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Published on: January 19, 2016
Functional Acrylic Resins Prepared via Photo-Induced Telomerization Using Tetrabromomethane as Telogen
Mateusz Weisbrodt1, Agnieszka Kowalczyk1, Beata Schmidt1
1Department of Chemical Organic Technology and Polymeric Materials, Faculty of Chemical Technology and Engineering, West Pomeranian University of Technology in Szczecin, 70-322 Szczecin, Poland.
This study presents a novel UV-initiated telomerization method for creating functional acrylic resins (FARs) with carboxyl and benzophenone groups. Higher tetrabromomethane content boosts monomer conversion and reduces viscosity without impacting key properties.
Area of Science:
- Polymer Chemistry
- Materials Science
- Organic Synthesis
Background:
- Functional acrylic resins (FARs) are versatile materials with applications in coatings, adhesives, and advanced composites.
- Developing efficient methods for in-chain functionalization and controlled molecular weight is crucial for tailoring FAR properties.
- Incorporating specific functional groups like carboxyl and benzophenone, along with terminal bromine atoms, enhances resin reactivity and performance.
Purpose of the Study:
- To develop and verify a novel, solution-free UV-initiated telomerization method for synthesizing functional acrylic resins (FARs).
- To investigate the impact of tetrabromomethane (CBr4) telogen content on the kinetics, molecular weight, and thermal properties of the synthesized FARs.
- To confirm the successful incorporation of carboxyl, benzophenone groups, and terminal bromine atoms into the acrylic telomer structure.
Main Methods:
- Solution-free UV-initiated telomerization using n-butyl acrylate, acrylic acid, and 4-acrylooxybenzophenone.
- Utilized tetrabromomethane (CBr4) as a telogen at varying concentrations.
- Employed photo-differential scanning calorimetry (photo-DSC) for kinetic studies, gel permeation chromatography (GPC) for molecular weight analysis, and differential scanning calorimetry (DSC) for thermal properties (Tg).
- Nuclear magnetic resonance (NMR) spectroscopy was used for structural confirmation.
Main Results:
- A telogen content exceeding 5 wt. parts did not significantly alter UV-telomerization rates, molecular weights, or glass transition temperatures (Tg).
- Increased tetrabromomethane content significantly enhanced monomer conversion, reaching up to 88%.
- Higher telogen concentrations effectively reduced the viscosity of the functional acrylic resins to approximately 6 Pa·s.
- NMR studies confirmed the successful incorporation of CBr4 into the functional acrylic telomer structure.
Conclusions:
- The developed UV-initiated telomerization offers an efficient route to functional acrylic resins with desirable in-chain and terminal functionalities.
- Tetrabromomethane content can be optimized to control monomer conversion and resin viscosity without compromising essential material properties.
- This method provides a pathway for producing tailored functional acrylic resins for advanced material applications.
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