Formation of Porous Polymer Morphology by Microsyneresis During Divinylbenzene Polymerization

0443627 - ÚCHP 2016 RIV US eng J - Článek v odborném periodiku
Hanková, Libuše - Holub, Ladislav - Jeřábek, Karel
Formation of Porous Polymer Morphology by Microsyneresis During Divinylbenzene Polymerization.
Journal of Polymer Science. Part B, Polymer Physics. Roč. 53, č. 11 (2015), s. 774-781. ISSN 0887-6266
Grant CEP: GA MŠMT LH12194
Institucionální podpora: RVO:67985858
Klíčová slova: crosslinking * macroporous polymers * mesopores
Kód oboru RIV: CI - Průmyslová chemie a chemické inženýrství
Impakt faktor: 3.318, rok: 2015

This article describes the investigation of the importance of various reaction conditions on microsyneretic pore formation during polymerization of divinylbenzene (DVB) under so-called “solvothermal” conditions. In order to induce microsyneretic pore formation, the most important parameter is an unusually high dilution of monomers with a “good” porogen solvating the polymer chains. High dilution and solvation of the growing poly(DVB) chains promotes the prolongation of the polymer chains rather than their interconnection by crosslinking. Consequently, when the polymer gel density reaches the point where syneresis starts, the polymer network is geometrically too extensive to be broken up into precipitating entities and, instead, porogen droplets are formed within the continuous polymer gel. The pore geometry created by microsyneresis offers high surface area in wide mesopores and hence, high capacity for supporting functional groups or reactions with much better accessibility than narrow pores between polymer microspheres produced by macrosyneresis in conventional styrenic polymer supports.
Trvalý link: http://hdl.handle.net/11104/0246642