81 resultados para 22-214


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随着社会的进步和医疗卫生水平的不断提高,人类获得了更高的平均寿 命,很多国家都步入了老龄化社会的行列。由于长寿具有遗传的倾向,所以 科学家们致力于人类长寿及衰老性疾病发生机理的研究,目的是为了使人类 在获得更长寿命的同时能够抵御或减缓老年性疾病的侵袭,远离衰老带来的 困扰,享受高质量的生活。 线粒体是真核生物的重要细胞器,具有长度为约为16569bp 的环状 DNA 分子。在人类群体,特别是欧洲群体的相关性研究中,线粒体DNA (mtDNA)编码区和控制区的一些多态性位点显示出与长寿及衰老性疾病的 相关。特别是mtDNA 控制区的C150T 变异除了在多个长寿人群中富集之外, 更是具有改变mtDNA 重链复制起始位点的功能。 为了探讨mtDNA 控制区多态性位点与中国汉族长寿人群是否存在相关 性,本研究在中国四川省都江堰地区采集了556 名年龄90 至108 岁的互无 关系的长寿老人血液样本,其中男性202 名,女性354 名。同时还采集了 214 名长寿老人的亲属和312 名无关对照的血液样本,年龄分别在10 至69 岁之间和22 到73 岁之间。我们对这些样本的mtDNA 通过测序和RFLP 等 手段进行了扫描,采集并记录了mtDNA 单倍型类群信息和控制区位点多态 信息。 在该人群中,本研究发现mtDNA 的主要单倍型类群与长寿没有显著的 相关性,总体单倍型类群频率分布在三个组别中基本一致(p=0.318)。对 mtDNA 控制区C150T 变异的频率在三个组别中做了包括总体频率差异,区 分mtDNA 单倍型类群的频率差异,区分样本性别的频率差异以及mtDNA 单倍型类群与性别信息联合的频率差异的分析。虽然在个别的比较中得到了 显著差异,但经过多重检验校正后,结果均变得不显著。此外,对146、152189 和195 等四个同样处于mtDNA 控制区复制起始区域的变异位点的初步 分析,同样没有获得显著的差异。不支持此前在欧洲长寿人群和日本长寿人 群得到的结论。 综上所述,本研究第一次在中国汉族人群中对mtDNA 控制区多态性与 长寿的相关性进行了研究。mtDNA 与人类长寿的关系还有待于更深层次的 机理性研究和功能性研究来揭示。

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讨论了目前有关2 2 Na(p ,γ) 2 3Mg反应的实验研究工作 ,结合兰州放射性束流线上的放射性束流2 3Al的β+延发质子衰变实验的测量结果 ,给出了2 3Al延发衰变的质子能谱 ,并比较了近期实验给出的相关能级的自旋、宇称值 ,正是由于这种自旋、宇称和能级部分宽度的不确定性 ,导致了反应率计算的不确定性 .计算了同位旋相似态的共振强度 .对于测量到的新的延发衰变能级Ed =8.91 6MeV ,由于没有相应的能级宽度值 ,实验仅给出其相对共振强度值

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The excited states in 22Mg have been investigated by the resonant elastic scattering of 21Na + p. A 4.0 MeV/nucleon 21Na beam was separated by the Center for Nuclear Study (CNS) radioactive ion beam separator (CRIB) and then used to bombard a thick (CH2)n target. The energy spectra of recoiled protons were measured at scattering angles of θc.m. ≈ 172◦ , 146◦, and 134◦, respectively. A wide energy-range of excitation function in 22Mg (up to Ex ∼ 8.9 MeV) was obtained simultaneously with a thick-target method, and a state at 7.06 MeV was newly observed. The resonant parameters were deduced from an R-matrix analysis of the center-of-mass (c.m.) differential cross-section data with a SAMMY-M6-BETA code. The astrophysical resonant reaction rate for the 18Ne(α,p)21Na reactionwas recalculated based on the present parameters. Generally speaking, the present rates are much smaller than the previous ones.

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An experiment of Mg-22 and Ne-20 beams bombarding on a C-12 target at an energy of 60 similar to 70 A MeV has been performed at the RIKEN projectile fragment separator (RIPS)in the RIKEN Ring Cyclotron Facility to study the two-proton correlated emission from Mg-22 and Ne-20 excited states. The two-protons momentum correlation functions have been obtained for Mg-22 and Ne-20, respectively. The trajectories of the Mg-22 decayed products (Ne-20 + p + p) were also measured to get the angular correlations between the two protons in Center of Mass of decaying system by relativistic-kinematics reconstruction. The results exhibit that Mg-22 has the features of He-2 cluster decay mechanism.

