2019
DOI: 10.1007/s10973-019-09143-2
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TG/DSC/FTIR study of porous copolymeric beads based on the dimethacrylate derivative of m-xylene

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Cited by 5 publications
(1 citation statement)
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“…For this purpose, both aliphatic and aromatic multifunctional monomers, can be successfully employed. The use of bifunctional glycidyl methacrylate (GMA) with a tetrafunctional cross-linking monomer, i.e., ethylene glycol dimethacrylate (EGDMA) [37,48,49] as well as bifunctional 4-vinylpyridine [50] or GMA [38] with hexafunctional trimethylolpropane trimethacrylate as a cross-linking agent resulted in porous microspheres resistant to about 200 • C. The improvement in thermal stability was obtained by replacing the aliphatic cross-linker, i.e., EGDMA with the aromatic one, i.e., di(methacryloyloxymethyl)naphthalene [51] or by using two tetrafunctional monomers, such as DVB and (4,6-dimethyl-1,3-phenylene)dimethylene bis(2-methylprop-2-enoate) [52] or DVB and dimethacrylate derivatives of naphthalene and diphenylmethanone [43].…”
Section: Introductionmentioning
confidence: 99%
“…For this purpose, both aliphatic and aromatic multifunctional monomers, can be successfully employed. The use of bifunctional glycidyl methacrylate (GMA) with a tetrafunctional cross-linking monomer, i.e., ethylene glycol dimethacrylate (EGDMA) [37,48,49] as well as bifunctional 4-vinylpyridine [50] or GMA [38] with hexafunctional trimethylolpropane trimethacrylate as a cross-linking agent resulted in porous microspheres resistant to about 200 • C. The improvement in thermal stability was obtained by replacing the aliphatic cross-linker, i.e., EGDMA with the aromatic one, i.e., di(methacryloyloxymethyl)naphthalene [51] or by using two tetrafunctional monomers, such as DVB and (4,6-dimethyl-1,3-phenylene)dimethylene bis(2-methylprop-2-enoate) [52] or DVB and dimethacrylate derivatives of naphthalene and diphenylmethanone [43].…”
Section: Introductionmentioning
confidence: 99%