Search

This work reports a study about the adsorption of the herbicides diquat and difenzoquat from aqueous medium employing polyurethane foam (PUF) as the adsorbent and sodium dodecylsulfate (SDS) as the counter ion. The adsorption efficiency was shown to be dependent on the concentration of SDS in solution, since the formation of an ion-associate between cationic herbicides (diquat and difenzoquat) and anionic dodecylsulfate is a fundamental step of the process. A computational study was carried out to identify the possible structure of the ion-associates that are formed in solution. They are probably formed by three units of dodecylsulfate bound to one unit of diquat, and two units of dodecylsulfate bound to one unit of difenzoquat. The results obtained also showed that 95% of both herbicides present in 45 mL of a solution containing 5.5 mg L −1 could be retained by 300 mg of PUF. The experimental data were well adjusted to the Freundlich isotherm (r 2 ≥ 0.95) and to the pseudo-second-order kinetic equation. Also, the application of Morris-Weber and Reichenberg equations indicated that an intraparticle diffusion process is active in the control of adsorption kinetics. [ABSTRACT FROM AUTHOR]

The cationic herbicides paraquat, diquat and difenzoquat are largely used in different cultures worldwide. With this, there is an intrinsic risk of environmental contamination when these herbicides achieve natural waters. The goal of this work was to propose a novel and low-cost sorbent for the removal of the cited herbicides from aqueous medium. The proposed sorbent was prepared by loading polyurethane foam with sodium dodecylsulfate. The influence of several parameters (SDS concentration, HCl concentration and shaking time) on the loading process was investigated. The results obtained in this work demonstrated that all studied variables influenced the loading process, having significant effect on the extraction efficiency of the resulted PUF-SDS. At optimized conditions, the PUF was loaded by shaking 200 mg of crushed foam with 200 mL of a solution containing 5.0×10 −3 mol L −1 SDS and 0.25 mol L −1 HCl, for 30 min. The obtained PUF-SDS was efficient for removing the three herbicides from aqueous medium, achieving extraction percentages higher than 90%. The sorption process followed a pseudo second-order kinetics, which presented excellent predictive capacity of the amount of herbicide retained with time. [ABSTRACT FROM AUTHOR]

The distribution and concentration of organic compounds in the environment have attracted great interest mainly due to their capability of bioaccumulation, dispersion, and danger to living organisms. Factors such as urbanization, population growth, and the emergence of new technologies contribute to the increase in pollutant emissions, especially volatile organic compounds (VOCs), such as benzene, toluene, ethylbenzene, and xylenes (BTEX). These compounds are emitted by several sources, becoming more common in work environments, influencing indoor air quality (IAQ), which can cause health damage, in addition to increasing the likelihood of cancer development. In this context, we developed a semipermeable membrane device (SPMD), consisting of low density polyethylene membrane (8 cm long × 3 cm wide), filled with 3 mL of acetonitrile, for passive sampling of toluene (and benzene) in gas phase. With this configuration, the SPMD needed 24 h exposure to the indoor air in order to achieve equilibrium. The target compounds were quantified in the acceptor phase by HPLC-DAD. The optimized SPMD was tested for the collection of toluene and benzene in six chemistry laboratories at Fluminense Federal University and in five nail salons in the city of Niterói, in the state of Rio de Janeiro, Brazil. The developed sampling method was able to identify the analytes in the indoor air of the studied environments, and was easy to operate, with no need to clean up the extracts, allowing their direct injection into the chromatographic system. • A passive sampler was developed for toluene (and benzene) collection from indoor air. • The sampler was constructed with a semipermeable membrane filled with acetonitrile. • Toluene and benzene were determined in the acceptor phase by HPLC-DAD. • We identified toluene and benzene in the indoor air of nail salons and chemistry laboratories. [ABSTRACT FROM AUTHOR]

