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Fullerene C60, Graphene-Oxide and Graphene-Oxide Foil with Fullerene and their Bromination

Received: 5 September 2014    Accepted: 23 September 2014    Published: 10 October 2014
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Abstract

A direct reaction with liquid bromine was used to prepare bromofullerene C60Br14-18. The brominated derivative reacted with previously prepared graphene-oxide (hereinafter GO), according to a method described by Hummer. The same method was used to oxidize graphite alone. The prepared graphite fullerene foil was brominated with liquid bromine and the graphene-oxide foil was reacted with bromofullerene. FT-IR analysis of all the obtained products was performed and also TGA analysis to investigate particularly their thermal stability. The brominated products demonstrate lower thermal effects when thermally decomposed which is caused by the retarding ability of bromine.

Published in International Journal of Materials Science and Applications (Volume 3, Issue 6)
DOI 10.11648/j.ijmsa.20140306.13
Page(s) 293-302
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Liquid Bromine, Graphene-Oxide Foil, Graphene-Oxide Foil with Fullerene, Brominated Fullerene, Fullerene C60

References
[1] Klouda, K., 1985. Interkalární sloučeniny grafitu. ( Intercalate compounds of graphite) Dissertation , VŠCHT Praha (available in the technical library in Prague 6 – Dejvice).
[2] Makharza, S., Cirillo, G., Bachmatiuk, A., Ibrahim, I., Ioannides, N., Trzebicka, B., Hampel, S., Rümmeli, M.H., 2013. Graphene oxide-based drug delivery vehicles: functionalization, characterization, and cytotoxicity evaluation. Journal of Nanopart Res, 15, 2099.
[3] Zhang, Y., Ren, L., Wang, S., Marathe, A., Chaudhuri, J. and Li, G., 2011. Functionalization of graphene sheets through fullerene attachment. Journal of Materials Chemistry, 21, 5386.
[4] Yoo, B.M., Shin, H.J., Yoon, H.W., Park, H.B., 2013. Graphene and graphene oxide and their uses in barrier polymers. Journal of Polymer Science: Polymer Physics.
[5] Kyzas, G. Z., Deliyanni, E. A. and Matis, K. A., 2014. Graphene oxide and its application as an adsorbent for wastewater treatment. J. Chem. Technol. Biotechnol., 89, 196-205.
[6] Fakhri, A., 2013. Adsorption characteristics of graphene oxide as a solid adsorbent for aniline removal from aqueous solutions: Kinetics, thermodynamics and mechanism studies. Journal of Saudi Chemical Society.
[7] Chabot, V., Higgins, D., Yu, A., Xiao, X., Chen, Z. and Zhang, J., 2014. A review of graphene and graphene oxide sponge: material synthesis and applications to energy and the environment. Energy Environ. Sci., 7, 1564-1596.
[8] Russo, P., Hu, A., Compagnini, G., 2013. Synthesis, Properties and Potential Applications of Porous Graphene: A Review. Nano-micro letters, 5(4), 260-273.
[9] Shen, H., Zhang, L., Liu, M., Zhang, Z., 2012. Biomedical Applications of Graphene. Theranostics, 2(3), 283-294.
[10] Troshin, P.A., Lyubovskaya, R.N., 2008. Organic chemistry of fullerenes: the major reactions, types of fullerene e derivatives and prospects for their practical use. Russian Chemical Reviews, 77(4), 305-349.
[11] Hummers, W.S., Offeman, R.E., 1958. Preparation of Graphitic Oxide. J. Am. Chem. Soc., 80 (6), 1339.
