945 resultados para Zr
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Compression, tension and high-velocity plate impact experiments were performed on a typical tough Zr41.2Ti13.8Cu10Ni12.5Be22.5 (Vit 1) bulk metallic glass (BMG) over a wide range of strain rates from similar to 10(-4) to 10(6) s(-1). Surprisingly, fine dimples and periodic corrugations on a nanoscale were also observed on dynamic mode I fracture surfaces of this tough Vit 1. Taking a broad overview of the fracture patterning of specimens, we proposed a criterion to assess whether the fracture of BMGs is essentially brittle or plastic. If the curvature radius of the crack tip is greater than the critical wavelength of meniscus instability [F. Spaepen, Acta Metall. 23 615 (1975); A.S. Argon and M. Salama, Mater. Sci. Eng. 23 219 (1976)], microscale vein patterns and nanoscale dimples appear on crack surfaces. However, in the opposite case, the local quasi-cleavage/separation through local atomic clusters with local softening in the background ahead of the crack tip dominates, producing nanoscale periodic corrugations. At the atomic cluster level, energy dissipation in fracture of BMGs is, therefore, determined by two competing elementary processes, viz. conventional shear transformation zones (STZs) and envisioned tension transformation zones (TTZs) ahead of the crack tip. Finally, the mechanism for the formation of nanoscale periodic corrugation is quantitatively discussed by applying the present energy dissipation mechanism.
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Porous Zr-based bulk metallic glass (PMG) with unidirectional opening pores is prepared by electrochemical etching of tungsten wires of the W/bulk metallic glass (BMG) composites. The porosity and pore size can be controlled by adjusting the tungsten wires. The PMG showed no measurable loss in thermal stability as compared to the monolithic Zr-based BMG by water quenching and is more ductile and softer than the pore-free counterpart. The specific surface area of the PMGs is calculated to be 0.65, 3.96, and 10.54 m(2)/kg for 20, 60, and 80 vol % porosity, respectively. (c) 2007 The Electrochemical Society.
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Velásquez M; JA. 2011. Análisis de las amenazas a deslizamiento de tierra e inundaciones y su influencia socio ambi ental en la gestión de riesgo en la microcuenca el Espinal, Municipio de Pueblo Nuevo, Departamento de Estelí , 2011 . El estudio se realizó en la micro cuenca El Espinal en el Municipio de Pueblo Nuevo en el Departamento de Estelí; El objetivo del estudio fue : 1) Delimitar zonas susceptibles a deslizamientos e inundaciones . 2) Analizar de manera integral la vulnerabilidad a deslizamientos e inundaciones en la zona . 3) Elaborar una propuesta de uso y manejo agroecológico usando criterios de uso de la tierra en función de las amenazas a deslizamiento de tierra e inundaciones. 4) Plantear líneas de acción con aportes de la población para el fortalecimiento de la gestión del riesgo a desastres naturales ante deslizamiento e inundaciones en la zona de estudio. La microcuenca El Espinal ha venido siendo afectada desde hace varios años por fenómenos de deslizamiento e inundaciones ; sin embargo , esto se ha venido intensificando en los últimos diez años a consecuencia de los efectos del cambio climático. Entre estas afectaciones tenemos grandes avenidas de agua que combinados con deslizamientos de tierra han causado pérdida y daños materiales, tal es el caso de las fuertes lluvias ocurridas en agosto del 2010, las cuales provocaron daños en la infraestructura a puentes vados, seis viviendas destruidas, afectaciones a cultivos, áreas de pasto, pero lo más importante es que no hubieron víctimas humanas. Debido a estas condiciones físicas, la vulnerabilidad socioeconómica y ambiental de esta micro cuenca y los efectos negativos que ha causado sobre el medio ambiente, economía y a las personas que habitan en estas áreas , surge el interés de esta investigación. La microcuenca El Espinal reúne una serie de condiciones física que la hace susceptible como: