Volume 132, Issue 7
Article

Flame retarding effect of graphite in rotationally molded polyethylene/graphite composites

Washington Mhike

Washington Mhike

Institute for Applied Materials, Department of Chemical Engineering, University of Pretoria, Private Bag X20, Hatfield, Pretoria, 0028 South Africa

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Ignatius V. W. Ferreira

Ignatius V. W. Ferreira

Institute for Applied Materials, Department of Chemical Engineering, University of Pretoria, Private Bag X20, Hatfield, Pretoria, 0028 South Africa

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Jing Li

Jing Li

Department of Fire Protection Engineering, University of Maryland, College Park, Maryland, 20742

Department of Mechanical Engineering, University of Maryland, College Park, Maryland, 20742

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Stanislav I. Stoliarov

Stanislav I. Stoliarov

Department of Fire Protection Engineering, University of Maryland, College Park, Maryland, 20742

Department of Mechanical Engineering, University of Maryland, College Park, Maryland, 20742

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Walter W. Focke

Corresponding Author

Walter W. Focke

Institute for Applied Materials, Department of Chemical Engineering, University of Pretoria, Private Bag X20, Hatfield, Pretoria, 0028 South Africa

Correspondence to: W. W. Focke (E-mail: [email protected])Search for more papers by this author
First published: 24 September 2014
Citations: 20

ABSTRACT

Linear low-density polyethylene (LLDPE) compounds containing 10 wt % graphite fillers were rotationally molded into flat sheets. Flame retardancy was studied using cone calorimeter tests conducted at a radiative heat flux of 35 kW/m2. Only the expandable graphite, an established flame retardant for polyethylene, significantly reduced the peak heat release rate. Compared with the neat polyethylene, it was easier to ignite the LLDPE composites containing carbon black, expandable graphite, and exfoliated graphite. However, rather unexpectedly, the inclusion of flake graphite increased the time to ignition by up to 80%. Simulations conducted with the ThermaKin numerical pyrolysis software suggest that increased reflectivity was mainly responsible for this effect. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41472.

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