Search Results (7)

A novel malachite green molecularly imprinted membrane (MG-MIM) with specific selectivity for malachite green (MG) and leucomalachite green (LMG) was prepared using a hydrophobic glass fiber membrane as the polymer substrate, methyl violet as a template analog, 4-vinyl benzoic acid as the functional monomer, and ethyleneglycol dimethacrylate as the crosslinking agent. MG-MIM and non-imprinted membrane (NIM) were structurally characterized using scanning electron microscopy, surface area analyzer, Fourier-transform infrared spectrometer and synchronous thermal analyzer. The results showed that MG-MIM possessed a fluffier surface, porous and looser structure, and had good thermal stability. Adsorption properties of MG-MIM were investigated under optimal conditions, and adsorption equilibrium was reached in 20 min. The saturated adsorption capacities for MG and LMG were 24.25 ng·cm⁻² and 13.40 ng·cm⁻², and the maximum imprinting factors were 2.41 and 3.20, respectively. Issues such as “template leakage” and “embedding” were resolved. The specific recognition ability for the targets was good and the adsorption capacity was stable even after five cycles. The proposed method was successfully applied for the detection of MG and LMG in real samples, and it showed good linear correlation in the range of 0 to 10.0 μg·L⁻¹ (R² = 0.9991 and 0.9982), and high detection sensitivity (detection limits of MG and LMG of 0.005 μg/kg and 0.02 μg·kg⁻¹ in shrimp, and 0.005 μg/kg and 0.02 μg/kg in fish sample). The recoveries and relative standard deviations were in the range of 76.31–93.26% and 0.73–3.72%, respectively. The proposed method provides a simple, efficient and promising alternative for monitoring MG and LMG in aquatic products. Full article

The study of the interactions between nanoparticles (NPs) and proteins has had a pivotal role in facilitating the understanding of biological effects and safe application of NPs after exposure to the physiological environment. Herein, for the first time, the interaction between L-methionine capped silver nanoparticles (AgMet), and bovine serum albumin (BSA) is investigated in order to predict the fate of AgMet after its contact with the most abundant blood transport protein. The detailed insights into the mechanism of interaction were achieved using different physicochemical techniques. The UV/Vis, TEM, and DLS were used for the characterization of the newly formed “entity”, while the kinetic and thermodynamic parameters were utilized to describe the adsorption process. Additionally, the fluorescence quenching and synchronous fluorescence studies enabled the prediction of the binding affinity and gave us insight into the influence of the adsorption on the conformation state of the BSA. According to the best of our knowledge, for the first time, we show that BSA can be used as an external stabilizer agent which is able to induce the peptization of previously agglomerated AgMet. We believe that the obtained results could contribute to further improvement of AgNPs’ performances as well as to the understanding of their in vivo behavior, which could contribute to their potential use in preclinical research studies. Full article

Conventional stabilization/solidification materials have defects in the simultaneous treatment of heavy metals (HMs) and phenanthrene (PHe). In order to solve this problem, a new functional material β-cyclodextrin modified biochar (β-CD-BC) was prepared by integrating the properties of biochar (BC) and the hydrophilic and hydrophobic properties of the β-CD surface and combined with Portland cement (PC) to cure and stabilize HMs and PHe. The effect of key parameters on the treatment effect was discussed by response surface method. The results showed that the minimum leaching concentration if HMs was 16.81 mg·L⁻¹, and the leaching concentration of PHe can be as low as 0.059 μg/kg under the conditions of β-CD-BC and Portland cement ratio of 9.75% and 11.4%, curing for 22.85 d. The weak acid soluble state reduced from 9~13% to 0.5~6%, the residual state was increased from 37~61% to 77~87%. The unconfined compressive strength of sample is more than 50 kPa. The results of this study can provide a new technical scheme for long-term curing and stabilization of HMs and PHe. Full article

