Removal of Copper,Nickel, and Zinc Ions from Electroplating Rinse Water

Removal of copper, nickel, and zinc ions from synthetic electroplating rinse water was investigated using cationic exchange resin (Ceralite IR 120). Batch ion exchange studies were carried out to optimize the various experimental parameters (such as contact time, pH, and dosage). Influence of co‐existing cations, chelating agent EDTA on the removal of metal ion of interest was also studied. Sorption isotherm data obtained at different experimental conditions were fitted with Langmuir, Freundlich, Redlich–Peterson, and Toth models. A maximum adsorption capacity of 164 mg g^?1 for Cu(II), 109 mg g^?1 for Ni(II), and 105 mg g^?1 for Zn(II) was observed at optimum experimental conditions according to Langmuir model. The kinetic data for metal ions adsorption process follows pseudo second‐order. Presence of EDTA and co‐ions markedly alters the metal ion removal. Continuous column ion exchange experiments were also conducted. The breakeven point of the column was obtained after recovering effectively several liters of rinse water. The treated rinse water could be recycled in rinsing operations. The Thomas and Adams–Bohart models were applied to column studies and the constants were evaluated. Desorption of the adsorbed metal ions from the resin column was studied by conducting a model experiments with Cu(II) ions loaded ion exchange resin column using sulfuric acid as eluant. A novel lead oxide coated Ti substrate dimensionally stable (DSA) anode was prepared for recovery of copper ions as metal foil from regenerated liquor by electro winning at different current densities (50–300 A cm^?2).     

H-implantation in SO2 and CO2 ices

Ices in the solar system are observed on the surface of planets, satellites, comets and asteroids where they are continuously subordinate at particle fluxes (cosmic ions, solar wind and charged particles caught in the magnetosphere of the planets) that deeply modify their physical and structural properties. Each incoming ion destroys molecular bonds producing fragments that, by recombination, form new molecules also different from the original ones. Moreover, if the incoming ion is reactive (H⁺, Oⁿ⁺, Sⁿ⁺, etc.), it can concur to the formation of new molecules.Those effects can be studied by laboratory experiments where, with some limitation, it is possible to reproduce the astrophysical environments of planetary ices.In this work, we describe some experiments of 15-100 keV H⁺ and He⁺ implantation in pure sulfur dioxide (SO₂) at 16 and 80 K and carbon dioxide (CO₂) at 16 K ices aimed to search for the formation of new molecules. Among other results we confirm that carbonic acid (H₂CO₃) is formed after H-implantation in CO₂, vice versa H-implantation in SO₂ at both temperatures does not produce measurable quantity of sulfurous acid (H₂SO₃). The results are discussed in the light of their relevance to the chemistry of some solar system objects, particularly of Io, the innermost of Jupiter's Galilean satellites, that exhibits a surface very rich in frost SO₂ and it is continuously bombarded with H⁺ ions caught in Jupiter's magnetosphere.     

A Method for Analyzing the Self-Supported Earth-Retaining Structure Using Stabilizing Piles

The self-supported earth-retaining structure using stabilizing piles (SSR is used from here) has the advantages of less deformation and less internal force compared with conventional cantilever retaining structure. It is easier to conduct the excavation when SSR is used for an excavation instead of using braced excavation with struts. The SSR is better than other methods to the 10 m shallow excavation depth in terms of economical and constructional efficiency when the ground is not very soft. However, this SSR method lacks a theoretical basis in terms of geotechnical engineering. The objective of this study is to develop a method of analysis by laboratory model tests. A variety of model tests were performed in order to analyze the behavior of SSR and the ground, and to measure the stress acting on stabilizing piles relative to excavation steps and earth pressures on the wall. The analysis reveals the failure mechanism of a wedge and then suggests a method for calculating a virtual supported point. These findings were incorporated into a method for analyzing retaining wall, stabilizing piles, and beams connecting two structures. Future research is geared toward developing a design program that uses the analytical methodology for this SSR.     

Estimation of base motion in instrumented steel buildings using output‐only system identification

A procedure to estimate the seismic motion at the base of a building from measured acceleration response at two or more floors is presented. The proposed method is comprised of two steps. In the first step, the dynamic characteristics of the building are inferred by using an output‐only system identification procedure. In the second step, the motion of the base of the building is estimated by using the transfer function of a simplified building model consisting of a shear and flexural continuous beam together with dynamic properties obtained in the first step. The proposed method is validated first with an analytical model subjected to the 1940 El Centro ground motion and then with an instrumented building in California that experienced the 1994 Northridge earthquake, and the ground motions at the base of the building are available. It is shown that the proposed method is capable of providing very good estimates of the motion at the base. The use of the proposed method is finally illustrated on an instrumented building, where the sensor at the base of the building did not function during the 1994 Northridge earthquake. Copyright © 2013 John Wiley & Sons, Ltd.     

Analysis of bromate and bromide in drinking water by ion chromatography-inductively coupled plasma mass spectrometry

A method for the detection of bromate and bromide in drinking water by ion chromatography-inductively coupled plasma mass spectrometry (IC-ICP-MS) was developed. The optimized conditions of IC including pH and concentration of the effluent were studied. The results showed that the above two species of bromine were baseline separated within nine minutes under the optimized conditions. The detection limits (S/N=3) of bromate and bromide were 0.23 and 0.12 μg/L, respectively. The RSD (n=6) of the peak areas was 1.2%-3.5%. The method has been successfully applied to the determination of the type bromide in drinking water samples. The recoveries were 95%-109%. The method can be used for the regular analysis of bromate and bromide in real drinking water samples.     

