Jin Kuk Kim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Jin Kuk Kim has a total of 104 co-authors. Here are the top co-authors by number of shared publications:
- Kaushik Pal
Indian Institute of Technology Roorkee
12 shared publications Zhen Xiu Zhang
School of Nano & Advanced Materials Engineering, Gyeongsang National University, Gyeongnam, Jinju, 660–701, South Korea
9 shared publicationsLin Li
Key Laboratory of Rubber–Plastics, Ministry of Education, College of Polymer Science and Engineering Qingdao University of Science and Technology Qingdao 266042 China
7 shared publicationsKanoktip Boonkerd
Department of Materials Science, Faculty of Science Chulalongkorn University Bangkok 10330 Thailand
6 shared publications- Vadahanambi Sridhar
Global Core Research Centre for Ships and Offshore Plants (GCRC-SOP), Pusan National University, Busan 46241, Republic of Korea
6 shared publications Jin Zhang
Polymer Science and Engineering, School of Materials Science and Engineering Gyeongsang National University Jinju Gyeongnam 660–701 Republic of Korea
5 shared publications
Latest Publications
- Open Access
A Comparative Analysis of Chemical, Plasma and In Situ Modification of Graphene Nanoplateletes for Improved Performance of Fused Filament Fabricated Thermoplastic Polyurethane Composites Parts
The limited number of materials and mechanical weakness of fused deposition modeling (FDM) parts are deficiencies of FDM technology. The preparation of polymer composites parts with suitable filler is a promising method to improve the properties of the 3D printed parts. However, the agglomerate of filler makes its difficult disperse in the matrix. In this work, graphene nanoplatelets (GnPs) were surface modified with chemical, low-temperature plasma and in situ methods, in order to apply them as fillers for thermoplastic polyurethane (TPU). Following its modification, the surface chemical composition of GnPs was analyzed. Three wt% of surface-modified GnPs were incorporated into TPU to produce FDM filaments using a melting compounding process. Their effects on rheology properties and electrical conductivity on TPU/GnPs composites, as well as the dimensional accuracy and mechanical properties of FDM parts, are compared. The images of sample facture surfaces were examined by scanning electron microscope (SEM) to determine the dispersion of GnPs. Results indicate that chemical treatment of GnPs with zwitterionic surfactant is a good candidate to significantly enhance TPU filaments, when considering the FDM parts demonstrated the highest mechanical properties and lowest dimensional accuracy.
Open AccessA Comparative Analysis of Chemical, Plasma and In Situ Modification of Graphene Nanoplateletes for Improved Performance of Fused Filament Fabricated Thermoplastic Polyurethane Composites Parts
The limited number of materials and mechanical weakness of fused deposition modeling (FDM) parts are deficiencies of FDM technology. The preparation of polymer composites parts with suitable filler is a promising method to improve the properties of the 3D printed parts. However, the agglomerate of filler makes its difficult disperse in the matrix. In this work, graphene nanoplatelets (GnPs) were surface modified with chemical, low-temperature plasma and in situ methods, in order to apply them as fillers for thermoplastic polyurethane (TPU). Following its modification, the surface chemical composition of GnPs was analyzed. Three wt% of surface-modified GnPs were incorporated into TPU to produce FDM filaments using a melting compounding process. Their effects on rheology properties and electrical conductivity on TPU/GnPs composites, as well as the dimensional accuracy and mechanical properties of FDM parts, are compared. The images of sample facture surfaces were examined by scanning electron microscope (SEM) to determine the dispersion of GnPs. Results indicate that chemical treatment of GnPs with zwitterionic surfactant is a good candidate to significantly enhance TPU filaments, when considering the FDM parts demonstrated the highest mechanical properties and lowest dimensional accuracy.
