969 resultados para 106-115 cm
Resumo:
用能量密度公式及小液滴模型给出的费米密度分布,并引入中子皮及中子分布弥散度随中子过剩自由度增加而增加这一因素,计算了重离子反应在相互作用势及熔合位垒。熔合位垒的计算值和实验值符合很好,特别是在中重核区域,改善了以前的计算结果。详细研究了亲近势标度,发现用中子皮及中子分布弥散度的变化能较好地解释中子过剩自由度对新近势标度偏离的影响。本工作对奇异核结构与核反应性质的研究无疑是有用的。我们利用HIRFL提供的46.7MeV/u ~(12)C束轰击~(58)Ni、~(115)In、~(197)Au研究了反应中发射的α粒子角分布和能谱。从速度表象中洛仑兹不变截面等高图中明显看到发射α粒子的三个源。用这三个源的运动模型成功拟合了α粒子能谱,所提取的参数符合费米气体模型计算结果,并讨论了能谱及拟合参数对靶的依赖关系。认为快速源实质上来自弹核碎裂或类弹核碎裂
Resumo:
重离子核反应机制的研究一直是人们关注的课题。入射能量较低时,集体效应占主要地位,反应为熔合反应及深部非弹性碰撞,实验可用平均场理论进行解释。当入射能量较高时,平均场效应消失,核子-核子碰撞起主要作用,实验可用参加者-旁观者模型来描述。中能区(10-100 MeV/u)的重离子反应既具有低能下一体耗散的特点,又具有高能下核子-核子碰撞的特征,由于作用时间短,非平衡现象变得很重要。在这一能区,多种反应机制共存并相互竞争。对这一能区的重离子核反应制的研究将有助于我们更清楚地了解原子核的结构。为此,我们在兰州重离子加速器HIRFL上进行了46.7 MeV/u ~(12)C引起的重离子反应中前方向出射产物的测量,着重讨论了周边反应中的弹核碎裂和转移反应以及它们的相互竞争。实验中用46.7 MeV/u ~(12)C束流轰击四种靶核:~(58)Ni、~(64)Ni、~(115)In和~(197)Au。通过对前方向出射的类弹碎片的测量,发现它们的平行动量分布宽度满足Goldhaber关系式,提取的约化平行动量分布宽度σ_0 = 80 ± 10 MeV/c,与相对论情形下的值接近,并且σ_0对于各种反应系统均相同。反应中弹核碎裂产物的最可几能量可用Abrasion图象来解释。对于质量接近弹核的类弹碎片,将碎裂部分和转移部分分开后,提取的转移部分的约化平行动量分布宽度为44 ± 10 MeV/c,这比弹核碎裂部分的宽度要窄,说明转移反应比弹核裂受到相空间中更严格的限制。弹核碎裂和转移反应的几率都随靶核质量增加而增加,并且与被转移结团的结构有关。转移反应主要对弹核附近的类弹碎片有贡献,当类弹碎片质量与弹核质量相差较大时,主要是弹核碎裂的贡献。对反应中的同位素产额分布也进行了分析,结果表明,类弹碎片的同位素分布对靶核有依赖关系,当靶核的N/Z增加时,产物的N/Z也增加,并且低能部分的N/Z比高能部分的N/Z要大。当角度变大时,~7Li/~6Li、~9Be/~7Be、~(11)B/~(10)B等同位素产额比随之变化,低能部分变化缓慢,高能部分则变化明显。产物的同位素产额分布或同位素产额比反映了系统由非平衡向平衡演化的过程。实验中对于BaF_2晶体与半导体组成的望远镜探测器的性能进行了测量。圆柱形BaF_2晶体后配以XP2020Q型光电倍增管,输出信号送入不同的QDC,以获得BaF_2中光输出的快慢成分。ΔE-E方法可以得到较好的元素鉴别,即使对低能的p、d、t也能分开,用快慢成分关联方法可对较高能量的轻带电粒子很好地鉴别。入射离子越重,相同能量的离子在BaF_2晶体中引起的光输出越小。BaF_2对入射离子的响应在较大的能区内是线性的,在低能时存在轻微的非线性。对80 cm大面积位置灵敏电离室与一维位置灵敏塑料闪烁体组成的探测系统首次在中能重离子反应中进行了测试。电离室可以测量较重的低能离子,有较好的粒子鉴别能力,能给出能量信息及两维位置信息。闪烁体则使得该系统可用于较高能量轻带电粒子的测量,它能给出能量吸一维位置信息,与电离室配合可以进行元素鉴别。它将在以后的中能重离子实验中得到广泛的应用
Resumo:
论文分为两个部分。第一部分:研究在25MeV/u ~(40)Ar+~(115)In反应中轻粒子发射机制。实验中,利用研制的轻粒子探测器测量了发射的P、#alpha#能谱。用三源模型拟合了轻粒子能谱,所提取的参数与费米气体模型的计算结果进行比较,分析了发射源形成和衰变的一些特点。第二部分:研制一种大面积幅度、时间、位置灵敏闪烁探测器。它是HIRFL上建成的第一阶段放射性核束物理实验终端的主要设备之一,在首次放射性核束调试中收到良好的效果。本文的目的是用经典理论研究了热核形成及衰变的一些性质,在即将开展的放射性核束物理研究中, 利用研制的大型探测器对经典理论普适性进行检验
Resumo:
Porous polytetrafluoroethylene (PTFE) membranes were used as support material for Nafion((R))/PTFE composite membranes. The composite membranes were synthesized by impregnating porous PTFE membranes with a self-made Nafion solution. The resulting composite membranes were mechanically durable and quite thin relative to traditional perfluorosulfonated ionomer membranes (PFSI); we expect the composite membranes to be of low resistance and cost. In this study, we used three kinds of porous PTFE films to prepare Nafion/PTFE composite membranes of different thickness. Scanning electron micrographs and oxygen permeabilities showed that Nafion resin is distributed uniformly in the composite membrane and completely plug the micropores, there is a continuous thin Nation film present on the PTFE surface. The variation in water content of the composite and Nafion 115 membranes with temperature was determined. At the same temperature, water content of the composite membranes was smaller than that of the Nafion 115. In both dry and wet conditions, maximum strength and break strength