基于线性规划的高温超导磁体线圈设计方法

电子真空回旋器件是一种对磁场精度要求较高的微波源装置, 一般采用超导磁体提供磁场环境. 超导磁体的应用中, 磁场分布的实现是超导磁体设计的核心问题. 提供回旋器件磁场的高温超导磁体包含较复杂的磁体绕组, 为了解决此类设计计算问题, 本文提出了一种包含设计区域约束的线性优化方法进行回旋器件高温超导绕组的设计优化, 通过分步的约束和线性优化计算, 可得到同时满足设计要求和绕组可实现的设计磁场电流分布设计. 计算实例的结果给出了一个提供磁场强度1 .3 Tesla, 长度285 mm 的均匀磁场区域, 同时满足多位置的磁场要求, 设计结果与要求一致度较好, 精度满足应用需求. 该计算方法是一种可适用于较复杂磁场要求和超导绕组结构的设计优化方法.     

Boosting Charge Transport in a 2D/3D Perovskite Heterostructure by Selecting an Ordered 2D Perovskite as the Passivator

We demonstrate that an ordered 2D perovskite can significantly boost the photoelectric performance of 2D/3D perovskite heterostructures. Using selective fluorination of phenyl-ethyl ammonium (PEA) lead iodide to passivate 3D FA_0.8Cs_0.2PbI₃, we find that the 2D/3D perovskite heterostructures passivated by a higher ordered 2D perovskite have lower Urbach energy, yielding a remarkable increase in photoluminescence (PL) intensity, PL lifetime, charge-carrier mobilities (ϕμ), and carrier diffusion length (L_D) for a certain 2D perovskite content. High performance with an ultralong PL lifetime of ≈1.3 μs, high ϕμ of ≈18.56 cm² V⁻¹ s⁻¹, and long L_D of ≈7.85 μm is achieved in the 2D/3D films when passivated by 16.67 % para-fluoro-PEA₂PbI₄. This carrier diffusion length is comparable to that of some perovskite single crystals (>5 μm). These findings provide key missing information on how the organic cations of 2D perovskites influence the performance of 2D/3D perovskite heterostructures.     

Promoting Photocatalytic H2 Evolution through Retarded Charge Trapping and Recombination by Continuously Distributed Defects in Methylammonium Lead Iodide Perovskite

Inspired by its great success in the photovoltaic field, methylammonium lead iodide perovskite (MAPbI₃) has recently been actively explored as photocatalysts in H₂ evolution reactions. However, the practical application of MAPbI₃ photocatalysts remains hampered by the intrinsically fast trapping and recombination of photogenerated charges. Herein, we propose a novel strategy of regulating the distribution of defective areas to promote charge-transfer dynamics of MAPbI₃ photocatalysts. By deliberately designing and synthesizing the MAPbI₃ photocatalysts featuring a unique continuation of defective areas, we demonstrate that such a feature enables retardation of charge trapping and recombination via lengthening the charge-transfer distance. As an outcome, such MAPbI₃ photocatalysts turn out to achieve an impressive photocatalytic H₂ evolution rate as high as 0.64 mmol ⋅ g⁻¹ ⋅ h⁻¹, one order of magnitude higher than that of the conventional MAPbI₃ photocatalysts. This work establishes a new paradigm for controlling charge-transfer dynamics in photocatalysis.     

Ultrasound-assisted polysaccharide extraction from Cercis chinensis and properites,antioxidant activity of polysaccharide

The purpose of the study was to improve the extraction of polysaccharide from the leaves of Cercis chinensis Bunge using ultrasound, and compare the difference between boiling and ultrasound extraction in terms of polysaccharide content, monosaccharide compounds, and evaluate how the factors affected the bioactivity. The best conditions, according to the single factor experiments and the Box-Bohnken design (BBD), were an intensity of ultrasound of 180 W, duration of extraction of 40 min, proportion of water to material of 15:1 (g/g), and a higher polysaccharide yield of 20.02 ± 0.55 (mg/g) than in boiling extraction (16.09 ± 0.82 mg/g). The antioxidative experiment suggested the polysaccharide by ultrasound exhibited higher DPPH, hydroxyl radical scavenging capacities, and reducing power at 1.2–1.4 mg/mL, which was superior to the boiling polysaccharide. Further analysis showed that the ultrasonic purified polysaccharides like Gla, N-Glu, and GluA contained more total sugar and uronic acids than the boiling method did. This may indicate that the ultrasonic isolation of the polysaccharides increase the antioxidant activity of the polysaccharides.     

