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根据安塞水土保持试验站1993~2002年林地径流小区的降雨产流产沙的定位观测资料及2002年土壤含水量资料,分析了不同树种对坡面尺度降雨产流产沙及土壤水分的影响。结果表明:场降雨径流小区的产流量、产沙量与降雨量具有较好的相关性;多元回归分析表明,场降雨产流量和产沙量与降雨量和最大30min雨强的乘积呈正相关,与植被覆盖度呈负相关,场降雨产沙量回归方程复相关系数为0.253,各处理场降雨产流量回归方程复相关系数的变化范围为0.465~0.723,均达到了极显著的水平(P<0.01)。同时,各树种均具有良好的减流减沙功能,与农地相比,年均产流量和产沙量分别减少4.8%~52.9%和26.8%~86.0%;沙棘纯林及其混交林的减流减沙效益优于油松纯林。同时,沙棘纯林及其各混交林在造林初期就表现出良好的减流减沙效益,随着树龄的增长,其作用更加明显;而油松纯林在造林初期作用不明显,甚至出现产流量和产沙量大于农地的现象,但随着树龄的增长,减流减沙作用逐渐呈现并增大。沙棘纯林及其混交林30cm以下土壤含水量在整个生长季中均呈递减趋势,生长季初(4月份)土壤含水量最高,而生长季末(10月份)降到最低值。2002年沙棘纯林的...

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在对遥感数据进行景观分类和对环境因子进行空间表达基础上 ,在地理信息系统的支持下 ,确定长白山自然保护区森林景观分布的环境 (包括年均温、年降水量、坡度和坡向 )范围 .结果表明 ,从苔原、岳桦、云冷杉到阔叶红松林 ,最适海拔高度范围依次为 1780~ 2 2 12、170 5~ 195 6、10 4 2~ 16 2 5、82 3~ 1184m ;最适温度范围分别为 - 4 .75~ - 2 .4 0℃、- 3.4 2~ - 2 .0 7℃、- 1.4 9~ 1.39℃、0 .71~ 2 .37℃ ;最适降水范围分别为 10 34~ 1110、10 14~ 10 6 0、883~ 10 17、82 4~ 92 5mm ;长白山自然保护区的森林景观主要分布在平、缓坡地上 ,并与坡向关系密切 ,苔原在各个坡向上均有分布 ,且在各个坡向上分布面积的变化不大 ;岳桦、云冷杉林、阔叶红松林、山杨白桦林主要呈现北、西北向分布 ,其次为东北、西向分布 ;落叶松林主要为东北向分布 ,其次为东和北向分布 ;疏林主要为西向分布 ,其次为西南、西北和南向分布 ;风倒区主要为西、西南、西北向分布 .

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Among complex oxides containing rare earth and manganese BaLn(2)Mn(2)O(7)( Ln = rare earth) with the layered perovskite type and Ln(2)(Mn, M)O-7 with pyrochlore-related structure were studied since these compounds show many kinds of phases and unique phase transitions. In BaLn(2)Mn(2)O(7) there appear many phases, depending on the synthetic conditions for each rare earth. The tetragonal phase of so-called Ruddlesden-Popper type is the fundamental structure and many kinds of deformed modification of this structure are obtained. For BaEu2Mn2O7 at least five phases have been identified from the results of X-ray diffraction analysis with the space group P4(2)/mnm, Fmmm, Immm and A2/m in addition to the fundamental tetragonal I4/mmm phase. In the pyrochlore-related type compounds, Ln(2)Mn(2-x)M(x)O(7)(M = Ta, Nb, W etc), there also appear several phases With different crystal structures. With regard to every rare earth, Ln(2)MnTaO(7) phase is stable only for excess Ta and can be obtained under high oxygen partial pressure process. This group has trigonal structure with zirkelite type ( P3(1)21 space group).

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通过环辛烯、环辛二烯和降冰片烯与ω-十一烯酸乙二醇二酯的易位共聚合及氢化反应合成了烯烃共聚酯 .改变聚合条件 ,可控制烯烃共聚酯的分子量、极性单体插入率和熔融温度等性质 .两段聚合过程适于制备高分子量的烯烃共聚酯 ,聚合物收率达 90 %,极性单体的插入率大于 1 0 %,熔融温度高达 120℃.

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Rhodamine B (RB)-doped organic-inorganic silica films and their patterning were fabricated by a sol-gel process combined with a soft lithography. The resulted film samples were characterized by atomic force microscope (AFM), optical microscope and UV/Vis absorption and photoluminescence excitation and emission spectra. The effects of the concentration of the RB dye and heat treatment temperature on the optical properties of the hybrid silica films have been studied. Four kinds of patterning structures with film line widths of 5, 10, 20 and 50 mum have been obtained by micromolding in capillaries by a soft lithography technique. The RB-doped hybrid silica films present a red color, with an excitation and emission bands around 564 and 585 mum, respectively. With increasing the RB concentration, the emission intensity of the RB-doped hybrid silica films increases and the emission maximum presents a red shift. The emission intensity of the films decreases with increasing the heat treatment temperatures.

