Good Dielectric Properties Research Articles

A Novel Mechano-Synthesized Zeolitic Tetrazolate Framework for a High-Performance Triboelectric Nanogenerator and Self-Powered Selective Neurochemical Detection.

Designing a high-performing triboelectric novel material with eco-friendly, rapid, and cost-effective synthesis is the future of material research in triboelectric nanogenerators (TENG). We report a mechanochemical ball mill synthesis of a zeolitic tetrazolate framework (ZTF-8) that is isostructural with the well-known zeolitic imidazolate framework ZIF-8. ZTF-8 is extremely stable in water, 0.1 M aqueous acid/base solutions for 75 days at 25 °C, and boiling water (100 °C) for 7 days. Kelvin probe force microscopy and molecular electrostatic surface potential computational analysis exhibited that ZTF-8 has a very high positive surface potential. Atomic force microscopy and three-dimensional digital microscopy studies reveal the high roughness profile in the ZTF-8 film. The unique structure, exceptional acid/base stability, good dielectric property, and high roughness profile combined with the extremely electropositive nature of ZTF-8 make it a suitable candidate as a polymer-free triboelectric positive material in TENG with outstanding performance (power density of 720 mW/m2). High triboelectric output was further validated using the COMSOL Multiphysics simulation tool. Simple mechanical hand tapping of the ZTF-based TENG (ZTF-TENG) device generates high electric output, which was practically used to power numerous low-powered devices like tally counter, clinical thermometer, and digital clock and also illuminates 125 light-emitting diodes. In addition, the efficiency of ZTF-TENG was utilized as a self-powered device for a selective dopamine (DA) sensor with good sensitivity (377.76 mV/μM/cm2), wide range linearity (5-120 μM), and excellent limit of detection (0.42 μM).

La3+ ion doped Cd0.5C0.5LaxFe2-xO4 nanomagnetic materials for high-frequency device applications

The sol-gel self-combustion technique was applied to form Cd–Co-based La-doped (Cd0.5Co0.5LaxFe2-xO4) spinel ferrite nanoparticles. A series of six samples was synthesized by varying lanthanum content from x = 0.00 to 0.20. The structural characteristics of the prepared nanoparticles were carried out using X-ray diffraction (XRD) analysis. The (311) plane verified that the prepared nanomaterials are in the spinel phase in all observed XRD patterns. The crystallite size for each sample was determined using the Scherrer formula found in the 8.7–17.8 nm range, which is well correlated with the SSP model. The crystallite size decreased while the lattice constant increased from 8.38 to 8.45 Å with increasing La-content. The increasing trend in the bulk density and X-ray density has been analyzed with the effects of La3+ contents. In Fourier-transform infrared spectroscopy (FTIR), the high-frequency absorption band (υ1) was found from 522.15 to 541.06 cm−1, whereas the low-frequency band (υ2) varied from 419.80 to 414.31 cm−1. The surface morphology was carried out by scanning electron microscope (SEM), which positively correlated with XRD analysis. Impedance analyzer (IA) assisted in observing the variations in complex dielectric properties of the compound in the frequency range from 1 MHz to 3 GHz. The dielectric constant and impedance plots depicted that the nano ferrites have good dielectric properties in low-frequency regions due contribution of polarization. While conduction can be made possible in the high-frequency areas as observed through AC conductivity. The electric modulus revealed the relaxation phenomenon at high frequency due to the hopping of electrons at the octa and tetrahedral sites. The magnetic properties were investigated to study the impact of La3+ ion under the applied magnetic field from −15 to 15 kOe. The saturation magnetization, and magnetic remanence were found from 40.6 to 27.7 emu/g and 19.6 to 2.7 emu/g, respectively. The synthesized nanoparticles can be utilized for microwave applications and magnetic storage devices.

