Compression behavior of carbon nanotube bundles and individual carbon nanotubes within the bundle has been studied by using the Suzuki, Shanker, and usual Tait formulations. It is found that the Suzuki formulation is not capable of explaining the compression behavior of nanomaterials. Shanker formulation slightly improves the results obtained by the Suzuki formulation, but only usual Tait’s equation (UTE) of state gives results in agreement to the experimental data. The present study reveals that the product of bulk modules and the coefficient of volume thermal expansion remain constant for carbon nanotubes. It has also been found that the individual carbon nanotubes are less compressible than bundles of carbon nanotubes. 1. Introduction After their discovery by Iijima [1] carbon nanotubes have got a lot of attention because of their unique electronic and mechanical properties, but the most important property of carbon nanotubes is their elastic response to the external force or stress [2, 3]. As a one-dimensional structure, carbon nanotubes can be thought of as one sheet or multiple sheets of graphene rolled into a cylinder. Single-walled carbon nanotube bundles typically consist of several nested tubes, each like a graphene sheet bent into the cylindrical form with an overall diameter of a few nanometers. According to different chiral angles, single-walled carbon nanotubes can be classified into zigzag ( ), armchair ( ), and chiral tubes ( ) [4]. The Young’s modulus and Poisson’s ratio of nanotube have been studied by the previous workers [5–9], while the hardness as one of the most important parameters characterizing the mechanical properties of single-walled carbon nanotubes has been intensively studied during the last decade [6, 10]. High pressures which are encountered from deep down the earth to the astrophysical objects may cause many effects such as compression, pressure ionization, modification in electronic properties, phase changes, and several phenomenons in applied fields [11]. For this, pressure versus volume relations of condensed matter known as equation of state is a vital input. Many equations of state exist in the literature, but still there is a need to judge on their suitability under whole range of compressions as most of them give the same result under small compression. In high pressure, generally used theory is the finite strain theory which means the theory due to Birch [12]. However, Birch’s theory rates no more than a passing mention as discussed in detail by Stacy [13]. The attention has also been given to the theory based
References
[1]
S. Iijima, “Helical microtubules of graphitic carbon,” Nature, vol. 354, no. 6348, pp. 56–58, 1991.
[2]
M. S. Dresselhaus, G. Dresselhaus, and P. C. Eklund, Science of Fullerenes and Carbon Nanotubes, Academic, New York, NY, USA, 1996.
[3]
B. Vigolo, A. Penicaud, C. Coulon et al., “Macroscopic fibers and ribbons of oriented carbon nanotubes,” Science, vol. 290, no. 5495, pp. 1331–1334, 2000.
[4]
M. S. Dresselhaus, G. Dresselhaus, and R. Saito, “Physics of carbon nanotubes,” Carbon, vol. 33, no. 7, pp. 883–891, 1995.
[5]
J. P. Lu, “Elastic properties of single and multilayered nanotubes,” Journal of Physics and Chemistry of Solids, vol. 58, no. 11, pp. 1649–1652, 1997.
[6]
J. P. Lu, “Elastic properties of carbon nanotubes and nanoropes,” Physical Review Letters, vol. 79, no. 7, pp. 1297–1300, 1997.
[7]
E. Hernandez, C. Goze, and A. Rubio, “Elastic properties of single-wall nanotubes,” Applied Physics A, vol. 68, pp. 287–292, 1999.
[8]
D. Sánchez-Portal, E. Artacho, J. M. Soler, A. Rubio, and P. Ordejón, “Ab initio structural, elastic, and vibrational properties of carbon nanotubes,” Physical Review B, vol. 59, no. 19, pp. 12678–12688, 1999.
[9]
G. van Lier, C. van Alsenoy, V. van Doren, and P. Geerlings, “Ab initio study of the elastic properties of single-walled carbon nanotubes and graphene,” Chemical Physics Letters, vol. 326, no. 1-2, pp. 181–185, 2000.
[10]
B. I. Yakobson, C. J. Brabec, and J. Bernholc, “Nanomechanics of carbon tubes: instabilities beyond linear response,” Physical Review Letters, vol. 76, no. 14, pp. 2511–2514, 1996.
