Abstract:Three types of polyhedral oligomeric silsesquioxane (POSS)—octaphenyl (OP), POSS@TESPT (TT), and MWCNT@POSS (VC)—were incorporated into natural rubber (NR) to fabricate nanocomposites. The transport properties of POSS–NR nanocomposites were studied through solvent diffusion techniques. Diffusion studies were done with toluene (aromatic solvent) and the influence of nanofiller structure, concentration and compatibility with the NR matrix on various diffusion parameters were analyzed. The fillers that have good … Show more
“…As the nano‐HA content increases, the blend matrix becomes more rigid due to the increased degree of reinforcement of the nanoparticles. Therefore, the rate of polymer blend chain relaxation becomes slow compared to the concurrent penetrant diffusion and the transport in filled system follow a relaxation‐controlled diffusion process 41 . As usual, the k values in the reinforced composite system are lower than the neat rubber blend due to the reduced solvent‐matrix interactions, which can be attributed to better 'across phase' adhesion through the improved interface.…”
Hydroxyapatite nanoparticles (HA) reinforced polymer blend based on chlorinated nitrile rubber (Cl‐NBR) and chlorinated ethylene propylene diene monomer rubber (Cl‐EPDM) were prepared. Resulting blend composites were analyzed with regard to their rheometric processing, crystallinity, glass transition temperature (Tg), mechanical properties, oil resistance, AC conductivity, and transport behavior. The decrease in optimum cure time with the addition of HA is more advantageous for the development of products from these blend nanocomposites. The XRD, FTIR, and SEM confirmed the attachment and uniform dispersion of HA nanoparticles in the Cl‐NBR/Cl‐EPDM blend. The good compatibility between polymer blend and nanoparticles was also deduced by the formation of spherically shaped HA particles in the blend matrix determined by TEM analysis. DSC analysis showed an increase in Tg of the blend with the filler loading. The addition of HA particles to the blend produced a remarkable increase in tensile and tear strength, hardness, AC conductivity, abrasion, and oil resistance. The diffusion of blend composites was decreased with an increase in penetrant size. The diffusion mechanism was found to follow an anomalous trend. Among the blend composites, the sample with 7 phr of HA not only showed good oil and solvent resistance but also a remarkable increase in AC conductivity and mechanical properties.
“…As the nano‐HA content increases, the blend matrix becomes more rigid due to the increased degree of reinforcement of the nanoparticles. Therefore, the rate of polymer blend chain relaxation becomes slow compared to the concurrent penetrant diffusion and the transport in filled system follow a relaxation‐controlled diffusion process 41 . As usual, the k values in the reinforced composite system are lower than the neat rubber blend due to the reduced solvent‐matrix interactions, which can be attributed to better 'across phase' adhesion through the improved interface.…”
Hydroxyapatite nanoparticles (HA) reinforced polymer blend based on chlorinated nitrile rubber (Cl‐NBR) and chlorinated ethylene propylene diene monomer rubber (Cl‐EPDM) were prepared. Resulting blend composites were analyzed with regard to their rheometric processing, crystallinity, glass transition temperature (Tg), mechanical properties, oil resistance, AC conductivity, and transport behavior. The decrease in optimum cure time with the addition of HA is more advantageous for the development of products from these blend nanocomposites. The XRD, FTIR, and SEM confirmed the attachment and uniform dispersion of HA nanoparticles in the Cl‐NBR/Cl‐EPDM blend. The good compatibility between polymer blend and nanoparticles was also deduced by the formation of spherically shaped HA particles in the blend matrix determined by TEM analysis. DSC analysis showed an increase in Tg of the blend with the filler loading. The addition of HA particles to the blend produced a remarkable increase in tensile and tear strength, hardness, AC conductivity, abrasion, and oil resistance. The diffusion of blend composites was decreased with an increase in penetrant size. The diffusion mechanism was found to follow an anomalous trend. Among the blend composites, the sample with 7 phr of HA not only showed good oil and solvent resistance but also a remarkable increase in AC conductivity and mechanical properties.
