996 resultados para 784
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农田防护林体系结构优化配置研究范志平,姜凤歧,林鹤鸣,朱教君(中国科学院沈阳应用生态研究所沈阳110015)为达到农田防护林防护效益和经济效益最大并永续利用,防护林体系必须具有在空间上布局的合理性及树种、群落和林分的多样性和稳定性特征。因此,构筑大面...
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通过对地带性常绿阔叶林、杉木人工林、农田、竹林等不同土地利用方式下土壤有机质总量、活性有机质及其组分的研究,发现土地利用方式对土壤有机质和活性有机质各组分的影响差异显著,其中阔叶林含量最高,杉木人工林低于阔叶林,竹林和农田最低。这些差别主要是由于凋落物的数量、质量以及各种管理措施不同所致
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根据东北沙质荒漠化地区呼伦贝尔沙地、科尔沁沙地的 72个沙地植物群落样地、2 76种植物的调查数据 ,进行双向指示种分析 (TWINSPAN) ,结合DCA排序得到符合客观实际的分类结果 ,初步建立了中国东北沙质荒漠化地区植被分类系统 ,6个植被型 ,11个植被亚型 ,40个群系 ,5 5个群丛
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It was reported for the first time that the electrocatalytic activity of the Carbon-supported Pd-Ir (Pd-Ir/C) catalyst with the suitable atomic ratio of Pd and Ir for the oxidation of formic acid in the direct formic acid fuel cell (DFAFC) is better than that of the Carbon-supported Pd (Pd/C) catalyst, although Ir has no electrocatalytic activity for the oxidation of formic acid. The potential of the anodic peak of formic acid at the Pd-Ir/C catalyst electrode with the atomic ratio of Pd and Ir = 5:1 is 50 mV more negative than that and the peak current density is 13% higher than that at the Pd/C catalyst electrode.
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The electrolytic deposition and diffusion of lithium onto bulk magnesium-9 wt pct yttrium alloy cathode in molten salt of 47 wt pct lithium chloride and 53 wt pct potassium chloride at 693 K were investigated. Results show that magnesium-yttrium-lithium ternary alloys are formed on the surface of the cathodes, and a penetration depth of 642 mu m is acquired after 2 hours of electrolysis at the cathodic current density of 0.06 A center dot cm(-2). The diffusion of lithium results in a great amount of precipitates in the lithium containing layer. These precipitates are the compound of Mg41Y5, which arrange along the grain boundaries and hinder the diffusion of lithium, and solid solution of yttrium in magnesium. The grain boundaries and the twins of the magnesium-9 wt pct yttrium substrate also have negative effects on the diffusion of lithium.
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series of a donor-acceptor-donor type of near-infrared (NIR) fluorescent chromophores based on [1,2,5]thiadiazolo[3,4-g]quinoxaline (TQ) as an electron acceptor and triphenylamine as an electron donor are synthesized and characterized. By introducing pendent phenyl groups or changing the pi-conjugation length in the TQ core, we tuned tile energy levels of these chromophores, resulting in the NIR emission in a range from 784 to 868 nm. High thermal stability and glass transition temperatures allow these chromophores to be used as dopant emitters, which can be processed by vapor deposition for the fabrication of organic light-emitting diodes (OLEDs) having the multilayered structure of ITO/MoO3/NPB/Alq(3):dopant emitter/BCP/Alq(3)/LiF/Al. The electroluminescence spectra of the devices based on these new chromophores cover a range from 748 to 870 nm. With 2 wt % of dopant 1, the LED device shows an exclusive NIR emission at 752 nm with the external quantum efficiency (EQE) as high as 1.12% over a wide range of current density (e.g., around 200 mA cm(-2)).
