Styrene and isoprene friction factors in styrene–isoprene matrices

Monomeric friction factors, Ξ, for polystyrene (PS), polyisoprene (PI), and a polystyrene–polyisoprene (SI) diblock copolymer have been determined as a function of temperature in four poly(styrene-b-isoprene-b-styrene-b-isoprene) tetrablock copolymer matrices. The Rouse model has been used to calculate the friction factors from tracer diffusion coefficients measured by forced Rayleigh scattering. Within the experimental temperature range the tetrablock copolymers are disordered, allowing for measurement of the diffusion coefficient in matrices with average compositions determined by the tetrablock copolymers (23, 42, 60, and 80% styrene by volume). Remarkably, for a given matrix composition the styrene and isoprene friction factors are essentially equivalent. Furthermore, at a constant interval from the system glass transition temperature, T_g, all of the friction factors (obtained from homopolymer, diblock copolymer, and tetrablock copolymer dynamics) agree to within an order of magnitude. This is in marked contrast to results for miscible polymer blends, where the individual components generally have distinct composition dependences and magnitudes at constant T − T_g. The homopolymer friction factors in the tetrablock matrices were systematically slightly higher than those of the diblock, which in turn were slightly higher than those of the homopolymers in their respective melts, when all compared at constant T − T_g. This is attributed to the local spatial distribution of styrene and isoprene segments in the tetrablocks, which presents a nonuniform free energy surface to the tracer molecules. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 3079–3086, 1998     

中国战略性新兴产业国际竞争力评价

以"新钻石模型"为基础,从产业环境、产业支撑和产业创新等3个维度构建战略性新兴产业国际竞争力评价指标体系.运用2005~2014年的面板数据对战略性新兴产业进行因子分析.评价结果显示,电子及通信设备制造业与医药制造业国际竞争力明显高于计算机及办公设备制造业与医疗仪器设备及仪器仪表制造业.航空航天器及设备制造业国际竞争力有很大提升潜力.电子及通信设备制造业创新能力表现突出,但战略性新兴产业整体创新能力较低.     

Improved Ligand-Field Theory with Effect of Electron-Phonon Interaction

Traditional ligand-field theory has to be improved by taking into account both “pure electronic” contribution and electron-phonon interaction one (including lattice-vibrational relaxation energy). By means of improved ligand-field theory, R₁, R₂, R₃', R₂', and R₁' lines, U band, ground-state zero-field-splitting (GSZFS), and ground-state g factors of ruby and/or GSGG:Cr³⁺ as well as thermal shifts of GSZFS, R₁ line and R₂ line of ruby have been calculated. The results are in very good agreement with the experimental data. Moreover, it is found that the value of cubic-field parameter given by traditional ligand-field theory is inappropriately large. For thermal shifts of GSZFS, R₁ line and R₂ line of ruby, several conclusions have also been obtained.     

锈蚀槽钢受弯承载力试验研究

通过7根锈蚀槽钢构件和2根未锈蚀槽钢构件的受弯试验,研究了锈蚀对槽钢受弯承载力的影响。试验表明:锈蚀槽钢的承载力随其点蚀因子的增大而降低;翼缘的锈蚀对钢构件受弯承载力的影响较腹板显著,其中受压翼缘与受拉翼缘影响程度基本相同。最后,结合试验结果,利用Matlab软件分别对锈蚀槽钢试件上、下翼缘点蚀因子与构件受弯承载力损失值进行数据拟合,定性地给出上、下翼缘点蚀因子与受弯承载力损失比之间的关系式。     

带有风险回避的最优消费模型研究

本文在文献[1]和[2]的基础上,把模型参数推广为时间t的变量,折扣因子β(t)为[0,T]上的有界可测函数,通过计算得出带有风险回避的最优消费条件和投资公式.     

脉冲压缩系统中气体开关对功率增益的影响

 对高功率微波脉冲压缩系统中气体开关对功率增益的一些重要影响进行了较详尽的理论分析,包括气体开关在导通过程中吸收微波能量,等离子体瞬间功率损耗使得谐振腔固有品质因数的下降,开关导通后等离子体并非理想良导体等,并将这些影响用修正系数来加以体现,对原有的用微波等效电路理论推导出的功率增益公式加以修正,使得理论公式的精确度由原来的60%提高至约85%。     

Sweeping with an Enhanced Electric Field of Neutral Analyte Zones in Electrokinetic Chromatography

The concept of sweeping has been used in electrokinetic chromatography to explain the concentrating mechanism in micellar electrokinetic chromatography when the sample matrix is a high resistivity non-micellar aqueous solution. Theoretical and experimental studies were undertaken. It was found that the total focusing effect is brought about by the cumulative effect of sweeping and sample stacking. For better analytical results, compounds showing low to moderate retention factors (k) and compounds showing high values of k must be dissolved in low and high conductivity matrices, respectively.     

