Estimation of power density in IMPATT using different materials

ABSTRACT

The RF output power dissipated per unit area is calculated using Runge-Kutta method for the high-moderate-moderate-high (n⁺-n-p-p⁺) doping profile of double drift region (DDR)-based impact avalanche transit time (IMPATT) diode by taking different substrate at Ka band. Those substrates are silicon, gallium arsenide, germanium, wurtzite gallium nitride, indium phosphide and 4H-silicon carbide. A comparative study regarding power dissipation ability by the IMPATT using different material is being presented thereby modelling the DDR IMPATT diode in a one-dimensional structure. The IMPATT based on 4H-SiC element has highest power density in the order of 10¹⁰ Wm^?2 and the Si-based counterpart has lowest power density of order 10⁶ Wm^?2 throughout the Ka band. So, 4H-SiC-based IMPATT should be preferable over others for the power density preference based application. This result will be helpful to estimate the power density of the IMPATT for any doping profile and to select the proper element for the optimum design of the IMPATT as far as power density is concerned in the Ka band. Also, we have focused on variation of power density with different junction temperatures and modelled the heat sink with analysis of thermal resistances.     

Mechanism of methanol decomposition on the Pd/WC(0001) surface unveiled by first-principles calculations

In this study, the decomposition of methanol into the CO and H species on the Pd/tungsten carbide (WC)(0001) surface is systematically investigated using periodic density functional theory (DFT) calculations. The possible reaction pathways and intermediates are determined. The results reveal that saturated molecules, i.e., methanol and formaldehyde, adsorb weakly on the Pd/ WC(0001) surface. Both CO and H prefer three-fold sites, with adsorption energies of −1.51 and −2.67 eV, respectively. On the other hand, CH₃O stably binds at three-fold and bridge sites, with an adsorption energy of −2.58 eV. However, most of the other intermediates tend to adsorb to the surface with the carbon and oxygen atoms in their sp³ and hydroxyl-like configurations, respectively. Hence, the C atom of CH₂OH preferentially attaches to the top sites, CHOH and CH₂O adsorb at the bridge sites, while COH and CHO occupy the three-fold sites. The DFT calculations indicate that the rupture of the initial C–H bond promotes the decomposition of CH₃OH and CH₂OH, whereas in the case of CHOH, O–H bond scission is favored over the C–H bond rupture. Thus, the most probable methanol decomposition pathway on the Pd/WC(0001) surface is CH₃OH → CH₂OH → trans-CHOH → CHO → CO. The present study demonstrates that the synergistic effect of WC (as carrier) and Pd (as catalyst) alters the CH₃OH decomposition pathway and reduces the noble metal utilization.     

Improving hydrogen evolution reaction and capacitive properties on CoS/MoS2 decorated carbon fibers

We report a facile method to transform abundantly dumped banana stem fibers into carbon fibers (CFs) useful for energy applications. The CFs surface area is increased by varying the quantity of KOH activation to 488 m²g^-1. The solvothermal method is used to synthesize CoS, CoS/MoS₂ and also grown on the activated carbon fibers (ACFs). Nano nodules of CoS arranged into sheets and layers of MoS₂ stacked together were found in FESEM analysis. The morphology of the CoS/MoS₂ differs when grown on ACFs. The growth of CoS/MoS₂ along the ACFs length prevents any stacking of the pseudocapacitance materials. The ternary composite ACFs/CoS/MoS₂ exhibits superior supercapacitor behavior as well as hydrogen evolution reaction (HER) due to the synergetic effect of the conducting ACF surface and redox active CoS/MoS₂. A maximum specific capacitance of 733 Fg^-1, energy and power density of 33 WhKg⁻¹ and 999 WKg^-1 respectively are obtained. A low Tafel slope value of 61 mVdec⁻¹ is obtained for the ACFs/CoS/MoS₂ ternary composite electrode. The present work therefore offers a fresh insight into the effective conversion of waste materials into electrode material for energy storage and conversion applications.     

非相变固体蓄热材料的蓄放热特性

搭建了低谷电蓄能蒸汽发生换热测试系统，采用数据记录仪、Hot Disk热常数分析仪等仪器检测了刚玉球等非相变固体蓄热材料的热物性。通过实验与模拟相结合的方式，研究了粉煤灰、氧化镁、刚玉砂、刚玉球等材料的蓄放热特性。分析了蓄热材料种类和粒径大小对蓄放热特性的影响，得到了不同材料的蓄热密度和综合换热系数等关键参数。结合FLUENT非稳态模拟方法，模拟了蓄热体在不同材料粒径下的蓄热和放热温度场变化规律。结果表明：刚玉球能够提供充足连续的热量，可以作为一种性能良好的蓄热材料进行应用；随着刚玉砂粒径的增大，其蓄热密度和综合换热系数会增大，有效放热时间也会延长。     

齐大山铁矿南帮含水构造带探测研究

为解决采空区突发涌水给矿山安全生产带来的安全威胁,以齐大山铁矿为研究对象,以高密度电阻率法含水构造带理论模型的正演模拟研究为基础,运用高密度电阻率法对采场南帮含水构造带的异常范围进行了圈定;运用瞬变电磁法进行了二次探测,并对高密度电阻率法所圈定的异常范围进行了验证。研究表明:含水构造带显示为低阻异常特征,在高密度电阻率法探测成果图中显示的两处低阻异常与含水构造带理论模型的正演模拟结果一致;同时,在瞬变电磁法探测成果图中显示的低阻区域均在高密度电阻率法所圈定的低阻异常范围内,二者相互验证,这两处低阻异常均为含水构造带的地球物理异常特征的显示,表明采用高密度电阻率法和瞬变电磁法组合识别技术可实现对隐伏含水构造带的先导性探测。     