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Crystal structure and polymorphism induced by uniaxial drawing of a poly(aryl ether ketone) [PEDEKmK] prepared from 1,3-bis(4-fluorobenzoyl)benzene and biphenyl-4,4'-diol have been investigated by means of transmission electron microscopy (TEM), electron diffraction (ED), wide-angle X-ray diffraction (WAXD), and differential scanning calorimetry (DSC) techniques. The melting and recrystallization process in the temperature range of 250-260 degrees C, far below the next melting temperature (306 degrees C), was identified and found to be responsible for the remarkable changes in lamellar morphology. Based on WAXD and ED patterns, it was found that crystal structure of isotropic-crystalline PEDEKmK obtained under different crystallization conditions (melt-crystallization, cold-crystallization, solvent-induced crystallization, melting-recrystallization, and crystallization from solution) keeps the same mode of packing, i.e., a two-chain orthorhombic unit cell with the dimensions a = 0.784 nm, b = 0.600 nm, and c = 4.745 nm (form I). A second crystal modification (form II) can be induced by uniaxial drawing above the glass transition temperature, and always coexists with form I. This form also possesses an orthorhombic unit cell but with different dimensions, i.e., a = 0.470 nm, b = 1.054 nm, c = 5.064 nm. The 0.32 nm longer c-axis of form II as compared with form I is attributed to an overextended chain conformation due to the expansion of ether and ketone bridge bond angles during uniaxial drawing. The temperature dependence of WAXD patterns for the drawn PEDEKmK suggests that form II can be transformed into the more stable form I by relaxation of overextended chains and relief of internal stress at elevated temperature in absence of external tension.
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The ultrafine LaFeO3 with particle size of 12 similar to 75nm was prepared by sol-gel method. In the process of gel to ultrafine powder, the weight loss reached 90%. The lowest forming temperature of single phase crystalline LaFeO3 ultrafine powder was ob
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本文使用溶胶-凝胶法制备了平均粒径为12~75nm的LaFeO_3超微粒子.从凝胶至超微粒子的过程中,失重达90%.纯相晶态的LaFeO_3超微粒子的最低生成温度为600℃.粒子平均粒径随着灼烧温度的升高而显著增大.通过对不同粒径的LaFeO_3超微粒子表面光电压光谱的研究发现,随着粒子粒径的增大,粒子内部逐渐形成长程有序的晶体结构和完整的能带结构.粒子粒径越小,表面特性越明显.
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REL3.H2O (RE=Y, La is similar to Lu; HL = o-chlorobenzoic acid) were synthesized. Their thermal decomposition and IR spectra were studied. The crystal structures of the complexes of neodymium, terbium and lutetium were determined by X-ray diffraction method. They crystallize in the monoclinic space group P2(1)/n and show infinite chain structures. The coordination numbers of rare earth ions are nine.
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本文合成了邻氯苯甲酸与十五种稀土的配合物REL_3·H_2O(RE=Y,La~Lu,HL=ClC_6H_4CO_2H),研究了它们的热分解及红外光谱.测定了钕、铽及镥三种稀土的配合物晶体结构,均属单斜晶系,空间群P2_1/n,稀土离子配位数为9,配合物呈无限链状聚合结构.
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Anti-lipopolysaccharide factor (ALF) represents one kind of basic proteins, which binds and neutralizes LPS and exhibits strong antibacterial activity against Gram-negative R-type bacteria. The ALF gene of Chinese mitten crab Eriocheir sinensis (Milne Edwards, 1853) (denoted as EsALF) was identified from haemocytes by expressed sequence tag (EST) and PCR approaches. The full-length cDNA of EsALF consisted of 700 nucleotides with a canonical polyadenylation signal-sequence AATAAA, a polyA tail, and an open-reading frame of 363 bp encoding 120 amino acids. The high similarity of EsALF-deduced amino acid sequence shared with the ALFs from other species indicated that EsALF should be a member of ALF family. The mRNA expression of EsALF in the tissues of heart, gonad, gill, haemocytes, eyestalk and muscle was examined by Northern blot analysis and mRNA transcripts of EsALF were mainly detected in haemocytes, heart and gonad. The temporal expression of EsALF in haemocytes after Vibrio anguillarum challenge was recorded by quantitative real-time RT-PCR. The relative expression level of EsALF was up-regulated rapidly at 2 h post-injection and reached 3-fold to that in blank group. After a drastic decrease to the original level from 4 to 8h, the expression level increased again and reached 4-fold to that in the blank group at 12 h post-injection. The genomic DNA sequence of EsALF gene consists of 1174bp containing three exons and two introns. The coding sequence of the EsALF mature peptide was cloned and expressed in Escherichia coli BL21(DE3)-pLysS to further elucidate its biological functions. The purified recombinant product showed bactericidal activity against both Gram-positive (G(+)) and Gram-negative (G(-)) bacteria, which demonstrated that the rEsALF was a broad-spectrum antibacterial peptide. All these results indicated that EsALF was an acute-phase protein involved in the immune responses of Chinese mitten crab, and provided a potential therapeutic agent for disease control in aquaculture. (c) 2007 Elsevier Ltd. All rights reserved.