.J., Xue C. Int. J. Hydrogen Energ. 2013, 38:1258-1266.
53. Yan S.C., Li Z.S., Zou Z.G. Langmuir 2010, 26:3894-3901.
54. Yan S.C., Li Z.S., Zou Z.G. Langmuir 2009, 25:10397-10401.
55. Butler M.A. J. Appl. Phys. 1977, 48:1914-1920.
56. Sing K.S.W., Everett D.H., Haul R.A.W., Moscou L., Pierotti R.A., Rouquerol J., Siemieniewska T. Pure Appl. Chem. 1985, 57:603-619.
57. Jin T., Yamaguchi T., Tanabe K. J. Phys. Chem. 1986, 90:4794-4796.
58. Ge L., Liu J. Appl. Catal. B: Environ. 2011, 105:289-297.
59. Chen S.F., Hu Y.F., Meng S.G., Fu X.L. Appl. Catal. B: Environ. 2014, 150-151:564-573.
60. Chen S.F., Yang Y.G., Liu W. J. Hazard. Mater. 2011, 186:1560-1567.
61. Ferry J.L., Glaze W.H. Langmuir 1998, 14:3551-3555.
62. Wei H.W., Jiang H.C., Zheng Z., Zhao Q.Q., Wu Q.Y., Zhan J.H. Mater. Res. Bull. 2013, 48:1352-1356.