Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/9720
Title: Mercury vapor sensor enhancement by nanostructured gold deposited on nickel surfaces using galvanic replacement reactions
Authors: Sabri, YM
Ippolito, SJ
Atanacio, AJ
Bansal, V
Bhargava, SK
Keywords: Mercury
Gold
Exhaust gases
Thin films
Toxicity
Morphology
Crystallography
X-ray diffraction
Issue Date: 16-Jul-2012
Publisher: Royal Society of Chemistry
Citation: Sabri, Y. M., Ippolito, S. J., Atanacio, A. J., Bansal, V., & Bhargava, S. K. (2012). Mercury vapor sensor enhancement by nanostructured gold deposited on nickel surfaces using galvanic replacement reactions. Journal of Materials Chemistry, 22(40), 21395-21404. doi:10.1039/C2JM33480A
Abstract: Anthropogenic mercury emission is a serious global environmental problem because of its toxicity to humans, plants and wildlife. In order to control these emissions, accurate and reliable online continuous mercury monitoring systems (CMMs) are critical. Such systems can notify appropriate authorities or provide feedback signals to a process control system in time, thus making them an integral part of monitoring and controlling Hg emissions. We demonstrate how nanostructured gold can easily be deposited in small quantities on nickel electrode based QCMs using galvanic replacement (GR) reactions with the resultant surface having excellent Hg monitoring properties. The developed GR surfaces were observed to have higher sensitivity and selectivity in the presence of interfering gas species (NH3 and H2O), as well as to have ∼80% higher mercury sorption capacity than the most efficient mercury sorbents reported to date. Investigations towards the Hg-sensing capabilities of the resultant Ni–Au surface based Hg sensors showed ∼50% better sensitivity and detection limit over control Au films. Furthermore, the GR based QCMs were found to self-regenerate without changing the operating temperature of the sensor, undergoing Hg desorption with sensor recoveries of 93.7–99.3% following Hg exposure at an operating temperature of 90 °C. Surface depth profile analysis of the Ni–Au electrode surfaces showed that the high recovery rate of the sensors was primarily due to the Ni–Au structures, which unlike continuous Au thin-films more commonly used for Hg sensing applications, do not accumulate Hg at the sensitive-layer–substrate interface. Furthermore, the GR Ni–Au surfaces were found to be highly selective towards Hg vapor in the presence of NH3 and H2O interfering gas species which makes them potentially suitable for operating in harsh industrial effluent environments.© The Royal Society of Chemistry 2012
Gov't Doc #: 9841
URI: https://pubs.rsc.org/en/content/articlehtml/2012/jm/c2jm33480a
http://apo.ansto.gov.au/dspace/handle/10238/9720
ISSN: 0959-9428
Appears in Collections:Journal Articles

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