Microstructure and interface-adhesion of thermally sprayed continuous gradient elastic modulus FeCrAl-ceramic coatings

The bond strength between thermally sprayed metal bond-coats and ceramic top-coats is a key factor in determining their service life. However, most studies focus on interface modifications. In this research, based on FeCrAl bond-coats prepared by arc spraying, top-coats (Al₂O₃-40 wt% TiO₂) were prepared by plasma spraying, and heat treatment was carried out in a hypoxic atmosphere. Continuous gradient elastic modulus FeCrAl-ceramic coatings were successfully prepared, and the microstructural and mechanical properties from the substrate to the top-coats were systematically investigated. The Al₂O₃ content gradually decreased from the top-coats to the substrate, forming continuous gradient elastic modulus FeCrAl-ceramic coatings. The oxide formed during the heat treatment filled the defects in the bond-coats and greatly improved the mechanical properties of the coating. The bonding strength of the continuous gradient elastic modulus coating was 21.7% greater than that of the as-received coating.     

含芳香氨基酸三肽及其衍生物自由基离子的形成和解离机理研究

铜-配体(L)-三肽组成的三元复合物［Cu(L)M］²⁺，其中，L表示4′-氯-2,2′:6′,2″-三联吡啶(缩写为4Cl-tpy)；M表示酪氨酰-甘氨酰-色氨酸(YGW)及其修饰型三肽(CH₃CO-YGW-OCH₃，缩写 Ac-YGW-OMe)。使用该复合物，通过碰撞诱导解离 (collision-induced dissociation, CID)产生两种自由基离子 (［YGW］^·+和［Ac-YGW-OMe］^·+)。采用串联质谱结合密度泛函理论 (density functional theory, DFT)得到气相稳定结构，并研究其气相解离行为。研究结果表明，［YGW］^·+和［Ac-YGW-OMe］^·+的气相解离行为截然不同，［YGW］^·+主要产生［M-CO₂-116］⁺和［M-CO₂］^·+碎片离子；而［Ac-YGW-OMe］^·+在气相中主要产生［M-CH₃OH］^·+碎片离子。推测这两种离子的气相裂解机理分别为：［YGW］^·+羧基上的质子重排到多肽骨架中羰基氧上，经历 C_α-C键的断裂产生［M-CO₂］^·+、断裂色氨酸侧链 C_β-C_γ键产生［M-CO₂-116］⁺离子；［Ac-YGW-OMe］^·+则先经历质子重排到酯基氧上，然后经过C-O酯键的断裂形成［M-CH₃OH］^·+离子。参与重排的质子可能有3个来源：Ac-YGW-OMe中甘氨酸的C_α-H、色氨酸的C_α-H 或C_β-H，该机理有待进一步验证。本研究将为其他类型多肽及衍生物的结构及气相反应机理研究提供参考。     

High breakdown strength and energy density in antiferroelectric PLZST ceramics with Al2O3 buffer

In this work, a new core-shell structure of antiferroelectric ceramic powder (Pb_0.97La_0.02Zr_0.85Sn_0.12Ti_0.03O₃-PLZST) coated with linear dielectric (Al₂O₃) has been successfully prepared to realize high energy density through tape-casting process. According to the experimental results of electron microscope, the sol-gel derived Al₂O₃ layer was uniformly coated on the PLZST particles and the Al₂O₃ layer can be taken as the buffer layer to effectively refine the grain growth as well. Therefore, the modified PLZST particles were fine and uniform compared with the pure PLZST. It was found that the buffer layer could undertake higher electric field and the electric field applied to PLZST particles was weakened based on finite element analysis, which can avoid the premature breakdown of PLZST. And the actual measured breakdown strength was significantly enhanced from 22.2 kV/mm to 35.5 kV/mm. Correspondingly, an extremely high recoverable energy storage density of 5.3 J/cm³ was obtained for PLZST with 0.5%wt Al₂O₃, an 204% enhancement over the pure PLZST ceramics (2.6 J/cm³), and the corresponding efficiency was up to 88.3%. In addition, impedance spectroscopy measurement was carried out to further confirm the better insulation of the ceramic with Al₂O₃ buffer.     

基于密闭爆发器试验的发射装药内弹道性能预估

为了预估发射装药的内弹道性能,建立了一种基于密闭爆发器试验检测发射药的静态燃烧性能参数进而预测其装药内弹道性能的方法,采用不同批次的单樟-5/7发射药进行了装药性能预估计算,并基于30 mm火炮对内弹道性能预估精度进行了试验验证。结果表明,采用所建立的基于密闭爆发器试验的发射装药内弹道性能预估方法计算获得的最大膛压为376.0 MPa,与试验测试的膛压平均值388.7 MPa的计算误差为3.27%;计算的炮口初速为1143.5 m/s,与试验测试的炮口初速平均值1156.3 m/s的计算误差为1.11%。所建立的基于密闭爆发器试验的发射装药内弹道性能预估方法具有较高的精度,可对发射药样品不同批次间的内弹道性能进行高效精确的预估,为长期贮存发射药使用寿命的判定及发射药产品的出厂校验提供了一种高效低成本的弹道性能评价方法。