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Polymer nanocomposites polyvinyl alcohol

The effect of polymer-filler interaction on solvent swelling and dynamic mechanical properties of the sol-gel-derived acrylic rubber (ACM)/silica, epoxi-dized natural rubber (ENR)/silica, and polyvinyl alcohol (PVA)/silica hybrid nanocomposites was described by Bandyopadhyay et al. [27]. Theoretical delineation of the reinforcing mechanism of polymer-layered silicate nanocomposites has been attempted by some authors while studying the micromechanics of the intercalated or exfoliated PNCs [28-31]. Wu et al. [32] verified the modulus reinforcement of rubber/clay nanocomposites using composite theories based on Guth, Halpin-Tsai, and the modified Halpin-Tsai equations. On introduction of a modulus reduction factor (MRF) for the platelet-like fillers, the predicted moduli were found to be closer to the experimental measurements. [Pg.7]

Zimmermann et al. [134] have used cellulose fibrils obtained from sulphite wood pulp to reinforce water soluble polymers such as polyvinyl alcohol (PVA) and hydroxypropyl cellulose (HPC). The mechanical properties of these nanocomposites were measured by tensile tests showing that the addition of fibrils increase the modulus of elasticity (E) up to three times and the tensile strength up to five times compared to the raw polymer. Zimmermann et al. [135] have determined the E values and the hardness of cellulose/HPC nanocomposites using nanoindentation technique. The results showed that the E values measured by nanoindentation were from two to three times higher than the E values measured by means of tensile tests. Stauss et al. [136] have explained that differences between tensile test and indentation results are due to the fact that they do not test the same material volumes and regions. The large volume used in tensile test includes defects such as pores, cracks and impurities. [Pg.40]

Roohani, M., Habibi, Y., Belgacem, N.M., Ebrahim, G., Karimi, A.N., Dufresne, A. Cellulose whiskers reinforced polyvinyl alcohol copolymers nanocomposites. Eur. Polym. J. 44, 2489-2498 (2008)... [Pg.50]

Roohani M, Habibi Y, Belgacem NM, Ebrahim G, Karimi AN, Dufresne A et al (2008) Cellulose whiskers reinforced polyvinyl alcohol copolymers nanocomposites. J Eur Polym 44 2489-2498... [Pg.41]

Ljungberg N, Cavaille J-Y, Heux L (2006) Nanocomposites of isotactic polypropylene reinforced with rod-like cellulose whiskers. Polymer 47 6285-6292 Lu Y, Weng L, Cao X (2005) Biocomposites of plasticized starch reinforced with cellulose crystallites from cottonseed linter. Macromol Biosci 5 1101-1107 Lu J, Wang T, Drzal LT (2008) Preparation and properties of microfibrillated cellulose polyvinyl alcohol composite materials. Compos Part A 39A 738-746 Magalhaes WLE, Cao X, Lucia LA (2009) Cellulose nanocrystals/cellulose core-in-shell nanocomposite assemblies. Langmuir. doi 10.1021Aa901928j Malainine ME, Mahrouz M, Dufresne A (2005) Thermoplastic nanocomposites based on cellulose microfibrils from Opuntiaficus-indica parenchyma cell. Compos Sci Technol 65 1520-1526 Marchessault RH, Sundararajan PR (1983) Cellulose. In Aspinall GO (ed) The polysaccharides. Academic, New York... [Pg.210]

Roohani M, Habibi Y, Belgacem NM et al (2008) Cellulose whiskers reinforced polyvinyl alcohol copol Tners nanocomposites. Eur Polym J 44 2489-2498 Ruiz MM, Cavaille JY, Dufresne A et al (2000) Processing and characterization of new thermoset nanocomposites based on cellulose whiskers. Compos Interface 7 117-131 Ruiz MM, Cavaille JY, Dufresne A et al (2001) New waterborne epoxy coatings based on cellulose nanofillers. Macromol Symp 16 211-222 Saito T, Nishiyama Y, Putaux JL et al (2006) Homogeneous suspensions of individualized microfibrils from TEMPO-catalyzed oxidation of native cellulose. Biomacromolecules 7 1687-1691... [Pg.585]

Electrical conductivity measurements have been reported on a wide range of polymers including carbon nanofibre reinforced HOPE [52], carbon black filled LDPE-ethylene methyl acrylate composites [28], carbon black filled HDPE [53], carbon black reinforced PP [27], talc filled PP [54], copper particle modified epoxy resins [55], epoxy and epoxy-haematite nanorod composites [56], polyvinyl pyrrolidone (PVP) and polyvinyl alcohol (PVA) blends [57], polyacrylonitrile based carbon fibre/PC composites [58], PC/MnCli composite films [59], titanocene polyester derivatives of terephthalic acid [60], lithium trifluoromethane sulfonamide doped PS-block-polyethylene oxide (PEO) copolymers [61], boron containing PVA derived ceramic organic semiconductors [62], sodium lanthanum tetrafluoride complexed with PEO [63], PC, acrylonitrile butadiene [64], blends of polyethylene dioxythiophene/ polystyrene sulfonate, PVC and PEO [65], EVA copolymer/carbon fibre conductive composites [66], carbon nanofibre modified thermotropic liquid crystalline polymers [67], PPY [68], PPY/PP/montmorillonite composites [69], carbon fibre reinforced PDMS-PPY composites [29], PANI [70], epoxy resin/PANI dodecylbenzene sulfonic acid blends [71], PANI/PA 6,6 composites [72], carbon fibre EVA composites [66], HDPE carbon fibre nanocomposites [52] and PPS [73]. [Pg.110]

