Polar Surface Energy Research Articles

Surface Thermodynamic Properties of Styrene–Divinylbenzene Copolymer Modified by Supramolecular Structure of Melamine Using Inverse Gas Chromatography

The surface thermodynamic properties of polymers and copolymers modified by supramolecular structures are used in several industrial processes, such as selective adsorption, paints, coatings, colloids, and adhesion applications. Background: Inverse gas chromatography at infinite dilution was proved to be the best technique to determine the surface properties of solid surfaces by studying the adsorption of some model polar and non-polar organic molecules adsorbed on solid surfaces at different temperatures. Methods: The retention volume of adsorbed solvents is a valuable parameter that was used to obtain the London dispersive and polar free energies and the London dispersive surface energy of styrene–divinylbenzene copolymer modified by supramolecular structure of melamine using both the Hamieh thermal model and our new methodology consisting of the separation of the two polar molecules and the dispersive free energy of their interaction. This led to the determination of the polar acid and base surface energy, and the Lewis acid–base constants of the various solid materials. Results: Following our new methodology, all surface energetic properties of styrene–divinylbenzene copolymer modified by melamine at different percentages were determined as a function of temperature. Conclusions: It was observed that the styrene–divinylbenzene copolymer exhibited the highest London dispersive surface energy, which decreased when the melamine percentage increased. All materials presented higher Lewis basicity and this Lewis basicity increased with the percentage of melamine.

Thermal Surface Properties, London Dispersive and Polar Surface Energy of Graphene and Carbon Materials Using Inverse Gas Chromatography at Infinite Dilution.

The determination of these surface properties is carried out using inverse gas chromatography at infinite dilution, which leads to the retention volume of organic solvents adsorbed on solid surfaces. This experimental and fundamental parameter actually reflects the surface thermodynamic interactions between injected probes and solid substrates. The London dispersion equation and the Hamieh thermal model are used to quantify the London dispersive and polar surface energy of graphenes and carbon fibers as well their Lewis acid-base constants by introducing the coupling amphoteric constant of materials. The London dispersive and polar acid-base surface energies, the free energy of adsorption, the polar enthalpy and entropy, and the Lewis acid-base constants of graphenes and carbon materials are determined. It is shown that graphene exhibited the highest values of London dispersive surface energy, polar surface energy, and Lewis acid-base constants. The highest characteristics of graphene justify its great potentiality and uses in many industrial applications.

Effect of Tacticity on London Dispersive Surface Energy, Polar Free Energy and Lewis Acid-Base Surface Energies of Poly Methyl Methacrylate by Inverse Gas Chromatography

This research was devoted to study the effect of the tacticity on the surface physicochemical properties of PMMA. (1) Background: The determination of the surface free energy of polymers is generally carried out by inverse gas chromatography (IGC) at infinite dilution. The dispersive, polar and surface acid-base properties of PMMA at different tacticities were obtained via IGC technique with the help of the net retention time and volume of adsorbed. (2) Methods: The London dispersion equation was used to quantify the polar free energy of adsorption, while the London dispersive surface energy γsd(T) of PMMAs was determined using the thermal model. (3) Results: The results showed non-linear variations of γsd(T) of atactic, isotactic, and syndiotactic PMMAs with three maxima characterizing the three transition temperatures of PMMAs. The obtained values of the enthalpic and entropic Lewis’s acid-base parameters showed that the basicity of the atactic PMMA was about four times larger than its acidity. (4) Conclusions: A large difference in the behavior of the various PMMAs was proven in the different values of the polar acid and base surface energies of the three PMMAs with an important effect of the tacticity of PMMA on its acid-base surface energies.

The Effect of Temperature on the London Dispersive and Lewis Acid-Base Surface Energies of Polymethyl Methacrylate Adsorbed on Silica by Inverse Gas Chromatography

