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Nanofillers organization

In order to reach a state of exfohation, a variety of protocols and formulatiorts have been tested. Nanofillers, organically modified by quaternary armnonirrm compoimds, which tend to be hydrophobic, have been incorporated into plasticized starch (wheat potato [CHE 05 a, b, PAR 03, PAR 02], or maize [ZHA 07]) in concentrations ranging from 0 to 9% per weight. It has clearly been demonstrated that the incorporation of clays bearing quaternary ammonittm compormds leads to the formation of microbiocomposites [CHE 05a, CHE 05b, CHI 05, PAR 02,... [Pg.188]

Nanofillers have a multiscale organization. The upper level of said organization refers to their distribution and dispersion in the rubber matrix. The lowest level of nanofiller organization refers to the structure of individual particles and of aggregates. In this section, the lowest level of nanofiller organization is discussed, presenting structural features of C, OC, CNT, GE and GNP, in their pristine state. [Pg.59]

Abstract Polymer electrolytes or gel-type polymer electrolytes are interesting alternatives to substitute liquid electrolytes in dye-sensitized solar cells (DSSC).The interest in this research field is growing, reflected in the increased number of papers published each year concerning these materials. This chapter presents a brief review of the history and development of polymer electrolytes aiming at the application in DSSC. Recent improvements achieved by modifications of the composition and by introduction of additives such as inorganic nanofillers, organic molecules and ionic Uquids are described. The stability of DSSC assembled with these materials, and scaling-up of such devices are also discussed. [Pg.381]

Organic modification of the nanofillers to obtain hydrophobic derivatives having improved compatibility with the polymer. [Pg.123]

ENGAGE is an ethylene-octene copolymer. Ray and Bhowmick [70] have prepared nanocomposites based on this copolymer. In this study, the nanoclay was modified in situ by polymerization of acrylate monomer inside the gallery gap of nanoclay. ENGAGE was then intercalated inside the increased gallery gap of the modified nanoclay. The nanocomposites prepared by this method have improved mechanical properties compared to that of the conventional counterparts. Preparation and properties of organically modified nanoclay and its nanocomposites with ethylene-octene copolymer were reported by Maiti et al. [71]. Excellent improvement in mechanical properties and storage modulus was noticed by the workers. The results were explained with the help of morphology, dispersion of the nanofiller, and its interaction with the mbber. [Pg.36]

Filler Carbon black Natural amorphous silica, precipitated silica, nonblack nanofiller Solvent Organic solvent Aqua-based solvent... [Pg.1024]

On the other hand, Bhattacharya et al. have reported the plasticization effect of organically modified layered silicates on dynamic mechanical properties [13]. In this work, nanocomposites of SBR have been prepared using various nanofillers like modified and unmodified montmorillonite, SP, hectorite etc. It has been observed that the Tg shifts to lower temperature in all the nanocomposites, except for systems from hectorite and NA. This is due to the fact that clay layers form capillaries parallel to each other as they become oriented in a particular direction. Due to wall slippage of the unattached polymer through these capillaries, the Tg is lowered, which could be even more in the absence of organo-modifiers [13]. A similar type of plasticization effect is also noted in the case of the low... [Pg.41]

Fig. 38 WAXD patterns of stearic acid, clay, and swollen clay. The swollen clay was prepared by mixing stearic acid and organically modified clay (Nanofil-15) at the ratio of 1 1... Fig. 38 WAXD patterns of stearic acid, clay, and swollen clay. The swollen clay was prepared by mixing stearic acid and organically modified clay (Nanofil-15) at the ratio of 1 1...
The sol-gel chemistry has also been used to prepare inorganic inhomogeneities in an organic matrix. Silane end-capped macrodiols can be used. Hydrolysis and condensation of alkoxy silane groups lead to inorganic hard clusters (Fig. 7.6b). Intramolecular reactions and the miscibility of the soft-segment chains with the relatively polar crosslinks determine the size distribution of the clusters (nanofillers). [Pg.226]

The pol5mier nanocomposite field has been studied heavily in the past decade. However, polymier nanocomposite technology has been around for quite some time in the form of latex paints, carbon-black filled tires, and other pol5mier systems filled with nanoscale particles. However, the nanoscale interface nature of these materials was not truly understood and elucidated until recently [2 7]. Today, there are excellent works that cover the entire field of polymer nanocomposite research, including applications, with a wide range of nanofillers such as layered silicates (clays), carbon nanotubes/nanofibers, colloidal oxides, double-layered hydroxides, quantum dots, nanocrystalline metals, and so on. The majority of the research conducted to date has been with organically treated, layered silicates or organoclays. [Pg.314]

Polyhedral oligomeric silsesquioxane (POSS) has been described as a three-dimensional "cage-shaped molecule composed of a silicon-oxygen framework bonded to organic groups that make it compatible with a polymer matrix. Unlike conventional nanofillers that must be dispersed and exfoliated to be useful, POSS molecules formulated in the resin are induced by shear to "self-assemble ... [Pg.112]

Along with the utilization of block copolymers as CNT dispersants, the role of an organic surfactant for the confinement of the nanotubes inside the self-assembled block copol5mier matrix was reported. More generally a surfactant consists of two parts, one hydrophilic and the other one hydrophobic, and due to this architecture it is used as a bridge between nanofillers and polymeric matrices. [Pg.240]


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Nanofillers organization nanocomposites properties

Nanofillers organization structures

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