[12] Dreyer, D.R., Park, S., Bielawski, Ch.W. and Ruoff, R.S., 2010. The chemistry of graphene oxide. Chemical Society Reviews, 19, 228-240.
[13] Peel, J.B., Rothwell, 1994. C60 Framework Response to Halogen Addition: The Stable Isomers of C60Br2m. Aust. J .Chem,47, 131-141.
[14] Resmi, M.R., Smitha, K., Pradeeo, T., 1997. Thermal Decomposition of C60Br24 and C60Br8: Absence of sequential elimination. Proc. Indian Acad Sci, 109, 221-228.
[15] Troshin, P.,A., Kemnitz, E., Troyanov, S., I., 2004. Characterization of reactions of fullerene e C60 with bromine. Crystal structures of bromofullerene es C60Br6, C60Br6•CS2, C60Br8•CHBr3•2Br2, and C60Br24• C6H4Cl2•Br2. Russ.chem.bull, Inter.ED, 53, 2787 – 2792.
[16] Troshin, P.,A., Kolesnikov, D., Burtsev, A.,V., Lubovskaya, R.,N., Denisenko, N.,I., Popov, A.,A., Troyanov, S., I., Boltalina, O., 2013. Bromination of 60 Fullerene e. High-Yielo Synthesi of C60Brx, (x = 6,8,24). Fullerenes, Nanotubes and Carbon Nanostructures 111, 47-60.
[17] Gayathri, S.S., Kamruddin, M., Tyagi, A.,K., Patnaik, A., 2003. Establishing a kinetic control regime for the decomposition of brominated fullerene e derivates: C60Br24 and C60Br6, Chem.Phys.Lett, 374, 33-40.
[18] Troyanov, S., I., Shustova, N., B., Popov, A., A., Sidorov, L., N., 2005. Synthesis and structures of C60 fullerene chlorides. Russ. Chem. Bull. Inter.ED, 54, 1656 – 1666.
[19] Troshin, P., A., Lyubovskaya, R., N., Ioffe, I., N., Shustova, N., B., Kemnitz, E., Troyanov, S., I., 2005. Synthesis and Structure of the Highly Chlorinated Fullerene C60Cl30 with a Drum-Shaped Carbon Cage. Angew. Chem. Inf. ED, 44, 234 – 237.
[20] Troshin, P.,A., Baskakov, S., A., Shulga, YU., M., Lyubovskaya, R., N., 2004. In the Chase of Mixed Halofullerenes: Remarkable Transformation of C60Cl n (n = 6, 8, 12, 14) to C60Br24. Full. Nanot. Carb. Nanostruct, 12, 159 – 163.
[21] Govindaraj, A. and Rao, C. N. R, 2013. Functionalization and Solubilization of Graphene. J Nanomater Mol Nanotechnol, S1.
[22] Park, J., Yan, M., 2013. Covalent functionalization of graphene with reactive intermediates. Acc Chem Res, 46, 181-189.
[23] Shanmugharaj, A. M., Yoon, J. H., Yang, W. J., Ryu, S. H., 2013. Synthesis, characterization and surface wettability properties of amine functionalized graphene oxide films with varying amine chain lengths. J Colloid Interface Sci, 401, 148-154.
[24] Marques, P. A. A. A., Golcalves, G., Cruz, S., Almeida, N., Singh, M. K., Grácio J. and Sousa, A. C. M., 2011. Functionalized Graphene Nanocomposites. Advances in Nanocomposite Technology, 374.
[25] Zhang, K., Zhang, Y. and Wang, S., 2013. Enhancing thermoelectric properties of organic composites through hierarchical nanostructures. Scientific Reports, 3, 3448.
[26] Kumar, R., Kumar, P., Naqvi, S., Gupta, N., Saxena, N., Gaur, J., Maurya, J. K. and Chand, S., 2014. Stable graphite exfoliation by fullereneol intercalation via aqueous route. New J. Chem., 2014.
[27] Zhang, X., Huang, Y., Wyng, Y., Ma, Y., Liu, Z. and Chen, Y., 2009. Synthesis and characterization of a graphene-C60 hybrid material. Carbon, 47, 1, 334-337.
[28] Zhang, Y., Ren, L., Wang, S., Marathe, A., Chaudhuri, J. and Li, G., 2011. Functionalization of graphene sheets through fullerene attachment. J. Mater. Chem., 21, 5386.
Cite This Article
  • APA Style

