Numerical investigation on dynamic characteristics of drilling shaft in deep hole drilling influenced by minimal quantity lubrication

The dynamic characteristics of drilling shaft in deep hole drilling influenced by minimal quantity lubrication (MQL) is investigated. According to the features of the compressible fluid Reynolds equation in oil/air feature, a time-dependent mathematical model is established to describe the pressure distribution of cutting fluid with nonlinearity in MQL deep hole drilling. By introducing the differential transformation approach, the time-dependent pressure equation arising from cutting fluid is solved by the use of direct integral method. The influences of the rotational speed, the transverse displacement ratio, and radial clearance on the hydrodynamic pressure distribution of cutting fluid are obtained. The advantage of this method is to overcome much of the computational cost and has its rapid convergence rate. Furthermore, the nonlinear responses of drilling shaft influenced by MQL are analyzed, and the instability rotational speeds of drilling tool are discussed while the design parameters of drilling shaft system changing.     

Influence of Macro-pores on DNAPL Migration in Double-Porosity Soil Using Light Transmission Visualization Method

Double porosity is a substantial microstructure characteristic in a wide range of geomaterials. It is a natural phenomenon that can be found in many types of soil, and it can result from biological, chemical or mechanical damage. In this paper, the influence of macro-pores on dense non-aqueous phase liquid (DNAPL) migration in double-porosity medium was investigated using light transmission visualization technique. Three experiments were carried out in two-dimensional flow chambers filled with a double-porosity medium composed of a mixture of local sand and sintered kaolin clay spheres arranged in a periodic manner. In each experiment, a different volumetric fraction of macro-pores and micropores was used. Tetrachloroethylene (PCE) was used to simulate DNAPL, and it was dyed using Oil-Red-O for better visualization. A predetermined amount of PCE was injected into the flow chambers and this amount was re-calculated using image analysis. A very strong correlation was found between the PCE amount injected and the amount calculated from image analysis in each experiment. The experiment was repeated by filling the flow chamber with silica sand to represent single-porosity medium. The results show that the macro-pores have a considerable effect on the PCE migration in double-porosity soil as the PCE movement was the fastest in the third experiment which contained the largest macro-pores volume. The accuracy of the method was validated using statistical analysis. The results show a slight difference between the means of the three experiments, indicating that the method is viable for monitoring NAPL migration in double-porosity medium under different volumetric fractions of macro-pores and micropores.     

熔盐堆空气换热器结构完整性分析

熔盐堆作为第四代核反应堆备选堆型之一,运行温度高,对材料高温性能要求严格;熔盐堆空气换热器作为实验堆关键设备,工作温度高,启停机次数多,长期运行后,材料许用应力松弛下降,应力、应变可能超出允许限值,或发生蠕变疲劳失效。使用Workbench软件,对熔盐堆空气换热器进行力学分析,并对A级使用载荷要求进行结构完整性评定,结果表明:熔盐堆空气换热器满足力学性能要求,其中疲劳损伤占比重较大,高温蠕变损伤也较为显著。     

Construction of Hybrid Bimetallic Uranyl Compounds Based on a Preassembled Terpyridine Metalloligand

