Asymptotic behavior of solutions for a class of predator-prey reaction-diffusion systems with time delays

The aim of this paper is to investigate the asymptotic behavior of solutions for a class of three-species predator-prey reaction-diffusion systems with time delays under homogeneous Neumann boundary condition. Some simple and easily verifiable conditions are given to the rate constants of the reaction functions to ensure the convergence of the time-dependent solution to a constant steady-state solution. The conditions for the convergence are independent of diffusion coefficients and time delays, and the conclusions are directly applicable to the corresponding parabolic-ordinary differential system and to the corresponding system without time delays.     

Visible-light-induced,autopromoted nickel-catalyzed three-component arylsulfonation of 1,3-enynes and mechanistic insights

A light-induced, nickel-catalyzed three-component arylsulfonation of 1,3-enynes in the absence of photocatalyst is reported.This methodology exhibited mild conditions, broad scope and high efficiency, and its synthetic utility has been demonstrated by a concise total synthesis of sulfone-containing drug molecule. Detailed mechanistic studies indicated that this light induced nickel catalysis is autopromoted by in situ produced allene, which plays a key role as co-ligand in the photoactive excite...     

Study on the Dynamics of Blending of Glucomannan with Carrageenan and Guaran Gum

In order to prove up the interaction between konjac glucomannan (KGM) and other amyloses, by using KGM, guaran gum and carrageenan as materials, their blending in different external conditions was modeled by means of molecular dynamics (MD) method. The result showed that 323 K was a significant turning point for the formation of hydrogen bond, and KGM and guaran gum were just juxtaposed together via intermolecular hydrogen bond; but with the addition of carrageenan, KGM, guaran gum and carrageenan were spirally twisted together, and when their blending proportion is 3:2:9 the combination was the most compact. Moreover, the research result has provided the sequent studies afterwards on amyloses with some references.     

水热法合成多金属氧酸盐棒状超细晶体

以SrCl₂·6H₂O、(NH₄)₆P₂Mo₁₈O₆₂·nH₂O为原料，在PEG-600/H₂O微乳体系中于80～130 ℃温度下水热反应8～12 h，从而制得一种多金属氧酸盐棒状超细晶体，组成是Sr₃P₂Mo₁₈O₆₂·nH₂O。该超细晶体具有长棒状形貌、高结晶度且分散性能较好，长度范围在10.0～20.0 μm，径度在1.0～2.0 μm。对反应体系中的PEG-600/H₂O体积比(V_PEC-600∶V_H2O)、水热温度以及(NH₄)₆P₂Mo₁₈O₆₂·nH₂O/SrCl₂·6H₂O质量比(W_POMs∶W_SrCl2·6H2O)3个影响因素进行了探讨，结果表明：V_PEC-600∶V_H2O主要对棒状超细晶体的形貌、长径比以及晶体结晶度有着重要影响，体积比在范围V_PEC-600∶V_H2O=(1.50～2.00)∶1.00有利于大长径比的棒状超细晶体的形成；水热温度则优选80～130 ℃范围，过低则不发生反应，过高则发生了多金属氧酸盐与PEG-600的氧化-还原反应；W_POMs∶W_SrCl2·6H2O基本上不影响超细晶体的形成。还初步探讨了该棒状超细晶体的形成机理。     

化学发光酶免疫法检测猪肉中氯丙嗪残留

采用棋盘滴定法确定包被抗原浓度和抗体稀释倍数,通过单因素实验优化了竞争反应时间、磷酸盐缓冲液浓度、甲醇含量、pH值等参数,建立了氯丙嗪的间接竞争化学发光酶免疫检测方法,并考察了方法的特异性、灵敏度和稳定性.结果表明,最佳反应条件为包被抗原浓度为0.05 μg/L;氯丙嗪抗体稀释32000倍;体系缓冲液为含10％甲醇、0.1 mol/L磷酸盐缓冲液(pH 7.0).本方法的IC50为0.12 μg/L;检出限为0.02 μg/L;线性范围0.02～24.78 μg/L;批内和批间相对标准偏差均小于10％.与其它结构类似物没有明显交叉反应.猪肉检测的平均回收率为87.4％～105.6％,与高效液相色谱方法的相关性良好.本方法具有较高的灵敏度和较好的稳定性.     

Cu2+离子A位取代对MgTiO3陶瓷结构及介电性能的影响

采用固相反应制备了Mg_1-xCu_x TiO₃(0.00≤x≤0.20)微波介电陶瓷,研究CuO烧结助剂对MgTiO₃陶瓷的微观结构和微波介电性能的影响。实验结果表明,CuO中的Cu²⁺离子会进入到MgTiO₃晶格中并取代Mg²⁺,形成Mg_1-xCu_x TiO₃固溶体。由于液相效应,适量的CuO可以促进MgTiO₃陶瓷的致密化烧结,降低其烧结温度。Cu²⁺离子的A位取代会改变样品的TiO₆八面体扭曲度。随着Cu²⁺离子含量的增加,会使MgTiO₃陶瓷的结构稳定性降低。随着CuO含量的增加,晶粒的不均匀生长和液相的出现导致样品的品质因数(Qf)下降。同时,Mg_1-xCu_x TiO₃陶瓷的相对密度、结构...     

BEPC-LINAC试验束上1GeV/c多粒子磁谱仪的设计和性能测量

试验束上2Q2D结构的磁谱仪系统由2块二极磁铁和2块四极磁铁以及位置灵敏探测器组成.该磁谱仪的接收立体角5×10^–4sr,动量范围0.2—1.3GeV/c.测量了聚焦面上的束流截面和动量谱.介绍了一种测量电子与质子飞行时间差的动量测量方法.     

叶酸-壳聚糖偶联物的制备及对人体血红细胞的影响

通过叶酸活性酯与壳聚糖的氨基反应,制备出叶酸-壳聚糖偶联物;经红外光谱、核磁共振表征该偶联物的化学结构,紫外分光光度法测定每个壳聚糖上叶酸的接枝量。通过溶血实验、扫描电镜、原子力显微镜观察比较了壳聚糖、叶酸-壳聚糖对人体红细胞的影响。结论:成功制备出叶酸-壳聚糖偶联物;与壳聚糖相比,接枝叶酸的壳聚糖对血红细胞的形貌没有改变。     

Controllable synthesis of ZnxCd1-xS@ZnO core-shell nanorods with enhanced photocatalytic activity

We report the synthesis of Zn(x)Cd(1-x)S@ZnO nanorod arrays via a facile two-step process and the implementation of these core-shell nanorods as an environmental friendly and recyclable photocatalyst for methyl orange degradation. The band gap of Zn(x)Cd(1-x)S@ZnO core-shell nanorods can be readily tunable by adjusting the ratio of Zn/Cd during the synthesis. These Zn(x)Cd(1-x)S@ZnO core-shell nanorods exhibit a high photocatalytic activity and good stability in the degradation of the methyl orange. Moreover, these films grown on FTO substrates make the collection and recycle of the photocatalyst easier. These findings may open new opportunities for the design of effective, stable, and easy-recyclable photocatalytic materials.