Transparency Properties Research Articles

Transparent, robust, and anti-fingerprint silicone coating with a three-dimensional cross-linked network enabled by hydrosilylation reaction

Silicone coatings with anti-smudge, anti-fingerprint, abrasion resistance, and ultraviolet (UV) resistance properties are increasingly demanded for touch screens as the development of artificial intelligence and human-computer interaction interfaces. Herein, a transparent, robust, and self-cleaning silicone coating was developed by incorporating cage-like structures and long carbon chains into a 3D cross-linked network via the rational combination of polymethylhydrosiloxane (PMHS), PSS-Octavinyl substituted (VPOSS), lauryl acrylate (LA), and 1,2-epoxy-4-vinylcyclohexane (EVCH) through hydrosilylation reaction with the presence of Karstedt catalysts. After introducing sealed diphenyliodonium phosphate (I-200), the silicone coating (PVLE-I-200) demonstrated excellent pencil hardness, anti-smudge, and abrasion resistance, and its average transmittance of visible light reached about 92 %. Owing to the low surface energy carbon chains, the coating showed amphiphobic properties and excellent anti-fingerprint property. The binding between cyclohexyl epoxy and glass substrate contributed to the high adhesion of the coating, which remained nearly intact and slightly reduced surface wettability after 500 friction cycles of sandpaper. In addition, the PVLE-I-200 coating demonstrated UV resistance which could withstand 200 h of UV irradiation attributed to the cage-like structure of VPOSS. The functional silicone coating provides insights into the development of environmentally friendly coatings for touch screens with high transparency, abrasion resistance, anti-smudge, and anti-fingerprint properties.

Bromine-containing copolymer polycarbonate for simultaneous thermal stability, transparency, and thin-wall flame-retardant polycarbonate

The incorporation of traditional low molecule bromine flame retardants can enhance the flame retardancy of polycarbonate (PC), yet their poor compatibility with PC impairs its transparency and mechanical properties. Here, brominated polycarbonate (B50PC) was synthesized by interfacial polycondensation method using bisphenol A, tetrabromobisphenol A, and triphosgene. The number average molecular weight (Mn) of B50PC reached 14,600, and compared to the low molecule bromine flame retardant tetrabromobisphenol A (TBBPA), its initial decomposition temperature increased by 38.7 % under air atmosphere. The PC composites containing 5 wt% B50PC achieved the V-0 rating in the UL-94 test, with LOI increased by 10.3 %. At the same time, the peak heat release rate (PHRR) was decreased by 28.6 % and the ignition time (TTI) was delayed by 21.3 %. Compared with that of samples with TBBPA, the composite with the same amount of B50PC maintained the original elongation at break of PC and the transmittance remained at 84.9 %. In summary, the composites with B50PC maintains outstanding transparency and mechanical properties while enhancing the flame retardancy. This work has developed a high molecular bromine flame retardant that combines flame retardancy and transparency, offering a strategy for expanding the application of PC in the electronics, construction, and aerospace sectors.

Achieving Ultrahigh Transparency and Superior Mechanical Properties in Flexible Polyimide Nanofoams Through CO2 Foaming for Thermal Insulation

Achieving Ultrahigh Transparency and Superior Mechanical Properties in Flexible Polyimide Nanofoams Through CO₂ Foaming for Thermal Insulation

Energy storage properties, transmittance and hardness of Er doped K0.5Na0.5NbO3-based ceramics

Transparent energy storage ceramics can balance energy storage characteristic and optical characteristic, and are expected to be used in areas such as transparent pulse capacitors. However, excellent energy storage performance and dramatic light transmittance are difficult to achieve simultaneously, limiting their subsequent development in the actual applications. The paper proposes a way to improve the transparent energy storage properties of KNN-based samples by regulating domain and grain size. By introducing an appropriate amount of Er2O3, fine cube grains and nanodomains are constructed. When doping 0.20 mol% Er2O3, the ceramics exhibited excellent recoverable energy storage density Wrec ∼ 6.2 J/cm3, superior energy-storage efficiency η ∼ 71.3 %, large dielectric breakdown strength Eb ∼ 670 kV/cm, ultrahigh hardness value of 6.9 GPa, and a maximum transmittance T ∼72 % at 880 nm. Dense microstructure, nanoscale grains, symmetrical lattice structure and relaxor behavior are the main reasons for obtaining high energy storage and transparency properties.

