Leaching behavior of V,Pb, Cd,Cr, and As from stone coal waste rock with different particle sizes

This paper investigates the leaching behavior of heavy metals (V, Pb, Cd, Cr, and As) from stone coal waste rocks with various particle sizes using dynamic leaching experiments. The results show that the dissolved concentrations of V and As initially increased and then slightly decreased as time progressed and that the dissolved concentrations of Pb, Cd, and Cr were high in the early stage before decreasing. The particle size of the stone coal waste rocks strongly influenced the heavy metal concentration in the leaching solutions. The effects of the particle size of the stone coal waste rocks on the dissolved concentrations of V, Pb, and As decreased in the order fine fraction > medium fraction > coarse fraction, and the effects of particle size on the dissolved concentrations of Cr and Cd decreased in the order medium fraction > coarse fraction > fine fraction and coarse fraction > medium fraction > fine fraction, respectively. The quantities of heavy metals dissolved from the stone coal waste rock with fine particle sizes were observed to decrease in the order V (17104.36 μg/kg) > As (609.41 μg/kg) > Pb (469.24 μg/kg) > Cr (56.35 μg/kg) > Cd (27.52 μg/kg), and the dissolution rates decreased in the order As (2.96%) > Pb (0.93%) > V (0.35%) > Cd (0.25%) > Cr (0.01%). The specific surface area, pore size of the stone coal waste rocks, and chemical forms of heavy metals also influenced the release of heavy metals from the stone coal waste rocks. Kinetic analysis showed that the dissolution of heavy metals fundamentally agreed with the rate equation controlled by the shrinking core model. The results of this study are expected to serve as a reference for the evaluation of heavy metals contamination from stone coal waste rocks.     

Microstructural characterization and oxidation resistance of multicomponent equiatomic CoCrCuFeNi-TiO high-entropy alloy

CoCrCuFeNi-TiO was prepared by arc melting of the pure elements and Ti₂CO powder under an Ar atmosphere. Both CoCrCuFeNi and CoCrCuFeNi-TiO alloys are composed of a face-centered cubic (fcc) solid solution, whereas the alloys of CoCrCuFeNi-TiO are basically composed of an fcc solid solution and TiO crystals. The microstructures of CoCrCuFeNi-TiO are identified as dendrite and interdendrite structures such as CoCrCuFeNi. The morphology of TiO is identified as an equiaxed crystal with a small amount of added Ti₂CO. By increasing the amount of Ti₂CO added, the TiO content was dramatically increased and part of the equiaxed crystals changed to a dendrite structure. A test of the oxidation resistance demonstrates that the oxidation resistance of CoCrCuFeNi-TiO is better than that of CoCrCuFeNi. However, as the TiO content increases further, a corresponding decrease is observed in the oxidation resistance.     

Effect of melting temperature on microstructural evolutions,behavior and corrosion morphology of Hadfield austenitic manganese steel in the casting process

In this study, the effect of melting temperature on the microstructural evolutions, behavior, and corrosion morphology of Hadfield steel in the casting process is investigated. The mold was prepared by the sodium silicate/CO₂ method, using a blind riser, and then the desired molten steel was obtained using a coreless induction furnace. The casting was performed at melting temperatures of 1350, 1400, 1450, and 1500℃, and the cast blocks were immediately quenched in water. Optical microscopy was used to analyze the microstructure, and scanning electron microscopy (SEM) and X-ray diffractrometry (XRD) were used to analyze the corrosion morphology and phase formation in the microstructure, respectively. The corrosion behavior of the samples was analyzed using a potentiodynamic polarization test and electrochemical impedance spectroscopy (EIS) in 3.5wt% NaCl. The optical microscopy observations and XRD patterns show that the increase in melting temperature led to a decrease of carbides and an increase in the austenite grain size in the Hadfield steel microstructure. The corrosion tests results show that with increasing melting temperature in the casting process, Hadfield steel shows a higher corrosion resistance. The SEM images of the corrosion morphologies show that the reduction of melting temperature in the Hadfield steel casting process induced micro-galvanic corrosion conditions.     

Mineral-phase evolution and sintering behavior of MO-SiO2-Al2O3-B2O3 (M=Ca,Ba) glass-ceramics by low-temperature liquid-phase sintering

In this work, network former SiO₂ and network intermediate Al₂O₃ were introduced into typical low-melting binary compositions CaO·B₂O₃, CaO·2B₂O₃, and BaO·B₂O₃ via an aqueous solid-state suspension milling route. Accordingly, multiple-phase aluminosilicate glass-ceramics were directly obtained via liquid-phase sintering at temperatures below 950℃. On the basis of liquid-phase sintering theory, mineral-phase evolutions and glass-phase formations were systematically investigated in a wide MO-SiO₂-Al₂O₃-B₂O₃ (M=Ca, Ba) composition range. The results indicate that major mineral phases of the aluminosilicate glass-ceramics are Al₂₀B₄O₃₆, CaAl₂Si₂O₈, and BaAl₂Si₂O₈ and that the glass-ceramic materials are characterized by dense microstructures and excellent dielectric properties.     

40-Gb/s all-optical digital 4-bit priority encoder employing cross-gain modulation in semiconductor optical amplifiers

High-speed all-optical logic circuits have attracted much attention because of their important roles in signal processing in next-generation optical networks.The digital encoder is widely used in binary calculation,multiplexing,demultiplexing,address recognition and data encryption.A priority encoder allows the existence of multiple valid inputs simultaneously,identifies the priority of the request signals and encodes the priority.We propose and experimentally demonstrate an all-optical 4-bit priority encoder for return-to-zero signals at 40 Gbit/s based on cross-gain modulation in semiconductor optical amplifiers.Detuning fil-ters after semiconductor optical amplifiers are employed to improve the output performance.Correct logic bit sequences and clear open eye patterns with extinction ratios exceeding 10 dB are achieved.     

