Sagisaka Masanobu, Fujii Tatsunori, Ozaki Yoshinobu, Yoda Satoshi, Takebayashi Yoshihiro, Kondo Yukishige, Yoshino Norio, Sakai Hideki, Abe Masahiko, Otake Katsuto
National Institute of Advanced Industrial Science and Technology, Institute for Green Technology, Higashi 1-1, Tsukuba, Ibaraki 305-8565, Japan.
Langmuir. 2004 Mar 30;20(7):2560-6. doi: 10.1021/la036074g.
We have examined the interfacial properties of several fluorinated surfactants in a water/CO2 mixture with a pendant drop tensiometer and revealed the relationships between the interfacial properties, the surfactant structure, and the microemulsifying power. We employed the following Aerosol-OT analogue surfactants that have two fluorinated tails: bis(1H,1H,5H-octafluoropentyl)-2-sulfosuccinate (di-HCF4), sodium bis(1H,1H,9H-hexadecafluorononyl)-2-sulfosuccinate (di-HCF8), sodium bis(1H,1H,2H,2H-heptadecafluorodecyl)-2-sulfosuccinate (8FS(EO)2), and sodium bis((1H,1H,2H,2H-heptadecafluorodecyl)-oxyethylene)-2-sulfosuccinate (8FS(EO)4). To discuss the effect of the fluorocarbon/hydrocarbon ratio in single surfactant molecules, water/CO2 interfacial tension (IFT) of a hybrid surfactant with one fluorocarbon and one hydrocarbon tail, that of a surfactant with a single fluorinated tail, and that of a hydrocarbon surfactant, Aerosol-OT (AOT), were examined. The hybrid surfactant employed was sodium 1-oxo-1-[4-(tridecafluorohexyl)phenyl]-2-hexanesulfonate (FC6-HC4), and the single-tailed surfactant was perfluoropolyether ammonium carboxylate (PFPECOONH4, CF3CF2(CF2OCF(CF3))4COONH4). All of the fluorinated AOT analogue surfactants exhibited an excellent level of activity at the water/CO2 interface compared with other fluorinated surfactants and AOT. With a larger hydrocarbon chain number in the CO2-philic tails (i.e., from 0 to 2), the IFT of the AOT analogue surfactants was increased. The area occupied by one surfactant molecule at the water/CO2 interface, A, and the critical microemulsion concentration, cmicroc, were determined and used to examine the water-to-surfactant molar ratio within a reversed micelle, W0c, of the surfactants. The surfactants that form W/scCO2 microemulsions with a large W0c were found to lower the interfacial tension efficiently irrespective of increases in temperature. To achieve the most desirable W0C, the surfactant needs not only a high CO2-philicity of the tails but also a high Krafft point, properties which induce a low hydrophilic/CO2-philic balance.
我们使用悬滴张力仪研究了几种含氟表面活性剂在水/二氧化碳混合物中的界面性质,并揭示了界面性质、表面活性剂结构和微乳化能力之间的关系。我们使用了以下具有两条氟化链的气溶胶-OT类似物表面活性剂:双(1H,1H,5H-八氟戊基)-2-磺基琥珀酸钠(二-HCF4)、双(1H,1H,9H-十六氟壬基)-2-磺基琥珀酸钠(二-HCF8)、双(1H,1H,2H,2H-十七氟癸基)-2-磺基琥珀酸钠(8FS(EO)2)和双((1H,1H,2H,2H-十七氟癸基)-氧乙烯)-2-磺基琥珀酸钠(8FS(EO)4)。为了讨论单个表面活性剂分子中碳氟/碳氢比的影响,我们研究了一种具有一条碳氟链和一条碳氢链的混合表面活性剂、一种具有单条氟化链的表面活性剂以及一种碳氢表面活性剂气溶胶-OT(AOT)在水/二氧化碳界面的界面张力(IFT)。所使用的混合表面活性剂是1-氧代-1-[4-(十三氟己基)苯基]-2-己烷磺酸钠(FC6-HC4),单链表面活性剂是全氟聚醚羧酸铵(PFPECOONH4,CF3CF2(CF2OCF(CF3))4COONH4)。与其他含氟表面活性剂和AOT相比,所有含氟AOT类似物表面活性剂在水/二氧化碳界面均表现出优异的活性水平。随着亲二氧化碳链中碳氢链数的增加(即从0增加到2),AOT类似物表面活性剂的IFT增大。测定了一个表面活性剂分子在水/二氧化碳界面所占的面积A和临界微乳液浓度cmicroc,并用于研究表面活性剂反胶束内的水与表面活性剂摩尔比W0c。发现形成具有大W0c的W/scCO2微乳液的表面活性剂无论温度升高都能有效降低界面张力。为了达到最理想的W0C,表面活性剂不仅需要链具有高亲二氧化碳性,还需要高克拉夫特点,这些性质会导致低亲水/亲二氧化碳平衡。