Polymer monoliths with open pores and median pore size of about 15 nm-3 lm have been successfully synthesized by photoinitiated polymerization of butyl methacrylate and ethylene glycol dimethacrylate monomers. The solubility of the monomers in a porogenic solvent is determined by Hildebrand solubility parameter, and it is found that it has great effect on the pore size of the polymers synthesized. Polymers with larger pores are usually generated with poorer solvents for the monomers. However, polymers with different pore sizes and porosities have been obtained using porogenic solvents with similar Hildebrand solubility parameters. The evaporation rate of the porogenic solvents might be another critical factor affecting the properties of the polymer monoliths. Moreover, the effect of water as a cosolvent on the pore size and porosity of the polymers have also been investigated. Polymers with larger pore size have been prepared with the presence of water due to the occurrence of earlier phase separation in the polymerization.
Porous polymer monoliths have been successfully prepared by photoinitiated polymerization of butyl methacrylate (BMA) and ethylene glycol dimethacrylate (EDMA) monomers in porogenic solvent of methanol. Mercury intrusion porosimetry and scanning electron microscope are used to characterize the porous properties; nevertheless, the pore size obtained from both techniques is not comparable. The porous structure of the porous polymers is controlled by the phase separation during the polymerization and crosslinking. By varying the composition of the starting solution such as initiator fraction, BMA/EDMA ratio, porogen fraction, and UV intensity, porous polymers with median pore size from about 140 nm to 3 lm can be obtained, and the pore size distribution for majority of the porous polymers is also narrow. The results present a very positive prospect to microfluidic applications. V C 2011 Wiley Periodicals, Inc. J Appl Polym Sci 120: [3190][3191][3192][3193][3194][3195] 2011
Collection of circumferentially aligned and 3D fibrous scaffold on a newly designed electrospinning auxiliary jig. The aligned fibres served as a signaling modality to induce cell alignment and the maintenance of a contractile phenotype for hSMCs.
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