Article

Quantum Chemical Study of Intercalation of Hydrazine Hydrate in Kaolinite

  • Zhang Chao ,
  • Wang Xing ,
  • Song Xiliang ,
  • Song Kaihui ,
  • Qian Ping ,
  • Yin Hongzong
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  • a Chemistry and Material Science Faculty, Shandong Agricultural University, Tai'an 271018, Shandong Province, China;
    b Linyi Yimin Experimental Middle School, Linyi 276025, Shandong Province, China

Received date: 2013-06-17

  Online published: 2013-07-24

Supported by

Project supported by the National Natural Science Foundation of China (No. 20903063) and the Postdoctoral Foundation of Shandong Agricultural University in China (No. 76335).

Abstract

Hydrazine hydrate is now drawn more attention with its alkalinity, adsorption and pollution in clay. In this paper, the cluster model of kaolinite Al6Si6O42H42 was constructed, and the B3LYP/6-31G(d,p), MP2/6-31G(d,p)//B3LYP/ 6-31G(d,p) and MP2/6-31++G(d,p)//B3LYP/6-31G(d,p) levels were used to explore the intercalation properties (such as optimal structures, structural parameters, binding energies, charge distributions, vibration spectrum, electrostatic potential, and so on) of hydrazine monohydrate and hydrazine dihydrate in kaolinite. During the optimization, geometries of hydrazine and water molecules and only the innermost part representative of the interaction sites of kaolinite cluster model, including the oxygen atoms on the tetrahedral layer and the hydroxyls on the octahedral layer, have been fully optimized, and the "dangling" valences of the border oxygen atoms were saturated with hydrogen atoms. Results show that the interaction between hydrazine and water molecules after intercalation is different from that before intercalation, when hydrazine monohydrate is intercalated into kaolinite. That is to say, water and hydrazine interact respectively with kaolinite by forming hydrogen bonds, and the interaction between hydrazine molecule and kaolinite is stronger than that between hydrazine and water molecules, and the intercalation points are almost in the active parts of kaolinite. These are the important factors that hydrazine hydrate is easily into the kaolinite layers and difficult to take off. When hydrazine dihydrate is intercalated into kaolinite, the cluster model with different layer spacing was optimized. And the interaction between hydrazine molecule and kaolinite is stronger than that between hydrazine and water molecules with the increase of the layer spacing. When the layer spacing is greater than 1.05 nm, the interaction between hydrazine and water molecules is stronger than that between hydrazine and kaolinite, which also further confirms the feasibility of hydrazine desorption. Specifically, the layer spacing could be increased to weaken the interaction of hydrazine and kaolinite, then the solvent is used to achieve hydrazine desorption.

Cite this article

Zhang Chao , Wang Xing , Song Xiliang , Song Kaihui , Qian Ping , Yin Hongzong . Quantum Chemical Study of Intercalation of Hydrazine Hydrate in Kaolinite[J]. Acta Chimica Sinica, 2013 , 71(11) : 1553 -1562 . DOI: 10.6023/A13060634

