Barium titanate (BT) recently gained new interest in the preparation of dielectric and piezoelectric lead-free materials for applications in sensors, electronics, energy harvesting and storage fields. Barium titanate nanocomposites can achieve attractive performance, provided that the compatibility between ceramic particles and polymeric matrices is enhanced to the benefit of the physical properties of the final composite. Tuning the particle–matrix interface through particle functionalization represents a viable solution. In this work, surface functionalization of BT nanoparticles (NPs), obtained by hydrothermal synthesis, with 3-glycidyloxypropyltrimethoxysilane, 2-[(acetoxy(polyethyleneoxy)propyl]triethoxysilane and triethoxysilylpropoxy(polyethyleneoxy)dodecanoate, was performed after optimizing the hydroxylation process of the NPs to improve their surface reactivity and increase the yield of grafting. Solid-state nuclear magnetic resonance and thermogravimetric analysis were used to quantify the molecules grafted onto the ceramic nanoparticles. Both bare and functionalized particles were employed in the realization of epoxy- and polydimethylsiloxane (PDMS)-based nanocomposites. Functionalization was proven to be beneficial for particle dispersibility and effective for particle alignment in the PDMS matrix. Moreover, the dielectric constant measurements revealed the potential of PDMS-based nanocomposites for applications in the field of dielectric elastomers. 相似文献
Over the past two decades polymer nanocomposites have received tremendous interest from industry and academia due to their advanced properties comparative to polymer blends. Many computational studies have revealed that the macroscopic properties of polymer nanocomposites depend strongly on the microscopic polymer structure and conformations. In this article we review computer simulation studies of the fundamental problem of homopolymers structure and dimensions in nanocomposites containing bare or grafted spherical or rod nanoparticles. Experimentally, there is controversy over whether the addition of nanoparticles in a polymer matrix can perturb the polymer chains. 相似文献
Coarse-grained molecular dynamics simulations were carried out to investigate the dewetting behavior of a polymer thin film on partial wetting solid surface at the early stage of the dewetting process. Spontaneous dewetting is initiated by removing a band of strip from both the ends of the liquid polymer film which has achieved equilibrium. The solid-liquid interaction and temperature were varied to show their influence on the dewetting dynamics during dewetting as well as the shape evolution of the liquid ... 相似文献
Polymers are crucial constituents of modern electronic devices. They can be used in their pristine, composite or nanocomposite forms for several domestic and industrial applications with innumerable unique possibilities. Polymer nanocomposites have gained wide theoretical interest and numerous practical applications in diverse fields of science and technology as they bestow the materials not only with virtuous processability but also with exceptional functionalities. It is evidenced that the electrical conductance of polymer nanocomposite is governed by the conductive filler networks within the polymer matrix. Hence, insignificant variation in the conductive networks can result in noteworthy variations in the output electric signal of polymer nanocomposite. Exploiting this stimuli-responsive performance of conductive networks to the physical parameters, polymer nanocomposites can be harnessed to fabricate novel sensitive sensors to detect vital physical parameters viz.strain/stress, pressure, temperature, solvent or vapor. Technical and phenomenological studies on polymer nanocomposites are still enduring.Advanced explanations are being sought but the mechanisms governing the formation of several polymer nanocomposites are still topics of debate in the material science community. Their in-depth investigation requires copious scientific work. This review analytically sketches the synthesis, microstructures, physiochemical properties and the underlying mechanisms for stimuli-responsiveness to the physical parameters of the polymer nanocomposites as well as their applications in various sensitive sensors and detectors. Thus, it became evocative for this review to focus on their processing methodologies, physiochemical physiognomies, classification and probable potentials of polymer nanocomposites.This review primarily presents the current literature survey on polymer composites and the gap areas in the study encourages the objective of the present review article. Finally, the status, perspectives and the advantages of specific polymer nanocomposites at present are summarized. The attention of this review is drawn to the present trends, challenges and future scope in this field of study. Finally, the vital concern and future challenge in utilizing the stimulus responsive behavior of polymer nanocomposites to design versatile sensors for real time applications are elaborately discussed. 相似文献
The diffusion of nanoparticles immersed in semidilute polymer solutions is investigated by a hybrid mesoscopic multiparticle collision dynamics method. Effects of polymer concentration and hydrodynamic interactions among polymer monomers are focused. Extensive simulations show that the dependence of diffusion coefficient D on the polymer concentration c agrees with Phillies equation D-exp (-αcδ) with a scaling exponent δ≈0.97 which coincides with the experimental one in literature. For increasing nanoparticle size, the scaling prefactor α increases monotonically while the scaling exponent always keeps fixed. Moreover, we also study the diffusion of nanoparticle without hydrodynamic interactions and find that mobility of the nanoparticle slows down, and the scaling exponent is obviously different from the one in experiments, implying that hydrodynamic interactions play a crucial role in the diffusion of a nanoparticle in semidilute polymer solutions. 相似文献
Using a unidirectional heat transfer apparatus, the roles of nanoparticle geometry, loading, dispersion and temperature on the thermal conductivity of polymer nanocomposites are investigated. The polymer nanocomposites (PNC) consist of epoxy matrices filled with silica nanopowder and carbon nanotubes, respectively, as well as poly (2-vinylpyridine) (P2VP) matrices loaded with silica nanoparticles. First, it is shown that thermal conductivity generally increases with nanofiller loading. These results are also reasonably described by the three phase Lewis-Nielsen or Halpin-Tsai analytical models. More importantly, it has been also demonstrated that the thermal conductivity of the polymer nanocomposites greatly depends on the dispersion state of the nanofillers. Furthermore, the effect of temperature on the thermal behavior of PNCs is briefly discussed. These results emphasize the important role of nanoparticles content and dispersion state on the thermal characteristics of polymer nanocomposites, which can be used to design composite materials with tunable thermal behavior. 相似文献
The effect of graphene (G) and graphene oxide (GO), used as the nanofiller in polymer nanocomposites (NC), on the structural and dynamic properties of polymer chains, has been studied by means of molecular dynamics (MD) simulations. Two polymers, i.e., poly(propylene) and poly(vinyl alcohol), are employed as matrices to cover a wider range of polymer–filler interactions. The local structural properties, e.g., density profile, average R g, and end‐to‐end distance as well as dynamic properties, e.g., estimated translational and orientational relaxation times, of polymer chains are studied. In addition, the interaction energies are estimated between polymers and nanofillers for different hybrid systems using MD pullout simulations. Strong heterogeneities in polymer structural and dynamic properties have been observed such that chains are more oriented and exhibit slower dynamics in the vicinity of the nanofillers (G and GO) as compared to bulk. It is also found that the orientation of polymer chains at the interface is more influenced by the nanofiller in such a way that the more oriented polymer chains are observed in G‐based NC for both polymers. However, the immobilization of polymer chains at the interface proves to be very much dependent on the polymer–filler interactions.
Nanoparticles in a flexible polymer melt film often segregate to the substrate due to attractive depletion interactions between the nanoparticles and the substrate. Here, molecular dynamics simulations are performed to study the effect of chain stiffness on this segregation. The nanoparticles are modeled as spheres and the polymers as semi‐flexible bead‐spring chains. Both purely repulsive and attractive forces are considered, while assuming non‐selective interactions among all species. The nanoparticles are found to be well‐dispersed in the system having repulsive forces only and aggregate into clusters in the completely attractive system. For the repulsive system, adding chain stiffness substantially decreases the nanoparticles' segregation, and hence their concentration, at the substrate.
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