Flexible and transparent polymer/cellulose nanocrystal nanocomposites with high thermal conductivity for thermal management application

Polymeric materials play important roles in semiconductor technology and modern electronic devices. However, the weak thermal management capability of polymer seriously restricts the service life, reliability, and efficiency of devices. Consequently, inorganic or metallic thermally conductive fillers are added into polymers to make up the low thermal conductivity, but the optical transparency and flexibility always decrease or even disappear. Herein, we report transparent polymer nanocomposites comprising poly(vinyl alcohol) (PVA) and cellulose nanocrystal (CNC) with highly lateral thermal conductivity [about 5.7 W/(m·K)]. Such a high thermal conductivity is attributed to the aligned structure of CNC in PVA matrix and hydrogen-bond interaction between CNC and PVA. All the organic nanocomposites also present excellent electrical insulating performance and tensile properties. The transparent and flexible nanocomposites are promising in the thermal management applications of displays, next-generation wearable devices, sensors, and LEDs. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48864.     

Graphene/polypropylene nanocomposites with improved thermal and mechanical properties

Small amount of large surface area graphene (G) is expected to significantly alter functional properties of polymers. The property enhancement is a function of degree of exfoliation and dispersion of G as well as its compatibility with base polymer. However, nonpolar nature of polyolefins such as polypropylene (PP) restricts homogeneous dispersion of G, leading to significant agglomeration and properties reduction. In this work, two compatibilizers, poly (ethylene-co-butyl acrylate) (EBA) (new compatibilizer) and PP-grafted-maleic anhydride (MA-PP) (conventional compatibilizer) were compared to enhance the dispersion efficacy of G in PP. The EBA-compatibilized nanocomposites exhibited 44% increase in the Young's modulus compared to 32% increment in MA-PP-compatibilized nanocomposites. Higher elongation at break for EBA-compatibilized nanocomposites is attributed to lower degree of crystallinity in these nanocomposites. On the other hand, EBA-compatibilized nanocomposites showed significantly improved thermal stability compared to MA-PP-compatibilized nanocomposites. The results indicate that EBA may act as a potential compatibilizer for G/PP nanocomposites.     

Processing,Dynamic mechanical thermal analysis,and dielectric properties of barium titanate/cellulosic polymer nanocomposites

High dielectric constant BaTiO₃/ethyl cellulose (BT/EC) nanocomposites having BT loadings of up to 13 vol% were fabricated through a simple casting technique. The BT filler powder, synthesized through an ultrasonic‐assisted solid‐state route, was revealed by X‐ray powder diffractometry (XRD) and Raman spectroscopy to be dominantly tetragonal. Scanning electron microscopy (SEM) showed good dispersion of the BT nanoparticles in the EC polymer matrix at lower BT concentrations. However, at higher concentrations, the BT particles form a continuous phase or a “filler network” leading to weak BT/EC interactions. This finding is well supported by the results of the tensile strength and storage modulus. The dielectric properties of the BT/EC nanocomposites were investigated over wide ranges of frequency and temperature. The addition of BT significantly increased the permittivity (ε ′) and dielectric loss (ε ″) and improved the ionic conductivity of the EC. The electric modulus (M″ ) results were analyzed in terms of the Havriliak–Negami function through three distinct relaxation mechanisms (namely α, β*, and β relaxations) in the temperature range 30–150°C. The dc conductivity (σ _dc) results suggest that the BT/EC nanocomposites formed at low BT loading (up to 7.0 vol%) and a temperature of ≤60°C are good candidates for antistatic applications while those formed at higher concentrations and temperatures are recommended for use in electrostatic dissipation applications. POLYM. COMPOS., 38:893–907, 2017. © 2015 Society of Plastics Engineers     

Functionalized graphene-reinforced polysiloxane nanocomposite with improved mechanical performance and efficient healing properties

It is a challenge to design nanofiller reinforced self-healing nanocomposites with both improved mechanical properties and highly efficient self-healing properties. In this work, we report a self-healing polysiloxane nanocomposite using furan-functionalized graphene (G-FA) as reinforcement based on Diels−Alder (DA) chemistry. The formed interactions between G-FA and polysiloxane chains were reversible DA bonds, which negligibly affected the nanocomposites healing efficiency. The self-healing polysiloxane nanocomposite with 6% G-FA has a tensile strength of 0.25 MPa that was improved by 140% when compared to an elastomer without G-FA. The healable polysiloxane nanocomposite recovered more than 90% of its tensile strength and 98% of its elongation-at-break, demonstrating that the nanocomposite exhibited highly efficient self-healing properties. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47725.     