Processing and characterisation of hot rolling pressed PVDF films with enhanced field-induced polarisation

Poly (vinylidene fluoride) (PVDF) based polymers are good candidates for high-power energy storage in dielectric capacitors. So far, most studies reporting PVDF with high energy density are based on solution casting, a method ill-suited for large-scale production. In this work, we develop PVDF films with high crystallinity (47%) and ultrahigh β-phase (∼97%) using Hot Rolling Press (HRP). During HRP, the crystallinity, fraction of β-phase, internal stress, and the piezoelectric coefficient d33 increased with rolling temperature. The anisotropic stress imposed by two rollers led to a highly preferred orientation of the HRP film along the rolling direction. Notably, the HRP film exhibits an enhanced field-induced polarisation Pin-max value (0.16 C m−2) compared to conventional PVDF films (0.10 C m−2), with an energy density of 32.6 J cm−3 at 871 kV mm-1. The good low field dielectric (εr ∼19 @ 1 kHz) and piezoelectric (d33 ∼30 pC N-1) properties with high-temperature stability (up to 100 °C), and its suitability for in-line continuous production, make HRP PVDF films promising for low field dielectric and piezoelectric applications.

Influence of the solvent removal method on the morphology of polystyrene porous structures prepared via thermally induced phase separation

Thermally induced phase separation (TIPS) allows preparation of nano and micro-porous structured materials for various applications. The literature thoroughly examines the impact of initial polymer solution concentration and cooling rate on the products morphology. On the contrary, the influence of the solvent removal methods was so far researched scarcely. Hence, we compare both qualitatively and quantitatively the effects of the solvent removal method on pore size distribution, structure, porosity, and thermal conductivity. Our study was carried out with samples prepared by TIPS from polystyrene/cyclohexane solutions employing either extraction agent or lyophilization at different solvent removal temperatures. Materials exhibited interconnected pore structure, implying good sound insulation properties, and had low thermal conductivity, offering the combination of thermal and sound insulation in one layer of material. Pore sizes after lyophilization were up to two times larger than after solvent removal by an extraction agent. On the other hand, the use of extraction agent led up to 10% porosity decrease with average porosity after lyophilization being above 82%. Our findings demonstrate that the solvent removal method is an important parameter during TIPS and that pros and cons of both methods should be carefully considered to obtain optimal material and TIPS process economy.

A New Experimental Setup to Characterize Binder–Vegetal Particle Compatibility in Plant-Based Concrete

The good insulation properties and the low carbon footprint of vegetal concretes make them promising materials whose use tends to grow continuously. To produce optimized building materials, a better understanding of the interfacial transition zone (ITZ) between vegetal particles and cement paste in terms of the reactions involved and the size of the impacted surface was investigated. This research led to the setting of a reliable visual test to observe ITZ, which enables the monitoring of its appearance and development. Different combinations of vegetal particles and cement pastes were tested to compare the formed ITZ: hemp, rapeseed, and bamboo into Portland and Prompt cement. Finally, a clear link was drawn between the sugar concentration and the size of ITZ. Thanks to image analysis, it was shown that ITZ is due to physico-chemical reactions, with the extraction of free saccharide molecules from the vegetal and water suction followed by their release into the cement paste.

Low-temperature synthesis and properties of high-purity boron nitride microspheres

Boron nitride (BN) has excellent high temperature resistance, thermal conductivity, strong insulation, and wave-transparent properties. Spherical BN is an essential filler in polymer matrix composites due to good particle mobility and high filler content. In this paper, we present a large-scale preparation for BN microspheres with uniform particle size distribution in the range of 1.0–2.8 μm via solvothermal method at low cost and high yield (∼90%), which is two orders of magnitude lower than the diameter of the spherical BN prepared by other methods. BN microspheres can achieve good crystallinity (>70%) and high purity (>99.9%) at 800 °C. The temperature resistance study showed that the BN microspheres could maintain the dense particle morphology at 1200 °C. In addition, the prepared BN microspheres have good dielectric and thermal conductivity properties (dielectric constant ∼3.4, dielectric loss ∼2.0 × 10−3, and thermal conductivity of 9.8 W m−1 K−1), which show great potential in the field of wave-transparent and thermal conductive composites. The synthesis process of BN microspheres proposed in this study provides a new idea for the preparation of ceramic micro or nano materials by polymer-derived ceramics.

