The Mechanism Study of Vortex Tools Drainage Gas Recovery of Gas Well

The liquid loading of gas well is an important issue in deep exploitation of natural gas. The technic of vortex drainage has good prospects because the tool construction and construction work is simple, the technic is environmental and efficient. Currently, the mechanism for the vortex drainage and the theory of fluid motion are still missing. Therefore, in order to further understand the downhole flow field, verify drainage mechanism and select best working conditions, based on computational fluid dynamics and mixture model of multiphase flow through Fluent, the study established a three-dimensional structural model of vortex tools and the numerical simulation has been done. By monitoring the wellhead and the radial distribution of the liquid content and observing the state of the gas-liquid flow and the path line, the study analyzed the influence on gas well flow field by vortex tool. The study revealed the working mechanism of vortex tools to facilitate understanding the nature of the vortex drainage process, guide how to select the preferred process conditions and provide theoretical basis for the application and the dynamics simulation of vortex drainage technology.Key words: The liquid loading of gas well; Vortex drainage; Multiphase flow; Numerical simulatio

Quantitative Analysis of Retinal Vasculature in Rhegmatogenous Retinal Detachment Based on Ultra-Widefield Fundus Imaging

PurposeTo quantitatively analyze retinal vascular morphological features, such as vascular density, caliber, and tortuosity, in rhegmatogenous retinal detachment (RRD). MethodsA total of 244 patients with RRD and 400 healthy controls (HC) were included. Retinal fundus images were collected using OPTOS PLC Daytona P200T. Retinal images were divided into RRD and non-RRD regions of interest (ROIs). All visible retinal fundus vessels were then extracted mainly based on edge detection within ROI to form the whole-vascular image. Retinal vasculature parameters, such as vascular density, caliber, and tortuosity, were calculated. ResultsFor the absolute density, the mean rank (MR) value of normal controls was significantly higher than that in non-RRD (p < 0.001). A consistent tendency of significant vascular density was increased from non-RRD to RRD (p < 0.001). The average and median diameters of normal controls were both significantly larger than RRD (p < 0.001). The average and median diameters were also appeared significantly thinner in non-RRD. Unweighted and width-inversely-weighted vascular tortuosity in RRD and non-RRD comparison exhibited non-significant differences. All types of tortuosity calculated from HC were significantly larger (p < 0.001) in values compared to RRD. All types of tortuosity values of HC were significantly higher than non-RRD. Compared with non-RRD, RRD was significantly larger in area-weighted, length-weighted, and width-weighted vascular tortuosity. ConclusionsThis study showed that RRD affects both the quantity and morphology of retinal vasculature, such as RRD and non-RRD areas. Smaller average and medium vascular diameters and tortuosity values were found in RRD. However, the absolute vascular density, the average and median diameter, and tortuosity values were also reduced in non-RRD although the retina is still attached. This work indicates that RRD may affect the retinal vasculature beyond the detached retina

Few-Layer Tin Sulfide: A New Black-Phosphorus-Analogue 2D Material with a Sizeable Band Gap, Odd–Even Quantum Confinement Effect, and High Carrier Mobility

As a compound analogue of black phosphorus, a new 2D semiconductor of SnS layers is proposed. Based on state-of-the-art theoretical calculations, we confirm that such 2D SnS layers are thermally and dynamically stable and can be mechanically exoliated from α-phase SnS bulk materials. The 2D SnS layer has an indirect band gap that can be tuned from 1.96 eV for the monolayer to 1.44 eV for a six-layer structure. Interestingly, the decrease of the band gap with increasing number of layers is not monotonic but shows an odd–even quantum confinement effect, because the interplay of spin–orbit coupling and lack of inversion symmetry in odd-numbered layer structures results in anisotropic spin splitting of the energy bands. It was also found that such 2D SnS layers show high in-plane anisotropy and high carrier mobility (tens of thousands of cm² V^–1 s^–1) even superior to that of black phosphorus, which is dominated by electrons. With these intriguing electronic properties, such 2D SnS layers are expected to have great potential for application in future nanoelectronics

