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3.6 AGGREGATION AND DISPERSION, CHARACTERIZATION AND CONTROL                 FUNDAMENTALS
                  vapor deposition process for nanoparticle synthesis [7].  3.6.2 Liquid phase
                  The deposited salt was dissolved during dispersion of
                  nanoparticles into liquid with surfactant or polymer  Fine particles including nanoparticles are generally
                  dispersant. By the adsorption of surfactant, nanopar-  supplied in the aggregated state, because they are eas-
                  ticles are dispersed in suspension.            ily aggregated during the drying process of produc-
                    The packing and assembling structure control of  tion and transportation due to pressure caused by
                  synthesized nanoparticles in the film or bulk material  stacking. Dispersion of these aggregates in the liquid
                  are being developed by the use of special technology.  phase requires the input of mechanical energy to
                  By Akedo et al. [8], aerosol gas containing fine parti-  break them.
                  cles with several hundreds of nanometers was jetted  Breaking the aggregates increases the surface
                  and collided on the surface of a substrate. By the col-  area of  the solid–liquid interface, which causes re-
                  lision of particles on the substrate, the particles were  aggregation to impede the dispersion process if the
                  dispersed to nanoparticles and formed dense powder  interface is unstable. Usually, the solid–liquid inter-
                  layer on the substrate. Gleiter’s group [9] prepared  face is stabilized in the liquid phase by forming an
                  almost fully densed nanopolycrystalline by the follow-  electric double layer or adsorption of the polymer
                  ing process. Nanometer-sized inorganic particles were  around fine particles. For the dispersion of fine parti-
                  prepared by PVD method in high-vacuum chamber.  cles in liquid, how to mechanically disperse fine par-
                  Prepared nanoparticles were packed into small metal  ticles in liquid and control their stability are very
                  mold, and consolidated by one axial pressing with  important together with the evaluation technique.
                  ultra high pressure up to 5 GPa in vacuum chamber.
                  Based on this work, the aggregated structure of oxide  (1) Mechanical dispersion
                  nanoparticles in atmosphere was able to be collapsed  The mechanical dispersion methods are classified
                  and packed to almost hexagonal closed-packing struc-  into stirring, high-speed revolution shearing, milling,
                  ture by cold isostatic pressing up to 1 GPa [10]. These  high-pressure jet, and ultrasonic waves. In these
                  closely packed green bodies were able to be sintered to  methods, a bead mill is mainly evaluated for dispers-
                  almost fully dense ceramic at several hundred degrees  ing nanoparticle aggregates. A schematic depiction of
                  lower than usual sintering temperature [11].   this apparatus is shown in Fig. 3.6.5 [1, 2]. The mech-
                    Based on the above research, if nanoparticles were  anism of this milling to break the aggregated particles
                  prepared in gas phase, it is necessary to develop new  is as follows [2]. In the milling, the beads stirred by
                  process engineering such as coating, packing, and
                  forming process for the preparation of new materials
                  with nanoparticles.


                                   References

                   [1] N.A. Fuchs:  The Mechanism of  Aerosol, p. 288
                      (1989).
                   [2] R.L. Drake: Topics in Current Aerosol Research, Part
                      2, Pergamon Press, p. 201 (1972).
                   [3] K. Okuyama, Y. Kousaka and T. Yoshida: J. Aerosol
                      Sci., 399 (1978).
                   [4] D.T. Shaw: Recent Development in Aerosol Science,
                      Wiley, p. 279 (1978).
                   [5] R.L.Carr: Chem. Eng. Jan., 163 (1965).
                   [6] H. Masuda, K. Goto:  J. Powder Technol., Jpn, 703
                      (1993).
                   [7] C. Panatarani, I.W. Lenggoro and K. Okuyama:
                      J. Nanoparticle. Res., 5(1), 47–54 (2003).
                   [8] J. Akedo, M. Lebedev: Jpn. J. Appl.Phys., 38 (P1-9B),
                      5397 (1999).
                   [9] J. Karch, R. Birringer and H. Gleiter:  Nature,  330,
                      556 (1987).
                  [10] H. Kamiya, H. Suzuki, D. Kato and G. Jimbo: J. Am.
                      Ceram. Soc. 76(1), 54 (1993).
                  [11] H. Kamiya, H. Suzuki,  T. Ichikawa,  Y.I. Cho and  Figure 3.6.5
                      M. Horio: J. Am. Ceram. Soc.81, 173 (1998).   Schematic illustration of a bead mill.

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