A new model for estimation of the thermal conductivity of polymer/clay nanocomposites

High density polyethylene– and polypropylene–clay nanocomposites are synthesized by melt blending, in which polyethylene glycol and polypropylene glycol are used as compatibilizers to increase the space of galleries. The morphology properties of nanocomposites are explored by X‐ray diffraction and transition electron microscopy. The thermal conductivity coefficient (K) of nanocomposites is also measured along with the thermal stability. A conventional model based on developed Maxwell‐Garnett formula is also established to predict the thermal conductivity of polymer/clay nanocomposites with clay loading. Morphology results indicate that two intercalated and exfoliated structures are formed. The established model satisfactorily predicts the K values of nanocomposites for low range of clay content. Thermogravimetric analysis shows remarkable thermal stability of nanocomposites with 10 wt % of clay content. The deviation of our model from experimental result for 10 wt % of clay can be attributed to the intercalated structure of layered silicates into the matrices. Although the K values do not considerably increase in 5 wt % with respect to the increase occurs for 10 wt % of clay, but it increases about 28 and 37% at 50°C for high density polyethylene– and polypropylene–clay nanocomposites, respectively. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Ferroelectric-thermoelectricity and Mott transition of ferroelectric oxides with high electronic conductivity

This paper reviews ferroelectric oxides in the unusual condition where the concentration of electronic carriers is close to a metal–insulator transition; in certain structures and compositions these materials have properties of interest for oxide based thermoelectric applications. In relaxor ferroelectrics, nanopolar regions associated with intrinsic localized phonon modes provide glass-like phonon characteristics due to the large levels of phonon scattering. The (Sr_1?xBa_x)Nb₂O_6?δ relaxor ferroelectric single crystals have a high thermoelectric power factor, S²σ ～ 40 μW/cm K² at 277 °C along the c-axis, which is competitive with the best thermoelectrics.In the heavily reduced, nonstoichiometric n-type perovskite BaTiO_3?δ and tungsten bronze (Sr_1?xBa_x)Nb₂O_6?δ, it is shown that metallic-like conductivity occurs in the paraelectric phase and the onset of ferroelectricity stabilizes semiconducting character. Both the phase transition temperature dependence on the carrier concentration and evidence for polarization coupling to the conductivity mechanism will be discussed.     

Improvement of thermal conductivity and dielectric constant of graphene-filled epoxy nanocomposites using colloidal polymerization approach

Polymer Bulletin - The effect of the polymeric cross-link density on the thermal conductivity of an oxidized graphene (OG)-filled epoxy nanocomposite was investigated by two different fabrication...     

Modeling electrical conductivity of polymer nanocomposites with aggregated filler

A mean-field model is developed for the electrical conductivity of microcomposites and nanocomposites with polymer matrices. The model accounts for aggregation of filler into clusters (involving both conducting and nonconducting particles) and rearrangement of these clusters with the growth of volume fraction of filler (which leads to a reduction in tunneling resistivity and an increase in the number of bridging contacts between conducting particles). The governing equations involve five material constants with transparent physical meaning: the depolarization factor of clusters, volume fraction of polymer in clusters of filler, effective conductivity of an individual filler particle, and two coefficients characterizing an increase in the effective electrical conductivity of filler driven by the growth of bridging contacts between neighboring particles in clusters. Good agreement is demonstrated between results of simulation and experimental data on the electrical conductivity of epoxy resin reinforced with carbon black and graphite particles, poly(vinyl chloride) reinforced with copper and nickel particles, polypropylene loaded with spherical and spheroidal tin particles, poly(butylene terephthalate) reinforced with graphene nanosheets, and polypropylene loaded with multiwalled carbon nanotubes.     

Thermal conductivity of polymer nanocomposites made with carbon nanofibers

An internal mixer was used to prepare polycarbonate (PC)‐based nanocomposites containing carbon fibers, carbon nanofibers (CNF), and mixtures of the two fillers. The influence of the filler volume fraction, the relative amounts of the two fillers, and the filler orientation relative to the direction of heat flow on the thermal conductivity was examined. Filler orientation was obtained by the extrusion of strands of the nanocomposite. The thermal conductivity was measured using a steady‐state heat conduction technique. The CNF were fragile, and their aspect ratio could be decreased during processing. In general, the composite thermal conductivity increased with increasing filler content. Fiber alignment in the heat flux direction resulted in a significant increase in thermal conductivity. Mixing of nanofibers with microfibers resulted contacts between the microfibers. This, together with fiber alignment provided large increases in the thermal conductivity. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Effects of carbon nanotubes and interphase properties on the interfacial conductivity and electrical conductivity of polymer nanocomposites

