Iodine speciation in deep eutectic solvents. Issue 39 (30th September 2022)

• Record Type: Journal Article
• Authors: Hartley, Jennifer M.; Scott, Sean; Dilruba, Zarfishan; Lucio, Anthony J.; Bird, Philip J.; Harris, Robert C.; Jenkin, Gawen R. T.; Abbott, Andrew P.
• Is Part Of: Physical chemistry chemical physics. Volume 24:Issue 39(2022)
• Page Start: 24105
• Page End: 24115
• Publication Date: 2022-09-30
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/d2cp03185j
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Iodine speciation in deep eutectic solvents is affected by chloride activity, which is controlled by the hydrogen bond donor. Abstract : Iodine has been shown to act as a good electrocatalyst for metal digestion in deep eutectic solvents (DESs) but little is known about its speciation or reactivity in these high chloride containing media. Extended X-ray absorption fine structure (EXAFS) spectroscopy measurements were made at the iodine K-edge in a range of DESs with different glycolic or acidic hydrogen bond donors (HBDs), along with examining the effect of iodine concentration between 0.01 and 0.5 mol dm −3 . Three groups of speciation were detected: mixed I2 Cl − /I3 − (glycol and lactic acid systems), mixed I3 − /I2 (oxalic acid and urea systems), and singular I3 − (levulinic acid system). UV-vis spectroscopy was used to confirm the speciation. Electrochemistry showed that iodine redox behaviour was unaffected by the changing speciation. Leaching data showed that metal oxidation was related not only to changing iodine speciation, but also the reactivity and coordination ability of the HBD.