Polymer nanocomposites dispersion

A nanocomposite is defined as the composite of two materials, one having the dimension of nanometric level at least in one dimension. In polymer nanocomposites (PNC), the fillers are dispersed on a nanolevel. 

CNTs can enhance the thermal properties of CNT-polymer nanocomposites. The reinforcing function is closely associated with the amount and alignment of CNTs in the composites. Well-dispersed and long-term stable carbon nanotubes/ polymer composites own higher modulus and better thermal property as well as better electronic conductivity (Valter et al., 2002 Biercuk et al., 2002). Both SWNT and MWNT can improve the thermal stability and thermal conductivity of polymer, the polymer-CNT composites can be used for fabricating resistant-heat materials. 

The dynamic mechanical thermal analyzer (DMTA) is an important tool for studying the structure-property relationships in polymer nanocomposites. DMTA essentially probes the relaxations in polymers, thereby providing a method to understand the mechanical behavior and the molecular structure of these materials under various conditions of stress and temperature. The dynamics of polymer chain relaxation or molecular mobility of polymer main chains and side chains is one of the factors that determine the viscoelastic properties of polymeric macromolecules. The temperature dependence of molecular mobility is characterized by different transitions in which a certain mode of chain motion occurs. A reduction of the tan 8 peak height, a shift of the peak position to higher temperatures, an extra hump or peak in the tan 8 curve above the glass transition temperature (Tg), and a relatively high value of the storage modulus often are reported in support of the dispersion process of the layered silicate. 

Kashiwagi, T., Du, F., Winey, K.I., Groth, K.M., Shields, J.R., Bellayer, S., Kim, S., and Douglas, J.F. 2005. Flammability properties of polymer nanocomposites with single-walled carbon nanotubes Effects of nanotube dispersion and concentration. Polymer 46(2) 471 181. 

Fabrication methods have overwhelmingly focused on improving nanotube dispersion because better nanotube dispersion in polyurethane matrix has been found to improve the properties of the nanocomposites. The dispersion extent of CNTs in the polyurethane matrix plays an important role in the properties of the polymer nanocomposites. Similar to the case of nanotube/solvent suspensions, pristine nanotubes have not yet been shown to be soluble in polymers, illustrating the extreme difficulty of overcoming the inherent thermodynamic drive of nanotubes to bundle. Therefore, CNTs need to be surface modified before the composite fabrication process to improve the load transfer from the polyurethane matrix to the nanotubes. Usually, the polyurethane/CNT nanocomposites can be fabricated by using four techniques melt-mixing (15), solution casting (16-18), in-situ polymerization (19-21), and sol gel process (22). 

Among the applications discussed in this chapter, the most prominent in recent years is CNT-reinforced polymer nanocomposites. The use of CNTs in polymers can provide superior mechanical properties (60). For instance, the addition of 1% CNTs might increase the stiffness of polymers by 10% and increase their resistance to fracture however, improvements in the properties of CNT-reinforced polymers largely depend on the dispersion of CNTs within the polymer matrix and the polymer-CNT interfacial properties. The following section highlights several studies regarding the processing of PLA-CNT nanocomposites. 

This chapter is an overview of the synthesis and properties of PVA/ nanotube composites. Various films and fibers have been processed from carbon nanotube and PVA dispersions. Compared to other polymers, PVA exhibit particularly strong interaction with single-walled as well as multiwalled carbon nanotubes. This leads to unique properties which are not observed in other nanotube polymer nanocomposites. In particular, this literature review confirms... 

This bicontinuous-microemulsion polymerization method can also be used to synthesize polymer nanocomposites containing Si02 [101], Ti02, ZnO and many other semiconductors. The advantage of this method is that the nanoparticles of inorganic materials can be dispersed in the polymer matrix fairly uniformly. The only requirement is that nanomaterials should be first stabihzed... 

A dispersion of nanoparticles of Au or other metals in a polymer matrix may also be obtained by a one-pot process of microemulsion polymerization. For instance, the UV-polymerization of a microemulsion of 35 wt% MMA, 35 wt% AUDMAA and 30 wt% of 0.1 M HAUCI4 aqueous solution would produce a Au-polymer nanocomposite, as shown in Fig. 12 [104]. This TEM micrograph shows a microtoned thin film of the sample. It is clearly apparent that Au particles of about 10-15 nm are well dispersed in the polymer matrix. 

It is reasonable that, in the synthesis of polymer nanocomposites, the y-ray irradiation method is convenient for growing nanofibers and nanowires of metal chalcogenides due to the shape-control of the macromolecules formed in situ. Figure 7.38 shows some of the resulting nanofiber-dispersed polymer composites,... 

The most commonly studied polymer nanocomposites are clay-based nanocomposites, mainly with montmorillonite (MMt) as layered silicate filler (Scheme 15.12). Upon incorporation of organomodihed clays (organoclays) into a polymer matrix, two nanomorphologies (Scheme 15.13) can be obtained, either intercalation of the polymer chain in between the clay platelets keeping the stacking of the sheets, or exfoliation of the clay platelets with a disordered dispersion of the inorganic sheets in the polymer. 

Polymer Nanocomposites The morphology and dispersion state of a filler-like sepiolite (lamella and fiber type) were determined using STEM [66]. 

Metal-polymer nanocomposites can be obtained by two different approaches, namely, in situ and ex situ techniques. In the in situ methods, metal particles are generated inside a polymer matrix by decomposition (e.g., thermolysis, photolysis, radiolysis, etc.) or chemical reduction of a metallic precursor dissolved into the polymer. In the ex situ approach, nanoparticles are first produced by soft-chemistry routes and then dispersed into polymeric matrices. Usually, the preparative scheme allows us to obtain metal nanoparticles whose surface has been passivated by a monolayer of -alkanethiol molecules (i.e., Crfiin+i-SH). Surface passivation has a fundamental role since it avoids aggregation and surface oxidation/contamination phenomena. In addition, passivated metal particles are hydrophobic and therefore can be easily mixed with polymers. The ex-situ techniques for the synthesis of metal/polymer nanocomposites are frequently preferred to the in situ methods because of the high optical quality that can be achieved in the final product. 

In this chapter, two new approaches for the synthesis of metal-polymer nanocomposite materials have been described. The first method allows the preparation of contact-free dispersions of passivated gold clusters in polystyrene, and it is based on a traditional technique for the colloidal gold synthesis—that is, the alcoholic reduction of tetrachloroauric acid in presence of poly(vinyl pyrrolidone) as polymeric stabilizer. The primary function of the stabilizer is to avoid cluster sintering, but it also allows us to isolate clusters by co-precipitation. It has been found that the obtained polymer-protected nanometric gold particles can be dissolved in alkane-thiol alcoholic solutions to yield thiol-derivatized gold clusters by thiol absorbtion on the metal surface. Differently from other approaches for thioaurite synthesis available in the literature, this method allows complete control over the passivated gold cluster structure since a number of thiol molecules can be equivalently used and the... 

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