Gabor‐frame‐based Gaussian packet migration

We present a Gaussian packet migration method based on Gabor frame decomposition and asymptotic propagation of Gaussian packets. A Gaussian packet has both Gaussian‐shaped time–frequency localization and space–direction localization. Its evolution can be obtained by ray tracing and dynamic ray tracing. In this paper, we first briefly review the concept of Gaussian packets. After discussing how initial parameters affect the shape of a Gaussian packet, we then propose two Gabor‐frame‐based Gaussian packet decomposition methods that can sparsely and accurately represent seismic data. One method is the dreamlet–Gaussian packet method. Dreamlets are physical wavelets defined on an observation plane and can represent seismic data efficiently in the local time–frequency space–wavenumber domain. After decomposition, dreamlet coefficients can be easily converted to the corresponding Gaussian packet coefficients. The other method is the Gabor‐frame Gaussian beam method. In this method, a local slant stack, which is widely used in Gaussian beam migration, is combined with the Gabor frame decomposition to obtain uniform sampled horizontal slowness for each local frequency. Based on these decomposition methods, we derive a poststack depth migration method through the summation of the backpropagated Gaussian packets and the application of the imaging condition. To demonstrate the Gaussian packet evolution and migration/imaging in complex models, we show several numerical examples. We first use the evolution of a single Gaussian packet in media with different complexities to show the accuracy of Gaussian packet propagation. Then we test the point source responses in smoothed varying velocity models to show the accuracy of Gaussian packet summation. Finally, using poststack synthetic data sets of a four‐layer model and the two‐dimensional SEG/EAGE model, we demonstrate the validity and accuracy of the migration method. Compared with the more accurate but more time‐consuming one‐way wave‐equation‐based migration, such as beamlet migration, the Gaussian packet method proposed in this paper can correctly image the major structures of the complex model, especially in subsalt areas, with much higher efficiency. This shows the application potential of Gaussian packet migration in complicated areas.     

Microanalysis of carbon isotope composition in organic matter by secondary ion mass spectrometry

An analytical procedure has been developed for the in situ measurement of carbon isotope composition of organic matter, with a spatial resolution of 20-30 μm, using a Cameca IMS 1270 ion microprobe. Instrumental mass fractionation (IMF) of carbon isotopes was observed to be independent of primary ion beam intensity and sputtering time, but did depend on vacuum conditions and on the chemical composition of the sample. To evaluate such “matrix effects”, a set of 9 standards representative of the natural chemical variability of organic matter was prepared, with H/C atomic ratios and organic carbon contents (C_org) ranging between 0.04 and 1.74 and between 41 and 100 wt.%, respectively. Under the analytical conditions tested, IMF was not found to be influenced by the presence of silicate mineral impurities in the organic matter, but variations in IMF up to 5‰ were observed over the set of standards with the magnitude of IMF negatively correlated to the H/C ratios of samples. Aliphaticity ratios determined using Fourier transform infrared microspectroscopy provided an in situ estimation of H/C ratios with a spatial resolution barely exceeding that of the ion microprobe and permit a correction for matrix effects with a standard error of ± 0.2‰ (1σ). Taking into account all sources of uncertainty, ion microprobe δ¹³C were accurately determined with a ± 0.7‰ (1σ) total uncertainty. The mechanism for the matrix effect of H/C ratios upon IMF is still to be determined but it is likely related to the difference in proportion of atomic vs. molecular carbon ions observed between samples of different H/C ratios.     

Rise and fall of road salt contamination of water-supply springs

A storage pile of de-icing agent consisting principally of sodium chloride was placed in the recharge area of two springs, and remained there for 2 years. Water flow is through fractures in rocks with low matrix permeability, along a hydraulic gradient developed along fracture zones. Salt contamination in the springs was noticed about 1 year after the salt was placed. When the salt was removed 1 year later, chloride concentrations in the springs exceeded 500 mg/L. Monitoring for the following 5 years showed salt contamination rising for the first year, but receding to normal background after 5 years. Chloride to sodium ratios of the spring waters indicated that some sodium was initially sequestered, probably by ion exchange on clay minerals, in the early part of the monitoring period, and released during the latter part; thereby extending the period of contamination.Richard S. diPretoro: deceased     

Observations of the electric fields that accelerate auroral particles

Electric fields accelerate electrons and ions in the auroral zone at altitudes below 8000 km to produce several distinctive particle distributions. The electric field of electrostatic shocks and double layers produces the inverted-V precipitating electron and up-flowing ion beams. Electrostatic ion cyclotron waves heat ion beams. The electric field in low frequency plasma waves and electrostatic shocks produces ion conics and field-aligned or counterstreaming electrons. Relationships between electric fields and particle distributions are illustrated with data from the S3-3 satellite.     

Multi-scale pore structure of COx claystone: Towards the prediction of fluid transport

We aim to relate the morphology of the pore network of finely porous claystones to their fluid transport properties. By using Focused Ion Beam in combination with Scanning Electron Microscopy (FIB/SEM), we image the pore network of COx claystone from 2D image stacks and as 3D reconstructed volumes. Our FIB/SEM samples are representative of the mesoscopic matrix clay. Porosity resolvable by this technique is in the range 1.7–5.9% with peak pore sizes of 50–90 nm. 3D pore network skeletonization provides connected pore volumes between end surfaces, tortuosity, density, and shortest pore paths with their pore size distribution. At higher resolution, 2D transmission electron microscopy (TEM) reveals large amounts of smaller pores (2–20 nm) between clay aggregates, associated to a local porosity of 14–25%, and peak sizes of 4–6 nm. Liquid permeability predictions with Katz–Thompson model, at the FIB/SEM volume scale and at the TEM surface scale, are in good agreement with macroscopic measurements (on the order of 10⁻²⁰ m²), showing that both mesopore sizes (peaks at 50–90 nm and 4–6 nm), located within the clay matrix, contribute to liquid transport.