Investigating the bio-rejuvenator effects on aged asphalt through exploring molecular evolution and chemical transformation of asphalt components during oxidative aging and regeneration

2021 ◽  
pp. 129711
Author(s):  
Dongliang Hu ◽  
Xingyu Gu ◽  
Qiao Dong ◽  
Lei Lyu ◽  
Bingyan Cui ◽  
...  
2021 ◽  
Author(s):  
Behzad Behnia

This chapter focuses on various applications of acoustic emissions (AE) technique in evaluation of cracking in asphalt pavements including (1) assessment of low-temperature cracking of asphalt binders and mixtures and (2) quantitative characterization of rejuvenators’ efficiency in restoring aged asphalt pavements to their crack-resistant state. The AE-based embrittlement temperature results of 24 different asphalt materials consisting of eight different binders, each at three oxidative aging levels are presented. Results show that embrittlement temperatures correlated well with corresponding bending beam rheometer (BBR-based) critical cracking temperatures with R2 = 0.85. This chapter also presents application of AE for evaluation of rejuvenators’ efficiency on asphalt materials at various oxidative aging levels. The Geiger’s iterative source location method was employed to accurately determine embrittlement temperatures throughout the thickness of rejuvenator-treated asphalt samples. Results showed that the low temperature cracking properties of oxidative aged materials after 2 weeks of dwell time of rejuvenator have been recuperated. Moreover, it was observed that cracking characteristics of aged asphalt 6–8 weeks after applying rejuvenator far exceeded that of the virgin materials. The promising results suggest that the AE technique can be considered as a viable approach for the assessment of low temperature behavior of asphalt pavements.


2021 ◽  
Author(s):  
Ansgar Bokel ◽  
Michael C. Hutter ◽  
Vlada B. Urlacher

Engineered cytochrome P450 monooxygenase CYP154E1 enables the effective synthesis of the potential antidepressant (2R,6R)-hydroxynorketamine via N-demethylation and regio- and stereoselective hydroxylation of (R)-ketamine.


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