Pressure Changes Across a Membrane Formed by Coacervation of Oppositely Charged Polymer-Surfactant Systems

被引:1
|
作者
Keshavarzi, Behnam [1 ,2 ]
Reising, Georg [2 ]
Mahmoudvand, Mohsen [3 ]
Koynov, Kaloian [4 ]
Butt, Hans-Jurgen [4 ]
Javadi, Aliyar [1 ,2 ]
Schwarzenberger, Karin [1 ,2 ]
Heitkam, Sascha [1 ,2 ]
Dolgos, Michelle [5 ]
Kantzas, Apostolos [3 ]
Eckert, Kerstin [1 ,2 ]
机构
[1] Helmholtz Zentrum Dresden Rossendorf, D-01314 Dresden, Germany
[2] Inst Proc Engn & Environm Technol, TU Dresden, D-01062 Dresden, Germany
[3] Univ Calgary, Dept Chem & Petr Engn, Calgary, AB T2N 1N4, Canada
[4] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[5] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
关键词
POLYELECTROLYTE/SURFACTANT MIXTURES; AIR/WATER INTERFACE; MECHANICAL-PROPERTIES; ADSORPTION BEHAVIOR; NEUTRON REFLECTION; DODECYL-SULFATE; PHASE-BEHAVIOR; XANTHAN; CAPSULES; TENSION;
D O I
10.1021/acs.langmuir.4c00049
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We investigate the mass transfer and membrane growth processes during capsule formation by the interaction of the biopolymer xanthan gum with C(n)TAB surfactants. When a drop of xanthan gum polymer solution is added to the surfactant solution, a membrane is formed by coacervation. It encapsulates the polymer drop in the surfactant solution. The underlying mechanisms and dynamic processes during capsule formation are not yet understood in detail. Therefore, we characterized the polymer-surfactant complex formation during coacervation by measuring the surface tension and surface elasticity at the solution-air interface for different surfactant chain lengths and concentrations. The adsorption behavior of the mixed polymer-surfactant system at the solution-air interface supports the understanding of observed trends during the capsule formation. We further measured the change in capsule pressure over time and simultaneously imaged the membrane growth via confocal microscopy. The cross-linking and shrinkage during the membrane formation by coacervation leads to an increasing tensile stress in the elastic membrane, resulting in a rapid pressure rise. Afterward, the pressure gradually decreases and the capsule shrinks as water diffuses out. This is not only due to the initial capsule overpressure but also due to osmosis caused by the higher ionic strength of the surfactant solution outside the capsule compared to the polymer solution inside the capsule. The influence of polymer concentration and surfactant type and concentration on the pressure changes and the membrane structure are studied in this work, providing detailed insights into the dynamic membrane formation process by coacervation. This knowledge can be used to produce capsules with tailored membrane properties and to develop a suitable encapsulation protocol in technological applications. The obtained insights into the mass transfer of water across the capsule membrane are important for future usage in separation techniques and the food industry and allow us to better predict the capsule time stability.
引用
收藏
页码:9934 / 9944
页数:11
相关论文
共 50 条
  • [41] Nanostructures of colloidal complexes formed in oppositely charged polyelectrolyte/surfactant dilute aqueous solutions
    Trabelsi, S.
    Guillota, S.
    Ritacco, H.
    Boue, F.
    Langevin, D.
    EUROPEAN PHYSICAL JOURNAL E, 2007, 23 (03): : 305 - 311
  • [42] Surfactant Self-Assembly in Oppositely Charged Polymer Networks. Theory
    Hansson, Per
    JOURNAL OF PHYSICAL CHEMISTRY B, 2009, 113 (39): : 12903 - 12915
  • [43] Insight into the structure of oppositely charged surfactant-polymer system by dielectric spectroscopy
    Wang, Shanshan
    Zhao, Kongshuang
    COLLOID AND POLYMER SCIENCE, 2017, 295 (11) : 2133 - 2140
  • [44] Oppositely charged surfactant-polyelectrolyte systems as model systems for mesoscopically ordered surfactant-silicates
    Friman, Rauno
    Backlund, Sune
    Hassan, Osman
    Alfredsson, Viveka
    Linden, Mika
    COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2006, 291 (1-3) : 148 - 154
  • [45] PHASE-BEHAVIOR OF ASSOCIATING AND SEGREGATING POLYMER-SURFACTANT SYSTEMS
    LINDMAN, B
    PICULELL, L
    KARLSTROM, G
    THALBERG, K
    ZHANG, KW
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 206 : 29 - MACR
  • [46] Development of combinatorial methods for formulation of polymer-surfactant systems.
    Huisinga, LR
    Lochhead, RY
    Welch, C
    Maggio, S
    McKay, T
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 227 : U561 - U561
  • [47] Organized assemblies in bolaamphiphile/oppositely charged conventional surfactant mixed systems
    Yan, Y
    Xiong, W
    Huang, JB
    Li, ZC
    Li, XS
    Li, NN
    Fu, HL
    JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (01): : 357 - 364
  • [48] Single polymer molecules adsorbed to mica and the oppositely charged polymer/surfactant complexes formed at the air-water interface visualized by atomic force microscopy
    Zhao, F
    Du, YK
    Yang, P
    Tang, J
    Li, XC
    COLLOID AND POLYMER SCIENCE, 2005, 283 (12) : 1361 - 1365
  • [49] Critical interaction strength for surfactant-induced mesomorphic structures in polymer-surfactant systems
    Ruokolainen, J
    Torkkeli, M
    Serimaa, R
    Vahvaselka, S
    Saariaho, M
    tenBrinke, G
    Ikkala, O
    MACROMOLECULES, 1996, 29 (20) : 6621 - 6628
  • [50] Critical interaction strength for surfactant-induced mesomorphic structures in polymer-surfactant systems
    Helsinki Univ of Technology, Espoo, Finland
    Macromolecules, 20 (6621-6628):