Adsorption of Mixed Dispersions of Silica Nanoparticles and an Amphiphilic Triblock Copolymer at the Water-Vapor Interface

被引:1
|
作者
Carbone, Carlo [1 ]
Rubio-Bueno, Alejandra [1 ]
Ortega, Francisco [1 ,2 ]
Rubio, Ramon G. [1 ,2 ]
Guzman, Eduardo [1 ,2 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Fis, Ciudad Univ S-N, Madrid 28040, Spain
[2] Univ Complutense Madrid, Inst Pluridisciplinar, Paseo Juan XXIII 1, Madrid 28040, Spain
来源
APPLIED SCIENCES-BASEL | 2023年 / 13卷 / 18期
关键词
adsorption; amphiphilic triblock copolymers; association; complexes; dilational rheology; fluid interfaces; hydrogen bonds; silica nanoparticles; OPTIMIZATION; PARTICLES; STABILITY; MIXTURES; RHEOLOGY; DELIVERY;
D O I
10.3390/app131810093
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study investigates the surface modification of hydrophilic silica nanoparticles by non-chemical adsorption of an amphiphilic triblock copolymer, Pluronic F-127, and elucidates its influence on the interfacial dispersion properties. The interaction between Pluronic F-127 and silica nanoparticles drives the formation of copolymer-decorated particles with increased hydrodynamic diameter and reduced effective charge as the copolymer concentration increases, while the opposite effect occurs as the particle concentration increases at a fixed polymer concentration. This indicates that increasing the copolymer concentration leads to an increase in the coating density, whereas increasing the particle concentration leads to a decrease. This is of paramount importance for modulating the reorganization of the Pluronic F-127 shell upon adsorption at fluid-fluid interfaces and, thus, the adsorption of the decorated nanoparticles at the interface and the rheological properties of the obtained layers. In fact, the relationship between copolymer concentration and interfacial tension, as well as the mechanical response of the interface, mirrors the patterns observed in Pluronic F-127 solutions, and only a shift mediated by the Pluronic F-127 concentration is found. This suggests that the presence of particles limits the space available for Pluronic F-127 molecules to reorganize at the interface but does not significantly affect the interfacial behavior of the particle-laden interface.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Alkane adsorption at the water-vapor interface
    Ashbaugh, HS
    Pethica, BA
    LANGMUIR, 2003, 19 (18) : 7638 - 7645
  • [2] Adsorption of Single and Multiple Graphene-Oxide Nanoparticles at a Water-Vapor Interface
    Gravelle, Simon
    Botto, Lorenzo
    LANGMUIR, 2021, 37 (45) : 13322 - 13330
  • [3] ADSORPTION OF WATER-VAPOR BY SILICA AND EFFECT OF SURFACE METHYLATION
    BARRACLOUGH, PB
    HALL, PG
    JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1978, 74 : 1360 - 1372
  • [4] Surface excess at water/air interface and micellization in solutions of an amphiphilic triblock copolymer
    Streck, L.
    da Cruz, P. I.
    Fonseca, J. L. C.
    JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 2020, 41 (14) : 2107 - 2115
  • [5] EFFECT OF THE COMPOSITION OF PYROGENIC TITANIUM SILICA ON WATER-VAPOR ADSORPTION
    VORONIN, EF
    PAKHLOV, EM
    TURUTINA, NV
    SUSHKO, RV
    JOURNAL OF APPLIED CHEMISTRY OF THE USSR, 1989, 62 (02): : 356 - 358
  • [6] REHYDROXYLATION ON SILICA-GEL AND POROUS SILICA GLASS BY WATER-VAPOR ADSORPTION
    NAONO, H
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1979, (APR): : 203 - 203
  • [7] Ions at the Water-Vapor Interface
    Tamashiro, M. N.
    Constantino, M. A.
    JOURNAL OF PHYSICAL CHEMISTRY B, 2010, 114 (10): : 3583 - 3591
  • [8] ADSORPTION OF WATER-VAPOR ON PLATINUM
    VORONINA, GF
    LARIN, LA
    KALISH, TV
    SOVIET ELECTROCHEMISTRY, 1980, 16 (02): : 146 - 148
  • [9] THE ADSORPTION OF NITROGEN AND WATER-VAPOR BY CARBON-COATED PRECIPITATED SILICA
    CARROTT, PJM
    SING, KSW
    RAISTRICK, JH
    COLLOIDS AND SURFACES, 1986, 21 : 9 - 15
  • [10] WATER-VAPOR ADSORPTION ON PHOSPHAZENES
    VASSILEVA, P
    LAKOV, L
    GOCHEVA, E
    PESHEV, O
    JOURNAL OF MATERIALS SCIENCE LETTERS, 1993, 12 (05) : 281 - 282