## Abstract From a phenomenological point of view, the Mayo‐Lewis terminal model can describe both copolymer composition and the variation of copolymerization rate for the ethyl α‐benzoyloxymethylacrylate/methyl methacrylate/benzene/2,2′‐azoisobutyronitrile system.
Radical polymerization of ethyl α-benzoyloxymethylacrylate in benzene
✍ Scribed by T. Sato; I. Kamiya; H. Tanaka; T. Ota
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 351 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The polymerization of ethyl ~t-benzoyloxymethylacrylate (EBMA), an ct-disubstituted monomer, initiated with azobisisobutyronitrile (AIBN) was studied kinetically in benzene. The polymerization rate (Rp) at 60 ° was expressed by Rp = k[AIBN] °'5 [EBMA] t'6. The overall activation energy was calculated to be 53 kJ/mol. Rate constants of propagation (kp) and termination (kt) of EBMA were estimated as 990 and 2.9 x 10 6 I/mol. sec respectively at 60 °, using the ESR-determined concentration of the propagating polymer radical. The large kp and rather low k t led to formation of poly(EBMA) with high molecular weight (A'Tn= 1-5 x 105). Thermogravimetry revealed that thermal degradation of poly(EBMA) began near 300 ° and the residue at 500 ° was only 2% of the initial polymer. Copolymerization of EBMA (M ~ ) with St (M 2) was also examined at 60 ° in benzene. The following copolymerization parameters were obtained according to the Kelen-Tiid6s method; r t = 0.27 + 0.01, r 2 = 0.30 + 0.02 giving Qi = 0.93 and e~ = +0.78.
📜 SIMILAR VOLUMES
Ethyl a-benzene-(EBSA) and a-toluenesulfonylmethylacrylate (ETSA) were found to show no homopolymerizability but to act as effective chain transfer reagents in radical polymerizations of methyl methacrylate (MMA), styrene (St) and n-butyl acrylate (BA), being coniugative monomers. The estimated chai
N-butadiene l-carboxylyl S(-)-ct-phenyl ethyl amine (Bu-I-CPA) was prepared and polymerized in various solvents such as acetonitrile, dimethylformamide (DMF), methanol, dioxane and benzene at 50 ° using AIBN as initiator. From the i.r. spectra of the polymers, it was confirmed that poly(Bu-l-CPA) wa
An integral relationship, first given by Nishimura, has been applied to the bulk and solution polymerizations (dead-end data) of ethyl methacrylate. The kinetic rate constants calculated by this method for the bulk and solution cases are compared. The results are also compared with those previously