Polydimethylsiloxane–PbZr0.52Ti0.48O3 nanocomposites with high permittivity: Effect of poling and temperature on dielectric properties

Polydimethylsiloxane (PDMS)/lead zirconate titanate (PbZr_0.52Ti_0.48O₃, PZT)-based nanocomposites with high dielectric constant (permittivity, k) are prepared through room temperature mixing. The effect of PZT loading on electrical and mechanical properties of the PDMS–PZT composites is extensively studied. It is found that there is significant increase in permittivity with PZT loading and decrease in volume resistivity. All the composites have low dielectric loss compared to permittivity value. It is observed that there is increase in permittivity and decrease in volume resistivity of composites after poling, which is due to the dipolar polarization. It is found that both permittivity (ε′) and alternating current conductivity (σ_ac) are increased with temperature at low frequency (1 Hz) and decreased with temperature at high frequency (1 MHz). The above composites are sensitive to external pressure and can be used as pressure/force sensor. The tensile strength and % elongation at break decreases with PZT loading, which is due to the nonreinforcing behavior of PZT ceramic. PZT particles distribution and dispersion in PDMS matrix are observed through field emission scanning electron microscopy, high resolution transmission electron microscopy, and atomic force microscopy/scanning probe microscopy. Thermal stability of composites increased with the PZT loading which is due to higher thermal stability of PZT particles compared to PDMS matrix. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47307.     

Influence of Ca[(Li1/3Nb2/3)0.8Ti0.2]O3‐δ filler on the microwave dielectric properties of polyethylene and polystyrene for microelectronic applications

Ceramic reinforced polyethylene and polystyrene composites were prepared by melt mixing and hot molding techniques. Temperature stable low‐loss Ca[(Li_1/3Nb_2/3)_0.8Ti_0.2]O_3‐δ (CLNT) ceramic was used as the filler to improve the dielectric properties of the polymers. The relative permittivity and dielectric loss in the microwave frequency range were increased with increase in the ceramic loading. As the filler content increased from 0 to 0.50 volume fraction, the relative permittivity increased from 2.3 to 9 and dielectric loss tangent from 0.0006 to 0.005 for polyethylene‐CLNT composite. In the case of polystyrene‐CLNT composite, the relative permittivity and dielectric loss tangent increased from 2.1 to 10.5 and 0.0005 to 0.0032 respectively with increase in filler content from 0 to 0.50 volume fractions. The thermal stability of the relative permittivity of polymer ceramic composites was also investigated. The experimentally observed relative permittivity was compared with theoretical models. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers     

Anodization of Al–Nd alloy films in nonaqueous electrolyte solutions for TFT-LCD application

The anodization behavior of Al–Nd alloys in nonaqueous electrolyte solutions and the electronic properties of the resultant anodic oxide films were studied for TFT-LCD application. Sputtered Al–Nd alloy films on glass substrates were anodized at 25 °C and 1 mA cm⁻² up to 100 V in ethylene glycol–water solutions containing 10 wt.% ammonium tartrate or salicylate to give uniform and flat oxide films. The incorporation of organic components into the anodic oxide films from the electrolyte solutions has lowered the relative permittivity and increased the breakdown electric field of the oxide films. This was performed by decreasing the water content in the electrolyte solutions. The tartrate solution caused higher carbon incorporation than the salicylate counterpart at the same water concentrations, giving lower relative permittivity, and higher forward breakdown electric field. The AlO stretching frequency of the oxide films decreased slightly as the amount of incorporated organic moieties increased. Nd was uniformly distributed in the oxide films and an increase in the Nd content was likely to increase both the relative permittivity and the forward breakdown electric field without any apparent change in the anodization behavior.     

Nanocomposites from fluoro‐oxygenated polyethylene: A novel route to organoclay exfoliation

We present a novel approach to improving organoclay exfoliation in a nonpolar matrix, polyethylene. High‐density polyethylene (HDPE) particles were modified by exposure to a reactive gas atmosphere containing F₂ and O₂. This treatment was aimed at increasing the polarity of the polymer with the formation of carboxyl, hydroxy, and ketone functionalities on the particle surface. The surface‐treated high‐density polyethylene (ST‐HDPE) particles were then melt‐mixed with an appropriate organoclay to form nanocomposites. Transmission electron microscopy (TEM), wide‐angle X‐ray scattering, stress–strain analysis, and Izod impact measurements were used to evaluate the nanocomposite morphology and physical properties. These data were compared to those of equivalent nanocomposites prepared from unmodified HDPE and high‐density polyethylene grafted with maleic anhydride (HDPE‐g‐MA). The nanocomposites prepared from the ST‐HDPE particles exhibited much better properties and organoclay dispersion than those prepared from unmodified HDPE. The level of reinforcement observed in ST‐HDPE‐based nanocomposites was comparable to, if not better than, that seen in HDPE‐g‐MA‐based nanocomposites. However, a comparison of the TEM micrographs suggested better organoclay exfoliation in HDPE‐g‐MA than the current version of ST‐HDPE. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2980–2989, 2006     

