4.2 Article

Controlling Crosslinking in Thermosets via Chain Transfer with Monoterpenes

Journal

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 49, Issue 17, Pages 3719-3727

Publisher

WILEY
DOI: 10.1002/pola.24808

Keywords

beta-pinene; carvone; chain transfer; crosslinking; d-limonene; DCPD; dicyclopentadiene; green polymerization; limonene oxide; metathesis; monoterpene; myrcene; renewable resources; ROMP; sustainable method; thermoset

Funding

  1. American Chemical Society
  2. DURIP

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Renewable resources have been utilized to control the degree of crosslinking during ring-opening metathesis polymerizations (ROMP). In this regard, the addition of monoterpenes to thermosets created a sustainable method for adjusting the physical properties and thermal stability. A number of monoterpenes with alkenes were examined as monofunctional reactants. The presence of these monoterpenes, such as beta-pinene, during the ROMP of dicyclopentadiene altered the degree of crosslinking and plasticized the thermoset. The resulting physical properties were tailored to obtain desired modulus and glass transition (T-g) temperatures. The influence of time, temperature, weight percent beta-pinene, and different metathesis catalysts was examined by dynamic mechanical analysis, thermogravimetric analysis, and FTIR spectroscopy. A comparison of beta-pinene with other monoterpenes, such as carvone, limonene oxide, myrcene, and d-limonene, resulted in a reactivity profile for this general method. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 3719-3727,2011

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