TY - JOUR
T1 - Nanoplastic production procedure for scientific purposes
T2 - PP, PVC, PE-LD, PE-HD, and PS
AU - Merdy, Patricia
AU - Delpy, Floriane
AU - Bonneau, Adrien
AU - Villain, Sylvie
AU - Iordachescu, Lucian
AU - Vollertsen, Jes
AU - Lucas, Yves
PY - 2023/8
Y1 - 2023/8
N2 - Studies on the environmental impact of nanoplastics face challenges in plastic analysis and a scarcity of nanoplastic materials necessary for the development of analytical techniques and experiments on biota impact. Here we provide detailed procedures for obtaining nanoparticles suspended in water for the most commonly used polymers: Polypropylene (PP), Polyvinylchloride (PVC), Low- and High-Density Polyethylene (PE-LD, PE-HD), and Polystyrene (PS). We dissolved larger size material to reprecipitate nanoparticles. For all plastic types, we obtained nanoparticles with a size between 50 and 300 nm, and a mainly spherical morphology. We verified that no irreversible agglomeration or coalescence of the particles occurred after 5 days of storage. The concentrations obtained in the final carrier solution were of the order of 109 particles mL−1. To prevent the persistence of reagents in the final carrier solution, a filtration step was implemented at the end of the process. The method proved unsuitable for Polyethylene Terephthalate (PET).
AB - Studies on the environmental impact of nanoplastics face challenges in plastic analysis and a scarcity of nanoplastic materials necessary for the development of analytical techniques and experiments on biota impact. Here we provide detailed procedures for obtaining nanoparticles suspended in water for the most commonly used polymers: Polypropylene (PP), Polyvinylchloride (PVC), Low- and High-Density Polyethylene (PE-LD, PE-HD), and Polystyrene (PS). We dissolved larger size material to reprecipitate nanoparticles. For all plastic types, we obtained nanoparticles with a size between 50 and 300 nm, and a mainly spherical morphology. We verified that no irreversible agglomeration or coalescence of the particles occurred after 5 days of storage. The concentrations obtained in the final carrier solution were of the order of 109 particles mL−1. To prevent the persistence of reagents in the final carrier solution, a filtration step was implemented at the end of the process. The method proved unsuitable for Polyethylene Terephthalate (PET).
KW - Dissolution-precipitation
KW - Nanoparticles production
KW - Nanoplastics
KW - Dissolution-precipitation
KW - Nanoparticles production
KW - Nanoplastics
U2 - 10.1016/j.heliyon.2023.e18387
DO - 10.1016/j.heliyon.2023.e18387
M3 - Journal article
AN - SCOPUS:85165961758
SN - 2405-8440
VL - 9
JO - Heliyon
JF - Heliyon
IS - 8
M1 - e18387
ER -