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Dispersion of nanoparticles

AOTF w/c RMs bearing the silver, silver iodide and silver sulfide nanoparticles were depressurized slowly and the nanoparticles in the cell were collected and re-dispersed in ethanol. Finally, the sample grids for the TEM (FEl TECNAl G ) measurements were prepared by placing a drop of ethanolic dispersion of nanoparticles on the copper grid. The morphology and size distribution of the silver, silver iodide, and silver sulfide nanoparticles were determined by TEM at an operation voltage of 200kV. The crystallinity of the silver, silver iodide, and silver sulfide nanoparticles was studied by electron diffraction techniques. [Pg.730]

Scheme 1. Inclusion of size-controlled PVP-protected Pt nanoparticles in calcined mesoporous SBA-15 silica matrices. Mechanical agitation by low-power sonication affords a high dispersion of nanoparticles ranging in size from 1 to 7nm in the mesopore channels. The method is referred to as capillary inclusion (Cl). The technique is limited by the size of nanoparticles that can fit into the 6-9 nm diameter mesopores [13]. (Reprinted from Ref [13], 2005, with permission from American Chemical Society.)... Scheme 1. Inclusion of size-controlled PVP-protected Pt nanoparticles in calcined mesoporous SBA-15 silica matrices. Mechanical agitation by low-power sonication affords a high dispersion of nanoparticles ranging in size from 1 to 7nm in the mesopore channels. The method is referred to as capillary inclusion (Cl). The technique is limited by the size of nanoparticles that can fit into the 6-9 nm diameter mesopores [13]. (Reprinted from Ref [13], 2005, with permission from American Chemical Society.)...
Figure 6.4 TEM image of the dispersion of nanoparticles obtained after evaporation of the solvent of a nanoemulsion with an O/S of 70 30 and a water content of 90wt% and negative staining with a phosphotungstic acid solution. Reproduced with permission from [54]. Figure 6.4 TEM image of the dispersion of nanoparticles obtained after evaporation of the solvent of a nanoemulsion with an O/S of 70 30 and a water content of 90wt% and negative staining with a phosphotungstic acid solution. Reproduced with permission from [54].
Carbon-based nanocomposite concepts have been successfully developed to limit or reduce these adverse effects and at the same time enhance the electron or ion transport [8]. CNT is an ideal building block in the carbon-inorganic composite/hybrid due to its mechanical, physical, chemical properties as mentioned above. CNTs are apparently superior to other carbonaceous materials such as graphite or amorphous carbon and are more adaptable to the homogeneous dispersion of nanoparticles than other carbonaceous materials [36],... [Pg.304]

Kumar P, Robins A, Britter R (2008) Fast response measurements for the dispersion of nanoparticles in a vehicle wake and a street canyon. Atmos Environ 43 6110-6118... [Pg.363]

In comparison to nematic liquid crystals, examples of smectic liquid crystals doped with quasi-spherical nanoparticles became more elusive over the last few years. This is surprising especially considering recent work by Smalyukh et al., who found that nanoscale dispersion (based on /V-vinyl-2-pyrrolidone-capped gold nanoparticles with 14 nm diameter) in a thermotropic smectic liquid crystal (8CB) are potentially much more stable than dispersions of nanoparticles in nematics [367]. [Pg.358]

Dispersions of nanoparticles in ferroelectric liquid crystals (FLCs) predominantly focused on induced or altered electro-optic effects, but also on the alignment of FLCs. Raina and co-workers reported on a gradual decrease of the dielectric permittivity, e, by doping with SiC>2 nanoparticles at frequencies up to 1 kHz and a rather minor increase of as well as an increase in optical transmission at frequencies above 2 kHz [279]. Liang et al. used BaTiC>3 nanoparticles (31 nm in diameter after grinding commercially available 90 nm nanoparticles Aldrich) and showed, perhaps expectably, a twofold increase in the spontaneous polarization... [Pg.360]

As shown by the results of processing of the TEM images of the structures, the relative size dispersion of nanoparticles formed by all the metals studied does not exceed 10% and their average size is only determined by the material of which the particles are composed. For example, the average sizes of Ni and Pd particles are 2.5 and 2nm, respectively. [Pg.734]

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. [Pg.278]