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The influences of different cations on plasmid DNA network structures on a mica substrate were investigated by atomic force microscopy (AFM). Interactions between the DNA strands and mica substrate, and between the DNA strands themselves were more strongly influenced by the complex cations (Fe(phen)(3)(2+), Ni(phen)(3)(2+), and Co(phen)(3)(3+)) than by the simple cations (Mg2+, Mn2+, Ni2+, Ca2+, Co3+). The mesh height of the plasmid DNA network was higher when the complex cations were added to DNA samples. The mesh size decreased with increasing DNA concentration and increased with decreasing DNA concentration in the same cation solution sample. Hence, plasmid DNA network height can be controlled by selecting different cations, and the mesh size can be controlled by adjusting plasmid DNA concentration.

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Persistent spectral hole burning spectroscopy is applied to evaluate the low-temperature relaxation around the dye molecules doped in several types of polymers. The doped dye is tetraphenylporphine, and the measured polymers are vinyl polymers and main chain aromatic polymers. The changes of microscopic environments around the dye are evaluated from the changes in the hole profiles during temperature cycling experiments. The relaxation behavior of the polymers is discussed in relation to their chemical structures. (C) 1999 John Wiley & Sons, Inc.

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The reaction of anhydrous PrCl3 with Na(C9H7) in 1.2 mole ratio in THF gives [(C9H7)(2)PrCl(THF)](2)1. 1 crystallized in monoclinic system, space group P2(1)/c with a = 7.808(2), b = 17.796(6), c = 14.070(4) Angstrom, beta = 93.97(2)degrees, V= 1950.3(9) Angstrom(3), Dcalcd = 1.63 g/cm(3) and Z = 2. Each Pr ion is surrounded by two indenyl, two Cl and one THF in a roughly trigonal bipyramid arrangement with average Pr-C(ring) and Pr-Cl distances of 2.81 and 2.84 Angstrom. The reaction of LaCl3 with Na(C9H7) in 1:3 mole ratio gives (C9H7)(3)LaTHF 2, which crystallizes in the monoclinic space group P2(1)/a with unit cell constants a = 21.871(8), b = 10.585(3), c = 23.652(7) Angstrom,beta = 114.62(2)degrees, V = 4977.9 Angstrom(3) and Z = 8. (C) 1997 Elsevier Science S.A.

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The crystal structure of thiamine iodide sesquihydrate has been determined by X-ray diffraction methods as a host-guest model for coenzyme-substrate interactions. The asymmetric unit contains two chemical units. Both the thiamine molecules A and B, which are crystallographically independent, assume the usual F conformation and have a disordered hydroxyethyl side chain. An iodide anion (or a water molecule) bridges the pyrimidine and thiazolium rings of molecule A (or B) by forming a hydrogen bond with the amino group and an electrostatic contact with the thiazolium ring to stabilize the molecular conformation. In the crystal the thiamine molecules self-associate to form a pipe-like polymeric structure, in which four thiamine hosts surround an iodide guest and hold it through C(2)-H...I hydrogen bonds and thiazolium...I electrostatic interactions. Crystal data: C12H17N4OS+.I- . 1.5 H2O, monoclinic, P2(1)/c, a = 12.585(2), b = 25.303(5), c = 12.030(2) angstrom, beta = 115.15(1)degrees, V = 3468(1) angtrom3, Z = 8, D(c) = 1.606 g cm-3, R = 0.045 for 3328 observed reflections.

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本文采用环氧乙烷与环氧丙烷共聚合成了一系列低分子量的聚醚(PEP),并用PEP的单烯丙基醚借助氢化硅烷基化反应(Hydrosilylation)制备出一种新型聚硅氧烷接枝聚醚的高分子电解质主体材料(PAEPS).分别讨论了共聚物组成、盐的种类和浓度等因素对交联PAEPS与碱金属盐络合物电解质膜离子电导的影响.结果表明,PAEPS与碱金属盐络合物的室温电导率较纯线型PEO提高两至三个数量级,电导率随温度变化关系基本上符合VTF方程,属于典型的非晶电解质行为.

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本文采用Cole-Cole,Fuoss-Kirkwood经验相关时间分布模型和构象跳跃,高聚物局部主链运动阻尼取向扩散分子模型,对1,2-聚丁二烯在溶液中的~(13)C-NMR自旋-晶格弛豫时间nT_1和核Overhauser效应(NOE)值进行了数值拟合。用拟合所得分子运动参数讨论了1,2-聚丁二烯微观分子运动对链结构和温度的依赖性。

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本文研究了在聚乙烯醇-124存在下,钨(V)-SCN~--乙基罗丹明B超高灵敏显色体系。缔合物λ_(max)=585nm,表观摩尔吸光系数ε_(585)=1.9×10~6L·mol~(-1)·cm~(-1)。钨浓度在0.1~1.5μg/25ml范围内符合比尔定律,方法曾用于水样及钢样中痕量钨的测定,结果较满意。