Studies of dynamic crack propagation and crack branching with peridynamics

In this paper we discuss the peridynamic analysis of dynamic crack branching in brittle materials and show results of convergence studies under uniform grid refinement (m-convergence) and under decreasing the peridynamic horizon (δ-convergence). Comparisons with experimentally obtained values are made for the crack-tip propagation speed with three different peridynamic horizons. We also analyze the influence of the particular shape of the micro-modulus function and of different materials (Duran 50 glass and soda-lime glass) on the crack propagation behavior. We show that the peridynamic solution for this problem captures all the main features, observed experimentally, of dynamic crack propagation and branching, as well as it obtains crack propagation speeds that compare well, qualitatively and quantitatively, with experimental results published in the literature. The branching patterns also correlate remarkably well with tests published in the literature that show several branching levels at higher stress levels reached when the initial notch starts propagating. We notice the strong influence reflecting stress waves from the boundaries have on the shape and structure of the crack paths in dynamic fracture. All these computational solutions are obtained by using the minimum amount of input information: density, elastic stiffness, and constant fracture energy. No special criteria for crack propagation, crack curving, or crack branching are used: dynamic crack propagation is obtained here as part of the solution. We conclude that peridynamics is a reliable formulation for modeling dynamic crack propagation.     

A new SiO/C anode composition for lithium-ion battery

A new anode composition comprising SiO and graphite(C) is prepared through a high-energy ball milling process. During the first cycle, the anode delivers high discharge and charge capacity values of 1556 and 693 mAh g⁻¹, respectively. The electrode shows a reversible charge capacity value of 688 mAh g⁻¹ at the 30th cycle with 99% Coulombic efficiency. X-ray diffraction analysis reveals that ball milling does not produce any new compound, but only causes a reduction in particle size. The irreversible and reversible capacities appear to be interdependent.     

Improvement of anaerobic digestion of sludge.

Anaerobic digestion improvement can be accomplished by different methods. Besides optimization of the process conditions, pretreatment of input sludge and increase of process temperature is frequently used. The thermophilic process brings a higher solids reduction and biogas production, a high resistance to foaming, no problems with odour, better pathogens destruction and an improvement of the energy balance of the whole treatment plant. Disintegration of excess activated sludge in a lysate centrifuge was proved to cause increase of biogas production in full-scale conditions. The rapid thermal conditioning of digested sludge is an acceptable method of particulate matter disintegration and solubilization.     

A new class of Sol–gel derived LiM1xM2yMn2?x?yO3.8F0.2 (M1?=?Cr, M2?=?V; x?=?y?=?0.2) cathodes for lithium batteries

A series of LiM_1xM_2yMn_2−x−yO_3.8F_0.2 (M₁ = Cr, M₂ = V; x = y = 0.2) cathodes, viz., LiMn₂O_3.8F_0.2, LiCr_0.2Mn_1.8O_3.8F_0.2 and LiCr_0.2V_0.2Mn_1.6O_3.8F_0.2 along with native LiMn₂O₄ have been synthesized by Citric Acid assisted Modified (CAM) sol–gel method, with a view to understand the effect of synthesis methodology and the effect of dual category dopants, viz., anion and/or cation upon spinel cathodes individually. An acceptable capacity retention (94%) observed up to 50 cycles for native LiMn₂O₄ cathodes is attributed to the significance of CAM sol–gel method. Similarly, the encouraging charge–discharge results of LiMn₂O_3.8F_0.2 (130 mAh g⁻¹) and LiCr_0.2Mn_1.8O_3.8F_0.2 (142 mAh g⁻¹) cathodes revealed a possible augmentation in the reversible capacity behavior of the spinels upon F⁻ substitution at 32e site and the simultaneous substitution of Cr³⁺ and F⁻ at 16d and 32e sites respectively.     

