983 resultados para 7140-237


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以掷孢酵母作为伴生菌与氧化葡萄糖酸杆菌组成新混菌体系 ,对其产酸性能和特点进行了研究。实验室摇瓶结果显示 :新菌系混菌状态不同 ,产酸不同 ,以KGA含量为 4 8,小菌 /掷孢酵母为 31∶1种液接种时 ,最有利于产酸 ,增加接种生物量可提高产酸速度 ,缩短发酵周期 ,但不影响最终产酸量。相同条件下 ,新菌系产酸能力高于现有菌系 ,酸量增加 5mg/ml~ 7mg/ml,发酵周期缩短 6h~ 8h ,酸转化率提高 3%~ 4 % ,最高产酸点pH值下降约 0 5,表现出较大的产酸潜力和可修饰性

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通过对中国东北部2555种种子植物种的分布进行对比研究,划分之为27个地理成分和34个地理成分亚型,统计分析表明,本地区的种子植物除少数的世界分布种之外,温带、寒带和热带的种数分别占88.5、6.8和4.7%,说明植物区系基本上属温带性质.本地区种子植物中的特有植物共有117种,分属于6个地理成分和4个地理成分亚型之中,其丰富度在国内是较为偏低的.

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该文重新评估了Zodiac算法抗Square攻击的能力。Zodiac算法存在8轮Square区分器,该文首先根据算法的结构特性,给出了Zodiac的4个等价结构,而后利用等价结构得到了两个新的9轮Square区分器。利用新的区分器,对不同轮数的Zodiac算法实施了Square攻击,对12轮,13轮,14轮,15轮和16轮Zodiac的攻击复杂度分别为237.3,262.9,296.1,2137.1和2189.5次加密运算,选择明文数分别为210.3,211,211.6,212.1和212.6。结果表明:完整16轮192bit密钥的Zodiac算法是不抗Square攻击的。

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大规模动态地形场景的建模与仿真是计算机图形学与虚拟显示领域的重要课题之一。本文提出了一种基于隐式限制四叉树的地形建模方法,用四叉树标记数组代替四叉树节点结构与指针操作,不但节省了大规模地形数据集所占的存储空间,而且提高了节点的索引效率。另外,提出了基于高程值的地形纹理图像合成方法,根据地形采样点的高程值实时合成匹配地形特征的纹理图像。本文还给出了弹坑与车辙的建模方法。仿真结果表明,本文描述的方法可以实时获得逼真的大规模动态地形仿真效果。

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用四氢呋喃(THF)络合还原法分别合成并比较了碳载金(Au/C)、碳载铱(Ir/C)、碳载金.铱(Au-Ir/c)催化剂对氧气还原和甲酸氧化的电催化活性.发现3种催化剂对甲酸氧化都没有电催化活性;Au-Ir/C催化剂对氧还原的电催化活性要远好于Au/C和Ir/C催化剂.表明Au-Ir/C催化剂适合作为直接甲酸燃料电池(DFAFC)的阴极催化剂.

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A novel hydrogen peroxide biosensor was fabricated that is based on horseradish peroxidase-Au nanoparticles immobilized on a viologen-modified glassy carbon electrode (GCE) by amino cation radical oxidation in basic solution. The immobilized BAPV acts as a mediator and a covalent linker between GCE and the Au nanoparticles. The biosensor exhibited fast response, good reproducibility, and long-term stability.

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用溶液相金属盐沉积法在苯乙烯与4-乙烯基吡啶嵌段共聚物(PS-b-P4VP)胶束中制备了平均直径为12 nm的PS-b-P4VP/Co、PS-b-P4VP/CoSm(nCo∶nSm=3.8∶1,13.0∶1)、PS-b-P4VP/Sm纳米粒子。胶束溶液通过高温回流使磁性成核粒子和磁性金属原子的流动能力和扩散能力提高而获得尺寸均一的颗粒。

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Two mononuclear neutral copper(I) complexes, Cu(L-1)PPh3 (1), Cu(L-2)(PPh3)(2) (2) ([L-1](-) = [{N((C6H3Pr2)-Pr-i-2,6)C(H)}(2)CPh](-); [L-2](-) = [{N(C6H5)C(H)}(2)CPh](-)) have been synthesized and structurally characterized by X-ray crystallography. In complex 1, the copper(I) atom is in a distorted three-coordinate trigonal planar environment, whereas in complex 2 with the less sterically hindered beta-dialdiminato ligand, the copper(I) atom is the centre of a four-coordinate distorted tetrahedron. At room temperature complexes 1 and 2 in a film of PMMA exhibit green emission at 543 and 549 nm with lifetimes of 5.28 and 5.32 ns, respectively.

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采用X射线光电子能谱(XPS)技术研究了二氧化碳与环氧丙烷共聚反应的稀土三元催化剂,探讨了中心金属的X射线光电子能谱与催化活性间的关系,指出稀土三元催化剂的活性中心在于配位活化后的锌氧键,稀土盐通过与烷氧基锌形成双金属桥键,改变了活性中心的电子云分布,从而提高了反应活性.

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Flat-sheet microporous membranes from F2.4 for membrane distillation (MD) were prepared by phase inversion process. Dimethylacetamide (DMAC) and LiClO(4)(.)3H(2)O/trimethyl phosphate (TMP) were, respectively, used as solvent and pore-forming additives. The effects of casting solution composition, exposure time prior to coagulation and temperature of precipitation bath on F2.4 membrane structure were investigated. The morphology of resultant porous membrane was observed by scanning electron microcopy. Some natures of F2.4 porous membrane after drying in air, such as mechanical properties and hydrophobicity, were exhibited and compared with poly(vinylidene fluoride) (PVDF) membrane prepared by the same ways. Stress-at-break and strength stress of F2.4 microporous membrane are higher than that of PVDF membrane, and elongation percentage of F2.4 membrane at break is about eight-fold as great as that of PVDF membrane. Contact angle of F2.4 microporous membrane to water (86.6 +/- 0.51degrees) was also larger than that of PVDF mernbrane (80.0 +/- 0.78degrees). MD experiment was carried out using a direct contact membrane distillation (DCMD) configuration as final test to permeate performance of resultant microporous membrane.

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Solvent free polyaniline emeraldine base(EB) corrosion protection coating was prepared, employing aliphatic polyamine as solvent of EB as well as hardener of epoxy resin. This coating passed 2000h of salt fog test when the EB loading was about 1 wt%. The interaction between EB and iron indicated that EB acted as a "quasi-catalyst" to cause the formation of densed iron oxide film in the interface.