alta intensidad en el uso de los suelos, altas pendientes, precipitaciones anuales altas; a ello se unen las con diciones mecánicas de las rocas y finalmente el factor humano, quien ha eliminado la cobertura vegetal, sustituida por pastizales, granos básicos y plantaciones de café que propicia los deslizamientos e inundaciones. Los resultados sobre la susceptibilidad a deslizamiento de tierra en la microcuenca El Espinal se describen de la siguiente manera: Las áreas con niveles de baja y muy baja susceptibilidad abarcan 54.70 Km2 que corresponde al 59 % del territ orio, el nivel moderado cubre 20.01km2 , correspondiente al 22 % del área, mientras que los niveles altos y mu y alta susceptibilidad cubren 16.82 Km2 correspondiente al 19% del área de la micro cuenca, siendo las comunidades más afectadas Macuelizo, El Chorro, San Pedro, Los Llanos y Horcones. Las áreas susceptibles con planicies de inundación abarcan una área de 2 . 40 Km 2 , siendo las comunidades que pueden sufrir mayor afec tación Paso Hondo, La Calera y E l Rosario, afectando áreas de cultivo, viviendas y puentes vados. De acuerdo a las entrevistas realizadas a los habitantes de la microcuenca El Espinal la percepció n de los fenómenos naturales ante inundación y deslizamiento son las amenazas de mayor probabilidad a que ocurran coincidiendo con la importancia del estudio. El análisis global por tipo de vulnerabilidad en la microcuenca El Espinal presentó vulnerabilidad muy alta en los aspectos económico, técnico, ecológico, institucional y físico , le siguen en orden de import ancia con vulnerabilidad alta los aspectos culturales, políticos, educativos e ideológicos y por ultimo con una vulnerabilidad moderada el aspecto social, siendo el capital humano una fortaleza que los tomadores de decisiones deben focalizar pa ra la implementación de acciones de prevención y mitigación de desastres naturales. Las comunidades que presentaron una vulnerabilidad muy alta son: San José, La Calera y El Horno. Con la delimitación de áreas susceptibles a deslizamiento de tierras e in undación se zonificaron 3 áreas para darle prioridad a los aspectos ambientales y manejo agroecológico, siendo estas: Zona Protectora de Restauración Ecológica (ZPRE), Zona de Rehabilitación (ZR) y Zona de Desarrollo Agrícola (ZDA) . Finalmente, en base a los resultados del estudio y con la participación activa de los actores locales, se propusieron acciones para la reducción del riesgo y la vulnerabilidad en la microcuenca. Estos lineamientos se agrupan en cinco líneas estratégicas: Educación, Manejo adecuado de los recursos naturales , fortalecimiento institucional local , participación comunitaria y mejoramiento de las condiciones socioeconómicas de la población Con este estudio se pretende que sirva de guía a la temática de riesgos a las amenazas de deslizamiento de tierra e inundaciones a las que está expuesta la microcuenca y sus habitantes en el Municipio de Pueblo Nuevo. Los resultados permitirán a los habitantes y los tomadores de decisiones a prepararse para reforzar los planes de emergencia ante eventos de esta naturaleza
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<正> 1.基本方程及其数值求解由于讨论的是轴对称问题,因此取柱坐标系中的θ坐标为任意曲线坐标系(q~1,q~2,q~3)中的q~2坐标,在轴纵剖面Z—R平面上取任意非正交曲线坐标q~3和q~1,则变截面圆轴扭转问题以无量纲应力函数ψ表达的求解方程为:
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本文研究了以PMBP-苯萃取稀土和钍、铀、钛、锆的萃取行为。测定了La、Ce、Pr、Nd、Sm、Gd、Dy、Yb、Y、U(Ⅵ)、Ti、Th和Zr的pH_(1/2)值,计算了它们的萃取平衡常数。并介绍了近十年来作者将此萃取剂应用于铀、钍、稀土、鋰、钢铁合金及岩石中痕量稀土、钍和钙的分离和测定方面的工作。实践证明,PMOP合成简便、价格低廉、萃取能力较强,是比TTA更为优越的萃取剂。
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We discuss the transversal heteroclinic cycle formed by hyperbolic periodic pointes of diffeomorphism on the differential manifold. We point out that every possible kind of transversal heteroclinic cycle has the Smalehorse property and the unstable manifolds of hyperbolic periodic points have the closure relation mutually. Therefore the strange attractor may be the closure of unstable manifolds of a countable number of hyperbolic periodic points. The Henon mapping is used as an example to show that the conclusion is reasonable.
