Dense inverse subsemigroups of a topological inverse semigroup

In this paper we study dense inverse subsemigroups of topological inverse semigroups. We construct a topological inverse semigroup from a semilattice. Finally, we give two examples of the closure of B _{( −∞, ∞ )}¹, a topological inverse semigroup obtained by starting with the real numbers as a semilattice with the operation a ∨ b=sup{a,b}. The author would like to thank to the referee for useful suggestions.     

Lipid diffusion in giant unilamellar vesicles is more than 2 times faster than in supported phospholipid bilayers under identical conditions

The lateral diffusion coefficients of a BODIPY tail-labeled lipid in two model systems, namely, free-standing giant unilamellar vesicles (GUVs) and supported phospholipid bilayers (SPBs), were determined by fluorescence correlation spectroscopy (FCS) using the Z-scan approach. For the first time, the performed measurements on 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) bilayers maintain exactly the same experimental conditions for both systems, which allows for a quantitative comparison of lipid diffusion in these two commonly used model membranes. The results obtained revealed that the lipid mobility in free-standing bilayers (D=7.8+/-0.8 microm2 s-1) is significantly higher than in the bilayer created on the solid support (mica) (D=3.1+/-0.3 microm2 s-1).     

Simple analysis of four bisphosphonates simultaneously by reverse phase liquid chromatography using n-amylamine as volatile ion-pairing agent

Volatile organic amine was used as the mobile phase addictive during the separation of four bisphosphonates (alendronate, pamidronate, zoledronic acid and etidronate). An isocratic liquid chromatography method with evaporative light-scattering detection (ELSD) was developed for these bisphosphonates which are not retained on non-polar column and lack chromophore for detection. The analytes have sufficiently separated from each other on a Phenomenex C18 column. The effects of mobile phase composition and instrumental parameters of ELSD were studied. This newly developed method enables direct measurement for analysis of bisphosphonates without the need of derivatization. This developed method provides high separation and specificity to bisphosphonate analysis. In quantitative analysis, the method showed satisfactory precision (less than 2.8%) and accuracy (higher than 94.4%), good linearity (r=0.9991-0.9997) and sufficient sensitivity (15-18 microg/ml). It can be easily and conveniently adopted for the routine quality control analysis.     

Hydrothermal synthesis and characterization of the first 1-D indiumphosphate chain In2(HPO4)2(H2PO4)2F2·C4N2H12, a precursor for high dimensional structures

The first one-dimensional (1-D) indiumphosphate chain, In₂(HPO₄)₂(H₂PO₄)₂F₂·C₄N₂H₁₂ (1), has been hydrothermally prepared using piperazine (PIP) as a template. The structure consists of infinite chains of trans,trans-corners-sharing InO₄F₂ octahedra with the adjacent octahedra being bridged by tetrahedral PO₃(OH) and PO₂(OH)₂ units, which are H-bonded with amine groups of the organic cations. Interestingly, this macroanionic chain InP₂O₈H₃F⁻ is similar to that found in the mineral tancoite-like chains and has potential to further set up higher-dimensional networks. On heating 1 in the presence of additional phosphoric acid at 180 °C under hydrothermal condition, compound 2, In₂(OH)(H₂O)(PO₄)₂·H₃O·H₂O, possessed a 3-D structure building from the repetition of a secondary building unit is obtained. When 1 is heated with additional PIP, an unknown phase, compound 3 is formed. Finally, on treatment with another amine, such as diethylenetriamine or 1,4-diaminobutane, at 180 °C, 1, as a precursor, can convert into a previously known 3-D framework structure with 16-membered ring compound 4. Compounds 1 and 2 are determined by single-crystal X-ray diffraction. Furthermore, 1 is characterized by X-ray powder diffraction, IR spectroscopy, inductively coupled plasma analysis, thermogravimetric analysis and differential thermal analysis.     

Static secondary ion mass spectrometry (S-SIMS) for the characterization of surface components in mineral particulates

The feasibility of static secondary ion mass spectrometry (S-SIMS) for the detection of molecule specific information from complex materials, such as natural clay and soil samples, has been investigated. Ion trap (IT), as well as triple quadrupole (TQ) instruments, have been used for mass analysis. Secondary ion images have been acquired using time-of-flight (TOF) S-SIMS. The generation of molecular adduct ions from thin and thick layers on the mineral substrates has been investigated using KBr as a simple model system. Results show that molecular adducts of KBr can be indeed detected from the spiked materials. However, the concentrations of the spiking solutions have to be significantly larger than expected from the surface area measured by gas adsorption techniques. In addition imaging analysis has evidenced that the detection of adduct ions in the mass spectra directly relates to the presence of local micro-crystallites.     

