Eti Pagar, Avinash V. Palodkar, Vimal Kumar, Hari Prakash Veluswamy
{"title":"Investigating the Effect of NaCl Concentration on CO2 Hydrate Formation Kinetics: Experimental and Modeling Insights for CO2 Sequestration","authors":"Eti Pagar, Avinash V. Palodkar, Vimal Kumar, Hari Prakash Veluswamy","doi":"10.1021/cbe.5c00092","DOIUrl":null,"url":null,"abstract":"<p>Gas hydrate-based CO<sub>2</sub> sequestration\r\nstands\r\nout as a\r\npotential approach for the permanent storage of CO<sub>2</sub> in\r\nmarine sediments, leveraging its exceptional capacity for CO<sub>2</sub> storage along with long-term stability and safety. This study presents\r\na systematic investigation of the kinetics of CO<sub>2</sub> hydrate\r\nformation in a silica sand matrix over a wide range of NaCl concentrations\r\n(0–5.0 wt %). While gas hydrates are typically stable in freshwater-saturated\r\nsilica sediments, the presence of NaCl (in seawater) poses significant\r\nchallenges by inhibiting hydrate growth, reducing thermodynamic stability,\r\nand lowering storage capacity. Previous studies often considered a\r\nsingle salt concentration, limiting our understanding of the salinity\r\neffect. This work provides a comprehensive kinetic analysis, supported\r\nby a chemical potential-driven model, to elucidate the impact of varying\r\nsalt content on CO<sub>2</sub> hydrate formation. The findings indicate\r\nthat higher NaCl concentrations (≥3 wt %) markedly hinder hydrate\r\nformation rates, reaffirming the suppressive effect of salt. To address\r\nthis challenge, biodegradable amino acid <span>l</span>-leucine (LL) was\r\nemployed as a kinetic hydrate promoter. In the presence of 5.0 wt\r\n% NaCl, incorporating 2.0 wt % LL boosted gas uptake by nearly 2.6\r\ntimes, highlighting its strong promotional impact. The proposed model,\r\nfirst of its kind, accurately represents the kinetics across diverse\r\nsalinity levels and additive scenarios, providing actionable insights\r\nfor advancing CO<sub>2</sub> hydrate-based sequestration.</p>","PeriodicalId":100230,"journal":{"name":"Chem & Bio Engineering","volume":"3 2","pages":"268–282"},"PeriodicalIF":8.4000,"publicationDate":"2026-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem & Bio Engineering","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/cbe.5c00092","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/9 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Gas hydrate-based CO2 sequestration
stands
out as a
potential approach for the permanent storage of CO2 in
marine sediments, leveraging its exceptional capacity for CO2 storage along with long-term stability and safety. This study presents
a systematic investigation of the kinetics of CO2 hydrate
formation in a silica sand matrix over a wide range of NaCl concentrations
(0–5.0 wt %). While gas hydrates are typically stable in freshwater-saturated
silica sediments, the presence of NaCl (in seawater) poses significant
challenges by inhibiting hydrate growth, reducing thermodynamic stability,
and lowering storage capacity. Previous studies often considered a
single salt concentration, limiting our understanding of the salinity
effect. This work provides a comprehensive kinetic analysis, supported
by a chemical potential-driven model, to elucidate the impact of varying
salt content on CO2 hydrate formation. The findings indicate
that higher NaCl concentrations (≥3 wt %) markedly hinder hydrate
formation rates, reaffirming the suppressive effect of salt. To address
this challenge, biodegradable amino acid l-leucine (LL) was
employed as a kinetic hydrate promoter. In the presence of 5.0 wt
% NaCl, incorporating 2.0 wt % LL boosted gas uptake by nearly 2.6
times, highlighting its strong promotional impact. The proposed model,
first of its kind, accurately represents the kinetics across diverse
salinity levels and additive scenarios, providing actionable insights
for advancing CO2 hydrate-based sequestration.