Comparative thermodynamic study of functional polymeric latex particles with different morphologies

被引:3
作者
Santillan, R. [1 ]
Nieves, E. [1 ]
Alejandre, P. [1 ]
Perez, E. [1 ]
del Rio, J. M. [2 ]
Corea, M. [1 ]
机构
[1] Inst Politecn Nacl, ESIQIE, UPALM, Mexico City, DF, Mexico
[2] Inst Mexicano Petr, Programa Aseguramiento Producc, Mexico City 07730, DF, Mexico
关键词
Functional polymers; Carboxylic groups; Functional particles; Emulsion polymerization and Specific partial properties; ISOTHERMAL TITRATION CALORIMETRY; PROTEIN HYDRATION; GLOBULAR-PROTEINS; INFINITE DILUTION; PARTIAL VOLUME; DRUG-DELIVERY; COMPRESSIBILITY; HYDROGELS; WATER; RELEASE;
D O I
10.1016/j.colsurfa.2013.12.004
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
In this work, the thermodynamic behavior of three series of functionalized polymeric particles with different morphologies and different functional group concentrations were compared. Partial volumes and partial adiabatic compressibilities of particles at infinite dilution were calculated from density and sound speed data. These properties were interpreted in terms of the atomic, free volume and hydration contributions. In addition, this interpretation was extended to the particle components (polar and non-polar groups), developing a new thermodynamic methodology. For homogeneous particles without forced gradient, functional groups are located from the surface to the interior and the voidness effect plays an important role in the swelling process. In multilayer particles, functional groups are located at the boundary of each layer and they are completely hydrated while non-polar groups behave as a permeable membrane at high functional groups concentrations. Homogeneous particles with forced gradient behave as homogeneous particles without forced gradient at low functional groups concentrations and as a multilayer particle at higher concentrations of functional groups. In conclusion the shown thermodynamic tool allowed understanding the role played by each particle component and its interactions inside the particle. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:189 / 208
页数:20
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