Control of pore environment in highly porous carbon materials for C2H6/C2H4 separation with exceptional ethane uptake

Adsorptive separation of C₂H₆ from C₂H₄ by adsorbents is an energy-efficient and promising method to boost the polymer grades C₂H₄ production. However, that C₂H₆ and C₂H₄ display very similar physical properties, making their separation extremely challenging. In this work, by regulating the pore environment in a family of chitosan-based carbon materials (C-CTS-1, C-CTS-2, C-CTS-4, and C-CTS-6)- we target ultrahigh C₂H₆ uptake and C₂H₆/C₂H₄ separation, which exceeds most benchmark carbon materials. Explicitly, the C₂H₆ uptake of C-CTS-2 (166 cm³/g at 100 kPa and 298 K) has the second-highest adsorption capacity among all the porous materials. In addition, C-CTS-2 gives C₂H₆/C₂H₄ selectivity of 1.75 toward a 1:15 mixture of C₂H₆/C₂H₄. Notably, the adsorption enthalpies for C₂H₆ in C-CTS-2 are low (21.3 kJ/mol), which will facilitate regeneration in mild conditions. Furthermore, C₂H₆/C₂H₄ separation performance was confirmed by binary breakthrough experiments. Under different ethane/ethylene ratios, C-CTS-X extracts a low ethane concentration from an ethane/ethylene mixture and produces high-purity C₂H₄ in one step. Spectroscopic measurement and diffraction analysis provide critical insight into the adsorption/separation mechanism. The nitrogen functional groups on the surface play a vital role in improving C₂H₆/C₂H₄ selectivity, and the adsorption capacities depend on the pore size and micropore volume. Moreover, these robust porous materials exhibit outstanding stability (up to 800 °C) and can be easily prepared on a large scale (kg) at a low cost (～$26 per kg), which is very significant for potential industrial applications.     

高效液相色谱-质谱联用法测定烟草中茉莉酸

采用高效液相色谱-质谱(HPLC-MS)联用法检测烟草中茉莉酸(JA)含量。样品研磨均质后经丙酮和柠檬酸萃取,离心分离,取上清液,氮气吹去丙酮后用乙醚萃取。经氨丙基固相萃取柱净化,吹干后用色谱流动相溶解,过0.45μm有机滤膜。利用高效液相色谱-质谱联用电喷雾负离子,选择离子监测模式进行检测,内标法定量。结果表明,待测样品JA浓度范围在5～1 000ng/mL之间,标准曲线具有良好的线性关系。方法检出限(S/N≥3)是2.0ng/mL。平均回收率为80.6%～101.1%,相对标准偏差为3.5%～14.6%。应用该方法检测烟草打顶与不打顶植株之间JA含量的差异,结果比较理想。     

A theoretical kinetics study on low-temperature oxidation of n-C4H9 radicals

The low-temperature oxidation mechanism of n?butyl radicals (n-C₄H₉) has been investigated by high level quantum chemical calculations coupled with the Rice–Ramsperger–Kassel–Marcus/Master Equation (RRKM/ME) theory. The potential energy surfaces (PES) were explored at the QCISD(T)/CBS//B3LYP/6-311++G(d,p) level. The temperature- and pressure-dependent rate constants were computed and fitted in modified Arrhenius parameters. The major reaction channels were discussed to more deeply understand the competing relationships between chain branching, chain propagation and termination reactions. The results show that the 1,5 H-shift reaction is more competitive than the 1,6 H-shift and 1,4 H-shift for isomerization reactions of n?butyl peroxy radicals, and the concerted HO₂ elimination channel to form butene becomes more important at high temperatures. Furthermore, based on our calculations, a revised kinetic model was developed to describe n-butane oxidation. Good consistency between model predictions and experimental data was shown. This study enhances our understanding of the combustion mechanism of n-butane and can be used as a reliable reference for mechanistic understanding of larger alkanes.     

Constituents of Essential Oil from Vinca major var. variegata and its Antibacterial Activity

Chemistry of Natural Compounds -     

硅胶表面修饰添加剂选择性降低卷烟烟气中的苯酚

分别以聚乙烯亚胺（PEI）、十六烷基三甲基溴化铵（CTMAB）对硅胶（SiO2）表面进行修饰,并以苯酚为模板,合成硅胶表面修饰分子印迹聚合物（MIP-SiO2）,制备获得功能添加剂PEI-SiO2、CTMAB-SiO2、MIP-SiO2。按不同剂量分别将功能添加剂加入到卷烟滤嘴中,考察对卷烟主流烟气中苯酚的截留效率。结果表明,各添加剂均可有效降低卷烟烟气中的苯酚释放量。当添加量达到20mg/支时,各功能材料对苯酚的截留效率均超过39%。且添加剂对烟气中苯酚的截留能力大于对烟气中焦油的吸附能力,表明功能添加剂具有选择性降低卷烟烟气中苯酚的作用。