The bonding performance between new and old concrete affects the reliability and service life of the repair structure. However, the bonding interface is complex and has many influencing factors, so selecting appropriate repair materials and evaluation methods for repair structures under different service environments is important. This paper presents a comprehensive overview of the factors that influence bonding properties. These include the choice of repair materials, the condition of the existing concrete, the type of interfacial agents used, the service environment, and the testing methods employed. The paper concludes by examining the challenges and opportunities in developing interface bonding properties to provide insights and research directions for future theoretical analysis and experimental research.

To increase performance and save costs when utilizing magnesium phosphate cements (MPC) to repair a damaged building structure or a cement pavement, MPC is typically combined with fly ash (FA) and metakaolin (MK). The influence of FA and MK on the workability, rheological characteristics, flexural strength, compressive strength, and drying shrinkage of MPC was investigated in this research. MPC samples with different percentages of FA and MK by weight replacement were prepared. The results indicate that an appropriate dosage of MK and FA could decrease MPC fluidity and delay the setting time. MPC’s yield stress and plastic viscosity were increased when MK was added. FA has a negative influence on flexural and compressive strength as compared to control MPC and the compressive strength of MPC with MK increases and then decreases. The drying shrinkage of MPC containing MK and FA is superior to control mixture. MPC with 10% FA and 10% MK has the best-modified performance in terms of the comprehensive performance of MPC at all test ages.

In this study, we developed a SYBR Green I real-time PCR method for the rapid and sensitive detection of novel porcine parvovirus 7 (PPV7). Specific primers were designed based on the highly conserved region within the Capsid gene of PPV7. The established method was 1,000 times more sensitive than the conventional PCR method and had a detection limit of 35.6 copies. This method was specific and had no cross-reactions with PCV2, PCV3, PRV, PEDV, PPV1, and PPV6. Experiments testing the intra and interassay precision demonstrated a high reproducibility. Testing the newly established method with 200 clinical samples revealed a detection rate up to 17.5% higher than that of the conventional PCR assay. The established method could provide technical support for clinical diagnosis and epidemiological investigation of PPV7.

A novel avian orthoreovirus (N-ARV) variant characterized with obvious arthritis and synovial inflammation, was isolated from Shandong, China in May 2016. It caused chicken poor growth and enormous economic losses to the poultry industry of China. However, there are few effective methods for detecting the antibody levels of N-ARV. In this study, a viral structural protein σC was expressed using the prokaryotic expression vector pET32a (+). The target protein was obtained by inducing for 6 hours at an IPTG concentration of 0.6mM. The optimal dilution of the coating antigen and serum antibody were determined to be 1000 fold and 10 fold respectively. A specificity test showed that there was no positive reactivity between N-ARV and other pathogens, and when the positive serum was diluted 100 times detection results were still checkable. The repeatability of this method was determined by the inter assay and intra assay tests with variability ranging from 4.85% to 7.93%. In conclusion, this indirect enzyme linked immunosorbent assay (ELISA) will be useful for large-scale serological surveys and monitoring antibody levels in N-ARV infection.