Thermal aging performance of soybean insulating oil mixed with glyceryl triacetate

A method of delaying the aging of natural ester oil-paper insulation systems by adding glyceryl triacetate is proposed in this work. A study was conducted on the thermal aging performance of soybean insulating oil mixed with glyceryl triacetate at a volume fraction of 7.5%. Through a 42-day accelerated thermal aging experiment, it was found that the addition of glyceryl triacetate effectively delayed the increase in kinematic viscosity of the insulating oil and reduced the generation of aging products such as moisture and acid. However, the polar compounds in glyceryl triacetate reduced the breakdown voltage of the mixed oil and made the dielectric loss factor higher than that of pure oil. In addition, tests were conducted on the insulating paper immersed in two types of oil, and it was found that the addition of glyceryl triacetate helps to distribute mixed oil molecules on the surface of insulating paper, which effectively helped absorb moisture from the paper, weakening the hydrolysis reaction of cellulose and delaying the aging of insulating paper. In addition, the insulating paper immersed in the mixed oil maintains good power frequency breakdown voltage and dielectric properties throughout the thermal aging experiment.

Ground tire rubber and coffee silverskin as sustainable fillers in EPDM compounds for rubber‐to‐steel bonded systems in roofing applications

AbstractIn this paper two waste fillers, namely ground tire rubber (GTR) and coffee silverskin (CSS, a waste bio‐product from the coffee‐making process), have been used to produce sustainable ethylene‐propylene‐diene monomer (EPDM) rubber compounds vulcanized on steel sheets to fabricate rubber‐to‐steel bonded systems for industrial roofing applications. The compounds have shown good mechanical performances, with elastic moduli in the range of 13–16 MPa, tensile strength of 13–20 MPa and elongation at break >400%, and strong adhesion to the metal substrate. Moreover, the rubber‐to‐steel bonded systems present good sound insulation properties (mean sound transmission loss [STL] of 39 dB and noise level reduction in simulated hailstones impact tests of 62 dB with respect to bare steel 73 dB). Accelerated UV‐ and thermal‐aging tests have shown excellent adhesion of the compounds to the metal substrate with the CSS acting as an antioxidant agent preventing excessive polymer degradation. The selected waste‐derived materials result in promising fillers for more sustainable rubber compounds.Highlights Waste fillers were used to produce sustainable rubber compounds. Rubber‐to‐steel bonded systems for roofing applications were produced. Rubber‐to‐steel bonded systems have good sound insulation properties. Rubber‐to‐steel bonded systems have excellent adhesion. Coffee silverskin filler acts as an antioxidant agent.

Synergistic enhancement of toughness and flame retardation for cyanate ester composites through hyperbranched polyborosiloxane

AbstractExcellent flame resistance is supposed to be taken into consideration for electronic packaging materials due to the spontaneous combustion of short circuits, except for good mechanical and dielectric properties. Herein, a hyperbranched polyborosiloxane (HPSiB) flame retardant was synthesized via a simple one‐pot transesterification as a multifunctional additive for cyanate ester (CE) resin. The HPSiB with many active terminals features good compatibility with the resin matrix, while catalyzing the curing reaction that conducts at a lower temperature. With as little as 2 wt% HPSiB incorporated, the HPSiB/bisphenol A cyanate ester (BADCy) resin achieves a UL‐94 V0 rating and 32.4% LOI value, and its peak heat release and total smoke production are simultaneously reduced. Its flexural strength and impact strength were significantly enhanced by 30.0% and 85.4%. Besides, the minimum values of dielectric constant and loss can reach 2.77 and 0.0024 at 10 GHz, which are, respectively, reduced by 7.9% and 88.5%. The integration of unique hyperbranched SiOB backbone of HPSiB with CE crosslinked network was responsible for the enhanced overall performance. This work paves a facile strategy to develop multifunctional flame retardant as a promising candidate for the high‐performance electronic packaging materials.Highlights A novel hyperbranched polyborosiloxane flame retardant was synthesized. HPSiB shows good compatibility and catalyzes the curing reaction of CE resin. HPSiB/CE resin with significantly enhanced flame retardancy was obtained. Simultaneously high toughness and low dielectric loss were achieved. Hyperbranched structure containing SiOB chains led to the great enhancement.