Inverse gas chromatography at infinite dilution was used to determine the surface thermodynamic properties of silica particles and PMMA adsorbed on silica, and more particularly, to quantify the London dispersive energy γsd, the Lewis acid γs+, and base γs− polar surface energies of PMMA/silica composites as a function of the temperature and the recovery fraction θ of PMMA. The polar acid-base surface energy γsAB and the total surface energy of the different composites were then deduced as a function of the temperature. In this paper, the Hamieh thermal model was used to quantify the surface thermodynamic energy of polymethyl methacrylate (PMMA) adsorbed on silica particles at different recovery fractions. A comparison of the new results was carried out with those obtained by applying other molecular models of the surface areas of organic molecules adsorbed on the different solid substrates. An important deviation of these molecular models from the thermal model was proved. The determination of γsd, γs+, γs−, and γsAB of PMMA in both the bulk and adsorbed phases showed an important non-linearity variation of these surface parameters as a function of the temperature. The presence of maxima in the curves of γsd(T) highlighted the second-order transition temperatures in PMMA showing beta-relaxation, glass transition, and liquid–liquid temperatures. These three transition temperatures depended on the adsorption rate of PMMA on silica. The proposed method gave a new relation between the recovery fraction of PMMA and its London dispersive energy, showing an important effect of the temperature on the surface energy parameters of the adsorption of PMMA on silica. A universal equation relating γsd(T,θ) of the systems PMMA/silica to the recovery fraction and the temperature was proposed.

Surface Thermodynamic Properties of Poly Lactic Acid by Inverse Gas Chromatography.

Poly lactic acid (PLA) is one of the most commonly used bio-derived thermoplastic polymers in 3D and 4D printing applications. The determination of PLA surface properties is of capital importance in 3D/4D printing technology. The surface thermodynamic properties of PLA polymers were determined using the inverse gas chromatography (IGC) technique at infinite dilution. The determination of the retention volume of polar and non-polar molecules adsorbed on the PLA particles filling the column allowed us to obtain the dispersive, polar, and Lewis's acid-base surface properties at different temperatures from 40 °C to 100 °C. The applied surface method was based on our recent model that used the London dispersion equation, the new chromatographic parameter function of the deformation polarizability, and the harmonic mean of the ionization energies of the PLA polymer and organic molecules. The application of this new method led to the determination of the dispersive and polar free surface energy of the adsorption of molecules on the polymeric material, as well as the glass transition and the Lewis acid-base constants. Four interval temperatures were distinguished, showing four zones of variations in the surface properties of PLA as a function of the temperature before and after the glass transition. The acid-base parameters of PLA strongly depend on the temperature. The accurate determination of the dispersive and polar surface physicochemical properties of PLA led to the work of adhesion of the polar organic solvents adsorbed on PLA. These results can be very useful for achieving reliable and functional 3D and 4D printed components.

Understanding the dynamic rheological property of cement paste blended with steel slag powder: From interparticle force and physico-chemical parameters of view

The blending of steel slag powder with cement can mitigate the carbon footprint of cementitious composites. The rheological properties of cement pastes are well known to be related to interparticle forces. However, the magnitude of the interparticle force depends on many physico-chemical factors. The influence of various factors on interparticle forces is not yet clear, making it difficult to control the rheological properties. In this paper, the interparticle force of steel slag powder blended cement paste was quantified and its relationships with dynamic rheological properties and basic physico-chemical parameters were explored. By means of this, the interparticle force was confirmed to could explain the effect of steel slag powder on the dynamic rheological properties of cement paste within 1 h. Moreover, how physico-chemical parameters affect the interparticle forces was clarified. A cement paste with large particle size and apolar surface energy, as well as small potential square, Debye length and small polar surface energy, can exhibit large interparticle force and high dynamic yield stress and plastic viscosity. A simple formula calculating interparticle force from basic parameters was proposed, which is believed to effectively and practically regulate the interparticle force. The relationships between interparticle forces, physico-chemical parameters, and rheological properties provide an effective reference for regulating the dynamic rheological properties of cement paste through fundamental parameters.

New Progress on London Dispersive Energy, Polar Surface Interactions, and Lewis's Acid-Base Properties of Solid Surfaces.

The determination of the polar surface free energy, polar properties, and Lewis's acid base of solid materials is of capital importance in many industrial processes, such as adhesion, coatings, two-dimensional films, and adsorption phenomena. (1) Background: The physicochemical properties of many solid particles were characterized during the last forty years by using the retention time of injected well-known molecules into chromatographic columns containing the solid substrates to be characterized. The obtained net retention time of the solvents adsorbed on the solid, allowing the determination of the net retention volume directly correlated to the specific surface variables, dispersive, polar, and acid-base properties. (2) Methods: Many chromatographic methods were used to quantify the values of the different specific surface variables of the solids. However, one found a large deviation between the different results. In this paper, one proposed a new method based on the London dispersion equation that allowed the quantification of the polar free energy of adsorption, as well as the Lewis's acid-base constants of many solid surfaces. (3) Results: The newly applied method allowed us to obtain the polar enthalpy and entropy of adsorption of polar model organic molecules on several solid substrates, such as silica, alumina, MgO, ZnO, Zn, TiO2, and carbon fibers. (4) Conclusions: our new method based on the separation between the dispersive and polar free surface energy allowed us to better characterize the solid materials.

