Conventional Polyimide Research Articles

Sandwich-Structured Fluorinated Polyimide Aerogel/Paraffin Phase-Change Composites Simultaneously Enables Gradient Thermal Protection and Electromagnetic Wave Transmission.

There is an emerging requirement of advanced functional materials for simultaneous thermal protection and electromagnetic wave-transparent transmission applications. A novel polyimide (PI) aerogel-based sandwich-structural composite is developed to meet such a requirement in this study. This composite is based on a unidirectional fluorinated PI (FPI) aerogel as a lower layer, a nondirectional conventional PI aerogel as a middle layer, and a nondirectional FPI aerogel/paraffin phase-change composite as an upper layer. The lower layer exhibits a unique unidirectional porous microstructure and an ultralow dielectric constant of 1.04. The upper layer possesses a dynamical temperature regulation capability thanks to its loaded paraffin having a high latent heat capacity of 242.7Jg-1. The presence of the nondirectional PI aerogel middle layer can effectively prevent against the leakage of paraffin from the upper layer to the surface of the composite. Through a rational integration of three functional layers, the developed sandwich-structured composite not only can provide gradient thermal protection for hot objects over a long period but also exhibits an excellent wave-transparent capability to establish communication between two electromagnetically shielded electronic devices. With such prominent thermal insulation and wave-transparent functions, the sandwich-structured composite exhibits great potential for specific applications in aircraft, spacecraft, radar systems, and satellite communication.

Synthesis and characterization of polyimides with rigid folded fragments

The macromolecular chain of conventional polyimide (PI) is a predominant linear extension, which is anticipated to uphold robust interchain interactions essential for preserving overall mechanical and thermal performance. This study is dedicated to the design and synthesis for the novel PIs containing folded chains, with a particular emphasis on modifying the chain conformational behavior with respect to the structure of the aggregation state and the corresponding gas separation properties. First, two unidirectional diamine monomers, dibenzo [c, g] phenanthrene-9,12-diamine (NPDA) and anthracene-1,8-diamine (ADA), were meticulously synthesized through a sequence of chemical reactions, including Witting olefination and photocyclization. These monomers possess distinctive spatial characteristics: NPDA adopts a helical conformation, while ADA maintains a planar structure. Subsequently, the corresponding folded chain-containing PIs, denoted as NPI and API, were successfully achieved by copolymerizing one of the unidirectional monomers with the 6FDA-TPDA system. API and NPI generally exhibit a propensity for enhanced molecular chain stacking, while retaining their good solubility and processability. Drawing from both experimental data and simulation results, it was ascertained that the inclusion of these two monomers produces a rearrangement of pore sizes with a decrease in large-size micropores and an increase in the percentage of ultra-micropores. Moreover, the PI membranes with the folded fragments have a much better CO2 plasticization resistance.

Enhancing the interlaminar property of carbon fiber/poly(aryl ether ketone) composites with water‐soluble polyimide oligomer sizing agent

AbstractNovel water‐soluble polymer‐based sizing agents for carbon fiber/poly(aryl ether ketone) composites (CF/PAEK) have gained attention. However, a challenge remains: the sized CF bundles lack flexibility, and the effect of this on the properties of the composite has not been discussed. Herein, a water‐soluble polyimide oligomer (OL) sizing agent was developed, and the sizing effect was comprehensively evaluated. The conventional molecular weight polyimide (HP) sizing agent was also assessed for comparison. Although the interfacial shear strength of the sized CF monofilaments is enhanced due to improved surface roughness and wettability, the effect of the OL sizing agent on the composite's interlaminar shear strength (ILSS) and tow's flexibility differed from that of the HP sizing agent. Compared with HP‐CF, the yarn spreading rate of OL‐CF tow is increased by about eight times, and the ILSS of OL‐CF/PAEK composites with 2 and 5 MPa molding pressure is increased by 69% and 222%, respectively. The HP sizing agent weakens the tow's flexibility and yarn spreading ability, which is not conducive to the resin penetration in the tow, resulting in lower ILSS. In contrast, the OL sizing agent considers the tow's flexibility and composite's interlaminar property, showing great application potential.Highlights Two PI‐based sizing agents with diverse film‐forming capacities were prepared. The ILSS of CF/PAEK with OL sizing agent was significantly improved. HP sizing agent weakened the tow flexibility and interlaminar property. The interaction of sizing layer—resin penetration—ILSS was proposed.

