J 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

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
Name: Cetocoen Plus
LM2015051, research and development project
Name: Centrum pro výzkum toxických látek v prostředí (Acronym: RECETOX RI)
Investor: Ministry of Education, Youth and Sports of the CR