Corrections to the cross-polarization dynamics in solids The effect of nonsecular terms of heteronuclear dipolar interaction on cross-relaxation

The dynamic theory of cross-polarization in solids is modified by considering the contribution of the nonsecular terms of the heteronuclear dipolar interaction Hamiltonian in the laboratory frame to cross-relaxation. This contribution is evaluated numerically and confirmed experimentally. It is shown that these nonsecular terms may play a considerable role in cross-relaxation in many systems, especially in those with fast internal molecular motion. The complication in the cross-polarization process is further revealed.     

Pokemon和p53在乳腺癌组织中的表达及其生物学意义

目的 探讨乳腺癌组织中Pokemon和p53蛋白的表达及其相关性，并分析其与乳腺癌患者临床病理特征的关系。方法 采用免疫组化En Vision 法检测90 例乳腺癌和相应癌旁组织中Pokemon 和p53 蛋白的表达情况。结果 乳腺癌组织中Pokemon和p53蛋白表达阳性率均明显高于癌旁组织（均P＜0.01）；Pokemon 和p53蛋白的表达与乳腺癌患者临床分期及淋巴结转移均有关（均P＜0.01），而与患者年龄、肿瘤大小、组织学类型及分级均无关（均P ＞0.05）。Spearman相关分析显示在乳腺癌组织中，Pokemon 和p53 蛋白表达呈正相关（P＜0.01）。结论 Pokemon 和p53蛋白异常表达可能与乳腺癌的发生、发展有关，联合检测两者对评估乳腺癌生物学行为及预后具有较重要的临床意义。     

Impact of environmental conditions on the sequestration of radionuclide 60Co(II) at Ca-rectorite/water interface

In this study, the removal of radionuclide ⁶⁰Co(II) from wastewater by Ca-rectorite was studied as a function of various environmental parameters such as contact time, pH, ionic strength, coexisting electrolyte ions, humic substances (HS) and temperature under ambient conditions. The results indicated that the sorption of Co(II) on Ca-rectorite was strongly dependent on pH and ionic strength. The Langmuir and Freundlich models were used to simulate the sorption isotherms of Co(II) at three different temperatures of 298.15, 318.15 and 338.15?K. The thermodynamic parameters ( $ \Updelta H^{0} ,\,\Updelta S^{0} $ and $ \Updelta G^{0} $ ) calculated from the temperature-dependent sorption isotherms indicated that the sorption process of Co(II) on Ca-rectorite was spontaneous and endothermic. At low pH, the sorption of Co(II) was dominated by outer-sphere surface complexation and ion exchange with Ca⁺/H⁺ on Ca-rectorite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. From the experimental results, it is possible to conclude that Ca-rectorite has good potentialities for cost-effective disposal of radiocobalt bearing wastewaters.     

Effect of bilayer structure and a SrRuO3 buffer layer on ferroelectric properties of BiFeO3 thin films

Effects of the BiFe_0.95Mn_0.05O₃ thickness and a SrRuO₃ (SRO) buffer layer on the microstructure and electrical properties of BiFeO₃/BiFe_0.95Mn_0.05O₃ (BFO/BFMO) bilayered thin films were investigated, where BFO/BFMO bilayered thin films were fabricated on the SRO/Pt/Ti/SiO₂/Si(100) substrate by a radio frequency sputtering. All thin films are of a pure perovskite structure with a mixture of (110) and (111) orientations regardless of the BFMO layer thickness. Dense microstructure is demonstrated in all thin films because of the introduction of BFMO layers. The SRO buffer layer can also further improve the ferroelectric properties of BFO/BFMO bilayered thin films as compared with those of these thin films without a SRO buffer layer. The BFO/BFMO bilayered thin film with a thickness ratio of 220/120 has an enhanced ferroelectric behavior of 2P _r??165.23???C/cm² and 2E _c??518.56?kV/cm, together with a good fatigue endurance. Therefore, it is an effective way to enhance the ferroelectric and fatigue properties of bismuth ferrite thin films by constructing such a bilayered structure and using a SRO buffer layer.     

