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Dive into the research topics where Kimiyoshi Naito is active.

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Featured researches published by Kimiyoshi Naito.


Applied Physics Letters | 2008

Tensile properties of carbon nanotubes grown on ultrahigh strength polyacrylonitrile-based and ultrahigh modulus pitch-based carbon fibers

Kimiyoshi Naito; Jenn-Ming Yang; Yoshihisa Tanaka; Yutaka Kagawa

The tensile properties and fracture behavior of carbon nanotubes (CNTs) grown on ultrahigh tensile strength polyacrylonitrile (PAN)-based (T1000GB) and ultrahigh modulus pitch-based (K13D) carbon fibers have been investigated. The CNTs were grown on the carbon fiber surface using chemical vapor deposition. The statistical scattering of the tensile strength was also evaluated. The results clearly show that grafting of CNTs improves the mechanical properties and the Weibull modulus of ultrahigh tensile strength PAN-based and ultrahigh modulus pitch-based carbon fibers.


Nanotechnology | 2011

Development of a pattern to measure multiscale deformation and strain distribution via in situ FE-SEM observations

Yoshihisa Tanaka; Kimiyoshi Naito; Satoshi Kishimoto; Yutaka Kagawa

We investigated a method for measuring deformation and strain distribution in a multiscale range from nanometers to millimeters via in situ FE-SEM observations. A multiscale pattern composed of a grid as well as random and nanocluster patterns was developed to measure the localized deformation at the specimen surface. Our in situ observations of a carbon fiber-reinforced polymer matrix composite with a hierarchical microstructure subjected to loading were conducted to identify local deformation behaviors at various boundaries. We measured and analyzed the multiscale deformation and strain localizations during various stages of loading.


RSC Advances | 2014

A novel high-temperature naphthyl-based phthalonitrile polymer: synthesis and properties

Fenghua Zhao; Ruojin Liu; Chao Kang; Xiaoyan Yu; Kimiyoshi Naito; Xiongwei Qu; Qingxin Zhang

A novel naphthyl-based phthalonitrile monomer, 1,6-bis(3,4-dicyanophenoxy) naphthalene (1,6-BDCN), was prepared, and the phthalonitrile resin was cured with 4,4′-diaminodiphenyl ether (ODA) via two steps, namely, preparation of prepolymer and postcuring prepolymer at elevated temperatures. The 1,6-BDCN polymer might form triazine and phthalocyanine rings as demonstrated by FTIR spectra. The prepolymer shows fine solubility in organic solvents. The 1,6-BDCN polymer exhibits excellent structural integrity and superior thermal stability as indicated by thermogravimetric analysis (TGA). Dynamic mechanical analysis (DMA) revealed that the phthalonitrile resin has a high storage modulus and glass transition temperature (Tg). The water uptake is about 3% by weight after submersion in boiling water for 50 hours. The influence of curing processes on thermal stability and flame retardancy was also explored.


High Performance Polymers | 2014

Synthesis and properties of a novel high-temperature diphenyl sulfone-based phthalonitrile polymer

Xuegang Peng; Haitong Sheng; Hui Guo; Kimiyoshi Naito; Xiaoyan Yu; Huili Ding; Xiongwei Qu; Qingxin Zhang

A novel high-temperature diphenyl sulfone-based phthalonitrile polymer is prepared from bis-[4-(3,4-dicyanophenoxy)phenyl]sulfone (BDS) monomer synthesized with high yield by a simple nucleophilic displacement of a nitro-substituent from 4-nitrophthalonitrile (NPN). The structure of BDS polymer is investigated by Fourier transform infrared spectroscopy and wide-angle X-ray diffraction. Curing behavior of BDS monomer with 1,3-bis(4-aminophenoxy)benzene (APB) is recorded by differential scanning calorimetry. The properties of BDS polymer are evaluated by thermogravimetric analysis, dynamic mechanical analysis, and tensile test. The results reveal that the BDS polymer exhibits excellent thermal and thermo-oxidative stabilities, high glass temperature (Tg = 337°C), and outstanding mechanical properties (Young’s modulus: 4.02 GPa and tensile strength: 64.16 MPa). Additionally, the BDS polymer exhibits high flame retardance and low water uptake.


