Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids

Formation of activated carbon from petroleum coke by KOH, results in high specific surface area materials that are predominantly microporous. This initial microporosity means that the adsorption kinetics of target species are not as rapid as they could be, thus limiting environmental remediation app...

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Main Authors: Oliver K.L. Strong, Elmira Nazari, Tyler Roy, Kevin Scotland, Paul R. Pede, Andrew J. Vreugdenhil
Format: Article
Language:English
Published: Elsevier 2023-02-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023007077
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author Oliver K.L. Strong
Elmira Nazari
Tyler Roy
Kevin Scotland
Paul R. Pede
Andrew J. Vreugdenhil
author_facet Oliver K.L. Strong
Elmira Nazari
Tyler Roy
Kevin Scotland
Paul R. Pede
Andrew J. Vreugdenhil
author_sort Oliver K.L. Strong
collection DOAJ
description Formation of activated carbon from petroleum coke by KOH, results in high specific surface area materials that are predominantly microporous. This initial microporosity means that the adsorption kinetics of target species are not as rapid as they could be, thus limiting environmental remediation applications for the material. To address this problem a series of additional heat cycles with no additional chemical inputs were applied after activation but prior to the removal of activating agents. This process resulted in the oxidation of residual potassium metal from the initial activation which allows it to function again as an activating agent for the subsequent cycles. The heat cycling resulted in an increase in mesoporosity by 10–25% with each successive cycle independent of the KOH to feedstock ratio. This was shown to be demonstrably different than equivalently extended heating times, thus identifying the importance of thermal cycling. Adsorption kinetics of three model naphthenic acids showed faster kinetics for the pore widened activated carbon. The t1/2 times dropped from 20 to 6.6 min for diphenyl acetic acid, 34.3 to 4.5 min for cyclohexane acetic acid, and 51.4 to 12.0 min for heptanoic acid.
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spelling doaj.art-a15ba115fb6e46e2babe6ae12d7de3342023-03-02T05:01:52ZengElsevierHeliyon2405-84402023-02-0192e13500Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acidsOliver K.L. Strong0Elmira Nazari1Tyler Roy2Kevin Scotland3Paul R. Pede4Andrew J. Vreugdenhil5Material Science, Department of Chemistry, Trent University, 1600 West Bank, Peterborough, Ontario K9L 0G2, CanadaMaterial Science, Department of Chemistry, Trent University, 1600 West Bank, Peterborough, Ontario K9L 0G2, CanadaMaterial Science, Department of Chemistry, Trent University, 1600 West Bank, Peterborough, Ontario K9L 0G2, CanadaMaterial Science, Department of Chemistry, Trent University, 1600 West Bank, Peterborough, Ontario K9L 0G2, CanadaCarbonix, 690 Mountain Rd, Suite 200, Fort William First Nation, Ontario P7J 1G8 CanadaMaterial Science, Department of Chemistry, Trent University, 1600 West Bank, Peterborough, Ontario K9L 0G2, Canada; Corresponding author.Formation of activated carbon from petroleum coke by KOH, results in high specific surface area materials that are predominantly microporous. This initial microporosity means that the adsorption kinetics of target species are not as rapid as they could be, thus limiting environmental remediation applications for the material. To address this problem a series of additional heat cycles with no additional chemical inputs were applied after activation but prior to the removal of activating agents. This process resulted in the oxidation of residual potassium metal from the initial activation which allows it to function again as an activating agent for the subsequent cycles. The heat cycling resulted in an increase in mesoporosity by 10–25% with each successive cycle independent of the KOH to feedstock ratio. This was shown to be demonstrably different than equivalently extended heating times, thus identifying the importance of thermal cycling. Adsorption kinetics of three model naphthenic acids showed faster kinetics for the pore widened activated carbon. The t1/2 times dropped from 20 to 6.6 min for diphenyl acetic acid, 34.3 to 4.5 min for cyclohexane acetic acid, and 51.4 to 12.0 min for heptanoic acid.http://www.sciencedirect.com/science/article/pii/S2405844023007077Activated carbonPetroleum cokeKOHMesoporosityNaphthenic acid
spellingShingle Oliver K.L. Strong
Elmira Nazari
Tyler Roy
Kevin Scotland
Paul R. Pede
Andrew J. Vreugdenhil
Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids
Heliyon
Activated carbon
Petroleum coke
KOH
Mesoporosity
Naphthenic acid
title Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids
title_full Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids
title_fullStr Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids
title_full_unstemmed Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids
title_short Transforming micropores to mesopores by heat cycling KOH activated petcoke for improved kinetics of adsorption of naphthenic acids
title_sort transforming micropores to mesopores by heat cycling koh activated petcoke for improved kinetics of adsorption of naphthenic acids
topic Activated carbon
Petroleum coke
KOH
Mesoporosity
Naphthenic acid
url http://www.sciencedirect.com/science/article/pii/S2405844023007077
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