基于功率谱分段对消频谱感知算法研究及性能分析

在实用的认知无线电系统中,频谱感知技术必须具备在噪声电平高动态变化和无线信道严重衰落电磁背景下,进行实时盲频谱感知的能力,这为经典的频谱感知算法带来巨大的挑战。该文提出的功率谱分段对消频谱感知算法,依据傅里叶变换的渐进正态性和相互独立性,计算出功率谱的统计特性,利用监测频带内部分谱线强度和与全部谱线强度和的比值作为检验统计量进行信号存在性的判断。该文推导了算法的虚警概率和不同信道模型下正确检测概率的数学表达式,并依据Neyman-Pearson准则得到判决门限的闭式表达式。理论分析和仿真结果均表明:功率谱分段对消频谱感知算法对噪声不确定度具有鲁棒性;固定信噪比,算法的频谱感知性能不受噪声电平改变的影响;应用于高斯白噪声和平坦慢衰落信道中,可在较宽的信噪比范围内获得较优越的频谱感知性能;算法计算复杂度低,可在微秒级时长内完成频谱感知。     

Neutrino Production via e-e+ Collision at Z-Boson Peak

The production of the three normal neutrinos via e^-e⁺ collision at Z-boson peak (neutrino production in a Z-factory) is investigated thoroughly. The differences of v_e-pair production from v_μ-pair and v_τ-pair production are presented in various aspects. Namely the total cross sections, relevant differential cross sections and the forward-backward asymmetry etc. for these neutrinos are presented in terms of figures as well as numerical tables. The restriction on the room for the mixing of the three species of light neutrinos with possible externals (heavy neutral leptons and/or sterile neutrinos) from refined measurements of the invisible width of Z-boson is discussed.     

CCD与CMOS像素传感器γ射线电离辐射响应特性对比研究

为了研究CCD与CMOS像素传感器对γ射线电离辐射的响应差异,对比研究了4类像素传感器的结构特点和辐射响应特性。通过辐射实验,对各传感器在不同辐射水平条件下的光子响应事件分布、平均灰度值以及典型光子响应事件进行研究。研究结果表明：光子响应程度均与辐射剂量率相关;CCD像素传感器的沟道传输方式使每列像元间的辐射响应更容易相互干扰;平均灰度值随剂量率的增大存在明显的梯度,各积分周期内输出信号灰度值围绕均值上下波动,CCD像素传感器输出信号灰度浮动范围较小;CMOS像素传感器各像元对光子的响应更加明显,CCD像素传感器各像元的响应信号易与相邻像元发生串扰;各类像素传感器典型辐射响应事件区域中发生光子响应的像元数量随剂量率的增大而增多,响应事件并非单个光子的行为,而是反映了多个光子在区域内同时沉积能量的过程。本研究为开发像素传感器的γ射线辐射探测技术和应用提供了重要的理论分析和实验数据支撑。     

基于改进射线描迹法的对流层斜延迟估计

该文针对传统对流层延迟模型和射线描迹法在估计对流层延迟方面的局限性,如效率低、成本高、精度受地表参数和探空数据限制等不足,提出一种基于改进射线描迹法的对流层斜延迟估计方法。该方法结合中纬度大气模式气象参数公式和UNB3m气象参数模型,改进了射线描迹法中折射率剖面的计算,克服了气象数据对射线描迹法的限制。选取亚洲地区10个站点2012年的气象数据,分别采用改进射线描迹法和传统对流层延迟模型估计各个站天顶方向至 高度角区间15个方向的对流层斜延迟,并与基于探空数据获取的对流层斜延迟真值进行比较,计算结果表明该方法的估计精度优于传统对流层延迟模型,为非气象数据情况下对流层斜延迟实时估计提供了新的思路。     

高效液相色谱-串联质谱法同时测定供港生猪尿液中29种限用兽药残留

建立了高效液相色谱-串联质谱(HPLC-MS/MS)同时测定生猪尿液中喹诺酮类、磺胺类、磺胺增效剂、四环素类、林可胺类、大环内脂共29种限用兽药残留量的检测方法。试样经乙酸铵和EDTA-Na缓冲液提取,HLB固相萃取小柱净化后,HPLC-MS/MS进行测定,其中β-受体激动剂类用内标法定量,其余兽药用外标法定量。在电喷雾电离正离子模式下,以多反应监测(MRM)方式采集数据进行定性与定量分析。29种兽药在猪尿基质中标准曲线的线性系数(r)均大于0.99,3个不同加标水平下的平均回收率为58%~108%,日内相对标准偏差(RSD)为1.9%~18.9%,日间RSD为3.4%~20.9%;定量下限(LOQ,S/N≥10)为1.0~10.0μg/L。该方法经济、高效、可靠,可用于生猪屠宰前兽药多残留的快速检测。