Development of Quantitative Structure-Activity Relationships for Nanoparticle Titanium Dioxide Aggregation in the Presence of Organic Contaminants

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Abstract

This study investigated the influence of organic wastewater contaminants (OWCs) on the aggregation of nanoparticle titanium dioxide (n-TiO2) because aggregation experiments are important to obtain fundamental information about the potential fate of n-TiO2 in environmental systems. Aggregation experiments showed that surface modification of n-TiO2 such as different aggregation behaviors and changes of zeta potentials was clearly influenced by the adsorption of OWCs based on t-test results. Largest diameter changes of n-TiO2 were observed by chlorothalonil (359 nm) at 0 h and alachlor (436 nm) at 12 h, while smallest diameter changes of n-TiO2 were observed by cyanazine (84 nm) at 0 h and butylate (53 nm) at 12 h. The most significant zeta potential changes of n-TiO2 were observed by pendimethalin and butylate with -15.2 mV at 0 h and with -16.7 mV and -17.1 mV at 12 h, respectively. These results may demonstrate insights into the microscopic and/or molecular interaction between n-TiO2 and OWCs that result in surface modification of n-TiO2. Thus, we developed quantitative structure-activity relationships (QSARs) between n-TiO2 aggregation rate kinetics and representative seven descriptors of OWCs including pKa, Solubility (Cw), log Kow, molecular weight, polar surface area (P.S.A.), molar volume, and # of H Bond Donor (# of H.B.D.). The developed QSARs showed that experimental n-TiO2 aggregation rate kinetics were strongly related to seven descriptors of all OWCs except for butylate. Particularly, some polarity descriptors such as Cw, log Kow, P.S.A., and # of H.B.D. seem to have influences on the developed QSARs. Therefore, our developed QSARs for n-TiO2 aggregation rate kinetics according to seven descriptors of OWCs provide solid information to the general nanoparticle (NP) researches and significant insights about the effects of emerging OWCs on microscopic and/or molecular interaction with NPs, which would demonstrate the roles of physicochemical descriptors of OWCs on n-TiO2 aggregation.

Original languageEnglish (US)
Pages (from-to)918-926
Number of pages9
JournalEnvironmental Engineering Science
Volume35
Issue number9
DOIs
StatePublished - Sep 2018

Fingerprint

Titanium dioxide
Wastewater
Agglomeration
Impurities
Nanoparticles
wastewater
pollutant
tetrachloroisophthalonitrile
Molecular interactions
Zeta potential
kinetics
Kinetics
Surface treatment
surface area
aggregation behavior
alachlor
titanium dioxide
nanoparticle
structure-activity relationship
Density (specific gravity)

Keywords

  • aggregation
  • n-TiO2
  • organic wastewater contaminants
  • quantitative structure activity relationships

ASJC Scopus subject areas

  • Environmental Chemistry
  • Waste Management and Disposal
  • Pollution

Cite this

@article{c62b8cbe0c94456e9d66f3cd868db8cd,
title = "Development of Quantitative Structure-Activity Relationships for Nanoparticle Titanium Dioxide Aggregation in the Presence of Organic Contaminants",
abstract = "This study investigated the influence of organic wastewater contaminants (OWCs) on the aggregation of nanoparticle titanium dioxide (n-TiO2) because aggregation experiments are important to obtain fundamental information about the potential fate of n-TiO2 in environmental systems. Aggregation experiments showed that surface modification of n-TiO2 such as different aggregation behaviors and changes of zeta potentials was clearly influenced by the adsorption of OWCs based on t-test results. Largest diameter changes of n-TiO2 were observed by chlorothalonil (359 nm) at 0 h and alachlor (436 nm) at 12 h, while smallest diameter changes of n-TiO2 were observed by cyanazine (84 nm) at 0 h and butylate (53 nm) at 12 h. The most significant zeta potential changes of n-TiO2 were observed by pendimethalin and butylate with -15.2 mV at 0 h and with -16.7 mV and -17.1 mV at 12 h, respectively. These results may demonstrate insights into the microscopic and/or molecular interaction between n-TiO2 and OWCs that result in surface modification of n-TiO2. Thus, we developed quantitative structure-activity relationships (QSARs) between n-TiO2 aggregation rate kinetics and representative seven descriptors of OWCs including pKa, Solubility (Cw), log Kow, molecular weight, polar surface area (P.S.A.), molar volume, and # of H Bond Donor (# of H.B.D.). The developed QSARs showed that experimental n-TiO2 aggregation rate kinetics were strongly related to seven descriptors of all OWCs except for butylate. Particularly, some polarity descriptors such as Cw, log Kow, P.S.A., and # of H.B.D. seem to have influences on the developed QSARs. Therefore, our developed QSARs for n-TiO2 aggregation rate kinetics according to seven descriptors of OWCs provide solid information to the general nanoparticle (NP) researches and significant insights about the effects of emerging OWCs on microscopic and/or molecular interaction with NPs, which would demonstrate the roles of physicochemical descriptors of OWCs on n-TiO2 aggregation.",
keywords = "aggregation, n-TiO2, organic wastewater contaminants, quantitative structure activity relationships",
author = "Jaewoong Lee and Bartelt-Hunt, {Shannon L} and Yusong Li",
year = "2018",
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language = "English (US)",
volume = "35",
pages = "918--926",
journal = "Environmental Engineering Science",
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T1 - Development of Quantitative Structure-Activity Relationships for Nanoparticle Titanium Dioxide Aggregation in the Presence of Organic Contaminants

