跌落冲击载荷下焊锡接点金属间化合物层的动态开裂

跌落冲击载荷作用下,含铅焊锡接点与无铅焊锡接点的破坏模式明显不同,而导致这种差异的原因目前尚不明朗.论文提出了一种可用于模拟焊锡接点在跌落冲击载荷下破坏行为的有限元模型,此模型中,金属间化合物(IMC)与焊料间的界面采用粘性区模型(CZM)来模拟其损伤开裂过程,而IMC层内的破坏程度则通过计算其能量释放率来判断.通过对板级封装跌落冲击过程的数值模拟发现,与无铅焊锡接点(Sn3.5Ag)相比,含铅焊锡接点(Sn37Pb)与IMC间的CZM层更容易发生损伤破坏,而该层的开裂会减小IMC层的应力,即降低了其内部的开裂驱动力,从而缓解了IMC层裂纹的起始和扩展.     

酱油中3-氯-1,2-丙二醇检测能力验证

为了解国内实验室在3-氯-1,2一丙二醇检测领域的能力,中国国家认证认可监督管理委员会(CNCA)组织了酱油中3一氯一1,2-丙二醇检测能力验证活动,有19个省、市、自治区的34个实验室参加.测试结果满意的实验室占73.5%.     

Strategies for the construction of supramolecular assemblies from poly-NHC ligand precursors

The field of supramolecular assemblies has developed rapidly in the last few decades, thanks in a large part to their diverse applications. These assemblies have been mostly based on Werner-type coordination motifs in which metal centres are coordinated by nitrogen or oxygen donors. Recently, N-heterocyclic carbene(NHC) ligands have been employed as carbon donors not only because of their appealing structures but also due to the extensive applications in catalysis, biomedicine and material science of the resulting assemblies. During the last decade, NHC-based supramolecular assemblies have witnessed rapid growth and extensive application in molecular recognition, luminescent materials and catalysis. For different topological systems, a diverse selection of poly-NHC precursors and synthetic strategies is crucial to precisely control the synthesis of supramolecular architectures. Several synthetic strategies have been developed to synthesise two-dimensional(2D) molecular metallacycles and three-dimensional(3D) metallacages from a wide range of poly-NHC precursors, including a straightforward one-pot strategy,supramolecular transmetalation, stepwise synthesis, an improved one-pot strategy involving self-sorting behaviour of 3D metallacages and a subtle variation strategy of poly-NHC ligand precursors. This review offers a summary of the synthetic strategies applied for the construction of different poly-NHC-based supramolecular assemblies, particularly emphasizes recent progress in the synthesis of large and complex supramolecular assemblies from poly-NHC precursors, and further attention is given to their application in postsynthetic modifications(PSMs), host-guest chemistry, luminescent properties and biomedical applications.     

毫米波回旋速调管放大器的自洽非线性数值模拟

为了实现回旋速调管放大器的快速设计,基于经典的回旋管的稳态单模非线性理论方法,开展了回旋速调管放大器的束波作用效率的理论模拟研究。由于单模理论无法匹配回旋速调管放大器的输入腔、中间腔两端的突变边界条件,所以输入腔与中间腔都只能采用给定场法进行求解。回旋速调管的输出腔的功率输出端通常采用缓变结构,这种腔体可以采用单模自洽理论进行求解。对两腔毫米波回旋速调管放大器进行了理论模拟,并与商业粒子模拟软件的结果进行对比,验证了该数值理论模拟方法的有效性。     

Lidar Sensor-Based Object Recognition Using Machine Learning

Journal of Russian Laser Research - Light detection and ranging (LIDAR) sensor provides complicated and large volume of environmental point cloud data that are essential for the target recognition....     

Efficient Ultraviolet Nanosources Based on Third-Harmonic Generation in Dielectric–Metal Composite Nanodisks

Dielectric materials with high indices have recently attracted much attention in the community of nanophotonics. Severe optical losses in visible–ultraviolet (UV) region, however, limit their applications. This article proposes dielectric–metal nanocomposites as alternative high-index materials for Mie-resonance-based applications. Such composite materials have high indices in the range of wavelength longer than plasmon resonance of inclusion metal nanoparticles, while they have much lower losses in the range from blue-violet down to near-UV compared with commonly used high-index materials such as silicon, enabling near-UV generation with high efficiency based on third-harmonic generation (THG). The numerical results show that ZnO nanodisk containing silver nanoparticles can generate near-UV radiation at 351.3 nm via THG with an efficiency about 20 times higher compared with silicon nanodisk under same pumping condition. Significantly high THG efficiency of 0.015% has been predicted with such a composite nanodisk supported by aluminum substrate under pumping with a peak intensity of 20 GW cm⁻², a spot size of 0.8 $\mu \mathrm{m}$, a duration of 50 fs at 1054 nm, respectively.     