Review of Systematic Tendencies in (001), (011) and (111) Surfaces Using B3PW as Well as B3LYP Computations of BaTiO3, CaTiO3, PbTiO3, SrTiO3, BaZrO3, CaZrO3, PbZrO3 and SrZrO3 Perovskites.

We performed B3PW and B3LYP computations for BaTiO3 (BTO), CaTiO3 (CTO), PbTiO3 (PTO), SrTiO3 (STO), BaZrO3 (BZO), CaZrO3 (CZO), PbZrO3 (PZO) and SrZrO3 (SZO) perovskite neutral (001) along with polar (011) as well as (111) surfaces. For the neutral AO- as well as BO2-terminated (001) surfaces, in most cases, all upper-layer atoms relax inwards, although the second-layer atoms shift outwards. On the (001) BO2-terminated surface, the second-layer metal atoms, as a rule, exhibit larger atomic relaxations than the second-layer O atoms. For most ABO3 perovskites, the (001) surface rumpling s is bigger for the AO- than BO2-terminated surfaces. In contrast, the surface energies, for both (001) terminations, are practically identical. Conversely, different (011) surface terminations exhibit quite different surface energies for the O-terminated, A-terminated and BO-terminated surfaces. Our computed ABO3 perovskite (111) surface energies are always significantly larger than the neutral (001) as well as polar (011) surface energies. Our computed ABO3 perovskite bulk B-O chemical bond covalency increases near their neutral (001) and especially polar (011) surfaces.

Polar and dispersive surface tension components of water-guanidinium chloride (Gdmcl) binary mixtures

Interfacial interaction of water with guanidinium chloride (GdmCl) is crucial to understanding protein solubility and denaturing mechanism. However, molecularly resolved parameters such as polar and dispersive surface energy components of water-GdmCl mixtures remain unknown. Here, we developed a method to determine water-GdmCl mixture surface tension and its components using four different substrates including polydimethylsiloxane (PDMS), silicone, polyethylene, and polystyrene. Results show all six combinations, PDMS-silicone, PDMS-polystyrene, PDMS-polyethylene, silicone-polyethylene, silicone-polystyrene, and polyethylene-polystyrene can estimate similar trend of total surface tension, polar and dispersive components with respect to salt concentration changes. Silicone-polyethylene pairs yield the most accurate surface tension compared to others because silicone and polyethylene have large distinctive surface energy differences. Results show that polar components increase from 51 mJ/m2 to 64 mJ/m2 when salt concentration increases; dispersive components decrease from 21 mJ/m2 to 15 mJ/m2 when salt concentration increases. Total surface tension increases from 72.8 mJ/m2 to 78.1 mJ/m2 when GdmCl increases from 0% to 40 wt%. The results of this study can elucidate molecular interaction between water and GdmCl.

Amido bisphosphonic acid as anchoring agent and photopolymerization initiator onto zirconium oxide surface

The surface modification of metal oxides by grafting an organic molecule allows the development of new specific properties on demand. In this work, we demonstrate the modification of the Yttria Tetragonal Zirconia Polycrystal (Y-TZP), which is a ceramic widely used in dental implantology, by polymer grafting of the surface in a three-steps protocol for tuning the wetting properties. The first step involved the preparation of zirconia pellet by sintering followed by their surface activation. In the second step, the organic initiator bearing a tertiary amine such as the N,N-dimethylamino group capable of initiating a radical photopolymerization reaction, was grafted onto the surface through a bisphosphonic acid functionality. In the last step, two monomers, namely methyl methacrylate and styrene, were photopolymerized on the zirconia surface by blue light irradiation.The chemical steps were monitored and characterized by X-ray photoelectron spectroscopy (XPS), spectroscopic ellipsometry (SE) and Atomic Force Microscopy (AFM). Wetting properties to different polar and nonpolar liquids and surface energies calculated with the Van Oss theory were found to vary systematically depending on the type of functionalization and grafting. This methodology is very promising for surface tuning of the dental ceramic.

