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dc.contributor.authorMurugappan, Krishnan
dc.contributor.authorKang, Colin
dc.contributor.authorSilvester, Debbie
dc.date.accessioned2017-01-30T14:58:39Z
dc.date.available2017-01-30T14:58:39Z
dc.date.created2014-09-30T20:00:22Z
dc.date.issued2014
dc.identifier.citationMurugappan, K. and Kang, C. and Silvester, D. 2014. Electrochemical Oxidation and Sensing of Methylamine Gas in Room Temperature Ionic Liquids. The Journal of Physical Chemistry C. 118 (33): pp. 19232-19237.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/42282
dc.identifier.doi10.1021/jp5061045
dc.description.abstract

The electrochemical behaviour of methylamine gas in several room temperature ionic liquids (RTILs), [C2mim][NTf2], [C4mim][NTf2], [C6mim][FAP], [C4mpyrr][NTf2], [C4mim][BF4], and [C4mim][PF6] has been investigated on a Pt microelectrode using cyclic voltammetry. A broad oxidation wave at approximately 3 V, two reduction peaks and another oxidation peak was observed. A complicated mechanism is predicted based on the voltammetry obtained, with ammonia gas as a likely by-product. The currents obtained suggest that methylamine has a high solubility in RTILs, which is important for gas sensing applications. The analytical utility of methylamine was then studied in [C4mpyrr][NTf2] and [C2mim][NTf2]. A linear calibration graph with an R2 value of 0.99 and limits of detection of 33 and 34 ppm were obtained respectively, suggesting that RTILs are favourable non-volatile solvents for the electrochemical detection of highly toxic methylamine gas.

dc.publisherAmerican Chemical Society
dc.subjectRoom temperature ionic liquids
dc.subjectGas sensing
dc.subjectReaction mechanism
dc.subjectCyclic Voltammetry
dc.subjectMethylamine oxidation
dc.subjectElectrochemistry
dc.titleElectrochemical Oxidation and Sensing of Methylamine Gas in Room Temperature Ionic Liquids
dc.typeJournal Article
dcterms.source.volume118
dcterms.source.startPage19232
dcterms.source.endPage19237
dcterms.source.issn1932-7447
dcterms.source.titleThe Journal of Physical Chemistry C
curtin.note

This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Physical Chemistry C, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://doi.org/10.1021/jp5061045.

curtin.note

This research was supported under Australian Research Council's Discovery Early Career Research Award (project number DE120101456)

curtin.departmentDepartment of Applied Chemistry
curtin.accessStatusOpen access


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