Hyunook Kim
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
Hyunook Kim has a total of 319 co-authors. Here are the top co-authors by number of shared publications:
- Byoung-In Sang
Department of Chemical Engineering, Hanyang University, Seoul 04763, Republic of Korea
10 shared publications - Ingyu Lee
Water-Energy Nexus Laboratory, Department of Environmental Engineering, University of Seoul, Seoul, 02504, Republic of Korea
9 shared publications Ingyu Lee
Department of Civil & Energy System Engineering, Kyonggi University, Suwon, Korea
8 shared publicationsMonu Verma
Department of Food Science and Technology, Graphic Era (Deemed to be University), Dehradun, India
8 shared publicationsYoungmin Hong
Water-Energy Nexus Laboratory, Department of Environmental Engineering, University of Seoul, Seoul, Republic of Korea
8 shared publications- Nisha Shabnam
Department of Environmental Engineering, University of Seoul, Seoul, Republic of Korea
7 shared publications
Latest Publications
- Open Access
- 11 July 2026
- Published by Elsevier in SSRN Electronic Journal
Global carbon isotope variability of commercial plastics: implications for microplastic source attribution and environmental forensics
Microplastic source attribution remains a major challenge because conventional analytical techniques primarily identify polymer types while providing limited information on the origin and environmental history of plastic materials. This study evaluates the potential and limitations of stable carbon isotope analysis (δ¹³C) for tracing common plastic polymers at the global scale. A total of 460 commercial plastic samples, including 233 polyethylene terephthalate (PET) bottles and 227 polyethylene (PE) caps, were collected from 59 countries across six continents and analysed by Elemental Analyzer - Isotope Ratio Mass Spectrometry (EA-IRMS). A preliminary thermal additive removal experiment showed systematic but minor isotopic shifts (~0.3‰ for PET and ~0.5‰ for PE), indicating a minor influence of additives on bulk δ¹³C values. Across all samples, PE exhibited a broad δ¹³C range from -35.2 ‰ to -24.0 ‰, with significant interregional variability and country-averaged values ranging from -33.88 ± 0.02‰ (Tunisia) to -25.93 ± 0.07‰ (New Zealand). Continental-scale comparisons revealed significant differences between several regions, consistent with regional differences in petrochemical feedstocks and production pathways. In contrast, PET displayed a narrower δ¹³C range (-33.1‰ to -26.2‰) and no significant interregional differences, consistent with a more homogeneous and globally integrated production system. Overall, the results demonstrate that stable carbon isotopes provide useful first-order constraints on broad PE source domains, while also highlighting important limitations related to overlapping isotopic domains and the globalization of polymer supply chains. Stable isotope analysis therefore represents a promising complementary tool for improving microplastic source attribution within multi-tracer environmental forensic frameworks.
- 11 July 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessGlobal carbon isotope variability of commercial plastics: implications for microplastic source attribution and environmental forensics
Microplastic source attribution remains a major challenge because conventional analytical techniques primarily identify polymer types while providing limited information on the origin and environmental history of plastic materials. This study evaluates the potential and limitations of stable carbon isotope analysis (δ¹³C) for tracing common plastic polymers at the global scale. A total of 460 commercial plastic samples, including 233 polyethylene terephthalate (PET) bottles and 227 polyethylene (PE) caps, were collected from 59 countries across six continents and analysed by Elemental Analyzer - Isotope Ratio Mass Spectrometry (EA-IRMS). A preliminary thermal additive removal experiment showed systematic but minor isotopic shifts (~0.3‰ for PET and ~0.5‰ for PE), indicating a minor influence of additives on bulk δ¹³C values. Across all samples, PE exhibited a broad δ¹³C range from -35.2 ‰ to -24.0 ‰, with significant interregional variability and country-averaged values ranging from -33.88 ± 0.02‰ (Tunisia) to -25.93 ± 0.07‰ (New Zealand). Continental-scale comparisons revealed significant differences between several regions, consistent with regional differences in petrochemical feedstocks and production pathways. In contrast, PET displayed a narrower δ¹³C range (-33.1‰ to -26.2‰) and no significant interregional differences, consistent with a more homogeneous and globally integrated production system. Overall, the results demonstrate that stable carbon isotopes provide useful first-order constraints on broad PE source domains, while also highlighting important limitations related to overlapping isotopic domains and the globalization of polymer supply chains. Stable isotope analysis therefore represents a promising complementary tool for improving microplastic source attribution within multi-tracer environmental forensic frameworks.
