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Photoinduced hydrophilicity and photocatalytic decomposition of endocrine-disrupting chemical pentachlorophenol on hollandite

Published online by Cambridge University Press:  31 January 2011

Toshiyuki Mori*
Affiliation:
Ecomaterials Center, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
Mamoru Watanabe
Affiliation:
Advanced Materials Laboratory, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
Hiromitsu Nakajima
Affiliation:
Advanced Materials Laboratory, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
Masaru Harada
Affiliation:
Advanced Materials Laboratory, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
Kenjiro Fujimoto
Affiliation:
Advanced Materials Laboratory, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
Satoshi Awatsu
Affiliation:
Advanced Materials Laboratory, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
Yoshio Hasegawa
Affiliation:
KAKEN Cooperation, Shikada 873-3, Asahi, Kashima, Ibaraki 311-1416, Japan
*
a)Address all correspondence to this author. e-mail: [email protected]
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Abstract

Surface properties and photocatalytic oxidation reactions on the hollandite-type compound K2Ga2Sn6O16 (KGSO) were examined for photoinduced hydrophilicity and oxidative decomposition of an endocrine-disrupting chemical, pentachlorophenol (C6Cl5OH, PCP), under ultraviolet (UV) illumination. The thin films and mesoporous powders of hollandite were used for examination of surface properties and photocatalysis, respectively. The photoinduced surface property was examined by measurement of the contact angle of water, ortho-chlorophenol (o-C6H4ClOH), and toluene on the surface of KGSO. The contact angle of H2O and o-C6H4ClOH decreased to 0° under UV illumination. The toluene showed little change in contact angle under UV irradiation. It is concluded that the surface of KGSO shows photoinduced hydrophilicity for H2O and aromatic compounds with hydroxyl groups (−OH). In addition, KGSO clearly showed a photo-oxidative decomposition of PCP under weak UV illumination at room temperature. The decomposition speed of C6Cl5OH on KGSO was much faster than that on previous reported nano-sized SnO2 photocatalysts. It is expected that photo-oxidative decomposition of aromatic compound will be controlled by a combination of optimum composition of the hollandite phase and control of the morphology of the hollandite particles. This suggests that hollandite would be a promising photocatalyst for decomposition of aromatic compounds in endocrine-disrupting chemicals.

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Articles
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

1.Data Base of Endocrine Disrupting Chemicals in Tokyo Metropolitan Research Laboratory of Public Health, 1998.Google Scholar
2.Colborn, T. and Mayer, J.P., Our Stolen Future: Are We Threatening Our Fertility, Intelligence and Survival? A Scientific Detective Story (Plume Books, New York, 1997).Google Scholar
3.Crain, D.A., Guillette, L.J., Jr., and Rooney, A.A., Environ. Health Prospect 105, 528 (1997).CrossRefGoogle Scholar
4.Harrison, P.T.C., Holmes, P., and Humfrey, C.D.N., Sci. Tot. Environ. 205, 97 (1997).CrossRefGoogle Scholar
5.Brandt, I., Berg, C., Halldin, K., and Brunstroem, B., Arch. Toxicol. 111 (1998).Google Scholar
6.Kamat, P.V., Chem. Rev. 93, 267 (1993); M.A. Fox and M.T. Dulay, Chem. Rev. 93, 341 (1993).CrossRefGoogle Scholar
7.Hashimoto, K. and Fujishima, A., Catalysis 36, 524 (1994).Google Scholar
8.Hashimoto, K. and Fujishima, A., Yosui and Haisui 36, 851 (1994).Google Scholar
9.Watanabe, M., Mori, T., Yamauchi, S., and Yamamura, H., Solid State Ionics 102, 376 (1994).Google Scholar
10.Mori, T., Yamauchi, S., Yamamura, H., and Watanabe, M., Appl. Catal. A 129, L1 (1995).CrossRefGoogle Scholar
11.Mori, T., Yamauchi, S., Yamamura, H., and Watanabe, M., J. Mater. Sci. 31, 1469 (1996).CrossRefGoogle Scholar
12.Mori, T., Suzuki, J., Fujimoto, K., and Watanabe, M., J. Mater. Synth. Process. 6, 329 (1998).CrossRefGoogle Scholar
13.Mori, T., Suzuki, J., Fujimoto, K., Watanabe, M., and Hasegawa, Y., Appl. Catal. B 23, 283 (1999).CrossRefGoogle Scholar
14.Mori, T., Suzuki, J., Fujimoto, K., Watanabe, M., and Hasegawa, Y., J. Sol-Gel Sci. Technol. 19, 505 (2000).CrossRefGoogle Scholar
15.Suzuki, J., Fujimoto, K., Mori, T., Watanabe, M., and Hasegawa, Y., J. Sol-Gel Sci. Technol. 19, 775 (2000).CrossRefGoogle Scholar
16.Fujimoto, K., Watanabe, M., Mori, T., and Ito, S., J. Mater. Res. 13, 926 (1998).CrossRefGoogle Scholar
17.Fujimoto, K., Suzuki, J., Mori, T., and Watanabe, M., J. Sol-Gel Sci.Technol. 19, 377 (2000).CrossRefGoogle Scholar
18.Awatsu, S., Mori, T., Fujimoto, K., and Watanabe, M., Abstract Book of the Third International Conference on Inorganic Materials, Sep 2002, Germany.Google Scholar
19.Wang, R., Hashimoto, K., Fujishima, A., Chikuni, M., Kojima, E., Kitamura, A., Shimohigoshi, M., and Watanabe, T., Nature 388, 431 (1997).CrossRefGoogle Scholar
20.Wang, R., Sasaki, N., Fujishima, A., Watanabe, T., and Hashimoto, K., J. Phys. Chem. B 103, 2188 (1999).CrossRefGoogle Scholar
21.Miyauchi, M., Nakajima, A., Watanabe, T., and Hashimoto, K., Chem. Mater. 14, 2812 (2002).CrossRefGoogle Scholar
22.Sakai, N., Fujishima, A., Watanabe, T., and Hashimoto, K., J. Phys. Chem. B 105, 3023 (2001).CrossRefGoogle Scholar
23.Wilcoxon, J.P., J. Phys. Chem. B 104, 7334 (2000).CrossRefGoogle Scholar