Planar amorphous silicon carbide microelectrode arrays for chronic recording in rat motor cortex

Chronic implantation of intracortical microelectrode arrays (MEAs) capable of recording from individual neurons can be used for the development of brain-machine interfaces. However, these devices show reduced recording capabilities under chronic conditions due, at least in part, to the brain's foreign body response (FBR). This creates a need for MEAs that can minimize the FBR to possibly enable long-term recording. A potential approach to reduce the FBR is the use of MEAs with reduced cross-sectional geometries. Here, we fabricated 4-shank amorphous silicon carbide (a-SiC) MEAs and implanted them into the motor cortex of seven female Sprague-Dawley rats. Each a-SiC MEA shank was 8 μm thick by 20 μm wide and had sixteen sputtered iridium oxide film (SIROF) electrodes (4 per shank). A-SiC was chosen as the fabrication base for its high chemical stability, good electrical insulation properties, and amenability to thin film fabrication. Electrochemical analysis and neural recordings were performed weekly for 4 months. MEAs were characterized pre-implantation in buffered saline and in vivo using electrochemical impedance spectroscopy and cyclic voltammetry at 50 mV/s and 50,000 mV/s. Neural recordings were analyzed for single unit activity. At the end of the study, animals were sacrificed for immunohistochemical analysis. We observed statistically significant, but small, increases in 1 and 30 kHz impedance values and 50,000 mV/s charge storage capacity over the 16-week implantation period. Slow sweep 50 mV/s CV and 1 Hz impedance did not significantly change over time. Impedance values increased from 11.6 MΩ to 13.5 MΩ at 1 Hz, 1.2 MΩ–2.9 MΩ at 1 kHz, and 0.11 MΩ–0.13 MΩ at 30 kHz over 16 weeks. The median charge storage capacity of the implanted electrodes at 50 mV/s was 58.1 mC/cm2 on week 1 and 55.9 mC/cm2 on week 16, and at 50,000 mV/s, 4.27 mC/cm2 on week 1 and 5.93 mC/cm2 on week 16. Devices were able to record neural activity from 92% of all active channels at the beginning of the study, At the study endpoint, a-SiC devices were still recording single-unit activity on 51% of electrochemically active electrode channels. In addition, we observed that the signal-to-noise ratio experienced a small decline of −0.19 per week. We also classified observed units as fast and slow repolarizing based on the trough-to-peak time. Although the overall presence of single units declined, fast and slow repolarizing units declined at a similar rate. At recording electrode depth, immunohistochemistry showed minimal tissue response to the a-SiC devices, as indicated by statistically insignificant differences in activated glial cell response between implanted brains slices and contralateral sham slices at 150 μm away from the implant location, as evidenced by GFAP staining. NeuN staining revealed the presence of neuronal cell bodies close to the implantation site, again statistically not different from a contralateral sham slice. These results warrant further investigation of a-SiC MEAs for future long-term implantation neural recording studies.

Dielectric elastomers with large actuation strain and high output force

AbstractDielectric elastomer actuator (DEA) is considered as an ideal artificial muscle with soft and light in nature, widespread application in soft robotics and sensors. Dielectric elastomer (DE), the core component of DEA, with high output force and large actuation strain under relatively low driving electric field is critical for high‐performance DEA. However, the widely used VHB series (3M) DE suffered from very large pre‐strain and high driving voltage to get their high actuation performance, limiting their scope of application. In this work, the DEs with good mechanical and dielectric properties were prepared via UV curing method consisting of acrylic acid (AA) with strong polar groups as functional monomer, n‐butyl acrylate (BA) as soft monomer and urethane acrylate as cross‐linker (c‐p(BA‐AA)). The c‐p(BA‐AA) DE films obtained the simultaneous increasing of dielectric constant and breakdown strength with the increasing content of AA, which guaranteed the good actuation performance. The c‐p(BA‐AA) film exhibited excellent actuating performance (44.11% actuation strain at 45 kV/mm) without pre‐strain. Besides, a simple linear actuator based on the c‐p(BA‐AA) film could easily output weight that is tens of times of its own active weight (654.1 mN/g at 30 kV/mm).

