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@ARTICLE{SchmittPauly:279321,
author = {Schmitt Pauly, Céline and Genix, Anne-Caroline and
Alauzun, Johan G. and Guerrero, Gilles and Appavou,
Marie-Sousai and Pérez, Javier and Oberdisse, Julian and
Mutin, P. Hubert},
title = {{S}imultaneous {P}hase {T}ransfer and {S}urface
{M}odification of {T}i{O} 2 {N}anoparticles {U}sing
{A}lkylphosphonic {A}cids: {O}ptimization and {S}tructure of
the {O}rganosols},
journal = {Langmuir},
volume = {31},
number = {40},
issn = {1520-5827},
address = {Washington, DC},
publisher = {ACS Publ.},
reportid = {FZJ-2015-07336},
pages = {10966 - 10974},
year = {2015},
note = {"final draft post referee" kann nicht beigebracht werden},
abstract = {An original protocol of simultaneous surface modification
and transfer from aqueous to organic phases of anatase TiO2
nanoparticles (NPs) using alkylphosphonic acids (PAs) is
studied. The influence of the solvent, the nature and
concentration of the PA, and the size, concentration, and
aggregation state of the TiO2 NPs was investigated. Complete
transfer was observed for linear alkyl chains (5, 8, 12, and
18 C atoms), even at very high sol concentrations. After
transfer, the grafted NPs were characterized by 31P
solid-state MAS NMR. The dispersion state of NPs before and
after phase transfer was monitored by dynamic light
scattering (DLS). Small-angle neutron scattering (SANS) was
used to characterize the structure of PA-grafted NPs in the
organic solvent. Using a quantitative core–shell model
cross-checked under different contrast conditions, it is
found that the primary particles making up the NPs are
homogeneously grafted with a solvated PA-layer. The
nanometric thickness of the latter is shown to increase with
the length of the linear carbon chain of the PA, independent
of the size of the primary TiO2 NP. Interestingly, a
reversible temperature-dependent aggregation was evidenced
visually for C18PA, and confirmed by DLS and SANS: heating
the sample induces the breakup of aggregates, which
reassemble upon cooling. Finally, in the case of NPs
agglomerated by playing with the pH or the salt
concentration of the sols, the phase transfer with PA is
capable of redispersing the agglomerates. This new and
highly versatile method of NP surface modification with PAs
and simultaneous transfer is thus well suited for obtaining
well-dispersed grafted NPs.},
cin = {JCNS (München) ; Jülich Centre for Neutron Science JCNS
(München) ; JCNS-FRM-II / Neutronenstreuung ; JCNS-1},
ddc = {670},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
I:(DE-Juel1)JCNS-1-20110106},
pnm = {6G15 - FRM II / MLZ (POF3-6G15) / 6G4 - Jülich Centre for
Neutron Research (JCNS) (POF3-623)},
pid = {G:(DE-HGF)POF3-6G15 / G:(DE-HGF)POF3-6G4},
experiment = {EXP:(DE-MLZ)KWS2-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000362920900005},
doi = {10.1021/acs.langmuir.5b02833},
url = {https://juser.fz-juelich.de/record/279321},
}