From Molecular Design to Practical Applications: Strategies for Enhancing the Optical and Thermal Performance of Polyimide Films.

Polyimide (PI) films are well recognized for their outstanding chemical resistance, radiation resistance, thermal properties, and mechanical strength, rendering them highly valuable in advanced fields such as aerospace, sophisticated electronic components, and semiconductors. However, improving their optical transparency while maintaining excellent thermal properties remains a significant challenge. This review systematically checks over recent advancements in enhancing the optical and thermal performance of PI films, focusing on various strategies through molecular design. These strategies include optimizing the main chain, side chain, non-coplanar structures, and endcap groups. Rigid and flexible structural characteristics in the proper combination can contribute to the balance thermal stability and optical transparency. Introducing fluorinated substituents and bulky side groups significantly reduces the formation of charge transfer complexes, enhancing both transparency and thermal properties. Non-coplanar structures, such as spiro and cardo configurations, further improve the optical properties while maintaining thermal stability. Future research trends include nanoparticle doping, intrinsic microporous PI polymers, photosensitive polyimides, machine learning-assisted molecular design, and metal coating techniques, which are expected to further enhance the comprehensive optical and thermal performance of PI films and expand their applications in flexible displays, solar cells, and high-performance electronic devices. Overall, systematic molecular design and optimization have significantly improved the optical and thermal performance of PI films, showing broad application prospects. This review aims to provide researchers with valuable references, stimulate more innovative research and applications, and promote the deep integration of PI films into modern technology and industry.

High-performance cellulose/thermoplastic polyurethane composites enabled by interaction-modulated cellulose regeneration

Strong interfacial adhesion between cellulose and other polymers is critical to achieve the properties required for specific applications in composite materials. Here, we developed a method for the simultaneous homogeneous dissolution of cellulose and thermoplastic polyurethane (TPU) in 1,8-diazabicyclo (5.4.0) undec-7-ene levulinate/dimethyl sulfoxide ([DBUH]Lev/DMSO) solvent. This process is essential for preparing cellulose/TPU composite films and fibers through interaction-modulated cellulose regeneration. Both cellulose and TPU can be easily dissolved together in [DBUH]Lev/DMSO solvent under mild conditions. The resulting cellulose/TPU solutions exhibited strong temperature sensitivity, shear-thinning behavior and viscoelasticity, making them suitable for cast films and continuous spinning. More importantly, research findings, including density functional theory calculations and experimental characterization, confirmed the high compatibility and interaction modulability of cellulose and TPU in the composite films. The representative C90T10 sample (cellulose/TPU, 90/10) showed high transparency (90 % at 800 nm) and excellent mechanical properties (tensile strength: 176 MPa; elongation at break: 8.1 %). Additionally, the maximum tensile strength and elongation at the break of the composite fiber from C90T10 were 214 MPa and 48.1 %, respectively. This method may provide a feasible approach to design and produce homogeneous environmentally friendly composites of cellulose and other polymers at the molecular level.

Sustainable PLA Bio-Nanocomposites: Integration of TPU Nanofibrils and CNC for Enhanced Crystallization, Toughness, Stiffness, Transparency, and Oxygen Barrier Properties

Sustainable PLA Bio-Nanocomposites: Integration of TPU Nanofibrils and CNC for Enhanced Crystallization, Toughness, Stiffness, Transparency, and Oxygen Barrier Properties

Defect engineering by annealing: Managing the trade-off relationship between photochromic and electrical properties in KNN-based translucent ceramics

Rare-earth-doped transparent ferroelectrics exhibit outstanding optical transparency, photoluminescence (PL), photochromic (PC) and various electrical properties, showing potential for use in optoelectronic applications. However, there is an inevitable trade-off relationship between optical and electrical coupling during the integration of multifunctionality. In this work, Ba2+, Ho3+ and Yb3+ were codoped in KNN translucent-ferroelectric ceramics (as a model material) to overcome the contradiction between optical (transparency/PC) and electrical properties (resistivity/ferroelectricity). The defects (mainly oxygen vacancies) within the ceramics can be effectively regulated through annealing under different atmospheres. At the cost of a slight decrease in PC performance, the electrical properties significantly improved; i.e., for the optimal ceramic annealed in an oxygen atmosphere, both the maximum and remnant polarizations nearly doubled, and the resistivity significantly decreased compared to that of the original sample. A mechanism for regulating these properties was proposed. This research serves as a valuable example for adjusting the optical and electrical properties of other ferroelectrics through annealing.