[11]
J. S. Schilling, “The use of high pressure in basic and materials science,” Journal of Physics and Chemistry of Solids, vol. 59, no. 4, pp. 553–568, 1998.
[12]
F. Birch, “Elasticity and constitution of the Earth's interior,” Journal of Geophysical Research, vol. 57, no. 2, pp. 227–286, 1952.
[13]
F. D. Stacy, “Finite strain, thermodynamics and the earth’s core,” Physics of the Earth and Planetary Interiors, vol. 128, pp. 179–193, 2001.
[14]
R. Rydberge, “Graphical representation of results of band spectroscopy,” Zeitschrift für Physik, vol. 73, pp. 376–385, 1931.
[15]
I. Suzuki, “Thermal expansion of periclase and olivine, and their anharmonic properties,” Journal of Physics of the Earth, vol. 23, no. 2, pp. 145–159, 1975.
[16]
I. Suzuki, S. Okajima, and K. Seya, “Thermal expansion of single-crystal manganosite,” Journal of Physics of the Earth, vol. 27, no. 1, pp. 63–69, 1979.
[17]
O. L. Anderson, Equation of State for Geophysics and Ceramic Science, Oxford University Press, Oxford, UK, 1995.
[18]
G. Helfrich, “Practical use of Suzuki's thermal expansivity formulation,” Physics of the Earth and Planetary Interiors, vol. 116, pp. 133–136, 1999.
[19]
M. Born and K. Huang, Dynamical Theory of Crystal Lattice, Oxford University Press, Oxford, UK, 1995.
[20]
J. Shanker, S. S. Kushwah, and P. Kumar, “Theory of thermal expansivity and bulk modulus for MgO and other minerals at high temperatures,” Physica B, vol. 233, no. 1, pp. 78–83, 1997.
[21]
M. Taravillo, V. G. Baonza, J. E. F. Rubio, J. Núez, and M. Cáceres, “The temperature dependence of the equation of state at high pressures revisited: a universal model for solids,” Journal of Physics and Chemistry of Solids, vol. 63, no. 9, pp. 1705–1715, 2002.
[22]
M. Singh, P. P. Singh, B. R. K. Gupta, and M. Kumar, “Temperature and pressure dependence of elastic constants,” High Temperatures, vol. 33, no. 2, pp. 199–206, 2001.
[23]
D. Kandpal, K. Y. Singh, and B. R. K. Gupta, “On pressure dependence of the relative compression (V/V0) at room temperature for the solids : copper and lead as prototypes,” Indian Journal of Physics A, vol. 78, no. 3, pp. 393–395, 2004.
[24]
S. Reich, C. Thomsen, and P. Ordejon, “Elastic properties of carbon nanotubes under hydrostatic pressure,” Physical Review B, vol. 65, no. 15, Article ID 153407, 4 pages, 2002.
[25]
M. Hanfland, H. Beister, and K. Syassen, “Graphite under pressure: equation of state and first-order Raman modes,” Physical Review B, vol. 39, no. 17, pp. 12598–12603, 1989.
[26]
K. Wang and R. R. Reeber, “The role of defects on thermophysical properties: thermal expansion of V, Nb, Ta, Mo and W,” Materials Science and Engineering R, vol. 23, no. 3, pp. 101–137, 1998.
[27]
M. Kumar, “A comparative study of Suzuki and Kumar formulations for thermal expansivity,” Indian Journal of Pure and Applied Physics, vol. 42, no. 1, pp. 67–70, 2004.
[28]
O. L. Anderson, D. G. Isaak, and H. Oda, “High-temperature elastic constant data on minerals relevant to geophysics,” Reviews of Geophysics, vol. 30, no. 1, pp. 37–90, 1992.
[29]
J. Shanker and M. Kumar, “Thermodynamic approximations in high-pressure and high-temperature physics of solids,” Physica Status Solidi B, vol. 179, no. 2, pp. 351–356, 1993.
[30]
H. Schlosser, J. Ferrante, and P. Vinet, “Pressure dependence of the melting temperature of metals,” Physical Review B, vol. 40, no. 9, pp. 5929–5935, 1989.
[31]
J. R. MacDonald, “Some simple isothermal equations of state,” Reviews of Modern Physics, vol. 38, no. 4, pp. 669–679, 1966.