Treatment of CrVI-containing Mg(OH)2 nanowaste

Angewandte Chemie - International Edition

Volumn 47, Issue 30, 2008, Pages 5619-5622

  Liu, Weizhen ^a   Huang, Feng ^a   Liao, Yiqun ^a   Zhang, Jing ^a   Ren, Guoqiang ^a   Zhuang, Zangyong ^a   Zhen, Jinsheng ^a   Lin, Zhang ^a   Wang, Chen ^b  

^a FUJIAN INSTITUTE OF RESEARCH ON THE STRUCTURE OF MATTER   (China)

^b NATIONAL CENTER FOR NANOSCIENCE AND TECHNOLOGY   (China)

Author keywords

Chromium; Green chemistry; Nanostructures; Waste prevention

Indexed keywords

CHROMIUM;

GREEN CHEMISTRY; NANOSTRUCTURES; WASTE PREVENTION;

WASTE TREATMENT;

EID: 53549086419     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800172     Document Type: Article

References (23)

1. a) S. Bag, P. N. Trikalitis, P. J. Chupas, G. S. Armatas, M. G. Kanatzidis, Science 2007, 317, 490-493;
2. b) A. Srivastava, O. N. Srivastava, S. Talapatra, R. Vajtai, P. M. Ajayan, Nat. Mater. 2004, 3, 610-614;
3. c) S. R. Kanel, B. Manning, L. Charlet, H. Choi, Environ. Sci. Technol. 2005, 39, 1291-1298.
4. Nanowaste refers to industrial sludge containing nanoparticles.
5. VI that is added intentionally to maintain the current efficiency during the electrolysis of NaCl.
6. J. A. Kent, Riegel's Handbook of Industrial Chemistry, Springer US, New York, 2003, pp. 429-430.
7. N. P. Cheremisinoff, Handbook of Solid Waste Management and Waste Minimization Technologies, Elsevier, Burlington, 2003, pp. 192-193.
8. K. Kannan, T. Imagawa, A. Blankenship, J. Giesy, Environ. Sci. Technol. 1998, 32, 2507-2514.
9. a) K. Viswanathan, B. V. Tilak, J. Electrochem. Soc. 1984, 131, 1551-1559;
10. b) G. Lindbergh, D. Simonsson, Electrochim. Acta 1991, 36, 1985-1994;
11. c) M. Li, Z. Twardowski, F. Mok, N. Tam, J. Appl. Electrochem. 2007, 37, 499-504.
12. A. D. Dayan, A. J. Paine, Hum. Exp. Toxicol. 2001, 20, 439-451.
13. a) C. F. Lin, W. Rou, K. S. Lo, Water Sci. Technol. 1992, 26, 2301-2304;
14. b) C. D. Palmer, P. R. Wittbrodt, Environ. Health Perspect. 1991, 92, 25-40;
15. c) A. Agrawal, V. Kumar, B. D. Pandey, Miner. Process. Extr. Metall. Rev. 2006, 27, 99-130.
16. a) J. Zhao, CN1799716A, 2007;
17. b) C. T. Li, W. J. Lee, K. L. Huang, S. F. Fu, Y. C. Lai, Environ. Sci. Technol. 2007, 41, 2950-2956.
18. J. Zhang, Z. Lin, Y. Z. Lan, G. Q. Ren, D. G. Chen, F. Huang, M. C. Hong, J. Am. Chem. Soc. 2006, 128, 12981-12987.
19. 2 nanomaterial in the nanowaste is positively charged.
20. F. Huang, J. F. Banfield, J. Am. Chem. Soc. 2005, 127, 4523-4529.
21. [13]
22. 2 is therefore extremely high. Such a high rate is not likely to be possible by oriented attachment growth due to the relatively large grain size or by classical Ostwald ripening growth due to slow precipitation/dissolution at the particle/matrix interface.
23. J. F. Banfield, S. A. Welch, H. Z. Zhang, T. T. Ebert, R. L. Penn, Science 2000, 289, 751-754.