Mapping of heavy metal pollution in stream sediments using combined geochemistry, field spectroscopy, and hyperspectral remote sensing: A case study of the Rodalquilar mining area, SE Spain

The aim of this study is to derive parameters from spectral variations associated with heavy metals in soil and to explore the possibility of extending the use of these parameters to hyperspectral images and to map the distribution of areas affected by heavy metals on HyMAP data. Variations in the spectral absorption features of lattice OH and oxygen on the mineral surface due to the combination of different heavy metals were linked to actual concentrations of heavy metals. The ratio of 610 to 500 nm (R_610,500 nm) in the visible and near-infrared (VNIR) range, absorption area at 2200 nm (Area_2200 nm), and asymmetry of the absorption feature at 2200 nm (Asym_2200 nm) showed significant correlations with concentrations of Pb, Zn, and As, respectively. The resulting spectral gradient maps showed similar spatial patterns to geochemical gradient maps. The ground-derived spectral parameters showed a reliable quantitative relationship with heavy metal levels based on multiple linear regression. To examine the feasibility to applying these parameters to a HyMAP image, image-derived spectral parameters were compared with ground-derived parameters in terms of R², one-way ANOVA, and spatial patterns in the gradient map. The R_1344,778 nm and Area_2200 nm parameters showed a weak relationship between the two datasets (R² > 0.5), and populations of spectral parameter values, Depth_500 nm, R_1344,778 nm, and Area_2200 nm derived from the image pixels were comparable with those of ground-derived spectral parameters along a section of the stream channel. The pixels classified in the rule image of Depth_500 nm, R_1344,778 nm, and Area_2200 nm derived from a HyMAP image showed similar spatial patterns to the gradient maps of ground-derived spectral parameters. The results indicate the potential applicability of the parameters derived from spectral absorption features in screening and mapping the distribution of heavy metals. Correcting for differences in spectral and spatial resolution between ground and image spectra should be considered for quantitative mapping and the retrieval of heavy metal concentrations from HyMAP images.     

Parameters affecting the efficiency of affinity-based reversed micellar extraction and separation (ARMES) in glycoprotein purification

The Bladder Neck Support Prosthesis (BNSP) was used in 21 women with combined genuine stress incontinence (GSI) and detrusor instability (DI). Outcomes included frequency volume charts, pad tests, voiding cystometry and quality of life scores, up to the sixth month. Of the 21 recruits, 5 never wore the BNSP home, leaving 16 participants. A further 2 did not reach week 4 because of poor efficacy or inability to fit the device. In the 14 who reached week 4, the median number of leaks/day declined from 4.3 to 1.0 (p = 0.002). Median pad test loss fell from 53 to 7 mL (p = 0.012). Cystometry showed an increase in maximum bladder capacity (p < 0.05) and a modest reduction in severity of detrusor instability, with no evidence of outflow obstruction. Three further women discontinued because of poor efficacy (2) or a poorly fitting device (1), leaving 11 of 16 participants (69%) at week 8, when median pad test loss fell to 2 mL. The BNSP is a useful option in patients with the unfortunate combination of an unstable bladder and an incompetent urethra, but requires careful fitting and attention to detail.     

Pile Driving Analysis for Top Hammering and Bottom Hammering

Piles are used for platform foundations and other offshore structures. Pile driving performance is predicted and analyzed using the wave equation analysis method. In general, the hammering point can be any part of the pile and the same analyses used for hammering at the top of the pile (top hammering) can be used for pile driving by hammering at the bottom of the pile (bottom hammering). Based on the numerical analyses in this research including residual stresses in the pile, there is little difference between the predictions of pile penetration per hammer blow by single- or multiple-blow analyses when soil resistance is low, such as 10 blows/m. The same is true for top hammering and bottom hammering when soil resistance is low. However, when soil resistance is high compared to that of the pile-hammer system, single-blow analysis predicts early refusal for top hammering and unrealistically high pile penetration for bottom hammering. Therefore, multiple-blow analysis, which considers residual stresses, should be used for better understanding of realistic pile driving performance and predictions. Additionally, this study shows that gravity is another controlling factor for pile driving in low-resistance soil.     

Chemical absorption of carbon dioxide into phenyl glycidyl ether solution containing THA-CP-MS41 catalyst

Carbon dioxide was absorbed into the phenyl glycidyl ether (PGE) solution within a range of 0–2.0 kmol/m³ in a stirred batch tank with a planar gas-liquid interface at 333–363 K and 101.3 kPa. Trihexylamine-immobilized on chloropropyl-functionalized MCM-41 (THA-CP-MS41) was used as a mesoporous catalyst, dispersed in organic liquid for the reaction between carbon dioxide and PGE. The measured absorption rates were analyzed to obtain the reaction kinetics of the consecutive chemical reactions which consisted of two steps using the mass transfer mechanism based on film theory. The overall reaction kinetics, analyzed with the pseudo-first-order reaction constant in the consecutive reaction model, was equivalent to the consecutive reaction kinetics. Effects of polar solvent, such as N, N-dimethylacetamide, N-methyl-2-pyrrolidinone, and dimethyl sulfoxide, on the reaction rate constants were observed using the solubility parameter of the solvent.     

