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为了探讨春小麦水肥耦合作用,采用312-D最优饱和设计,于2000~2003年在辽西半干旱区开展了水肥耦合对春小麦产量效应的田间试验研究。结果表明:在该试验条件下水分对产量的作用最大,磷肥次之,氮肥最小;水肥耦合的产量效应是:中水中肥效应最高,高水高肥次之,低水低肥最低;水肥交互耦合效应大小顺序是:氮水耦合>氮磷耦合>磷水耦合。产量超过4000kg/hm2的水肥管理方案为:施氮量240.1~361.2kg/hm2,施磷量103.1~152.6kg/hm2,灌水量337.5~450.0mm。获得最高产量4610kg/hm2的施氮量为315.1kg/hm2、施磷量111.1kg/hm2、灌水量354.6mm。

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采用土壤淤浆方法对丹麦农田和山毛榉森林土壤反硝化过程中N2 O的产生与还原进行了研究 ,同时考察了硝酸根和铵离子对反硝化作用的影响 .结果表明 ,森林土壤反硝化活性大于农田土壤 ,但农田土壤中N2 O还原活性大于森林土壤 ,表现在农田和森林土壤中N2 O/N2 的产生比率分别为 0 .11和 3 .65 .硝酸根和铵离子能促进两种土壤中的N2 O产生 ,但可降低农田土壤中的N2 O还原速率 .与农田土壤相比 ,硝酸根可降低森林土壤N2 O的还原能力 ,而铵离子却表现出对N2 O还原的促进作用 .培养 1周内尽管农田土壤中硝酸根始终存在 ,但几乎所有产生的N2 O都被还原成N2 .然而 ,只有当硝酸根几乎耗尽 ,森林土壤中N2 O的还原才开始进行 .由于两种土壤 pH值的不同造成硝酸根对N2 O还原抑制作用的差异 ,因为酸性条件下硝酸根对N2O还原的抑制较强 .因此 ,土壤消耗大气N2 O的适宜条件为厌氧 ,pH中性和硝酸根含量低 .

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对日光温室渗灌和沟灌的土壤环境、室内空气环境、作物生育及病害状况、水分利用效率等进行了研究.结果表明,与沟灌相比,渗灌可增加土壤水稳性团粒81.4%,降低土壤容重21.2%,增加土壤孔隙度29.0%,提高土壤温度1.1~1.7℃,降低空气湿度13.4%,节约灌溉用水36.7%,而且能促使作物早熟,提高作物产量,减少作物病害,降低生产成本,是目前日光温室理想的灌溉技术.

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Melt-spun ribbon and bulk samples in cylindrical rod form with diameter ranging from 2 mm to 4 mm of Ti40Cu40Zr10Ni10 alloy were prepared by melt-spinning technique and copper mould casting method, respectively. The microstructure, thermal stability and mechanical properties of the bulk samples were investigated. A completely glassy single phase is formed in the 2 mm rod sample. Increasing the diameter of the rod samples resulted in the formation of CuTi crystalline phase in the 3 mm and 4 mm rod samples.

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Structure and crystallization behavior of amorphous and quasicrystalline Ti45Zr35Ni17Cu3 alloy have been studied. DSC trace of the amorphous alloy obtained during continuous heating to 1300 K shows distinctly an exothermic peak and two endothermic peaks.

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Preparation of monodispersed platinum nanoparticles with average size 2.0 nm stabilized by amino-terminated ionic liquid was demonstrated. The resulting platinum nanoparticles (Pt-IL) retained long-term stability without special protection. The Pt-IL nanoparticles exhibited high electrocatalytic activity toward reduction of oxygen and oxidation of methanol. Rotating disk electrode voltammetry and rotating ring-disk electrode voltammetry confirmed that the Pt-IL films could catalyze an almost four-electron reduction of dioxygen to water.

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This work describes the design and assembly of multifunctional and cost-efficient composite fiber nonwovens as semi-occlusive wound dressings using a simple electrospinning process to incorporate a variety Of functional components into an Ultrathin fiber. These components include non-hydrophilic poly(L-lactide) (PLLA) as fibrous backbone, hydrophilic poly(vinyl pyrrolidone)iodine (PVP-I), TiO2 nanoparticles, zinc chloride as antimicrobial, odor-controlling, and antiphlogistic agents, respectively. The process of synthesis starts with a multicomponent solution Of PLLA, PVP, TiO2 nanoparticles plus zinc chloride, in which TiO2 nanoparticles are synthesized by in situ hydrolysis of TiO2 precursors in a PVP Solution for the sake of obtaining the particle-uniformly dispersive solution. Subsequent electrospinning generates the corresponding composite fibers. A further iodine vapor treatment to the composite fibers combines iodine with PVP to produce the PVP-I complexes. Experiments indicate that the assembled composite fibers (300-400 nm) possess the ointment-releasing characteristic and the phase-separate, core-sheath structures in which PVP-I residing in fiber Surface layer becomes the sheath, and PLLA distributing inside the fiber acts as the core.

