986 resultados para 1995_01090439 TM-4 4300203
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土壤有机碳是陆地生态系统的一个动态组成部分,其储量、分布及其转化在陆地碳循环中起着重要的作用,是土壤肥力的核心指标之一。土壤有机碳含量的多少及其空间分布特性受气候、母质、地形等结构性因子以及施肥、耕作等随机性因子的影响。作为陆地生态系统中的一个区域化随机变量,土壤有机碳在系统内部垂直和水平方向上发生变化的同时,参与大气圈和生物圈这两个碳库之间的循环。为了揭示土壤有机碳的空间分布特性,传统统计学、地统计学、遥感与地理信息系统等方法被相继引入且逐渐走向成熟,其中,利用遥感与地理信息系统相结合的方法来反演土壤有机碳库储量及其空间分布格局为越来越多的专家学者所重视。本文在对不同方法基本理论进行简单阐述的基础上,对利用Landsat TM影像分析表层土壤有机碳格局的可行性进行了分析,并就遥感技术在反演表层土壤有机碳的空间分布格局中的应用前景进行了展望。 以黑龙江省部分黑土地区为研究对象,在不同时空尺度下分析了表层土壤有机碳与Landsat TM影像的TM1-TM5、TM7六个波段以及由其计算出的NDVI、NDTI、NDI5、NDI7、NDSVI、SAVI、RDVI和MSAVI 8个遥感指数之间的相关性。结果表明当Landsat TM影像的成像时间为2002年9月份时:(1)小尺度下表层土壤有机碳与TM1极显著相关(r=0.32, p<0.01),与TM2、TM3和NDSVI显著相关(p<0.05),相关系数分别为r=0.27,r=-0.29,r=0.26。(2)大尺度下,表层土壤有机碳与TM1、TM2、TM5和NDI5存在极显著的正相关(p<0.01),相关系数分别为r=0.30,r=0.34,r=0.35,r=0.32;而与NDI7之间存在显著相关性(r=0.27, p=0.02)。(3)当空间尺度一定时,在不同的时间尺度下与表层土壤有机碳具有显著相关性的遥感指标不同。(4)在大尺度下利用遥感技术测定法得到的回归模型对表层土壤有机碳空间分布格局具有较好的预测效果(R2=0.7097, p<0.05);(5)在大尺度下海拔高于200 m的地区表层土壤有机碳浓度显著高于海拔低于200 m的地区(p<0.05)。 通过分别利用地统计方法和遥感技术测定法分析海伦市表层土壤有机碳的空间分布格局,以步长为6170m时球状模型对表层土壤有机碳进行了拟合并利用Kriging插值方法得到了海伦市表层土壤有机碳分布格局;将这一结果与我们利用Landsat TM影像通过遥感技术测定方法得到表层土壤有机碳空间格局进行比较发现:在精度一致的前提下,遥感技术测定法在所需样本数量约为地统计方法的一半,同时在所消耗的人力、物力以及在时间上的循环周期等方面,遥感技术测定方法与地统计方法相比也有着明显的优势。
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The large uncertainties in estimates of cropland area in China may have significant implications for major cross-cutting themes of global environmental change-food production and trade, water resources, and the carbon and nitrogen cycles. Many earlier studies have indicated significant under-reporting of cropland area in China from official agricultural census statistics datasets. Space-borne remote sensing analyses provide an alternative and independent approach for estimating cropland area in China. In this study, we report estimates of cropland area from the National Land Cover Dataset (NLCD-96) at the 1:100,000 scale, which was generated by a multi-year National Land Cover Project in China through visual interpretation and digitization of Landsat TM images acquired mostly in 1995 and 1996. We compared the NLCD-96 dataset to another land cover dataset at I-km spatial resolution (the IGBP DIScover dataset version 2.0), which was generated from monthly Advanced Very High Resolution Radiometer (AVHRR)-derived Normalized Difference Vegetation Index (NDVI) from April, 1992 to March, 1993. The data comparison highlighted the limitation and uncertainty of cropland area estimates from the DIScover dataset. (C) 2003 Elsevier Science B.V. All rights reserved.