Antivenom allergy disease mediated by patient IgE is an important public health care concern. To improve detection of hypersensitive individuals prior to passive antibody therapy, an amperometric immunosensor was developed to detect reactive human IgE. Whole horse IgG3 (hoIgG3) was immobilized onto the surface of carbon or gold screen-printed electrodes through a cross-linking solution of glutaraldehyde on a chitosan film. Sera from persons with a known allergic response to hoIgG3 or non-allergic individuals was applied to the sensor. Bound human IgE (humIgE) was detected by an anti-humIgE antibody through a quantitative amperometric determination by tracking via the electrochemical reduction of the quinone generated from the hydroquinone with the application of a potential of 25 mV. The optimal immunosensor configuration detected reactive humIgE at a dilution of 1:1800 of the human sera that represent a detection limit of 0.5 pg/mL. Stability testing demonstrated that through 20 cycles of a scan, the specificity and performance remained robust. The new immunosensor successfully detected humIgE antibodies reactive against hoIgG3, which could allow the diagnosis of potential allergenic patients needing therapeutic antivenom preparations from a horse. [ABSTRACT FROM AUTHOR]

We studied the adsorption of paraquat onto polyurethane foam (PUF) when it was in a medium containing sodium dodecylsulfate (SDS). The adsorption efficiency was dependent on the concentration of SDS in solution, because the formation of an ion-associate between the cationic paraquat and the dodecylsulfate anion was found to be a fundamental step in the process. A computational study was carried out to identify the possible structure of the ion-associate in aqueous medium. The obtained data demonstrated that the structure is probably formed from four units of dodecylsulfate bonded to one paraquat moiety. The results showed that 94% of the paraquat present in 45 mL of a solution containing 3.90 × 10 −5 mol L −1 could be retained by 300 mg of PUF, resulting in the removal of 2.20 mg of paraquat. The experimental data were reasonably adjusted to the Freundlich isotherm and to the pseudo-second-order kinetic model. Also, the application of Morris–Weber and Reichenberg models indicated that both film-diffusion and intraparticle-diffusion processes were active during the control of the adsorption kinetics. [ABSTRACT FROM AUTHOR]

Abstract: In the present work, the determination of the total protein concentration in hyperimmune serum samples was performed through a partial least-squares near-infrared (NIR-PLS) method. The method was based on the chemometric treatment of the NIR spectra of samples. The influences of spectra preprocessing and spectral window utilized in the construction of PLS model were studied. Models were built using reference data of 19 samples selected through the use of hierarchical cluster analysis (HCA) of NIR spectra of samples and another 24 samples were employed for external validation of the method. A model with better prediction capacity was obtained after whole spectra preprocessing by multiplicative scattering correction (MSC) algorithm and using data in the spectral range of 2158–2209nm. Under optimized conditions a RMSEP of 0.21gdl−1 and a quality coefficient value (QC) of only 5.8% were obtained for the prediction of total protein content in the samples used for external validation. Also, a determination coefficient, r 2, of 0.97 was obtained in the correlation of predicted and reference data of samples situated in the validation set. [Copyright &y& Elsevier]

Abstract: This work presents a detailed study about the adsorption of iron(III)–thiocyanate complexes onto unloaded polyether-type polyurethane foam (PUF). A novel strategy was employed for this purpose, utilizing the adjustment of the plug cylinder of PUF to the arm of an overhead stirrer. The system was characterized in relation to equilibrium and kinetic aspects and it was modeled by applying Langmuir and Freundlich isotherms. The results obtained showed that adsorption occurs on a monolayer and that external transport of the solute from solution to adsorbent was the rate-determining mechanism. A maximum adsorption capacity of was obtained under established experimental conditions (0.5 mol L−1 SCN− and 0.005 mol L−1 HCl). Sequential extraction experiments were carried out by changing PUF in time intervals previously defined (5, 20, and 40 min), and the obtained results showed that it is possible to remove around 95% of the Fe(III) in solution through five consecutive extractions of 5 min with five 200 mg PUF cylinders. [Copyright &y& Elsevier]