Six hybrid uranyl–transition metal compounds [UO₂Ni(cptpy)₂(HCOO)₂(DMF)(H₂O)] ( 1 ), [UO₂Ni(cptpy)₂(BTPA)₂] ( 2 ), [UO₂Fe(cptpy)₂(HCOO)₂(DMF)(H₂O)] ( 3 ), [UO₂Fe(cptpy)₂(BTPA)₂] ( 4 ), [UO₂Co(cptpy)₂(HCOO)₂(DMF)(H₂O)] ( 5 ), and [UO₂Co(cptpy)₂(BTPA)₂] ( 6 ), based on bifunctional ligand 4′-(4-carboxyphenyl)-2,2′:6′,2′′-terpyridine (Hcptpy) are reported (H₂BTPA = 4,4′-biphenyldicarboxylic acid). Single-crystal XRD revealed that all six compounds feature similar metalloligands, which consist of two cptpy⁻ anions and one transition metal cation. The metalloligand M(cptpy)₂ can be considered to be an extended linear dicarboxylic ligand with length of 22.12 Å. Compounds 1 , 3 , and 5 are isomers, and all of them feature 1D chain structures. The adjacent 1D chains are connected together by hydrogen bonds and π–π interactions to form a 3D porous structure, which is filled with solvent molecules and can be exchanged with I₂. Compounds 2 , 4 , and 6 are also isomers, and all of them feature 2D honeycomb (6,3) networks with hexagonal units of dimensions 41.91×26.89 Å, which are the largest among uranyl compounds with honeycomb networks. The large aperture allows two sets of equivalent networks to be entangled together to result in a 2D+2D→3D polycatenated framework. Remarkably, these uranyl compounds exhibit high catalytic activity for cycloaddition of carbon dioxide. Moreover, the geometric and electronic structures of compounds 1 and 2 are systematically discussed on the basis of DFT calculations.     

3D photon counting imaging at 1550 nm with 1.5-GHz sine-wave-gated InGaAs/InP GAPD

We demonstrated a 3D laser imaging system at 1550 nm with a 1.5-GHz sine-wave gated Geiger-mode InGaAs/InP avalanche photodiode (APD). An optical fiber bundle with 100 individual fiber outputs was implemented at the focal plane of the telescope, providing a 2.5-mrad imaging view. The system used single-pixel near-infrared single-photon detector to measure photons at fiber outputs instead of a photon counting array. The 1.5-GHz gated Geiger-mode InGaAs/InP APD with a timing jitter of 290 ps was operated in quasi-continuous mode with detection efficiency of ∼4.3%. We achieved higher than 6-cm surface-to-surface resolution at single-photon level, showing a potential of low-energy and eye-safe laser imaging system for long-distance measurements.     

Simultaneous determination of 75 abuse drugs including amphetamines,benzodiazepines, cocaine,opioids, piperazines,zolpidem and metabolites in human hair samples using liquid chromatography–tandem mass spectrometry

A liquid chromatography–tandem mass spectrometric method for the simultaneous determination of 75 abuse drugs and metabolites, including 19 benzodiazepines, 19 amphetamines, two opiates, eight opioids, cocaine, lysergic acid diethylamide, zolpidem, three piperazines and 21 metabolites in human hair samples, was developed and validated. Ten‐milligram hair samples were decontaminated, pulverized using a ball mill, extracted with 1 mL of methanol spiked with 28 deuterated internal standards in an ultrasonic bath for 60 min at 50°C, and purified with Q‐sep dispersive solid‐phase extraction tubes. The purified extracts were evaporated to dryness and the residue was dissolved in 0.1 mL of 10% methanol. The 75 analytes were analyzed on an Acquity HSS T3 column using gradient elution of methanol and 0.1% formic acid and quantified in multiple reaction monitoring mode with positive electrospray ionization. Calibration curves were linear (r ≥ 0.9951) from the lower limit of quantitation (2–200 pg/mg depending on the drug) to 2000 pg/mg. The coefficients of variation and accuracy for intra‐ and inter‐assay analysis at three QC levels were 4.3–12.9% and 89.2–109.1%, respectively. The overall mean recovery ranged from 87.1 to 105.3%. This method was successfully applied to the analysis of 11 forensic hair samples obtained from drug abusers.     

Sparse Multicategory Generalized Distance Weighted Discrimination in Ultra-High Dimensions

Distance weighted discrimination (DWD) is an appealing classification method that is capable of overcoming data piling problems in high-dimensional settings. Especially when various sparsity structures are assumed in these settings, variable selection in multicategory classification poses great challenges. In this paper, we propose a multicategory generalized DWD (MgDWD) method that maintains intrinsic variable group structures during selection using a sparse group lasso penalty. Theoretically, we derive minimizer uniqueness for the penalized MgDWD loss function and consistency properties for the proposed classifier. We further develop an efficient algorithm based on the proximal operator to solve the optimization problem. The performance of MgDWD is evaluated using finite sample simulations and miRNA data from an HIV study.     

