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Yasushi Okamoto

Bio: Yasushi Okamoto is an academic researcher from Denso. The author has contributed to research in topics: Epoxy & Adhesive. The author has an hindex of 3, co-authored 11 publications receiving 34 citations.

Papers
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Journal ArticleDOI
09 Jul 2015-Polymer
TL;DR: In this paper, an ordered topography was fabricated on a spin-coated thin film of a polymethacrylate-based copolymer with polymerization initiating sites [P(MMA-co-BIEM)] by NI.

16 citations

Journal ArticleDOI
TL;DR: In this article, the microscopic dynamics in the curing process of a catalytic epoxy resin were investigated under different temperature conditions utilizing X-ray photon correlation spectroscopy, which revealed that the temperature conditions greatly affected the dynamical heterogeneity and cross-linking density of the cured materials.
Abstract: Epoxy resin is indispensable for modern industry because of its excellent mechanical properties, chemical resistance, and excellent moldability. To date, various methods have been used to investigate the physical properties of the cured product and the kinetics of the curing process, but its microscopic dynamics have been insufficiently studied. In this study, the microscopic dynamics in the curing process of a catalytic epoxy resin were investigated under different temperature conditions utilizing X-ray photon correlation spectroscopy. Our results revealed that the temperature conditions greatly affected the dynamical heterogeneity and cross-linking density of the cured materials. An overview of the microscopic mechanism of the curing process was clearly presented through comparison with the measurement results of other methods, such as 1H-pulse nuclear magnetic resonance spectroscopy. The quantification of such heterogeneous dynamics is particularly useful for optimizing the curing conditions of various materials to improve their physical properties.

10 citations

Journal ArticleDOI
TL;DR: The morphology of ordered heterojunction organic photovoltaics (OPVs) interfaces was evaluated using synchrotron radiation small angle X-ray scattering and grazing incidence Xray diffraction as mentioned in this paper.
Abstract: The morphology of ordered heterojunction organic photovoltaics (OHJ-OPVs) interfaces was evaluated using synchrotron radiation small angle X-ray scattering and grazing incidence X-ray diffraction. [6,6']-phenyl C61-butyric acid methyl ester (PCBM) was deposited on the line/space patterned poly(3-hexylthiophene-2,5-diyl) (P3HT) thin film fabricated by nano-imprinting. After deposition of the PCBM film, the P3HT thin film retained the rectangular edge features of the imprinted mold, with some Gaussian broadening due to interdiffusion and partial phase mixing at the P3HT/PCBM interface. The P3HT main chains were oriented vertically in the nano-imprinted line pattern and showed π–π stacking along the line direction. PCBM nano-crystals exist throughout the OHJ-OPV thin film.

5 citations

Patent
18 Jun 2009
TL;DR: In this paper, a method for adhering polyacetal resin molded products to an adherend by an adhesive comprises: a step of treating the surface of the polyacetel resin molded product to generate hydroxyl groups on the surface and to react the generated hydroxym groups with an organosilicone compound.
Abstract: PROBLEM TO BE SOLVED: To provide an adhering method of a polyacetal resin molded product for expressing an excellent adhesiveness while maintaining the original property of the polyacetal resin. SOLUTION: The method for adhering the polyacetal resin molded product to an adherend by an adhesive comprises: a step of treating the surface of the polyacetal resin molded product to generate hydroxyl groups on the surface of the polyacetal resin molded product and to react the generated hydroxyl groups with an organosilicone compound; and a step of expressing the adhesiveness by an interaction between the functional groups of the organosilicone compound reacted with the hydroxyl groups generated on the surface of the polyacetal resin molded product and the functional groups of the adhesive. COPYRIGHT: (C)2009,JPO&INPIT

4 citations

Patent
06 Sep 2006
TL;DR: In this paper, an epoxy-based adhesive is applied to polyester resins and an oxygen-containing functional group is formed in an area in thickness of 3-10 nm from the polyester surface.
Abstract: PROBLEM TO BE SOLVED: To provide a resin bonding method for bonding a polyester resin to an epoxy-based adhesive, having excellent adhesiveness. SOLUTION: The method is for bonding a polyester resin 2 to an epoxy-based adhesive 3. The epoxy-based adhesive 3 is bonded to an adhesive surface 202 after surface treatment for providing the surface 201 of the polyester resin 2 with an oxygen-containing functional group. The oxygen-containing functional group is a hydroxy group, a carbonyl group or a carboxy group. The method is for bonding the polyester resin 2 after annealing treatment to the epoxy-based adhesive 3. The oxygen-containing functional group is formed in an area in thickness of 3-10 nm from the surface 201 of the polyester resin 2. COPYRIGHT: (C)2008,JPO&INPIT

