Deposition and release kinetics of nano-TiO2 in saturated porous media: Effects of solution ionic strength and surfactants
The aggregation, transport and deposition kinetics (i.e. attachment and release) of TiO2 nanoparticles (nano-TiO2) were investigated as a function of ionic strength and the presence of anionic (sodium dodecylbenzene sulfonate, SDBS) and non-ionic (Triton X-100) surfactants in 100% critical micelle c...
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Published in: | Environmental pollution (1987) Vol. 174; pp. 106 - 113 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Kidlington
Elsevier Ltd
01-03-2013
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | The aggregation, transport and deposition kinetics (i.e. attachment and release) of TiO2 nanoparticles (nano-TiO2) were investigated as a function of ionic strength and the presence of anionic (sodium dodecylbenzene sulfonate, SDBS) and non-ionic (Triton X-100) surfactants in 100% critical micelle concentration (CMC). The electrolyte concentration of the suspensions dictated the kinetic stability of nano-TiO2 thus influencing the transport and retention of the nanoaggregates in the saturated porous medium. With increasing ionic strength, the interaction between approaching nano-TiO2 and nano-TiO2 already deposited onto collectors surfaces seemed to be more favorable than the interaction between approaching nano-TiO2 and bare collectors surfaces. The abrupt and gradual reduction in electrolyte concentration during the flushing cycles of the column experiments induced the release of previously deposited nano-TiO2 suggesting attachment of nano-TiO2 through secondary energy minimum.
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► This study focuses on aggregation, transport and deposition kinetics of nano-TiO2. ► Ionic strength and surfactants impact nano-TiO2 transport in saturated porous media. ► Previously deposited nano-TiO2 serve as preferential sites for subsequent deposition. ► Changes in solution chemistry cause nanodeposits to release a portion of nano-TiO2.
Previously deposited nano-TiO2 serve as preferential sites for subsequent deposition and changes in solution chemistry cause nanodeposits to release a portion of nano-TiO2. |
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Bibliography: | http://dx.doi.org/10.1016/j.envpol.2012.11.002 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0269-7491 1873-6424 |
DOI: | 10.1016/j.envpol.2012.11.002 |