Detailed Information on Publication Record
2017
Investigations into titanium dioxide nanoparticle and pesticide interactions in aqueous environments
ILINA, Svetlana M., Patrick OLLIVIER, Danielle SLOMBERG, Nicole BARAN, Anne PARIAT et. al.Basic information
Original name
Investigations into titanium dioxide nanoparticle and pesticide interactions in aqueous environments
Authors
ILINA, Svetlana M. (250 France), Patrick OLLIVIER (250 France), Danielle SLOMBERG (250 France), Nicole BARAN (250 France), Anne PARIAT (250 France), Nicolas DEVAU (250 France), Nicole SANI-KAST (756 Switzerland), Martin SCHERINGER (756 Switzerland, guarantor, belonging to the institution) and Jerome LABILLE (250 France)
Edition
ENVIRONMENTAL SCIENCE-NANO, CAMBRIDGE, ROYAL SOC CHEMISTRY, 2017, 2051-8153
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10511 Environmental sciences
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.087
RIV identification code
RIV/00216224:14310/17:00100151
Organization unit
Faculty of Science
UT WoS
000412904200013
Keywords in English
TIO2 NANOPARTICLES; ENGINEERED NANOPARTICLES; AGGREGATION KINETICS; ORGANIC-MATTER; PHOTOCATALYTIC DEGRADATION; OXIDE NANOPARTICLES; SURFACE SPECIATION; ACID ADSORPTION; IONIC-STRENGTH; HUMIC-ACID
Tags
International impact, Reviewed
Změněno: 5/4/2018 15:55, Ing. Nicole Zrilić
Abstract
V originále
The influence of three pesticides (glyphosate, aminomethylphosphonic acid (AMPA) and 2,4-dichlorophenoxyacetic acid (2,4-D)) on the colloidal fate of TiO2 nanoparticles (NPs; anatase and rutile) has been investigated under aqueous conditions of variable chemical composition (Na+ or Ca2+), ionic strength (IS, 10(-4) -10(-1) M), and pH (5 or 8). Sorption and degradation of these pesticides in the presence of the NPs were evaluated. In the absence of the pesticides, increasing IS, the presence of the divalent cation Ca2+ and a pH value close to the NP isoelectric point favored NP homoaggregation as expected. However, at low IS (<= 10(-2) M in NaCl; <= 10(-3) M in CaCl2), in the presence of a few mu g L-1 of glyphosate and rutile in the mg L-1 range, NP homoaggregation was prevented, despite the pH = 5 close to the NP isoelectric point (4.0-4.2). The phosphonate group of the pesticide drove glyphosate adsorption onto the NP, while the carboxylic group was responsible for the electrostatic stabilization of the NP. The stabilizing effect of glyphosate on NP aggregation however appears to be temporary. Furthermore, TiO2 NPs also adsorbed AMPA and promoted degradation of glyphosate to AMPA. These results highlight new evidence of NP-pesticide interactions and the differences in their fate and potential co-migration behavior in aquatic environments.
Links
EF15_003/0000469, research and development project |
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LM2015051, research and development project |
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