Microwave-absorbing building materials: Assessing thickness and antenna separation in fly ash-ladle furnace slag one-part geopolymer

This paper aims to examine the effect of thickness (20, 40, 60, 80, and 100 mm) and antenna separation (20, 40, 60, 80, and 100 mm) on microwave absorption ability of fly ash-ladle furnace slag one-part geopolymer. The one-part geopolymers exhibited a dense structure with a good compressive strength of 39.2 MPa, which satisfies the minimum requirement for structural building (>28.0 MPa). The geopolymers had good dielectric properties with a low dielectric constant and increased dielectric loss and loss tangent, subsequently contributing to the microwave absorption properties. The microwave absorption ability increased from 60.0% to >80.0% at an optimal thickness of 100.0 mm and antenna separation of 20.0 mm. The presence of calcium-silicate-hydrate (C–S–H) refined the microstructure and enhanced the microwave absorption performance. This work offered an optimal thickness and antenna separation to maximize the microwave absorption ability, which is crucial for reducing microwave interference and preventing public exposure in regions with widespread deployment of Wi-Fi and 5G networks.

Modeling the impact of high thermal conductivity paper on the performance and life of power transformers

Degradation of insulation paper is a key contributor to the failure of power transformers. Insulation degradation accelerates at elevated temperatures, which highlights the potential for better thermal management to prolong life. While several studies have analyzed the benefits of high thermal conductivity oil for reducing temperatures inside a transformer, this study is an initial assessment of the benefits of high thermal conductivity paper on transformer life. Blending particulates with cellulosic fibers offers a pathway for high thermal conductivity paper (with good dielectric properties), which can reduce internal temperatures. Presently, life extensions that can be achieved by the use of such thermally conducting papers were estimated, with the thermal conductivity of the paper being the key parameter under study. The analytical-numerical thermal model used in this study was validated against experimental measurements in a distribution transformer, adding confidence to the utility of the model. This model was then used to provide estimates of hot-spot temperature reduction resulting from the use of papers with higher thermal conductivity than baseline. Transformer life was predicted conventionally by tracking the degree of polymerization of paper over time, based on an Arrhenius model. Results indicate that increasing the thermal conductivity of paper from 0.2 W/mK (baseline) to 1 W/mK reduces the hot spot temperature by 10 °C. While degradation significantly depends on the moisture and oxygen content, the model shows that such a temperature reduction can increase life for all conditions, by as much as a factor of three.

Reusable, high specific surface areas, and excellent thermal stability Al2O3–SiO2 aerogel composites as high-temperature thermal insulators for radome applications

In this study, monolithic Al2O3–SiO2 aerogels with excellent thermal stability and high specific surface area were synthesized using boehmite nanorods (L=20–30 nm, D=3–5 nm). The high specific surface area of aerogels was maintained after calcination at 800 °C (663.54 m2/g), 1000 °C (486.91 m2/g), and 1100 °C (230.76 m2/g). The anti-sintering mechanism of the Al2O3-SiO2 aerogels was discussed. Thanks to the composite of Al2O3-SiO2 aerogel and mullite fibers, the disadvantages of brittleness and low strength of aerogel are overcome. The thermal conductivity of the composite is extremely low at 0.034 W/(m·K)-0.089 W/(m·K) (25 °C-1000 °C). Five muffle cycle back-temperature tests at 1000 °C and a butane blowtorch back-temperature test at 1350 °C also proved that the composites have excellent thermal insulation properties. Composites with excellent thermal insulation properties combined with lightweight, thinness, machinability, and good dielectric properties meet the need for high-temperature thermal insulating-wave transmitting integrated materials for hypersonic missile radomes.

