Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates

In this study, four ammonium hydroxide ionic liquids (AHILs) with varying alkyl chains were evaluated for their kinetic hydrate inhibition (KHI) impact on pure carbon dioxide (CO<sub>2</sub>) and methane (CH<sub>4</sub>) gas hydrate systems. The constant cooling technique was...

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Main Authors: Muhammad Saad Khan, Cornelius Borecho Bavoh, Mohammad Azizur Rahman, Bhajan Lal, Ato Kwamena Quainoo, Abdulhalim Shah Maulud
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Energies
Subjects:
Online Access:https://www.mdpi.com/1996-1073/13/12/3272
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spelling doaj-9ef1d119a4fa4de2821fd4e24077bf032020-11-25T01:20:26ZengMDPI AGEnergies1996-10732020-06-01133272327210.3390/en13123272Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide HydratesMuhammad Saad Khan0Cornelius Borecho Bavoh1Mohammad Azizur Rahman2Bhajan Lal3Ato Kwamena Quainoo4Abdulhalim Shah Maulud5Petroleum Engineering Department, Texas A&M University at Qatar, Doha PO Box 23874, QatarCO2 Research Centre (CO2RES), Universiti Teknologi PETRONAS, Perak 32610, MalaysiaPetroleum Engineering Department, Texas A&M University at Qatar, Doha PO Box 23874, QatarCO2 Research Centre (CO2RES), Universiti Teknologi PETRONAS, Perak 32610, MalaysiaPetroleum Engineering Department, Universiti Teknologi PETRONAS, Perak 32610, MalaysiaChemical Engineering Department, Universiti Teknologi PETRONAS, Perak 32610, MalaysiaIn this study, four ammonium hydroxide ionic liquids (AHILs) with varying alkyl chains were evaluated for their kinetic hydrate inhibition (KHI) impact on pure carbon dioxide (CO<sub>2</sub>) and methane (CH<sub>4</sub>) gas hydrate systems. The constant cooling technique was used to determine the induction time, the initial rate of hydrate formation, and the amount of gas uptake for CH<sub>4</sub>-AHILs and CO<sub>2</sub>-AHILs systems at 8.0 and 3.50 MPa, respectively, at 1 wt.% aqueous AHILs solutions. In addition, the effect of hydrate formation sub-cooling temperature on the performance of the AHILs was conducted at experimental temperatures 274.0 and 277.0 K. The tested AHILs kinetically inhibited both CH<sub>4</sub> and CO<sub>2</sub> hydrates at the studied sub-cooling temperatures by delaying the hydrate induction time and reducing the initial rate of hydrate formation and gas uptake. The hydrate inhibition performance of AHILs increases with increasing alkyl chain length, due to the better surface adsorption on the hydrate crystal surface with alkyl chain length enhancement. TPrAOH efficiently inhibited the induction time of both CH<sub>4</sub> and CO<sub>2</sub> hydrate with an average inhibition percentage of 50% and 84%, respectively. Tetramethylammonium Hydroxide (TMAOH) and Tetrabutylammonium Hydroxide (TBAOH) best reduced CH<sub>4</sub> and CO<sub>2</sub> total uptake on average, with TMAOH and Tetraethylammonium Hydroxide (TEAOH) suitably reducing the average initial rate of CH<sub>4</sub> and CO<sub>2</sub> hydrate formation, respectively. The findings in this study could provide a roadmap for the potential use of AHILs as KHI inhibitors, especially in offshore environs.https://www.mdpi.com/1996-1073/13/12/3272ammonium hydroxide ionic liquids (AHILs)CH<sub>4</sub> hydrateCO<sub>2</sub> hydratealkyl chainionic liquidskinetic hydrate inhibition (KHI)
collection DOAJ
language English
format Article
sources DOAJ
author Muhammad Saad Khan
Cornelius Borecho Bavoh
Mohammad Azizur Rahman
Bhajan Lal
Ato Kwamena Quainoo
Abdulhalim Shah Maulud
spellingShingle Muhammad Saad Khan
Cornelius Borecho Bavoh
Mohammad Azizur Rahman
Bhajan Lal
Ato Kwamena Quainoo
Abdulhalim Shah Maulud
Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates
Energies
ammonium hydroxide ionic liquids (AHILs)
CH<sub>4</sub> hydrate
CO<sub>2</sub> hydrate
alkyl chain
ionic liquids
kinetic hydrate inhibition (KHI)
author_facet Muhammad Saad Khan
Cornelius Borecho Bavoh
Mohammad Azizur Rahman
Bhajan Lal
Ato Kwamena Quainoo
Abdulhalim Shah Maulud
author_sort Muhammad Saad Khan
title Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates
title_short Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates
title_full Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates
title_fullStr Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates
title_full_unstemmed Assessing the Alkyl Chain Effect of Ammonium Hydroxides Ionic Liquids on the Kinetics of Pure Methane and Carbon Dioxide Hydrates
title_sort assessing the alkyl chain effect of ammonium hydroxides ionic liquids on the kinetics of pure methane and carbon dioxide hydrates
publisher MDPI AG
series Energies
issn 1996-1073
publishDate 2020-06-01
description In this study, four ammonium hydroxide ionic liquids (AHILs) with varying alkyl chains were evaluated for their kinetic hydrate inhibition (KHI) impact on pure carbon dioxide (CO<sub>2</sub>) and methane (CH<sub>4</sub>) gas hydrate systems. The constant cooling technique was used to determine the induction time, the initial rate of hydrate formation, and the amount of gas uptake for CH<sub>4</sub>-AHILs and CO<sub>2</sub>-AHILs systems at 8.0 and 3.50 MPa, respectively, at 1 wt.% aqueous AHILs solutions. In addition, the effect of hydrate formation sub-cooling temperature on the performance of the AHILs was conducted at experimental temperatures 274.0 and 277.0 K. The tested AHILs kinetically inhibited both CH<sub>4</sub> and CO<sub>2</sub> hydrates at the studied sub-cooling temperatures by delaying the hydrate induction time and reducing the initial rate of hydrate formation and gas uptake. The hydrate inhibition performance of AHILs increases with increasing alkyl chain length, due to the better surface adsorption on the hydrate crystal surface with alkyl chain length enhancement. TPrAOH efficiently inhibited the induction time of both CH<sub>4</sub> and CO<sub>2</sub> hydrate with an average inhibition percentage of 50% and 84%, respectively. Tetramethylammonium Hydroxide (TMAOH) and Tetrabutylammonium Hydroxide (TBAOH) best reduced CH<sub>4</sub> and CO<sub>2</sub> total uptake on average, with TMAOH and Tetraethylammonium Hydroxide (TEAOH) suitably reducing the average initial rate of CH<sub>4</sub> and CO<sub>2</sub> hydrate formation, respectively. The findings in this study could provide a roadmap for the potential use of AHILs as KHI inhibitors, especially in offshore environs.
topic ammonium hydroxide ionic liquids (AHILs)
CH<sub>4</sub> hydrate
CO<sub>2</sub> hydrate
alkyl chain
ionic liquids
kinetic hydrate inhibition (KHI)
url https://www.mdpi.com/1996-1073/13/12/3272
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