Magnetic and Dielectric Properties of YIG/HDPE Composites for High-Frequency Applications

A low loss high-frequency magnetic composite with Y₃Fe₅O₁₂ (YIG) ultrafine particles embedded in a high-density polyethylene (HDPE) matrix was fabricated by using a simple low-temperature hot-pressing technique. The magnetic and dielectric properties of the as-prepared composites were investigated in detail. The results indicate that as the volume of the ceramic fillers increases, the permittivity, permeability, dielectric and magnetic loss of the composite all increase. The cut-off frequencies of the composites are all above 700 MHz. Since the low resistivity of YIG, the dielectric losses of the composites are high and decrease with frequency in the lower frequency range. Good frequency stability of the permittivities and permeabilities, and low dielectric and magnetic losses within the measurement range have been observed.     

Structure of blown film from blends of polyethylene and high melt strength polypropylene

The structure of blown film processed from linear low density polyethylene blended with up to 30 wt[percnt] of a high melt strength polypropylene (hmsPP) was examined using primarily atomic force microscopy and wide angle X-ray scattering. The study focused on two polyethylene resins with the same density: a conventional Ziegler-Natta catalyzed linear low density polyethylene (znPE) and a blend of a Ziegler-Natta catalyzed and a metallocene catalyzed linear low density polyethylene (zn/mPE). Parallel characterization was performed on blown film of the hmsPP and blown film of each of the polyethylene resins. In films of the blends, the hmsPP was well-dispersed in the polyethylene matrix as elongated domains. In the domains, the hmsPP crystallized as planar row-nucleated structures with the long axis of the lamellae perpendicular to the extrusion direction. Row-nucleated hmsPP lamellae provided a template for epitaxial crystallization of polyethylene lamellae. The 42° angle of the lattice match imparted a characteristic herringbone texture to the polyethylene. Blending with hmsPP increased the tensile modulus and strength of polyethylene film without significantly affecting the ultimate elongation.     

Limitation of the Young-Dupré Equation in the Analysis of Adhesion Forces Involving Surfactant Solutions

The atomic force microscope was used to measure adhesion forces between polyethylene particles, serving as model oil droplets, and mineral substrates (fluorite and quartz) in aqueous solutions of ethoxylated alcohols. Also, contact angles were measured in the kerosene–ethoxylated alcohol solution–mineral systems. Correlations obtained between adhesion and surfactant concentration for the polyethylene–aqueous solution–quartz system differs significantly from those predicted by the Young-Dupré equation for the kerosene–aqueous solution–quartz system. Interactions, characteristic for such aqueous systems, which contribute to the pull-off forces measured by atomic force microscopy are not included in the Young-Dupré equation, and are primarily responsible for the inconsistency in the adhesion versus surfactant concentration relationship obtained from contact angle measurements.     

Reinforcement of maleated polyethylene/ground tire rubber thermoplastic elastomers using talc and wood flour

Maleated polyethylene (MAPE)/Ground tire rubber (GTR) thermoplastic elastomer with 50 vol % GTR was reinforced by incorporation of talc powder and wood flour. Scanning electron microscopy (SEM) reveals that maleated polyethylene (MAPE) has good compatibility with wood flour, but the adhesion with talc particles is weak. Tensile moduli of MAPE/GTR increase more significantly after inclusion of talc particles compared to wood flour. Prediction of the tensile modulus of hybrid MAPE/GTR/particle composites is successfully performed using a combination of Kerner and Halpin‐Tsai models. Elastic moduli are shown to depend strongly on both aspect ratio and level of particle dispersion in the matrix. Measurement of compression sets shows that elastic recovery of the compounds decreases after addition of solid particles. Samples having better particles/matrix compatibility show higher elastic recovery. Thermogravimetric analysis shows that inclusion of wood flour decreases thermal stability of compounds. Density and hardness of MAPE/GTR are also shown to increase after inclusion of particulate reinforcements. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40195.     

