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傅里叶变换红外光谱法评估人工老化和环境风化微塑料的老化程度

Fourier Transform Infrared Spectroscopy to Assess the Degree of Alteration of Artificially Aged and Environmentally Weathered Microplastics.

作者信息

Campanale Claudia, Savino Ilaria, Massarelli Carmine, Uricchio Vito Felice

机构信息

Italian National Council of Research-Water Research Institute, CNR-IRSA, 70132 Bari, Italy.

出版信息

Polymers (Basel). 2023 Feb 11;15(4):911. doi: 10.3390/polym15040911.

DOI:10.3390/polym15040911
PMID:36850194
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9961336/
Abstract

Fourier transform infrared (FTIR) is a spectroscopy technique widely used to identify organic materials. It has recently gained popularity in microplastic (MP) pollution research to determine the chemical composition of unknown plastic fragments. However, it could also be used to evaluate the degree of ageing of MPs collected from the environment. In this context, the principal aim of our research has been to qualitatively evaluate the natural weathering of environmental MPs collected in an Italian freshwater body (the Ofanto River) using ATR-FTIR technology. Furthermore, we compared environmental particles to weathered artificial MPs under controlled light and temperature conditions and to unaltered pristine materials to assess the results. FTIR spectra were acquired using a Nicolet Summit FTIR (ThermoFisher Scientific) equipped with an Everest ATR with a diamond Crystal plate and a DTGS KBr detector (wavenumber range 4000-500 cm, 32 scans per spectrum, spectral resolution of 4 cm). The degree of ageing was assessed using three different indexes known to be related to changes in MPs: Carbonyl Index (CI), Hydroxyl Index (HI), and Carbon-Oxygen Index (COI). The overall results showed that the regions reflecting changes (hydroxyl groups, peaks from 3100 to 3700 cm, alkenes or carbon double bonds, 1600 and 1680 cm, and carbonyl groups, 1690 and 1810 cm) appeared significantly modified in artificial and natural weathered particles compared to the pristine materials. The indexes calculated for polymers degraded under the artificial photo and thermo ageing conditions displayed a general tendency to increase with the time in contact with irradiation time. Particular enhancements of CI of PS fragment and PE pellet, HI of PE and PS fragments and PE pellet, and COI of PS fragment were observed. Otherwise, the following incubation of the same particles at a constant temperature of 45 °C did not further affect the chemical composition of the particles. Moreover, new unique peaks were also observed in the freshwater particles, almost all in the fingerprint region (1500-500 cm). Differences in CI, HI, and COI were evidenced among the different morphological MP shapes. On the one hand, the CI calculated for the environmental PE pellets showed values ranging from 0.05 to 0.26 with a mean value of 0.17 ± 0.10. Most samples (57%) presented a CI with values between 0.16 and 0.30. On the other hand, fragments presented slicer modifications in the carbonyl region with CI values lower than pellets (0.05 ± 0.05). This index helps evaluate the degradation of PE MPs by UV light, increasing with enhancing residence time in the environment. Conversely, fragments showed greater values of HI (5.90 ± 2.57) and COI (1.04 ± 0.48) than pellets, as well as lines, which presented the maximum value of HI (11.51). HI is attributed to the bond vibrations of hydroxyl, carboxyl, or phenol groups. In contrast, COI is frequently attributed to the vibrations of C_O bonds found in carbohydrates, alkanes, secondary alcohols, and ketones. In conclusion, our results showed characteristics spectra acquired from environmental particles compared to pristine and artificial aged ones. The interpretation of our main results emphasizes the need to conduct ecotoxicological experimental studies using naturally weathered particles due to the unicity of their properties, which are more helpful for understanding microplastic pollution effects.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/5a3fb8b9ea99/polymers-15-00911-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/586088245707/polymers-15-00911-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/ff22ca428beb/polymers-15-00911-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/7cdb334e0e66/polymers-15-00911-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/3097cad5aa23/polymers-15-00911-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/864b6c2de109/polymers-15-00911-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/25e616f31d6a/polymers-15-00911-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/5a3fb8b9ea99/polymers-15-00911-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/586088245707/polymers-15-00911-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/ff22ca428beb/polymers-15-00911-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/7cdb334e0e66/polymers-15-00911-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/3097cad5aa23/polymers-15-00911-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/864b6c2de109/polymers-15-00911-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/25e616f31d6a/polymers-15-00911-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fae/9961336/5a3fb8b9ea99/polymers-15-00911-g007.jpg
摘要

傅里叶变换红外光谱(FTIR)是一种广泛用于识别有机材料的光谱技术。最近,它在微塑料(MP)污染研究中受到欢迎,用于确定未知塑料碎片的化学成分。然而,它也可用于评估从环境中收集的微塑料的老化程度。在此背景下,我们研究的主要目的是使用衰减全反射傅里叶变换红外光谱(ATR-FTIR)技术对在意大利淡水水体(奥凡托河)中收集的环境微塑料的自然风化进行定性评估。此外,我们将环境颗粒与在受控光照和温度条件下风化的人造微塑料以及未改变的原始材料进行比较,以评估结果。使用配备有金刚石晶体板的埃佛勒斯峰衰减全反射附件和DTGS KBr探测器(波数范围4000 - 500 cm,每个光谱扫描32次,光谱分辨率4 cm)的尼高力峰会傅里叶变换红外光谱仪(赛默飞世尔科技公司)采集傅里叶变换红外光谱。使用已知与微塑料变化相关的三个不同指标评估老化程度:羰基指数(CI)、羟基指数(HI)和碳氧指数(COI)。总体结果表明,与原始材料相比,在人造和自然风化颗粒中,反映变化的区域(羟基基团,3100至3700 cm的峰,烯烃或碳双键,1600和1680 cm,以及羰基基团,1690和1810 cm)出现了显著变化。在人工光老化和热老化条件下降解的聚合物计算出的指数总体上显示出随着与辐照时间接触时间的增加而增加的趋势。观察到聚苯乙烯(PS)碎片和聚乙烯(PE)颗粒的羰基指数、PE和PS碎片以及PE颗粒的羟基指数以及PS碎片的碳氧指数有特别增强。否则,将相同颗粒在45℃恒温下进一步孵育不会进一步影响颗粒的化学成分。此外,在淡水颗粒中也观察到新的独特峰,几乎所有峰都在指纹区域(1500 - 500 cm)。在不同形态的微塑料形状之间,羰基指数、羟基指数和碳氧指数存在差异。一方面,计算得出的环境PE颗粒的羰基指数值范围为0.05至0.26,平均值为0.17±0.10。大多数样品(57%)的羰基指数值在0.16至0.30之间。另一方面,碎片在羰基区域呈现出比颗粒更低的羰基指数值(0.05±0.05)的更明显变化。该指数有助于评估紫外线对PE微塑料的降解,随着在环境中的停留时间增加而增加。相反,碎片的羟基指数(5.90±2.57)和碳氧指数(1.04±0.48)比颗粒以及线条更高,线条呈现出羟基指数的最大值(11.51)。羟基指数归因于羟基、羧基或酚基团的键振动。相比之下,碳氧指数通常归因于碳水化合物、烷烃、仲醇和酮中发现的C - O键的振动。总之,我们的结果显示了与原始和人工老化颗粒相比从环境颗粒获得的特征光谱。我们主要结果的解释强调了由于自然风化颗粒性质的独特性,需要使用它们进行生态毒理学实验研究,这对于理解微塑料污染影响更有帮助。

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