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HUANG YUAN

Faculty of Environmental Earth Science Integrated Environmental Science Environmental Adaptation ScienceSpecially Appointed Assistant Professor

Researcher basic information

■ Degree
  • Master (Environmental Science), Hokkaido University, Sep. 2020
  • Doctor (Environmental Science), Hokkaido University, Sep. 2024
■ URL
researchmap URLホームページURL■ Various IDs
J-Global ID■ Research Keywords and Fields
Research Keyword
  • ガス吸着、分離
  • 金属錯体
  • 多孔性材料
  • 触媒化学
Research Field
  • Nanotechnology/Materials, Inorganic/coordination chemistry
  • Manufacturing Technology (Mechanical Engineering, Electrical and Electronic Engineering, Chemical Engineering), Catalyst and resource chemical process

Career

■ Career
Educational Background
  • Oct. 2020 - Oct. 2023, 北海道大学
  • Oct. 2018 - Sep. 2020, 北海道大学

Research activity information

■ Papers
  • Photoredox Cascade Catalysis for Hydrogen Production With Wacker Oxidation of Olefin Gases
    Atsushi Kobayashi; Yuan Huang; Shin‐ichiro Noro
    ChemSusChem, 19, 7, Wiley, 08 Apr. 2026
    Scientific journal, Solar‐light‐driven photocatalytic coproduction of hydrogen (H 2 ) and valuable organic compounds is a promising technique for realizing sustainable carbon neutral society. In this work, we fabricate a new dual‐product photocatalytic system for the coproduction of H 2 and acetaldehyde/acetone by combining a dual Ru (II) dye‐sensitized Pt‐cocatalyst‐loaded TiO 2 nanoparticles photocatalyst with a Pd(II)‐acetate/9‐azanoradamantane N‐oxyl (nor‐AZADO ) double‐mediatory Wacker oxidation catalytic system. This photoredox cascade catalytic system successfully converts gaseous ethylene/propylene substrates into H 2 and acetaldehyde/acetone under blue‐light irradiation owing to the electron mediation of nor‐AZADO between the two (photo)catalytic cycles. The maximum turnover number per one photosensitizer and apparent quantum yield for the initial 1 h of irradiation in the presence of 5.0 vol% ethylene gas are estimated to be 1533 and 1.23%, respectively. These findings open a new avenue for simultaneously supplying clean energy resources, H 2 and organic valuables via oxidative organic transformations.
  • Zeolite X Loaded with Ag + as a Slow Ethylene-Releasing Nanoporous Material to Suppress Potato Sprouting
    Yuan Huang; Akira Yamamoto; Ryoichi Otomo; Shin-ichiro Noro; Yuichi Kamiya
    ACS Applied Nano Materials, 9, 4, 1996, 2006, American Chemical Society (ACS), 15 Jan. 2026
    Scientific journal
  • Coexisting gases regulate the rates of water adsorption by a flexible one-dimensional coordination polymer
    Anqi Wang; Xin Zheng; Yuki Saito; Arata Tateishi; Yuan Huang; Yuichi Kamiya; Hiroyasu Sato; Atsushi Kondo; Kiyonori Takahashi; Takayoshi Nakamura; Shin-ichiro Noro
    CHEMICAL SCIENCE, 16, 39, 18135, 18140, 08 Oct. 2025
    English, Scientific journal
  • Removal and complete combustion of 1,4-dioxane in water by a two-step reaction combining adsorption and catalytic combustion
    Jieqiong Zhang; Yuan Huang; Miyu Sato; Xin Zheng; Shin-ichiro Noro; Ryoichi Otomo; Yuichi Kamiya
    Journal of Water Process Engineering, 64, 105658, 105658, Elsevier BV, Jul. 2024
    Scientific journal
  • Uniformly Distributed Palladium Nanoparticles on NH2‐MIL‐53 Fabricated by an Equilibrium Adsorption Method for Reduction of Nitrite in Water
    Yuan Huang; Wontae Kim; Ryoichi Otomo; Shuhei Shimoda; Kevin C.‐W. Wu; Yuichi Kamiya
    ChemCatChem, 16, 16, Wiley, 02 May 2024, [Lead author]
    Scientific journal, Abstract

    Metal particle on a support material should be small and homogeneous in size, which is desirable when using it as a catalyst. In this study, we investigated to introduce Pd nanoparticles (NPs) with narrow size distribution into NH2‐MIL‐53, which was prepared by the reaction of aluminum(III) nitrate with 2‐aminoterephthalic acid. Only by immersing it in an aqueous PdCl2 solution, followed by the reduction with NaBH4, Pd NPs of about 2 nm with unform distribution were formed in NH2‐MIL‐53 up to 3.5 wt.% Pd loadings. Amino group on the linkers in NH2‐MIL‐53 played a critical role for the introduction of (PdCl3) as a precursor for Pd NPs, while no Pd was introduced into MIL‐53 without amino group. The obtained catalysts (Pd@NH2‐MIL‐53) showed high catalytic performance for reduction of nitrite in water. The specific activity per Pd site exposed on the surface changed greatly depending on the Pd loadings despite the size of Pd NPs unchanged. Pd@NH2‐MIL‐53 with low Pd loadings showed higher specific activity (TOF=2.9×102 h−1), which might be due to the preferential exposure of Pd(111) facet on Pd NPs.