Thermal and dielectric properties of the aluminum particle reinforced linear low‐density polyethylene composites

The possibility of obtaining relatively high thermal conductivity and dielectric constant but low dielectric loss polymeric composites by incorporating the core‐shell‐structured aluminum (Al) particles in a linear low‐density polyethylene (LLDPE) by melt mixing and hot pressing was demonstrated in this study. The morphology, thermal and dielectric properties of the composites were characterized using X‐ray diffractions, thermal analysis, scanning electron microscope, and dielectric analyzer. The Al particle decreases the degree of crystallinity and has no appreciable influence on the melting temperature of LLDPE. The thermal conductivity, dielectric constant and loss factor of the composites increase with an increase in Al content at all the frequencies (1 ～ 10⁶ Hz). The thermal conductivity and dielectric constant of the 70 wt% flaky Al particles filled LLDPE are 1.63 W/mK and 50, much higher than those of the spherical Al reinforced one. Moreover, the surface treatment of Al particles with γ‐Aminopropyltriethoxysilane silane coupler improves the thermal conductivity. The dielectric loss factors of the composites still remain at relatively low levels in the measured frequency range. Further, the dielectric permittivity frequency independence in the measured frequency range was observed due to the nanoscale‐Al‐oxide insulating shell of Al. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Composition dependence of dielectric properties,elastic modulus,and electroactivity in (carbon black‐BaTiO3)/silicone rubber nanocomposites

The dielectric properties, elastic modulus, and electromechanical responses of dielectric elastomers (DEs) consisting of silicone rubber and carbon black (CB) incorporated with BaTiO₃ (BT) were studied. When compared with single filler/rubber composites, the resulting three‐component nanocomposites yielded very abnormal phenomena. They might be attributed to the interactions between the two kinds of fillers. The increase in concentration of CB (BT) would play a destructive role to the network structure formed by BT (CB) particles. The maximum electromechanical strain of the nanocomposites achieved at mass fraction m_CB = 0.03 and m_BT = 0.06. The resultant electromechanical strain would be attributed to the large dielectric permittivity in the three‐component nanocomposites, in which the BT particles themselves have a high dielectric permittivity and the electrical networks of CB particles have a contribution on the increase in dielectric permittivity of the three‐component nanocomposites. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Dielectric performance of composites of BaTiO3 and polymers for capacitor applications under microwave frequency

Composites of nano-sized barium titanate (BaTiO₃) with volume fractions up to 0.5 and poly(butylene terephthalate) (PBT) or linear low-density polyethylene (LLDPE) were made via extrusion. Scanning electron microscopy demonstrated that BaTiO₃ is well dispersed in the polymer matrices. The crystalline content (DSC) and thermal stability (TGA) of both polymers decreased with increasing BaTiO₃ loading. Dielectric properties of the composites were measured using a vector network analyzer. Both dielectric permittivity and tangent loss increased with increasing BaTiO₃ content. At 2.45 GHz, the dielectric permittivity for 48 vol% BaTiO₃-filled LLDPE and 43 vol% BaTiO₃-filled PBT was 25 and 21.2, respectively. There was a good fit between the Lichtenecker model and experimental data obtained up to a certain value, with the permittivity variations being dependent on volume fraction. The improved dielectric performance achieved on inclusion of BaTiO₃ confirms both composite systems as potential candidates for microwave frequency capacitor applications.     

Corona Discharge Treatment of Polyolefins

The effects of corona discharge treatment on polyethylene and polypropylene homopolymers have been studied. X-ray photoelectron spectroscopy was used to determine surface compositions which were related to surface free energy estimates from contact angle measurements. Changes in composition and surface free energy were measured as a function of treatment level. The work of adhesion was seen to increase with oxygen incorporation. The increase was not linear and this is attributed to an increase in the degree of sub-surface to near-surface oxidation at intense treatment levels. Aging of samples followed by XPS and contact angle measurement showed that surface wettability is reduced whereas a slight increase in surface oxygen was found. This phenomenon was attributed to the reorientation/migration of functional groups. Morphological examination by scanning electron microscopy indicated no surface roughening at any power level.     