L_c is the minimum length of carbon nanotubes (CNTs) required for efficient transfer of filler conductivity to polymer matrix in polymer CNT nanocomposites (PCNTs). In this work, L_c is correlated with the dimensions of the CNTs and the interphase thickness. Subsequently, the interfacial conductivity as well as the effective length and concentration of CNTs are expressed by CNT and interphase properties. Moreover, a simple model for the tunneling conductivity of PCNTs is developed with these effective terms. The impacts of all parameters on L_c, the interfacial conductivity, the fraction of CNTs in the networks and the conductivity of the PCNT are explained and justified. In addition, the predictions of the percolation threshold and conductivity are compared with the experimental results of several samples. The desirable values of interfacial conductivity are achieved by thin, short and super‐conductive CNTs, high waviness and a thick interphase. However, thin and long CNTs, low waviness, a thick interphase, poor tunneling resistivity due to the polymer matrix and a short tunneling distance advantageously affect the conductivity of PCNTs, because they produce large conductive networks. The predictions also show good agreement with the experimental measurements of percolation threshold and conductivity, which confirms the developed equations. © 2020 Society of Chemical Industry     

Comparative study of dielectric and electro-optical properties of pure and polymer ferroelectric liquid crystal composites

The ferroelectric liquid crystals (FLCs) displays normally suffer from less contrast ratio and vision angle. To produce high optical contrast and colors in FLC displays, Guest-host mode is widely used. Addition of a small amount of polymer in the pure FLC results in considerable change in its dielectric and electro-optical properties. In the present paper we have investigated the effect of adding polymer (PMMA) on the FLC material (Felix 17/100). Polymer doped FLC composites (FLCPC) has been prepared by the dispersion of 1% wt/wt concentration of polymer in pure FLC. Planar aligned cells have been used to study dielectric and electro-optical properties in SmC* phase of both the samples i.e. pure FLC and FLCPC. Considerable change in various properties like spontaneous polarization, anchoring parameters, Goldstone mode relaxation time and relaxation strength have been noticed for both the samples. These changes have been explained by considering polymer network formed in the FLC matrix.     

Insulating enamels with improved dielectric properties

The effect of the content of alkali oxides on the physicomechanical and dielectric properties of glasses of the SiO₂ - B₂O₃ - R₂O - BaO system is studied. The optimum ratio of (Na + K) : Li providing for manifestation of the polyalkali effect at different concentrations of B₂O₃ is established. The considered compositions can be used as an insulating coating on ozonizer parts. Translated from Steklo i Keramika, No. 4, pp. 27 – 29, April, 1999.     

Simultaneously enhanced thermal conductivity and dielectric properties of borosilicate glass-based LTCC with AlN and h-BN additions

Microwave devices with reduced dielectric loss and electronic components with increased integration density necessitate the higher performance of electronic packaging materials. The h-BN/AlN/CaCO₃-MgO-B₂O₃-SiO₂-Li₂CO₃ glass composites were prepared via tape-casting and then sintered by pressureless and hot-pressing, respectively. The thermal conductivity of pressureless sintered composite was increased to 6.55 W/(m·K) by incorporating 3 wt% h-BN, and the thermal expansion of 4.47 ppm/K was achieved along with low dielectric constant of 5.76 and dielectric loss of 7.02 × 10⁻⁴ at 24 GHz. In contrast, the hot-pressing sintered composite containing 4 wt% h-BN exhibited higher thermal conductivity of 10.3 W/(m·K) and lower dielectric loss of 4.77 × 10⁻⁴. The microstructure characterization indicated the construction of heat conduction networks, and XRD analysis illustrated the formation of crystallization in the glass. Such low-temperature co-fired ceramic (LTCC) with high thermal conductivity and low dielectric loss would be a promising candidate for electronic packaging and 5G communication applications.     

Electrically insulating ZnOs/ZnOw/silicone rubber nanocomposites with enhanced thermal conductivity and mechanical properties

In this work, hybrids of surface modified zinc oxide spherical (ZnOs) nanoparticles and tetrapod‐shaped whiskers (ZnOw) were incorporated into the silicon rubber (SR) to prepare the ZnOs/ZnOw/SR nanocomposites. The incorporation of the ZnOs/ZnOw facilitated the formation of three‐dimensional thermally conducting network. It was found that the thermal conductivity of the ZnOs/ZnOw/SR reached up to 1.309 W m^?1 K^?1 when the ZnOs/ZnOw content was 20 vol % (V_m‐ZnOs:V_ZnOw = 7:3), which was nearly 6.5 times that of the pristine SR. The dielectric and resistivity measurements showed that the incorporation of the ZnOs/ZnOw hybrids did not cause much change in the electrical properties. In addition, the results show that the tensile strength of ZnOs/ZnOw/SR nanocomposites is higher than that of pristine SR. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46454.     