A renewable lignin-based thermoplastic adhesive for steel joining

Adhesive bonding of metals has become increasingly relevant in recent years due to the demand for reducing weight and improving performance in structural applications such as automobiles and aerospace. We developed renewable thermoplastic adhesives from technical organosolv lignin isolated from hardwood biomass and acrylonitrile butadiene co-polymer rubber (NBR) for joining steel substrates. NBR33, NBR41 and NBR51 with acrylonitrile molar ratios of 33, 41 and 51%, respectively, were blended with lignin to form two-phase thermoplastic adhesives, and their adhesion, viscoelastic and surface properties were measured. Lignin content in the compositions were varied, ranging from 40% to 80% (w/w), to alter toughness, stiffness, and surface energy characteristics of the material. Better interaction or reactivity between the lignin and NBR phases was observed with greater nitrile content in NBR, leading to greater modulus and stiffness of the adhesive. Simultaneously, increasing the proportion of lignin reduced toughness and improved stiffness, with the highest adhesive strength of 13.1 MPa measured in a 60% lignin loading ratio with NBR51. Surface energy measurements revealed that total surface energy (sum of polar and dispersive surface energy) raised with lignin loading, suggesting that both surface energy and matrix strength play a critical role in the adhesive properties of the synthesized materials. A finite element-based cohesive zone model (CZM) was developed and implemented to study the failure strength of the adhesively bonded joint. This study demonstrates the viability of lignin as a valuable building block for adhesives, not only due to its inherent chemical structure and rigidity, but also for its surface energy characteristics.

Modeling liquid penetration into porous materials based on substrate and liquid surface energies

HypothesisThe widely used Lucas-Washburn (LW) equation depends on the contact angle as the driving force for liquid penetration. However, the contact angle depends on both, the liquid and the substrate. It would be desirable to predict the penetration into porous materials, without the requirement to measure the solid–liquid interaction. Here, we propose a novel modeling approach for liquid penetration from mutually independent substrate- and liquid properties. For this purpose, the contact angle in the LW-equation is replaced by polar and dispersive surface energies, utilizing the theories of Owens-Wendt-Rabel-Kaelble (OWRK), Wu, or van Oss, Good, Chaudhury (vOGC). ExperimentsThe proposed modelling approach is validated exhaustively by measuring penetration speed for 96 substrate-liquid pairings and comparing the results to model predictions based on literature- and measured data. FindingsLiquid absorption is predicted very well (R2 = 0.8–0.9) with all three approaches, spanning a wide range of penetration speed, substrate- and liquid surface energy, viscosity, and pore size. The models for liquid penetration without measurement of solid–liquid interaction (contact angle) performed well. Modeling calculations are entirely relying on physical data of the solid and the liquid phase (surface energies, viscosity and pore size), which can be measured or retrieved from databases.

Investigating the Effects of Nitric Acid Treatments on the Properties of Recycled Carbon Fiber.

In this study, the chemical state change of recycled carbon fiber (rCF) surfaces and the mechanism of the oxygen functional groups according to nitric acid treatment at various times and temperatures were investigated to upcycle the carbon fiber recovered from used carbon composite. When treated with nitric acid at 25 °C, the carbon fiber surface demonstrated the same tensile properties as untreated carbon fiber (CF) for up to 5 h, and the oxygen functional group and polar surface energy of C-O (hydroxyl group) and C=O (carbonyl group) increased slightly compared to the untreated CF up to 5 h. On the other hand, at 100 °C, the tensile properties slightly decreased compared to untreated CF up to 5 h, and the amount of C-O and C=O decreased and the amount of O=C-O (lactone group) started to increase until 1 h. After 1 h, the amount of C-O and C=O decreased significantly, and the amount of O=C-O increased rapidly. At 5 h, the amount of oxygen functional groups increased by 92%, and the polar surface energy increased by 200% compared to desized CF. It was determined that the interfacial bonding force increased the most because the oxygen functional group, O=C-O, increased greatly at 100 °C and 5 h.