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The ligands 4,4,4-trifluoro-1-phenyl-1.3-butanedione (Hbfa) and 1,10-phenanthroline (phen) were used to prepare ternary lanthanide (Ln) complexes [Dy(bfa)(3)phen and Tm(bfa)(3)phen]. Crystal data: Dy(bfa)(3)phen C(42)H(26)FqN(2)O(6)Dy, triclinic, P (1) over bar, a= 9.9450(6) angstrom, b = 14.0944(9) angstrom, c = 14.6043(9) angstrom, alpha = 82.104(1)degrees, beta = 87.006(1)degrees, gamma = 76.490(1)degrees, V = 1971.1(2)angstrom(3), Z = 2; Tm(bfa)(3)phen C42H26F9N2O6Tm, triclinic, P (1) over bar, a = 9.898(5)angstrom, b = 13.918(5)angstrom, c = 14.753(5)angstrom, a = 83.517(5)degrees, alpha = 86.899(5)degrees, gamma = 76.818(5)degrees, V = 1965.3(14)angstrom(3), Z = 2. The coordination number of the central Ln(3+) (Ln = Dy, Tm) ion is eight, with six oxygen atoms from three Hbfa ligands and two nitrogen atoms from the phen ligand.
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LaAlO3:Tm3+ and LaAlO3:Tb3+ phosphors were prepared through a Pechini-type sol-gel process. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), photoluminescence, and cathodoluminescence (CL) spectra were utilized to characterize the synthesized phosphors. The XRD results reveal that the fully crystalline pure LaAlO3 Phase can be obtained at 800 degrees C. The FE-SEM image indicates that the phosphor samples are composed of aggregated spherical particles with sizes ranging from 40 to 80 nm. Under the excitation of ultraviolet light (230 nm) and low-voltage electron beams (1-3 kV), the LaAlO3:Tm3+ and LaAlO3:Tb3+ phosphors show the characteristic emissions of Tb3+ (D-1(2)-> H-3(6,4),F-3(4) transitions) and Tm3+ (D-5(3,4)-> F-7(6,5,4,3) transitions) respectively. The CL of the LaAlO3:Tm3+ phosphors have high color purity and comparable intensity to the Y2SiO5:Ce3+ commercial product, and the CL colors of Tb3+-doped LaAlO3 phosphors can be tuned from blue to green by changing the doping concentration of Tb3+ to some extent.
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Five new complexes based on rare-earth-radical [Ln(hfac)(3)(NIT-5-Br-3py)](2) (Ln=Pr (1), Sm (2), Eu (3), Tb (4), Tm (5); hfac = hexafluoroacetylacetonate; NIT-5-Br-3py = 2-(4,4,5,5-tetramethyl-3-oxylimidazoline-1-oxide)-5-bromo-3-pyridine) have been synthesized and characterized by X-ray crystal diffraction. The single-crystal structures show that these complexes have similar structures, in which a NIT-5-Br-3py molecule acts as a bridging ligand linking two Ln(III) ions through the oxygen atom of the N-O group and nitrogen atom from the pyridine ring to form a four-spin system. Both static and dynamic magnetic properties were measured for complex 4, which exhibits single-molecule magnetism behavior.
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beta-NaYF4:Ln(3+) (Ln = Eu, Tb, Yb/Er, and Yb/Tm) hexagonal microprisms with remarkably uniform morphology and size have been synthesized via a facile hydrothermal route. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) spectra as well as kinetic decays were used to characterize the samples. It is found that sodium citrate as a shape modifier introduced into the reaction system plays a critical role in the shape evolution of the final products. Furthermore, the shape and size of the products can be further manipulated by adjusting the molar ratio of citrate/RE3+ (RE represents the total amount of Y3+ and the doped rare earth elements such as Eu3+, Tb3+, Yb3+/Er3+, or Yb3+/Tm3+). Under the excitation of 397 nm ultraviolet light, NaYF4:xEu(3+) (x = 1.5, 5%) shows the emission lines of Eu3+ corresponding to D-5(0-3) -> F-7(J) (J = 0-4) transitions from 400 to 700 nm (whole visible spectral region) with different intensity, resulting in yellow and red down-conversion (DC) light emissions, respectively.
