Adsorption of Sterically Stabilized Latex Particles at Liquid Surfaces: Effects of Steric Stabilizer Surface Coverage, Particle Size, and Chain Length on Particle Wettability

被引:29
|
作者
Reed, K. M. [1 ]
Borovicka, J. [1 ]
Horozov, T. S. [1 ]
Paunov, V. N. [1 ]
Thompson, K. L. [2 ]
Walsh, A. [2 ]
Armes, S. P. [2 ]
机构
[1] Univ Hull, Dept Chem, Surfactant & Colloid Grp, Kingston Upon Hull HU6 7RX, N Humberside, England
[2] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
DISPERSION POLYMERIZATION; CONTACT-ANGLE; METHYL-METHACRYLATE; COLLOID PARTICLES; BLOCK-COPOLYMERS; MOLECULAR-WEIGHT; EMULSION COPOLYMERIZATION; RADICAL POLYMERIZATION; POLYSTYRENE PARTICLES; POLYPYRROLE PARTICLES;
D O I
10.1021/la300735u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of five near-monodisperse sterically stabilized polystyrene (PS) latexes were synthesized using three well-defined poly(glycerol monomethacrylate) (PGMA) macromonomers with mean degrees of polymerization (DP) of 30, 50, or 70. The surface coverage and grafting density of the PGMA chains on the particle surface were determined using XPS and H-1 NMR spectroscopy, respectively. The wettability of individual latex particles adsorbed at the air water and n-dodecane water interfaces was studied using both the gel trapping technique and the film calliper method. The particle equilibrium contact angle at both interfaces is relatively insensitive to the mean DP of the PGMA stabilizer chains. For a fixed stabilizer DP of 30, particle contact angles were only weakly dependent on the particle size. The results are consistent with a model of compact hydrated layers of PGMA stabilizer chains at the particle surface over a wide range of grafting densities. Our approach could be utilized for studying the adsorption behavior of a broader range of sterically stabilized inorganic and polymeric particles of practical importance.
引用
收藏
页码:7291 / 7298
页数:8
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