Polymer weathering under simulated solar radiation and comparison to stormwater and estuarine microplastics

Accurate spectral identification of weathered plastics and analyses that provide insight into environmental degradation and age are desirable for source tracking and understanding hazards. The objectives of this study were to (1) evaluate the kinetics of spectral changes for lab-weathered polymers and compare to spectra from environmental microplastics (MPs), and (2) assess the accuracy of spectral databases in identifying weathered polymers. For objective 1, polyethylene (PE) and polypropylene (PP) fragments were exposed to simulated solar radiation in water for 90 days. FTIR spectra were collected periodically and degradation was quantified using carbonyl and hydroxyl bond indices. Significant linear increases in carbonyl indices for PP, but not PE, were observed as a function of exposure time. Spectra (via principal component analysis) and bond indices from lab-weathered polymers were then compared to environmental MPs collected from urban stormwater and the Delaware Bay estuary. Estuarine PP carbonyl and hydroxyl indices varied as a function of spectral collection mode (i.e., ATR vs. transmission) and by sampling site, potentially indicating the bond indices provide insight into sources/fate/transport of PP and are worthy of further study. In contrast, no significant differences were observed for PP in stormwater samples, possibly due to the close proximity of collection locations. PE exhibited non-linear trends in bond indices in the laboratory study and showed no significant association with sampling location in environmental samples, suggesting these indices may be less useful for PE degradation analysis. For objective 2, 14 different polymers, eight of which were polymer blends, were exposed to simulated solar radiation for up to 90 days, in dry and wet conditions. FTIR spectra were collected periodically and analyzed with two spectral identification software. OpenSpecy achieved an 88 % true positive rate compared to siMPle's 57 % at a 70 % hit quality threshold. Expanding reference libraries, to include weathered polymers and polymer blends, could improve spectral identification accuracy, and manual interpretation of FTIR spectra is recommended for low-confidence matches.

Authors

Institutions

Publication Details

Journal
Chemosphere
Published
2025-04-25
DOI
https://doi.org/10.1016/j.chemosphere.2025.144379
Citations
3
Primary Topic
Microplastics and Plastic Pollution
Type
article
Field-Weighted Citation Impact
1.51
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Polymer weathering under simulated solar radiation and comparison to stormwater and estuarine microplastics

Robert J. Chant, Georgia Arbuckle‐Keil, Nicole Fahrenfeld, Erik J Nitzberg et al.
3 citations
Chemosphere
Microplastics and Plastic Pollution
1.51
article

Polymer weathering under simulated solar radiation and comparison to stormwater and estuarine microplastics

Robert J. Chant, Georgia Arbuckle‐Keil, Nicole Fahrenfeld, Erik J Nitzberg, Lilia Ochoa
article en
3 citations

Abstract

Accurate spectral identification of weathered plastics and analyses that provide insight into environmental degradation and age are desirable for source tracking and understanding hazards. The objectives of this study were to (1) evaluate the kinetics of spectral changes for lab-weathered polymers and compare to spectra from environmental microplastics (MPs), and (2) assess the accuracy of spectral databases in identifying weathered polymers. For objective 1, polyethylene (PE) and polypropylene (PP) fragments were exposed to simulated solar radiation in water for 90 days. FTIR spectra were collected periodically and degradation was quantified using carbonyl and hydroxyl bond indices. Significant linear increases in carbonyl indices for PP, but not PE, were observed as a function of exposure time. Spectra (via principal component analysis) and bond indices from lab-weathered polymers were then compared to environmental MPs collected from urban stormwater and the Delaware Bay estuary. Estuarine PP carbonyl and hydroxyl indices varied as a function of spectral collection mode (i.e., ATR vs. transmission) and by sampling site, potentially indicating the bond indices provide insight into sources/fate/transport of PP and are worthy of further study. In contrast, no significant differences were observed for PP in stormwater samples, possibly due to the close proximity of collection locations. PE exhibited non-linear trends in bond indices in the laboratory study and showed no significant association with sampling location in environmental samples, suggesting these indices may be less useful for PE degradation analysis. For objective 2, 14 different polymers, eight of which were polymer blends, were exposed to simulated solar radiation for up to 90 days, in dry and wet conditions. FTIR spectra were collected periodically and analyzed with two spectral identification software. OpenSpecy achieved an 88 % true positive rate compared to siMPle's 57 % at a 70 % hit quality threshold. Expanding reference libraries, to include weathered polymers and polymer blends, could improve spectral identification accuracy, and manual interpretation of FTIR spectra is recommended for low-confidence matches.

ChemosphereVol. 379
Rutgers, The State University of New Jersey (US)
Life below water
Openalex Percentile: Top 20%
Microplastics and Plastic Pollution
1.51
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.