COMPENSATING ROLE OF SELF-EQUILIBRATED STRESS FIELDS IN CONSTRUCTING NON-SINGULAR SOLUTIONS USING A NON-EUCLIDEAN CONTINUUM MODEL FOR AN INCOMPRESSIBLE SPHERE

Journal of Applied Mechanics and Technical Physics - A self-equilibrated stress field for an incompressible sphere is constructed based on a non-Euclidean continuum model. The...     

LWE from non-commutative group rings

Designs, Codes and Cryptography - The Learning-With-Errors (LWE) problem (and its variants including Ring-LWE and Module-LWE), whose security are based on hard ideal lattice problems, has proven to...     

Stability of Multiplier Ideal Sheaves

Chinese Annals of Mathematics, Series B - In the present article, the authors find and establish stability of multiplier ideal sheaves, which is more general than strong openness.     

季铵盐改性蒙脱石的制备与表征

采用十六烷基三甲基氯化铵(CTAC)对钠基蒙脱石(MMT)进行季铵化改性,制备有机蒙脱石(CMMT),对改性后的蒙脱石进行X射线衍射(XRD)、电位分析法(PA)、红外光谱(FT-IR)和热分析(TGA)等分析表征,并用改性后的蒙脱石吸附五氟尿嘧啶(5-FU)后测定并比较其载药量.结果表明,改性剂已成功插入到蒙脱石的层间;相比于钠基蒙脱石,有机蒙脱石的层间距和热稳定性均有所增大;当制备季铵盐有机改性蒙脱石时,反应温度为80℃,且CTAC的用量是MMT的2.5倍阳离子交换容量时,形成的有机蒙脱石的阳离子化程度和对5-FU的载药量最高.此外,考察并比较了有机蒙脱石和钠基蒙脱石的体外细胞毒性,结果显示有机蒙脱石具有更好的生物相容性和更低的细胞毒性.     

聚变堆相关的液态金属膜流初步实验研究

在磁约束核聚变堆的面对等离子部件设计中,液态金属锂膜流因具有带走杂质、保护面对等离子固壁等优点而被认为是优选方案之一. 然而,如何克服聚变堆中强磁场环境下产生的磁流体力学效应并形成大面积均匀铺展锂膜流动是目前亟需解决的问题.本文通过搭建室温液 态镓铟锡回路和高温液态锂回路,开展了两种不同特性的液态金属膜流实验, 并采用传统可视化方法获得了展向磁场存在时镓铟锡和锂在导电底板形成的液膜流动表面特征.实验结果 表明: 无磁场时,两种液态金属膜流流动表面波动特性与常规流体膜流均一致, 即随着流动雷诺数的增加表面波动变得更为混乱; 而展向磁场存在时,镓铟锡膜流表面波动变得更为规则, 且沿着磁场方向平行排列,表现为拟二维波动的特征; 而锂膜流却产生了明显的磁流体 力学阻力效应,表现为在流动方向局部产生锂滞留现象, 且滞留点随雷诺数增大向下游移动. 最后通过膜流受力分析,进一步阐述了锂膜流受到比镓铟锡膜流更为严重磁流体力学效应影响的原因.      

Nanoporous Gold Embedded ZIF Composite for Enhanced Electrochemical Nitrogen Fixation

The electrochemical nitrogen reduction reaction (NRR) offers an energy‐saving and environmentally friendly approach to produce ammonia under ambient conditions. However, traditional catalysts have extremely poor NRR performances because of their low activity and the competitive hydrogen evolution reaction. The high catalytic activity of nanoporous gold (NPG) and the hydrophobicity and molecular concentrating effect of the zeolitic imidazolate framework‐8 (ZIF‐8) were incorporated in the NPG@ZIF‐8 nanocomposite so that the ZIF‐8 shell could weaken hydrogen evolution and retard reactant diffusion. A highest Faradaic efficiency of 44 % and an excellent rate of ammonia production of (28.7±0.9) μg h^?1 cm^?2 were achieved, which are superior to traditional gold nanoparticles and NPG. Moreover, the composite catalyst shows high electrochemical stability and selectivity (98 %). The superior NRR performance makes NPG@ZIF‐8 one of the most promising water‐based NRR electrocatalysts for ammonia production.     

Scaled‐Up Synthesis of Amorphous NiFeMo Oxides and Their Rapid Surface Reconstruction for Superior Oxygen Evolution Catalysis

The anode oxygen evolution reaction (OER) is known to largely limit the efficiency of electrolyzers owing to its sluggish kinetics. While crystalline metal oxides are promising as OER catalysts, their amorphous phases also show high activities. Efforts to produce amorphous metal oxides have progressed slowly, and how an amorphous structure benefits the catalytic performances remains elusive. Now the first scalable synthesis of amorphous NiFeMo oxide (up to 515 g in one batch) is presented with homogeneous elemental distribution via a facile supersaturated co‐precipitation method. In contrast to its crystalline counterpart, amorphous NiFeMo oxide undergoes a faster surface self‐reconstruction process during OER, forming a metal oxy(hydroxide) active layer with rich oxygen vacancies, leading to superior OER activity (280 mV overpotential at 10 mA cm^?2 in 0.1 m KOH). This opens up the potential of fast, facile, and scale‐up production of amorphous metal oxides for high‐performance OER catalysts.     

In Situ Observation of Dynamic Galvanic Replacement Reactions in Twinned Metallic Nanowires by Liquid Cell Transmission Electron Microscopy

Galvanic replacement is a versatile approach to prepare hollow nanostructures with controllable morphology and elemental composition. The primary issue is to identify its fundamental mechanism. In this study, in situ liquid cell transmission electron microscopy was employed to monitor the dynamic reaction process and to explore the mechanism of galvanic replacement. The detailed reaction process was revealed based on in situ experiments in which small Au particles first appeared around Ag nanowires; they coalesced, grew, and adhered to Ag nanowires. After that, small pits grew from the edge of Ag nanowires to form tubular structures, and then extended along the Ag nanowires to obtain hollowed structures. All of our experimental observations from the viewpoint of electron microscopy, combined with DFT calculations, contribute towards an in‐depth understanding of the galvanic replacement reaction process and the design of new materials with hollow structures.     

A hydrophobic deep eutectic solvent‐based vortex‐assisted dispersive liquid–liquid microextraction combined with HPLC for the determination of nitrite in water and biological samples

In recent years, hydrophobic deep eutectic solvents as new generation of green solvents have attracted wide attention in liquid microextraction technique. In this article, four hydrophobic deep eutectic solvents composed of trioctylmethylammonium chloride and oleic acid were designed and prepared firstly. Combined with high‐performance liquid chromatography, these deep eutectic solvents were used as an extraction solvent in vortex‐assisted dispersive liquid–liquid microextraction for the selective enrichment and indirect determination of trace nitrite from real water and biological samples. This method is based on the diazotization‐coupling reaction of nitrite with p‐nitroaniline and diphenylamine in acidic water, and then the nitrite is quantified indirectly by measuring the obtained azo compounds. Some factors influencing the extraction efficiency, including the reaction and extraction conditions, were investigated. Under the optimized conditions, the method has a linear range of 1–300 μg/L with a correlation coefficient of 0.9924, limit of detection of 0.2 μg/L, limit of quantitation of 1 μg/L, intraday and interday relative standard deviations of 4.0 and 6.0%. This method was successfully applied in determination of nitrite from three environmental water and two biological samples with the recovery in the range of 90.5–115.2%. In addition, these results were well agreement with those obtained by the conventional Griess method.