Effect of Water–Soluble Polyimide (w-PI) Type Binders on the Performance of High-Capacity Silicon Anodes of Lithium-Ion Batteries

In order to enhance rapid charging and driving range for electric vehicles, the high-capacity of lithium-ion batteries (LIBs) is imperative. Commercially available graphite as an anode material has long cycle life, abundance, and low cost. However, it has a limitation in its theoretical specific capacity (372 mAh g−1).To overcome this limitation, much attention has been paid to silicon (Si), which offers a high theoretical specific capacity of 4,200 mAh g−1. Nevertheless, silicon suffers from excessive volume expansion, resulting in issues such as pulverization of active alloy particles, delamination, and the formation of an unstable Solid Electrolyte Interphase layer. This lead to a limitation to use the silicon in large amount in an electrode. A polymeric binder has a critical role in improving the high-capacity Si anode. Conventional polyimide (PI), one of various super-engineering plastics, was applied to the Si anodes, but it is still challenged to water-insolublity and high temperature imidization process around 300 oC. In this study, a water-soluble PI (w-PI) is designed by the polycondensation between dianhydrides and diamine in water environment. In addition, a relatviely low-temperature imidization temperature below 200 oC will be appled by the introduction of dimethylimidazole. This study will briefly outline the direction for implementing a w-PI binder and improving electrochemical performance of high-capacity anode compared to conventional binders such as PVdF and CMC/SBR. Keyword: high-capacity Si anode; dianhydrides and diamine; Polyimide (PI); and water-soluble PI Figure 1

Nano/microgroove zirconium‐doped lanthanum oxide film with self‐aligned molecules for liquid crystal device application

Herein, we propose a brush‐coated zirconium‐doped lanthanum oxide (ZrLaO) film as a liquid crystal (LC) alignment layer. The film‐curing temperature was adjusted to 70, 150, and 230°C. Polarized optical microscopy and pre‐tilt angle analysis confirmed that there was uniform and homogeneous LC alignment on the 230°C cured ZrLaO film. Atomic force microscopy revealed that the surface had a nano/microgroove structure, which was caused by the shear stress generated by the brush‐coating process. This structure induced the uniform LC alignment. X‐ray photoelectron spectroscopy verified that the ZrLaO film was well‐formed on a glass substrate. The ZrLaO film displayed hydrophilic characteristics, and its surface energy increased as the film‐curing temperature increased. The ZrLaO alignment layer displayed suitable optical transmittance for LC device applications. The ZrLaO layer‐based twisted‐nematic LC cell exhibited more stable switching properties and better threshold voltage characteristics than conventional polyimide layers. Therefore, we expect that this brush‐coated ZrLaO layer will be a suitable LC alignment layer for LC device applications.

Negative-tone Photo-definable Polyimide with High Thermal Stability and Thick Film Processability

High voltage power semiconductor requires higher polyimide insulation properties. We have designed a polyimide with high thermal stability, high light transparency and alkali dissolvable polyimide that is capable of passivating thick layer of polyimide with large topographys. A novel negavitve-tone photo-definable polyimide was formulated with cross linking reagent that can easily decompose during cure and a photo-initiator that initiates well during lithography. Our novel Negative photo sensitive polyimide, PSPI-1, has a patternable capability up to 16 mm thickness on silicon with 350 mj/cm2. PSPI-1 showed higher patternability than of the conventional polyimide. The cured film showed excellent properties as follows: 310C glass transition temperature (Tg), 500C 5% weight loss temperature, 40% elongation, no short observation during bias-HAST (130C. 96%, 100hr, 100V 15/30 mm line & space) and good adhesion to Si and Cu substrates. These results indicated a possibility for this novel PSPI-1 to be applicable for passivating power semiconductor.

Poly(ester imide)s with Low Linear Coefficients of Thermal Expansion and Low Water Uptake (VII): A Strategy to Achieve Ultra-Low Dissipation Factors at 10 GHz.