Journal of Reinforced Plastics and Composites | 2011

Synthesis, tensile, and thermal properties of polyimide/diamond nanocomposites

Xiaoyan Yu; Xiongwei Qu; Kimiyoshi Naito; Qingxin Zhang

Polyimide/diamond nanocomposites were prepared using 4,4′-diaminoiphenyl ether and 3,3 ′,4,4′-benzophenonetetracarboxylic dianhydride. The structure of the polyimide/diamond nanocomposites was characterized by Fourier transform infrared, ultraviolet and transmission electron microscopy. Agglomeration of nano diamond particles is observed in polyimide matrix as revealed by transmission electron microscopy micrographs which is ascribed to the high surface free energy of particles. Both tensile strength and failure strain of polyimide are obviously enhanced with incorporation of nano diamond particles though tensile modulus only shows slight increase. The reinforcing effect of nano diamond on polyimide is discussed. Thermal stabilities of the polyimide/diamond nanocomposites are evaluated using a thermogravimetric analyzer. The thermal stability of nanocomposites is slightly reduced as indicated by a small decrease in onset degradation temperature.


Journal of Materials Engineering and Performance | 2014

Tensile Properties of Polyimide Composites Incorporating Carbon Nanotubes-Grafted and Polyimide-Coated Carbon Fibers

Kimiyoshi Naito

Abstract The tensile properties and fracture behavior of polyimide composite bundles incorporating carbon nanotubes-grafted (CNT-grafted) and polyimide-coated (PI-coated) high-tensile-strength polyacrylonitrile (PAN)-based (T1000GB), and high-modulus pitch-based (K13D) carbon fibers were investigated. The CNT were grown on the surface of the carbon fibers by chemical vapor deposition. The pyromellitic dianhydride/4,4′-oxydianiline PI nanolayer coating was deposited on the surface of the carbon fiber by high-temperature vapor deposition polymerization. The results clearly demonstrate that CNT grafting and PI coating were effective for improving the Weibull modulus of T1000GB PAN-based and K13D pitch-based carbon fiber bundle composites. In addition, the average tensile strength of the PI-coated T1000GB carbon fiber bundle composites was also higher than that of the as-received carbon fiber bundle composites, while the average tensile strength of the CNT-grafted T1000GB, K13D, and the PI-coated K13D carbon fiber bundle composites was similar to that of the as-received carbon fiber bundle composites.


Advanced Composite Materials | 2016

Mechanical property enhancement of aligned multi-walled carbon nanotube sheets and composites through press-drawing process

Tran Huu Nam; Ken Goto; Kahori Oshima; E.V.A. Premalal; Yoshinobu Shimamura; Yoku Inoue; Kimiyoshi Naito; Shinji Ogihara

A solid-state drawing and winding process was done to create thin aligned carbon nanotube (CNT) sheets from CNT arrays. However, waviness and poor packing of CNTs in the sheets are two main weaknesses restricting their reinforcing efficiency in composites. This report proposes a simple press-drawing technique to reduce wavy CNTs and to enhance dense packing of CNTs in the sheets. Non-pressed and pressed CNT/epoxy composites were developed using prepreg processing with a vacuum-assisted system. Effects of pressing on the mechanical properties of the aligned CNT sheets and CNT/epoxy composites were examined. Pressing with distributed loads of 147, 221, and 294 N/m showed a substantial increase in the tensile strength and the elastic modulus of the aligned CNT sheets and their composites. The CNT sheets under a press load of 221 N/m exhibited the best mechanical properties found in this study. With a press load of 221 N/m, the pressed CNT sheet and its composite, respectively, enhanced the tensile strength by 139.1 and 141.9%, and the elastic modulus by 489 and 77.6% when compared with non-pressed ones. The pressed CNT/epoxy composites achieved high tensile strength (526.2 MPa) and elastic modulus (100.2 GPa). Results show that press-drawing is an important step to produce superior CNT sheets for development of high-performance CNT composites.


