ABSTRACT
Organic-inorganic materials have attracted attention because of the advantages of both organic and inorganic resins. Among their disadvantages, hard coating films made of organic-inorganic mixtures of resins have opacity and interface peeling problems because of organic-inorganic phase separation and surface segregation of inorganic resins. Although an organic-inorganic gradient-structured material comprising an inorganic-rich domain at the air interface and an organic-rich domain at the organic substrate has the potential to solve these problems, the fabrication of a gradient-structured material has not yet been achieved. Here, we describe the fabrication of an organic-inorganic gradient film by impeding the movement of organic and inorganic resins through radical photopolymerization of organic and inorganic oligomers. Moreover, we successfully enhanced gouge hardness by cross-linking with photobase-catalyzed sol-gel reactions of inorganic resins at the air interface. As a result, the organic-inorganic gradient coating contributed excellent gouge hardness (pencil hardness >9H), adhesion to an organic substrate such as polycarbonate, and transparency (visible light transmittance >99%T). In addition, we demonstrated that the formation of organic-inorganic gradient structures is dominated by the surface free energy and viscosity of each resin. Achieving a gradient structure required a significant difference in surface free energy (>20 mJ/m2) and high mixture viscosity (>65 mPa·s).
ABSTRACT
Ionic interactions in ionic polymers, such as ionomers, polyelectrolytes, and polyampholytes, contribute to toughness in systems with high mobility and active ion dynamics, such as hydrogels and elastomers. However, it remains challenging to toughen rigid polymers through ionic interactions without lowering their elastic modulus through plasticization. Here, we present a strategy for toughening without sacrificing the elastic modulus by combining a comb polymer with bulky ammonium counterions. We designed and synthesized ionic comb polymers with oligoethylene glycol side chains and carboxylic acids in each monomer unit of the polynorbornene backbone, neutralized by trialkylamines, ranging from ethyl to octyl. The counterion size in ionic comb polymers influenced the mechanical properties of tensile testingânot the elongation at break and the elastic modulus but the ultimate strength and toughness. The ionic comb polymer containing heptylammonium counterions displayed the highest toughness of 77 MJ m-3. Tensile studies at various strain rates demonstrated a rate-dependent difference between heptyl- and octylammonium counterions. This result suggests that the heptylammonium counterion acted as a sacrificial bond by providing a moderate dissociation rate that was slightly slower than that of the octylammonium counterion, leading to toughening.
ABSTRACT
A cross-linking reagent having two adenine units was mixed with polymers bearing thymine units to form adhesive materials utilizing both intermolecular hydrogen bonding and in situ formation of covalent bonds. In the case of 58 mol % of adenine units relative to thymine units, formation of intermolecular hydrogen bonds because of a thymine-adenine interaction was observed at room temperature using FT-IR. The peel strength became weak with heating above 60 °C, indicating breakup of intermolecular bonds between thymine and adenine units. On the other hand, UV-vis spectral measurements showed that heating at 80 °C with 254 nm light irradiation facilitated the photodimerization reaction between thymine units even in the presence of adenine cross-linking reagents. This result was consistent with a large value for the peel strength (6.5 N/10 mm) after the dual treatment, heating at 80 °C with 400 mJ/cm2 of UV irradiation.
ABSTRACT
Epoxy resins are important thermosetting resins widely used in industrial applications. Though imidazoles as curing agents have attracted particular attention because of their high reactivity in chain polymerizations with epoxides, polymerization of a liquid epoxy resin containing imidazoles proceeds gradually even at room temperature. This makes it difficult to use such mixtures as one-component materials for industrial applications. To improve the shelf life of the mixutures, we have developed a very simple and powerful thermal latent curing agent, a 2-(2-hydroxyphenyl)imidazole derivative (1), having an intramolecular hydrogen bond between the phenolic hydroxyl group and the nitrogen atom of the imidazole ring, leading to suppression of reactivity of 1 toward epoxy resins at room temperature. It was confirmed that high reactivity of 1 toward epoxy resins at 150 °C was based on breakage of the intramolecular hydrogen, whereas the epoxy resin composition showed long-term storage stability at room temperature.
ABSTRACT
We have developed a novel cinnamic acid-type photo-cleavable surfactant. This surfactant experiences photo-cleavage through UV-induced cyclization in aqueous solutions. The photo-cleavage not only reduces its capabilities as a surfactant but also yields two functional materials including a coumarin derivative and an aminated polyoxyethylene compound. This means that the photo-cleavable surfactant synthesized in this study is a photo-responsive function-exchangeable material. In our current study, we have characterized the photo-cleavable behavior that occurs in aqueous solutions and a resulting change in interfacial properties. The photo-cleavage induces an increased interfacial tension of a squalane/water interface and a decreased solubilization capability of the surfactant micelles.
