Synthesis and characterisation of highly branched polyisoprene: exploiting the “Strathclyde route” in anionic polymerisation
Document Type
Article
Publication Date
1-1-2018
Abstract
This work aimed at developing a synthetic route towards highly branched poly(isoprene) from commercially available raw materials, in good yield and devoid of microgelation, i.e., to prepare a completely soluble polymer via the versatile technique anionic polymerisation. The polymerisations were conducted under high vacuum conditions using sec-butyllithium as initiator at 50 °C in toluene. Toluene served both as a solvent and as a chain-Transfer agent. The polar modifier used was tetramethylethylenediamine (TMEDA), and a commercial mixture of divinylbenzene (DVB) was employed as the branching agent for the "living" poly(isoprenyl)lithium anions. The nature of the reaction was studied on the TMEDA/Li ratio as well as the DVB/Li ratio. The obtained branched polymers were characterised by triple detection size exclusion chromatography (SEC), proton nuclear magnetic resonance spectroscopy (1H NMR), differential scanning calorimetry (DSC) and melt rheology. Broad molecular weight distributions have been obtained for the highly branched polymer products. 1H NMR spectroscopy reveals the dominance of 3,4-polyisoprene microstructure. It was found that the complex viscosities and dynamic moduli of the branched samples were much lower compared to their linear counterparts. The results conform with earlier findings by the "Strathclyde team" for radical polymerisation systems. This methodology has the potential of providing soluble branched vinyl polymers at low cost using the readily available raw materials.
Keywords
1H NMR spectroscopy, Broad molecular weight distribution, Chain transfer agents, Commercial mixtures, High-vacuum conditions, Highly branched polymers, Proton nuclear magnetic resonance spectroscopy, Tetramethylethylenediamine
Divisions
CHEMISTRY
Funders
University of Malaya (UM): Fundamental Research Grant Scheme, FRGS (FP031-2014B) and Postgraduate Research Fund, PPP (PG193-2015B)
Publication Title
RSC Advances
Volume
8
Issue
21
Publisher
Royal Society of Chemistry