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FUNDAMENTALS                                           CH. 4 CONTROL OF NANOSTRUCTURE OF MATERIALS
                  methacrylate monomer and palladium or platinum  [9] K. Chujo:  Nanokonpojitto No Sekai  (in Japanese,
                  acetyl acetate is polymerized and reduced at the same  World of Nanocomposite, Kogyo Chosakai Publishing,
                  time at 60°C to obtain metal nanoparticle/poly methyl  Tokyo, p. 161 (2000).
                  methacrylate composite [16]. Since the polymerization  [10] S. Choi, K. Lee and S. Park: Stud. Surf. Sci. Catal.,
                  of the monomer capable of forming the complex and the  146, 93 (2003).
                  particle formation reaction proceed at the same time,  [11] J. Fang, L.D. Tung, K.L. Stokes, J. He, D. Caruntu,
                  this process can be defined as one of the Pechini meth-  W.L. Zhou and C.J. O’Commor:  J. Appl. Phys.,  91,
                  ods, although the esterification reaction does not occur.
                  In the simultaneous syntheses of polymers and particles  8816 (2002).
                  (or particle syntheses in polymers), the stability is con-  [12] M.S. Pechini: US Patent No. 3, 330, 697 (1967).
                  sidered important for inorganic compounds as precur-  [13] B.L. Cushing, V.L. Kolesnichenko and C.J. O’Connor:
                  sors of particles and complex compounds to be formed.  Chem. Rev., 104(9), 3893 (2004).
                    In this field, many reports concentrate on acrylic  [14] S. Yamamoto, M. Kakihana and S. Kato:  J. Alloys
                  polymer and polyalkylene glycol, the reason being,  Compos., 297, 81–86 (2000).
                  probably, that the stability of the complex is a key  [15] P.  Duran, F. Capel, D. Gutierrez, J.  Tarataj and
                  issue. Other examples of polymer systems include a  C. Moure: J. Euro. Ceram. Soc., 22, 1711–1721 (2002).
                  study on the preparation of nanocomposites in the  [16] Y. Nakao:  Kobunshi: High Polymers, Japan,  43,
                  PET synthesis reaction field [17]. They may be clas-  852–855 (1994).
                  sified as organic/inorganic hybrid materials rather
                  than polymer/particle nanocomposites.          [17] T. Morimoto, M. Yoshida and K. Okuyama: J. Soc.
                                                                     Mater. Sci., Jpn., 54, 393–398 (2005).

                                   References
                                                                 4.4.5 ECAP
                   [1] The Chemical Society of Japan: Kikan Kagaku
                      Sosetsu No.42, Organic–Inorganic Hybrid Material,  (1) ECAP Process
                      Japan Scientific Society Press, Tokyo, p. 35 (1999).  Figure 4.4.18 shows the schematic representation of
                   [2] L. Liu, Z. Qi and X. Zhu:  J. Appl. Polym. Sci.,  71,  side extrusion processes, which are a kind of the
                      1133–1138 (1999).                          double-action extrusion. In this figure, (d) and (e)
                   [3] J. Chang, D. Park:  J. Polym. Sci. Part B,  39,  indicate the process in which pure shear deformation
                      2581–2588 (2001).                          can be repeatedly imposed on materials so that an
                   [4] K. Chujo:  Nanokonpojitto No Sekai  (in Japanese,  intense plastic strain is produced with the materials
                                                                 within any change in the cross-sectional dimensions
                      World of Nanocomposite), Kogyo Chosakai Publishing,
                                                                 of the workpiece.  This processes are named as an
                      Tokyo, p. 113 (2000).
                                                                 equal channel angular extrusion (ECAE) or an equal
                   [5] Z. Ke, B. Yongping: Mater. Lett., 59 (27), p. 3348–3351
                                                                 channel angular press (ECAP).
                      (2005).
                                                                  Segal [1] proposed this process in 1977. In 1990s,
                   [6] Y. Ke, C. Long and Z. Qui: J. Appl. Polym. Sci., 71,  many studies for the development of ultra-fine
                      1139–1146 (1999).                          grained materials were carried out by Valiev et al. [2],
                   [7] Y. Ke, Z. Yang and C. Zhu: J. Appl. Polym. Sci, 85,  Horita et al. [3, 4], and Azushima et al. [5]. Azushima
                      2677–2691 (2001).                          et al. proposed the repetitive side extrusion process. It
                   [8] M.W. Weimer, H. Chen, E.P. Giannelis and D.Y. Sogah:  is a process in which a high back pressure is applied
                      J. Am. Chem. Soc., 1615–1616 (1999).       in the process of (d) type as shown in Fig. 4.4.18 in
















                  Figure 4.4.18
                  Schematic representation of side extrusion processes in double-acting extrusion.

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