Measurement of laminar burning velocities of iso-butanol-air mixtures

The laminar burning velocity of iso-butanol-air mixtures was measured under different initial pressures, initial temperatures and equivalence ratios using high-speed schlieren photography and outwardly propagation flame in a constant volume combustion bomb. Based on the analysis of stretched flame propagation speed and stretch rate, the laminar burning velocities and Markstein lengths of iso-butanol-air flames are obtained. In accordance, with photos of flame, an analysis of flame stability and the influencing factors is carried out. The results show that the laminar burning velocity is decreased with the increase of initial pressure and is increased with the increase of initial temperature. The maximum value of laminar burning velocity is presented at the equivalence ratio of 1.2. The Markstein length is decreased with the increase of equivalence ratio. For specified equivalence ratio, the Markstein length is decreased with the increase of initial temperature and initial pressure. Thus, the flame instability is increased with the increase of equivalence ratio, initial temperature and initial pressure.     

Predicting the spread of nuclear radiation from the damaged Fukushima Nuclear Power Plant

Japan suffered a M9.0 earthquake and massive tsunami on March 11, 2011, which seriously damaged the Fukushima Nuclear Power Plant and caused a nuclear crisis. The spread of nuclear radiation from the power plant through the atmosphere and ocean was predicted with a short-term climate forecasting model and an ocean circulation model under some idealized assumptions. If nuclear matter were leaked in the near-ground layer of 992 hPa, the climate model results show that the nuclear radiation would cover North America 10 days after the initial leakage, with the concentration at the forefront dramatically reduced to 10 millionths of the initial model concentration at the source. The radiation would span Europe in 15 days and cover much of the Northern Hemisphere in 30 days. If the initial leakage was assumed to occur in the layer 5000-m above the ground, the radiation would cover Europe in 10 days and cover much of the Northern Hemisphere in 15 days. Moreover, under the assumption that the nuclear matter leaked in the 10000-m layer, the radiation would affect much of China after 10 days. The ocean circulation model indicates that the nuclear material would be slowly transported northeast of Fukushima and reach 150°E in 50 days, and the nuclear debris in the ocean would be confined to a narrow band. Compared with the spread in the ocean, the area affected by leaked nuclear radiation in the atmosphere would be very large. Atmospheric monitors in North America and Europe will be helpful for estimating the effect in China of any leaked nuclear material.     

Development and application of flexible substrate sensors in instantaneous heat flux measurement

A new type of sensor with the flexible substrate is introduced. It is applicable in measuring instantaneous heat flux on the model surface in a hypersonic shock tunnel. The working principle, structure and manufacture process of the sensor are presented. The substrate thickness and the dynamic response parameter of the sensor are calculated. Because this sensor was successfully used in measuring the instantaneous heat flux on the surface of a flat plate in a detonation-driven shock tunnel, it may be effective in measuring instantaneous heat flux on the model surface.     

C-isotope composition and correlation of the Upper Neoproterozoic in Keping area, Xinjiang

C-isotope analysis of the carbonates in the Upper Neoproterozoic in Keping, Xinjiang indicates that the Qigebrak Formation and the Upper Sugaitbrak Formation mainly record positive C-isotope values, and a distinct positive excursion occurs in the lower part of the Qigebrak Formation. There are three negative excursions in the boundary between the Qigebrak Formation and the Cambrian, the uppermost and lowermost Upper Sugaitbrak Formation. These characters resemble those of the Upper Neoproterozoic in the Three-Gorge area, which suggests that the Upper Sugaitbrak Formation and Qigebrak Formation can be correlated with the middle and upper parts of the Doushantuo Formation and Dengying Formation, respectively. The negative excursion at the top of the Upper Sugaitbrak Formation corresponds to that at the top of the Doushantuo Formation, while the negative excursion at the bottom of the Sugaitbrak Formation can be correlated with that at the middle part of the Doushantuo Formation in the Three-Gorge area and that at the top of the Hangelchaok diamictites in the Quruqtagh area.     

Solvent effects on photophysical properties of copper and zinc porphyrins

The photophysics of Zn（tetraphenylporphyrin,TPP）, Zn（tetra-2,4,6-trimethylphenyl porphyrin, TMP）, Zn （tetra-（o-dichlorophenyl） porphyrin, TPPCI8）, Cu（tetraphenylporphyrin,TPP）, Cu（tetra-2,4,6-trimethyl- phenyl porphyrin,TMP）, and Cu（tetra-（o-dichlorophenyl） porphyrin, TPPCIE, TPPCI8） in several solvents have been investigated on steady state and time-resolved spectroscopy. The Cu（TPPCI8 ） is normal and shows no evidence of CT transition in the visible or near UV regions in nonpolar solvent. However, Cu（TPPCI8）shows a blue shift in the absorption spectrum and intramolecular CT bands at absorption spectra in polar solvent, which shows a fluorescence maximum emission at 650 nm and 8.4 ns lifetime. The reason can be attributed to two points. Firstly, the increase of solvent polarity can enlarge outer reorganisational energy, which is favorable to reduce the activation free energy of charger-transfer transition based on Marcus theory of electron transfer. Moreover, the internal heavy-atom effect on Cu（TPPCIE） is encouraging to stabilize the 2T1 state also, which increases the possibility of population to CT band from 2T1 state. This result is in accord with an earlier estimate of a 10 ns lifetime and CT absorption at 640 nm bands for the CT state of Cu （11） octethylporphyrins. Other possible reasons arousing unusual fluorescence like H-bonding, axial ligands, molecular aggregation are excluded.