Akane Miyazaki
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Akane Miyazaki has a total of 31 co-authors. Here are the top co-authors by number of shared publications:
- Ioan Balint
Institute of Physical Chemistry “Ilie Murgulescu”, 202 Splaiul Independentei, 060021 Bucharest, Romania
5 shared publications Ioan Balint
Institute of Physical Chemistry of the Romanian Academy, Spl. Independentei, 202, 060021 Bucharest, Romania
3 shared publicationsHiroshi Okochi
Graduate School of Creative Science and Engineering, Waseda University, Tokyo, Japan
2 shared publications- Ken-Ichi Aika
Tokyo Institute of Technology
2 shared publications Takushi Yokoyama
Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395 , Japan
2 shared publicationsToru Asakawa
Japan Women's University, Department of Chemical and Biological Sciences, 2-8-1 Mejirodai, Bunkyo-ku, Tokyo 112-8681, Japan
2 shared publications
Latest Publications
- 20 March 2024
- Published by Springer Nature in Environmental Chemistry Letters
- Vol. 22 (4) , 1599-1606
Alkaline extraction yields a higher number of microplastics in forest canopy leaves: implication for microplastic storage
- 20 March 2024
- Published by Springer Nature in Environmental Chemistry Letters
- Vol. 22 (4) , 1599-1606
Alkaline extraction yields a higher number of microplastics in forest canopy leaves: implication for microplastic storage
- Open Access
- 29 November 2023
- Published by Springer Nature in Research Square
Accumulation of Airborne Microplastics on Forest Canopy Leaves: Insights from Trichomes and Epicuticular Waxes
Airborne microplastics (AMPs) on konara oak (Quercus serrata Murray) leaves collected at a small forest in the Tokyo metropolitan area were analyzed. The leaves underwent a three-step treatment process: (i) washing with Milli-Q water, (ii) sonication in Milli-Q water, and (iii) extraction with a 10% KOH solution. The average number of AMPs found in solutions (i), (ii), and (iii) were 0.01, 0.05, and 0.07 microplastics (MP) /cm2 leaf, respectively. More than 50% of the total AMPs recovered from the aqueous samples were detected in the KOH solution. Scanning electron microscopy (SEM) observation revealed that the KOH solution significantly altered the leaf surfaces, while rinsing and ultrasonication with Milli-Q water had little effect. These results emphasize the strong adsorption of AMPs to epidermal waxes and the importance of using KOH solutions in addition to conventional water washing methods to prevent underestimation of AMPs intercepted by forest canopy leaves. Using data from the growing season, it was estimated that a small forest in the metropolitan area captures approximately 2.2 billion AMP particles per year. This indicates that forests may play an important role as sinks for AMPs in the terrestrial environment.
- 29 November 2023
- Published by Springer Nature in Research Square
Open AccessAccumulation of Airborne Microplastics on Forest Canopy Leaves: Insights from Trichomes and Epicuticular Waxes
Airborne microplastics (AMPs) on konara oak (Quercus serrata Murray) leaves collected at a small forest in the Tokyo metropolitan area were analyzed. The leaves underwent a three-step treatment process: (i) washing with Milli-Q water, (ii) sonication in Milli-Q water, and (iii) extraction with a 10% KOH solution. The average number of AMPs found in solutions (i), (ii), and (iii) were 0.01, 0.05, and 0.07 microplastics (MP) /cm2 leaf, respectively. More than 50% of the total AMPs recovered from the aqueous samples were detected in the KOH solution. Scanning electron microscopy (SEM) observation revealed that the KOH solution significantly altered the leaf surfaces, while rinsing and ultrasonication with Milli-Q water had little effect. These results emphasize the strong adsorption of AMPs to epidermal waxes and the importance of using KOH solutions in addition to conventional water washing methods to prevent underestimation of AMPs intercepted by forest canopy leaves. Using data from the growing season, it was estimated that a small forest in the metropolitan area captures approximately 2.2 billion AMP particles per year. This indicates that forests may play an important role as sinks for AMPs in the terrestrial environment.
- Open Access
Band-Gap Engineering of Layered Perovskites by Cu Spacer Insertion as Photocatalysts for Depollution Reaction
A multi-step ion-exchange methodology was developed for the fabrication of Cu(LaTa2O7)2 lamellar architectures capable of wastewater depollution. The (001) diffraction line of RbLaTa2O7 depended on the guest species hosted by the starting material. SEM and TEM images confirmed the well-preserved lamellar structure for all intercalated layered perovskites. The UV–Vis, XPS, and photocurrent spectroscopies proved that Cu intercalation induces a red-shift band gap compared to the perovskite host. Moreover, the UV–Vis spectroscopy elucidated the copper ions environment in the Cu-modified layered perovskites. H2-TPR results confirmed that Cu species located on the surface are reduced at a lower temperature while those from the interlayer occur at higher temperature ranges. The photocatalytic degradation of phenol under simulated solar irradiation was used as a model reaction to assess the performances of the studied catalysts. Increased photocatalytic activity was observed for Cu-modified layered perovskites compared to RbLaTa2O7 pristine. This behavior resulted from the efficient separation of photogenerated charge carriers and light absorption induced by copper spacer insertion.