Injectable dual glucose-responsive hydrogel-micelle composite for mimicking physiological basal and prandial insulin delivery

For type 1 and advanced type 2 diabetic patients, insulin replacement therapy with simulating on-demand prandial and basal insulin secretion is the best option for optimal glycemic control. However, there is no insulin delivery system yet could mimic both controlled basal insulin release and rapid prandial insulin release in response to real-time blood glucose changes. Here we reported an artificial insulin delivery system, mimicking physiological basal and prandial insulin secretion, to achieve real-time glycemic control and reduce risk of hypoglycemia. A phenylboronic acid(PBA)/galactosyl-based glucose-responsive insulin delivery system was prepared with insulin-loaded micelles embedded in hydrogel matrix. At the hyperglycemic state, both the hydrogel and micelles could swell and achieve rapid glucose-responsive release of insulin, mimicking prandial insulin secretion.When the glucose level returned to the normal state, only the micelles partially responded to glucose and still released insulin gradually. The hydrogel with increased crosslinking density could slow down the diffusion speed of insulin inside, resulting in controlled release of insulin and simulating physiological basal insulin secretion. This hydrogel-micelle composite insulin delivery system could quickly reduce the blood glucose level in a mouse model of type 1 diabetes, and maintain normal blood glucose level without hypoglycemia for about 24 h. This kind of glucose-responsive hydrogel-micelle composite may be a promising candidate for delivery of insulin in the treatment of diabetes.     

Achieving Ultrahigh Molecular Weights with Diverse Architectures for Unconjugated Monomers through Oxygen-Tolerant Photoenzymatic RAFT Polymerization

Achieving well-defined polymers with ultrahigh molecular weight (UHMW) is an enduring pursuit in the field of reversible deactivation radical polymerization. Synthetic protocols have been successfully developed to achieve UHMWs with low dispersities exclusively from conjugated monomers while no polymerization of unconjugated monomers has provided the same level of control. Herein, an oxygen-tolerant photoenzymatic RAFT (reversible addition-fragmentation chain transfer) polymerization was exploited to tackle this challenge for unconjugated monomers at 10 °C, enabling facile synthesis of well-defined, linear and star polymers with near-quantitative conversions, unprecedented UHMWs and low dispersities. The exquisite level of control over composition, MW and architecture, coupled with operational ease, mild conditions and environmental friendliness, broadens the monomer scope to include unconjugated monomers, and to achieve previously inaccessible low-dispersity UHMWs.     

Synthesis and investigation of surface active properties of green glucosyl esters

We here reported on the regioselective biosynthesis of green glucosyl monoesters surfactants which were confirmed by chemical analysis methods using immobilized enzyme catalysis with N-fatty acyl amino acid and D-glucose as substrate. Lipozyme 435 was the most efficient lipase to catalyze the transesterification reaction in t-butanol at 50?°C. The target compounds showed good surface properties. The CMC values of glucosyl esters 15-22 were 4.97, 3.96, 1.87, 0.48?mmol/L, and 4.70, 3.53, 1.58 and 0.42?mmol/L at 25?°C, respectively. It was noteworthy that the micellization physiochemical parameters were calculated and the micellization was exothermic process. Meanwhile, it was entropy driven in the formation of micelles related to the structure of glucosyl esters at different temperature.     

Novel structurally characterized hetero-bimetallic [Zn(II)2M(II)] (M = Ca and Sr) bis(salamo)-type complexes: DFT calculation,Hirshfeld analyses,antimicrobial and fluorescent properties

Two hetero-bimetallic [Zn(II)₂M(II)] (M = Ca and Sr) complexes [Zn₂Ca(L)(OAc)₂] ( 1 ) and [Zn₂Sr(L)(OAc)₂] ( 2 ) with a novel asymmetrical bis(salamo)-type tetraoxime ligand (H₅L) were designed and synthesized, and characterized by elemental analyses, FT-IR spectra, UV–vis absorption spectra, Density Functional Theory (DFT) calculation, Hirshfeld surface analyses and X-ray single crystal diffractions. Compared with the symmetric bis(salamo)-type ligands, the ligand H₅L and its [Zn(II)₂M(II)] (M = Ca and Sr) asymmetrical bis(salamo)-type complexes synthesized for the first time in this paper have more novel structures and better properties. The results of ultraviolet titration show that the coordination ratio of ligand, alkaline earth metal and transition metal is 1:1:2. Complexes 1 and 2 have good luminescent properties and obvious antimicrobial activities.