The copolymerization of styrene ( M 1 ) with N-phenylmaleimide ( M 2 ) in chloroform with 2,2 -azobis(isobutyronitrile) as an initiator was investigated. The kinetic parameters, such as reactivity ratios, overall activity energy, and the effect of molar fraction of monomers on the initial copolymeri
Emulsion copolymerization of N-phenylmaleimide with styrene
โ Scribed by Y. Yuan; A. Siegmann; M. Narkis; J. P. Bell
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 435 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
Emulsion copolymerization of N-phenylmaleimide (PMI) with styrene (St) was conducted via semibatch and batch methods. The effect of monomer mixture composition and method of copolymerization on copolymer structure-property relationships was investigated. The semibatch copolymers have a homogeneous molecular structure, exhibiting a single Tg which increases linearly with increasing PMI content. The batch copolymers have a heterogeneous molecular structure, exhibiting two Tg's, assigned to the polystyrene (PSt) and poly( PMI-co-St) components. The composition drift in the batch-copolymerized product, at different conversion levels, was examined by DSC and FTIR techniques. In general, the inherent viscosity of the semibatch copolymers is lower than that of the corresponding batch ones. The Young's modulus increases for the semibatch copolymers, with increasing PMI content, while a clear trend for the batch copolymers is not found. The tensile strength tends to decrease for both types of copolymers when PMI content increases. The thermal stability increases with increasing PMI content in the copolymers.
๐ SIMILAR VOLUMES
Terpolymers of N-phenylmaleimide (PMI), styrene, and acrylonitrile (AN) were synthesized by emulsion polymerization. The thermal properties of terpolymers at different PMI and AN feed contents were investigated by differential scanning calorimetry, torsional braid analysis, thermogravimetric analysi
## Abstract Freeโradicalโinitiated copolymerization of __N__โphenylmaleimide (NPMI) with styrene (St) at 110ยฐC in a toluene solution initiated by AIBN was carried out by a semibatch method. The compositions of the copolymers were determined by using an elemental analyzer. The glassโtransition tempe
The spontaneous copolymerization of N-phenylmaleimide (NPMI) (M 1 ) with ethyl โฃ-phenylacrylate (EPA)(M 2 ) were carried out in dioxane at 85ยฐC. A high alternating tendency was observed. The monomer reactivity ratios were r 1 ฯญ 0.07 ฯฎ 0.01 and r 2 ฯญ 0.09 ฯฎ 0.02. The maximum copolymerization rate and
The copolymerization and addition reaction of styrene (S) with N-phenylmaleimide (PMI), either neat or in xylene, have been found to proceed at 125ยฐC in the presence of 2,2,6,6-tetramethylpiperidin-1-yloxy (TEMPO) radicals. TEMPO-terminated alternating S-PMI copolymers and comonomer adducts were obt