Search

Deep-buried tunnels with weak surrounding rock are frequently encountered issues in traffic engineering. It plays an important role in the excavation process and the project operation. This paper applies the theoretical analysis and laboratory test related to four different conditions in terms of their thickness to determine the mechanical response of deep-buried tunnel lining. Then, the energy dissipative structure theory is employed to explain the experimental results. This paper has made the following achievements: firstly, it is found that the toughness of the secondary lining was found to be often the most important indicator of tunnel safety, with better-toughness linings having higher tensile strength and crack resistance. Secondly, it suggests that the inclusion of steel reinforcement in the concrete lining can effectively improve the secondary lining toughness. Finally, it proves that the more ductile liner had more energy, higher load-carrying capacity, and was better able to maintain the overall stability of the structure. [ABSTRACT FROM AUTHOR]

This study aimed to predict the outcome of patient specific quality assurance (PSQA) in IMRT for breast cancer using complexity metrics, such as MU factor, MAD, CAS, MCS. Several breast cancer plans were considered, including LBCS, RBCS, LBCM, RBCM, left breast, right breast and the whole breast for both Edge and TrueBeam LINACS. Dose verification was completed by Portal Dosimetry (PD). The receiver operating characteristic (ROC) curve was employed to determine whether the treatment plans pass or failed. The area under the curve (AUC) was used to assess the classification performance. The correlation of PSQA and complexity metrics was examined using Spearman’s rank correlation coefficient (Rs). For LINACS, the most suitable complexity metric was found to be the MU factor (Edge Rs = − 0.608, p < 0.01; TrueBeam Rs = − 0.739, p < 0.01). Regarding the specific breast cancer categories, the optimal complexity metrics were as follows: MAD (AUC = 0.917) for LBCS, MCS (AUC = 0.681) for RBCS, MU factor (AUC = 0.854) for LBCM and MAD (AUC = 0.731) for RBCM. On the Edge LINAC, the preferable method for breast cancers was MCS (left breast, AUC = 0.938; right breast, AUC = 0.813), while on the TrueBeam LINAC, it became MU factor (left breast, AUC = 0.950) and MCS (right breast, AUC = 0.806), respectively. Overall, there was no universally suitable complexity metric for all types of breast cancers. The choice of complexity metric depended on different cancer types, locations and treatment LINACs. Therefore, when utilizing complexity metrics to predict PSQA outcomes in IMRT for breast cancer, it was essential to select the appropriate metric based on the specific circumstances and characteristics of the treatment. [ABSTRACT FROM AUTHOR]

Modifying the position and numbers of lateral fluorine substituent is a common method to design and adjust the mesophase of liquid crystal compounds. Here, a series of 2-(2,2ʹ-difluoro-4ʹ-alkoxy-1,1ʹ-biphenyl-4-yl)-5-substituted benzoxazole with both non-polar (H, CH3) and polar (NO2) groups (coded as nPF(2)PF(2)Bx) is synthesised and characterised. All of the compounds show a conspicuous inter-ring twist angle of 38° compared with corresponding reference compounds I and II which are calculated by density functional theory method, and it is interesting to note that the final compounds nPF(2)PF(2)Bx show only nematic mesophase during heating or cooling. Meanwhile, the UV-vis absorption bands and photoluminescence emission peaks both display remarkable blue-shifted. The aforementioned results reveal that lateral difluoro substituents play a key role to stable the nematic mesophase by increasing the dihedral angle of biphenyl. [ABSTRACT FROM AUTHOR]

Terminal vinyl-based benzoxazole liquid crystalline compounds, 2-(3-fluoro-4ʹ-alkoxy-1,1ʹ-biphenyl −4-yl)-5-(2-propenyloxymethyl)-benzoxazole (nPPF(2)BP), were synthesised and their structures were confirmed by infrared (IR) spectra, proton nuclear magnetic resonance (1H-NMR) spectra, gas chromatography with electron impact-mass spectrometry (GC/EI-MS), matrix-assisted laser desorption/ionisation-time of flight (MALDI-TOF) mass spectrometry and elemental analysis (EA). The compounds show enantiotropic smectic/nematic phases with mesophase ranges are 71–97 °C and 87–136°C on heating and cooling processes for nPPF(2)BP, respectively. They give low melting points due to lateral fluoro substituent and flexible terminal 2-propenyloxymethyl chain. It is found that the compounds nPPF(2)BP with shorter alkoxy chain (n = 3, 4) exhibit a wide range of nematic mesophase, which is ascribed to enhanced π–π interaction caused by terminal vinyl moiety, whereas further elongation of the terminal alkoxy chain results in supressing nematic phase and increasing smectic mesophase. Compared with methyl terminated analogues, 2-propenyloxymethyl terminated compounds nPPF(2)BP display much lower melting points and wider or comparable mesophase range both in heating and cooling. [ABSTRACT FROM AUTHOR]