- 24 April 2026
- Published by Elsevier in Chemosphere
- Vol. 404, 144922
Molecular-level green chemistry based design of a custom binding site for targeted Cu (II) ion removal in bio-retention system
- 24 April 2026
- Published by Elsevier in Chemosphere
- Vol. 404, 144922
Molecular-level green chemistry based design of a custom binding site for targeted Cu (II) ion removal in bio-retention system
- 30 March 2026
- Published by Springer Nature in Fibers and Polymers
- Vol. 27 (6) , 3049-3060
Rapid Assessment of Synthetic Fibers Released During Laundering Using Total Organic Carbon-Based Analysis
- 30 March 2026
- Published by Springer Nature in Fibers and Polymers
- Vol. 27 (6) , 3049-3060
Rapid Assessment of Synthetic Fibers Released During Laundering Using Total Organic Carbon-Based Analysis
- Open Access
- 10 March 2026
- Published by Elsevier in SSRN Electronic Journal
Rainfall Deposition of Atmospheric Microplastics and Urban Freshwater Contamination: Insights from a Seoul Case Study
Atmospheric wet deposition is a critical scavenger of microplastics (MPs); yet, its contribution to urban hydrologic cycles remains under-quantified. In this study, we investigated the MP characteristics and flux in rainfall across 21 events in Seoul, South Korea, utilizing a cascade filtration protocol coupled with dual-spectroscopy (Fourier Transform-Infrared for ≥20 µm and Raman Spectroscopy for 5–20 µm). Results revealed an average MP abundance of 197 MPs L-1 with a dominance of fragments (> 96%). A critical "mass-count paradox" was observed: while fine particles (< 50 µm) were numerically dominant, larger particles (> 50 µm) accounted for approximately 90% of the total mass. Polymer composition also exhibited size-dependence, with brittle polymers (polystyrene and polyethylene terephthalate) prevalent in the finer fraction detected by Raman, whereas polypropylene and polyethylene dominated the larger fraction. The Conditional Fragmentation Model showed a fragmentation exponent (α) of approximately 1.08, characterizing the particles as an extensively weathered “aged atmospheric pool”. Furthermore, a strong correlation (r = 0.87) between MP flux and Antecedent Dry Days confirmed a "first-flush" mechanism, whereas meteorological analysis identified inertial impaction as the dominant scavenging driver (r = 0.97 with rainfall depth). Box model simulations demonstrated that although wet deposition contributes a minor fraction (1.8%–8.8%) of the annual load, it generates acute "shock loading" during storm events, accounting for up to 81% of the total influx. The findings underscore the necessity of integrating atmospheric deposition into urban water quality management strategies.
- 10 March 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessRainfall Deposition of Atmospheric Microplastics and Urban Freshwater Contamination: Insights from a Seoul Case Study
Atmospheric wet deposition is a critical scavenger of microplastics (MPs); yet, its contribution to urban hydrologic cycles remains under-quantified. In this study, we investigated the MP characteristics and flux in rainfall across 21 events in Seoul, South Korea, utilizing a cascade filtration protocol coupled with dual-spectroscopy (Fourier Transform-Infrared for ≥20 µm and Raman Spectroscopy for 5–20 µm). Results revealed an average MP abundance of 197 MPs L-1 with a dominance of fragments (> 96%). A critical "mass-count paradox" was observed: while fine particles (< 50 µm) were numerically dominant, larger particles (> 50 µm) accounted for approximately 90% of the total mass. Polymer composition also exhibited size-dependence, with brittle polymers (polystyrene and polyethylene terephthalate) prevalent in the finer fraction detected by Raman, whereas polypropylene and polyethylene dominated the larger fraction. The Conditional Fragmentation Model showed a fragmentation exponent (α) of approximately 1.08, characterizing the particles as an extensively weathered “aged atmospheric pool”. Furthermore, a strong correlation (r = 0.87) between MP flux and Antecedent Dry Days confirmed a "first-flush" mechanism, whereas meteorological analysis identified inertial impaction as the dominant scavenging driver (r = 0.97 with rainfall depth). Box model simulations demonstrated that although wet deposition contributes a minor fraction (1.8%–8.8%) of the annual load, it generates acute "shock loading" during storm events, accounting for up to 81% of the total influx. The findings underscore the necessity of integrating atmospheric deposition into urban water quality management strategies.