In this study, a series of ester-linked tetracarboxylic dianhydrides (TCDAs) with 2,6-naphthalene-containing longitudinally extended structures consisting of different numbers of aromatic rings (NAr = 6-8) was synthesized to obtain novel modified polyimides, poly(ester imide)s (PEsIs). These TCDAs were fully compatible with the conventional manufacturing processes of conventional polyimide (PI) systems. As an example, the PEsI film obtained from the ester-linked TCDA (NAr = 8) and an ester-linked diamine achieved unprecedented outstanding dielectric properties without the support of fluorinated monomers, specifically an ultra-low dissipation factor (tan δ) of 0.00128 at a frequency of 10 GHz (50% RH and 23 °C), in addition to an extremely high glass transition temperature (Tg) of 365 °C, extremely low linear coefficient of thermal expansion (CTE) of 6.8 ppm K-1, suppressed water uptake (0.24%), requisite film ductility, and a low haze. Consequently, certain PEsI films developed in this study are promising candidates for heat-resistant dielectric substrates for use in 5G-compatible high-speed flexible printed circuit boards (FPCs). The chemical and physical factors denominating tan δ are also discussed.

Liquid Crystal-Filled 60 GHz Coaxially Structured Phase Shifter Design and Simulation with Enhanced Figure of Merit by Novel Permittivity-Dependent Impedance Matching

This work serves as the first simulation investigation to tackle the liquid crystal (LC)-filled coaxially structured continuously variable phase shifter at 60 GHz, wherein the LCs act as single tunable dielectrics fully occupying the millimeter-wave (mmW) power transmitted (i.e., free of leakage or interference). Impedance and effective dielectric constant computations are settled, followed by the quantification of the interplay between the dielectric thickness and the dielectric constant (Dk) for a controlled 50 Ω impedance. Geometry’s aspect ratio (AR) effects are exploited for the coaxially accommodating topology filled with mmW-tailored LCs with an operatable Dk range of 2.754 (isotropic state) to 3.3 (saturated bias state). In addition to the proposed structure’s noise-free advantages, a novel figure of merit (FoM) enhancement method based on Dk-selection-based impedance matching is proposed. The optimum FoM design by simulation exhibits a 0–180.19° continuously variable phase shift with a maximum insertion loss of 1.75871 dB, i.e., a simulated FoM of 102.46°/dB when the LC-filled coaxial geometry is 50 Ω and matched with the Dk of 2.8, corresponding to the dielectric thickness of 0.34876 mm and line length of 15.92 mm. The envisioned device fabrication and assembly processes are free of the conventional polyimide alignment agent and the related thermal and electrical concerns. Significant cost reduction and yield improvement can hence be envisaged. The topology can also serve as a test structure for broadband characterizations of LC materials and new electro-optical effects.

Spontaneously homogeneous alignment of liquid crystals on self-assembly organic rubrene

A novel spontaneously homogeneous liquid crystal (LC) alignment with self-assembled organic rubrene layer on the substrate surface has been reported. The spontaneous alignment technique without surface pre-treatment results in low cost, short processing time, and the room-temperature processing extends application to plastic device. The rubrene-nematic LC mixture is used to fabricate the LC cell. During the capillary filling, the LC molecules align in the flow direction. Meanwhile, the flow-induced LC alignment enforces the tetracene of the rubrene dopants along the flow direction because of the van der Waals and π–π interactions between the rubrene and LC molecules. Afterwards, the rubrene dopants spontaneously migrate onto substrate surface and self-assemble as the triclinic crystalline rubrene (TCR) with ribbon morphology. The LC alignment on TCR has a low pretilt angle, thereby providing a homogeneous LC alignment spontaneously. LC alignment on TCR shows a higher thermal stability compared to conventional polyimide due to the strong interactions of the rubrene and LC molecules. Moreover, the rubrene molecules remain in the bulk suppress the free-ions, decrease the rotational viscosity of LCs and hence shortening the response time of cell. The suppressed free-ions also decrease the screening effect on the substrate surfaces and hence the operation voltage of cell. The TCR structure on the substrate surface and the residual rubrene molecules dispersed in the bulk simultaneously contribute to the enhancement in electro-optical performance of the LC cell.

