Abstract:Summary: Radical homopolymerizations and copolymerizations of styrene were performed in toluene and N,N‐dimethylformamide (DMF) as solvents using different initiators with and without microwave irradiation. Only the homopolymerization of styrene under microwave irradiation in DMF with DtBP showed significantly enhanced styrene conversion whereas other initiators resulted in no or only slight increase of styrene conversion under microwave irradiation. In any case, DMF was required to gain in styrene conversion … Show more
“…[42] Free Radical Copolymerizations Greiner and coworkers investigated the free radical polymerization of styrene and copolymerization of styrene and MMA with and without MW irradiation (monomode MW reactor, temperature control) by using different organic peroxide initiators in a solution of toluene and N,N -dimethylformamide (DMF). [44] It was found that the homopolymerizations of styrene in DMF showed a significantly higher monomer conversion under MW conditions compared with experiments performed in an oil bath. However, the conversions of polymerizations performed in toluene were not influenced by MW irradiation.…”
In the past few years the use of microwave irradiation in polymer science has become a well-established technique to drive and promote chemical reactions. The main advantages of microwave heating are a strong reduction in reaction time and a high potential to contribute to green and sustainable chemistry. This article provides a short review of recent examples in the field of microwave-assisted polymer synthesis with special emphasis on radical polymerizations, step-growth polymerizations, ring-opening polymerizations, and polymer modifications.
“…[42] Free Radical Copolymerizations Greiner and coworkers investigated the free radical polymerization of styrene and copolymerization of styrene and MMA with and without MW irradiation (monomode MW reactor, temperature control) by using different organic peroxide initiators in a solution of toluene and N,N -dimethylformamide (DMF). [44] It was found that the homopolymerizations of styrene in DMF showed a significantly higher monomer conversion under MW conditions compared with experiments performed in an oil bath. However, the conversions of polymerizations performed in toluene were not influenced by MW irradiation.…”
In the past few years the use of microwave irradiation in polymer science has become a well-established technique to drive and promote chemical reactions. The main advantages of microwave heating are a strong reduction in reaction time and a high potential to contribute to green and sustainable chemistry. This article provides a short review of recent examples in the field of microwave-assisted polymer synthesis with special emphasis on radical polymerizations, step-growth polymerizations, ring-opening polymerizations, and polymer modifications.
“…Solvent effects for free-radical polymerizations were investigated in detail by Greiner and coworkers. [15,16] Given the example of the tert-butyl perbenzoate (tBPB)-initiated radical copolymerization of styrene and methyl methacrylate (MMA), no significant effects were observed in toluene, but in DMF. tBPB was the initiator with the lowest decomposition rate of all peroxides investigated in this comparative study, comprising also dibenzoyl peroxide and dicumyl peroxide.…”
The application of microwave irradiation in polymer syntheses and modifications is of continuously growing interest and has received significant international interest since the beginning of the millennium. Preceded by a review that was published 6 years ago, the present paper summarizes the most recent trends in this research area. Radical as well as step-growth and ring-opening polymerizations will be addressed; furthermore, the evolution from microwave-assisted polymerizations to microwave-assisted material fabrication will be described on the examples of polymeranalogous reactions, polymer/metal composites and bio-based materials.
“…Hence six different homopolymers of myristyl acrylate, P-1, P-2, P-3, P-4, P-5, and P-6 correspond to reaction times 25, 20, 15, 10, 8, and 2 min, respectively, are obtained (Stange et al, 2006).…”
Homopolymer of myristyl acrylate was prepared by microwave assisted free radical polymerization method using BZP as initiator with variation of time at a fixed power without any solvent. Characterization of the polymers was done by IR, NMR, and viscometric analysis. Additive performances of each of them (pour point depressant [PPD] and viscosity modifier [VM]) for lubricating oil (lube oil) were also evaluated by standard ASTM methods. A comparison of their performances has also been reported. The molecular weights of the polymers were determined from viscosity measurements in toluene at 313 K and thermal stability was measured by thermogravimetric analysis.
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