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Ceramic Matrix Composites (CMCs) have many interesting properties, mainly light weight, cost efficiency, low density, high compressive strength, high hardness and durability. Hence, they emerged as a boon to the development of personnel armors in the past. The current work aims to review various new methodologies adapted for the reinforcement of Alumina (Al2O3) CMCs in recent times, including some of the interesting results obtained with respect to mechanical properties, suitability of the synthesized composites for armor applications, and the upcoming reinforcement trends. Finally, studies related to reinforcement in Al2O3 CMCs, specifically towards armor applications have been consolidated to arrive at some of the important inferences for concluding reasonably.  相似文献   
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Iranian Polymer Journal - Poly(vinyl alcohol) (PVA) nanocomposites incorporated with ZnO nanofiller were prepared and examined to study the influence of nanofiller on their properties. All the...  相似文献   
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Structurally stable β-Ca3(PO4)2/t-ZrO2 composite mixtures with the aid of Dy3+ stabilizer were accomplished at 1500°C. The precursors comprising Ca2+, P5+, Zr4+, and Dy3+ have been varied to obtain five different combinations. The results revealed the fact that complete phase transformation of calcium-deficient apatite to β-Ca3(PO4)2 occurred only at 1300°C, whereas the evidence of t-ZrO2 crystallization is obvious at 900°C. The dual occupancy of Dy3+ at β-Ca3(PO4)2 and t-ZrO2 structures was evident; however, Dy3+ initially prefers to occupy β-Ca3(PO4)2 lattice until its saturation limit and thereafter accommodates at the lattice site of ZrO2. The typical absorption and emission behavior of Dy3+ were noticed in all the systems and, moreover, the surrounding symmetry of Dy3+ domains has been determined from the luminescence study. All the systems ensured paramagnetic response that is generally contributed by the presence of Dy3+. A gradual increment in the phase content of t-ZrO2 in the composite mixtures ensured a significant improvement in the hardness and Young's modulus of the investigated compositions.  相似文献   
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The electrochemical reduction of carbon dioxide (CO2) to hydrocarbons is a challenging task because of the issues in controlling the efficiency and selectivity of the products. Among the various transition metals, copper has attracted attention as it yields more reduced and C2 products even while using mononuclear copper center as catalysts. In addition, it is found that reversible formation of copper nanoparticle acts as the real catalytically active site for the conversion of CO2 to reduced products. Here, it is demonstrated that the dinuclear molecular copper complex immobilized over graphitized mesoporous carbon can act as catalysts for the conversion of CO2 to hydrocarbons (methane and ethylene) up to 60%. Interestingly, high selectivity toward C2 product (40% faradaic efficiency) is achieved by a molecular complex based hybrid material from CO2 in 0.1 m KCl. In addition, the role of local pH, porous structure, and carbon support in limiting the mass transport to achieve the highly reduced products is demonstrated. Although the spectroscopic analysis of the catalysts exhibits molecular nature of the complex after 2 h bulk electrolysis, morphological study reveals that the newly generated copper cluster is the real active site during the catalytic reactions.  相似文献   
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International Journal of Information Security - Context-aware network logging is becoming more prevalent for enterprise networks, data centers, and forensics. Monitoring agents are strategically...  相似文献   
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Journal of Materials Science: Materials in Electronics - In the recent years, metal oxides have attracted more interest for researchers because of their applications in energy and...  相似文献   
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