Modulating Properties of Piroxicam,Meloxicam and Oxicam Analogues against Macrophage-Associated Chemokines in Colorectal Cancer

The mechanisms underlying the antineoplastic effects of oxicams have not been fully elucidated. We aimed to assess the effect of classic and novel oxicams on the expression/secretion of macrophage-associated chemokines (RTqPCR/Luminex xMAP) in colorectal adenocarcinoma cells, and on the expression of upstream the non-steroidal anti-inflammatory drug (NSAID)-activated genes NAG1, NFKBIA, MYD88, and RELA, as well as at the chemokine profiling in colorectal tumors. Meloxicam downregulated CCL4 9.9-fold, but otherwise the classic oxicams had a negligible/non-significant effect. Novel analogues with a thiazine ring substituted with arylpiperazine and benzoyl moieties significantly modulated chemokine expression to varying degree, upregulated NAG1 and NFKBIA, and downregulated MYD88. They inhibited CCL3 and CCL4, and their effect on CCL2 and CXCL2 depended on the dose and exposure. The propylene linker between thiazine and piperazine nitrogens and one arylpiperazine fluorine substituent characterized the most effective analogue. Only CCL19 and CXCL2 were not upregulated in tumors, nor was CXCL2 in tumor-adjacent tissue compared to normal mucosa. Compared to adjacent tissue, CCL4 and CXCL2 were upregulated, while CCL2, CCL8, and CCL19 were downregulated in tumors. Tumor CCL2 and CCL7 increased along with advancing T and CCL3, and CCL4 along with the N stage. The introduction of arylpiperazine and benzoyl moieties into the oxicam scaffold yields effective modulators of chemokine expression, which act by upregulating NAG1 and interfering with NF-κB signaling.     

不同手机屏幕对青少年生理节律和蓝光危害的影响

针对市场上三款常见的不同材质的手机屏幕（LED背光LCD、OLED、SUPER AMOLED）,在黑暗中、屏幕距离瞳孔15 cm处4种不同色温的条件下,研究不同手机对青少年生理节律和蓝光危害的影响。在充分考虑年龄、人眼受光面积、透射率的情况下,改进传统计算蓝光危害因子的公式,并计算节律因子和蓝光危害因子。结果表明,不管何种手机,节律因子和蓝光危害因子都随色温升高而增大,并且均呈现出良好的线性关系。在7 425~9 201 K色温下,节律因子由大到小依次为:OLED > SUPER AMOLED > LED背光LCD;而蓝光危害因子由大到小依次为:LED背光LCD > SUPER AMOLED > OLED,由此可以根据不同需求,选择相对更健康合适的手机。     

Observation of 18O/16O isotope effects at the cathode of a polymer electrolyte membrane fuel cell

¹⁸O/¹⁶O isotope effects were observed at the cathode of a polymer electrolyte membrane fuel cell at 25 and 35°C. Results of experiments in which the ¹⁸O/¹⁶O isotope ratios of the oxygen gases supplied to and exhausted from the cell were measured revealed that the lighter isotope ¹⁶O reacted more preferentially to form water molecules at the cathode than the heavier one, ¹⁸O. The value of the oxygen isotope separation factor, S₁, defined as the ratio of the ¹⁸O/¹⁶O isotope ratios of the oxygen gases supplied to and exhausted from the cell, ranged from 1.0030 to 1.0139, and tended to decrease with decreasing rate of oxygen utilisation (θ) and with increasing flow rate of the feed oxygen gas (D_F). The value of another separation factor, S₂, defined as the ratio of the ¹⁸O/¹⁶O isotope ratios of the exhausted oxygen gas and oxygen having reacted to form water molecules at the cathode, ranged from 1.0049 to 1.0304. The S₂ value was much less affected by the change in θ and D_F than the S₁ value with the majority of the S₂ value being in the range of 1.0240–1.0304.