The large-scale production of waste plastics has brought serious environmental pollution problems and its recycling and high value-added utilization technology remains a global challenge. Therefore, this study uses waste polyethylene (PE) to prepare high-performance polyethylene composite modified asphalt (HPEA), solving the problem of poor stability and low temperature performance of traditional plastic modified asphalt, while achieving high value-added utilization of waste plastics. A high-performance polyethylene composite modifier (HPE) was prepared through mechanochemical and thermochemical interactions. Then HPEA with different HPE content and styrene-butadiene-styrene (SBS) modified asphalt (SBSMA) with different SBS content were prepared. Compare and analyze the conventional performance, storage stability, anti-aging performance and microscopic properties of HPEA and SBSMA. The results are as follows: (1) the conventional performance of HPEA is comparable to, or superior to, that of SBSMA. The addition of HPE resulted in a significant decrease in asphalt penetration. The modification effect achieved by adding 3–5% SBS to Kunlun 70# asphalt is equivalent to that achieved by incorporating 4–6% HPE. (2) HEPA exhibits good storage stability and no obvious segregation phenomenon. When the HPE content changes from 4% to 8%, the maximum difference in 48 h softening point of HPEA is 1.1 °C, which is significantly smaller than the 48 h softening point difference of SBSMA when the SBS content changes from 3% to 5%. (3) When HPE attains a specific concentration, HPEA can exhibit an anti-aging performance that is comparable to, or superior to, that of SBSMA. (4) The infrared spectrum of HPEA closely resembles that of SK70# matrix asphalt. The modification of HPEA primarily involves physical blending, with HPE undergoing development and re-crosslinking within the system, leading to interactions between smaller particles and asphalt, resulting in the formation of a relatively stable three-dimensional spatial structure.

In response to the complex pretreatment processes (e.g., solvent dissolution and high-temperature melting) of direct coal liquefaction residue (DCLR) in asphalt, its low-dosage limitation for high-value utilization in asphalt pavement, and the unclear interaction mechanisms between high-proportion DCLR and asphalt, this study comprehensively analyzed the molecular composition and structural characteristics of DCLR at multiple scales using FTIR, GPC, SEM, BET, Tg-FTIR, and XRD. DCLR was crushed to a particle size of 0.15 mm and mixed with 70# base asphalt at mass ratios of 10:100, 15:100, 20:100, 25:100, 30:100, 40:100, and 45:100 at 185 °C to prepare high-proportion DCLR-modified asphalt. The conventional and rheological properties of DCLR-modified asphalt at various dosages were evaluated and compared with those of Buton rock asphalt (BRA)-modified asphalt at equivalent dosages. The results indicated that DCLR and BRA significantly improved the high-temperature performance and PG grade of the base asphalt but reduced its low-temperature performance and grade. At equivalent dosages, DCLR exhibited a more pronounced enhancement in high-temperature performance and a greater reduction in low-temperature performance compared to BRA. High-proportion DCLR-modified asphalt meets the technical requirements for high-modulus asphalt. Using FTIR, GPC, four-component analysis, and elemental analysis, the chemical composition and performance variation trends of high-proportion DCLR-modified asphalt were investigated at multiple scales. The interfacial physical, chemical, and mechanical behaviors between DCLR and base asphalt were characterized. The interaction mechanisms between high-proportion DCLR and asphalt were elucidated, and a novel application strategy for DCLR in asphalt was proposed, significantly enhancing its resource utilization rate in road engineering.