Ultrahigh-permeance polyamide thin-film composite membranes enabled by interfacial polymerization on a macro-porous substrate toward organic solvent nanofiltration

Organic solvent nanofiltration (OSN) membranes have become a powerful separation platform in a myriad of chemical and pharmaceutical fields owing to their superior merits in high separation efficiency and low energy consuming. Despite extensive progress in exploiting polyamide thin film composite (TFC) membranes for OSN, they are heavily limited by inferior solvent permeability, especially when using conventional low-porous polyimide as TFC substrate. Herein, we report a facile substrate engineering strategy to leverage macro-porous Nylon66 microfiltration membrane to replace the conventional low-porous polyimide substrates for fabricating TFC membranes by interfacial polymerization, enabling high and robust solvent permeability during OSN. Distinct from conventional polyimide, Nylon66 substrates take advantage of their high porosity, macro-porous size and excellent hydrophilicity to realize more monomers storage and uniform monomers distribution, allowing to create crumpled and defect-free polyamide layers. With this method, the polyamide TFC membranes show a 2.1-fold increase in ethanol permeance (up to 16.0 L h−1 m−2 bar−1) meanwhile possessing 98 % rejection of dye, surpassing the most reported TFC membranes. We also demonstrate that the TFC membranes exhibit excellent long-term stability in both polar and non-polar solvent, as well as hold huge promise in the precise separation of dye mixture, pharmaceutical ingredient, and catalyst.

Fluorinated polyimide with enhanced ultraviolet-resistant radiation via a self-sacrificial strategy

High-performance polyimide (PI) films with excellent ultraviolet (UV)-resistant radiation and low dielectric constant (k) properties are ideal spacecraft antenna substrates in space applications. However, conventional commercial PI films like Kapton® applied in the aerospace field are inevitably subjected to the harsh UV radiation environment, leading to their structural damage and performance failure. Herein, a type of “self-sacrificial” micro-branched crosslinked PI films were fabricated by employing tris(4-aminophenyl)amine (TAPA) intrinsically containing the C-N bonds to crosslink linear pure fluorinated PI (FPI), where TAPA functioned as the dual roles of crosslinker and creating “self-sacrificial” local deep traps of C-N bonds in crosslinked sites. Consequently, abundant local deep traps of C-N bonds in crosslinked sites could capture energy from UV-rays to prevent the destruction of PI molecular main chains, thus the crosslinked FPI-TAPA films exhibited better UV-resistant radiation properties than that of pure FPI films and commercial PI films. And the crosslinked film showed least k of 2.53 and least dielectric loss of 0.006 at frequency of 1 MHz owing to the introduction of micro-branched crosslinked structure. Additionally, a high breakdown strength of 522 MV/m, as well as a high tensile modulus of 3.03 ± 0.07 GPa, was achieved, much better than the value of pure FPI film. This work provides a novel and facile approach to fabricate high-performance PI films with excellent UV-resistant properties, exhibiting great potential application in aerospace and microelectronics industries.

Laser‐Induced Carbon Nanofiber‐Based Redox Cycling System

AbstractRedox cycling is a powerful amplification strategy for reversible redox species within miniaturized electrochemical sensors. Herein, we generate three‐dimensional (3D) porous carbon nanofiber electrodes by CO2 laser‐writing on electrospun polyimide (PI) nanofiber mats, referred to as laser‐induced carbon nanofibers (LCNFs). The technique allowed the fabrication of interdigitated electrode (IDE) arrays with finger width and gap distance of ~400 μm and ~40 μm, respectively, offering approximately 3.5 times amplification efficiency (AF) and 95 % collection efficiency (CE). Such dimensions could not be achieved with IDEs fabricated on conventional PI film because the devices were short‐circuited. Stacked electrodes were also constructed as an alternative to the IDE design. Here, nanofiber mats as thin as ~20 μm were fabricated and used as vertical insulation between two LCNF band electrodes. While redox cycling efficiency was similar, the IDE design is more favorable considering the lower complexity and better signal reproducibility. Our strategy thus paves the way for creating flexible 3D porous electrodes with redox cycling ability that can be integrated into microfluidics and lab‐on‐a‐chip systems. In particular, the devices offer inherent flow‐through features in miniaturized analytical devices where separation and sensitive detection could be further realized.