Fluorescent hydrogen-bonded organic framework act as a multifunctional platform for Fe3+ and F− sensing, and for information encryption

Due to their exceptional optical properties and adjustable functional characteristics, hydrogen-bonded organic frameworks (HOFs) demonstrate significant potential in applications such as sensing, information encryption. However, studies on the synthesis of HOFs designed to construct multifunctional platforms are scant. In this work, we report the synthesis of a new fluorescent HOF by assembling melem and isophthalic acid (IPA), designated as HOF-IPA. HOF-IPA exhibited good selectivity and sensitivity towards Fe3+, making it suitable as a fluorescent sensor for Fe3+ detection. The sensor achieved satisfactory recoveries ranging from 97.79 % to106.42 % for Fe3+ sensing, with a low relative standard deviation (RSD) of less than 3.33 %, indicating significant application potential for HOF-IPA. Due to the ability of F− to mask the electrostatic action on the surface of Fe3+ and inhibit the photoelectron transfer (PET) of HOF-IPA, the HOF-IPA − Fe3+ system can be utilized as a fluorescent “off–on” sensor for F− detection. Additionally, owing to the colorless, transparent property of HOF-IPA in aqueous solution under sunlight and its blue fluorescence property under UV light (color) or microplate reader (fluorescence intensity), HOF-IPA based ink can be used for various types of information encryption, and all yielding favorable outcomes.

Knittable hydrogel fiber with physically amorphous structure for multi-mode sensing capacities

Integrating both green forming character and multifunctionality for physically crosslinked hydrogel fibers is challenging, but intensively desirable for emerging applications. Herein, the amorphous multi-scale structure for continuously spinning polyvinyl alcohol (PVA) hydrogel fibers is achieved with an innovatively suppressed-freezing strategy. In particular, the antifreezing salt with salting-in effect is introduced into precursor solution, in which an exceptionally homogeneous yet weak approach of polymer chains is available under weakened repelling behavior of ice crystals using liquid nitrogen as the coagulation bath. Hence, a totally amorphous network with release of free hydroxyl groups is constructed for freeze-thawed PVA hydrogel fibers, which is further stabilized by water evaporation induced densification of polymer network. Such particular multi-scale structure interestingly endows the physical hydrogel fibers with tunable mechanical properties of superior extendibility, flexibility and elasticity in a wide range, along with integrated properties of excellent transparency, antifreezing and long-term stability. Moreover, the hydrogel fibers could be knitted into fabric-like materials with arbitrary shapes, of which the extendibility and toughness are tremendously improved. Notably, benefiting from the high transparency and homogeneous structure, the physical fibers and the corresponding fabrics demonstrate light transmittance ability and deformation responsiveness, which retains even in extreme condition (−196 °C). Together with ionic-conductivity, the PVA hydrogel fibers/fabrics as strain sensors intriguingly represent conductive/optical multi-mode sensations, which are capable of dynamically monitoring subtle and sophisticated human movements. The combined advantages enable this new generation of physical hydrogel fibers to promise potential for applications in wearable electronics, biomedicine, and information transmission.

Transparent bamboo as a replacement for glass: Effects of lignin decolorisation methods on weatherability

Transparent bamboo proved to be a promising substitute for glass due to its high light transmittance and excellent mechanical properties. Nevertheless, it was susceptible to outdoor weathering, which negatively affected its physical and mechanical properties. In this study, two decolorisation methods, namely the delignification method and the lignin modification method, were used to produce transparent bamboos with epoxy resin, referred to as DL-TB and LM-TB, respectively. The changes in surface color, optical and mechanical properties, wettability, thermal stability, and thermal insulation properties of transparent bamboo during accelerated UV weathering were evaluated. Additionally, the deterioration mechanism of DL-TB and LM-TB was investigated. The findings revealed that DL-TB demonstrated better transparency and mechanical properties than LM-TB, although it exhibited lower thermal insulation properties. Furthermore, DL-TB demonstrated enhanced color stability and higher hydrophobicity on weathered surfaces than LM-TB. Unexpectedly, the tensile properties of both two transparent bamboos significantly improved after weathering, especially for LM-TB, which was due to the EP post-curing and the formation of more hydrogen bonds between lignin and EP. These observations revealed that lignin played a key role in the photodegradation process of transparent bamboo, but further attempts should be made in future studies to improve its color stability.