Graphene Nanoribbons Derived from Zigzag Edge-Encased Poly(para-2,9-dibenzo[bc,kl]coronenylene) Polymer Chains

In this work, we demonstrate the bottom-up on-surface synthesis of poly(para-dibenzo[bc,kl]-coronenylene) (PPDBC), a zigzag edge-encased analog of poly(para-phenylene) (PPP), and its lateral fusion into zigzag edge-extended graphene nanoribbons (zeeGNRs). Toward this end, we designed a dihalogenated di(meta-xylyl)anthracene monomer displaying strategic methyl groups at the substituted phenyl ring and investigated its applicability as precursor in the thermally induced surface-assisted polymerization and cyclodehydrogenation. The structure of the resulting zigzag edge-rich (70%) polymer PPDBC was unambiguously confirmed by scanning tunneling microscopy (STM) and non-contact atomic force microscopy (nc-AFM). Remarkably, by further thermal treatment at 450 °C two and three aligned PPDBC chains can be laterally fused into expanded zeeGNRs, with a ribbon width of nine (N = 9) up to 17 (N = 17) carbon atoms. Moreover, the resulting zeeGNRs exhibit a high ratio of zigzag (67%) vs armchair (25%) edge segments and feature electronic band gaps as low as 0.9 eV according to gaps quasiparticle calculations

Tuning Li-enrichment in high-Ni layered oxide cathodes to optimize electrochemical performance for Li-ion battery

To understand what and how structural properties affect battery performance, and to optimize the structural properties accordingly are of crucial importance to improve the performance of cathode materials for advanced Li-ion batteries. Herein, we investigated the influence of Li-enrichment in Li1+x(Ni0.8Co0.2)1-xO2 transition metal (TM) oxide cathodes, obtained by sintering Ni0.8Co0.2(OH)2 precursor with different amount of Li sources. Compared with stoichiometric Li1+x(Ni0.8Co0.2)1-xO2 (i.e. x = 0, Li:TM = 1:1), the improvements of cycling stability and rate performance were observed in material with moderate degree of Li-enrichment with respect to TMs (i.e. x = 0.019, Li:TM = 1.04:1). Further increase in Li:TM ratio up to 1.07 diminishes the electrochemical performance. Multi-scale structural characterizations including neutron diffraction and aberration-corrected transmission electron microscopy measurements show that the Li-enrichment leads to a monotonical increase in both Li/Ni exchange ratio and Li slab space. Based on the results, we argue that, in material with moderate Li-enrichment, larger Li slab space can facilitate the diffusion of Li ions and a certain amount of Li/Ni disordering can also mitigate the contraction of layered structure, therefore resulting in an optimized electrochemical performance; while in material with excessive Li:TM ratio, the diffusion path can be partially blocked due to the presence of redundant Ni ions in Li layers

Excess Li-Ion Storage on Reconstructed Surfaces of Nanocrystals To Boost Battery Performance

Because of their enhanced kinetic properties, nanocrystallites have received much attention as potential electrode materials for energy storage. However, because of the large specific surface areas of nanocrystallites, they usually suffer from decreased energy density, cycling stability, and effective electrode capacity. In this work, we report a size-dependent excess capacity beyond theoretical value (170 mA h g^–1) by introducing extra lithium storage at the reconstructed surface in nanosized LiFePO₄ (LFP) cathode materials (186 and 207 mA h g^–1 in samples with mean particle sizes of 83 and 42 nm, respectively). Moreover, this LFP composite also shows excellent cycling stability and high rate performance. Our multimodal experimental characterizations and ab initio calculations reveal that the surface extra lithium storage is mainly attributed to the charge passivation of Fe by the surface C–O–Fe bonds, which can enhance binding energy for surface lithium by compensating surface Fe truncated symmetry to create two types of extra positions for Li-ion storage at the reconstructed surfaces. Such surface reconstruction nanotechnology for excess Li-ion storage makes full use of the large specific surface area of the nanocrystallites, which can maintain the fast Li-ion transport and greatly enhance the capacity. This discovery and nanotechnology can be used for the design of high-capacity and efficient lithium ion batteries