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HERO ID
5847410
Reference Type
Journal Article
Title
A simple treatment of electronic-waste plastics to produce asphalt binder additives with improved properties
Author(s)
Mohd Hasan, MR; Colbert, B; You, Z; Jamshidi, A; Heiden, PA; Hamzah, MO
Year
2016
Is Peer Reviewed?
Yes
Journal
Construction and Building Materials
ISSN:
0950-0618
EISSN:
1879-0526
Volume
110
Page Numbers
79-88
URL
http://www.sciencedirect.com/science/article/pii/S0950061816300769
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Abstract
This study evaluated the performance of e-waste modified asphalt binders. E-waste modifiers Acrylonitrile Butadiene Styrene (ABS), Acrylonitrile Butadiene Styrene-Polycarbonate (ABS-PC) and High Impact Polystyrene (HIPS) were used after 100% of the material passed through a #50 (300μm) sieve. A conventional asphalt binder, PG58-28 binder, was used as a control. The e-wastes were blended with the control binder as untreated (UT) and chemically treated (T) modified binders. Chemically treated (T) modifiers were processed with cumene hydroperoxide before blending into PG58-28, to promote covalent molecular bonding between the e-waste plastic and asphalt. Results showed that untreated e-waste modified asphalt binders were stiffer and more elastic behavior than the control binder, but when these same e-waste plastics were first treated with cumene hydroperoxide, the increases were significantly higher. Use of chemically treated e-waste modifiers also significantly improves the resistance to rutting of asphalt binders, as shown by the work dissipated per loading based on the analysis conducted at 1.59Hz. The improved results are attributed to the cumene hydroperoxide promoting direct covalent molecular bonding between e-waste plastic powders and the asphalt binder. These results suggest that when polymer modifiers are used in asphalt, radical reactions, at least at the interface with the modifier, should be promoted rather than prevented by added radical inhibitors.
Keywords
Recycled electronic-waste plastic; Asphalt modification; Rheological; Free radical initiator; Peltier system; Activation energy
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