Synthesis and properties of modified thermoplastic polyimide films with good dielectric properties at high frequency and enhanced thermal stability via incorporation of rigid ester and biphenyl structural units

AbstractA series of ester‐ and fluoro‐containing thermoplastic polyimide (PI) films, PEsI‐1 ~ PEsI‐4 have been prepared by the two‐step thermal imidization procedure via the soluble poly(amic acid) (PEsAA) precursors from the copolymerization of four monomers, including the dianhydrides of bisphenol A dibenzoate‐3,3′,4,4′‐tetracarboxylic acid dianhydride (TMBPA) and 3,3′, 4,4′‐biphenyl tetracarboxylic acid dianhydride (BPDA) and the diamine monomers of 4‐aminophenyl‐4′‐ aminobenzoate (APAB) and 2,2′‐bis(trifluoromethyl)‐4,4′‐diamino biphenyl (TFMB) in the polar aprotic solvent of N‐methyl‐2‐pyrrolidinone (NMP). The PI films obtained from the high‐temperature dehydration of the PEsAA solutions exhibited the good thermal stabilities with the glass transition temperatures (Tg) over 269°C, the 5% weight loss temperatures (T5%) higher than 480°C, and the linear coefficients of thermal expansion (CTE) values in the range of 17.7 × 10−6/K–33.6 × 10−6/K in the temperature range of 50–250°C. Meanwhile, the PI films showed good thermoplasticity in the dynamic mechanical analysis (DMA) tests, in which the storage modulus of the PI films dropped sharply in the temperature range of glass transition of the polymers. At last, the PI films exhibited the good dielectric properties with the breakdown voltages (Vb) over 5200 V, the dielectric strength (Ds) higher than 210 V/μm, the dielectric constants (Dk) in the range of 3.26 ~ 3.32 at the frequency of 10 GHz, and the dielectric dissipation factors (Df) of 0.0038 ~ 0.0047. Compared with the commonly used PEsI‐ref film for high‐frequency flexible copper clad laminates (FCCL), the currently developed PI films exhibited the obviously increased Tg values, decreased CTE values, and comparable dielectric properties.

The Aging Effects of Ultraviolet Irradiation on the Optical Properties of Glass

Glass is known for its high mechanical strength, resistance to high temperatures, corrosion resistance, excellent transparency, thermal stability, and good electrical insulation properties, making it widely used in various fields such as construction, household, and automotive applications. In this study, three types of glass samples were exposed to three different environments: outdoor, ultraviolet (UV) irradiation, and UV irradiation in water vapor. The influence of these different environments on light transmittance and surface morphology was investigated using UV-visible-near infrared spectroscopy and scanning electron microscopy. The experimental results indicate that lead-containing glass exhibits excellent resistance to UV irradiation, sodium-calcium glass samples exhibit significant variations in transmittance in the UV and infrared regions, possibly related to iron content, and high borosilicate glass samples show a noticeable decrease in transmittance in the infrared region.

Sintering behavior and mechanism of Bi‐Zn‐Nb‐O microwave dielectric ceramics

AbstractBi‐Zn‐Nb‐O‐based microwave dielectric ceramics are promising candidates for wireless communication. Investigations have concentrated on their fabrication methods and doping modification. In this work, the densification mechanism and grain growth kinetics of the Bi‐Zn‐Nb‐O‐based microwave dielectric ceramics were explored. A significantly wide sintering temperature window (800–1000°C) of the monoclinic Bi2Zn2/3Nb4/3O7 (BZN) was found. High‐density stacking faults were observed in BZN grains at the initial stage of sintering, which could act as paths for mass transport, thus remarkably accelerating the densification process and decreasing the densification temperature. On the other hand, BZN possesses a high grain growth exponent and activation energy, which indicates a slow grain growth rate and a high threshold for abnormal grain growth, corresponding to the wide sintering temperature window. Moreover, the BZN ceramics display good microwave dielectric properties stability over a wide temperature range (25–450°C).