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A new class of high-performance materials, fluorinated poly(phenylene-co-imide)s, were prepared by Ni(0)-catalytic coupling of 2,5-dichlorobenzophenone with fluorinated dichlorophthalimide. The synthesized copolymers have high molecular weights ((M) over bar (W)= 5.74 x 10(4)-17.3 x 10(4) g center dot mol(-1)), and a combination of desirable properties such as high solubility in common organic solvent, film-forming ability, and excellent mechanical properties. The glass transition temperature (T(g)s) of the copolymers was readily tuned to be between 219 and 354 degrees C via systematic variation of the ratio of the two comonomers. The tough polymer films, obtained by casting from solution, had tensile strength, elongation at break, and tensile modulus values in the range of 66.7-266 MPa, 2.7-13.5%, and 3.13-4.09 GPa, respectively. The oxygen permeability coefficients (P-O2) and permeability selectivity of oxygen to nitrogen (P-O2/P-N2) of these copolymer membranes were in the range of 0.78-3.01 barrer [1 barrer = 10(-10) cm(3) (STP) cm/(cm(2) center dot s center dot cmHg)] and 5.09-6.2 5, respectively. Consequently, these materials have shown promise as engineering plastics and gas-separation membrane materials.

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直接甲醇燃料电池(DMFC)是以固体聚合物为电解质,阳极以液相甲醇或蒸气相甲醇进料,阴极以空气或氧气为氧化剂.DMFC具有原料甲醇易储存、电池的理论电压高和能量效率高等特点,适于作电动车电源和便携式电源,具有广阔的发展前景.然而,在DMFC中,甲醇的阳极氧化涉及6个电子的传递过程,比氢气的氧化更困难,由于存在较高的阳极过电位,使得电池的实际输出电压低于理论电压;更为重要的是甲醇的部分氧化中间产物(CO)易使电催化剂中毒,因此,高效的阳极电催化剂一直是DMFC中的重要研究领域之一[1~7].目前解决这一问题的途径主要集中在对电催化剂的研究和改进上,如性能较好的Pt/Metal(oxide),即Pt复合金属或金属氧化物催化剂.稀土元素Ln系位于元素周期表中的B族,具有丰富的d轨道和f轨道电子,因此可以作为催化剂中的第二种金属元素加以研究.将稀土元素及其氧化物用于较低温度(250℃)下催化CO的化学氧化反应已早有研究[8].目前,已经有将Rh/Sm和Pt/Sm合金应用于CO的催化氧化反应的研究报道[9].本文选择几种稀土离子作为添加剂,研究了稀土离子对甲醇电氧化反应的影响.1实验部分1.1试剂与仪器甲醇(优级纯),...

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The crystal structure, hydrogen storage property and electrochemical characteristics of the La0.7Mg0.3Ni3.5-x(Al0.5Mo0.5), (x=0-0.8) alloys have been investigated systematically. It can be found that with X-ray powder diffraction and Rietveld analysis the alloys are of multiphase alloy and consisted of impurity LaNi phase and two main crystallographic phases, namely the La(La, Mg)(2)Ni-9 phase and the LaNi5 phase, and the lattice parameter and the cell volume of both the La(La, Mg)(2)Ni-9 phase and the LaNi5 phase increases with increasing A] and Mo content in the alloys. The P-C isotherms curves indicate that the hydrogen storage capacity of the alloy first increases and then decreases with increasing x, and the equilibrium pressure decreases with increasing x. The electrochemical measurements show that the maximum discharge capacity first increases from 354.2 (v = 0) to 397.6 mAh g(-1) (x = 0.6) and then decreases to 370.4 mAh g(-1) (x= 0.8). The high-rate dischargeability of the alloy electrode increases lineally from 55.7% (x=0) to 73.8% (x=0.8) at the discharge current density of 1200 mA g(-1). Moreover, the exchange current density of the alloy electrodes also increases monotonously with increasing x.

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Fourier-transform (FT)-Raman and -infrared (IR) spectroscopy were employed to investigate the function of the aqueous 2-hydroxyethylmethacrylate/glutaraldehyde solution (Gluma) as a desensitizer. 2-Hydroxyethylmethacrylate (HEMA), glutaraldehyde (GA), and the mixture of HEMA/GA (i.e. Gluma) were used to interact with dentin, collagen, hydroxyapatite (HAP), and bovine serum albumin (BSA) individually. All the interactions were monitored by an FT-Raman spectrometer. FT-IR spectroscopy was also used in this study. The results show that HEMA could be absorbed by dentin and collagen; GA could cross-link collagen and BSA; and when BSA was added to Gluma, polymerization of HEMA occurred. The results suggest that Gluma acts as a desensitizer whereby, first, GA reacts with part of the serum albumin in dentinal fluid, which induces a precipitation of serum albumin, then, second, a reaction of GA with serum albumin induces polymerization of HEMA. The function of Gluma as a desensitizer to block dentinal tubules occurs via these two reactions.

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Assisted by a mechanical alloying and high-pressure technique, a new W4Mg intermetallic was formed. W4Mg amorphous mixture was obtained by mechanically alloying the pure metal powder mixtures at designated composition for 20 h. A new compound was found after the subsequent high-pressure and high-temperature treatment. W4Mg intermetallic was identified as a cubic structure and the lattice parameter was a=0.4150 nm. The synthesis mechanism is also discussed in this paper.