A blockchain-based solution for transparent intellectual property rights management: smart contracts as enablers

PurposeThe purpose of this study is to address the limitations of traditional methods for managing intellectual property rights (IPRs) by proposing a blockchain-based solution. By leveraging blockchain technology and smart contracts, the aim is to create a comprehensive ecosystem that offers advantages such as reduced transaction costs, improved transparency, enhanced security and increased liquidity levels for IP assets.Design/methodology/approachThis paper proposes using blockchain technology to manage intellectual property rights (IPRs) through a smart contract-based ecosystem. It outlines the use of non-fungible tokens (NFTs) on the blockchain to represent IPRs, with smart contracts automating interactions and encoding rules for various processes such as applications, licensing, transfers and royalty distribution. Governance mechanisms, such as decentralized autonomous organizations (DAOs), are employed to allow stakeholders to propose and vote on contract changes, ensuring adaptability. This approach aims to streamline IPR workflows, reduce transaction costs, improve transparency and enhance security.FindingsThe findings of this study suggest that implementing a blockchain-based ecosystem for managing intellectual property rights (IPRs) can lead to various benefits. These include reduced transaction costs, improved transparency, enhanced security, increased liquidity levels for IP assets and streamlined automated processes. The use of non-fungible tokens (NFTs) on the blockchain allows for detailed management, valuation and trading of IPRs. Furthermore, simulation results demonstrate the robustness and efficiency of our proposed ecosystem, outperforming traditional IP management systems in terms of transaction speed and cost-effectiveness. These simulations highlight the practical viability of integrating blockchain technology into IP management workflows.Practical implicationsThe practical implications of adopting this blockchain-based ecosystem for managing intellectual property rights (IPRs) are significant. By streamlining processes, reducing transaction costs and improving transparency and security, organizations can expedite the protection and commercialization of their IP assets. Additionally, the increased liquidity levels and accessibility of IP assets to investors and financiers can spur innovation and economic growth.Originality/valueThis paper contributes to the field by proposing a novel approach to managing intellectual property rights (IPRs) using blockchain technology and smart contracts. By leveraging non-fungible tokens (NFTs) on the blockchain, the proposed ecosystem offers a more efficient and transparent way of managing IPRs, reducing reliance on costly and opaque traditional methods. The potential benefits include improved efficiency, transparency, security and collaboration in the management and commercialization of IPRs.

Atomic layer deposition of SnO2 enables fast-dynamics in electrochromic vanadium oxide/polyaniline films

Heterostructure materials hold great promise for electrochromism, but the complexity in coupling the optical and electronic properties of multiple materials remains a challenge. Herein, SnO2 film with excellent transparency and electronic properties is deposited on electro-deposited inorganic-organic vanadium oxide-polyaniline composite films by atomic layer deopisiton (ALD). As a result, the heterostructure strategy stimulated the reaction dynamics, significantly reducing the response time (from 30 s to 5 s). In addition, the thickness of the SnO2 films is found to have a crucial influecne on the electrochromic performance of heterostructure electrodes. Our work highlights the potential of semiconductor films in improving the electrochoromic materials.

High-performance epoxy resin with flame-retardant, transparent, and ultraviolet shielding properties based on a vanillin-based multifunctional macromolecule

Flame-retardant epoxy resins with tough, transparent, ultraviolet shielding, and low dielectric properties have fascinating prospects in electronic and electrical applications, but it is still challenging at present. In this work, a bio-based macromolecule was synthesized from vanillin (a lignin derivative), phenyl dichlorophosphate, 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO), and poly(propylene glycol) bis(2-aminopropyl ether). The bio-based macromolecule, namely, MFR, was designed and added to the epoxy resin (EP). The cured EP containing 15 wt% MFR (i.e., EP/MFR15) exhibits excellent flame retardancy with an Underwriter Laboratory 94 (UL-94) V-0 rating and a limiting oxygen index (LOI) of 29.2 %. Furthermore, the peak heat release rate (PHRR) and total heat release rate (THR) are drastically reduced by 59.5 % and 40.7 %, respectively. Meanwhile, EP/MFR15 shows 20.3 % and 43.8 % improvements in tensile strength and toughness, respectively. Moreover, MFR simultaneously endows EP with accessional ultraviolet shielding performance and low dielectric constant without sacrificing transparency. This work provides a promising strategy for fabricating a bio-based macromolecular flame retardant and preparing a high-performance EP composite with versatile properties.