Cross-linked PI membranes with simultaneously improved CO2 permeability and plasticization resistance via tunning polymer precursor orientation degree

Polyimides (PIs) have gained recognition as highly desirable membrane materials for efficient CO2/CH4 separation. However, the practical utilization of these materials has been impeded by the issue of the substantial susceptibility to plasticization when exposed to high-feed-pressure conditions. Although thermal cross-linking has been widely employed to enhance plasticization resistance in PI membranes, cross-linking will normally sacrifice CO2 permeability. Thus, the advancement of PI membranes that exhibit both remarkable CO2 permeability and exceptional plasticization resistance is highly desired. The current work designed a series of cross-linkable PIs with different polymer chain orientation degrees. Different from conventional PIs, by properly controlling the polymer chain orientation, the CO2 permeability can be enhanced by 2.3 times without compromising the membrane plasticization resistance. Various techniques, including FTIR, WAXD, TGA, and DMA, were employed to thoroughly characterize the obtained membranes. These characterizations verified that optimizing the polymer chain orientation constitutes an efficacious strategy to enhance the resistance of PI membranes against plasticization, while simultaneously preserving their CO2 permeability. Additionally, the thermally cross-linked membranes exhibited good long-term stability during an 1100-h test.

Surface alignment of nematic liquid crystals by direct laser writing of photopolymer alignment layers

ABSTRACT We demonstrate the fabrication of good quality surface alignment layers on glass by Direct Laser Writing method using a 2-photon polymerisation technique. We use commercially available photosensitive resins to print alignment layers by scanning the focal point of a femtosecond laser near the resin-glass interface. This results in down to ~ 100 nm thin alignment layers that provide good planar anchoring of 5CB and MLC13300, with the easy axis of alignment along the scanning direction. The azimuthal anchoring strength is ~ 5 × 10−6 J/m2 and is an order of magnitude weaker compared to commercial rubbed polyimide alignment layer. The threshold voltage for Fréedericksz transition in a 90° twisted nematic cell is slightly increased compared to conventional rubbed polyimide for printed alignment layers. The turn-on switching time is longer for printed layers compared to polyimide alignment layers, whereas the turn-off time is shorter for printed alignment layers. The advantage of this new method is in its flexibility, as we demonstrate printing of complex surface alignment patterns with alignment layer thickness below 100 nm.

Fluorinated polyimide for controlling pretilt angle of liquid crystals by plasma treatment

ABSTRACT The pretilt angles of LC molecules can be controlled by tetrafluoromethane (CF4) plasma treatment. For conventional polyimide layers, the homogeneous alignment turns homeotropic owing to the invasion of fluoride atoms, which leads to the wettability transition from being hydrophilic to hydrophobic. The different treatment times generate variable pretilt angles such that the values of pretilt angles can be changed from 7.21ο to 79.53ο, and the polar anchoring energy can be tuned continuously. This technique can provide a reversible alignment layer that can be controlled by applying different plasmas of CF4 and O2. Moreover, a hybrid-aligned LC cell with patterned displays based on different pretilt angles, was proposed herein.

Achieving both low thermal expansion and low birefringence for polyimides by regulating chain structures

The synthesis of polyimides (PIs) with both low coefficient of thermal expansion (CTE) and low birefringence still faces a big challenge. In this study, we prepared a new kind of PI (PI-c-P), derived from a diamine monomer (cis-diamine-DBCOD) that contains dibenzocyclooctadiene (DBCOD) units, which exhibits near-zero thermal expansion with a CTE value of 1.5 ppm/K in the temperature range of 0–150 °C due to the unique conformation transition of DBCOD unit. The increase in chain rigidity and cis-diamine-DBCOD content could effectively reduce the CTE values by promoting conformation transition. Cross-linking could restrict chain conformation transition and impair thermal contraction, leading to higher CTE values. Unlike the conventional low CTE PIs with high orientation or crystallization, the birefringence of DBCOD-containing PI films was in the range of 0.0021 ∼ 0.0094, showing both low birefringence and low thermal expansion, this property is extremely important for its application in optical and electronic devices.

Long-term atomic oxygen resistant polyimide films containing carborane nanocage structure in the main chains

High-temperature durable polymer films with long-term atomic oxygen (AO) resistant capabilities are highly desired for the development of spacecraft with long-servicing lifetimes in low earth orbit (LEO). The relatively poor AO resistance of conventional polyimide (Kapton® H) film severely limited its applications in LEO spacecraft. In this work, carborane nanocage rich in boron element was introduced into polyimide molecular chain to prolong the atomic oxygen resistance life of polyimide film. A series of carborane-containing polyimide (CBPI) nanocomposite films with ultrahigh AO resistance have been prepared by casting precursor polyamic acid (PAA) solution on a glass plate, followed by thermal imidization at several elevated temperatures. The AO exposure experiments were tested in a ground-based AO effects simulation facility in our laboratory with the filament discharge and bound of magnetic field. Incorporation of carborane nanocage structure apparently improved the thermal stability and AO resistance of the PI nanocomposite films. The CBPI-50 film exhibited the lowest AO average erosion yield (Es) of 2.3 × 10−25 cm3·atom−1 under AO exposure with a fluence of 3.33 × 1020 atoms·cm−2, which is more than one order of magnitude lower than the reference Kapton® H film. The protective mechanism of CBPI nanocomposite films during AO exposure was proposed.