A series of 1-methyl-1H-benzimidazole-based compounds, 2-(4ʹ-alkoxy-1,1ʹ-biphenyl-4-yl)-1-methyl- 1H-1,3-benzimidazole derivatives (nPPMx-M) with terminal hydrogen, methyl and nitro moieties (coded as nPPMH-M, nPPMM-M and nPPMN-M, respectively), were prepared and their structures were characterised. The compounds display enantiotropic smectic mesophases for hydrogen and methyl terminated compounds (nPPMH-M and nPPMM-M), and enantiotropic nematic mesophases for nitro terminated compounds (nPPMN-M) with short alkoxy chain below than 10 carbon atoms, where the mesophase ranges are 24-72°C and 74-104°C on heating and cooling processes for nPPMH-M, 90-119°C and 110-135°C for nPPMM-M, and 102-129°C and 113-207°C for nPPMN-M, respectively. It is noted that the compounds nPPMx-M exhibit much lower melting points and much wider mesophase range both in heating and cooling than non-1-methyl substituted analogs, which are ascribed to the disruption of hydrogen bonding among the molecules caused by methyl substitution at 1-position of benzimidazole. Meanwhile, among the compounds nPPMx-M, much wider mesophase ranges are obtained for nPPMM-M and nPPMN-M, indicating a much high mesophase stability for the compounds bearing terminal moiety (CH3 and NO2). [ABSTRACT FROM AUTHOR]

Fluorinated aromatics is generally chosen as mesogenic cores to design novel liquid crystal compounds. Here, a series of benzoxazole derivatives with laterally multifluorinated biphenyl units, 2-(3′,3-difluoro −4′-alkoxy-1,1′-biphenyl-4-yl)-benzoxazole derivatives (coded as nPF(3)PF(3)Bx), are synthesized and characterized, where methyl and nitro moieties are selected as terminal groups to investigate the effects of different polar substituents on the liquid crystal properties. The compounds nPF(3)PF(3)Bx show enantiotropic mesophases with mesophase ranges of 0-40°C and 0-63°C on heating and cooling for hydrogen-terminated derivatives (nPF(3)PF(3)BH), 43-93°C and 54-123°C for methyl-terminated ones (nPF(3)PF(3)BM), 60-108°C and 74-152°C for nitro terminated ones (nPF(3)PF(3)BN), respectively. They exhibit photoluminescence emission peaks at 390-392 nm and UV-vis absorption bands with maxima at 327-330 nm, respectively. The results reveal that lateral multifluoro substituents lead to a decrease in melting/clearing points, while electron-withdrawing terminal nitro moiety results in increases in both melting point and mesophase range. [ABSTRACT FROM AUTHOR]

Series of laterally multifluorinated heterocyclic compounds, 2-(2ʹ,3-difluoro-4ʹ-alkoxy-1,1ʹ-biphenyl-4-yl)-benzoxazole derivatives (nPF(2)PF(3)Bx), are prepared and characterised. They mainly display enantiotropic nematic mesophases with wider mesophase ranges of 12–107°C (heating process) and 22–134°C (cooling process) than the corresponding analogues. The enhanced nematic mesophase stability is achieved via slightly increasing inter-ring twist angle with inter-ring lateral fluorine substitute in biphenyl unit, as well as through improving the molecular polarity with multifluorine substitutes. Meanwhile, two inter-ring lateral fluorine atoms lead to a decrease in melting/clearing points and a wide nematic mesophase range, which makes it possible for heterocyclic mesogens nPF(2)PF(3)Bx to use in nematic liquid crystal display mixtures. [ABSTRACT FROM PUBLISHER]

Series of laterally monofluorinated compounds, 2-(4ʹ-alkoxy-3-fluorobiphenyl-4-yl)-1H-benzimidazole derivatives (nPPF(3)Mx) bearing different substituents (H, CH3, NO2, coded as nPPF(3)MH, nPPF(3)MM and nPPF(3)MN, respectively) at 5-position, were prepared and their structures were characterised. According to the results from differential scanning calorimetry and polarising optical microscopy, the present compounds nPPF(3)Mx exhibit enantiotropic smectic mesophases, for which the mesophase ranges are 13–67 and 47–111°C on heating and cooling for nPPF(3)MH, 84–112 and 126–154°C for nPPF(3)MM, and 23–102 and 49–117°C for nPPF(3)MN, respectively. Compared to non-fluorinated analogues, monofluorinated nPPF(3)Mx have low melting/clearing points and display enhanced mesophase range both in heating and cooling, which are attributed to the disruption of the side-to-side intermolecular packing caused by theortholateral fluoro substituents and the increased dipole–dipole interaction between the polar fluoro-substituted molecules, respectively. It is noted that nPPF(3)MM and nPPF(3)MN show a much wider mesophase range than nPPF(3)MH, which suggest that the substituent at benzimidazole moiety can improve the mesophase stability. [ABSTRACT FROM PUBLISHER]