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The thermal conductivity of periodic composite media with spherical inclusions embedded in a homogeneous matrix is discussed. Using Green's function, we show that the Rayleigh identity can be generalized to deal with the thermal properties of these systems. A technique for calculating effective thermal conductivities is proposed. Systems with cubic symmetries (including simple cubic, body centered cubic and face centered cubic symmetry) are investigated in detail, and useful formulae for evaluating effective thermal conductivities are derived.
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通过充氢和未充氢缺口拉伸试样和三点弯曲试样在SEM下的原位加载,研究了氢对Zr65Al7.5Ni10Cu17.5块体非晶合金形变和开裂过程的影响.结果表明,无论是否有氢,块体非晶的剪切带发展到临界尺寸,剪切裂纹就沿剪切带形核、扩展,它一旦张开就导致快速的断裂.断口边缘观察到的无特征区是剪切带,而不是剪切裂纹断口;剪切断口形貌和拉伸断口形貌没有本质区别.只有当长时间充氢才能形成氢鼓泡,如鼓泡很小或尚未形成,则氢对剪切带以及裂纹的形核、扩展没有明显影响;如存在较大的氢鼓泡,则当剪切带尚未充分发展时微裂纹就形核,导致低应力脆断.
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利用脉冲辐照研究超高温度梯度下表层预轩ZrO_2纳米颗粒涂层的18-8奥氏体不锈钢的快凝组织形态、微结构特征及力学性质,结果表明,在表层约15μm范围内形成Zr的合金化微区,Zr最大含量(原子分数)为43.3%,但Zr成分分布存在不连续特征;预置纳米ZrO_2陶瓷涂层明显提高了激光作用深度。超高温梯度和高冷却速度显著细化了快凝亚组织并得到超细枝晶及胞晶,并观察到位错胞及栅栏孪晶两类亚晶,而激光熔区的外延生长机制未使晶粒细化。激光辐照后,合金化区硬度增加而弹性模量降低,其余部分硬度增加而弹性模量无变化。
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The surface mechanical attrition treatment (SMAT) technique was developed to synthesize a nanocrystalline (NC) layer on the surface of metallic materials for upgrading their overall properties and performance. In this paper, by means of SMAT to a pure zirconium plate at the room temperature, repetitive multidirectional peening of steel shots (composition (wt%): 1C, 1.5Cr, base Fe) severely deformed the surface layer. A NC surface layer consisting of the intermetallic compound FeCr was fabricated on the surface of the zirconium. The microstructure characterization of the surface layer was performed by using X-ray diffraction analysis, optical microscopy, scanning and transmission electron microscopy observations. The NC surface layer was about 25 mu m thick and consisted of the intermetallic compound FeCr with an average grain size of 25 +/- 10 nm. The deformation-induced fast diffusion of Fe and Cr from the steel shots into Zr occurred during SMAT, leading to the formation of intermetallic compound. In addition, the NC surface layer exhibited an ultrahigh nanohardness of 10.2 GPa.
