Research on the Failure Characteristics of a Spherical Bearing

Strength of Materials - In order to study the failure process of a large-scale spherical bearing, the finite element simulation method was used to establish the full-scale finite element model of...     

双功能催化剂上四氢萘加氢裂化生成单环芳烃的反应网络研究

Conversion of LCO (light cycle oil) to BTX (benzene, toluene, and xylene) is an economically valuable method for refineries. However, this approach still faces difficulties as the main reactions are not clearly understood. Here we study the detailed hydrocracking pathway of typical reactants, 1-methylnaphthalene and tetralin, through molecular simulations and experiments to improve our understanding of the conversion process of LCO to BTX. Molecular simulations demonstrate that the rate-determining step is the isomerization pathway of six-membered ring to five-membered ring in tetralin as its activation energy (ΔEa) is the highest among all the reactions and the order of ΔEa of reactions is isomerization > ring-opening ≈ side-chain cleavage. The results of experiments show that with the increase in reaction depth, i.e., through a high temperature (350 – 370 °C) and low LHSV (4.5 – 6.0 h−1), isomerization, ring-opening, and side-chain  cleavage reactions occurred, thus improving the selectivity and yield of alkyl aromatics.     

Optimal Design of Novel Electromagnetic-Ring Active Balancing Actuator with Radial Excitation

Imbalance vibration is a typical failure mode of rotational machines and has significant negative effects on the effii-ciency,accuracy,and service life of equipment.To automatically reduce the imbalance vibration during the opera-tional process,different types of active balancing actuators have been designed and widely applied in actual produc-tion.However,the existing electromagnetic-ring active balancing actuator is designed based on an axial excitation structure which can cause structural instability and has low electromagnetic driving efficiency.In this paper,a novel radial excitation structure and the working principle of an electromagnetic-ring active balancing actuator with a combined driving strategy are presented in detail.Then,based on a finite element model,the performance param-eters of the actuator are analyzed,and reasonable design parameters are obtained.Self-locking torque measurements and comparative static and dynamic experiments are performed to validate the self-locking torque and driving effi-ciency of the actuator.The results indicate that this novel active balancing actuator has sufficient self-locking torque,achieves normal step rotation at 2000 r/min,and reduces the driving voltage by 12.5％.The proposed novel balancing actuator using radial excitation and a combination of permanent magnets and soft-iron blocks has improved electro-magnetic efficiency and a more stable and compact structure.     

Hollow multi-nanochannel carbon nanofiber/MoS2 nanoflower composites as binder-free lithium-ion battery anodes with high capacity and ultralong-cycle life at large current density

The electrode materials with high pseudocapacitance can enhance the rate capability and cycling stabil-ity of lithium-ion storage devices.Herein,we fabricated MoS2 nanoflowers with ultra-large interlayer spacing on N-doped hollow multi-nanochannel carbon nanofibers(F2-MoS2/NHMCFs)as freestanding binder-free anodes for lithium-ion batteries(LIBs).The ultra-large interlayer spacing(0.78～1.11 nm)of MoS2 nanoflowers can not only reduce the internal resistance,but also increase accessible active sur-face area,which ensures the fast Li+intercalation and deintercalation.The NHMCFs with hollow and multi-nanochannel structure can accommodate the large internal strain and volume change during lithi-ation/delithiation process,it is beneficial to improving the cycling stability of LIBs.Benefiting from the above combined structure merits,the F2-MoS2/NHMCFs electrodes deliver a high rate capability 832 mA h g-1 at 10 A g-1 and ultralong cycling stability with 99.29 and 91.60％capacity retention at 10 A g-1 after 1000 and 2000 cycles,respectively.It is one of the largest capacities and best cycling stability at 10 A g-1 ever reported to date,indicating the freestanding F2-MoS2/NHMCFs electrodes have potential applications in high power density LIBs.     

Theoretical study on a kind of cyclization mechanism of boron trichloride and hexamethyldisilazane to form the borazine ring for SiBCN ceramics precursor

Borazine rings act as a pivotal part in siliconboroncarbonitride ceramics (SiBCN) for high-temperature stability and great resistance to crystallization. A detailed investigation of the ring formation mechanism will guide the design and synthesis of SiBCN to meet application requirements under extreme conditions. Boron trichloride (BCl₃) and hexamethyldisilazane (HN(SiMe₃)₂) are common raw materials for the synthesis of precursors for SiBCN. In this paper, quantum chemical calculation was used to study the cyclization reaction mechanism between BCl₃ and HN(SiMe₃)₂ to form trichloroborazine (TCBZ) at the MP2/6-31G (d,p) level of theory. We discussed the structure properties, reaction pathways, energy barriers, reaction rates, and other aspects in detail. The results show that BCl₃ and HN(SiMe₃)₂ alternately participate in the reaction process, accompanied by the release of trimethylchlorosilane (TMCS), and that the entire reaction shows an absolute advantage in terms of energy. In the Step by step reaction, lower reaction barriers are formed due to the introduction of BCl₃ with more heat released compared to that for the introduction of HN(SiMe₃)₂. The final single-molecule cyclization and TMCS elimination steps are found to be faster compared to all previous bimolecular reactions.     