As expected, the formation of ZnS-(GSH) nanoclusters is analogous to CdS. Beginning with the Zn(II)(GSH)2 precursor complex, nanocluster formation is initiated by the addition of the sulfide. Mehra et al. has shown that the precursor Zn(II)GSH complex does indeed closely follow the synthetic route of CdS-(GSH) nanoparticles. Considering the similarities between the thiol chemistry of zinc and cadmium, studies to optimize ZnS nanocluster formation primarily focused on the ratio of zinc to sulfide ions in solution. Varying equivalents of sulfide (0.1-2.0) were studied for the formation of nanoclusters. An optimal ratio of Zn + S was obtained at 1 1. The average size of nanoparticles prepared at this ratio was shown to be about 3.45 0.5nm. Elution profiles from SEC highlighted the dispersity of nanoparticle populations synthesized in aqueous solutions. By size dependent absorption, the reaction mixtures revealed two cluster populations with an approximate diameter of 22.6 A and 19.54 A, respectively. Any excess of sulfide added greater than 1 equivalent was volatilized and not incorporated into the nanoclusters. ... [Pg.5362]

Industrial interest in nanomaterials derives from the novel properties they exhibit. These are defined for this entry as materials having engineered discrete particulate domains with diameters in the range of 1 nm to a few hundred nanometers. These domains may appear in many forms, such as dispersions of nanoparticles in a liquid, on surfaces, or embedded in a continuous matrix. The unique properties of nanomaterials are a consequence of the small size and extremely large interfacial areas. In this regime, dramatic variations in the chemical and physical properties of a material may be effected. Representative examples of size-critical properties, enabling new industrial applications, reviewed in this entry include surface and interfacial, catalytic, optical, and mechanical. [Pg.1803]

Infiltration with a second material (the matrix, e.g., an ultraviolet (UV) or thermally curable prepolymer [27,28], an ordinary organic precursor with initiators [29], a sol-gel precursor [30,31], or a dispersion of nanoparticles (1-50 nm) [32-34]) into the interstices of the colloidal template, followed by soHdification and the removal of colloidal template via dissolution, pyrolysis, or chemical etching. [Pg.138]

Nanocomposite aerogels mainly consist as homogeneous dispersions of nanoparticles in an aerogel matrix. The preparation of nanocomposite aerogels can be... [Pg.162]

Figure 9.2 is a schematic representation of CdSe QDs dispersed in poly(hexyl methacrylate) by in situ polymerization. The polymer with long alkyl branches is expected to prevent or reduce phase separation of the QDs from the polymer matrix during polymerization. This technique resulted in the preparation of a series of QD-based nanocomposite materials for which laser scanned confocal microscopy imaging revealed a nearly uniform dispersion of nanoparticles within the polymethacrylate matrix (Fig. 9.3). Notably, the resulting macroscopic QD-polymer composites appeared to be clear and uniformly colored. Figure 9.2 is a schematic representation of CdSe QDs dispersed in poly(hexyl methacrylate) by in situ polymerization. The polymer with long alkyl branches is expected to prevent or reduce phase separation of the QDs from the polymer matrix during polymerization. This technique resulted in the preparation of a series of QD-based nanocomposite materials for which laser scanned confocal microscopy imaging revealed a nearly uniform dispersion of nanoparticles within the polymethacrylate matrix (Fig. 9.3). Notably, the resulting macroscopic QD-polymer composites appeared to be clear and uniformly colored.
In order to achieve the desired fluidity and better dispersion of nanoparticles, the polycarboxylate ether based superplastisiser was incorporated into all mixes. The content of superplastisiser was adjusted for each mixture to keep the fluidity of the mortars constant. Natural river sand was used with the fraction of sand, which passed through a 1.18 mm sieve and... [Pg.325]

Homogeneous dispersion of nanoparticles of nanofibers in plastic — a problem yet to be solved satisfactorily - results, assuming equal parts by volume of nanoparticles and microparticles, in a significantly larger number of particles (10 with 1 pm to 1 nm particles), producing a polymer entity based entirely on interfacial interactions. Miilhaupt et al. [77] have called these materials interfacial polymers. This approach opens up new opportunities to modify the properties of older plastic types with low volumes of reinforcing nanomaterials. [Pg.138]


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See also in sourсe #XX -- [ Pg.58 , Pg.63 , Pg.256 ]




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