Enhancement in Photoluminescence of Nematic Liquid Crystals Doped with CsPbBr3 Quantum Dots

We report the enhancement in photoluminescence (PL) of nematic liquid crystals (NLCs) doped with CsPbBr3 (perovskite) quantum dots (QDs). QDs play a vital role to enhance the PL intensity, which has been attributed to the increase in the planar alignment of NLC molecules by reducing light leakage centres and intrinsic defects. QDs were synthesized by the hot injection chemical method. The structural properties of QDs were examined by X-ray Diffraction (XRD) and Transmission Electron Microscopic (TEM) measurements. Orthorhombic crystallite structure of CsPbBr3 QDs without secondary phase formation was confirmed from XRD pattern. The particle size of QDs was calculated by TEM and found to be 7.3 (± 1.1) nm. The optical properties of QDs were studied by recording UV-Visible absorption and PL spectra at room temperature. The absorption spectrum reveals the excitonic peak at 509 nm and PL emission is observed at 514 nm. The chemically prepared QDs were further used to enhance the emission of NLC. Firstly, liquid crystal sample cells were fabricated by conventional polyimide technique. NLC doped with CsPbBr3 QDs were inserted into the sample cell via the capillary action. The filled sample cells were characterized by polarising optical microscope (POM) images and PL spectra measurements. The dark and bright state images of POM demonstrate the uniform alignment and homogeneous texture of liquid crystal molecules in both cells. The molecular alignment is further improved while the light leakage centres and defects were reduced after doping QDs in the host NLC material. This leads to a significant enhancement in absorption and hence the emission of NLC. We found the enhancement in PL intensity by 11% compared to pure NLC. The improved emission of NLC is attributed to modified molecular alignment in presence of QDs. Results based on present work will help to fabricate QDs based display devices with improved the optical contrast and lower the operating voltage

Hierarchically self-constructed alignment layer of comb-shaped amphiphilic copolymers for spontaneous and stable vertical orientation of liquid crystals

Hierarchically self-constructed ordered nanoarchitectures for precise control of molecular alignment has received much attention in a wide range of applications from optoelectronic devices to flexible biosensors. Herein, we present a facile and effective fabrication strategy to create a hierarchically constructed self-alignment layer of comb-shaped amphiphilic copolymers for spontaneous vertical molecular orientation of liquid crystals (LCs). Amphiphilic poly(vinyl 4-heptylbenzoate)-g-poly(vinyl alcohol) (PVHB-g-PVA) as a comb-shaped copolymer was doped to an LC medium, and its interfacial self-assembly on indium tin oxide electrode induced the hierarchical self-constructed alignment layer through hydrophilic interactions of hydroxy groups. In addition, hydrophobic and cooperative interactions of alkyl phenyl moieties in amphiphilic copolymers ensured the stable vertical self-alignment of LC molecules. Compared to conventional polyimide layer, the proposed self-constructed alignment layer afforded high vertical alignment ability for LCs and outstanding device performance in terms of the threshold voltage and response speed. Furthermore, the long-term alignment reliability of the proposed copolymeric self-assemblies was comparable to that of commercial alignment layer.

Negative Photo-Definable Polyimide Dry Films for Fine and High Aspect Ratio Patterning

We newly developed a negative photo-definable polyimide dry films with higher photoreactivity than conventional ones. We succeeded in fine and high aspect ratio patterning with 90 μm thickness and 8 μm width by using new polyimide dry films. When compared after curing, the tensile breaking strength and share strength of new and conventional polyimide dry films were almost the same. However, when compared after PEB and exposure, the new ones showed clearly higher properties than conventional one. Using this polyimide dry film as an inter-layer dielectrics or a permanent resist was effective in improving the wiring density of electric devices.