3 citations


Cited by
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Journal ArticleDOI
TL;DR: The generation of polymer brushes by surface-initiated controlled radical polymerization (SI-CRP) techniques has become a powerful approach to tailor the chemical and physical properties of interfaces and has given rise to great advances in surface and interface engineering as mentioned in this paper.
Abstract: The generation of polymer brushes by surface-initiated controlled radical polymerization (SI-CRP) techniques has become a powerful approach to tailor the chemical and physical properties of interfaces and has given rise to great advances in surface and interface engineering. Polymer brushes are defined as thin polymer films in which the individual polymer chains are tethered by one chain end to a solid interface. Significant advances have been made over the past years in the field of polymer brushes. This includes novel developments in SI-CRP, as well as the emergence of novel applications such as catalysis, electronics, nanomaterial synthesis and biosensing. Additionally, polymer brushes prepared via SI-CRP have been utilized to modify the surface of novel substrates such as natural fibers, polymer nanofibers, mesoporous materials, graphene, viruses and protein nanoparticles. The last years have also seen exciting advances in the chemical and physical characterization of polymer brushes, as well as an ev...

681 citations

Journal ArticleDOI
TL;DR: In this article, the anti-fouling mechanism was considered on the basis of the wetting, lubrication, hydrated chain dimension and hydrogen-bonding structure of hydrated water in the polyelectrolyte brushes.
Abstract: Nature-inspired material design concepts and recent progress on anti-fouling polymer materials are reviewed, and our recent researches on anti-fouling studies with polymer brushes are summarized. Zwitterionic polyelectrolyte brush immobilized surfaces represent significant anti-fouling for bio-macromolecules, oil foulants, marine fouling organisms and pipeline foulants. The anti-fouling mechanism was considered on the basis of the wetting, lubrication, hydrated chain dimension and hydrogen-bonding structure of hydrated water in the polyelectrolyte brushes.

124 citations

Journal ArticleDOI
TL;DR: Layer-by-layer (LL) processes are widely used in the fabrication of organic solar cells (OSCs) as mentioned in this paper, where the charge carriers dissociated from excitons at the donor-acceptor interface are confined to each phase so bimolecular recombination losses can be reduced.
Abstract: Layer-by-layer (LL) processes, i.e., sequential deposition of different active layers, are widely used in the fabrication of organic solar cells (OSCs). Recently, LL vacuum deposition and LL solution processes have attracted considerable attention. LL processing presents some advantages over the blend method: a) donor and acceptor layers can be easily and independently controlled and optimized; b) the charge carriers dissociated from excitons at the donor–acceptor interface are confined to each phase, so bimolecular recombination losses can be reduced; c) bilayer geometries enable an easier way for understanding the physical processes taking place at the donor–acceptor interface; d) desired vertical phase separation for charge extraction can be obtained through changing the sequence of donor and acceptor deposition. This report summarizes the recent developments of LL processed OSCs. The remaining problems and challenges, and the key research direction in near future are discussed.

83 citations

Journal ArticleDOI
TL;DR: It is believed that the prepared fluorinated copolymers are potential candidates to replace the fluoroalkylated polymers with long perfluorinated chains in nonstick and self-cleaning applications in the authors' daily life.
Abstract: Because the emission of perfluorooctanoic acid (PFOA) was completely prohibited in 2015, the widely used poly- and perfluoroalkyl substances with long perfluoroalkyl groups must be substituted by environmentally friendly alternatives. In this study, one kind of potential alternative (i.e., fluorinated polymers with short perfluorobutyl side chains) has been synthesized from the prepared monomers {i.e., (perfluorobutyl)ethyl acrylate (C4A), (perfluorobutyl)ethyl methacrylate (C4MA), 2-[[[[2-(perfluorobutyl)]sulfonyl]methyl]amino]ethyl acrylate (C4SA), and methacrylate (C4SMA)}, and the microstructure, super wetting performance, and applications of the synthesized fluorinated polymers were systematically investigated. The thermal and crystallization behaviors of the fluoropolymer films were characterized by differential scanning calorimetry and wide-angle X-ray diffraction analysis, respectively. Dynamic water-repellent models were constructed. The stable low surface energy and dynamic water- and oil-repell...

66 citations

Journal ArticleDOI
Yanli Qi1, Zhangbin Yang1, Tingting Chen1, Yulin Xi1, Jun Zhang1 
TL;DR: In this paper, a super-hydrophobic surface was successfully obtained via the combination of specific micro/nano-structures and chemical modification, where the surface was covered with many more micro-nano structures and organic groups.

49 citations