脉冲离子束作用下靶面次级电子的抑制

论述了离子束作用下固体表面次级电子产生的机制,介绍了特种真空器件中次级电子抑制的各种方法及其优缺点,提出了脉冲离子束作用下靶面次级电子抑制的自偏势法和曲面靶法等设计思路,并在实验上进行了初步验证。实验结果表明,自偏势电压大于80 V后,次级电子得到很好的抑制。在相同束流情况下,曲面靶较平面靶的次级电子产额少。利用实验结果进行估算得到了近似的次级电子产额约为0.67,比文献中的结果(0.58)偏大。对实验中自偏势法抑制反峰电子电流的效果进行了分析和讨论,结果表明:自偏势法不但能够有效抑制离子打靶产生的次级电子,还能抑制由功率源不稳定带来的入射反峰电子流。     

Arrangement, conformation, and mobility of surfactant molecules intercalated in montmorillonite prepared at different pillaring reagent concentrations as studied by solid-state NMR spectroscopy

The arrangement, conformation, and mobility of dodecyltrimethylammonium cations (DDTMA+) intercalated in montmorillonite prepared with different pillaring reagent concentrations have been studied by 13C relaxation time measurement, cross-polarization dynamics, and two-dimensional proton wide-line separation (2D WISE) spectroscopy, as well as X-ray powder diffraction (XRD). We demonstrate that the arrangement of DDTMA+ and the mobility of various groups are different, depending on the pillaring concentration, but the conformations of alkyl chains are similar. XRD experiments illustrate that at three different pillaring concentrations (DDmt0.2, DDmt0.5, and DDmt1.0), the organic cations adopt a lateral-monolayer, lateral-monolayer, and pseudotrilayer arrangement, respectively. 13C MAS NMR reveals that the alkyl chains at the three concentrations uniformly display a large amount of mixed trans and gauch conformation (disordered) and a small amount of trans conformation (ordered). 13C spin-lattice relaxation time and 1H-13C cross-polarization dynamics measurement, along with 2D WISE NMR experiments, indicate that the mobility is much different for various groups at a given concentration and for a given group at different concentrations. At each concentration N-methyl unusually possesses the highest mobility, even exceeding that of the terminal methyl; at different concentrations the N-methyl and terminal methyl in DDmt1.0 exhibit the highest mobility compared with the other two samples.     

Focusing surface acoustic waves assisted electrochemical detector in microfluidics

This article demonstrates a novel electrochemical detection device. The device is composed by two focusing interdigital transducers for exciting focused surface acoustic waves by applying an AC signal, a three-electrode system for electrochemical measurement, and a liquid pool for holding liquid on a LiNbO₃ wafer. The amperometry current of ferrocenecarboxylic acid and potassium phosphate buffer solution is used to characterize the detection sensitivity. Two experiments are carried out to optimize the device design. The result shows that the two focusing interdigital transducers with arc degree 30° and distance 5 mm can remarkably enhance the liquid mixing rate. Under this condition, the oxidation current is about 27 times larger than that without surface acoustic wave stirring.     

Investigation of sequestration mechanisms of radionuclide 63Ni(II) on kaolinite in aqueous solutions

To better understand the application of kaolinite as an adsorbent for the decontamination of Ni(II) from radionuclide contaminated aqueous systems, herein, the sorption behavior of radionuclide ⁶³Ni(II) on kaolinite as a function of contacting time, pH, coexistent electrolyte ions, adsorbent concentration, fulvic acid and humic acid was investigated using batch technique. At low pH values, ion exchange and/or outer-sphere surface complexation was the main mechanism of Ni(II) sorption on kaolinite, whereas, the sorption of Ni(II) was dominated by inner-sphere surface complexation at high pH values. The presence of different electrolyte ions can enhance or inhibit the sorption of Ni(II) on kaolinite to some extent. The Langmuir and Freundlich models were used to simulate the sorption isotherms of Ni(II) at three different temperatures of 288, 313 and 338 K. The thermodynamic parameters (i.e., ΔS°, ΔH°, and ΔG°) calculated from the temperature-dependent sorption isotherms indicated that the sorption reaction of Ni(II) on kaolinite was endothermic and spontaneous. The findings in this present study demonstrates that the kaolinite can be used as a cost-effective adsorbent for the solidification and pre-concentration of Ni(II) from large volumes of aqueous systems.     

曲率渐近非负流形

本文主要研究了在曲率渐近非负流形上的一些性质：其上不存在非常数的正调和函数；若其调和函数是对一固定指数d的多项式增长,那么由这些调和函数所组成的空间的维数≤Cd~(CD),而且此流形的体积为无穷大等．     

镜煤吡啶不溶物及其热解加氢产物的NMR研究

本文对镜煤吡啶不溶物、热解加氢后吡啶及四氢呋喃不溶物进行了固体NMR研究,获得了12种结构参数,并对热解加氢产物中的苯可溶各馏份进行了一维、二维液体NMR研究,归属了其¹³C和¹H谱,计算了各馏份的平均分子结构.