Carbon contamination analysis and its effect on extreme ultra violet mask imaging performance using coherent scattering microscopy/in-situ accelerated contamination system

The coherent scattering microscopy/in-situ accelerated contamination system (CSM/ICS) is a developmental metrology tool designed to analyze the impact of carbon contamination on the imaging performance. It was installed at 11B EUVL beam-line of the Pohang Accelerator Laboratory (PAL). Monochromatized 13.5 nm wavelength beam with Mo/Si multilayer mirrors and zirconium filters was used. The CSM/ICS is composed of the CSM for measuring imaging properties and the ICS for implementing acceleration of carbon contamination. The CSM has been proposed as an actinic inspection technique that records the coherent diffraction pattern from the EUV mask and reconstructs its aerial image using a phase retrieval algorithm. To improve the CSM measurement accuracy, optical and electrical noises of main chamber were minimized. The background noise level measured by CCD camera was approximately 8.5 counts (3 sigma) when the EUV beam was off. Actinic CD measurement repeatability was <1 A (3 sigma) at 17.5 nm line and space pattern. The influence of carbon contamination on the imaging properties can be analyzed by transferring EUV mask to CSM imaging center position after executing carbon contamination without a fine alignment system. We also installed photodiode and ellipsometry for in-situ reflectivity and thickness measurement. This paper describes optical design and system performance observed during the first phase of integration, including CSM imaging performance and carbon contamination analysis results.     

Characterizations and electrochemical performance of pure and metal-doped Li4Ti5O12 for anode materials of lithium-ion batteries

Pure and metal (Cu, Al, Sn, and V)-doped Li₄Ti₅O₁₂ powders are prepared with solid-state reaction method. The effects of dopants on the physical and electrochemical properties are characterized by using TGA, XRD, and SEM. Compared with pure Li₄Ti₅O₁₂, metal-doped Li₄Ti₅O₁₂ powders show structural stability and enhanced lithium ion diffusivity brought by doped metal ions. Voltage characteristics and initial charge–discharge characteristics according to the C rates in pure and metal-doped Li₄Ti₅O₁₂ electrode materials are studied. Pure Li₄Ti₅O₁₂ powder shows a relatively good discharge capacity of 164 mAh/g at a rate 0.2C, and some of metal-doped Li₄Ti₅O₁₂ powders show higher discharge capacities. Metal-doped Li₄Ti₅O₁₂ powders are promising candidates as anode materials for lithium-ion batteries.     

Analysis and prevention of DRAM latch-up during power-on

The occasional power-on latch-up phenomenon of DRAM modules with a data bus shared by multiple DRAM chips on different modules was investigated and the circuit techniques for latch-up prevention were presented. Through HSPICE simulations and measurements, the latch-up triggering source was identified-to be the excessive voltage drop at the n-well pick-up of the CMOS transmission gate of read data latch circuit due to the short-circuit current which flows when the bus contention occurs during power-on. By extracting the HSPICE Gummel-Poon model parameters of the parasitic bipolar transistors of DRAM chips from the measured I-V and C-V data, HSPICE simulations were performed for the power-on latch-up phenomenon of DRAM chips. Good agreements were achieved between measured and simulated voltage waveforms. In order to prevent the power-on latch-up even when the control signals (RAS, GAS) do not track with the power supply, two circuit techniques were presented to solve the problem. One is to replace the CMOS transmission gate by a CMOS tristate inverter in the DRAM chip design and the other is to start the CAS-BEPORE-RAS (CBR) refresh cycle during power-on and thus disable all the Dout buffers of DRAM chips during the initial power-on period     

Consolidation and mechanical properties of nanostructured MoSi2-SiC-Si3N4 from mechanically activated powder by high frequency induction heated sintering

A dense nanostructured MoSi₂-SiC-Si₃N₄ composite was sintered by the high frequency induction heating method within 2 min from mechanically activated powder of Mo₂N, Mo₂C and Si. Highly dense MoSi₂-SiC-Si₃N₄ composite was produced under simultaneous application of a 80 MPa pressure and the induced current. Mechanical properties and grain size of the composite were investigated. The average hardness and fracture toughness values obtained were 1420 kg/mm² and 4.5 MPa m^1/2, respectively.