“…They have concluded that equilibrium solvent uptake decreases with increase of CB content due to reduction in free volume 20 . Influence of POSS fillers on transport characteristics of NR was determined by Priya et al 21 wherein fillers with good interaction in polymer matrix showed lowest solvent uptake, which supports studies reported by Maria et al Aminabhavi et al studied the effect of organic liquids on Polyurethane (PU), Chloroprene (CR), NR, NBR, SBR, and ethylene propylene diene rubber. They reported dependency of diffusion parameters on the choice of a solvent molecule and chemical structure of the polymer membrane 22–25 .…”
Section: Introductionmentioning
confidence: 56%
“…One may observe that “k” value for 50phr CB filled rubber vulcanizates decreases in comparison to neat rubber vulcanizates. As the concentration of CB in 70NR/30BR increases, the “k” values shows a decreasing trend for interaction with benzene and toluene but varies when xylene is used as solvent 21 …”
Knowledge of solvent effect on the polymer is a need, for a large number of industrial and laboratory purposes. It is well known that swelling is a serious drawback for rubber products such as seals and O‐rings. The flexible rubber chains are highly prone to diffusion and allow easy penetration of solvent molecules through it, which causes swelling in rubber products. The flexibility and molecular mobility of rubber chains are reduced by either cross‐linking/blending/ adding inclusions. This reduces the swelling of rubber products. In the present work, blending rubbers and adding inclusions are experimented and reported. Various compositions of natural rubber (NR) / butadiene rubber (BR) i.e., 70NR/30BR, 50NR/50BR,30NR/70BR with and without carbon black (CB) were compounded, cured and characterized for diffusion analysis using benzene, toluene, and xylene. To determine the effect of varying filler concentration, 70NR/30BR blend was filled with 10, 20, 30, 40, and 50phr of CB and analyzed for diffusion characteristics. Loading of CB into rubbers reduces the chain flexibility as a result of rubber/filler interactions and this leads to a dramatic reduction in the diffusion of the solvent into rubber compounds. Diffusion characteristics of CB filled rubber blends were compared with their neat counterparts and CB filled blends showed less solvent uptake. Swelling characteristics for the neat and filled rubbers and their blends were calculated to determine coefficients and index of swelling. The experimental diffusion data obtained were fitted with mathematical models for predicting the diffusion behavior through the rubber vulcanisates to understand the mechanism of transport phenomena.
“…Polyhedral oligomeric silsesquioxane (POSS), a special type of crystalline silsesquioxane with regular cage-like structures, is often applied as a nanofiller for polymer materials, aiming to improve their mechanical, thermal, and fire retardancy properties. [1][2][3][4][5][6][7] However, though various POSS are commercially available, the cost of POSS remains quite high (one or several US dollar[s] per gram). This highly restricts their real-world applications as nanofillers for commodity polymers, such as polyolefin.…”
A novel commercial available and inexpensive long-chain alkyl (C30-45) modified silsesquioxane, namely (C30-45 alkyl)dimethylsilyl polypropylsilsesquioxane (C30PSS), was applied as a functional filler for linear low density polyethylene (LLDPE). For comparison, LLDPE/octaisobutyl polyhedral oligomeric silsesquioxane (BuPOSS) nanocomposites were also prepared via melt blending. The chemical and crystalline structures of C30PSS and BuPOSS were first identified by Fourier transform infrared spectroscopy, solid 29 Si NMR, and X-ray diffraction. The dispersion of two fillers in the polymer matrix was analyzed via scanning electron microscopy and X-ray energy dispersive spectroscopy. The rheological, tensile, and thermal properties of pristine LLDPE, LLDPE/C30PSS, and LLDPE/BuPOSS composites were systematically studied. Our results showed that C30PSS can serve as a promising and low-priced filler for LLDPE with respect to its fine dispersion in LLDPE and its abilities to improve the rheological and mechanical properties of LLDPE.
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