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Organically modified clay was used as reinforcement for HDPE using maleated polyethylene (PEMA) as a compatibilizer.
Due to high thermal resistance along with excellent specific surface area and porosity, modified clay was therefore gained many interests.
By virtue of these reasons, modified clay was therefore prepared from many synthetic routes for significant enhancement on specific surface area and porosity.
MMT was pre-modified with cationic amphiphilic block copolymer of poly styrene-b-2-hydroxyethyl acrylate) (poly styrene-b-2-hydroxyethyl(poly styrene-b-2-hydroxyethylwas used as stabilizer in dispoly styrene-b-2-hydroxyethyl
It was found that the increase in d-spacing of organically modified clay was due to starch molecular intercalation while the increase in d-spacing of pristine clay was mostly caused by glycerol intercalation because of the narrow valid d-spacing of pristine clay and special ring-like monomer of starch.
Interactions AB, BC and AC showed that the modified clay was the factor of greater significance.
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The ramification of these phenomena on blending of PP, PA6, and organically modified clay is discussed.
Polypropylene (PP) was selected as a model polymer, and nanocomposites of PP with organically modified clay were prepared by a master batch dilution technique in a twin-screw extruder.
The preparation, structure and properties of polymer nanocomposites using the modified clays are discussed.
The modified clays were dispersed in the epoxy resin (5 wt.%) and subjected to the UV-curing process.
Organofunctional silane-modified clay was synthesized using an ion exchange technique.
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