Polyethylene/sepiolite fibers. Influence of drawing and nanofiller content on the crystal morphology and mechanical properties

The influence of sepiolite content (1, 2, and 3 wt%) and successive drawing steps on the final properties of polyethylene/sepiolite nanocomposite fibers are reported. Particularly the effects of these variables on crystallinity, fiber macroscopic morphology, and tensile mechanical properties are analyzed applying different experimental techniques: differential scanning calorimetry, wide angle x‐ray diffraction, scanning electronic microscopy, and tensile mechanical characterization. The study evidenced the important role of both sepiolite content and stretching on the crystalline morphology and mechanical properties of the nanocomposites fiber. Both variables favor the appearance of the monoclinic phase during polyethylene crystallization, and produce an increase of crystallinity degree (35 % with drawing steps and 10 % by the sepiolite incorporation in non drawing fiber). This change of crystal morphology influences mechanical properties enhancing with both sepiolite content and drawing steps. Thus, Young Modulus increases 17 times with drawing in pure PE fibers and 1.5 times because sepiolite presence. The strength shows similar behavior, but the elongation at break decreases 14 timed with draw steps and to a half by the sepiolite influence. The final properties of drawing nanocomposite fibers are so acceptable for textile applications and they content particles that enhance their moisture and odors absorptive capacities. POLYM. ENG. SCI., 55:1096–1103, 2015. © 2014 Society of Plastics Engineers     

Dielectric properties of Permalloy granular composite materials

Dielectric and electrical properties of Permalloy granular composite materials have been studied considering the application to left-handed meta-materials. Surface oxidized Permalloy particles have high surface electrical resistance; the eddy current effect in the composite structure is suppressed. The electrical conductivity of compacted Permalloy particles increases with increasing temperature and indicates the semiconductive layer formation on the particle. The low frequency ac electrical conductivity of Permalloy composite materials shows a drastic increase in the particle content between 50 and 60 vol.%. Electrical permittivity spectra of Permalloy composites show a non-metallic characteristic and the enhancement of permittivity is observed with increase of Permalloy particle content.     

Thermal and dielectric properties of low-density polyethylene/NaA zeolite composites

The effect of the weight fraction of NaA zeolite on thermal properties (specific heat capacity, thermal diffusivity, thermal conductivity) and dielectric properties (electrical conductivity, real and imaginary electric permittivity) of composites based on low-density polyethylene (LDPE) and NaA zeolite is examined. Composite samples containing from 5 to 30 wt% zeolite are prepared using the compression molding technique. The degree of dispersion and the weight fraction of filler in the LDPE/NaA zeolite composites are determined using X-ray diffraction. A linear decrease in the values of the specific heat capacity with an increase in the weight fraction of zeolite is observed using differential scanning calorimetry. The laser flash method is used to determine the thermal diffusivity of the composites. An increase in effective thermal diffusivity and abrupt increase in the range from 15 to 20 wt% of zeolite are established. It is demonstrated that effective thermal conductivity increases with an increase in the weight fraction of zeolite, and an abrupt increase in the range from 15 to 20 wt% is observed. Dielectric spectroscopy measurements are performed to determine the real and imaginary parts of permittivity. An increase of real and imaginary parts of permittivity of LDPE/NaA zeolite composites, with increasing weight fraction of zeolite, is established. Two relaxation peaks of the imaginary parts of permittivity of LDPE/NaA zeolite composites are detected. An increase of electrical conductivity with increasing weight fraction of zeolite and abrupt increase in the range 15 to 20 wt% are noticed. © 2021 Society of Industrial Chemistry.     

Surface modification of microcrystalline cellulose (MCC) and its application in LDPE‐based composites

Microcrystalline cellulose (MCC) was modified by grafting onto its surface ferulic acid, methacryloyl chloride and oleoyl chloride. The efficacy of the chemical modification was confirmed by X‐ray photoelectron spectroscopy. In addition, the size distribution of the cellulosic particles was investigated by optical microscopy and laser granulometry and its hydrophobicity was evaluated using a contact angle method. Finally, to investigate the affinity of modified MCC with a nonpolar polymer and to assess its potential as a biobased reinforcing filler, the modified MCC was compounded into low‐density polyethylene. An organic peroxide, dicumyl peroxide, was added at selected formulations to see if it could further enhance mechanical bonding between the polymer and the particulates. The dispersion was assessed by scanning electron microscopy. Mechanical properties were investigated through tensile testing while the melt rheology of the composites was monitored by small angle oscillatory shear rheology. The acylation modification of the MCC improved the dispersion within LDPE and enhanced the mechanical properties of the composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44348.     