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Characteristics of supersonic combustion by injecting kerosene vapor into a Mach 2.5 crossflow at various preheat temperatures and pressures were investigated experimentally. A two-stage heating system has been designed and tested, which can prepare heated kerosene of 0.8 kg up to 820 K at pressure of 5.5 Mpa with minimum/negligible fuel coking. In order to simulate the thermophysical properties of kerosene over a wide range of thermodynamic conditions, a three-component surrogate that matches the compound class of the parent fuel was employed. The flow rate of kerosene vapor was calibrated using a sonic nozzle. Computed flow rates using the surrogate fuel are in agreement with the experimental data. Kerosene jets at various preheat temperatures injecting into both quiescent environment and Mach 2.5 crossflow were visualized. It was found that at injection pressure of 4 Mpa and preheat temperature of 550 K the kerosene jet was completely in vapor phase, while keeping almost the same penetration depth as compared to the liquid kerosene injection. Supersonic combustion tests were also carried out to compare the combustor performance for the cases of vaporized kerosene injection, liquid kerosene injection, and effervescent atomization with hydrogen barbotage, under the similar stagnation conditions. Experimental results demonstrated that the use of vaporized kerosene injection leads to better combustor performance. Further parametric study on vaporized kerosene injection in a supersonic model combustor is needed to assess the combustion efficiency as well as to identify the controlling mechanism for the overall combustion enhancement.
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The reactivity of permethylzirconocene and permethylhafnocene complexes with various nucleophiles has been investigated. Permethylzirconocene reacts with sterically hindered ketenes and allenes to afford metallacycle products. Reaction of these cummulenes with permethylzirconocene hydride complexes affords enolate and σ-allyl species, respectively. Reactions which afford enolate products are nonstereospecific, whereas reactions which afford allyl products initially give a cis-σ-allyl complex which rearranges to its trans isomer. The mechanism of these reactions is proposed to occur either by a Lewis Acid-Lewis Base interaction (ketenes) or by formation of a π-olefin intermediate (allenes).
Permethylzirconocene haloacyl complexes react with strong bases such as lithium diisopropylamide or methylene trimethylphosphorane to afford ketene compounds. Depending on the size of the alkyl ketene substituent, the hydrogenation of these compounds affords enolate-hydride products with varying degrees of stereoselectivity. The larger the substituent, the greater is the selectivity for cis hydrogenation products.
The reaction of permethylzirconocene dihydride and permethylhafnocene dihydride with methylene trimethylphosphorane affords methyl-hydride and dimethyl derivatives. Under appropriate conditions, the metallated-ylide complex 1, (η^5-C_5(CH_3)_5)_2 Zr(H)CH_2PMe_2CH_2, is also obtained and has been structurally characterized by X-ray diffraction techniques. Reaction of 1 with CO affords (η^5-C_5(CH_3)_5)_2 Zr(C,O-η^2 -(PMe_3)HC=CO)H which exists in solution as an equilibrium mixture of isomers. In one isomer (2), the η^2-acyl oxygen atom occupies a lateral equatorial coordination position about zirconium, whereas in the other isomer (3), the η-acyl oxygen atom occupies the central equatorial position. The equilibrium kinetics of the 2→3 isomerization have been studied and the structures of both complexes confirmed by X-ray diffraction methods. These studies suggest a mechanism for CO insertion into metal-carbon bonds of the early transition metals.
Permethylhafnocene dihydride and permethylzirconocene hydride complexes react with diazoalkanes to afford η^2-N, N' -hydrazonido species in which the terminal nitrogen atom of the diazoalkane molecule has inserted into a metal-hydride or metal-carbon bond. The structure of one of these compounds, Cp*_2Zr(NMeNCTol_2)OH, has been determined by X-ray diffraction techniques. Under appropriate conditions, the hydrazonido-hydride complexes react with a second equivalent of diazoalkene to afford η' -N-hydrazonido-η^2-N, N' -hydrazonido species.
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We measured spectroscopic and laser action properties of a novel 8-position substituted pyrromethene-BF2, namely 1,3,5,7-tetramethyl-2,6-diethyl-8-n-propyl pyrromethene-BF2 complex. The laser action was performed with the corresponding dye solution in ethanol, which was placed in a Littman-type laser cavity pumped by the second harmonic of a Q-switched Nd:YAG laser. The spectroscopic measurements clearly indicated that the corresponding dye solution in ethanol exhibited intense absorption in the visible spectral region with large fluorescence quantum yield. It possesses rather low triplet-triplet absorption in the spectral region 460-550 nm and almost negligible triplet-triplet absorption in the lasing spectral region. As a consequence, it lases nearly as efficiently as commercially available benchmark laser dyes such as Rhodamine-6G and outperformed them in wavelength tunability in our laser cavity and pump geometry. (C) 2002 Optical Society of America.
