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This paper aims to investigate the variation rule of coarse aggregate and pore structure of shotcrete by adding MWCNTs. In the paper, X-ray computed tomography scans are used to study the coarse aggregate distribution and pore structure of the preparation of shotcrete, high-temperature curing shotcrete and shotcrete with MWCNTs. The distribution pattern of coarse aggregate and pore of shotcrete is obtained. The results show that: the coarse aggregate loss of shotcrete is serious within 30 mm from the wall and the coarse aggregate increases significantly in 30–70 mm. The addition of 0.03% MWCNTs increased the coarse aggregate of shotcrete by 36.63% and the volume of coarse aggregate by 25.64%. The largest increase is in coarse aggregates of 5–7 mm. This show that MWCNTs can improve mortar adhesion and reduce aggregate rebound. The number of shotcrete pores decreases with the increase of pore diameter. The proportion of small pores is up to 85%, the proportion of large pores is only 2%, but the volume of large pores reaches 87%. The addition of 0.03% MWCNTs can reduce the number of small pores in the shotcrete and reduce the mean pore diameter, resulting in a decrease in the porosity of the shotcrete. When the curing temperature is 80℃, the porosity of shotcrete increases, and the pores decrease due to interconnection. The pores around the coarse aggregate account for over 70% of the total porosity, with pores larger than 1 mm accounting for 75%. This paper has a good reference value for the development of shotcrete and the selection of coarse aggregate in the actual working conditions. • The coarse aggregate distribution and pore structure characteristics of shotcrete were revealed. • The influence of MWCNTs on the rebound of shotcrete coarse aggregate was analyzed. • The relationship between pore distribution of shotcrete and coarse aggregate distribution is discussed. [ABSTRACT FROM AUTHOR]

The inhalation route has a substantial influence on the fate of inhaled particles. An outbreak of infectious diseases such as COVID-19, influenza or tuberculosis depends on the site of deposition of the inhaled pathogens. But the knowledge of respiratory deposition is important also for occupational safety or targeted delivery of inhaled pharmaceuticals. Simulations utilizing computational fluid dynamics are becoming available to a wide spectrum of users and they can undoubtedly bring detailed predictions of regional deposition of particles. However, if those simulations are to be trusted, they must be validated by experimental data. This article presents simulations and experiments performed on a geometry of airways which is available to other users and thus those results can be used for intercomparison between different research groups. In particular, three hypotheses were tested. First: Oral breathing and combined breathing are equivalent in terms of particle deposition in TB airways, as the pressure resistance of the nasal cavity is so high that the inhaled aerosol flows mostly through the oral cavity in both cases. Second: The influence of the inhalation route (nasal, oral or combined) on the regional distribution of the deposited particles downstream of the trachea is negligible. Third: Simulations can accurately and credibly predict deposition hotspots. The maximum spatial resolution of predicted deposition achievable by current methods was searched for. The simulations were performed using large-eddy simulation, the flow measurements were done by laser Doppler anemometry and the deposition has been measured by positron emission tomography in a realistic replica of human airways. Limitations and sources of uncertainties of the experimental methods were identified. The results confirmed that the high-pressure resistance of the nasal cavity leads to practically identical velocity profiles, even above the glottis for the mouth, and combined mouth and nose breathing. The distribution of deposited particles downstream of the trachea was not influenced by the inhalation route. The carina of the first bifurcation was not among the main deposition hotspots regardless of the inhalation route or flow rate. On the other hand, the deposition hotspots were identified by both CFD and experiments in the second bifurcation in both lungs, and to a lesser extent also in both the third bifurcations in the left lung. • Limits of current methods in prediction of flow and high-resolution deposition in an airway geometry were investigated. • Experiments and simulations performed on a replica of airways - nasal and oral cavity and seven generations of TB branching. • The influence of the inhalation route on the flow field was negligible downstream of the glottis. • The carina of the first bifurcation was not among the main deposition hotspots regardless of the inhalation route. • Deposition hotspots identified in the second bifurcation in both lungs, and in both third bifurcations in the left lung. [ABSTRACT FROM AUTHOR]