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Paper Title

Kinetic studies of semibatch emulsion copolymerization of methyl methacrylate and styrene in the presence of high intensity ultrasound and initiator

Keywords

  • Kinetic Studies
  • Semibatch Emulsion Copolymerization
  • Methyl Methacrylate
  • Styrene
  • Ultrasound-Assisted Polymerization
  • High-Intensity Ultrasound
  • Sodium Dodecyl Sulfate
  • SDS
  • Potassium Persulfate
  • External Initiator
  • Acoustic Intensity
  • Polymerization Rate
  • Temperature Effect
  • Initiator Loading
  • Surfactant Concentration
  • Monomer Conversion
  • Cavitational Activity
  • Micro Jets
  • Monomer Droplet Stabilization
  • Fine Polymer Particles
  • Nanoparticle Formation
  • Polymer Particle Size
  • Ultrasound-Induced Polymerization
  • Emulsion Polymerization Mechanism
  • Process Optimization
  • Sustainable Polymer Synthesis

Article Type

Research Article

Research Impact Tools

Issue

Volume : 85 | Page No : 168-177

Published On

November, 2014

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Abstract

The present work deals with kinetic studies of copolymerization of methyl methacrylate and styrene using ultrasound assisted semibatch emulsion copolymerization in the presence of sodium dodecyl sulfate (emulsifier) and potassium persulfate (external initiator). The effect of temperature, acoustic intensity, initiator loading, surfactant concentration and monomer concentration on the extent of conversion has been investigated. The extent of polymerization was observed to increase with an increase in the temperature, and concentrations of initiator, monomer and surfactant. Further, the initial polymerization rate increased with an increase in the acoustic intensity from 11.2 to 23.1 W cm−2 and then it was found to decrease with a further increase to 33.80 W cm−2. The novelty of this work lies in the fact that there have been only limited kinetic studies for the approach of ultrasound assisted emulsion copolymerization. It has been also established in the present work that the formation of fine and stable monomer droplets, due to the cavitational activity at/near the interface of immiscible monomer phase and subsequent disruption by micro jets, leads to the smaller final polymer particle size and under optimized conditions, it was found to be about 40 nm.

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