- 30 January 2026
- Published by Elsevier in Molecular Catalysis
- Vol. 592
Synthesis of iron nanoparticles for heterogeneous electrocatalytic oxidation of acid orange dye: In situ and stepwise mechanism
- 30 January 2026
- Published by Elsevier in Molecular Catalysis
- Vol. 592
Synthesis of iron nanoparticles for heterogeneous electrocatalytic oxidation of acid orange dye: In situ and stepwise mechanism
- Open Access
- 13 October 2025
- Published by Springer Nature in npj Clean Water
- Vol. 8 (1) , 93
Cyclodextrin polymer networks synthesis via amine-functionalized tripodal crosslinker for ultra-rapid removal of PFAS from water
- 13 October 2025
- Published by Springer Nature in npj Clean Water
- Vol. 8 (1) , 93
Open AccessCyclodextrin polymer networks synthesis via amine-functionalized tripodal crosslinker for ultra-rapid removal of PFAS from water
- Open Access
- 25 March 2025
- Published by Copernicus GmbH
Production of Sustainable Aviation Fuel from CO2-fed Algae Farm: A beneficial way of achieving both green-energy production and CO2 reduction simultaneously
It is expected that about 600-GT CO2 is expected to be emitted by the industrial sector for the next 50 years. In order to achieve the goal to reduce the industrial CO2 emission by 75%, an innovative carbon capture and utilization technology should be urgently developed and implemented. From 2050, all the flights taking off from any airport in the Europe should be fueled with jet-oils more than 70% of which should be sustainable aviation fuel (SAF). By the same year, all the petrol-based jet-fuel consumed in the US will be replaced with SAF. Therefore, 190 private companies located in 330 cities, 73% of which are in the EU or the US, are planning to produce SAF. As one of the most important jet-fuel providers in the world, Korea is finding a stable biomass source for producing SAF. Growing algae for oil extraction has attracted interest from engineers, since its lipid content is 40-60%. If CO2 is supplemented to the algae-growing farm, a higher yield is expected. Moreover, CO2 is supplied to the farm as HCO3-, the yield can double. In this presentation, an innovative and economical strategy to produce SAF via utilizing CO2 from industry will be presented. The feasibility of the strategy will evaluated in a holistic way.
- 25 March 2025
- Published by Copernicus GmbH
Open AccessProduction of Sustainable Aviation Fuel from CO2-fed Algae Farm: A beneficial way of achieving both green-energy production and CO2 reduction simultaneously
It is expected that about 600-GT CO2 is expected to be emitted by the industrial sector for the next 50 years. In order to achieve the goal to reduce the industrial CO2 emission by 75%, an innovative carbon capture and utilization technology should be urgently developed and implemented. From 2050, all the flights taking off from any airport in the Europe should be fueled with jet-oils more than 70% of which should be sustainable aviation fuel (SAF). By the same year, all the petrol-based jet-fuel consumed in the US will be replaced with SAF. Therefore, 190 private companies located in 330 cities, 73% of which are in the EU or the US, are planning to produce SAF. As one of the most important jet-fuel providers in the world, Korea is finding a stable biomass source for producing SAF. Growing algae for oil extraction has attracted interest from engineers, since its lipid content is 40-60%. If CO2 is supplemented to the algae-growing farm, a higher yield is expected. Moreover, CO2 is supplied to the farm as HCO3-, the yield can double. In this presentation, an innovative and economical strategy to produce SAF via utilizing CO2 from industry will be presented. The feasibility of the strategy will evaluated in a holistic way.
- 28 February 2025
- Published by Springer Nature in Frontiers of Environmental Science & Engineering
- Vol. 19 (4) , 1-15
Highly recyclable EDTA-crosslinked chitosan-gelatin biopolymer adsorbent for separation and recovery of rare earth elements from aqueous solution
- 28 February 2025
- Published by Springer Nature in Frontiers of Environmental Science & Engineering
- Vol. 19 (4) , 1-15
Highly recyclable EDTA-crosslinked chitosan-gelatin biopolymer adsorbent for separation and recovery of rare earth elements from aqueous solution