987 resultados para orientamento :: 341 :: Orientamento A
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运用在二维不对称谐振子势加八极形变势中传播的二维不对称谐振子相 干态,研究了不同强度耦合作用下密度矩阵的复杂性及对干扰动强度微小变动 的敏感性。发现相应于对应经典系统作规则、部分混沌、及整体混沌运动的相空 间区域,量子系统有对应的特征性的表现,它们与势能面上负曲率的存在及负 曲率的大小有关系.
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用双核模型研究超重核的合成机制,最主要的部分是由双核系统演化到复合核的熔合机制研究。双核模型认为超重复合核的形成是由弹核的核子全部转移到靶核所致。核子分中子和质子,在以前的研究中,描述熔合过程的主方程是一维的,以类弹核的质量数 为变量,与此对应的驱动势也是一维的。对确定的 ,其同位旋的确定是由较低的势能面确定的,这样确定的同位旋与反应系统的同位旋很接近。但是我们的研究发现,对入射道同位旋与复合系统同位旋相差较大的情况,入射道在双核系统势能面比较高的位置,有时甚至在最高位置,这时核子转移的同位旋路径比较复杂,以致一维主方程的描述给出错误的结果。为此,建立了以类弹碎片中子数 和质子数 为变量的二维主方程,并建立了二维主方程的分步差分的解法,完成了解二维主方程的程序编写。并对一些典型的弹核、靶核同位旋与复合系统同位旋相差较大的系统进行了研究。对这些反应道的研究表明,无论1D主方程对这些反应道的蒸发剩余截面的研究给出了过高、或过低的估计,2D主方程都能给出与实验值一致地结果。二维主方程适用于所有的弹靶组合入射道。对确定的超重核目标,可以较准确的对各种弹靶组合的合成几率给出预言,特别是研究合成超重核的同位素依赖性,因而极大增加了预言合成预期超重岛区域超重核的弹靶组合的选择性。本工作还检验了一维主方程的适用条件:入射点必须在比较接近二维驱动势谷底时才适用,这时一维主方程预言的蒸发剩余截面的结果与二维主方程的结果很接近
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生态足迹是评价可持续发展状况和能力的重要指标之一。本文以统计年鉴和林业年鉴为主要数据来源,对延边林区1996~2002年的生态足迹进行了计算和分析。结果表明,该区人均生态足迹逐年下降,人均生态承载力波动较小,而人均生态盈余逐年增长。人均万元GDP生态足迹逐年递减,同西部地区相当,而明显高于东部。人均林地生态足迹变化平稳,天然林保护工程实施前后林地生产足迹和林地出口足迹的平均值分别降低了0.341和0.327 hm2.人-1,降幅分别为46.32%和54.94%。延边区域和林业的发展是可持续的,天然林保护工程的实施有助于增强其可持续发展能力,但同林业发达国家相比,仍有很大差距。依靠科技,提高单位面积林地产量和资源利用率,合理经营和管理森林生态系统是今后的工作重点。
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采用田间微区试验和分级提取测定的方法研究了褐土中P、Zn形态转化问题.发现褐土中Ca2-P和Ca8-P是转化最活跃的P素形态.而且Ca8-P的流通容量很大,可超过作物需P量9倍以上;在Zn的各种形态中转化最活跃的是EX-Zn和CARB-Zn,其中CARB-Zn的流通容量亦很大,可超过作物需Zn量19倍以上.Ca8-P库和CARB-Zn库形成了褐土中调控P、Zn养分供蓄以适应旱地水分波动的主要机构.合理施肥和培肥土壤以丰富Ca8-P和CARB-Zn库将有利于增强作物抵御干旱能力,提高水分养分利用效率,促使旱地农业持续向高产优质高效方向发展.
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在经济高速增长的新形势下,能源保障风险日益凸现。全国能源保障分区研究不仅是能源风险管理的基本要求,也是经济发展对能源产业提出的新要求。本文阐述了全国能源资源的基础形势,并对1996年~2005年间我国一次能源生产和消费情况进行了分析;构建了由能源储量比、对外依存度、库存增减量、能源生产弹性系数、能源消费弹性系数、运输线路长度6个指标组成的能源保障指标体系,采用因子分析法确定各个指标的权重;并根据灰色聚类方法对全国30个省(市、区)"十五"期间的能源保障能力进行了评估与分区。结果表明:我国能源保障水平具有南
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Polyaniline/magnetite nanocomposites consisting of polyaniline (PANI) nanorods surrounded by magnetite nanoparticles were prepared via an in situ self-assembly process in the presence of PANI nanorods. The synthesis is based on the well-known chemical oxidative polymerization of aniline in an acidic environment, with ammonium persulfate (APS) as the oxidant. An organic acid (dodecylbenzenesulfonic acid, DBSA) was used to replace the conventional strong acidic (1 M HCl) environment. Here, dodecylbenzenesulfonic acid is used not only as dopant, but also as surfactant in our reaction system.