In this paper, we investigate implications of running a cooling system of two silicagel/water adsorption chillers powered by a district heating network. The devices are connected in series, i.e., the heating water output from the primary chiller is directed to the secondary one. In consequence, the secondary device must deal with an even lower driving temperature and with temperature fluctuations caused by the primary device. We have evaluated three factors that influence the operation of those coupled devices: synchronization of their operating cycles, selection of their cycle time allocations (CTAs), and changing the heating water mass flow rate. Numerical analyses indicate that the performance of the secondary chiller drops significantly if the coupled devices that use the same CTA run asynchronously. The decrease is largest if the shift between the operating cycles is $x=0.375$ and $x=0.875$. We found that it is possible to reduce the negative influence of the asynchronous operation by implementing different CTA in each chiller. The best performance is achieved if the primary chiller uses an adsorption time to desorption time ratio $f=1.0$ and the secondary chiller uses f = 0.6–0.7. Full article

Cobalt ferrite (CoFe₂O₄) nanoparticles were synthesized and investigated as a catalyst in the reaction of nitrous oxide (N₂O) decomposition. Cobalt ferrite was synthesized by solid–phase interaction at 1100 °C and by preliminary mechanochemical activation in a roller-ring vibrating mill at 400 °C. The nanoparticles were characterized by X-ray diffraction (XRD), synchronous thermal analysis (TG and DSC) and scanning electron microscopy (SEM). A low-temperature nitrogen adsorption/desorption test was used to evaluate the catalytic activity of the cobalt ferrite nanoparticles. Correlations between the structure and catalytic properties of the catalysts are reported. The highest catalytic activity of CoFe₂O₄ in the reaction of nitrous oxide decomposition was 98.1% at 475 °C for cobalt ferrite obtained by mechanochemical activation. Full article

Surface plasmon resonance (SPR) and Love wave (LW) surface acoustic wave (SAW) sensors have been established as reliable biosensing technologies for label-free, real-time monitoring of biomolecular interactions. This work reports the development of a combined SPR/LW-SAW platform to facilitate simultaneous optical and acoustic measurements for the investigation of biomolecules binding on a single surface. The system’s output provides recordings of two acoustic parameters, phase and amplitude of a Love wave, synchronized with SPR readings. We present the design and manufacturing of a novel experimental set-up employing, in addition to the SPR/LW-SAW device, a 3D-printed plastic holder combined with a PDMS microfluidic cell so that the platform can be used in a flow-through mode. The system was evaluated in a systematic study of the optical and acoustic responses for different surface perturbations, i.e., rigid mass loading (Au deposition), pure viscous loading (glycerol and sucrose solutions) and protein adsorption (BSA). Our results provide the theoretical and experimental basis for future application of the combined system to other biochemical and biophysical studies. Full article

Using impedance spectroscopy the electrical response of sensors with various porous Y-stabilized ZrO₂ (YSZ) microstructures was measured for gas concentrations containing 0–100 ppm NO with 10.5%O₂ at temperatures ranging from 600–700 °C. The impedance response increased substantially as the sensor porosity increased from 46%–50%. Activation energies calculated based on data from the impedance measurements increased in magnitude (97.4–104.9 kJ/mol for 100 ppm NO) with respect to increasing YSZ porosity. Analysis of the oxygen partial pressure dependence of the sensors suggested that dissociative adsorption was the dominant rate limiting. The PWC/DNP theory level was used to investigate the gas-phase energy barrier of the 2NO+O₂→2NO₂ reaction on a 56-atom YSZ/Au model cluster using Density Functional Theory and Linear Synchronous Transit/Quadratic Synchronous Transit calculations. The reaction path shows oxygen surface reactions that begin with NO association with adsorbed O₂ on a Zr surface site, followed by O₂ dissociative adsorption, atomic oxygen diffusion, and further NO₂ formation. The free energy barrier was calculated to be 181.7 kJ/mol at PWC/DNP. A qualitative comparison with the extrapolated data at 62% ± 2% porosity representing the YSZ model cluster indicates that the calculated barriers are in reasonable agreement with experiments, especially when the RPBE functional is used. Full article