Morphology and Pore Size Distribution of Biocompatible Interconnected Porous Poly(L-lactic acid) Foams with Nanofibrous Structure Prepared by Thermally Induced Liquid–Liquid Phase Separation

2010 ◽  
Vol 49 (5) ◽  
pp. 897-919 ◽  
Author(s):  
Shirong Li ◽  
Kemin Wang ◽  
Muzi Li
2012 ◽  
Vol 512-515 ◽  
pp. 403-406 ◽  
Author(s):  
Gang Zhang ◽  
Ze Wen Xiao ◽  
Guan Jun Qiao

The preparation of interconnected mesoporous carbon monoliths (MCMs) derived from phenolic resin/ethylene glycol mixtures based on polymerization-induced phase separation have been investigated for fabrication of complex-shape SiC ceramics. The effect of the ethylene glycol content, curing catalyst and the curing temperature on the pore structure and pore distribution of carbon monoliths has also been studied, with emphasis on controlling the apparent porosity and pore size distribution. Fractal dimensions (DF) was proposed to evaluate the morphologies of carbon monoliths by using the box counting method. The results show that interconnected mesoporous carbon monoliths with narrow pore size distribution were obtained by changing the curing temperature and the content of ethylene glycol, curing catalyst in the resin mixtures and its mechanism was discussed in this paper. In this paper, interconnected mesoporous structure was attributed to the mechanism of spinodal decomposition (SD), which was discussed in detail. Carbon monoliths inherit their porosity from cured resins where it was formed as a result of phase separation of resin-rich and glycol- rich phases.


1996 ◽  
Vol 431 ◽  
Author(s):  
J. Kiefer ◽  
R. Porouchani ◽  
D. Mendels ◽  
J. B. Ferrer ◽  
C. Fond ◽  
...  

AbstractWe have explored a new technology based on chemically induced phase separation that yields porous epoxies and cyanurates with a closed cell morphology and micrometer sized pores with a narrow pore size distribution. When the precursor monomers are cured in the presence of a low molecular weight liquid, the desired morphology results from a phase separation and a chemical quench. After phase separation, the porosity is achieved by thermal removal of the secondary liquid phase, specifically by diffusion through the crosslinked matrix. In respect to the thermodynamics and kinetics, the origin of the phase separation process can be identified as nucleation and growth. The influence of internal and external reaction parameters, such as chemical nature of the low molecular weight liquid, its concentration and the curing temperature on the final morphology are presented. Thus, the morphology can be controlled ranging from a monomodal to bimodal pore size distribution with pore sizes inbetween 1 to 10 μm. These porous thermosets are characterized by a significantly lower density, without any loss in thermal stability compared to the neat matrix. Such new materials demonstrate great interest for lowering the dielectric constant and for improving the fundamental understanding of the role of voids in stress relaxation and toughening.


Author(s):  
Harish Chinnasami ◽  
Frank Breeden ◽  
Daniel Hayes ◽  
Ram Devireddy

Bio-degradable Poly (l-lactic acid) (PLLA) scaffolds were prepared by using thermal liquid-liquid phase separation method. A solution of PLLA-Dioxane was prepared by dissolving PLLA in dehydrated 1,4-Dioxane. This PLLA-Dioxane solution was then directionally frozen in vials of similar dimensions but made of different materials (borosilicate glass, aluminum and copper). The frozen solution was then placed in a freeze-dryer to allow for the frozen dioxane to sublimate or lyophilized. The porosities of the resulting PLLA scaffolds were calculated and their porous structures were studied and compared between the three different vials (and the corresponding cooling rates).


Author(s):  
H. Chinnasami ◽  
R. Devireddy

Bio-degradable Poly (l-lactic acid) (PLLA) scaffolds synthesized using thermally induced phase separation (TIPS) method was used to load cryo-preserved human adipose derived stem cells (hASCs). To make the scaffolds, PLLA-Dioxane solutions were formed by dissolving PLLA in 1,4-Dioxane with three different compositions (wt/vol). These PLLA-Dioxane solutions, frozen in three different cooling rates were lyophilized at 0.037bar and −70°C for 48hrs resulting in porous PLLA scaffolds. Based on the porosity, pore size and compressive strength, a suitable scaffold was chosen to investigate its bio-compatibility and osteo-inductive potential.


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