具阻尼的Gross-Pitaevskii(GP)方程的整体解

考虑临界的具阻尼的Gross-Pitaevskii(GP)方程iψt=-Δψ+|x|2ψ+g|ψ|4/Dψ+iaψ, t≥0, x∈RD, g＜0, a＜0,这里D是空间维数.这个方程很好地描述了吸引的玻色-爱因斯坦凝聚(BEC).通过偏微分方程的严格理论和变分方法,获得了整体解的一个充分条件,而这个条件利用了非线性数量场方程-Δu+(2)/(b)u-|u|4/Du=0的唯一正解.     

关于环的广义内射性的一点注记

定义了完全YJ(GP)—内射环及强完全YJ(GP)—内射环，推广了完全P—内射环及强完全P—内射环的有关结果，并给出了强正则环的一个等价刻画。     

两个玻色-爱因斯坦凝聚体间相互作用的数值研究

本文采用辛算法数值求解一维含时Gross-Pitaevskii(GP)方程.研究了存在陷俘势和撤掉陷俘势时两个凝聚体间的相互作用.发现当存在陷俘势时两个凝聚体间发生弹性碰撞;在零时刻撤掉陷俘势时两个凝聚体间发生干涉现象;当t=2时撤掉陷俘势两个凝聚体间发生了复杂现象.     

电子竞价在高校政府采购中的应用

介绍了电子政府采购在高校的作用,分析了电子竞价的特点和优势,针对高校电子政府采购的现状,提出了高校电子竞价采购系统的基本构架和优先建设电子竞价采购系统的策略.     

电力线载波通讯火灾报警网络系统的研究开发

研究开发一种以电力线载波通讯为基础的新型火灾报警网络系统，对网络系统结构、网络协议、逻辑组件和传输方式进行优化设计，分析了主要干扰因素对系统可靠性的影响以及技术对策。     

形变对铁铜合金时效析出的影响

对铁铜合金分别进行50%和80%冷变形,利用金相显微镜以及高分辨投射电镜研究形变热处理过程中的微观组织与沉淀析出,分析形变量对时效析出的影响. 结果表明:变形有助于第二相的析出,大的冷变形量时沉淀相粒子形成的速率更快,所占体积分数更大. 优先析出为富铜过渡相,这种富铜过渡相所形成的GP区对合金起强化作用,其后随时效时间延长这种富铜相逐渐转转变成ε-Cu.     

具阻尼的Gross-Pitaevskii(GP)方程在二维空间中的稳定性

本文讨论出现在吸引玻色-爱因斯坦凝聚中的一类带调和势的阻尼非线性Schr dinger方程.对照玻色-爱因斯坦凝聚的物理性质,证明了阻尼参数存在一个门槛值,即当阻尼参数大于该门槛值时,初值问题的解整体存在;当阻尼参数小于该门槛值时,其初值问题的解将在有限时间内坍塌.     

YAG激光器的计算机闭环控制

介绍了采用ＩＥＥＥ－４８８接口组建的ＹＡＧ激光器的计算机闭环控制系统，实现了激光波长连续扫描和数据同步采集，改进了传统实验手段     

Bulk derivatization and cation exchange restricted access media-based trap-and-elute liquid chromatography–mass spectrometry method for determination of trace estrogens in serum

Estrone (E1), estradiols (α/β-E2), and estriol (E3) are four major metabolically active estrogens exerting strong biological activities at very low circulating concentrations. This paper reports a sensitive and efficient method with automated, on-line clean-up and detection to determine trace estrogens in a small volume of serum samples using liquid chromatography–electrospray ionization–tandem mass spectrometry directly, without off-line liquid–liquid or solid-phase extraction pretreatments. Serum aliquots (charcoal stripped fetal bovine serum, 100 μL) were spiked with four estrogen standards and their corresponding isotope-labeled internal standards, then bulk derivatized with 2-fluoro-1-methyl-pyridium p-toluenesulfonate (2-FMP) to establish the calibration curves and perform method validation. Calibration was established in the concentration ranges of 5–1000 pg mL⁻¹, and demonstrated good linearity of R² from 0.9944 to 0.9997 for the four derivatized estrogens. The lower detection limits obtained were 3–7 pg mL⁻¹. Good accuracy and precision in the range of 86–112% and 2.3–11.9%, respectively, were observed for the quality control (QC) samples at low, medium, and high concentration levels. The stability tests showed that the derivatized serum samples were stable 8 h after derivatization at room temperature and at least to 48 h if stored at −20 °C. The method was applied to measure trace estrogens in real human and bovine serum samples, and three of four estrogen compounds studied were observed and quantified.