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Attosecond-pulse extreme-ultraviolet (XUV) photoionization in a two-color laser field is investigated. Attosecond pulse trains with different numbers of pulses are examined, and their strong dependence on photoelectronic spectra is found. Single-color driving-laser-field-assisted attosecond XUV photoionization cannot determine the number of attosecond pulses from the photoelectronic energy spectrum that are detected orthogonally to the beam direction and the electric field vector of the linearly polarized laser field. A two-color-field-assisted XUV photoionization scheme is proposed for directly determining the number of attosecond pulses from a spectrum detected orthogonally. (C) 2005 Optical Society of America.
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Two major topics are covered: the first chapter is focused on the development of post-metallocene complexes for propylene polymerization. The second and third chapters investigate the consequences of diisobutylaluminum hydride (HAliBu2) additives in zirconocene based polymerization systems.
The synthesis, structure, and solution behavior of early metal complexes with a new tridentate LX2 type ligand, bis(thiophenolate)pyridine ((SNS) = (2-C6H4S)2-2,6-C5H3N) are investigated. SNS complexes of Ti, Zr, and Ta having dialkylamido coligands were synthesized and structurally characterized. The zirconium complex, (SNS)Zr(NMe2)2, displays C2 symmetry in the solid state. Solid-state structures of tantalum complexes (SNS)Ta(NMe2)3 and (SNS)TaCl(NEt2)2 also display pronounced C2 twisting of the SNS ligand. 1D and 2D NMR experiments show that (SNS)Ta(NMe2)3 is fluxional with rotation about the Ta N(amide) bonds occurring on the NMR timescale. The fluxional behavior of (SNS)TaCl(NEt2)2 in solution was also studied by variable temperature 1H NMR. Observation of separate signals for the diastereotopic protons of the methylene unit of the diethylamide indicates that the complex remains locked on the NMR timescale in one diastereomeric conformation at temperatures below -50 °C.
Reduction of Zr(IV) metallocenium cations with sodium amalgam (NaHg) produces EPR signals assignable to Zr(III) metallocene complexes. Thus, chloro-bridged heterobinuclear ansa-zirconocenium cation [((SBI))Zr(μ-Cl)2AlMe2]+B(C6F5)4¯ (SBI = rac-dimethylsilylbis(1-indenyl)), gives rise to an EPR signal assignable to the complex (SBI)ZrIII(μ-Cl)2AlMe2, while (SBI)ZrIII-Me and (SBI)ZrIII(-H)2AliBu2 are formed by reduction of [(SBI)Zr(μ-Me)2AlMe2]+B(C6F5)4¯ and [(SBI)Zr(μ-H)3(AliBu2)2]+B(C6F5)4¯, respectively. These products are also formed, along with (SBI)ZrIII-iBu and [(SBI)ZrIII]+ AlR4¯ when (SBI)ZrMe2 reacts with HAliBu2, eliminating isobutane en route to the Zr(III) complex. Studies concerning the interconversion reactions between these and other (SBI)Zr(III) complexes and reaction mechanisms involved in their formation are also reported.
The addition of HAliBu2 to precatalyst [(SBI)Zr(µ-H)3(AliBu2)2]+ significantly slows the polymerization of propylene and changes the kinetics of polymerization from 1st to 2nd order with respect to propylene. This is likely due to competitive inhibition by HAliBu2. When the same reaction is investigated using [(nBuCp)2Zr(μ-H)3(AliBu2)2]+, hydroalumination between propylene and HAliBu2 is observed instead of propylene polymerization.