Improved Adhesion, Growth and Maturation of Vascular Smooth Muscle Cells on Polyethylene Grafted with Bioactive Molecules and Carbon Particles

High-density polyethylene (PE) foils were modified by an Ar⁺ plasma discharge and subsequent grafting with biomolecules, namely glycine (Gly), polyethylene glycol (PEG), bovine serum albumin (BSA), colloidal carbon particles (C) or BSA and C (BSA + C). As revealed by atomic force microscopy (AFM), goniometry and Rutherford Backscattering Spectroscopy (RBS), the surface chemical structure and surface morphology of PE changed dramatically after plasma treatment. The contact angle decreased for the samples treated by plasma, mainly in relation to the formation of oxygen structures during plasma irradiation. A further decrease in the contact angle was obvious after glycine and PEG grafting. The increase in oxygen concentration after glycine and PEG grafting proved that the two molecules were chemically linked to the plasma-activated surface. Plasma treatment led to ablation of the PE surface layer, thus the surface morphology was changed and the surface roughness was increased. The materials were then seeded with vascular smooth muscle cells (VSMC) derived from rat aorta and incubated in a DMEM medium with fetal bovine serum. Generally, the cells adhered and grew better on modified rather than on unmodified PE samples. Immunofluorescence showed that focal adhesion plaques containing talin, vinculin and paxillin were most apparent in cells on PE grafted with PEG or BSA + C, and the fibres containing α-actin, β-actin or SM1 and SM2 myosins were thicker, more numerous and more brightly stained in the cells on all modified PE samples than on pristine PE. An enzyme-linked immunosorbent assay (ELISA) revealed increased concentrations of focal adhesion proteins talin and vinculin and also a cytoskeletal protein β-actin in cells on PE modified with BSA + C. A contractile protein α-actin was increased in cells on PE grafted with PEG or Gly. These results showed that PE activated with plasma and subsequently grafted with bioactive molecules and colloidal C particles, especially with PEG and BSA + C, promotes the adhesion, proliferation and phenotypic maturation of VSMC.     

Electrical properties of composites in the vicinity of the percolation threshold

The electrical response of thermoplastic composites composed of carbon black and high‐density polyethylene near the electrical percolation threshold (p_c) has been investigated through the study of the volume resistivity and complex permittivity. The change in conductivity beyond p_c exhibited a critical exponent that was greater than predicted from percolation theory. Composites with carbon black contents slightly larger than p_c exhibited the greatest sensitivity in volume resistivity with temperature variations under the melting point of polyethylene. In addition, percolating composites with low carbon black contents exhibited significant “negative temperature coefficient” (NTC) effects and improvements in conductivity with annealing. Maxwell–Wagner interfacial polarization resulted in moderate increases in both the permittivity (ϵ′) and dielectric loss factor (ϵ″) below p_c, while at percolation, an abrupt and dramatic increase was observed for both components of the complex permittivity. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 1573–1582, 1999     

Adhesion of flame-treated polyolefins to styrene butadiene rubber

Samples of polyethylene and polypropylene have been submitted to repeated short duration (75 ms) flame treatments, at optimum flaming conditions. Surface energies of untreated and flamed specimens were determined by liquid contact angle measurements. It appears that the surface energy of polyethylene increases much more than that of polypropylene after flame treatment. The flamed polymer surfaces were further examined by electron spectroscopy, Fourier Transform IR spectroscopy and secondary ions mass spectrometry. The adhesion properties of modified polymer surfaces were studied by testing in peel the bonded Styrene Butadiene Rubber/polyolefins assemblies. Scanning electron microscopy (SEM) and water contact angle measurements have been used to observe the locus of failure. Good correlations were obtained between surface energy and adhesion strength, the increase in adhesion strength being particularly important for flamed PE/SBR assemblies. In addition, the peeling in a liquid medium allowed the determination of the respective contribution to adhesion of chemical and physical interactions. It is shown that a major part of the adhesion strength increase is of chemical origin, particularly for the bonded flamed PE/SBR assemblies.     

Microwave dielectric properties of ceramics based on CaTiO3–LnMO3 System (Ln–La,Nd; M–Al,Ga)

Structural features and microwave dielectric properties of LnMO₃–CaTiO₃ samples (where Ln stands for La or Nd, M stands for Al or Ga) are studied. Solid solutions with the rhombic perovskite structure are shown to be formed with increasing molar concentration of LnMO₃ up to ∼35% (for Ln–Nd, M–Al) or ∼40% (for Ln–La, M–Ga). Further increase of the neodymium aluminate or lanthanum gallate molar content in the solid solution up to 70% leads to formation of solid solutions with the tetragonal perovskite structure. A family of promising ceramics for application in the microwave technology with dielectric permittivity lying within the range from 43 to 48, the dielectric permittivity temperature coefficient being near to zero, and heightened quality factor (Q·f ⩾40,000 GHz) are obtained.