Silicate clays as recovered from nature do not lead to the formation of nanocomposites by simply physically mixing them with a polymer. Except with few hydrophilic polymers like polyethylene oxide [49-52] or polyvinyl alcohol [53,54], which have good interaction with the inorganic, highly hydrophilic, layered silicates, the surfaces of the silicates have... [Pg.37]

The homogeneous dispersion of cellulose nanoparticles in a polymer matrix in order to obtain nanomaterials is due to their size, which allows penetration in hydrosoluble or at least hydrodispersible structures (as latex-form polymers) as well as dispersion of polysaccharide nanocrystals in nonaqueous media especially using surfactants and chemical grafting. Thus, one of the processing techniques of polymer nanocomposites reinforced with polysaccharide nanocrystals was carried out using hydrosoluble or hydrodispersible polymers. In this respect, the literature has reported preparation of polysaccharide particles with reinforced starch (Svagan et al. 2009), silk fibroin (Noishiki et al. 2002), poly(oxyethylene) (POE) (Samir et al. 2006), polyvinyl alcohol (PVA) (Zimmermann et al. 2005), hydroxypropyl cellulose (HPC) (Zimmermann et al. 2005), carboxymethyl cellulose (CMC) (Choi and Simonsen 2006), or soy protein isolate (SPI) (Zheng et al. 2009). [Pg.100]

Extrusion and impregnation, electrospinning, and multilayer films are other processes applicable for reinforced nanocomposites. Thus, preparation of cellulose whiskers reinforced with polylactic acid nanocomposites (by melt extrusion carried out by pumping the suspension of nanocrystals into the polymer melt during the extrusion process), using polyvinyl alcohol as a compatibilizer for the dispersion of cellulose whiskers within the polylactic acid matrix, was reported (de Menezes et al. 2009) bacterial cellulose whiskers incorporated into poly(oxyethylene) nanofibers by electrospinn to enhance the mechanical properties of electrospun fibers (Peresin et al. 2010) or the use of the layer-by-layer assembly technique, which maximizes the interaction between cellulose whiskers and a polar polymeric matrix (Bruno et al. 2009 Aulin et al. 2010), are some examples of nanocomposites reinforced by the last three methods. [Pg.102]

Biodegradation indicates degradation of a polymer in natural environment. This implies loss of mechanical properties, changing in the chemical structure, and into other eco-friendly compounds (Jamshidian et al. 2010). Degradable polymers from natural sources (such as lignin, cellulose acetate, starch, polylactic acid (PLA), polyhydroxylaUcanoates, polyhydroxylbutyrate (PHB)), and some synthetic sources (polyvinyl alcohol, modified polyolefins, etc.) are classified as biopolymers (John and Thomas 2008). It is noticeable that the nanocomposite from nonrenewable synthetic sources is neither wholly degradable nor renewable. [Pg.3]

Due to the feet, that metal ions are active, in the polymer medium they immediately appear in flic environment of the PVA molecules and form bonds with the hydroxyl groups of this polymer. Polyvinyl alcohol replicates the stmeture of the particle that it surrounds however, due to the tendency of the molecules of the metal salts or other metal compounds to combine, PVA as if envelopes the powder particles, and therefore the forms of the obtained nanostmetures can be different. The optical microscopy method allows to determine the stmeture of the nanocomposite at the early stage. [Pg.30]

Tang, X. and Alavi, S. (2011) Recent advances in starch, polyvinyl alcohol based polymer blends, nanocomposites and their biodegradabilily. Carbohydr. Polym.,... [Pg.388]

There has been increasing interest in polyvinyl alcohol (PVA) nanocomposites recently [66]. For bone-regeneration purposes, PVA-based biomimetic phosphate compounds were produced by electrospinning [67]. The polymer solution aimed at electrospinning was treated by Ca(N03)2 addition to incorporate Ca ions in PVA. Such an introduction of Ca + ions into PVA nanofibers was reported beneficial for the distribution, the nucleation and the crystallinity of subsequent HA forming when alternately... [Pg.295]


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See also in sourсe #XX -- [ Pg.361 , Pg.364 , Pg.367 , Pg.369 , Pg.378 , Pg.379 , Pg.382 , Pg.383 , Pg.384 ]




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