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Nanocomposite degradability

In recyding, low temperatures may limit nanocomposite degradation, which may be condudve to lowering future releases of nanoparticulate materials. Also, contained processing might reduce the release of nanopartides, and thereby reduce risk [77]. [Pg.290]

Studies of the photochemical behavior of polyamides based nanocomposites were run using MMT [116] or silica [10, 144]. As in other thermoplastics, MMT enhanced the photooxidative processes and accelerated the nanocomposite degradation [116]. In poly(trimethylhexamethylene terephthalamide)-silica nanocomposites, the silica enhanced the light transmittance and the effect decreased gradually when its amount increased over 5 wt% [144]. [Pg.129]

Presence of nanosilica and its interaction with the rubber matrices strongly affect the low and high temperature degradation behaviour of the hybrid nanocomposites. Figure 3.24 shows the post-aging swelling analysis of the cross-linked ACM-sihca and ENR-silica hybrid nanocomposites. The data points are collected after aging of the samples at 50°C, 70°C, and 90°C for 72 h. [Pg.80]

Figure 4.6 Example of the recovery of Ti02- advantage of the magnetic nature of the CoFe204 nanocomposite from an aqueous material. Reprinted from [102] (2010) with suspension after its use as a photocatalyst in the permission from Elsevier, degradation of atrazine. The separation takes... Figure 4.6 Example of the recovery of Ti02- advantage of the magnetic nature of the CoFe204 nanocomposite from an aqueous material. Reprinted from [102] (2010) with suspension after its use as a photocatalyst in the permission from Elsevier, degradation of atrazine. The separation takes...
Recently, nanocomposites of calcium and bismuth mixed oxides obtained by flame synthesis were used for the degradation of organic dyes under visible light, with good activity due to the formation of relatively high surface area materials and oxygen vacancy formation in the flame process [119]. [Pg.104]

Zhao, H. and H, R.K.Y. (2006) A study on the photo-degradation of zinc oxide (ZnO) filled polypropylene nanocomposites. Polymer, 47,3207-3217. [Pg.243]

Except for the PBS/SAP-qC16 (n-hexadecyl tri-n-butyl phosphonium cation modified saponite) system, the degree of degradation is the same for other samples. This indicates that MMT or alkylammonium cations, and at the same time other properties, have no effect on the biodegradability of PBS. The accelerated degradation of PBS matrix in the presence of SAP-qC16 may be due to the presence of alkylpho-sphonium surfactant. This kind of behavior is also observed in the case of PLA/MMT-based nanocomposite systems. [Pg.294]


See other pages where Nanocomposite degradability is mentioned: [Pg.304]    [Pg.596]    [Pg.231]    [Pg.29]    [Pg.301]    [Pg.102]    [Pg.62]    [Pg.166]    [Pg.202]    [Pg.36]    [Pg.145]    [Pg.182]    [Pg.304]    [Pg.596]    [Pg.231]    [Pg.29]    [Pg.301]    [Pg.102]    [Pg.62]    [Pg.166]    [Pg.202]    [Pg.36]    [Pg.145]    [Pg.182]    [Pg.36]    [Pg.37]    [Pg.43]    [Pg.47]    [Pg.57]    [Pg.80]    [Pg.80]    [Pg.81]    [Pg.1101]    [Pg.661]    [Pg.715]    [Pg.162]    [Pg.232]    [Pg.99]    [Pg.102]    [Pg.102]    [Pg.103]    [Pg.103]    [Pg.104]    [Pg.232]    [Pg.434]    [Pg.66]    [Pg.17]    [Pg.26]    [Pg.29]    [Pg.168]    [Pg.290]    [Pg.291]    [Pg.292]    [Pg.293]    [Pg.293]    [Pg.294]   
See also in sourсe #XX -- [ Pg.318 ]




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