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This paper presents the results of the adsorption of heavy rare earth ions (Gd(III), Tb(III), Dy(III), Ho(III), Er(III), Tm(III), Yb(III), Lu(III) and Y(III)) from hydrochloric acid solutions at 30 degreesC by the extraction resin containing 1-hexyl-4-ethyloctyl isopropylphosphonic acid (HEOPPA), which has higher steric hindrance, higher selectivities and lower extraction and stripping acidity than di(2-ethylhexyl)phosphoric acid (DERPA) or 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (HEH/EHP). The dependence of acid concentration, flow rate and amounts of rare earth ions sorbed on the separation of Er-Tm, Tm-Yb and Er-Tm-Yb mixtures has been studied. The baseline chromatographic separation of Er-Tm-Yb mixture has been observed. Satisfactory results with purity and yield of Tm2O3>99.71% and >71.25%, Er2O3>99-81% and >94.17%, and Yb2O3>99.74% and >89.83%, respectively, have been obtained. The parameters such,as resolution, separation factors and efficiencies have been determined as a function of acidity, loading of rare earth elements and flow rates. The stoichiometry of the extraction of rare earth ions has been suggested as well.
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Chemical bond parameters in RBa2Cu4O8(R = Dy, Ho, Er, Tm, Yb) and Y2Ba4Cu7O14.3 were calculated by using complex chemical bond theory. The results indicated that the bond covalency in CuO chain was larger than that in CuO2 plane. For metal atoms, the bond covalency of five coordinated case was larger than that of six coordinated case.
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使用复杂晶体上化学键理论计算了 RBa2 Cu4 O8(R=Dy,Ho,Er,Tm ,Yb)和 Y2 Ba4 Cu7O14 .3 的化学键参数 .结果表明 ,Cu O链上的 Cu O键共价性大于它们在 Cu O2 面的共价性 .当金属元素与氧形成五配位时 ,其共价性的数值大于这些元素在六配位时的情形
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Extraction resins, of the type of;levextrel, (which is a collective term for styrene/divinylbenzene based copolymers of predominantly macroporous structure that contain a selective extractant) are important for the recovery and separation of metal ions, as they combine features of solvent extraction and ion exchange resins. This paper presents the results of the adsorption of heavy rare earth ions (Ho(III), Er(III), Tm(III), Yb(III), Lu(III) and Y(III)) from hydrochloric acid solutions at 0.2 mol/L ionic strength and 50 degrees C by the extraction resin containing di (2,4,4-trimethyl pentyl) phosphinic acid (Cyanex 272) and the chromatographic separation of (Er(III), Tm(III) and Yb(III)). Technological separation products, with purity and yield of Tm2O3 >99.97%, >80%, Er2O3 >99.9%, >94% and Yb2O3 >99.8%, >80% respectively, have been obtained from a feed having the composition Tm2O3 60%, Er2O3 10%, and Yb2O3 3%, the others 27%. The distribution coefficients, extraction equilibrium constants and separation factors have been determined as a function of acidity, loading of the resin and rare earths, flow rates and column ratios. The resolutions and efficiencies of separation of Er/Tm/Yb each other have been calculated. The stoichiometry of the extraction of rare earth ions has been suggested as well.
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RBa2Cu3O7 (R = Pr, Sm, Eu, Gd, Dy, Y, Ho, Er, Tm) has been studied using complex chemical bond theory. The results indicated that with the decreasing of R radius, the ionicities for all considered types of bond decrease. This is in good agreement with the experimental fact that T-c decreases with the decreasing of R radius. PrBa2Cu3O7 with no Ba-site Pr in this calculation is also predicted to be a superconductor. This supports the conclusion obtained by Blackstead et al. The ionicity for each bond obeys the following order: Ba-O > R-O > Cu(2)-O(1) > Cu(2)-O(2,3) > Cu(1)-O(4) similar to Cu(1)-O(1).
