01984nas a2200253   4500008004100000022001400041245006900055210006800124260009900192300001400291490000700305520111100312653000901423653001801432653002401450653001801474100002901492700002201521700002301543700002001566700001801586700002401604856010201628       2006                        eng d  a0141-391000aPhotooxidation of vulcanized EPDM/montmorillonite nanocomposites0 aPhotooxidation of vulcanized EPDMmontmorillonite nanocomposites  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLANDbELSEVIER SCI LTDcDEC  a3033-30390 v913 a<p>The photooxidation of a vulcanized ethylene-propylene-diene monomer (EPDM)/montmorillonite nanocomposite as well as EPDM/nanocomposite with stabilizers was studied under accelerated UV-light irradiation (lambda &gt;= 300 nm, 60 degrees C) for different times. The development of functional groups during oxidation was monitored by infrared spectroscopy. Photodegradation of the neat polymer and composites took place and the increases of absorbance in hydroxyl and carbonyl groups with irradiation times and also the decreases of the EPDM unsaturations were measured. The data indicated that the photooxidation products were not changed in the presence of the nanofiller. However, the presence of MMt was observed to dramatically enhance the rate of photooxidation of EPDM with a shortening of the oxidation induction time, leading to a decrease of the durability of the nanocomposites. On the other hand, it was observed that addition of stabilizers, either Tinuvin P or 2-mercaptobenzimidazole, was efficient in inhibiting the degradative effect of MMt. (c) 2006 Elsevier Ltd. All rights reserved.</p>10aEPDM10aNanocomposite10aphotooxidation rate10astabilization1 aMorlat-Therias, Sandrine1 aFanton, Elisabeth1 aTomer, Namrata, S.1 aRana, Sravendra1 aSingh, R., P.1 aGardette, Jean, Luc  uhttps://library.ncl.res.in/content/photooxidation-vulcanized-epdmmontmorillonite-nanocomposites-002692nas a2200241   4500008004100000022001400041245011600055210006900171260009900240300001400339490000700353520173200360653002902092653004302121653003302164100002202197700002902219700001602248700002002264700002402284700001802308856012402326       2009                        eng d  a0032-386100aPreparation and nonisothermal crystallization behavior of polypropylene/layered double hydroxide nanocomposites0 aPreparation and nonisothermal crystallization behavior of polypr  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLANDbELSEVIER SCI LTDcMAR  a1505-15150 v503 a<p>Polypropylene (PP)/layered double hydroxide (LDH) nanocomposites were prepared via melt intercalation using dodecyl sulfate anion modified LDH and maleated PP as compatibilizing agent. Evidently the interlayer anions in LDH galleries react with maleic anhydride groups of PP-g-MA and lead to a finer dispersion of individual LDH layers in the PP matrix. The nanostructure was characterized by XRD and TEM; the examinations confirmed the nanocomposite formation with exfoliated/intercalated layered double hydroxides well distributed in the PP matrix. The nonisothermal crystallization behavior of resulting nanocomposites was extensively studied using differential scanning calorimetry (DSC) technique at various cooling rates. In nonisothermal crystallization kinetics, the Ozawa approach failed to describe the crystallization behavior of nanocomposites, whereas the Avrami analysis and Jeziorny method well define the crystallization behavior of PP/LDH nanocomposite. Combined Avrami and Ozawa analysis (Liu model) also found useful. The results revealed that very small amounts of LDH (1%) could accelerate the crystallization process relative to the pure PP and increase in the crystallization rates was attributed to the nucleating effect of the nanoparticles. Polarized optical microscopy (POM) observations also support the DSC results. The effective crystallization activation energy was estimated as a function of the relative degree of crystallinity using the isoconversional analysis. Overall, results indicated that the LDH particles in nanometer size might act as nucleating agent and distinctly change the type of nucleation, growth and geometry of PP crystals. (C) 2009 Elsevier Ltd. All rights reserved.</p>10aLayered double hydroxide10aNonisothermal crystallization kinetics10aPolypropylene nanocomposites1 aLonkar, Sunil, P.1 aMorlat-Therias, Sandrine1 aCaperaa, N.1 aLeroux, Fabrice1 aGardette, Jean, Luc1 aSingh, R., P.  uhttps://library.ncl.res.in/content/preparation-and-nonisothermal-crystallization-behavior-polypropylenelayered-double-0