人工降雨条件下谷子地留茬的水土保持效应研究

通过人工模拟降雨试验研究了谷子地不同留茬高度及不同坡度的水土保持效应。结果表明,15cm留茬高度相对于未留茬处理径流量减少了18.6%,留茬5cm与10cm无显著减少径流作用;留茬能够减小产沙量14.36%～19.47%;5,10,及15cm留茬高度对产流时间没有显著影响,坡度的变化对产流时间无显著影响;坡度为10°时,径流对土壤的侵蚀最明显;留茬高度为15cm的处理水土保持效应最佳。

水体质量综合评价的物元模型

对水体的可拓性做了充分地分析和研究,说明了利用可拓学方法对水体质量进行分析评价的适宜性。并且应用可拓学的理论和方法,对水体的物征和质量特性进行了全面分析,建立了相应的物元模型,为水体的质量评价提供了一种新的科学方法。

黄土高原典型土壤矿物固定态铵变化的南北差异

采集从北向南依次分布的干润砂质新成土(神木)、黄土正常新成土(延安)和土垫旱耕人为土(杨陵)等典型土壤剖面0—200 cm土层土样,通过测定土样全氮和矿物固定态铵,以阐明黄土高原典型区域土壤全氮和矿物固定态铵及二者比率随地理位置和土层的变异规律,为全面了解黄土高原土壤相对稳定氮库累积提供科学数据。结果表明,不同地理位置、不同土层全氮和矿物固定态铵含量存在显著差异。从南到北全氮和矿物固定态铵呈下降趋势,但各土壤全氮和矿物固定态铵的分布显著不同,全氮含量在0—60 cm随土层深度增加下降很明显,60—120 cm有一定下降,120 cm以下低而稳定。矿物固定态铵在全剖面上的分布比较均匀,随土层深度的变化差异不显著,不同土层间的差异基本在误差范围内,土垫旱耕人为土、黄土正常新成土和干润砂质新成土表层(0—10 cm)矿物固定态铵平均含量分别为215.80±7.45、165.80±8.73和146.50±1.83 mg/kg,表层以下(10—200 cm)平均含量分别为193.40±9.67、157.14±5.75和142.02±5.47 mg/kg。从地理位置分析,干润砂质新成土、黄土正常新成土和土垫旱耕人为土表层...

干旱和复水条件下转基因甘薯的光合特性

以转铜锌超氧化物歧化酶(Cu/Zn SOD)和抗坏血酸过氧化物酶(APX)基因甘薯(TS)及未转基因甘薯(NT)为实验材料,研究在旱后复水条件下转基因甘薯及未转基因甘薯抗氧化酶活性和光合特性变化。结果显示,连续36 h胁迫条件下,TS和NT的SOD活性都先降低后升高,但TS的SOD活性始终高于NT。胁迫至24 h时,TS的SOD活性约为NT的1.2倍,复水后二者SOD活性都下降。持续胁迫,TS的APX活性先升高后降低,NT与之相反,复水后TS和NT的APX活性都是先升高后降低,复水12 h,TS的APX活性是NT的1.5倍。水分胁迫条件下TS的膜质受伤害程度要轻于NT,胁迫24 h,复水12 h,NT的MDA含量均约为TS的1.2倍。胁迫12 h,TS和NT净光合速率都下降,继续胁迫,TS净光合速率开始上升,NT几乎保持不变,胁迫36 h,TS的净光合速率约为NT的1.5倍。复水后二者净光合速率都开始上升,复水12 h,TS净光合速率约为NT的3倍。胁迫时TS、NT胞间CO2浓度(Ci)都逐渐增大,胁迫36 h时NT胞间CO2浓度显著高于TS,是其1.4倍。实验结果表明,同时转入SOD、APX抗氧化基因后,在...

改善生态与富民增收是黄土高原生态建设的中心

黄土高原发展要以生态建设为核心 ,寓富民增收于生态建设之中 ,把恢复植被作为突破口 ,带动土地利用结构调整 ,开发替代产业 ,实现黄土高原可持续发展。通过科学问题研究、关键技术开发、典型试验示范和推广 (RDDE) ,为黄土高原生态建设提供科学依据与技术支撑

雨水资源集蓄利用研究综述

由于干旱、人口增长、地表水地下水污染等问题 ,人们对雨水资源的开发利用产生了极大的兴趣并进行了广泛的研究 ,而且已初步显示出雨水资源开发利用的巨大潜力。文中对雨水的汇集、蓄存、利用技术,雨水利用对区域环境的影响,雨水资源的评价,雨水利用的效益评估等方面的最新研究进行了全面的分析总结 ,同时 ,提出了目前研究中亟待解决的问题。

流域水土资源优化配置的几种方法比较

目前关于流域水土资源优化配置研究的特点表现为:对单项的水、土资源优化配置研究较多,把两者结合起来的研究较少;分别从宏观和微观两个尺度研究的较多,将两种尺度结合起来研究的较少;越来越重视资源配置模式下的生态系统服务功能状况及其能否满足特定区域可持续发展的需要;研究方法逐渐由定性向定量化转变,在定量研究中,较多使用一般线性规划、灰色线性规划、动态规划、多目标决策和系统动力学等方法;越来越重视以3S技术为基础,结合专业模型进行模拟,为水土资源配置和管理提供高质量的科学决策支持,但目前还没有建立完善的区域性的支持

