Physical Properties of Thermally Crosslinked Fluorinated Polyimide and Its Application to a Liquid Crystal Alignment Layer

This study demonstrated the use of a thermally crosslinked polyimide (PI) for the liquid crystal (LC) alignment layer of an LC display (LCD) cell. Polyamic acid was prepared using 4,4′-oxydianiline (ODA) and 4,4′-(hexafluoroisopropylidene) diphthalic anhydride (6FDA). The 6FDA−ODA-based polyimide (PI) prepared by the thermal cyclic dehydration of the polyamic acid (PAA) was soluble in various polar solvents. After forming a thin film by mixing trifunctional epoxide [4-(oxiran-2-ylmethoxy)-N,N-bis(oxiran-2-ylmethyl)aniline] with the 6FDA−ODA-based PAA, it was confirmed that thermal curing at −110 °C caused an epoxy ring opening reaction, which could result in the formation of a networked polyimide not soluble in tetrahydrofuran. The crosslinked PI film showed a higher rigidity than the neat PI films, as measured by the elastic modulus. Furthermore, based on a dynamic mechanical analysis of the neat PI and crosslinked PI films, the glass transition temperatures (Tgs) were 217 and 339 °C, respectively, which provided further evidence of the formation of crosslinking by the addition of the epoxy reagent. After mechanical rubbing using these two PI films, an LC cell was fabricated using an anisotropic PI film as an LC alignment film. LC cells with crosslinked PI layers showed a high voltage holding ratio and low residual direct current voltage. This suggests that the crosslinked PI has good potential for use as an LC alignment layer material in advanced LCD technologies that require high performance and reliability.

Effective Epoxidation of Fatty Acid Methyl Esters with Hydrogen Peroxide by the Catalytic System H3PW12O40/Quaternary Phosphonium Salts

Six quaternary phosphonium salts (QPSs) in combination with phosphotungstic heteropolyacid, H3PW12O40, were tested in the epoxidation of rapeseed oil fatty acid methyl esters with a hydrogen peroxide aqueous solution. The QPSs consisted of trihexyl(tetradecyl)phosphonium [P6], tributyl-tetradecylphosphonium [P4] or tetraoctylphosphonium [P8] cation and different anions—chloride (Cl−), bromide (Br−), tetrafluoroborate (BF4−), bis(trifluoromethylsulfonyl)amide (NTf2−), bis(2,4,4-trimethyl-pentyl)phosphinate (Phosf−). The influence of the kind of QPS and temperature on the epoxy number, iodine number, glycol content has been determined. The epoxidation was confirmed using Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance (NMR) and elemental analysis CHO. Two QPSs with a trihexyltetradecyphosphonium cation—[P6][Fosf] and [P6][Cl]—were selected as the most effective in the studied epoxidation process. The proposed kinetic model takes into consideration the two reactions, namely, epoxidation and epoxy ring opening involving the formation of hydroxyl groups. The rate constants and activation energies for epoxidation fatty acid methyl esters were determined.

Degradable branched polycationic systems are promising gene therapy vectors

Degradable branched polycationic systems have exhibited exceptional potential for nucleic acid delivery due to their good responsive degradability and exceptional transfection efficacy. We focused on current work on the development of ARP for nucleic acid delivery in this study. The results of numerous responsive degradable branching polycationic systems were assembled. For the synthesis of ARP, the typical amino-epoxy ring-opening procedure was primarily presented. For nucleic acid delivery, the properties of redox- and pH-responsive degradable branching systems were addressed. Despite great development, there are still a lot of barriers to overcome in this discipline. The step growth strategy is more convenient than the chain growth technique. However, the polydispersity index (PDI) of most branched polymers generated by the step growth process is relatively high, making biological investigations hard. As a result, regulating the batch-to-batch quality of branched polycations is important for the translation of ARP from laboratories to clinics. Furthermore, as diseases develop more complicated and treatment processes get more diversified, single-function nucleic acid carriers are increasingly unable to satisfy complicated needs. Nucleic acid carriers must be manufactured in a precise and multifunctional method. In nucleic acid-based therapy, branched polycations must have degradability, targeting capability, and multimodal therapeutic properties in addition to degradability. In the future, one problem will be how to develop degradable, targeted, and multifunctional branching polycations for nucleic acid delivery in a regulated manner. Degradable branching polycationic systems will have a substantial effect on nucleic acid delivery and will become key instruments for nucleic acid treatment as research improves and allied areas such as materials science and medicine improve quickly.