Bioactivity-Guided Isolation of Phytochemicals from Vaccinium dunalianum Wight and Their Antioxidant and Enzyme Inhibitory Activities

Vaccinium dunalianum Wight, usually processed as a traditional folk tea beverage, is widely distributed in the southwest of China. The present study aimed to investigate the antioxidant, α-glucosidase and pancreatic lipase inhibitory activities of V. dunalianum extract and isolate the bioactive components. In this study, the crude extract (CE) from the buds of V. dunalianum was prepared by the ultrasound-assisted extraction method in 70% methanol and then purified with macroporous resin D101 to obtain the purified extract (PM). Five fractions (Fr. A–E) were further obtained by MPLC column (RP-C18). Bioactivity assays revealed that Fr. B with 40% methanol and Fr. D with 80% methanol had better antioxidant with 0.48 ± 0.03 and 0.62 ± 0.01 nM Trolox equivalent (TE)/mg extract for DPPH, 0.87 ± 0.02 and 1.58 ± 0.02 nM TE/mg extract for FRAP, 14.42 ± 0.41 and 19.25 ± 0.23 nM TE/mg extract for ABTS, and enzyme inhibitory effects with IC₅₀ values of 95.21 ± 2.21 and 74.55 ± 3.85 for α-glucosidase, and 142.53 ± 11.45 and 128.76 ± 13.85 µg/mL for pancreatic lipase. Multivariate analysis indicated that the TPC and TFC were positively related to the antioxidant activities. Further phytochemical purification led to the isolation of ten compounds (1–10). 6-O-Caffeoylarbutin (7) showed significant inhibitory effects on α-glucosidase and pancreatic lipase enzymes with values of 38.38 ± 1.84 and 97.56 ± 7.53 µg/mL, and had the highest antioxidant capacity compared to the other compounds.     

Theoretical investigation into coordination and selectivity of uranyl-unilateral benzotriazole salophens (X = O/S) for R/S-triadimefons

The design of new uranyl-ligands (uranyl-Ls) is of great significance for the separation and utilization of uranium. In this paper, the triazole group was introduced into uranyl-salophen (uranyl-S) to form new asymmetric uranyl-unilateral benzotriazole salophen (uranyl-UBS); we further replaced two oxygen atoms of uranyl-UBS with two sulfur atoms to generate uranyl-unilateral benzotriazole thio-salophen (uranyl-UBTS) as a new receptor. Then, we comprehensively explored coordination models of uranyl-UBS and uranyl-UBTS with R/S-triadimefons (R/S-TDFs) enantiomers as the guests using density functional theory calculations at the B3LYP//RECP/6-311G** level; we then investigated enantioselectivity recognition of the new receptors to the guests R/S-TDFs. The results indicated that the uranium atoms of the receptors uranyl-S, uranyl-UBS and uranyl-UBTS could coordinate with the carbonyl oxygens in guests R/S-TDFs to form complexes of guest-receptors R/S-TDFs-uranyl-Ls that exhibited two stable V-shaped structures with quite different properties. It was found that the coordination ability to the guests R/S-TDFs is uranyl-UBTS > uranyl-UBS > uranyl-S, while the enantioselectivity for the guests is uranyl-UBTS > uranyl-S > uranyl-UBS and, when the receptor is the same, R-TDF has stronger coordination ability than S-TDF. These results provide information and theoretical supports for the experiments of asymmetric uranyl-UBS with R/S-TDFs, and produce a reference for further exploring the coordination characteristics of asymmetric uranyl-salophen with the triazole derivatives.