Surface functionalization of SBA-15 particles for ibuprofen delivery

We have synthesized SBA-15 particles and functionalized their surface with different functional groups (amine, diamine, and sulfonic acid groups) to use them as carrier materials in drug delivery. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen sorption, and zeta potential measurements were used to characterize the synthesized particles. After surface functionalization, the surface of the sulfonic acid-functionalized particles was more acidic than that of the other particles. Using ibuprofen as a model drug, we found that the release rate increased at higher pH. Furthermore, the particles with the sulfonic acid groups exhibited higher release rate than those with the amine and diamine groups. We explained the difference in the release rate using different electrostatic interaction between drug and particle surface that was caused by the surface functionalization. These results should enable design of drug carrier materials based on the SBA-15 particles with the desired release rate.     

"Outer-sphere to inner-sphere" redox cycling for ultrasensitive immunosensors

This paper reports chemical-chemical (CC) and electrochemical-chemical-chemical (ECC) redox cycling, for use in ultrasensitive biosensor applications. A triple chemical amplification approach using an enzymatic reaction, CC redox cycling, and ECC redox cycling is applied toward electrochemical immunosensors of cardiac troponin I. An enzymatic reaction, in which alkaline phosphatase converts 4-aminophenyl phosphate to 4-aminophenol (AP), triggers CC redox cycling in the presence of an oxidant and a reductant, and electrochemical signals are measured with ECC redox cycling after an incubation period of time in an air-saturated solution. To obtain high, selective, and reproducible redox cycling without using redox enzymes, two redox reactions [the reaction between AP and the oxidant and the reaction between the oxidized form of AP (4-quinone imine, QI) and the reductant] should be fast, but an unwanted reaction between the oxidant and reductant should be very slow. Because species that undergo outer-sphere reactions (OSR-philic species) react slowly with species that undergo inner-sphere reactions (ISR-philic species), highly OSR-philic Ru(NH(3))(6)(3+) and highly ISR-philic tris(2-carboxyethyl)phosphine (TCEP) are chosen as the oxidant and reductant, respectively. The OSR- and ISR-philic QI/AP couple allows fast redox reactions with both the OSR-philic Ru(NH(3))(6)(3+) and the ISR-philic TCEP. Highly OSR-philic indium-tin oxide (ITO) electrodes minimize unwanted electrochemical reactions with highly ISR-philic species. Although the formal potential of the Ru(NH(3))(6)(3+)/Ru(NH(3))(6)(2+) couple is lower than that of the QI/AP couple, the endergonic reaction between Ru(NH(3))(6)(3+) and AP is driven by the highly exergonic reaction between TCEP and QI (via a coupled reaction mechanism). Overall, the "outer-sphere to inner-sphere" redox cycling in the order of highly OSR-philic ITO, highly OSR-philic Ru(NH(3))(6)(3+)/Ru(NH(3))(6)(2+) couple, OSR- and ISR-philic QI/AP couple, and highly ISR-philic TCEP allows high, selective, and reproducible signal amplification. The electrochemical data obtained by chronocoulometry permit a lower detection limits than those obtained by cyclic voltammetry. The detection limit of an immunosensor for troponin I in serum, calculated from the anodic charges in chronocoulometry, is ca. 10 fg/mL.     

Usability evaluation of symbols in digital cluster for drivers with color vision deficiency

Universal Access in the Information Society - Digital clusters have been adopted as displays in vehicles, and various driving information is presented through the digital clusters with different...     

Perchlorate adsorption and desorption on activated carbon and anion exchange resin

The mechanisms of perchlorate adsorption on activated carbon (AC) and anion exchange resin (SR-7 resin) were investigated using Raman, FTIR, and zeta potential analyses. Batch adsorption and desorption results demonstrated that the adsorption of perchlorate by AC and SR-7 resin was reversible. The reversibility of perchlorate adsorption by the resin was also proved by column regeneration test. Solution pH significantly affected perchlorate adsorption and the zeta potential of AC, while it did not influence perchlorate adsorption and the zeta potential of resin. Zeta potential measurements showed that perchlorate was adsorbed on the negatively charged AC surface. Raman spectra indicated the adsorption resulted in an obvious position shift of the perchlorate peak, suggesting that perchlorate was associated with functional groups on AC at neutral pH through interactions stronger than electrostatic interaction. The adsorbed perchlorate on the resin exhibited a Raman peak at similar position as the aqueous perchlorate, indicating that perchlorate was adsorbed on the resin through electrostatic attraction between the anion and positively charged surface sites.     

Control of serial sampling systems

In industrial multivariable plants, it is often the case that the plant outputs are detected not simultaneously but serially. The problem of estimating the state vector of the plant based on the data obtained from such a detection scheme is considered, and a special type of observer (referred to as a serial-sampling type) which renews its internal state whenever new data are obtained is proposed. The constructability of a serial-sampling observer and the stability of the closed-loop system which includes such an observer are theoretically studied