Synthesis of N-doped mesoporous carbons under different carbonization temperature and their application in supercapacitors

We have synthesized N-doped mesoporous carbon by the in-suit doping template method under the carbonized temperature of 900?°C. We found that the electrochemical performance of mesoporous carbon was enhanced by N-doping. So, we tried to increase the content of nitrogen to further optimize the electrochemical performance of the mesoporous carbon as electrode materials. During the process of synthesizing mesoporous carbon, the carbonized temperature played an important role in the formation of the carbon structure and its morphology, as well as in determining the content of nitrogen. We attained a considerable electrochemical performance enhancement by changing the carbonized temperature from 900 to 700?°C. We found the content of Nitrogen decreased with the increase of the carbonized temperature and the content of Nitrogen is 6.11% at 700?°C, 5.39% at 800?°C, 3.9% at 900?°C, respectively. The best electrochemical performance was observed in the product carbonized at 700?°C, which exhibited high specific capacitance (245.6 F/g at 0.5 A/g) and good cycle ability (more than 90% of the initial capacitance after 5000 cycles) in 6 M KOH electrolyte.     

Hybrid JND model-guided watermarking method for screen content images

Multimedia Tools and Applications - With the prevalence of digital products like cellphone, tablet and personal computer, the screen content images (SCIs) consisting of text, graphic, and natural...     

SnSe+Ag_2Se composite engineering with ball milling for enhanced thermoelectric performance

Earth-abundant IV-VI semiconductor SnSe is regarded as a promising thermoelectric material due to its intrinsic low thermal conductivity. In this report, the highly textured SnSe/Ag2 Se composites were first designed by solid solution method followed by spark plasma sintering(SPS) and their thermoelectric properties in two directions were investigated, and then, the performance of composites was further optimized with an additional ball milling. The coexistence of SnSe and Ag2 Se phases is clearly confirmed by energy-dispersive X-ray spectroscopy(EDX) in transmission electron microscopy(TEM). After ball milling, the size of SnSe grains as well as the incorporated Ag2 Se particles reduces effectively, which synergistically optimizes the electrical and thermal transport properties at high temperature range. As a result, a maximum ZT of ～0.74 at 773 K for SnSe+1.0%Ag_2 Se in the direction vertical to the pressing direction is achieved. Composite engineering with additional ball milling is thus proved to be an efficient way to improve the thermoelectric properties of SnSe, and this strategy could be applicable to other thermoelectric systems.     

Matrilin-3-Primed Adipose-Derived Mesenchymal Stromal Cell Spheroids Prevent Mesenchymal Stromal-Cell-Derived Chondrocyte Hypertrophy

Adipose-derived mesenchymal stromal cells (Ad-MSCs) are a promising tool for articular cartilage repair and regeneration. However, the terminal hypertrophic differentiation of Ad-MSC-derived cartilage is a critical barrier during hyaline cartilage regeneration. In this study, we investigated the role of matrilin-3 in preventing Ad-MSC-derived chondrocyte hypertrophy in vitro and in an osteoarthritis (OA) destabilization of the medial meniscus (DMM) model. Methacrylated hyaluron (MAHA) (1%) was used to encapsulate and make scaffolds containing Ad-MSCs and matrilin-3. Subsequently, the encapsulated cells in the scaffolds were differentiated in chondrogenic medium (TGF-β, 1–14 days) and thyroid hormone hypertrophic medium (T3, 15–28 days). The presence of matrilin-3 with Ad-MSCs in the MAHA scaffold significantly increased the chondrogenic marker and decreased the hypertrophy marker mRNA and protein expression. Furthermore, matrilin-3 significantly modified the expression of TGF-β2, BMP-2, and BMP-4. Next, we prepared the OA model and transplanted Ad-MSCs primed with matrilin-3, either as a single-cell suspension or in spheroid form. Safranin-O staining and the OA score suggested that the regenerated cartilage morphology in the matrilin-3-primed Ad-MSC spheroids was similar to the positive control. Furthermore, matrilin-3-primed Ad-MSC spheroids prevented subchondral bone sclerosis in the mouse model. Here, we show that matrilin-3 plays a major role in modulating Ad-MSCs’ therapeutic effect on cartilage regeneration and hypertrophy suppression.     

Preparation and properties of Eu and Dy co-doped strontium aluminate long afterglow nanomaterials

The long afterglow nanomaterials of strontium aluminate co-doped by Eu and Dy have been synthesized by co-precipitation combined hydrothermal method. The effects of hydrothermal time, calcination time, pH value, the amount of aluminum nitrate, activator, co-activator and flux H₃BO₃ on the fluorescence properties of the product were investigated by means of single factor optimization experiment. Then the orthogonal experiment was employed to obtain the optimal synthesis conditions that are as follows: n_Dy/n_Eu = 2.5, t_c = 2.5?h, n_Eu/n_Sr = 0.02, t_h = 8?h. Subsequently, the optimal synthesis conditions were verified by three repeated experiments, and the obtained products were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX) and fluorescence spectrometer. The results showed that the synthesized target products all were the mixed crystal phase of SrAl₂O₄ and Sr₄Al_l4O₂₅. The particles presented regular spherical-like with size ~ 100?nm. The dopants Eu and Dy were confirmed existed in the SrAl₂O₄ powders. The fluorescence and afterglow data of the target products were better than that in the orthogonal experiment scheme. The primary emission spectra band was in the range of 400–600?nm with characteristic peak located at ~ 460?nm corresponding to the transitions of Eu²⁺ ions from 4f⁶5d→4f⁷, and the blue light can be observed by naked eyes. The similar fast-decaying and slow-decaying processes were displayed in all the afterglow curves, and the initial afterglow brightness of the target product is apparently higher than that of products synthesized by the orthogonal experiment. The synthesized target products, which show excellent long afterglow performance, present a great application prospects in the aspects of ceramics, plastics, arts and crafts, ink and coating.