Polar-surface-dominated zigzag GaN nanowires with alternate H2 and O2 evolution sites for photocatalytic overall water splitting

Photocatalytic overall water splitting is an ideal green technology to produce the clean and renewable hydrogen energy. Herein, high crystalline zigzag GaN nanowires (NWs) are successfully synthesized through an Au-catalyzed chemical vapor deposition process. The single-crystalline zigzag nanowire is a polar-surface-dominated nanostructure composed of Ga and N atoms alternately as a result of the inherent surface atomic termination and polar charges. Compared with the non-polar-dominated smooth-surfaced nanowires, the zigzag nanowires attain multifold H2 and O2 evolutions in the presence of respective sacrificial reagents. More importantly, the zigzag nanowires realize the stoichiometric overall pure water splitting, due to the synergistic effect of the internal electric field between Ga-terminated and N-terminated facets that drives the spatial charge separation, the high charge mobility and polar surface energy. This work suggests that constructing polar surface on one-dimensional nanomaterial with spatially separated H2 and O2 evolution sites could be employed as a new crystal engineering strategy for designing efficient photocatalysts towards overall water splitting.

The Surface Energy of Hydrogenated and Fluorinated Graphene

The surface energy of graphene and its chemical derivatives governs fundamental interfacial interactions like molecular assembly, wetting, and doping. However, quantifying the surface energy of supported two-dimensional (2D) materials, such as graphene, is difficult because (1) they are so thin that electrostatic interactions emanating from the underlying substrate are not completely screened, (2) the contribution from the monolayer is sensitive to its exact chemical state, and (3) the adsorption of airborne contaminants, as well as contaminants introduced during transfer processing, screens the electrostatic interactions from the monolayer and underlying substrate, changing the determined surface energy. Here, we determine the polar and dispersive surface energy of bare, fluorinated, and hydrogenated graphene through contact angle measurements with water and diiodomethane. We accounted for many contributing factors, including substrate surface energies and combating adsorption of airborne contaminants. Hydrogenating graphene raises its polar surface energy with little effect on its dispersive surface energy. Fluorinating graphene lowers its dispersive surface energy with a substrate-dependent effect on its polar surface energy. These results unravel how changing the chemical structure of graphene modifies its surface energy, with applications for hybrid nanomaterials, bioadhesion, biosensing, and thin-film assembly.

Order−disorder interfaces in a graphitic carbon nitride-nanoclay composite for improved photodynamic antibiotics

Antibiotic-resistant microorganisms are a threat to human health. Despite efforts to treat bacterial and fungal infections with photodynamic therapy, it suffers from low light absorption and low singlet oxygen yield. Here, we observe order-disorder interfaces in graphitic carbon nitride (g-C3N4) modified by kaolinite nanoclay via polar interactions, decreasing the band gap of g-C3N4. The polar interactions originate from interactions between the basic amine surface moieties and hydrogen-bonding motifs of g-C3N4 and the hydroxyl groups on the nanoclay surface. Surface free energy theory demonstrates that the electron-acceptor displayed by the nanoclay surface could form a couple with g-C3N4 due to its nucleophilic property. The polar interactions accelerate electron transfer, and the nanoclay surface functions as an electron sink due to its polar surface and free energy. This promotes spin-orbit coupling and intersystem crossing resulting in a higher singlet oxygen yield, even in the dark. The graphitic carbon nitride-kaolinite composite showed improved and faster would healing in rat animal models.

Experimental and numerical studies of polyamide 11 and 12 surfaces modified by atmospheric pressure plasma treatment

Polyamide 11 and 12 (PA11 and PA12) have been applicable in various industries, including automotive, oil and gas, and sporting goods, over the past 70 years. Although they have good dyeability, their adhesion to other materials is limited due to relatively poor surface properties, which can be promoted by good wettability and high surface energy. This study aims to improve the surface properties of PA11 and PA12 by employing the advanced method of Atmospheric Pressure Plasma Torch (APPT) treatment. In this regard, the adhesion strengths of four commercially available adhesives were evaluated with the pull-off test on PAs plates before and after APPT treatment. The numerical simulation of this test was carried out in commercial finite element software using a cohesive zone model (CZM) to predict the fracture of adhesively bonded joints. Moreover, the modified PAs were analyzed using XPS, DSC, ATR-FTIR, optical profilometer and surface energy measurement. The results indicated that the surface properties, including wettability, polar surface energy and adhesion bonding, improved by employing the plasma treatment on PAs surfaces. The numerical simulation outcomes showed that the pull-off test might be a viable alternative to determine the CZM laws for fracture mode I.

