| description abstract | The thermo-photo coupling aging of high-viscosity modified asphalt (HVMA) is essentially a complicated chemical reaction process, and the chemical reaction kinetics theory can provide a novel chemical perspective to elucidate the aging mechanism of HVMA. The aim of this study is to achieve kinetics decoupling of the thermo-photo coupling aging process at different aging times and depths based on chemical reaction kinetics theory, with the purpose of clarifying the spatiotemporal distribution characteristics of thermal aging and photoaging. Firstly, Fourier transform infrared spectroscopy was conducted to investigate the chemical composition changes of HVMA at different aging times and depths. Then, the aging gradient distribution submodel, as well as thermal aging and photoaging kinetics submodels, were constructed to calculate the contribution rates of thermal aging and photoaging at different aging times and depths, thus achieving the kinetics decoupling of the thermo-photo coupling aging process. The results showed that the proposed aging kinetics combination model can ideally fit the thermal aging and photoaging characteristics of HVMA. No notable aging gradient phenomena were detected during thermal aging, but a significant aging gradient characteristic was observed during photoaging. At the surface, the photoaging rate constant was the highest, and it slowed down after the aging depth reached 200 μm. The photoaging exhibited a dominant effect at the surface, with a contribution rate exceeding 96%. As the aging depth increased, the contribution rate of photoaging decreased, whereas that of thermal aging increased. With extended aging time, the aging dominant depth of photoaging gradually increased. A decoupling cloud map was constructed to achieve the kinetics decoupling of the thermo-photo coupling aging process under various aging conditions, durations, and depths. | |