    Klouda Karel, Zemanova Eva, Friedrichova Romana, Weisheitova Marketa. (2014). Fullerene C60, Graphene-Oxide and Graphene-Oxide Foil with Fullerene and their Bromination. International Journal of Materials Science and Applications, 3(6), 293-302. https://doi.org/10.11648/j.ijmsa.20140306.13

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    ACS Style

    Klouda Karel; Zemanova Eva; Friedrichova Romana; Weisheitova Marketa. Fullerene C60, Graphene-Oxide and Graphene-Oxide Foil with Fullerene and their Bromination. Int. J. Mater. Sci. Appl. 2014, 3(6), 293-302. doi: 10.11648/j.ijmsa.20140306.13

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    AMA Style

    Klouda Karel, Zemanova Eva, Friedrichova Romana, Weisheitova Marketa. Fullerene C60, Graphene-Oxide and Graphene-Oxide Foil with Fullerene and their Bromination. Int J Mater Sci Appl. 2014;3(6):293-302. doi: 10.11648/j.ijmsa.20140306.13

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  • @article{10.11648/j.ijmsa.20140306.13,
      author = {Klouda Karel and Zemanova Eva and Friedrichova Romana and Weisheitova Marketa},
      title = {Fullerene C60, Graphene-Oxide and Graphene-Oxide Foil with Fullerene and their Bromination},
      journal = {International Journal of Materials Science and Applications},
      volume = {3},
      number = {6},
      pages = {293-302},
      doi = {10.11648/j.ijmsa.20140306.13},
      url = {https://doi.org/10.11648/j.ijmsa.20140306.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijmsa.20140306.13},
      abstract = {A direct reaction with liquid bromine was used to prepare bromofullerene C60Br14-18. The brominated derivative reacted with previously prepared graphene-oxide (hereinafter GO), according to a method described by Hummer. The same method was used to oxidize graphite alone. The prepared graphite fullerene foil was brominated with liquid bromine and the graphene-oxide foil was reacted with bromofullerene. FT-IR analysis of all the obtained products was performed and also TGA analysis to investigate particularly their thermal stability. The brominated products demonstrate lower thermal effects when thermally decomposed which is caused by the retarding ability of bromine.},
     year = {2014}
    }
    

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    T1  - Fullerene C60, Graphene-Oxide and Graphene-Oxide Foil with Fullerene and their Bromination
    AU  - Klouda Karel
    AU  - Zemanova Eva
    AU  - Friedrichova Romana
    AU  - Weisheitova Marketa
    Y1  - 2014/10/10
    PY  - 2014
    N1  - https://doi.org/10.11648/j.ijmsa.20140306.13
    DO  - 10.11648/j.ijmsa.20140306.13
    T2  - International Journal of Materials Science and Applications
    JF  - International Journal of Materials Science and Applications
    JO  - International Journal of Materials Science and Applications
    SP  - 293
    EP  - 302
    PB  - Science Publishing Group
    SN  - 2327-2643
    UR  - https://doi.org/10.11648/j.ijmsa.20140306.13
    AB  - A direct reaction with liquid bromine was used to prepare bromofullerene C60Br14-18. The brominated derivative reacted with previously prepared graphene-oxide (hereinafter GO), according to a method described by Hummer. The same method was used to oxidize graphite alone. The prepared graphite fullerene foil was brominated with liquid bromine and the graphene-oxide foil was reacted with bromofullerene. FT-IR analysis of all the obtained products was performed and also TGA analysis to investigate particularly their thermal stability. The brominated products demonstrate lower thermal effects when thermally decomposed which is caused by the retarding ability of bromine.
    VL  - 3
    IS  - 6
    ER  - 

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Author Information
  • V?B-Technical University of Ostrava, Faculty of Safety Engineering, Ostrava, CZ; State Office for Nuclear Safety, Prague, CZ

  • State Office for Nuclear Safety, Prague, CZ

  • Ministry of the Interior – General Directorate of the Fire Rescue Service of the Czech Republic, Technical Institute of Fire Protection, Prague, CZ

  • National Institute for Nuclear, Chemical and Biological Protection, Kamenna, CZ

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