Efficient red organic light-emitting diode sensitized by phosphorescent Ir compound

The efficiencies of red organic light-emitting diode (OLED) using tris-(8-hydroxy-quinoline)aluminum (Alq(3)) as host and 4-(dicyanomethylene)-2-t-butyl-6-(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJTB) as dopant were greatly increased by adding a small amount (0.3 wt%) of Ir compound, iridium(III) bis(3-(2-benzothiazolyl)-7-(diethylamino)-2H-1-benzopyran-2-onato-N-',C-4) (acetyl acetonate) (Ir(C6)(2)(acac)), as a sensitizer

Pt和Ir催化剂在中性电解液中对NH_3电氧化性能

比较了Pt和Ir催化剂在中性NaClO4电解液中对NH3氧化的电催化活性和选择性。发现NH3和NH4OH在Pt和Ir催化剂上的电氧化性能相似,因而可用NH4OH代替NH3进行研究。NH4OH在Pt和Ir催化剂上氧化峰峰电流密度与NH4OH浓度呈很好的线性关系,因而Pt和Ir均能作为控制电位电解型NH3传感器的催化剂。当NH4OH浓度为0.013 mol/L时,NH3在Pt和Ir催化剂上的氧化峰分别位于0.4和0.8 V,NH4OH在Pt催化剂上的氧化峰峰电位负于在Ir催化剂上的,这是Pt催化剂的优点,但NH4OH在Ir催化剂上的氧化峰峰电流密度为Pt催化剂上的2.5倍以上,说明NH4OH在Ir催化剂上的检测灵敏度远高于在Pt催化剂上的。

超细Ir催化剂对氨氧化的电催化性能

报道了一种新型的、用NH4F作络合剂的络合还原法制备的Ir催化剂及其对氨氧化的电催化性能.结果表明,由于溶液中的Ir3+和NH4F形成络合物,因此用这种络合法制得Ir催化剂中Ir粒子的平均粒径为2.8nm,要比不加络合剂时制得的Ir催化剂中Ir粒子的平均粒径(7.5nm)小很多.所以,用络合还原法制得的Ir催化剂对氨氧化的电催化活性和稳定性都比不加络合剂时制得的Ir催化剂好很多.且该制备方法简单、实用,适用于催化剂的实际生产.

Microstructure and mechanical property of Mg-8.31Gd-1.12Dy-0.38Zr alloy

The Mg-8.31Gd-1.12Dy-0.38Zr (mass%) alloy was prepared by casting technology, and the microstructure, age hardening behavior and mechanical property have been investigated. It is noted that the alpha-Mg and the different Mg-RE (RE = Gd/Dy) compounds are subsistent in the as-cast and annealed state samples. The age hardening behavior is observed during the investigated temperature range, and the alloy exhibits high Vickers hardness, excellent ultimate tensile strength and yield strength at peak hardness.

Syntheses, crystal structures, visible and near-IR luminescent properties of ternary lanthanide (Dy3+, Tm3+) complexes containing 4,4,4-trifluoro-1-phenyl-1,3-butanedione and 1,10-phenanthroline

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.

Design and synthesis of near-IR luminescent mesoporous materials covalently linked with tris(8-hydroxyquinolinate) lanthanide(III) complexes

By using the bifunctional ligand, 8-hydroxyquinoline-functionalized organosilane (Q-Si), the new mesoporous material Q-MCM-41 covalently bonded with 8-hydroxyquinoline was synthesized. Through the ligand exchange reaction, the new near-infrared (NIR) luminescent mesoporous LnQ(3)-MCM-41 (Ln = Er, Nd, Yb) materials were prepared by linking the lanthanide quinolinate complexes to the ordered mesoporous Q-MCM-41 material. The LnQ(3)-MCM-41 materials were characterized by powder X-ray diffraction and N-2 adsorption/desorption, and they all show the characteristic mesoporous structure of MCM-41 with highly uniform pore size distributions.

Injection, Transport, Absorption and Phosphorescence Properties of a Series of Blue-Emitting Ir(III) Emitters in OLEDs: a DFT and Time-Dependent DFT Study

Quantum-chemistry methods were explored to investigate the electronic structures, injection and transport properties, absorption and phosphorescence mechanism of a series of blue-emitting Ir(III) complexes {[(F-2-ppy)(2)Ir(pta -X/pyN4)], where F-2-ppy = (2,4-difluoro)phenylpyridine; pta = pyridine-1,2,4-triazole; X = phenyl(1); p-tolyl (2); 2,6-difluororophenyl (3); -CF3 (4), and pyN4 = pyridine-1,2,4-tetrazolate (5)}, which are used as emitters in organic light-emitting diodes (OLEDs). The mobility of hole and electron were studied computationally based on the Marcus theory. Calculations of Ionization potentials (IPs) and electron affinities (EAs) were used to evaluate the injection abilities of holes and electrons into these complexes.