Resumo:
近二十多年来,在异成二烯的络合催化聚合中,由Ni、Co、Ti及稀土等过渡金属元素络合物组成的催化体系,研究报道得很多,有些已投入工业生产。但由最常见的过渡金属元素铁络合物组成的催化体系,对异成二烯聚的聚合却不多见。本工作研究了三乙酰基丙酮铁为主催化剂,烷基铝为助催化剂,添加含氮类给电子试剂组成三元体系,对异成二烯聚合的催化作用。Fe(a cac)_3 - Al(i-Bu)_3二元体系不能引起异成二烯聚合,而加入少量的含氮类给电子试剂如邻菲啰啉、α,α'-联吡啶等,催化活性显著提高。聚合活性与含氮类给电子试剂的性质有关,并随着下列顺序依次递减:邻菲啰啉、α,α'-联吡啶、对苯二胺、邻苯二胺,对硝基苯胺、邻硝基苯胺;吡啶和已二胺对催化活性的提高几乎没有贡献。烷基铝的不同对催化活性也有明显的影响。其活性顺序为:Al(i-Bu)_3 approx Al Eτ_3 > Al(i-Bu)_2H。首次合成了结晶的3,4-聚异成二烯,3,4-链节含量为70%左右时,Tm为121 ℃左右, Tc为65 ℃左右,透射电镜下观察到结晶的3,4-聚异成二烯具有球晶状结构。初步研究了铁系三元催化体系的反应机理,设想铁化合物和烷基铝生成的烷基铁必须与含氮类给电子试剂作用才能形成活性中心;可见光谱和催化活性实验数据证实了含氮类给电子试剂参与活性中心的形成,并起着稳定活性中心的作用。本文详细地研究了Fe(a cac)_3 - phen - Al(i-Bu)_3催化体系对异成二烯的聚合,考察了起始单体浓度、聚合温度,催化剂总用量以及催化剂各组分配比对聚合速率、聚合物的特性粘数和链节结构的影响,从实验结果讨论了Fe(a cac)_3 - phen - Al(i-Bu)_3体系催化异成二烯的聚合机理,并进行了一些动力学的基本计算,得到了与实验结果基本相符的结果,解释了一些实验现象。铁系聚异成二烯橡胶的表征工作未见诸文献,本工作对铁系聚异成二烯生胶的结晶、力学、流变及阻尼性能作了较系统的研究,并对硫化胶的物理机械性能,弹性及阻尼性能作了初步的表征。铁系聚异成二烯橡胶在室温具有较好的阻尼性能,并且生热值和冲击弹性均较低,可作为室温阻尼材料使用。
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A new series of fully aromatic thermotropic liquid crystalline copolyesters were synthesized by thermal polycondensation of p-hydroxybenzoic acid (PHB), terephthalic acid (TPA), resorcinol (RES) and bis (4-hydroxyphenyl) methanone (BHP). The DSC traces of copolyesters exhibited two or three endotherms, the low temperature endotherm(Tm) of which indicated the transition from solid state to anisotropic phase. Observation under polarizing microscope and WAXD measurements suggested that the LC-phase formed immediately above Tm had a nematic character.
Resumo:
A partir dos anos 1970, a ocupação pelo homem do espaço do centro-oeste brasileiro apresentou um elevado crescimento devido a políticas de expansão agrícola. Este fato ocorreu por meio do alto grau de mecanização agrícola e aplicação de fertilizantes, visando elevados níveis de produção em diversas localidades, como o sudoeste do Estado de Goiás. Tal predicado da alta produtividade mantém-se até os dias atuais, indicando a grande intensidade da dinâmica de uso e cobertura das terras nesta região. Desta forma, tornase necessário o conhecimento da dinâmica e distribuição espacial dos padrões de uso e cobertura da terra, podendo fornecer subsídios a ações de planejamento agrícola sobre o espaço em alguns municípios do sudoeste goiano. Para isto, imagens orbitais do satélite Landsat TM-5 foram adquiridas em diferentes períodos do ciclo agrícola ao longo de 2007. Informações complementares acerca do uso regional foram utilizadas para apoiar a interpretação e classificação, principalmente a partir dos dados obtidos em campo. Os mapas de uso e cobertura da terra para os municípios de Rio Verde, Acreúna, Santo Antônio da Barra, Santa Helena de Goiás, Montividiu e Paraúna foram obtidos utilizando ferramentas do programa Spring 4.3.3 como a segmentação de imagens, bem como o classificador semi-automático Bhattacharya Distance, sendo estabelecidas dez classes temáticas, com base na legenda proposta pelo IBGE e Corine. A análise multitemporal, assim como a segmentação mostraram-se eficientes na distinção das classes de uso e cobertura da terra da região. A classe de uso destinada ao plantio da soja apresentou o maior percentual da área, mudando para culturas safrinha, solo exposto ou pousio no inverno. Outras classes também merecem destaque como a Pastagem e a Cana-de-açúcar, que apresentaram distribuição espacial bastante concentrada. Este mapeamento fornece subsídios ao planejamento do uso e ocupação das terras na região, considerando os aspectos ambientais e sociais, assegurando maior produtividade agrícola, visando um manejo sustentável das terras e a qualidade de vida ao homem do campo.