Open AccessBand-Gap Engineering of Layered Perovskites by Cu Spacer Insertion as Photocatalysts for Depollution Reaction
A multi-step ion-exchange methodology was developed for the fabrication of Cu(LaTa2O7)2 lamellar architectures capable of wastewater depollution. The (001) diffraction line of RbLaTa2O7 depended on the guest species hosted by the starting material. SEM and TEM images confirmed the well-preserved lamellar structure for all intercalated layered perovskites. The UV–Vis, XPS, and photocurrent spectroscopies proved that Cu intercalation induces a red-shift band gap compared to the perovskite host. Moreover, the UV–Vis spectroscopy elucidated the copper ions environment in the Cu-modified layered perovskites. H2-TPR results confirmed that Cu species located on the surface are reduced at a lower temperature while those from the interlayer occur at higher temperature ranges. The photocatalytic degradation of phenol under simulated solar irradiation was used as a model reaction to assess the performances of the studied catalysts. Increased photocatalytic activity was observed for Cu-modified layered perovskites compared to RbLaTa2O7 pristine. This behavior resulted from the efficient separation of photogenerated charge carriers and light absorption induced by copper spacer insertion.
- 15 May 2018
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 91 (8) , 1249-1251
Morphological Development and Coordination Change in the Course of Cd2+ Hydrolysis
Morphological development from nanowire to hexagonal platelet was observed for hydrolysis products of Cd(NO3)2 aqueous solution. 113Cd cross-polarization magic-angle spinning nuclear magnetic resonance spectroscopy and X-ray diffraction revealed that the morphological development corresponds to the change of coordination environment around Cd2+ from double salts containing nitrate ions to β-Cd(OH)2.
- 15 May 2018
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 91 (8) , 1249-1251
Morphological Development and Coordination Change in the Course of Cd2+ Hydrolysis
Morphological development from nanowire to hexagonal platelet was observed for hydrolysis products of Cd(NO3)2 aqueous solution. 113Cd cross-polarization magic-angle spinning nuclear magnetic resonance spectroscopy and X-ray diffraction revealed that the morphological development corresponds to the change of coordination environment around Cd2+ from double salts containing nitrate ions to β-Cd(OH)2.
- 7 December 2012
- Published by Elsevier in Colloids and Surfaces A: Physicochemical and Engineering Aspects
- Vol. 420, 115-121
Evidence for tetrahedral AlO4 formation induced by Zn2+ adsorption onto Al(OH)3 gel
- 7 December 2012
- Published by Elsevier in Colloids and Surfaces A: Physicochemical and Engineering Aspects
- Vol. 420, 115-121
Evidence for tetrahedral AlO4 formation induced by Zn2+ adsorption onto Al(OH)3 gel
- Open Access
- 1 April 2011
- Published by IntechOpen
Purification of Waste Water Using Alumina as Catalysts Support and as an Adsorbent
- 1 April 2011
- Published by IntechOpen
Open AccessPurification of Waste Water Using Alumina as Catalysts Support and as an Adsorbent
- 31 May 2010
- Published by Elsevier in Applied Catalysis A: General
- Vol. 380 (1-2) , 186
Reply to the comments on “NO2− adsorption onto denitration catalysts”
- 31 May 2010
- Published by Elsevier in Applied Catalysis A: General
- Vol. 380 (1-2) , 186
Reply to the comments on “NO2− adsorption onto denitration catalysts”
- 1 July 2009
- Published by Elsevier in Applied Catalysis A: General
- Vol. 363 (1-2) , 81-85
NO2− adsorption onto denitration catalysts
- 1 July 2009
- Published by Elsevier in Applied Catalysis A: General
- Vol. 363 (1-2) , 81-85
NO2− adsorption onto denitration catalysts
- 13 December 2007
- Published by Springer Nature in Catalysis Letters
- Vol. 122 (1-2) , 183-187
The Influence of Rh Addition on the Catalytic Activity of Cubic Pt Nanocrystals Supported on Alumina for NO/CH4 Reaction
- 13 December 2007
- Published by Springer Nature in Catalysis Letters
- Vol. 122 (1-2) , 183-187
The Influence of Rh Addition on the Catalytic Activity of Cubic Pt Nanocrystals Supported on Alumina for NO/CH4 Reaction
- 6 March 2004
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 33 (4) , 418-419
Efficient Catalytic Reduction of Concentrated Nitric Acid on the Adsorption Sites of Activated Carbon
The adsorption sites of active carbon were found to promote efficiently the catalytic reduction of concentrated HNO3 by HCOOH at low temperature.
- 6 March 2004
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 33 (4) , 418-419
Efficient Catalytic Reduction of Concentrated Nitric Acid on the Adsorption Sites of Activated Carbon
The adsorption sites of active carbon were found to promote efficiently the catalytic reduction of concentrated HNO3 by HCOOH at low temperature.