Unveiling the effect of phase separation on crystallization of calcium borosilicate glass-ceramics

The CaO–B2O3–SiO2(CBS) glass-ceramics with low sintering temperature and good microwave dielectric properties have been applied on the famous commercial low temperature co-fired ceramics (LTCC) Tape for passivation substrate materials for 5G/6G technology. However, the phase separation and its relationship with the crystallization is rarely studied but extremely important for understanding and designing the high-performance CBS glass-ceramics. Herein, we find that the phase separation type of CBS glass-ceramics changes from metastable immiscibility to stable immiscibility with the increase of B2O3 content. In the metastable immiscible glass-ceramics, three phases are observed, including continuous borate-rich and silicate-rich phases as well as spherical silicate-rich phases. In the stable immiscible glass-ceramics, the silicate-rich phases transform into petal-liked shapes. β-CaSiO3 nuclei are formed in fractions with BO3/SiO4 equaling to 0.56. Notably the β-CaSiO3 nucleus do not grow after heat treatment at 850 °C, but grow at higher temperatures. Phase separation hinders the precipitation of β-CaSiO3 and promoted the formation of CaB2O4 and SiO2. In addition, interfacial defects caused by phase separation alter the crystal barrier and promote the formation of α-CaSiO3. However, α-CaSiO3 dissolves at 1000 °C and may provide Ca2+ cations together with the borate-rich phase for the regrowth of β-CaSiO3. Our work provides another perspective for understanding the effects of phase separation on crystallization in CBS glass-ceramics, contributing to improving the microwave dielectric performance by structural design.

High throughput synthesis of SiO2 microspheres enhancing dielectric properties of quartz fibers insulation composites for high temperature resistant communication cable

The development of the digital society has led to an urgent demand for high-temperature-resistant, low-dielectric cable insulation materials. In order to meet the stable high temperature service performance, it is necessary to use inorganic materials instead of the traditional organic insulating materials as the cable insulation layer. Silicon dioxide (SiO2) as a widely used inorganic dielectric material has great potential for application, and quartz fiber is another wave-transparent material with good dielectric properties. The combination of SiO2 and quartz fiber can provide a feasible path for pure inorganic composite insulation materials. In this work, the high-throughput (>50 g) synthesis of SiO2 was investigated to explore the factors affecting the dielectric properties. The effects of different quartz fiber composite amounts and sintering temperatures on the dielectric properties of the composites were investigated by testing the dielectric properties of the composite powders after pressing. The composite powders doped with 20 wt% quartz fibers at 600 °C sintering temperature were found to have better dielectric properties with dielectric constant of 2.48 and dielectric loss of 0.0109 at 20 M Hz. Furthermore, the composite powders were filled into the cables and measured for electrical properties by a network analyzer. And dielectric properties of the cables preliminarily meet the performance requirements for the applications of high temperature (900 °C) radio frequency (RF) communication cables with dielectric constant of 1.731 and insertion loss of 2.02 dB at 18 G Hz. Therefore, this inorganic composite material can be used as the insulation layer for RF high-temperature-resistant communication cables for aerospace, nuclear power plants and energy fields.

High toughness, healable, self-cleaning polydimethylsiloxane elastomers with "rigid-while-flexible" mutual network structure.

Polydimethylsiloxane (PDMS) elastomers with high mechanical and healing properties are developed as smart materials for electrical power systems and electronic devices to address electrical or mechanical damage. However, the challenge is to reconcile the conflicting molecular mechanisms of mechanical and healing properties in the development of PDMS elastomers. This study adopts the "rigid-while-flexible" mutual network structure by copolymerizing the rigid polyimide (PI) with flexible segments with dynamic reversible crosslinking designed on the PDMS backbones. This elastomer (designated PSiPI) exhibits high toughness, tensile strength and elongation at break, as well as excellent healing efficiency and recyclability. Moreover, the PSiPI elastomer also exhibits good insulation and corona damage healing properties. Taking advantage of the recyclability and healing properties of PSiPI elastomers, healable superhydrophobic coatings with contact angles greater than 150° have been prepared by compositing PSiPI elastomers with SiO2. Likewise, combining the elastomer with conductive materials can create a healing flexible conductor. This "rigid-while-flexible" design approach provides important inspiration for the development of high-performance, sustainable and environmentally friendly PDMS elastomers for electrical and electronic applications.