Polymers composites, with nanodiamonds

The preparation of composite materials in general is a very important appHca-tion of the mechanical properties of nanodiamond. With many polymers like caoutchouc, polysiloxanes, fluoroelastomers polymethacrylates, epoxy resins, etc., composites with markedly improved mechanical characteristics have already been obtained from the noncovalent incorporation of nanodiamond by simple admixing during polymerization. The modulus of elasticity, the tensile strength, and the maximal elongation of the material all increase upon this modification. Depending on the basic polymer, just 0.1-0.5% (w/w) of nanodiamond are required to achieve this effect (Table 5.3). Polymer films can also be reinforced by the addition of nanodiamond. For a teflon film with ca. 2% of nanodiamond added, for example, friction is reduced at least 20%, and scratches inflicted by mechanical means are only half as deep as in neat teflon. 

Owing to its remarkable properties nanodiamond suits very well to being part of composite materials. In particular it is the small particle size, the hardness, the large chemical inertness, its nontoxicity and the high refractive index that may beneficially complement the properties of the polymer matrix. The latter may be connected to the diamond particles either by covalent bonding or by noncovalent interaction. Numerous examples of noncovalently bound composites have been reported in the literature (Section 5.6.1). StiU the interaction with the matrix is by far more complex than discussed for the nanotubes and fullerenes. This is due to the more variable surface structure that features not only graphitized domains, but also a variety of polar and nonpolar functional groups. 

From the hydrogenation or fluorination of a diamond material, a very hydro-phobic surface results that may then enter into an exchange with rather nonpolar compounds. A connection via Jt-stadting, however, plays just a minor role because graphitic fragments are only found in small domains on the particle surface. In the case of thermally graphitized nanodiamond particles, on the other hand, the conditions largely resemble those observed for multiwalled nanotubes. The interaction of the 7t-electrons with the polymer molecule causes a stable noncovalent incorporation into the composite. 

Carbon-based polymer nano composites represent an interesting type of advanced materials with structural characteristics that allow them to be applied in a variety of fields. Functionalization of carbon nanomaterials provides homogeneous dispersion and strong interfacial interaction when they are incorporated into polymer matrices. These features confer superior properties to the polymer nanocomposites. This chapter focuses on nanodiamonds, carbon nanotubes and graphene due to their importance as reinforcement fillers in polymer nanocomposites. The most common methods of synthesis and functionalization of these carbon nanomaterials are explained and different techniques of nanocomposite preparation are briefly described. The performance achieved in polymers by the introduction of carbon nanofillers in the mechanical and tribological properties is highlighted, and the hardness and scratching behavior of the nanocomposites are also discussed. 

In Chapter 2, the development of composite materials based on improved nanodiamonds is reported by P. Ya Detkov, V. A. Popov, V. G. Kuhchikhin and S. I. Chukhaeva. The authors describe methods for improving the quality of diamond nanopowders obtained by detonation synthesis, as well as some commercial applications of nanodiamonds. The authors prove that the synthetic detonation diamond is a promising material that can be used in many fields. Of special interest are its applications in compos ite materials both with a metal and polymer matrix. Commercial production of ultradisperse diamonds (or nanodiamonds) has been developed, and it is synthesized on a scale sufficient for particular industries. 

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