References

[1] Zhang, J.; Li, D. Chemical Intermediates 2006, (3), 8. (张杰, 李丹, 化工中间体, 2006, (3), 8).
[2] Poso, A.; von Wright, A.; Gynther, J. Mutation Research- Fundamental and Molecular Mechanisms of Mutagenesis 1995, 332, 63.
[3] Pan, X. B.; Li, Y. F.; Liu, G.; Men, X. H. Chemistry 2004, 67, 630. (潘晓兵, 李彦锋, 刘刚, 门学虎, 化学通报, 2004, 67, 630.)
[4] Ge, Q.; Zhao, M.; Guo, F.; Niu, D. L.; Wu, F. H. Agrochemicals 2009, 48, 157. (葛青, 赵敏, 郭飞, 牛德良, 吴范宏, 农药, 2009, 48, 157.)
[5] Zhang, X.; Fan, D.; Xu, Z. J. Tongji Univ. 2005, 33, 1646.
[6] Franco, F.; Cecila, J.; Pérez-Maqueda, L.; Pérez-Rodríguez, J.; Gomes, C. Appl. Clay Sci. 2007, 35, 119.
[7] Yan, L.; Kong, H.; Li, Z. J. Acta Chim. Sinica 2013, 71, 822. (严琳, 孔惠, 李在均, 化学学报, 2013, 71, 822.)
[8] Fan, H. B.; Yang, R. J.; Li, D. H. Acta Chim. Sinica 2012, 70, 429. (范海波, 杨荣杰, 李定华, 化学学报, 2012, 70, 429.)
[9] Chen, Z. X.; Yan, W.; Wang, J.; Ji, C. Y. J. Building Materials 2000, 3(3), 240. (陈祖熊, 颜卫, 王坚, 季春勇, 建筑材料学报, 2000, 3(3), 240.)
[10] Tao, J. J. Zhongguo Lvjian 2007, 11, 30. (陶建军, 中国氯碱, 2007, 11, 30.)
[11] Zhu, P.; Shen, M.; Xiao, S.; Zhang, D. Physica B: Condensed Matter 2011, 406, 498.
[12] Horvath, E.; Kristof, J.; Frost, R. L.; Redey, A.; Vágvölgyi, V.; Cseh, T. J. Therm. Anal. Calorim. 2003, 71, 707.
[13] Gao, X.; Jang, J.; Nagase, S. J. Phys. Chem. C 2009, 114, 832.
[14] Mattevi, C.; Eda, G.; Agnoli, S.; Miller, S.; Mkhoyan, K. A.; Celik, O.; Mastrogiovanni, D.; Granozzi, G.; Garfunkel, E.; Chhowalla, M. Adv. Funct. Mater. 2009, 19, 2577.
[15] Park, S.; An, J.; Potts, J. R.; Velamakanni, A.; Murali, S.; Ruoff, R. S. Carbon 2011, 49, 3019.
[16] Stankovich, S.; Dikin, D. A.; Dommett, G. H. B.; Kohlhaas, K. M.; Zimney, E. J.; Stach, E. A.; Piner, R. D.; Nguyen, S. B. T.; Ruoff, R. S. Nature 2006, 442, 282.
[17] Becerril, H. A.; Mao, J.; Liu, Z.; Stoltenberg, R. M.; Bao, Z.; Chen, Y. ACS Nano 2008, 2, 463.
[18] Robinson, J. T.; Zalalutdinov, M.; Baldwin, J. W.; Snow, E. S.; Wei, Z.; Sheehan, P.; Houston, B. H. Nano Lett. 2008, 8, 3441.
[19] Tung, V. C.; Chen, L. M.; Allen, M. J.; Wassei, J. K.; Nelson, K.; Kaner, R. B.; Yang, Y. Nano Lett. 2009, 9, 1949.
[20] Ren, P. G.; Yan, D. X.; Ji, X.; Chen, T.; Li, Z. M. Nanotechnology 2011, 22, 055705.
[21] Costanzo, P.; Giese, R. Clays Clay Miner. 1990, 38, 160.
[22] Tunega, D.; Haberhauer, G.; Gerzabek, M. H.; Lischka, H. Langmuir 2002, 18, 139.
[23] Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, Jr. J. A.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, Revision A.01, Gaussian Inc., Pittsburgh, PA, 2003.
[24] Flükiger, P.; Lüthi, H.; Portmann, S.; Weber, J. Molekel 4.0, Swiss Center for Scientific Computing, Manno, Switzerland, 2000.
[25] Zhang, C.; Song, K. H.; Wang, X.; Yin, H. Z.; Qian, P. J. Mol. Sci. 2013, (2), 134. (张超, 宋开慧, 王幸, 尹洪宗, 钱萍, 分子科学学 报, 2013, (2), 134.)
[26] Hu, X. L.; Michaelides, A. Surf. Sci. 2008, 602, 960.
[27] Neder, R. B.; Burghammer, M.; Grasl, T.; Schulz, H.; Bram, A.; Fiedler, S. Clays Clay Miner. 1999, 47, 487.
[28] Bish, D. L. Clays Clay Miner. 1993, 41, 738.
[29] Zhao, S. P.; Wang, T.; Xu, H.; Guo, Y. Non-Metallic Mines 2009, (4), 37. (赵顺平, 王涛, 许衡, 郭玉, 非金属矿, 2009, (4), 37.)
[30] Anakli, D.; Çetinkaya, S. Curr. Appl. Phys. 2010, 10, 401.
[31] Gardolinski, J.; Lagaly, G. Clay Miner. 2005, 40, 537.
[32] Hayes, M.; Isaacson, P.; Chia, K.; Lees, A.; Yormah, T. Interactions of Hydrazine and of Hydrazine Derivatives with Soil Constituents and with Soils, DTIC Document, 1984.
[33] Ren, X. H. Agro-Environmental Protection 2001, 20, 31. (任向红, 农业环境保护, 2001, 20, 31.)
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