HL－1托卡马克杂质注入实验及杂质输运特性的研究

本文给出了ＨＬ－１托卡马克在通常欧姆放电和偏压诱发Ｈ模放电条件下，脉冲注入杂质气体的实验结果以及对杂质在通常欧姆等离子体和偏压诱发Ｈ模等离子体中的输运研究结果。实验结果表明，在ＨＬ－１上偏压诱发Ｈ模等离子体中对杂质的约束性能明显优于在通常欧姆等离子体中对杂质的约束性能。杂质输运的数值模拟结果说明，无论在通常欧姆等离子体中，还是在偏压诱发Ｈ模等离子体中，杂质的输运系数都比新经典理论预计的要大得多，输运是反常的。在偏压诱发的Ｈ模等离子体中引入杂质输运“位阱”概念，能够对杂质离子约束时间长的实验现象进行很好的描述。合理地解释了在偏压杂质注入实验中杂质辐射上升时间长、衰减慢的现象。     

原位制备SrSb2O6/g-C3N4新型二维异质结用于可见光催化降解四环素的研究

本文采用高温固相原位制备新型二维SrSb2O6/g-C3N4异质结光催化复合材料,并将其用于可见光催化降解四环素.通过XRD和FT-IR谱对其结构进行表征.光催化降解实验表明,异质结复合材料较母体g-C3N4和SrSb2O6而言,光催化效率均得到了提升.其中,异质结样品SSO-CN-2对四环素溶液具有最优的光催化降解效...     

Interfacial Nanobubbles on Atomically Flat Substrates with Different Hydrophobicities

The dependence of the morphology of interfacial nanobubbles on atomically flat substrates with different wettability ranges was investigated by using PeakForce quantitative nanomechanics. Interfacial nanobubbles were formed and imaged on silicon nitride (Si₃N₄), mica, and highly ordered pyrolytic graphite (HOPG) substrates that were partly covered by reduced graphene oxide (rGO). The contact angles and sizes of those nanobubbles were measured under the same conditions. Nanobubbles with the same lateral width exhibited different heights on the different substrates, with the order Si₃N₄≈mica>rGO>HOPG, which is consistent with the trend of the hydrophobicity of the substrates.     

Structure elucidation and NMR assignments for curcuminoids from the rhizomes of Curcuma longa

Thirteen curcuminoids (1–13) were isolated from the rhizomes of Curcuma longa. Among them, 1,5‐dihydroxy‐1,7‐bis(4‐hydroxyphenyl)‐4,6‐heptadiene‐3‐one (1), 1,5‐dihydroxy‐1‐(4‐hydroxy‐3‐methoxyphenyl)‐7‐(4‐hydroxyphenyl)‐4,6‐heptadiene‐3‐one (2), 1,5‐dihydroxy‐1‐(4‐hydroxyphenyl)‐7‐(4‐hydroxy‐3‐methoxyphenyl)‐4,6‐heptadiene‐3‐one (3), and 3‐hydroxy‐1,7‐bis‐(4‐hydroxyphenyl)‐6‐heptene‐1,5‐dione (4) are new compounds, and 1‐(4‐hydroxyphenyl)‐7‐(3, 4‐dihydroxyphenyl)‐1, 6‐heptadiene‐3, 5‐dione (5) is isolated from natural sources for the first time. The structures of these compounds were elucidated by extensive spectroscopic analyses, especially 1D and 2D NMR spectroscopy. The ¹³C NMR data and complete ¹H and ¹³C NMR assignments of some known compounds are reported for the first time. In addition, the errors of ¹H and ¹³C assignments reported in the literature were corrected. Copyright © 2009 John Wiley & Sons, Ltd.     

用离子对色谱分离氨基酸衍生物的对映体

通过在由（Ｓ）－（Ｎ）－（２萘基）丙氨酸衍生而成的“刷型”手性固定相上采用离子对色谱分离氨基酸的３,５－二硝基苯甲酰衍生物,探讨了非手性离子对试剂的浓度对溶质保留和选择性的影响。使用甲醇与磷酸盐缓冲溶液组成的溶剂为流动相,考察了甲醇含量对手性分离的影响,另外,通过在不同构型的和性固定相上做对照实验,证明在结构相同、构型相反的手性固定相上,对映体的出峰顺序是相反的。     

Investigation of the luminescence properties and thermal stability of dysprosium,terbium, and europium ions singly- and co-doped strontium yttrium borate phosphors

A series of trivalent rare-earth element ions (europium, terbium, dysprosium) singly- and co-doped strontium yttrium borate phosphors was synthesized via the sol–gel method. The phase formation, luminescence properties, decay times, and energy transfer behaviors from terbium ions to europium ions, the thermal stability, and the Commission Internationale de L’Eclairage coordinates were investigated. Under the excitation of ultraviolet light, the singly doped phosphors exhibited green emission of terbium ions, white emission of dysprosium ions, and red emission of europium ions, respectively. For the terbium and europium ions co-doped strontium yttrium borate samples, a white emission can be realized by blending the doping concentration of terbium and europium ions. The critical distance between terbium and europium ions has been calculated to be about 14.52?Å and the energy transfer from terbium to europium occurred through the dipole–quadrupole interaction. At 150°C, the emission intensity of terbium and europium in the 12?mol% terbium and 14?mol% europium co-doped strontium yttrium borate sample was maintained at about 74% and 87% of their corresponding initial values, respectively, and the dysprosium ions singly doped strontium yttrium borate sample showed about 70% of its initial emission intensity at room temperature. The above results suggested that europium, terbium, dysprosium ions singly- and co-doped strontium yttrium borate phosphors have potential applications as ultraviolet-convertible phosphors.     

葛根提取物高效液相色谱分析方法的优化

针对葛根提取物的复杂体系,分别从色谱模式、流动相、添加剂以及梯度洗脱条件几个方面对其高效液相色谱分析 方法进行了优化。其中梯度洗脱条件的优化是根据各组分在5次线性梯度下的保留时间并借助于CSASS软件快速准确地计 算出各组分的液相色谱保留参数a,c值以及峰形参数σ和τ,在此基础上使用CSASS软件对葛根提取物的色谱分离情况进行 高精度仿真预测,从而优化了梯度洗脱条件。考察了优化条件下的分析方法的精密度和重现性,结果表明该方法稳定、可 靠、重现性好。     

Monovalent Cation–Phenolic Crystals with pH-Driven Reversible Crystal Transformation

The conversion of renewable plant polyphenol to advanced materials with tailorable properties and various functions is desirable and challenging. In this work, monovalent cation-phenolic crystals contained K⁺ or Na⁺ ions were synthesized by using plant polyphenol as an organic source in alkaline solution. The crystal structure was resolved, showing a laminar crystal structure with M⁺ as connecting nodes. The morphologies (e.g., rod-like and spindle-shaped) and chemical compositions of crystals could be tuned by changing the cations. Interestingly, these polymer crystals exhibited a pH-driven reversible crystal transformation. They transformed into their protonated crystalline form under acidic conditions (e.g., pH 2) and went back to the cation-bound crystalline form in alkaline solutions. Furthermore, the crystals proved excellent antioxidants and heavy metal ion adsorbents.     

Spontaneous reactions of potassium phenoxide with dibromoperflouroalkanes· first evidence for bromophilic attack on C-Br bonds by the phenoxide·

In contrast to earlier reports, It has been found that dibromoperfluoroalkanes actually can react spontaneously with PhOK, yielding fluoroalkyl phenyl ethers as products. Evidence for an anionic chain mechanism involving a bromophilic attack by the phenoxide ion is presented.