The stable latex of poly(4-vinylpyridine-co-n-butyl acrylate) (P4VP/nBA) with a solid content as high as 10 wt % was prepared by a modified soap-free emulsion polymerization. A mixture of water and organic solvents was employed as the continuous phase for increasing the solid content of the latex. S
Novel method of preparation of a charged mosaic membrane by using dipole-like microspheres. II. Preparation of dumbbell/egg-like microspheres
✍ Scribed by Henmei Ni; Guanghui Ma; Masatoshi Nagai; Shinzo Omi
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 491 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0021-8995
- DOI
- 10.1002/app.1298
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✦ Synopsis
Abstract
The dumbbell‐like/egglike microspheres of poly(4‐vinylpyridine/n‐butyl acrylate)/polystyrene [P(4VP/nBA)/PS] were prepared by soap‐free seed emulsion polymerization. The effects of various polymerization parameters, such as the amount of ethyl acetate (EA) in the continuous phase, swelling time, degree of crosslinking of seed polymer, polymerization temperature, and compatibility of seed polymer and the secondary polymer, and so forth, on the formation of dumbbell‐like/egglike morphology were investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). It was found that secondary particles could be eliminated either by drastically increasing the number of seed particles or by stripping EA from the seed latex by dialysis and evaporation under a vacuum. Swelling the seed particle with the secondary monomer was essential for the preparation of egglike microspheres. For the localization of PS domains on one side of the egglike particle, the most effective factors were to elevate the polymerization temperature up to 90°C and simultaneously to lower the compatibility of the polymer on the seed particle surface with the phase of PS, while using the uncrosslinked seed latex. Crosslinking the seed latex was not suitable for localizing the PS domains in the seed particle, especially when the degree of crosslinking exceeded 0.5 wt % of EGDMA. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 2002–2017, 2001
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