水合物
动能
蛋氨酸
化学
笼状水合物
化学工程
无机化学
生物化学
有机化学
氨基酸
工程类
物理
量子力学
作者
Huazheng Xu,Yingying Liu,Siyuan He,Jia‐nan Zheng,Lanlan Jiang,Yongchen Song
出处
期刊:Energy
[Elsevier BV]
日期:2024-01-19
卷期号:291: 130280-130280
被引量:28
标识
DOI:10.1016/j.energy.2024.130280
摘要
One promising proposal for CO2 capture and storage is based on hydrate technology, which grapples with challenges related to stringent formation conditions and slow formation rates. In this study, the induction time, gas uptake and the rate of CO2 hydrate formation were measured with varying concentrations (ranging from 0.05 wt% to 0.2 wt%) of L-Methionine (L-Met) and sodium dodecyl sulfate (SDS). Remarkably, the novel additive hydrogen-rich stone significantly reduced the induction time by 89.74 % and 85.16 %, even under static conditions. The morphology analysis reveals that L-Met foster the creeping growth of hydrates, resulting in an approximate 41.89 % increase in the initial 1 h gas uptake. The efficient heat diffusion further enables the rapid formation of hydrates, resulting in a high gas uptake in a short period. L-Met outperforms SDS in terms of induction time and gas uptake, with the optimal choice for CO2 hydrate formation being 0.1 wt% L-Met. This study briefly describes the mechanisms of three different kinetic promoters for hydrate formation, which provides new ideas for subsequent studies on CO2 capture and storage via hydrate technology.
科研通智能强力驱动
Strongly Powered by AbleSci AI