of C-325(#) and C-345(#) were larger than those of Nafion 112 due to the reinforcing effect of the porous PTFE films. And the PEMFC performances and the lifetime of the composite membranes were also tested on the self-made apparatus. Results showed that the bigger the porosity of the substrate PTFE films, the better the fuel cell performance; the fuel cell performances of the thin composite membranes were superior to that of Nation 115 membrane; and after 180 h stability test at 500 mA/cm(2), the cell voltage showed no obvious drop. (C) 2002 Published by Elsevier Science B.V.
Resumo:
The dual-phase membrane of La0.15Sr0.85Ga0.3Fe0.7O3-delta-Ba0.5Sr0.5Fe0.2Co0.8O3-delta (LSGF-BSCF) was prepared successfully. This membrane was characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM) and electron probe micro-analyzer (EPMA). This membrane has a dense dual-phase structure: LSGF being the dense body of this membrane and BSCF as another phase running along the LSGF body. This structure is favorable for the oxygen permeation through the membrane. The oxygen permeation test shows that the oxygen permeation flux of LSGF-BSCF membrane (Jo(2) = 0.45 ml/min cm(2), at 915 degreesC) is much higher than that of LSGF membrane (Jo(2) = 0.05 ml/min cm(2)). Thickness dependence of oxygen permeation indicates that the oxygen permeation is controlled by the bulk diffusion. Compared to pure BSCF the dual-phase membrane of LSGF-BSCF is stable in reducing atmosphere. (C) 2003 Elsevier B.V. All rights reserved.
Resumo:
A 2-kW-class chemical oxygen-iodine laser (COIL) using nitrogen buffer gas has been developed and tested since industrial applications of COIL devices will require the use of nitrogen as the buffer gas. The laser, with a gain length of 11.7 cm, is energized by a square pipe-array jet-type singlet oxygen generator (SPJSOG) and employs a nozzle bank with a designed Mach number of 2.5. The SPJSOG has advantages over the traditional plate-type JSOG in that it has less requirements on basic hydrogen peroxide (BHP) pump, and more important, it has much better operational stability. The SPJSOG without a cold trap and a gas-liquid separator could provide reliable operations for a total gas flow rate up to 450 mmol/s and with a low liquid driving pressure of around 0.7 atm or even lower. The nozzle bank was specially designed for a COIL using nitrogen as the buffer gas. The cavity was designed for a Mach number of 2.5, in order to provide a gas speed and static temperature in the cavity similar to that for a traditional COIL with helium buffer gas and a Mach 2 nozzle. An output power of 2.6 kW was obtained for a chlorine flow rate of 140 mmol/s, corresponding to a chemical efficiency of 20.4%. When the chlorine flow rate was reduced to 115 mmol/s, a higher chemical efficiency of 22.7% was attained. Measurements showed that the SPJSOG during normal operation could provide a singlet oxygen yield Y greater than or equal to 55%, a chlorine utilization U greater than or equal to 85%, and a relative water vapor concentration w = [H2O]/([O-2] + [Cl-2]) less than or equal to 0.1.