- 14 September 2021
- Published by Springer Nature in Colloid and Polymer Science
- Vol. 299 (11) , 1703-1715
Facile preparation of hydrogenated nitrile butadiene rubber/reduced graphene oxide nanocomposite with one-pot reduction approach via the latex way
- 14 September 2021
- Published by Springer Nature in Colloid and Polymer Science
- Vol. 299 (11) , 1703-1715
Facile preparation of hydrogenated nitrile butadiene rubber/reduced graphene oxide nanocomposite with one-pot reduction approach via the latex way
- 19 December 2020
- Published by American Chemical Society (ACS) in ACS Applied Electronic Materials
- Vol. 3 (1) , 248-259
Temperature–Pressure Hybrid Sensing All-Organic Stretchable Energy Harvester
The design and development of intrinsically stretchable all-organic self-powered sensors concurrently perceiving temperature and pressure remain a challenge but deliver an exciting platform to realize environmentally friendly wearable electronics. In this approach, a biomimetic all-organic stretchable energy harvester is designed by a xylitol-added poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS/Xyl) film as a compatible overlay electrode with polyaniline-reinforced one-dimensional aligned poly(vinylidene fluoride) hybrid electroactive soft nanowires. The gradient of elastic modulus between the electrode and the active nanowire component enables the all-organic device to manifest excellent power-generating performance under external temperature fluctuation (∼3 μW/m2 under ΔT ∼ 92 K) and mechanical force (∼31 μW/cm2 at 30 N). Importantly, the device renders simultaneous energy scavenging of temperature and pressure changes under pressing and stretching conditions (∼20%). The excellent mechanosensitivity (∼100 mV/N), fast response time (∼1 ms), outstanding mechanical and thermal stability, and good temperature resolution <10 K enable the harvester to act as an epidermal sensor, which simultaneously detects and discriminates both subtle pressure and thermal deviations exposed to an epidermis surface. The real-time recording and wireless transferring of physiological signals to a smartphone indicate an effective way to realize remote healthcare monitoring for early intervention.
- 19 December 2020
- Published by American Chemical Society (ACS) in ACS Applied Electronic Materials
- Vol. 3 (1) , 248-259
Temperature–Pressure Hybrid Sensing All-Organic Stretchable Energy Harvester
The design and development of intrinsically stretchable all-organic self-powered sensors concurrently perceiving temperature and pressure remain a challenge but deliver an exciting platform to realize environmentally friendly wearable electronics. In this approach, a biomimetic all-organic stretchable energy harvester is designed by a xylitol-added poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS/Xyl) film as a compatible overlay electrode with polyaniline-reinforced one-dimensional aligned poly(vinylidene fluoride) hybrid electroactive soft nanowires. The gradient of elastic modulus between the electrode and the active nanowire component enables the all-organic device to manifest excellent power-generating performance under external temperature fluctuation (∼3 μW/m2 under ΔT ∼ 92 K) and mechanical force (∼31 μW/cm2 at 30 N). Importantly, the device renders simultaneous energy scavenging of temperature and pressure changes under pressing and stretching conditions (∼20%). The excellent mechanosensitivity (∼100 mV/N), fast response time (∼1 ms), outstanding mechanical and thermal stability, and good temperature resolution <10 K enable the harvester to act as an epidermal sensor, which simultaneously detects and discriminates both subtle pressure and thermal deviations exposed to an epidermis surface. The real-time recording and wireless transferring of physiological signals to a smartphone indicate an effective way to realize remote healthcare monitoring for early intervention.
- 1 August 2018
- Published by Elsevier in Waste Management
- Vol. 78, 980-991
Devulcanization of waste rubber powder using thiobisphenols as novel reclaiming agent
- 1 August 2018
- Published by Elsevier in Waste Management
- Vol. 78, 980-991
Devulcanization of waste rubber powder using thiobisphenols as novel reclaiming agent
- 5 July 2018
- Published by Wiley in Advanced Materials Interfaces
- Vol. 5 (19)
Melt‐Compounded Keratin‐TPU Self‐Assembled Composite Film as Bioinspired e‐Skin
Inspired by the keratin–elastin composition of human skin, here an artificial skin (alias electronic (e)‐skin) is developed through solvent‐free extrusion based melt mixing of thermoplastic polyurethane (TPU) with the biowaste human hair keratin. Self‐assembled composite film of TPU and keratin (i.e., PUK) shows leg skin equivalent coefficient of friction value of 0.26 ± 0.05, cheek skin equivalent average surface roughness (Ra) of 0.047 ± 0.07 µm, cytoskeletal keratin intermediate filament network like rheological behavior, porous morphology, and skin like positive triboelectric property, when the keratin content is 10 wt%. H‐bonded self‐assembled network and lubricating behavior of cysteine‐rich keratin provide such tribological and rheological behaviors of the PUK. Single electrode triboelectric nanogenerator (STENG) made of PUK containing 10 wt% keratin (i.e., 10% PUK) not only shows clear discrimination between the touch feeling sensations of bare, and glove protected human finger, by producing output voltage of ≈1 and ≈16 V cm−2, respectively, but it also can discriminate the tactile sensations of different objects viz., aluminum foil, cotton glove, wood, polyimide, and poly(tetrafluoroethylene) by producing different output voltages, resembling that the PUK composite film is well fitted for e‐skin applications.
