Effects of the geometric characteristics of graphene nanoplatelets on the physico-rheological properties of asphalt binder

被引:4
|
作者
Almashaqbeh, Hashem Khaled [1 ,2 ]
Rushing, Grace [1 ,2 ]
Doyle, Jesse [3 ]
Sengottuvelu, Dineshkumar [1 ]
Majdoub, Mohammed [1 ]
Al-Ostaz, Ahmed [1 ,2 ]
Alkhateb, Hunain [1 ,2 ]
Nouranian, Sasan [1 ,4 ]
Ucak-Astarlioglu, Mine G. [3 ]
机构
[1] Univ Mississippi, Ctr Graphene Res & Innovat, University, MS 38677 USA
[2] Univ Mississippi, Dept Civil Engn, University, MS 38677 USA
[3] US Army Corps Engineers, Engineer Res & Dev Ctr, Vicksburg, MS 39180 USA
[4] Univ Mississippi, Dept Chem Engn, University, MS 38677 USA
关键词
Graphene nanoplatelets; Asphalt binder; Particle diameter; Rheological properties; Multiple stress creep and recovery test; Atomic force microscopy; PERFORMANCE EVALUATION; MIXTURES;
D O I
10.1617/s11527-024-02302-4
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
While graphene nanoplatelets (GnPs) have emerged as promising nano-modifiers of asphalt binder in recent years, much is still unknown in terms of the existing correlations between the physical, chemical, and geometric characteristics of this nanofiller and observed asphalt binder properties. In this work, we investigate the important correlation between the geometric characteristics of GnPs and the rheological properties of the GnP-modified asphalt binder at high temperatures. Our results indicate that, in general, incorporating GnPs with large mean particle diameters (> 14 mu m) and thicknesses (> 8 nm) enhances the high-temperature performance of the asphalt binder. The results of the multiple stress creep and recovery tests confirm that including GnPs in asphalt binder can decrease its permanent deformation by 33.2% and enhance its elastic recovery by 53.9%. Phase contrast images obtained by atomic force microscopy further indicate that the presence of GnPs with large mean particle diameters alters the morphology of the asphalt binder, leading to improved temperature stability and less susceptibility to permanent deformation.
引用
收藏
页数:15
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