Reinforcement of Epoxy Resin by Additives of Amine-Functionalized Graphene Nanosheets

In this study, graphene oxide (GO) nanosheets were modified with an amine functional group to obtain amine-functionalized graphene (AMG) nanosheets and then blended with the aniline curing agent of bisphenol-A (BPA) epoxy resin to crosslink BPA epoxy resin. The AMG-blended curing agent and BPA epoxy resin formed an intermolecular hydrogen bond that was stronger than the π–π stacking force between benzene rings of graphene nanosheets. Therefore, AMG nanosheets exhibited excellent dispersion in the aniline curing agent. The amine group of AMG-blended curing agents and the epoxy functional group of BPA epoxy resin exhibited strong chemical activity and underwent crosslinking and polymerization. AMG nanosheets were mixed with BPA epoxy resin to form a crosslinked structure through the epoxy ring-opening polymerization of the resin. The mechanical properties of the epoxy resin nanocomposites were significantly improved by the added 1 wt.% AMG nanosheets. The tensile strength was enhanced by 98.1% by adding 1 wt.% AMG in epoxy. Furthermore, the impact resistance of the epoxy resin was enhanced by 124.4% after adding 2.67 wt.% of AMG nanosheets. Compared with other reinforced fillers, AMG nanosheets are very light and can therefore be used as nanocomposite materials in coating applications, the automotive industry, aerospace sheet materials, wind power generation, and other fields.

Hydrogenation of High Molecular Weight Bisphenol A Type Epoxy Resin BE503 in a Functional and Greener Solvent Mixture Using a Rh Catalyst Supported on Carbon Black

A functional greener solvent mixture containing water, isopropyl alcohol (IPA) and ethyl acetate with the ratio 10:20:70 (wt%) was found to accelerate hydrogenation of bisphenol A type epoxy resin BE503 with a molecular weight of 1500 through an on-water mechanism, and led to an increased H2 availability, due to high solubility of H2 in IPA. Different carbon-based supports were tested and VulcanXC72 was found as the best support among the tested carbon-based ones as it possessed the highest amount of electron deficient promoter, RhOx. The catalyst, Rh5/VulcanXC72-polyol, synthesized by the microwave assisted polyol method, yielded a 100% hydrogenation of aromatic rings with an epoxy ring opening below 20.0% at 50 °C and a H2 pressure of 1000 psi in 2.25 h. Intrinsic activation energies for the hydrogenation of aromatic rings and epoxy ring opening were experimentally estimated and a mechanism for the hydrogenation of BE503 was proposed, wherein the hydrogenation of aromatic rings and epoxy ring opening in BE503 proceeded simultaneously in parallel and in-series with parallel being the major pathway.

Tailored Crosslinking Process and Protective Efficiency of Epoxy Coatings Containing Glycidyl-POSS

Versatile product protective coatings that deliver faster drying times and shorter minimum overcoat intervals that enable curing at faster line speeds and though lower energy consumption are often desired by coating manufacturers. Product protective coatings, based on silsesquioxane-modified diglycidyl ether of bisphenol-A (DGEBA) epoxy resin, are prepared through a glycidyl ring-opening polymerization using dicyandiamide (DICY) as a curing agent. As silsesquioxane modifier serves the octaglycidyl-polyhedral oligomeric silsesquioxane (GlyPOSS). To decrease the operational temperature of the curing processes, three different accelerators for crosslinking are tested, i.e., N,N-benzyl dimethylamine, 2-methylimidazole, and commercial Curezol 2MZ-A. Differential scanning calorimetry, temperature-dependent FT-IR spectroscopy, and rheology allow differentiation among accelerators’ effectiveness according to their structure. The former only contributed to epoxy ring-opening, while the latter two, besides participate in crosslinking. The surface roughness of the protective coatings on aluminum alloy substrate decreases when the accelerators are applied. The scanning electron microscopy (SEM) confirms that coatings with accelerators are more homogeneous. The protective efficiency is tested with a potentiodynamic polarization technique in 0.5 M NaCl electrolyte. All coatings containing GlyPOSS, either without or with accelerators, reveal superior protective efficiency compared to neat DGEBA/DICY coating.