Effect of heat treatment and zircon addition on the properties of low-cement castables based on recycled alumina grog

In this investigation, low-cement castables were prepared using 70% alumina grog aggregates obtained from crushed alumina brick waste. The aggregates were thermally treated at 1550 °C for 3 h. Four types of low-cement castables were prepared with various types of aggregates (alumina grog with or without thermal treatment) and fillers (with or without zircon addition), and they were evaluated in terms of their physical, thermal, and chemical properties. Microstructural analysis via scanning electron microscopy (SEM) was performed on the castables before and after slag attack. Compared to the other fabricated castables, the thermally treated alumina grog castables with zircon showed better physical properties, such as a higher bulk density, cold crushing strength, and modulus of rupture and a lower apparent porosity and water absorption. In addition, they had a higher positive linear thermal expansion, refractoriness under load, permanent linear change, and hot modulus of rupture. The results of the SEM with energy dispersive X-ray analysis of the prepared castables confirmed that the mullite and anorthite phases were predominant when zircon was not added and the zircon–mullite phase additionally appeared upon the incorporation of zircon. A quantitative elemental analysis via X-ray fluorescence spectroscopy was employed to determine the composition of the castables. X-ray diffraction analysis showed that the alumina grog castables had a high mullite and low anorthite content, and the thermally treated alumina grog had a high anorthite, low mullite, and high zircon content. The improvement in the mechanical and thermo-mechanical properties of the castables with thermally treated alumina grog and added zircon can be attributed to the formation of the zircon–mullite phase with a low mullite phase content.     

Boron-doped activated carbon from the stems of Prosopis juliflora as an effective electrode material in symmetric supercapacitors

For a supercapacitor electrode, carbon-based materials have received great attention for their high surface area and stability. In this work, sustainable and cost-effective synthesis of boron-doped activated biomass-derived carbon from the stems of Prosopis juliflora has been reported for supercapacitor applications. The activation by KOH creates pores and boron induces p-type doping in the carbon matrix. The material gave a higher specific capacitance of 307.14 F/g at a current density of 0.5 A/g. The symmetric supercapacitor device delivered 156.29 F/g of specific capacitance with 98.1% of energy efficiency. The observed energy and power densities were 7.81 Wh/Kg and 150 W/Kg, respectively. The device was further studied with stability test for 1000 charge/discharge cycles and showed 98.6% of capacitance retention and 97.9% of coulombic efficiency.

     

A New Route for the Synthesis of Tungsten Carbide–Cobalt Nanocomposites

Synthesis of WC–Co nanocomposites generally involves gas-phase carburization. A novel approach in which a polymer precursor such as polyacrylonitrile serves as an in situ carbon source has been developed. The WC–Co nanocomposites formed are characterized by X-ray powder diffraction and electron microscopy. Nearly phase pure WC–Co nanocomposites with a particle size of 50–80 nm have been obtained. The phase purity of the products is strongly influenced by the synthesis and processing conditions such as the firing temperature, time, and atmosphere.     

Ageing studies of pineapple leaf fiber–reinforced polyester composites

This experimental study evaluated the water absorption characteristics of pineapple leaf fiber (PALF)–polyester composites of different fiber content. The degree of water absorption was found to increase with fiber loading. The mechanism of diffusion was analyzed and the effect of fiber loading on the sorption kinetics was studied. The diffusion coefficient was calculated and found to increase with fiber content. Studies were also made to correlate water absorption with the cross‐sectional areas of the specimens. The effects of ageing on the tensile properties and dimensional stability of PALF polyester composites were studied under two different ageing conditions. Ageing studies showed a decrease in tensile strength of the composites. The composite specimens subjected to thermal ageing showed only a slight deterioration in strength. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 503–510, 2004     

Ultra-Thin Single-Particle-Layer Sodium Beta-Alumina-Based Composite Polymer Electrolyte Membrane for Sodium-Metal Batteries

Inorganic/organic composite polymer electrolytes (CPEs) with good flexibility and electrode contact have been pursued for solid−state sodium-metal batteries. However, the application of CPEs for high energy density solid−state sodium-metal batteries is still limited by the low Na⁺ conductivity, large thickness, and low ion transference number. Herein, an ultra-thin single-particle-layer (UTSPL) composite polymer electrolyte membrane with a thickness of ≈20 µm straddled by a sodium beta−alumina ceramic electrolyte (SBACE) is presented. A ceramic Na⁺-ion electrolyte that bridges or percolates across an ultra-thin and flexible polymer membrane provides: 1) the strength and flexibility from the polymer membrane, 2) excellent electrolyte/electrode interfacial contact, and 3) a percolation path for Na⁺-ion transfer. Owing to this novel design, the obtained UTSPL-35SBACE membrane exhibits a high Na⁺-ion conductivity of 0.19 mS cm⁻¹ and a transference number of 0.91 at room temperature, contributing to long−term cycling stability of symmetric sodium cells with a small overpotential. The assembled quasi-solid-state cell with the as−prepared UTSPL-35SBACE membrane displays superior cycling performance with a discharge capacity of 105 mAh g⁻¹ at 0.5 °C rate after 100 cycles and excellent rate performance (82 mAh g⁻¹ at 5 °C rate) at room temperature with the potassium manganese hexacyanoferrate (KMHCF)@CNTs/CNFs cathode, where KMHCF refers to potassium manganese hexacyanoferrate.     