Development and characterization of flaxseed mucilage and elastin/collagen biofilms

Flaxseed mucilage (FSM)-based biofilms were prepared with varying compositions of the elastin/collagen (ELN/COL) protein matrix. These biofilms were characterized by using fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimeter (DSC), and X-ray diffraction (XRD). The thickness, water solubility, moisture content, transparency, and mechanical properties of biofilms were investigated. The biofilms were observed to be homogeneous and flexible. The addition of 40 % w/w ELN/COL to the FSM biofilms (FSM-ELN/COL biofilms) enhanced the thickness from 0.127 to 0.142 mm, water solubility from 59.30 to 84.60 % and elongation at break from 91.4 to 188.6 %. However, the reductions in the tensile strength from 6.56 to 4.69 MPa and melting point from 140 °C to 134 °C of the biofilms were observed. The transparency value of 40 % w/w FSM-ELN/COL biofilms increased from 5.42 to 7.19 due to the presence of ELN/COL within the FSM matrix that hinders the light transmission passing through the biofilm. FTIR and XRD tests indicated hydrogen bonding and electrostatic interactions occurred between FSM and ELN/COL, giving rise to a good compatibility of the system. FSM-ELN/COL biofilms fabricated in this work had appropriate mechanical and thermal stability, thus the promising potential to be employed as food packaging and coating.

Development of crosslinked gelatin films through Maillard reaction and reinforced with poly(vinyl alcohol) for active food packaging

In order to improve the functionality of natural gelatin films for active food packaging applications, a combined strategy of crosslinking via Maillard reaction and blending enhancement incorporated with poly(vinyl alcohol) (PVA) was explored. In this study, when the mass ratio of gelatin to glucose was 10:1, Maillard reaction of crosslinked gelatin films was the highest, UV absorption and browning index reached the maximum. Infrared analysis showed that PVA could form strong interfacial interactions with gelatin matrix. The presence of PVA could significantly improve the toughness, water absorption, transparency, and oxygen barrier properties of crosslinked gelatin films. When the amount of PVA reached 5 %, elongation at break and oxygen barrier properties of crosslinked gelatin films were improved by 76.7 % and 47.9 % compared with pure crosslinked gelatin film. Even when the amount of PVA reached 10 %, UV absorption (at 315 nm) of crosslinked gelatin films still exceeded 98.7 %. The addition of PVA could accelerate the dissolution and swelling of crosslinked gelatin films, promoting the migration and release of active substances (Maillard reaction products (MRPs)). The two antioxidant activities tests (DPPH and ABTS method) achieved the highest radical scavenging rates of 71.6 % and 91.2 %, respectively, with corresponding PVA addition of 5 % and 7.5 %. After continuing to add PVA, antioxidant activities began to significantly decrease, which was directly related to the decrease in the generation of MRPs. Therefore, crosslinked gelatin films reinforced with appropriate amount of PVA can be considerable potential as active films for renewable food packaging applications.

Characterization of Composite Film Containing Polyvinyl Alcohol Cross‐Linked With Dialdehyde Cellulose Using Citric Acid as a Catalyst for Sustainable Packaging

ABSTRACTThis study is aimed at fabricating composite films by cross‐linking polyvinyl alcohol (PVA) and dialdehyde cellulose (DAC) in varying ratios using citric acid as a catalyst. The acetal formation between the two components was studied using FTIR. Characterizations of the physiochemical properties revealed that increasing the DAC ratio of the composite film improved the hydrophobicity, tensile strength and barrier properties (water vapour, UV and oxygen) of the films while reducing elongation at break (flexibility), swelling and solubility of the film in water. When the DAC ratio was elevated to 50%, the tensile strength was enhanced to 98 MPa. In comparison, flexibility diminished to 29%, the solubility of the film reduced to 10% and water vapour permeability was lower by two orders of magnitude than that of the control PVA film. The peroxide value of linoleic acid decreased from 21.2% ± 7.6 (packed with PVA film) to 9.9% ± 0.9 (packed with 50% DAC composite film) after 15 days. Furthermore, the composite films demonstrated effective absorption of UV radiation, with the order of effectiveness being UV‐C > UV‐B > UV‐A radiation. No significant difference in biodegradability was detected in the composite films with an increase in DAC ratio during indoor soil burial tests for 30 days. This study implies that the composite film could serve as an alternative sustainable packaging option, especially when transparency and high oxygen barrier properties are desired.

