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Interfacial Behavior of Orthoborate Ionic Liquids at Inorganic Oxide Surfaces Probed by NMR, IR and Raman Spectroscopy
Luleå tekniska universitet, Institutionen för samhällsbyggnad och naturresurser, Kemiteknik.ORCID-id: 0000-0003-3652-7798
Luleå tekniska universitet, Institutionen för samhällsbyggnad och naturresurser, Kemiteknik.ORCID-id: 0000-0001-9794-8305
Surface and Corrosion Science, Department of Chemistry, KTH Royal Institute of Technology.
System and Component Design, KTH Royal Institute of Technology.
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2018 (Engelska)Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 122, nr 34, s. 19687-19698Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Absorption modes and reactivity of non-halogenated ionic liquids (ILs) at inorganic oxide surfaces of γ-Al2O3, MgO and SiO2 particles were characterized using multinuclear (11B, 31P and 29Si) solid-state magic-angle-spinning NMR, FTIR and Raman spectroscopy. ILs are composed of the trihexyl(tetradecyl)phosphonium cation, [P6,6,6,14]+, and bis(mandelato)borate, [BMB]-, or bis(salicylato)borate, [BScB]-, anions. Spectroscopic measurements were performed on room temperature (298 K) samples and samples exposed to 15 hours of heating at 373 K. The single pulse 11B NMR data of heated [P6,6,6,14][BMB] mixed with the inorganic oxides showed a significant change in spectra of the anion for all three oxides. In contrast, no such spectral changes were detected for heated [P6,6,6,14][BScB] mixed with the inorganic oxides. 31P MAS NMR data for the IL/metal oxide systems revealed interactions between [P6,6,6,14]+ and the surfaces of oxides. A significant intensity of 31P CP-MAS NMR signals indicated a low mobility of cations in these systems. The existence of strongly adhered surface layers of ILs on SiO2 particles was also confirmed by 1H-29Si CP-MAS NMR spectroscopy. FTIR and Raman spectroscopic data revealed strong interactions between the anions and the inorganic surfaces and there is strong correlation with the data obtained from NMR spectroscopy. Although their chemical structures are rather similar, the [BScB]- anion is more stable than the [BMB]- anion at the inorganic oxide surface.

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American Chemical Society (ACS), 2018. Vol. 122, nr 34, s. 19687-19698
Nationell ämneskategori
Fysikalisk kemi Kemiska processer
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Gränsytors kemi; Kemisk teknologi
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URN: urn:nbn:se:ltu:diva-70194DOI: 10.1021/acs.jpcc.8b06049ISI: 000443923500041Scopus ID: 2-s2.0-85052316588OAI: oai:DiVA.org:ltu-70194DiVA, id: diva2:1236346
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Validerad;2018;Nivå 2;2018-10-05 (johcin)

Tillgänglig från: 2018-08-01 Skapad: 2018-08-01 Senast uppdaterad: 2018-12-14Bibliografiskt granskad

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Shah, Faiz UllahHolmgren, AllanAntzutkin, Oleg

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The Journal of Physical Chemistry C
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