Using iron sulphate to form both n-type and p-type pseudo -thermoelectrics: non-hazardous and ‘second life’ thermogalvanic cells

Thermogalvanic cells can act like ‘liquid thermoelectrics’ to convert a thermal energy gradient to electrical energy. Such cells are typically combined electrically in-series in devices to boost the output voltage (as thermocells). However, the typical system involves a potentially fatal combination...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2020-09, Vol.22 (18), p.6062-6074
Hauptverfasser: Buckingham, Mark A., Laws, Kristine, Sengel, Jason T., Aldous, Leigh
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container_title Green chemistry : an international journal and green chemistry resource : GC
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creator Buckingham, Mark A.
Laws, Kristine
Sengel, Jason T.
Aldous, Leigh
description Thermogalvanic cells can act like ‘liquid thermoelectrics’ to convert a thermal energy gradient to electrical energy. Such cells are typically combined electrically in-series in devices to boost the output voltage (as thermocells). However, the typical system involves a potentially fatal combination of inherently acidic or acidified Fe 2+/3+ and [Fe(CN) 6 ] 3−/4− electrolytes; mixing and heating is expected to trigger extremely toxic HCN gas release. Here we demonstrate that benign aqueous iron( ii / iii ) sulphate can be combined with equally benign sodium sulphate and sodium hydrogen sulphate; the first leads to an [Fe(SO 4 ) 2 ] −/2− thermocell (Seebeck coefficient, S e = −0.4 mV K −1 ), and the second to a thermocell with intermediate [FeSO 4 ] 0/+ and [Fe(HSO 4 )] +/2+ character ( S e = +0.57 mV K −1 ). Their fundamental thermoelectrochemistry was explored, and their speciation elucidated. It was demonstrated that these can be utilised electrically in-parallel and in-series in thermogalvanic devices. When connected electrically in-series the thermocells presented here displayed temperature-dependent open circuit potentials only ca. one-third that typically reported for the ‘conventional’ combination of Fe 2+/3+ - and [Fe(CN) 6 ] 3−/4− -based thermocells (0.8 mV K −1 vs. ca. 3 mV K −1 , respectively). However, whereas the latter thermocells cannot be safely mixed, when the iron-sulphate cells were ‘accidently’ mixed they safely form a mixed thermocell electrolyte ( S e = +0.19 mV K −1 ), enabling a ‘second life’ of both the electrolyte and thermocell devices. This novel ‘all-iron sulphate’ thermocell was compared against the typically employed Fe 2+/3+ and [Fe(CN) 6 ] 3−/4− combination using the 12 principles of green chemistry and of green engineering, further demonstrating the inherent sustainability, safety and ‘green’ credentials of this system (but not yet efficiency). This work demonstrates how functionality and complexity can be introduced in a safe manner, while also preventing potential accidents and enabling new ‘end-of-life’ opportunities.
doi_str_mv 10.1039/D0GC01878C
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When connected electrically in-series the thermocells presented here displayed temperature-dependent open circuit potentials only ca. one-third that typically reported for the ‘conventional’ combination of Fe 2+/3+ - and [Fe(CN) 6 ] 3−/4− -based thermocells (0.8 mV K −1 vs. ca. 3 mV K −1 , respectively). However, whereas the latter thermocells cannot be safely mixed, when the iron-sulphate cells were ‘accidently’ mixed they safely form a mixed thermocell electrolyte ( S e = +0.19 mV K −1 ), enabling a ‘second life’ of both the electrolyte and thermocell devices. This novel ‘all-iron sulphate’ thermocell was compared against the typically employed Fe 2+/3+ and [Fe(CN) 6 ] 3−/4− combination using the 12 principles of green chemistry and of green engineering, further demonstrating the inherent sustainability, safety and ‘green’ credentials of this system (but not yet efficiency). 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When connected electrically in-series the thermocells presented here displayed temperature-dependent open circuit potentials only ca. one-third that typically reported for the ‘conventional’ combination of Fe 2+/3+ - and [Fe(CN) 6 ] 3−/4− -based thermocells (0.8 mV K −1 vs. ca. 3 mV K −1 , respectively). However, whereas the latter thermocells cannot be safely mixed, when the iron-sulphate cells were ‘accidently’ mixed they safely form a mixed thermocell electrolyte ( S e = +0.19 mV K −1 ), enabling a ‘second life’ of both the electrolyte and thermocell devices. This novel ‘all-iron sulphate’ thermocell was compared against the typically employed Fe 2+/3+ and [Fe(CN) 6 ] 3−/4− combination using the 12 principles of green chemistry and of green engineering, further demonstrating the inherent sustainability, safety and ‘green’ credentials of this system (but not yet efficiency). 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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Acidification
Circuits
Electrolytes
Electrolytic cells
End of life
Energy gradient
Ferricyanide
Green chemistry
Green development
Iron
Iron sulfates
Seebeck effect
Sodium sulfate
Speciation
Sulfates
Sustainability
Temperature dependence
Thermal energy
Thermoelectricity
title Using iron sulphate to form both n-type and p-type pseudo -thermoelectrics: non-hazardous and ‘second life’ thermogalvanic cells
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