Interconnectivity of Macroporous Hydrogels Prepared via Graphene Oxide-Stabilized Pickering High Internal Phase Emulsions

Interconnected macroporous poly­(acrylic acid) (PAA) hydrogels are prepared via oil-in-water (o/w) Pickering high internal phase emulsion (HIPE) templates stabilized by graphene oxide (GO). The amphiphilicity of GO is adjusted by slight modification with cetyltrimethylammonium bromide (CTAB). The morphology of macroporous PAA is observed by a field-emission scanning electron microscope (FE-SEM). The gas permeability is characterized to evaluate the interconnectivity of polymer foams. The pore and pore throat size can be tailored by varying the wettability and concentration of GO. The selective adsorption toward dyes of PAA hydrogels is proved. Macroporous PAA hydrogels with an open-cell structure show enhanced adsorption behavior of both methylene blue (MB) and copper­(II) ions

Macroporous Graphene Oxide–Polymer Composite Prepared through Pickering High Internal Phase Emulsions

Macroporous polymer–graphene oxide (GO) composites were successfully prepared using Pickering high internal phase emulsion (HIPE) templates. GO flakes were modified by the cationic surfactant cetyltrimethylammonium bromide (CTAB) and used as the stabilizer of water-in-oil (W/O) Pickering emulsions. CTAB-modified GO is effective at stabilizing W/O Pickering HIPEs, and the lowest GO content is only about 0.2 mg mL^–1 (relative to the volume of the oil phase). The close-cell morphology of the resulting poly-Pickering HIPEs is observed, and the void size of the porous polymers is tuned by varying the concentration of GO. Three-dimensional macroporous chemically modified graphene (CMG) monoliths with a high specific surface area of about 490 m² g^–1 were obtained after removing the cellular polymer substrates through calcination. The micropores were also found in CMGs, which may be caused by the decomposition of CTAB adsorbed on the surface of GO

Interconnected Macroporous Polymers Synthesized from Silica Particle Stabilized High Internal Phase Emulsions

<i>n</i>-Octadecyltrimethoxysilane (ODS)-modified silica particles were used as sole Pickering stabilizer to prepare water-in-oil Pickering high internal phase emulsions (HIPEs) with an internal phase volume of 80%. After polymerization of the continuous phase of HIPEs, interconnected macroporous polymers were obtained when modified silica was initially dispersed in water to form a micelle-like structure. However, silica particles in oil phase resulted in closed-cell pores. The pore size, the pore wall morphology, and the interconnectivity of polymer foams could be adjusted finely by the grafted amounts of ODS, modified silica concentrations, and the initial location of Pickering stabilizer. The gas permeation of interconnected porous polymers increased dramatically with the increase of the hydrophobicity of silica particles from 3 to 153 mL/min

Interconnected Porous Polymers with Tunable Pore Throat Size Prepared via Pickering High Internal Phase Emulsions

Interconnected macroporous polymers were prepared by copolymerizing methyl acrylate (MA) via Pickering high internal phase emulsion (HIPE) templates with modified silica particles. The pore structure of the obtained polymer foams was observed by field-emission scanning electron microscopy (FE-SEM). Gas permeability was characterized to evaluate the interconnectivity of macroporous polymers. The polymerization shrinkage of continuous phase tends to form open pores while the solid particles surrounding the droplets act as barriers to produce closed pores. These two conflicting factors are crucial in determining the interconnectivity of macroporous polymers. Thus, poly-Pickering HIPEs with high permeability and well-defined pore structure can be achieved by tuning the MA content, the internal phase fraction, and the content of modified silica particles