Journal of Materials Engineering and Performance | 2016

Effect of Hybrid Surface Modifications on Tensile Properties of Polyacrylonitrile- and Pitch-Based Carbon Fibers

Kimiyoshi Naito

Recent interest has emerged in techniques that modify the surfaces of carbon fibers, such as carbon nanotube (CNT) grafting or polymer coating. Hybridization of these surface modifications has the potential to generate highly tunable, high-performance materials. In this study, the mechanical properties of surface-modified polyacrylonitrile (PAN)-based and pitch-based carbon fibers were investigated. Single-filament tensile tests were performed for fibers modified by CNT grafting, dipped polyimide coating, high-temperature vapor deposition polymerized polyimide coating, grafting-dipping hybridization, and grafting-vapor deposition hybridization. The Weibull statistical distributions of the tensile strengths of the surface-modified PAN- and pitch-based carbon fibers were examined. All surface modifications, especially hybrid modifications, improved the tensile strengths and Weibull moduli of the carbon fibers. The results exhibited a linear relationship between the Weibull modulus and average tensile strength on a log-log scale for all surface-modified PAN- and pitch-based carbon fibers.


Applied Adhesion Science | 2016

Fracture toughness of adherends bonded with two-part acrylic-based adhesive: double cantilever beam tests under static loading

Hyun-Bum Kim; Kimiyoshi Naito; Hiroyuki Oguma

Adhesives are used in various industries to bond materials. The failure criteria of adhesive joints are based on the strength (peel) and fracture mechanisms of the materials. It is important to investigate these criteria in relation to the propagation and separation of Mode I, II, and III cracks. The purpose of this study is to use double cantilever beam (DCB) tests to measure fracture toughness in aluminum alloy (5052-H34), glass fiber-reinforced polypropylene matrix composite, and carbon fiber-reinforced epoxy matrix composite adherends bonded with a two-part acrylic-based adhesive. The fracture behaviors of the specimens are also discussed. DCB tests are carried out to measure fracture toughness under Mode I loading of adhesively bonded joints with different types of adherends. The fracture toughnesses of the aluminum alloy, glass-fiber-reinforced polypropylene matrix composite (GF/PP), and carbon fiber-reinforced epoxy matrix composite (CF/EP) specimens are 1071, 1438, and 1652 Jm−2, respectively. The fracture surfaces of the aluminum alloy, GF/PP, and CF/EP specimens are observed to be of the interfacial, adherend, and cohesive types, respectively.


Computational methods and experimental measurements, 2013, ISBN 978-1-84564-732-2, págs. 275-284 | 2013

Increasing the interfacial strength in carbon fiber/polypropylene composites by growing CNTs on the fibers

S. Yumitori; Yoshihiko Arao; Tatsuya Tanaka; Kimiyoshi Naito; Kazuto Tanaka; Tsutao Katayama

Carbon nanotubes (CNTs) were grown uniformity on the surface of carbon fibers to create hierarchical fibers by use of floating catalyst chemical vapor deposition. The tensible properties of CNTs grafted fibers were measured. The strength of grafted fibers decreased approximately 12% compared to raw carbon fibers in this process. A fiber pull-out test revealed that the interfacial shear strength (IFSS) in polypropylene composites improved by 35% by grafting CNTs onto carbon fibers. It indicates the use of hierarchical fibers in thermoplastic composites is effective due to the improvement of IFSS by mechanical interlocking between CNTs and the matrix. The CNT/fiber joint strength is the most critical property, and the experimental observations also revealed that the joint fracture was the major failure mode.

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Yoshihisa Tanaka

National Institute for Materials Science

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Satoshi Kishimoto

National Institute for Materials Science

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Jenn-Ming Yang

University of California

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Xiongwei Qu

Hebei University of Technology

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Qingxin Zhang

National Institute for Materials Science

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Qingxin Zhang

National Institute for Materials Science

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Hiroyuki Oguma

National Institute for Materials Science

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