AU - Lee, Jaewoong

AU - Bartelt-Hunt, Shannon L

AU - Li, Yusong

PY - 2018/9

Y1 - 2018/9

N2 - This study investigated the influence of organic wastewater contaminants (OWCs) on the aggregation of nanoparticle titanium dioxide (n-TiO2) because aggregation experiments are important to obtain fundamental information about the potential fate of n-TiO2 in environmental systems. Aggregation experiments showed that surface modification of n-TiO2 such as different aggregation behaviors and changes of zeta potentials was clearly influenced by the adsorption of OWCs based on t-test results. Largest diameter changes of n-TiO2 were observed by chlorothalonil (359 nm) at 0 h and alachlor (436 nm) at 12 h, while smallest diameter changes of n-TiO2 were observed by cyanazine (84 nm) at 0 h and butylate (53 nm) at 12 h. The most significant zeta potential changes of n-TiO2 were observed by pendimethalin and butylate with -15.2 mV at 0 h and with -16.7 mV and -17.1 mV at 12 h, respectively. These results may demonstrate insights into the microscopic and/or molecular interaction between n-TiO2 and OWCs that result in surface modification of n-TiO2. Thus, we developed quantitative structure-activity relationships (QSARs) between n-TiO2 aggregation rate kinetics and representative seven descriptors of OWCs including pKa, Solubility (Cw), log Kow, molecular weight, polar surface area (P.S.A.), molar volume, and # of H Bond Donor (# of H.B.D.). The developed QSARs showed that experimental n-TiO2 aggregation rate kinetics were strongly related to seven descriptors of all OWCs except for butylate. Particularly, some polarity descriptors such as Cw, log Kow, P.S.A., and # of H.B.D. seem to have influences on the developed QSARs. Therefore, our developed QSARs for n-TiO2 aggregation rate kinetics according to seven descriptors of OWCs provide solid information to the general nanoparticle (NP) researches and significant insights about the effects of emerging OWCs on microscopic and/or molecular interaction with NPs, which would demonstrate the roles of physicochemical descriptors of OWCs on n-TiO2 aggregation.

AB - This study investigated the influence of organic wastewater contaminants (OWCs) on the aggregation of nanoparticle titanium dioxide (n-TiO2) because aggregation experiments are important to obtain fundamental information about the potential fate of n-TiO2 in environmental systems. Aggregation experiments showed that surface modification of n-TiO2 such as different aggregation behaviors and changes of zeta potentials was clearly influenced by the adsorption of OWCs based on t-test results. Largest diameter changes of n-TiO2 were observed by chlorothalonil (359 nm) at 0 h and alachlor (436 nm) at 12 h, while smallest diameter changes of n-TiO2 were observed by cyanazine (84 nm) at 0 h and butylate (53 nm) at 12 h. The most significant zeta potential changes of n-TiO2 were observed by pendimethalin and butylate with -15.2 mV at 0 h and with -16.7 mV and -17.1 mV at 12 h, respectively. These results may demonstrate insights into the microscopic and/or molecular interaction between n-TiO2 and OWCs that result in surface modification of n-TiO2. Thus, we developed quantitative structure-activity relationships (QSARs) between n-TiO2 aggregation rate kinetics and representative seven descriptors of OWCs including pKa, Solubility (Cw), log Kow, molecular weight, polar surface area (P.S.A.), molar volume, and # of H Bond Donor (# of H.B.D.). The developed QSARs showed that experimental n-TiO2 aggregation rate kinetics were strongly related to seven descriptors of all OWCs except for butylate. Particularly, some polarity descriptors such as Cw, log Kow, P.S.A., and # of H.B.D. seem to have influences on the developed QSARs. Therefore, our developed QSARs for n-TiO2 aggregation rate kinetics according to seven descriptors of OWCs provide solid information to the general nanoparticle (NP) researches and significant insights about the effects of emerging OWCs on microscopic and/or molecular interaction with NPs, which would demonstrate the roles of physicochemical descriptors of OWCs on n-TiO2 aggregation.

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