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Using recycled concrete fines (RFs) as a supplementary cementitious material in blended cement systems offers potential benefits for the construction industry. This study investigated the mechanical properties, hydration development, and microstructural evolutions of blended Portland cement systems incorporating different particle-size distributions of untreated RFs. The results highlighted that finer RFs improved the compressive strength of mortar and influenced hydration by promoting monocarbonate formation. The incorporation of RFs optimizes the pore structure in the early stage but increases porosity. RFs affected the distribution of capillary pores and created a rougher and more complex surface compared to inert mineral admixtures. Furthermore, the particle size of RFs impacted the fractal dimension of multi-scale pore sizes.

Radiotherapy (RT) has been used to control tumors by physically damaging DNA and inducing apoptosis; it also promotes antitumor immune responses via neoantigens release and augmenting immune-oncology agents to elicit systemic response. Tumor regression after RT can recruit inflammatory cells, such as tumor-associated macrophages and CD11b+ myeloid cell populations, a major subset of which may actually be immunosuppressive. However, these inflammatory cells also express Toll-like receptors (TLRs) that can be stimulated to reverse suppressive characteristics and promote systemic antitumor outcomes. Here, we investigated the effects of adding CMP-001, a CpG-A oligodeoxynucleotide TLR9 agonist delivered in a virus-like particle (VLP), to RT in two murine models (344SQ metastatic lung adenocarcinoma and CT26 colon carcinoma). High-dose RT (12Gy x 3 fractions) significantly increased the percentages of plasmacytoid dendritic cells within the tumor islets 3- and 5-days post-RT; adding CMP-001 after RT also enhanced adaptive immunity by increasing the proportion of CD4+ and CD8+ T cells. RT plus CMP-001-mediated activation of the immune system led to significant inhibition of tumor growth at both primary and abscopal tumor sites, thereby suggesting a new combinatorial treatment strategy for systemic disease.