一种基于感兴趣区域提取的医学图像检索技术

针对胸部CT扫描图像库,提出了一种基于感兴趣区域提取的图像检索方法．首先为了提取感兴趣区域,提出一种基于灰度层共现矩阵的区域增长算法,分割出病灶区域,再通过闽值算法进行边界的磨合,然后针对感兴趣区域提取形状和分布特性作为图像匹配准则的客观依据．最后,将该算法与其他底层特征算法进行比较和分析．实验结果表明,该算法能够比较有效地应用于基于内容的医学图像检索系统中．     

不同水胶比混凝土内部温湿度长期变化规律研究

鉴于混凝土内部温湿度显著影响混凝土耐久性, 为研究混凝土内部温湿度长期的变化规律, 将不同水胶比混凝土放置于室内大气环境中, 并测量其距离表面3cm、5cm、7cm及9cm处140d内温湿度的演变规律. 研究结果表明: 正常室温条件下, 混凝土内部温度变化主要受环境温度影响, 且与环境温度变化趋势基本相同, 浇筑完成7d后内部温度与环境温度温差大约为2℃, 60d以后内外温差基本消失. 高水灰比混凝土内部含水量充足, 140d内部相对湿度一直保持在85%以上; 低水灰比混凝土内部含水量较少, 早期相对湿度变化受水化耗水影响明显, 混凝土内部相对湿度存在明显梯度差, 5cm、7cm处相对湿度最低分别为60.18%和29.83%; 随着水化作用进行, 长期来看混凝土内部湿度逐步与环境湿度趋于一致.     

Unconventional transport in the "hole" regime of a si double quantum dot

Studies of electronic charge transport through semiconductor double quantum dots rely on a conventional "hole" model of transport in the three-electron regime. We show that experimental measurements of charge transport through a Si double quantum dot in this regime cannot be fully explained using the conventional picture. Using a Hartree-Fock (HF) formalism and relevant HF energy parameters extracted from transport data in the multiple-electron regime, we identify a novel spin-flip cotunneling process that lifts a singlet blockade.     

烯烃聚合高性能FI催化剂的进展

FI催化剂系一近几年发展起来的烯烃聚合高性能催化剂。以它的极高的活性、聚合物分子结构的可控性、多重活性聚合等特性而引人注目。本评述首先进行该催化剂的化学描述,然后分别介绍该催化剂的主要特征、活性中心结构、聚合机理和应用,重点介绍该催化剂的五大特征。     

微视频在无机化学实验教学中的应用

To improve the students' autonomous learning ability and learning enthusiasm in practice course,we introduce micro video,which is short,fast,precise,easy,and fun,into inorganic chemistry laboratory teaching.As an important supplementary means of teaching,micro videos will solve the repeated problems,help students promote study efficiency,provide students with a good way for communication,and improve the students' study enthusiasm.     

Chaos in an Ar+ Composite Resonator Laser Using KNSBN;Cu Crystal Self-Pumped Phase-Conjugator

Observation of the dynamics in a single-mode Ar⁺ composite resonator laser using KNSBN;Cu crystal self-pumped phase-conjugator is reported. The sequence of instabilities occurring on gain change corresponds to the transition the chaos of the logistic equation. Period-doubling route to chaos, and period-5, -3,-3×2, and -2 together with -3 windows in the chaotic range were observed. The strange attractor which is similar to that of the forced Duffing equation is obtained by reconstructing phase-space pictures of the system.     

横向磁场导致CO2激光器混沌运转及其奇异吸引子的观测

在外加磁场的情况下,对单模均匀展宽CO₂激光器进行了实验研究。改变磁场的大小,观察到了自脉动和混沌现象,同时还获得了该系统的奇异吸引子,并对其物理机制进行了探讨。     

The statistics of continued fractions for polynomials over a finite field

Given a finite field of order and polynomials of degrees respectively, there is the continued fraction representation . Let denote the number of such pairs for which and for . We give both an exact recurrence relation, and an asymptotic analysis, for . The polynomial associated with the recurrence relation turns out to be of P-V type. We also study the distribution of . Averaged over all and as above, this presents no difficulties. The average value of is , and there is full information about the distribution. When is fixed and only is allowed to vary, we show that this is still the average. Moreover, few pairs give a value of that differs from this average by more than

     

SYNTHESIS AND NMR CHARACTERIZATION OF PRECURSORS OF EPOXY NETWORK AS POLYMER HOST FOR SOLID ELECTROLYTE

To raise the room temperature ionic conductivity and improve the mechanical strength of a PEO-based polymer electrolyte, a noncrystalline two-component epoxy electrolyte system has been prepared. The diglycidyl ether of polyethylene glycols as precursors of the system were synthesized by a two-step process. The presumed structure of the product was characterized, by ~(13)C, ~1H NMR and IR spectroscopy. It was found that a side-reaction occurred between the secondary hydroxyl group of PEG-chlorohydrin and epichlorohydrin in some degree, resulting in a by- product containing—CH_2Cl side group. By selecting a characteristic signal, which is undistorted by the increase in the length of CH_2 CH_2—O segment, a ~1H NMR approach of determining the equivalent epoxy weight (EEW) was proposed. The method is valid to specimens even though the EEW is as high as 2,000. The examination of the specimens by DSC showed that epoxidation greatly depressed the crystallinity of the PEG's, whereas the T_g was raised.     

Solvent dependence of intramolecular electron transfer in a helical oligoproline assembly

The helical oligoproline assembly CH3-CO-Pro-Pro-Pro-Pra(Ptzpn)-Pro-Pro-Pra(RuIIb2m2+ -Pro-Pro-Pra(Anq)-Pro-Pro-Pro-NH2, having a spatially ordered array of functional sites protruding from the proline backbone, has been prepared. The 13-residue assembly formed a linear array containing a phenothiazine electron donor, a tris(bipyridine)ruthenium(II) chromophore, and an anthraquinone electron acceptor with the proline II secondary structure as shown by circular dichroism measurements. Following RuII --> b2m metal-to-ligand charge-transfer (MLCT) excitation at 457 nm, electron-transfer quenching occurs, ultimately to give a redox-separated (RS) state containing a phenothiazine (PTZ) radical cation at the Pra(Ptzpn) site and an anthraquinone (ANQ) radical anion at the Pra(Anq) site. The redox-separated state was formed with 33-96% efficiency depending on the solvent, and the transient stored energy varied from -1.46 to -1.71 eV at 22 +/- 2 degrees C. The dominant quenching mechanism is PTZ reductive quenching of the initial RuIII(b2m*-) MLCT excited state which is followed by m*- --> ANQ electron transfer to give the RS state. Back electron transfer is highly exergonic and occurs in the inverted region. The rate constant for back electron transfer is solvent dependent and varies from 5.2 x 10(6) to 7.7 x 10(6) s-1 at 22 +/- 2 degrees C. It is concluded that back electron transfer occurs by direct ANQ*- --> PTZ*+ electron transfer. Based on independently evaluated kinetic parameters, the electron-transfer matrix element is HDA approximately 0.13 cm-1.