Synthesis of phosphonate-functionalized polystyrene and poly(methyl methacrylate) particles and their kinetic behavior in miniemulsion polymerization

被引:47
作者
Ziegler, Anke [1 ,2 ]
Landfester, Katharina [1 ,2 ]
Musyanovych, Anna [1 ,2 ]
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[2] Univ Ulm, Inst Organ Chem Macromol Chem & Organ Mat 3, D-89081 Ulm, Germany
关键词
Miniemulsion; Radical copolymerization; Functionalized nanoparticles; Phosphonate groups; Calorimetric measurements; POLY(VINYLPHOSPHONIC ACID); CORROSION INHIBITION; METHYL-METHACRYLATE; OXIDE SURFACES; NANOPARTICLES; MONOLAYERS; HYDROGELS; CARBOXYL; ADHESION; ABILITY;
D O I
10.1007/s00396-009-2087-z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Phosphonate-functionalized polymer nanoparticles were synthesized by free-radical copolymerization of vinylphosphonic acid (VPA) with styrene or methyl methacrylate (MMA) using the miniemulsion technique. The influence of different parameters such as monomer and surfactant type, amount of vinylphosphonic acid on the average particle size, and size distribution was studied using dynamic light scattering and transmission electron microscopy. Depending on the amount and type of the surfactant used (ionic or non-ionic), phosphonate-functionalized particles in a size range from 102 to 312 nm can be obtained. The density of the phosphonate groups on the particle surface was higher in the case of using MMA as a basis monomer than polystyrene. The kinetic behavior of VPA copolymerization with styrene or MMA using a hydrophobic initiator was investigated by reaction calorimetry. Different kinetic curves were observed for miniemulsion (co)polymerization of styrene- and MMA-based nanoparticles indicating different nucleation mechanisms.
引用
收藏
页码:1261 / 1271
页数:11
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