Tailoring of nanozeolite NaX for enhanced removal of a phytoestrogen from its aqueous solutions

This study represents the application of nanozeolite NaX (NZX) synthesized by hydrothermal treatment without addition of any expensive structure directing agent for the highly effectual adsorption of biochanin A from aqueous solution. The characteristics and surface morphology of NZX were determined using FT-IR, SEM, TEM, BET, and XRD. The adsorption performance of NZX was analyzed at different conditions such as temperature, pH, contact time, adsorbent dose, and initial adsorbate concentration. The adsorption mechanism was well verified by pseudo-second-order kinetic and Redlich–Peterson isotherm models. The thermodynamic parameters revealed that the removal process was exothermic and spontaneous.     

Role of interface on dynamic modulus of high‐performance poly(etheretherketone)/ceramic composites

High‐performance printed circuit board or electronic packaging substrate with low warping particularly at high frequency is the key demand of manufacturers. In the present work, poly(etheretherketone) (PEEK) matrix composites reinforced with untreated micron size aluminum nitride (AlN) and alumina (Al₂O₃) particles have been studied for dynamic modulus in the temperature range varying from 30 to 250°C. At 48 vol % particles, the room temperature modulus of the PEEK/AlN composites increased by approximately fivefold (～ 23 GPa), whereas it increased by twofold for PEEK/Al₂O₃ composite. The reinforcing efficiency is more pronounced at higher temperatures. The significant improvement in modulus was attributed to the better adhesion between the matrix and the AlN particles. Scanning electron microscope (SEM) and Kubat parameter showed that the poor adhesion between the matrix and the Al₂O₃ particles resulted in comparatively smaller increase in modulus of PEEK/Al₂O₃, despite higher intrinsic modulus of Al₂O₃ than that of AlN. SEM showed almost uniform distribution of particles in the matrix. The experimental data were correlated with several theoretical models. The Halpin–Tsai model with ξ (xi) is equal to four correlates well up to 48 vol % AlN composites while ξ is equal to two correlates only up to 18 vol % Al₂O₃ composites. Guth–Smallwood model also correlates well up to 28 vol % AlN and 18 vol % Al₂O₃‐filled composites. Thereafter, data deviated from it due to the particles tendency to aggregate formation. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Enhanced upconversion study of Er3+-Yb3+ codoped NaYF4 phosphors synthesized by the reverse microemulsion method

Herein, nanocrystals of Er³⁺ and Er³⁺, Yb³⁺ co-doped NaYF₄ upconversion (UC) phosphor were prepared via the reverse-microemulsion method. The impact of different concentrations of Er³⁺ ions on the UC emission intensity after 980?nm diode laser excitation is discussed. The structure, morphology and composition of the nanophosphors were confirmed by X-ray diffraction, transmission electron microscopy, scanning electron microscopy and the results showed the presence of NaYF₄ nanocrystals with hexagonal phases of NaYF₄. The UC spectra revealed two emission bands including a green and a red emission band and the CIE coordinate for the samples were estimated. The present research revealed that the reverse-microemulsion approach will be suitable for the synthesis of efficient upconversion nanophosphors.     

Carbon nanotube-based electrochemical sensor for the determination of halobetasol propionate, a topical corticosteroid

Electrocatalytic reduction of halobetasol propionate (HBP) at single-walled carbon nanotube (SWCNT) modified edge plane pyrolytic graphite electrode (EPPGE) was performed by square wave voltammetry and cyclic voltammerty in phosphate buffer of pH 7.2. The surface morphology of SWCNT/EPPGE was characterized by field emission scanning electron microscopy. The enhanced peak current (i _p) and lower reduction peak potential (E _p) at modified electrode as compared to bare electrode were obvious evidences for the electrocatalytic ability of SWCNT toward the reduction of HBP. The cathodic peak current varied linearly with concentration of HBP in the range 0.02 to 1 mM with sensitivity of 2.432 μA mM⁻¹ and detection limit (3σ/slope) of 10 μM. The product of electrochemical reduction of HBP was characterized using FT-IR and ¹H-NMR spectroscopic techniques. A tentative mechanism for the formation of product was suggested and it was found that reduction of >C=O occurred at position three. The proposed methodology was successfully applied to the detection of HBP in pharmaceutical preparations.     

Electrochemical and peroxidase-catalyzed oxidation of epinephrine

Electrochemical and peroxidase-catalyzed oxidation of epinephrine (EPI) has been studied. In the electrochemical studies a single well-defined, 4e, 4H⁺, pH-dependent oxidation peak was observed in square wave and cyclic sweep voltammetry at edge plane pyrolytic graphite electrode. In the reverse sweep a redox couple was observed. The decay of the UV-absorbing intermediate generated and the first-order rate constants were calculated at different pH and were found to be ～6.3 × 10^?3 s^?1. The detection limit and sensitivity are found to be 17 × 10^?8 M and 2.325 μA μM^?1 respectively. At pH 7.2, the electro-oxidation product was characterized using NMR and DEPT studies as leucoadrenochrome. The peroxidase-catalyzed oxidation was carried out using horseradish peroxidase and initiated by adding H₂O₂. The identical spectral changes, rate constants and product formed during electrochemical and enzymatic oxidation suggest that the same intermediate species is generated during both the oxidations. A tentative pathway for the oxidation of EPI has been suggested. It is concluded that the electrochemical and peroxidase-catalyzed oxidation of EPI proceed by an identical pathway.     

Enhanced Photovoltaic Performance of PEDOT:PSS/Si Heterojunction Solar Cell with ZnO BSF Layer: A Simulation Study using SCAPS-1D

Silicon - Here, we report an enhanced photovoltaic (PV) performance including open circuit voltage (Voc), short circuit current (Jsc), fill factor (FF) and power conversion efficiency (PCE) of...     

MoS2-Polyaniline Based Flexible Electrochemical Biosensor: Toward pH Monitoring in Human Sweat

Wearable pH sensors for sweat analysis have garnered significant scientific attention for the detection of early signs of many physiological diseases. In this study, a MoS₂-polyaniline (PANI) modified screen-printed carbon electrode (SPCE) is fabricated and used as a sweat biosensor. The exfoliated MoS₂ nanosheets are drop casted over an SPCE and are functionalized by a conducting polymer, polyaniline (PANI) via the electropolymerization technique. The as-fabricated biosensor exhibits high super-Nernstian sensitivity of −70.4 ± 1.7 mV pH⁻¹ in the linear range of pH 4 to 8 of 0.1 m standard phosphate buffer solution (PBS), with outstanding reproducibility. The sensor exhibits excellent selectivity against the common sweat ions including Na⁺, Cl⁻, K⁺, and NH₄⁺ with tremendous long-term stability over 180 min from pH 4 to 6. The enhanced active surface area and better electrical conductivity as a consequence of the synergistic effect between MoS₂ and PANI are correlated with the boosted performance of the as-produced biosensor. The feasibility of the sensor is further examined using an artificial sweat specimen and the successful detection confirms the potential of the biosensor for a real-time noninvasive, skin attachable, and flexible wearable pH sensor.     

Sodium silicate as a coke inhibitor during naphtha pyrolysis

Rates of coke formation during steam pyrolysis of naphtha have been investigated in a jet-stirred reactor both for sodium silicate coated and uncoated Inconel 600 surfaces in the temperature range of 1078–1108 K. Coke formation rates were significantly reduced on sodium silicate coated plates due to the passivation of the metal surface. However, the coking rates gradually increased with successive decokings of the coated surface.