Interfacial properties of liquid metal immersed in various liquids

HypothesisWhen gallium-based liquid metal (LM) droplets are injected through different solvent media, the oxygen solubility of the environment influences the droplet eccentricity. The formation of an oxide membrane in solvents can determine whether a bulk-scale droplet behaves in a liquidlike or solidlike manner. In the case of LM emulsions, the solvent’s oxygen solubility leads to varying degrees of organic solvent adsorption. The adsorption of solvent molecules changes the surface energy of the oxide layer. ExperimentsThe pinch-off frames of LM droplets immersed in liquids with differing oxygen solubility were captured using a high-speed camera. Through scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), the surface composition of micro and nanoscale LM emulsions in different solvents was investigated. The van Oss-Good model was implemented to determine the polar and nonpolar surface energy components of LM layers with adsorbates. FindingsPear-shaped LM droplets displaying solidlike behavior are created when the mole fraction of dissolved oxygen in the ambient solution is above approximately 2.43×10-4. For LM emulsions sonicated in organic solvents, Carbon/Oxygen (C/O) and Carbon/Gallium (C/Ga) atomic percent ratios display an increasing trend with increasing oxygen solubility. The nonpolar component of surface energy shows a logarithmic relationship with the oxygen solubility of the solvent used to treat the LM layer. The polar component of surface energy is more susceptible to the chemical properties of the solvent.

Deciphering the Reduced Loss in High Fill Factor Inverted Perovskite Solar Cells with Methoxy-Substituted Poly(Triarylamine) as the Hole Selective Contact.

A dopant-free polymeric hole selective contact (HSC) layer is ubiquitous for stable perovskite solar cells (PSCs). However, the intrinsic nonwetting nature of the polymeric HSC impedes the uniform spreading of the perovskite precursor solution, generating a terrible buried interface. Here, we dexterously tackle this dilemma from the perspective of dispersive and polar component surface energies of the HSC layer. A novel triarylamine-based HSC material, poly[bis(4-phenyl)(2,4-dimethoxyphenyl)amine] (2MeO-PTAA), was designed by introducing the polar methoxy groups to the para and ortho positions of the dangling benzene. These nonsymmetrically substituted electron-donating methoxy groups enhanced the polar components of surface energy, allowing more tight interfacial contact between the HSC layer and perovskite and facilitating hole extraction. When utilized as the dopant-free HSC layer in inverted PSCs, the 2MeO-PTAA-based device with CH3NH3PbI3 as the absorber exhibited an encouraging power conversion efficiency of 20.23% and a high fill factor of 84.31% with negligible hysteresis. Finally, a revised detailed balance model was used to verify the drastically lessened surface defect-induced recombination loss and shunt resistance loss in 2MeO-PTAA-based devices. This work demonstrates a facile and efficient way to modulate the buried interface and shed light on the direction to further improve the photovoltaic performance of inverted PSCs with other types of perovskites.

Vertical Alignment of Liquid Crystals on Phenylphenoxymethyl-Substituted Polystyrene-PS Derivatives Structurally Similar to LC Molecules.

A series of polystyrene derivatives containing precursors of liquid crystal (LC) molecules, phenylphenoxymethyl-substituted polystyrene (PPHE#; # = 5, 15, 25, 50, 75, and 100)—where # is the molar content of 4-phenylphenol using polymer modification reactions—were prepared in order to examine the effect of the polymer film, which possess similar LC molecular structure on the LC alignment properties. It was found that the Tg values of the PPHE# were higher than 100 °C due to their aromatic structure in the biphenyl-based PHE moiety. The LC cells fabricated with PPHE5 and PPHE15 films exhibited planar LC alignment. Conversely, LC molecules showed a vertical alignment in LC cells made using the polymer films with phenylphenoxymethyl side groups in the range of 25–100 mol %. The polar surface energies on the PPHE# films can be associated with the vertical LC alignment on the PPHE# films. For example, vertical LC alignment was exhibited when the polar surface energy of the polymer films was less than approximately 4.2 mJ/m2. Aligning stability was observed at 200 °C and UV irradiation of 20 J/cm2 for LC cells made using the PPHE100 film. Therefore, it was found that biphenyl, one of the LC precursors, modified polystyrene derivatives and can produce a next-generation vertical LC alignment system.