Core‐shell structured Al/PVDF nanocomposites with high dielectric permittivity but low loss and enhanced thermal conductivity

Surface modification of core‐shell structured Al (Al@Al₂O₃) nanoparticles was performed using γ‐(Aminopropyl)‐triethoxysilane (APS) and dopamine (DA), respectively, and the microstructures, dielectric properties and thermal conductivities of the Al/poly(vinylidene fluoride) (PVDF) nanocomposites were investigated. Both DA and APS enhance the interfacial bonding strength between the fillers and the matrix, leading to homogeneous dispersion of Al nanoparticles in PVDF matrix. Compared with raw Al nanoparticles, surface‐treated Al/PVDF exhibit much higher dielectric permittivity due to the enhanced interfacial interactions between the two components, whereas, the dielectric loss and electric conductivity of the nanocomposites still remain at rather low levels owing to the insulating alumina shell preventing effectively core Al from direct contact. The dynamic dielectric properties results reveal that dielectric constant and loss increase with temperature due to the gradually enhanced mobility of molecular chain segments of PVDF for the raw Al/PVDF and treated Al/PVDF nanocomposites. Additionally, the PVDF nanocomposites with Al treated with APS and DA show enhanced thermal conductivities compared with raw Al/PVDF under the same filler loading because of reduced thermal interfacial resistance promoting phonon transfer across the interfaces. POLYM. ENG. SCI., 59:103–111, 2019. © 2018 Society of Plastics Engineers     

New composites with high thermal conductivity and low dielectric constant for microelectronic packaging

Three composites based on cyanate (CE) resin, aluminum nitride (AlN), surface‐treated aluminum nitride [AlN(KH560)], and silicon dioxide (SiO₂) for microelectronic packaging, coded as AlN/CE, AlN(KH560)‐SiO₂(KH560)/CE, and AlN‐SiO₂/CE composite, respectively, were developed for the first time. The thermal conductivity and dielectric constant of all composites were investigated in detail. Results show that properties of fillers in composites have great influence on the thermal conductivity and dielectric constant of composites. Surface treatment of fillers is beneficial to increase the thermal conductivity or reduce dielectric constant of the composites. Comparing with binary composite, when the filler content is high, ternary composites possess lower thermal conductivity and dielectric constant. The reasons leading to these outcomes are discussed intensively. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

In situ thermal reduction of graphene oxide forming epoxy nanocomposites and their dielectric properties

The electrical properties of epoxy based composites modified by low amounts of graphite oxide, below the conduction threshold, have been investigated. The composites have been prepared without the use of solvents by direct sonication of graphite oxide (GO) powders and of chemically modified and partially reduced GO powders in the based epoxy monomer. Through a mild thermal treatment, in situ reduction of the previously dispersed GO has been obtained directly inside the epoxy resins. The changes in the electrical response of the materials thus obtained have been compared to that of pristine unmodified epoxy resin. Data so far collected underline the possibility to tune the electrical conductivity of the composites within two orders of magnitude and to increase the values of permittivity without significantly worsening dielectric losses. POLYM. COMPOS., 36:294–301, 2015. © 2014 Society of Plastics Engineers     

Polyimide nanocomposites: Comparison of their properties with precursor polymer nanocomposites

A precursor poly(amic acid) was obtained by solution polymerization of pyromellitic dianhydride and benzidine in N, N‐dimethylacetamide. Poly(amic acid)/Organoclay hybrids were prepared by the solution intercalation method with dodecylamine‐montmorillonite. A polyimide hybrid was obtained from poly(amic acid) hybrid by heat treatment at various temperatures. The film type polyimide hybrids showed better thermal properties than poly(amic acid) hybrids. Also, the thermal stability of the two polymer hybrids were enhanced linearly with increasing clay content from 0 to 8 wt%. Tensile properties and gas barriers of the hybrids, however, were enhanced remarkably compared to pristine polymers. Intercalations of the polymer chains in clar were examined through wide angle X‐ray diffraction (XRD) and electron microscopy (SEM and TEM). Transmission electron microscopy revealed that a partially exfoliated structure had been obtained from polyimide/organo‐clay hybrids.     

Electrical conductivity of interphase zone in polymer nanocomposites by carbon nanotubes properties and interphase depth

In this work, carbon nanotubes (CNT) properties and interphase depth define the interphase conductivity in polymer CNT nanocomposites (PCNT). In addition, the operative CNT length and volume portion are linked to the conductivity transportation between CNT and insulated polymer medium to propose a simple model for conductivity. The significances of various terms on the interphase conductivity and conductivity of PCNT are justified and the model's predictions are examined using the experimental outputs of certain examples. Thin CNT and dense interphase obtain the extraordinary conductivity transportation, while CNT length and conductivity are ineffective. Moreover, thin, small, and high-conductive CNT as well as dense interphase introduce the high interphase conductivity. The estimations of conductivity appropriately follow the experimental data authorizing the established model. This model is capable to substitute the conventional models owing to the assumption of innovative nanocomposite's terms.