Self-Assembly of Polymers and Their Applications in the Fields of Biomedicine and Materials.

Polymer self-assembly can prepare various shapes and sizes of pores, making it widely used. The complexity and diversity of biomolecules make them a unique class of building blocks for precise assembly. They are particularly suitable for the new generation of biomaterials integrated with life systems as they possess inherent characteristics such as accurate identification, self-organization, and adaptability. Therefore, many excellent methods developed have led to various practical results. At the same time, the development of advanced science and technology has also expanded the application scope of self-assembly of synthetic polymers. By utilizing this technology, materials with unique shapes and properties can be prepared and applied in the field of tissue engineering. Nanomaterials with transparent and conductive properties can be prepared and applied in fields such as electronic displays and smart glass. Multi-dimensional, controllable, and multi-level self-assembly between nanostructures has been achieved through quantitative control of polymer dosage and combination, chemical modification, and composite methods. Here, we list the classic applications of natural- and artificially synthesized polymer self-assembly in the fields of biomedicine and materials, introduce the cutting-edge technologies involved in these applications, and discuss in-depth the advantages, disadvantages, and future development directions of each type of polymer self-assembly.

Ultra-Fast-Healing Glassy Hyperbranched Plastics Capable of Restoring 26.4 MPa Tensile Strength within One Minute at Room Temperature.

The growing concern regarding widespread plastic pollution has propelled the development of sustainable self-healing plastics. Although considerable efforts have been dedicated to fabricating self-healing plastics, achieving rapid healing at room temperature is extremely challenging. Herein, we have developed an ultra-fast-healing glassy polyurethane (UGPU) by designing a hyperbranched molecular structure with a high density of multiple hydrogen bonds (H-bonds) on compliant acyclic heterochains and introducing trace water to form water bridge across the fractured surfaces. The compliant acyclic heterochains allow the dense multiple hydrogen bonds to form a frozen network, enabling tensile strength of up to 70 MPa and storage modulus of 2.5 GPa. The hyperbranched structure can drive the reorganization of the H-bonding network through the high mobility of the branched chains and terminals, thereby leading to self-healing ability at room temperature. Intriguingly, the presence of trace water vapor facilitates the formation of activated layers and the rearrangement of networks across the fractured UGPU sections, thereby enabling ultra-fast self-healing at room temperature. Consequently, the restored tensile strength after healing for 1 minute achieves a historic-record of 26.4 MPa. Furthermore, the high transparency (>90 %) and ultra-fast healing property of UGPU make it an excellent candidate for advanced optical and structural materials.

A comparative study of comprehensive performances for transparent plasticized polyvinyl chloride films with different plasticizers

AbstractFor flexible polyvinyl chloride (PVC) films with excellent mechanical performances and high transparency, the demand for antistatic properties is becoming increasingly urgent in textile and electronic fields. This study compares the effects of 60 phr bis (2‐(2‐butoxyethoxy) ethyl) adipate (DBEEA) with other five equal amounts of plasticizers on the conductivity, electrical stability, transparency, and mechanical properties of plasticized PVC. The infrared spectra of plasticizers indicate that there are unique ether groups exist in DBEEA. Then the calculated solubility parameters suggest the good compatibility between DBEEA and PVC. For conductivity, the volume resistivity and surface resistivity of the PVC sample with DBEEA (PVC/DBEEA) are 107 Ω· m and 1010 Ω, respectively, which are both lower by 3–4 orders of magnitude than that of other plasticized PVC. For electrical stability, the results indicate that PVC/DBEEA placed in air still maintains lowest resistivities. Under 10, 23, and 30°C, PVC/DBEEA keeps high and stable electrical properties. The similar refractive indices of DBEEA and PVC resin prepared by suspension method indicate good transparency for PVC/DBEEA. Moreover, PVC/DBEEA still has good mechanical property.