{"title":"CTAB serves as the best kinetic promoters of H2/DIOX mixed hydrates for moderate solidified hydrogen storage via clathrates","authors":"Honglin Yu, Peng Zhang, Mengqi Liu, Daiming Liu, Guodong Zhang, Fei Wang","doi":"10.1016/j.cej.2025.159818","DOIUrl":null,"url":null,"abstract":"Although clathrate hydrates were thought to open the Pandora box of hydrogen moderate storage, poor hydration efficiency of hydrogen hydrates impedes its application in hydrogen economy. To improve the situation, an efficient kinetic promoter of cetyltrimethylammonium bromide (CTAB) was proposed to enhance the hydration efficiency of mixed H<sub>2</sub> and 1,3-dioxolane (DIOX) hydrates, the micro structures of which were characterized via Raman spectra. In DIOX system, when CTAB was introduced, hydrate induction time reduces by 91.4 %, hydrate growth rate increases by 185.2 %, and the storage capacity of hydrogen in hydrates is up to 0.582 wt% under a moderate condition (12 MPa, 274.15 K), which increases by 99.32 %. Potential mechanisms behind the enhancement were proposed, and it was deduced that CTAB changes the arrangement of interfacial water molecules and induces hydration shells, which decrease the nucleation energy barrier as confirmed by the profiles of differential scanning calorimetry (DSC), giving rise to fast hydrate nucleation. In addition, hydrogen molecules were thought to enter the cavity of CTAB micelles, which serve as hydrogen vehicles to enhance the mass transfer of hydrogen by interfacial capture and inner release, resulting in fast hydrate formation. To the best of our knowledge, CTAB presents the best promotion effect on the nucleation and growth of H<sub>2</sub>/DIOX mixed hydrates among known kinetic promoters, and this finding promotes the application of clathrate hydrates on hydrogen moderate storage a small step forward.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"2 1","pages":""},"PeriodicalIF":13.3000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.159818","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Although clathrate hydrates were thought to open the Pandora box of hydrogen moderate storage, poor hydration efficiency of hydrogen hydrates impedes its application in hydrogen economy. To improve the situation, an efficient kinetic promoter of cetyltrimethylammonium bromide (CTAB) was proposed to enhance the hydration efficiency of mixed H2 and 1,3-dioxolane (DIOX) hydrates, the micro structures of which were characterized via Raman spectra. In DIOX system, when CTAB was introduced, hydrate induction time reduces by 91.4 %, hydrate growth rate increases by 185.2 %, and the storage capacity of hydrogen in hydrates is up to 0.582 wt% under a moderate condition (12 MPa, 274.15 K), which increases by 99.32 %. Potential mechanisms behind the enhancement were proposed, and it was deduced that CTAB changes the arrangement of interfacial water molecules and induces hydration shells, which decrease the nucleation energy barrier as confirmed by the profiles of differential scanning calorimetry (DSC), giving rise to fast hydrate nucleation. In addition, hydrogen molecules were thought to enter the cavity of CTAB micelles, which serve as hydrogen vehicles to enhance the mass transfer of hydrogen by interfacial capture and inner release, resulting in fast hydrate formation. To the best of our knowledge, CTAB presents the best promotion effect on the nucleation and growth of H2/DIOX mixed hydrates among known kinetic promoters, and this finding promotes the application of clathrate hydrates on hydrogen moderate storage a small step forward.
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.