Design and analysis of text document clustering using salp swarm algorithm

The Journal of Supercomputing - In the technological era, exponential increase of unorganized text documents offers increased difficulties retrieving the most relevant data. The document clustering...     

Cost Effective Optimal Task Scheduling Model in Hybrid Cloud Environment

In today’s world, Cloud Computing (CC) enables the users to access computing resources and services over cloud without any need to own the infrastructure. Cloud Computing is a concept in which a network of devices, located in remote locations, is integrated to perform operations like data collection, processing, data profiling and data storage. In this context, resource allocation and task scheduling are important processes which must be managed based on the requirements of a user. In order to allocate the resources effectively, hybrid cloud is employed since it is a capable solution to process large-scale consumer applications in a pay-by-use manner. Hence, the model is to be designed as a profit-driven framework to reduce cost and make span. With this motivation, the current research work develops a Cost-Effective Optimal Task Scheduling Model (CEOTS). A novel algorithm called Target-based Cost Derivation (TCD) model is used in the proposed work for hybrid clouds. Moreover, the algorithm works on the basis of multi-intentional task completion process with optimal resource allocation. The model was successfully simulated to validate its effectiveness based on factors such as processing time, make span and efficient utilization of virtual machines. The results infer that the proposed model outperformed the existing works and can be relied in future for real-time applications.     

Inkjet‐Printed Lithium–Sulfur Microcathodes for All‐Printed,Integrated Nanomanufacturing

Improved thin‐film microbatteries are needed to provide appropriate energy‐storage options to power the multitude of devices that will bring the proposed “Internet of Things” network to fruition (e.g., active radio‐frequency identification tags and microcontrollers for wearable and implantable devices). Although impressive efforts have been made to improve the energy density of 3D microbatteries, they have all used low energy‐density lithium‐ion chemistries, which present a fundamental barrier to miniaturization. In addition, they require complicated microfabrication processes that hinder cost‐competitiveness. Here, inkjet‐printed lithium–sulfur (Li–S) cathodes for integrated nanomanufacturing are reported. Single‐wall carbon nanotubes infused with electronically conductive straight‐chain sulfur (S@SWNT) are adopted as an integrated current‐collector/active‐material composite, and inkjet printing as a top‐down approach to achieve thin‐film shape control over printed electrode dimensions is used. The novel Li–S cathodes may be directly printed on traditional microelectronic semicoductor substrates (e.g., SiO₂) or on flexible aluminum foil. Profilometry indicates that these microelectrodes are less than 10 µm thick, while cyclic voltammetry analyses show that the S@SWNT possesses pseudocapacitive characteristics and corroborates a previous study suggesting the S@SWNT discharge via a purely solid‐state mechanism. The printed electrodes produce ≈800 mAh g^?1 S initially and ≈700 mAh g^?1 after 100 charge/discharge cycles at C/2 rate.     

Rechargeable Aluminum‐Ion Batteries Based on an Open‐Tunnel Framework

Rechargeable batteries based on an abundant metal such as aluminum with a three‐electron transfer per atom are promising for large‐scale electrochemical energy storage. Aluminum can be handled in air, thus offering superior safety, easy fabrication, and low cost. However, the development of Al‐ion batteries has been challenging due to the difficulties in identifying suitable cathode materials. This study presents the use of a highly open framework Mo_{2.5 + y} VO_{9 + z} as a cathode for Al‐ion batteries. The open‐tunnel oxide allows a facile diffusion of the guest species and provides sufficient redox centers to help redistribute the charge within the local host lattice during the multivalent‐ion insertion, thus leading to good rate capability with a specific capacity among the highest reported in the literature for Al‐based batteries. This study also presents the use of Mo_{2.5 + y} VO_{9 + z} as a model host to develop a novel ultrafast technique for chemical insertion of Al ions into host structures. The microwave‐assisted method employing diethylene glycol and aluminum diacetate (Al(OH)(C₂H₃O₂)₂) can be performed in air in as little as 30 min, which is far superior to the traditional chemical insertion techniques involving moisture‐sensitive organometallic reagents. The Al‐inserted Al _x Mo_{2.5 + y} VO_{9 + z} obtained by the microwave‐assisted chemical insertion can be used in Al‐based rechargeable batteries.