Development of a Cure Model for Unsaturated Polyester Resin Systems Based on Processing Conditions

Author:

Barakat Abdallah1ORCID,Al Ghazal Marc1,Fono Tamo Romeo Sephyrin1ORCID,Phadatare Akash1,Unser John2,Hagan Joshua3,Vaidya Uday145

Affiliation:

1. Department of Mechanical, Aerospace, and Biomedical Engineering, University of Tennessee, Knoxville, TN 37996, USA

2. Composite Applications Group (CAG), 3137 Waterfront Dr, Chattanooga, TN 37419, USA

3. Research and Development Department, Wabash National Corporation, 3550 Veterans Memorial Pkwy S, Lafayette, IN 47909, USA

4. Manufacturing Sciences Division (MSD), Oak Ridge National Laboratory (ORNL), 2350 Cherahala Blvd, Knoxville, TN 37932, USA

5. The Institute for Advanced Composites Manufacturing Innovation, 2370 Cherahala Blvd, Knoxville, TN 37932, USA

Abstract

Unsaturated polyester resin (UPR) systems are extensively used in composite materials for applications in the transportation, marine, and infrastructure sectors. There are continually evolving formulations of UPRs that need to be evaluated and optimized for processing. Differential Scanning Calorimetry (DSC) provides valuable insight into the non-isothermal and isothermal behavior of UPRs within a prescribed temperature range. In the present work, non-isothermal DSC tests were carried out between temperatures of 0.0 °C and 250 °C, through different heating and cooling ramp rates. The isothermal DSC tests were carried out between 0.0 and 170 °C. The instantaneous rate of cure of the tested temperatures were measured. The application of an autocatalytic model in a calculator was used to simulate curing behaviors under different processing conditions. As the temperature increased from 10 °C up to 170 °C, the rate of cure reduced, and the heat of reaction increased. The simulated cure behavior from the DSC data showed that the degree of cure (α) maximum value of 71.25% was achieved at the highest heating temperature of 85 °C. For the low heating temperature, i.e., 5 °C, the maximum degree of cure (α) did not exceed 12% because there was not enough heat to activate the catalyst to crosslink further.

Funder

Wabash National Corporation

Advanced Materials and Manufacturing Technologies Office

University of Tennessee’s Open Publishing Support Fund

Publisher

MDPI AG

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