Related Experiment Video
Updated: May 13, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Pentaerythritol and Glycerol Ester-Based Rosin-Modified Hydroxyl-Terminated Polybutadiene (HTPB)
Frank Lee1, Aran Guner1, Ken Lewtas1,2
1International Institute for Nanocomposites Manufacturing (IINM), WMG, University of Warwick, WarwickCV4 7AL, U.K.
Abstract:
Hydroxyl-terminated polybutadiene (HTPB) has widespread applications such as in adhesives, coatings, and solid propellants due to its durability and excellent mechanical strength when cross-linked, which can be maintained at low temperatures. However, many of the additives used to modify the properties of HTPB are not sustainably sourced nor have the functionality such that tailoring of HTPB properties can be achieved. Here, we describe the use of the pentaerythritol ester of rosin (PER) and glycerol ester of rosin (GER), sourced from gum rosin (pine trees), to modify the rheology and mechanical properties of uncross-linked and cross-linked HTPB. Both rosin esters are compatible with HTPB resulting in a change in the glass transition temperature (T g) of HTPB, which is concentration-dependent. The inclusion of PER increased the viscosity of uncross-linked HTPB more than GER due to the additional abietic functionality per molecule. The rosin esters also compete with the terminal hydroxyl groups of HTPB during cross-linking with toluene diisocyanate (HTPB-PU). Consequently, the cross-link density of HTPB-PU decreases and the molecular mass between cross-links increases with increasing PER/GER content. This competition results in a decrease in Young's modulus and tensile strength of HTPB but a significant increase in elongation at break (+153%) and tensile toughness (+76%) of HTPB.
Related Concept Videos
Types of Step-Growth Polymers: Polyesters
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the...
Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene
Hydroboration-Oxidation of Alkenes
Polymer Classification: Architecture