Resumo:
研究表明 ,5~ 7年生沙棘林冠层可截留降水 8 5%~ 4 9 0 % ,并降低雨滴动能 ;枯枝落叶层重5 4 6t·hm- 2 ,其最大持水量可达 15 31t·hm- 2 ,有 1cm厚枯枝落叶层覆盖地表 ,即可基本控制水土流失 ;根系可以提高土壤的抗冲性和抗蚀性 ,与无根系土壤相比 ,可减少土壤冲刷量 55%~ 88% .据1988~ 1994年雨季径流小区测定 ,沙棘林在栽植后 4~ 5年可充分发挥水土保持作用 ,与农地相比 ,可减少地表径流量 87 1% ,减少土壤流失量 99 0 % .此外 ,它还可以每 4~ 5年提供薪材 10~ 30t·hm- 2 ,提高土壤中有机质和氮素含量 115%和 90 % ,生产沙棘果实 50 0kg·hm- 2 .所有这些表明了沙棘在治理黄土高原水土流失和改善人民生活条件 ,在实现由“恶性循环”向“良性循环”转变等方面 ,具有十分重要的作用 .目前 ,黄土地区已建立起若干利用沙棘固坡、防洪、解决燃料短缺和综合治理小流域的成功典型
Resumo:
In this work, both the thermal expansion and electrical conductivity of nanocrystalline La2Mo2O9 were studied. The nanocrystalline powder of La2Mo2O9 was obtained by sol-gel method, and with the help of SHP (superhigh pressure) up to 4.5 x 10(4) atm at 700 degrees C for a short time, and the nanocrystalline powder was densified without obvious particle size growth. The electrical conductivity of nanocrystalline La2Mo2O9 was one order of magnitude lower than that of the microcrystalline sample at the same temperature. Owing to the phase transition, the microcrystalline La2MO2O9 has an abrupt increase of thermal expansion with a peak value of 48 x 10(-6) K-1 at 556 degrees C. For the nanocrystalline material, the peak value increases to 112 x 10(-6) K-1 at 520 degrees C. On the other hand, above 600 degrees C the significant growth of particle size of the nanocrystalline La2Mo2O9 was observed, accompanying by a tremendous increase of thermal expansion with a peak value of 1565 x 10(-6) K-1 at 620 degrees C. The electrical conductivity of La1.6Nd0.4Mo2O9 at 800 degrees C is 0.14 S center dot cm(-1) which is about one third higher than that of La2Mo2O9.
Resumo:
The crystal of the title compound (C10H18N2O9SZn M-r=407.69) belongs to the hexagonal system, space group P 6(5) with cell parameters: a=11.411 (2), c=20.908(4) Angstrom, V=2357.7(7) Angstrom(3), Z=6, D-c=1.723g/cm(3), F(000)=1260, mu(MoKa)=1.743mm(-1). The final R and omega R factors are 0.072 and 0.178 respectively for 1335 observed reflections. in the structure, zinc ions are bridged by 4,4'-bipyridine to form infinite chains. The sheets containing parallel chains stack along a 65 screw axis to give a helical staircase motif. The helical structure is mainly controlled by the hydrogen bonds.
Resumo:
We report the measurement of 112 new high-lying odd-parity excited levels of U I in the energy region 35 678-36 696 cm(-1). These levels were obtained with a setup composed of a Nd:YAG-laser-pumped pulsed dye laser system, an atomic beam device, a time-of-flight mass spectrometer, and a boxcar integrator. (C) 2000 Optical Society of America [S0740-3224(99)02309-7] OCIS code: 300.0300.
Resumo:
The Ophiophagus hannah (King Cobra) neurotoxin CM-11 is a small protein with 72 amino acid residues, Based on complete assignments of H-1-NMR resonances and determination of secondary structures of CM-11, 349 distance and 27 dihedral angle constraints including 19 phi's and 8 chi's were collected from NOESY and DQF-COSY , and the chemical stereospecific assignment of beta(1)H was partially achieved, Twelve structures with lower energy was obtained via metric matrix distance geometry and refinement with simulated annealing, These structures have a low RMSD of 0.14 nm for backbone atoms and 0.20 nm for heavy atoms, with no distance constraint violation more than 0.05 nm, and no dihedral angle violation more than 3 degrees.
Resumo:
在完成了眼镜王蛇毒液抽提物CM-11的残基质子谱峰归属和二级结构的判定后,利用1H的NOESY谱和DQF-COSY谱选取了距离约束、测定了Φ角和χ1,并做了部分β1H的立体归属。利用度量矩阵距离几何法计算了其三维空间结构,并进行了结构的优化。同一个系列中挑选的12个低能分子结构中,骨架的RMSD为0.14nm,所有重原子的RMSD为0.20nm,所有的距离约束偏差不超过0.05nm,二面角的偏差不超过3°
Resumo:
2DNMR谱的自动归属是核磁共振发展的一个方向,CAPRI即是蛋白质1H谱的计算机辅助谱峰归属的一种程序。作者将其应用于眼镜王蛇神经毒素CM-111H谱的归属,讨论了CAPRI的功能和特点以及运用在CM-11后得到的分析结果。
Resumo:
The king cobra(Ophiophagus hannah) neurotoxin CM-11 is long-chain peptide with 72 amino acid residues. Its complete assignment of H-1-NMR resonances was obtained using various 2D-NMR technologies, including DQF-COSY, clean-TOCSY and NOESY.
Resumo:
The king cobra neuotoxin CM-11 is a small protein with 72 amino acid residues. After its complete assignments of H-1-NMR resonance's were obtained using various 2D-NMR technologies, including of DQF-COSY, clean-TOCSY AND NOESY, the secondary structure was analysed by studying the various NOEs extracted from the NOESY spectra and the distribution of chemical shifts. The secondary structure was finally determined by MCD as follows: a triple-strand antiparallel beta sheet with I20-W36, R37-A43 and V53--S59 as its beta strands, a short alpha helix formed by W30-G35 and four turns formed by P7-K10, C14-G17, K50-V53 and D61-N64.