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A new blend system consisting of an amorphous sulfonated poly[bis(benzimidazobenzisoquinolinones)] (SPBIBI) and the semi-crystalline poly(vinylidene fluoride) (PVDF) was prepared for proton exchange membranes. The miscibility behavior of a series of blends of SPBIBI with PVDF at various weight ratios was studied by WXRD, DSC and FTIR. The properties of the blend membranes were investigated, and it was found that the introduction of PVDF in the SPBIBI matrix altered the morphological structure of the blend membranes, which led to the formation of improved connectivity channels. For instance, the conductivity of the blend membrane containing 10 wt% PVDF displayed the highest proton conductivity (i.e., 0.086 S cm(-1)) at room temperature, a value almost twofold that of the pristine SPBIBI membranes (i.e., 0.054S cm(-1)) under identical conditions.
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Mg-5Al-0.3Mn-xCe (x = 0-3, wt.%) alloys were prepared by metal mould casting method. The microstructures and mechanical properties were investigated. The results revealed that the main phases of as-cast Mg-5Al-0.3Mn alloy consist of alpha-Mg matrix and beta-Mg17Al12 phase. With the addition of Ce element, Al11Ce3 precipitates were formed and mainly aggregated along the grain boundaries. The amount of the Al11Ce3 precipitates increased with increasing addition of Ce, but the amount of beta-Mg17Al12 phase decreased. The highest tensile strength was obtained in Mg-5Al-0.3Mn-1.5Ce alloy. The ultimate tensile strength (UTS), yield strength (YS) and elongation at room temperature are 203 MPa, 88 MPa and 20%, separately.
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Effect of cerium on the microstructure and electrochemical performance of the Ti0.25V0.35-xCexCr0.1Ni0.3 (x = 0, 0.005) electrode alloy was investigated by X-ray diffraction (XRD), field emission scanning electron microscopy/energy dispersive X-ray spectrometry (FESEM-EDS), and electrochemical impedance spectroscopy (EIS) measurements. On the basis of XRD and FESEM-EDS analysis, the alloy was mainly composed of V-based solid solution with body-centered-cubic structure and TiNi-based secondary phase. Ce did not exist in two phases, instead, it existed as Ce-rich small white particles, with irregular edges, distributed near the grain boundaries of the V-based solid solution phase. Discharge capacity, cycle stability, and high-rate discharge ability of the alloy electrode were effectively improved with the addition of Ce at 293 K. It was very surprising that the charge retention was abnormal with larger discharge capacity after standing at the open circuit for 24 h. EIS indicated that addition of Ce improved the dynamic performance, which caused the charge transfer resistance (R-T) to decrease and exchange current density (I-0) to increase markedly. The exchange current density of the electrochemical reaction on the alloy surface with Ce addition was about 2.07 and 3.10 times larger than that of the alloy without Ce at 303 and 343 K, respectively.
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采用氯化原位接枝法合成主链为氯化聚乙烯(CPE)、支链为丙烯酸-2-羟基乙酯(HEA)的官能化接枝聚合 物(CPE-g-HEA),制备CPE-g-HEA/2,4-二异氰酸甲苯酯(TDI)热塑性弹性体,并对其性能进行研究。结果表明, CPE-g-HEA/TDI热塑性弹性体的物理性能较好;与溶液法产物相比,共混法CPE-g-HEA/TDI热塑性弹性体的强度 较大、相对分子质量较小、相对分子质量分布较宽,热行为基本无变化;共混法CPE-g-HEA/TDI热塑性弹性体的反 应温度应控制在60~70℃,共混次数(即打三角包次数) 为150次时拉伸强度较高、80次时拉断伸长率较高,HEA/TDI摩尔比为1/0.5时拉伸强度较高。
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Negative differential resistance (NDR) and memory effect were observed in diodes based on 1,4-dibenzyl C60 (DBC) and zinc phthalocyanine doped polystyrene hybrid material. Certain negative starting sweeping voltages led to a reproducible NDR, making the hybrid material a promising candidate in memory devices. It was found that the introduction of DBC enhanced the ON/OFF current ratio and significantly improved the memory stability. The ON/OFF current ratio was up to 2 orders of magnitude. The write-read-erase-reread cycles were more than 10(6), and the retention time reached 10 000 s without current degradation.