Ken Kojio

ORCID: 0000-0002-6917-7029
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About
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Research Areas
  • Polymer composites and self-healing
  • Polymer Nanocomposites and Properties
  • Polymer crystallization and properties
  • Polymer Surface Interaction Studies
  • Molecular Junctions and Nanostructures
  • Force Microscopy Techniques and Applications
  • Silicone and Siloxane Chemistry
  • Advanced Polymer Synthesis and Characterization
  • Block Copolymer Self-Assembly
  • Epoxy Resin Curing Processes
  • Fiber-reinforced polymer composites
  • biodegradable polymer synthesis and properties
  • Conducting polymers and applications
  • Synthesis and properties of polymers
  • Mechanical Behavior of Composites
  • Analytical Chemistry and Sensors
  • Polymer Science and Applications
  • Surface Modification and Superhydrophobicity
  • Advanced Sensor and Energy Harvesting Materials
  • Photopolymerization techniques and applications
  • Material Properties and Applications
  • Adhesion, Friction, and Surface Interactions
  • Structural Engineering and Vibration Analysis
  • Polymer Nanocomposite Synthesis and Irradiation
  • Polymer Foaming and Composites

Kyushu University
2016-2025

Interface (United States)
2025

Japan Graduate School of Education University
2024

Japan Science and Technology Agency
2024

Graduate School USA
2006-2019

Nagasaki University
2005-2014

University of Tsukuba
2012

Engineering (Italy)
2009

Faculty (United Kingdom)
2009

Materials Science & Engineering
2006-2008

Octadecyltrichlorosilane (OTS) and [2-(perfluorooctyl)ethyl]trichlorosilane (FOETS) monolayers their mixed monolayer were polymerized on a water subphase subsequently immobilized onto silicon wafer surface by covalent bonding. Atomic force microscopic (AFM) observation of the (OTS/FOETS) revealed formation phase-separated structure. Protein-adsorption behavior was investigated in situ basis an attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectroscopic flow cell method...

10.1163/156856298x00479 article EN Journal of Biomaterials Science Polymer Edition 1998-01-01

A series of eight aliphatic polycarbonate (PC) glycols with various methylene numbers (HO−[(CH2)mOC(═O)O]n−(CH2)m−OH, m = 3, 4, 5, 6, 7, 8, 9, and 10) were employed as a soft segment for synthesis polyurethane elastomers (PUEs). First all, viscosity, glass transition temperature, melting point, crystalline structure these new PC-glycols investigated. The PC-glycol-based PUEs synthesized using the PC-glycols, 4,4′-diphenylmethane diisocyanate, 1,4-butanediol by one-shot method. Differential...

10.1021/ma901317t article EN Macromolecules 2009-11-03

Polyurethane elastomers (PUEs) containing trans-1,4-bis(isocyanatomethyl)cyclohexane (1,4-H6XDI) have been synthesized by polymerizing 1,4-H6XDI with poly(oxytetramethylene) glycol and 1,4-butanediol. The molecular aggregation state mechanical properties of these PUEs compared those exhibited PUE analogues made MDI diols. hard segment chains in the 1,4-H6XDI-based are found to readily crystallize form strong hydrogen bonds due a high symmetry molecule. Consequently, exhibit well-organized...

10.1021/acs.macromol.6b02044 article EN Macromolecules 2017-01-20

A novel diisocyanate, 1,2-bis(isocyanate)ethoxyethane (TEGDI), whose backbone is ether bonds was used for the preparation of polyurethane elastomers (PUEs). 1,6-Hexamethylene diisocyanate (HDI) also as a control. The PUEs were prepared with either TEGDI or HDI, poly(oxytetramethylene) glycol (PTMG), and curing agent by prepolymer method. Differential scanning calorimetry, infrared spectroscopy, wide-angle X-ray diffraction revealed that phase separation network TEGDI-based much weaker...

10.1021/ma0359988 article EN Macromolecules 2004-03-27

Liquid crystal elastomers can vary their shape freely with no extra mechanical energy like liquids when deformed in the plane.

10.1126/sciadv.abe9495 article EN cc-by-nc Science Advances 2021-06-18

Organoclay, such as organo-modified montmorillonite (MMT), is one of the potential filler candidates in preparation epoxy nanocomposite adhesives for automotive and civil engineering industries. However, there no systematic research on effect organoclay reinforcement its adhesion fatigue behaviors shear loading. Here, single-lap joints (SLJs) stainless steel substrates bonded with epoxy/MMT adhesives, consisting diglycidyl ether bisphenol A poly(oxypropylene) diamine various weight contents...

10.1021/acsapm.1c00347 article EN ACS Applied Polymer Materials 2021-06-09

Molecular arrangement of polymerized n-octadecyltrichlorosilane (OTS, CH3(CH2)17SiCl3) monolayer transferred onto hydrophilic substrate by an upward drawing method was investigated with a transmission electron microscope (TEM) and atomic force (AFM). The diffraction (ED) pattern the OTS revealed that molecules were regularly arranged in hexagonal array (10) spacing ca. 0.42 nm. high-resolution AFM image scan area 10 × nm2 exhibited individual methyl group which packing similar molecular...

10.1021/la970040p article EN Langmuir 1998-02-10

Abstract A network structure and the mechanical properties, such as stretching adhesive properties of low cross-linking density cured epoxy resin (CER-L), were investigated by swelling test, tensile temperature dependence dynamic viscoelastic properties. CER-Ls synthesized with three different primary monoamines diepoxy. Even though was low, they showed modulus, strength comparable those high-cross linking CER.

10.1093/chemle/upaf001 article EN Chemistry Letters 2025-03-01

Alkyltrichlorosilanes, [2-(perfluorooctyl)ethyl]trichlorosilane (FOETS) and their mixed monolayers were polymerized on the water subphase subsequently immobilized onto silicon wafer surface by covalent bonding. Atomic force microscopic (AFM) observation of [n-octadecyltrichlorosilane(OTS)/FOETS] monolayer revealed that crystalline OTS formed circular domains ∼1–2 μm in diameter surrounded an amorphous FOETS matrix. Lateral (LFM) scanning viscoelasticity (SVM) observations (OTS/FOETS) could...

10.1116/1.580331 article EN Journal of Vacuum Science & Technology A Vacuum Surfaces and Films 1996-05-01

Abstract Randomly copolymerized poly(carbonate) glycols were employed as starting materials for the synthesis of polyurethane elastomers (PUEs). The had hexamethylene (C 6 ) and tetramethylene 4 units between carbonate groups in various composition ratios /C = 0/100, 50/50, 70/30, 90/10), number‐average molecular weights these 1000 2000. PUEs synthesized with glycols, 4,4′‐diphenylmethane diisocyanate, 1,4‐butanediol by a prepolymer method. Differential scanning calorimetry measurements...

10.1002/polb.20303 article EN Journal of Polymer Science Part B Polymer Physics 2004-11-03

An amphiphilic polymer bearing glutamic acid in the side chain was used as a surface modifier to produce an amino acid-based zwitterionic with pH-responsive and selective protein properties.

10.1039/c5py00783f article EN Polymer Chemistry 2015-01-01
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