Adsorption and Desorption Behaviour of Polychlorinated Biphenyls onto Microplastics' Surfaces in Water/Sediment Systems.
adsorption
marine microcosm
microplastics (MPLs)
polychlorinated biphenyls
polyethylene
polyethylene terephthalate
polystyrene
Journal
Toxics
ISSN: 2305-6304
Titre abrégé: Toxics
Pays: Switzerland
ID NLM: 101639637
Informations de publication
Date de publication:
17 Aug 2020
17 Aug 2020
Historique:
received:
23
07
2020
revised:
12
08
2020
accepted:
13
08
2020
entrez:
23
8
2020
pubmed:
23
8
2020
medline:
23
8
2020
Statut:
epublish
Résumé
The potential of microplastics (MPLs) in marine ecosystems to adsorb and transport other micropollutants to biota, contributing to their entry in the food chain, is a primary cause of concern. However, these interactions remain poorly understood. Here, we have evaluated the adsorption/desorption behaviour of marker polychlorinated biphenyls (PCBs), onto MPL surfaces of three widely used polymers-polystyrene (PS), polyethylene (PE), and polyethylene terephthalate (PET). The range of MPL sizes ranged from 1 to 600 μm. The adsorption/desorption was evaluated in sediment/water systems in marine microcosms emulating realistic environmental conditions for 21 days. The adsorption percentages ranged from 20 to 60%. PCBs with a lower degree of chlorination showed higher adsorption percentages because of conformational impediments of PCBs with high-degree chlorination, and also by their affinity to be adsorbed in sediments. Glassy plastic polymers as PET and PS showed a superior affinity for PCBs than rubbery polymers, such as PE. The polymers that can bond PCBs by π-π interactions, rather than van der Waals forces showed better adsorption percentages, as expected. Finally, the adsorption/desorption behaviour of selected PCBs onto MPLs was fitted to a Freundlich isotherm model, with correlations higher than 0.8 in most of the cases.
Identifiants
pubmed: 32824499
pii: toxics8030059
doi: 10.3390/toxics8030059
pmc: PMC7560274
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Ministerio de Ciencia, Innovación y Universidades
ID : CTM 2017-89701C3-1-R
Références
Environ Toxicol Chem. 2016 Jul;35(7):1667-76
pubmed: 27093569
Environ Pollut. 2013 Jul;178:483-92
pubmed: 23545014
Mar Pollut Bull. 2020 Feb;151:110806
pubmed: 32056600
Environ Sci Technol. 2016 Apr 5;50(7):4037-44
pubmed: 26963589
Environ Sci Technol. 2007 Nov 15;41(22):7759-64
pubmed: 18075085
Sci Total Environ. 2019 Nov 10;690:565-572
pubmed: 31301497
Environ Sci Technol. 2014 May 6;48(9):4869-76
pubmed: 24689832
Chemosphere. 2017 Nov;186:10-16
pubmed: 28759812
Environ Pollut. 2017 Jan;220(Pt A):150-158
pubmed: 27650963
Mar Pollut Bull. 2011 Aug;62(8):1596-605
pubmed: 21742351
Environ Pollut. 2010 Aug;158(8):2672-8
pubmed: 20605296
Mar Pollut Bull. 2014 Oct 15;87(1-2):286-291
pubmed: 25172614
Mar Pollut Bull. 2007 Aug;54(8):1230-7
pubmed: 17532349
Sci Rep. 2014 Mar 31;4:4528
pubmed: 24681661
Mar Pollut Bull. 2020 Jan;150:110697
pubmed: 31753557
Environ Pollut. 2016 Jul;214:194-201
pubmed: 27086075
Mar Pollut Bull. 2010 Nov;60(11):1988-92
pubmed: 20800853
Sci Total Environ. 2019 Jan 10;647:20-28
pubmed: 30077159
J Agric Food Chem. 2005 Jan 12;53(1):164-9
pubmed: 15631524
Environ Pollut. 2018 Apr;235:680-691
pubmed: 29339337
J Environ Monit. 2005 Jun;7(6):612-20
pubmed: 15931424
Environ Sci Technol. 2013 Feb 5;47(3):1646-54
pubmed: 23270427
Environ Sci Technol. 2018 Mar 6;52(5):2677-2685
pubmed: 29420017