- 5 July 2018
- Published by Wiley in Advanced Materials Interfaces
- Vol. 5 (19)
Melt‐Compounded Keratin‐TPU Self‐Assembled Composite Film as Bioinspired e‐Skin
Inspired by the keratin–elastin composition of human skin, here an artificial skin (alias electronic (e)‐skin) is developed through solvent‐free extrusion based melt mixing of thermoplastic polyurethane (TPU) with the biowaste human hair keratin. Self‐assembled composite film of TPU and keratin (i.e., PUK) shows leg skin equivalent coefficient of friction value of 0.26 ± 0.05, cheek skin equivalent average surface roughness (Ra) of 0.047 ± 0.07 µm, cytoskeletal keratin intermediate filament network like rheological behavior, porous morphology, and skin like positive triboelectric property, when the keratin content is 10 wt%. H‐bonded self‐assembled network and lubricating behavior of cysteine‐rich keratin provide such tribological and rheological behaviors of the PUK. Single electrode triboelectric nanogenerator (STENG) made of PUK containing 10 wt% keratin (i.e., 10% PUK) not only shows clear discrimination between the touch feeling sensations of bare, and glove protected human finger, by producing output voltage of ≈1 and ≈16 V cm−2, respectively, but it also can discriminate the tactile sensations of different objects viz., aluminum foil, cotton glove, wood, polyimide, and poly(tetrafluoroethylene) by producing different output voltages, resembling that the PUK composite film is well fitted for e‐skin applications.
- 5 April 2018
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 10 (16) , 14008-14016
Soft and Flexible Bilayer Thermoplastic Polyurethane Foam for Development of Bioinspired Artificial Skin
Inspired by the epidermis–dermis composition of human skin, here we have simply developed a lightweight, robust, flexible, and biocompatible single-electrode triboelectric nanogenerator (S-TENG)-based prototype of bilayer artificial skin, by attaching one induction electrode with unfoamed skin layer of microcellular thermoplastic polyurethane (TPU) foam, which shows high-performance object manipulation [by responding differently toward different objects, viz., aluminum foil, balloon, cotton glove, human finger, glass, rubber glove, artificial leather, polyimide, poly(tetrafluoroethylene) (PTFE), paper, and wood], due to electrification and electrostatic induction during contact with the objects having different chemical functionalities. Comparative foaming behavior of ecofriendly supercritical fluids, viz., CO2 over N2 under variable temperatures (e.g., 130 and 150 °C) and constant pressure (15 MPa), have been examined here to pursue the soft and flexible triboelectric TPU foam. The foam derived by CO2 foaming at 150 °C has been prioritized for development of S-TENG. Foam derived by CO2 foaming at 130 °C did not respond as well due to the smaller cell size, higher hardness, and thicker skin. Inflexible N2-derived foam was not considered for S-TENG fabrication. Object manipulation performance has been visualized by principal component analysis (PCA), which shows good discrimination among responses to different objects.
- 5 April 2018
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 10 (16) , 14008-14016
Soft and Flexible Bilayer Thermoplastic Polyurethane Foam for Development of Bioinspired Artificial Skin
Inspired by the epidermis–dermis composition of human skin, here we have simply developed a lightweight, robust, flexible, and biocompatible single-electrode triboelectric nanogenerator (S-TENG)-based prototype of bilayer artificial skin, by attaching one induction electrode with unfoamed skin layer of microcellular thermoplastic polyurethane (TPU) foam, which shows high-performance object manipulation [by responding differently toward different objects, viz., aluminum foil, balloon, cotton glove, human finger, glass, rubber glove, artificial leather, polyimide, poly(tetrafluoroethylene) (PTFE), paper, and wood], due to electrification and electrostatic induction during contact with the objects having different chemical functionalities. Comparative foaming behavior of ecofriendly supercritical fluids, viz., CO2 over N2 under variable temperatures (e.g., 130 and 150 °C) and constant pressure (15 MPa), have been examined here to pursue the soft and flexible triboelectric TPU foam. The foam derived by CO2 foaming at 150 °C has been prioritized for development of S-TENG. Foam derived by CO2 foaming at 130 °C did not respond as well due to the smaller cell size, higher hardness, and thicker skin. Inflexible N2-derived foam was not considered for S-TENG fabrication. Object manipulation performance has been visualized by principal component analysis (PCA), which shows good discrimination among responses to different objects.
- 27 August 2016
- Published by Springer Nature
- p. 13-36
Design for Multicomponent Materials
- 30 November 2014
- Published by Springer Nature in Fibers and Polymers
- Vol. 15 (11) , 2345-2354
Effect of photodegradation of lignocellulosic fibers transesterified with vegetable oil
- 30 November 2014
- Published by Springer Nature in Fibers and Polymers
- Vol. 15 (11) , 2345-2354
Effect of photodegradation of lignocellulosic fibers transesterified with vegetable oil