化学
十二烷基硫酸钠
肺表面活性物质
笼状水合物
水合物
动力学
胶束
水溶液
无机化学
成核
化学工程
有机化学
生物化学
量子力学
物理
工程类
作者
Parisa Naeiji,Farshad Varaminian
标识
DOI:10.1016/j.molliq.2017.11.087
摘要
In the present study, formation kinetics of carbon dioxide hydrate has been investigated by thermal analysis. Since differential scanning calorimetry has no agitation, a small amount of two surfactants of sodium dodecyl sulfate (SDS) and lauryl alcohol ethoxylate (LAE) has been used to improve gas/aqueous solution interface and increase gas diffusion into the solution. A central composite design of experiment has evaluated the hydrate formation kinetics aiming to maximize the heat ratio and heat flow rate, while minimizing of the relaxation time is desirable. The optimal values of CO2 hydrate formation has been found to be at gas pressure of 3.045 MPa and surfactant concentration of 29 ppm in the presence of LAE2. It is clear that the kinetics of hydrate formation is promoted at higher pressure. The driving force is the key component of a hydrate nucleation and growth. On the other hand, LAE2 leads to a more increased the kinetics hydrate formation because it can represent lower gas-liquid interfacial tension than SDS. Moreover, the surfactant concentration considerably affected the kinetics hydrate formation after CMC value of surfactants. That means the formation of surface micelles helps diffuse the gas into the bulk.
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