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固体/水界面处二氧化碳纳米气泡形成的动力学

Kinetics of CO2 nanobubble formation at the solid/water interface.

作者信息

Yang Jingwu, Duan Jinming, Fornasiero Daniel, Ralston John

机构信息

Ian Wark Research Institute, University of South Australia, Mawson Lakes Campus, Adelaide, SA 5095, Australia.

出版信息

Phys Chem Chem Phys. 2007 Dec 28;9(48):6327-32. doi: 10.1039/b709624k. Epub 2007 Aug 29.

Abstract

The kinetics of adsorption of CO(2) molecules dissolved in aqueous solution onto a hydrophobised silica surface were investigated using a quartz crystal microbalance (QCM). The results of this investigation were compared with those obtained earlier from tapping mode atomic force microscopy (TMAFM) under the same experimental conditions (J. Yang, J. Duan, D. Fornasiero, J. Ralston, J. Phys. Chem. B., 2003, 107(25), 6139-6147; ref. 1). The QCM results represent the early stage of CO(2) gas adsorption (<20 min), before CO(2) gas bubbles adsorbed on the surface can be directly observed by TMAFM. The QCM results confirmed our observation from TMAFM imaging: that CO(2) gas molecules present in solution only adsorb on silica when its surface is hydrophobic. More importantly, the results showed that gas adsorption/bubble growth undergoes two consecutive kinetic processes: a slow and a fast adsorption process.

摘要

利用石英晶体微天平(QCM)研究了溶解在水溶液中的CO₂分子在疏水化二氧化硅表面的吸附动力学。将该研究结果与之前在相同实验条件下通过敲击模式原子力显微镜(TMAFM)获得的结果进行了比较(J. Yang、J. Duan、D. Fornasiero、J. Ralston,《物理化学杂志B》,2003年,107(25),6139 - 6147;参考文献1)。QCM结果代表了CO₂气体吸附的早期阶段(<20分钟),此时TMAFM还无法直接观察到吸附在表面的CO₂气泡。QCM结果证实了我们从TMAFM成像中观察到的现象:溶液中存在的CO₂气体分子仅在二氧化硅表面疏水时才会吸附。更重要的是,结果表明气体吸附/气泡生长经历两个连续的动力学过程:一个缓慢的吸附过程和一个快速的吸附过程。

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