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MCM-22 zeolite with mid-strong acidity and openings of 10-membered ring channels may obtain a high catalytic activity and selectivity for alkylation of toluene with methanol. The acidic sites, for catalyzing alkylation of toluene with methanol, are weaker than that for catalyzing toluene disproportionation. Compared with silicon as a modifier, modification of MCM-22 with La(NO3)(3) is a promising way to improve the catalytic selectivity of para-xylene. In addition, the experimental results also clearly indicate the characteristics of MCM-22 structure consisting of large intracrystalline cages, some of which may locate on surface of MCM-22. (C) 2004 Elsevier B.V. All rights reserved.

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A comprehensive study on physical and chemical properties of Mo/MCM-22 bifunctional catalysts has been made by using combined analytic and spectroscopic techniques, such as adsorption, elemental analysis, and Xe-129 and P-31 NMR of adsorbed trialkylphosphine oxide probe molecules. Samples prepared by the impregnation method with Mo loadings ranging from 2-10 wt.% have been examined and the results are compared with that obtained from samples prepared by mechanical mixing using MoO3 or Mo2C as agents. Sample calcination treatment is essential in achieving a well-dispersed metal species in Mo/MCM-22. It was found that, upon initial incorporation, the Mo species tend to inactivate both Bronsted and Lewis sites locate predominantly in the supercages rather than the 10-membered ring channels of MCM-22. However, as the Mo loading exceeds 6 wt.%, the excessive Mo species tend to migrate toward extracrystalline surfaces of the catalyst. A consistent decrease in concentrations of acid sites with increasing Mo loading < 6 wt.% was found, especially for those with higher acid strengths. Upon loading of Mo > 6 wt.%, further decreases in both Bronsted and Lewis acidities were observed. These results provide crucial supports for interpreting the peculiar behaviors previously observed during the conversion of methane to benzene over Mo/MCM-22 catalyst under non-oxidative conditions, in which an optimal performance was achieved with a Mo loading of 6 wt.%. The effects of Mo incorporation on porosity and acidity features of the catalyst are discussed. (C) 2004 Published by Elsevier B.V.

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The density functional theory has been used to study the isomorphously substituted MCM-22 zeolite for the first time. The effect of the basis sets on the calculation results is discussed in details. Data of several index properties for characterizing the relative acidity of T-MCM-22 (T = B, Al, Ga, and Fe), including proton affinity, bond length and bond angle, OH stretching frequency, and charge on the acidic proton, show that the acidity of T-MCM-22 increases in the sequence of B-MCM-22 < Fe-MCM-22 < Ga-MCM-22 < Al-MCM-22. After making a correction, the calculated OH stretching frequencies for Al-MCM-22 and Fe-MCM-22 show a reasonable agreement with the experimental data. On the basis of an equilibrium structure of the B-MCM-22 zeolite, the effect of the B element in the synthesis of the Ti-MCM-22 is also discussed. The adding of the B element during the synthesis of the Ti-MCM-22 can decrease greatly the Ti substitution energy because of the forming of a structure quite similar to the terminal silanol group. The results can provide some constructively information for zeolite synthesis.

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By characterizing fresh and used Mo/HMCM-22 catalysts with ICP-AES, XRD, NH3-TPD technique, UV - Vis DRS and UV Raman spectroscopy, the reactivity of Mo species for methane partial oxidation into formaldehyde were directly studied with a new point of view. By comparing the fresh and used catalysts, it was found that the tetrahedral Mo species bonding chemically to the support surface were practically unchanged after the reaction, while the polymolybdate octahedral Mo species, which had a rather weak interaction with the MCM-22 zeolite, leached out during the reaction, especially when the Mo loading was high. Correspondingly, it was found from the time-on-stream reaction data that the HCHO yield remained unchanged, while COx decreased with the reaction time during the reaction. By combining the characterization results and the reaction data, it can be drawn that the isolated tetrahedral molybdenum oxo-species (T-d) is responsible for HCHO formation, while the octahedral polyoxomolybdate species (O-h) will lead to the total oxidation of methane.