Modification of glassy carbon electrode with multi-walled carbon nanotubes and iron(III)-porphyrin film: Application to chlorate, bromate and iodate detection

In this study, multi-wall carbon nanotubes (MWCTs) is evaluated as a transducer, stabilizer and immobilization matrix for the construction of amperometric sensor based on iron-porphyrin. 5,10,15,20-Tetraphenyl-21H,23H-porphine iron(III) chloride (Fe(III)P) adsorbed on MWCNTs immobilized on the surface of glassy carbon electrode. Cyclic voltammograms of the Fe(III)P-incorporated-MWCNTs indicate a pair of well-defined and nearly reversible redox couple with surface confined characteristics at wide pH range (2-12). The surface coverage (Γ) and charge transfer rate constant (k_s) of Fe(III)P immobilized on MWCNTs were 7.68 × 10⁻⁹ mol cm⁻² and 1.8 s⁻¹, respectively, indicating high loading ability of MWCNTs for Fe(III)P and great facilitation of the electron transfer between Fe(III)P and carbon nanotubes immobilized on the electrode surface. Modified electrodes exhibit excellent electrocatalytic activity toward reduction of ClO₃⁻, IO₃⁻ and BrO₃⁻ in acidic solutions. The catalytic rate constants for catalytic reduction of bromate, chlorate and iodate were 6.8 × 10³, 7.4 × 10³ and 4.8 × 10² M⁻¹ s⁻¹, respectively. The hydrodynamic amperometry of rotating-modified electrode at constant potential versus reference electrode was used for detection of bromate, chlorate and iodate. The detection limit, linear calibration range and sensitivity for chlorate, bromate and iodate detections were 0.5 μM, 2 μM to 1 mM, 8.4 nA/μM, 0.6 μM, 2 μM to 0.15 mM, 11 nA/μM, and 2.5 μM, 10 μM to 4 mM and 1.5 nA/μM, respectively. Excellent electrochemical reversibility of the redox couple, good reproducibility, high stability, low detection limit, long life time, fast amperometric response time, wide linear concentration range, technical simplicity and possibility of rapid preparation are great advantages of this sensor. The obtained results show promising practical application of the Fe(III)P-MWCNTs-modified electrode as an amperometric sensor for chlorate, iodate and bromate detections.     

Kinetic study of radical polymerization. II. Solid‐state bulk polymerization of sodium methacrylate by differential scanning calorimetry

The solid‐state radical polymerization of sodium methacrylate was investigated. It was initiated by azobisisobutyronitrile, which was used as a radical initiator. Differential scanning calorimetry (DSC) was used to observe the endothermic and exothermic transitions during the polymerization reaction. Structural studies were performed with the DSC thermograms and Fourier transform infrared and ultraviolet–visible spectra, and all of the results confirmed the progress of the reaction. The obtained data revealed that the polymerization reaction proceeded completely with a 100% conversion. ΔH of this reaction was calculated with various amounts of the initiator, and the peak temperatures were determined at different heating rates. The activation energy (19.7 kcal mol^?1) was also obtained by the Kissinger method for this type of solid polymerization reaction. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1648–1654, 2003     

Electrochemical and microstructural characteristics of nanoperovskite oxides Ba0.2Sr0.8Co0.8Fe0.2O3−δ (BSCF) for solid oxide fuel cells

Nanoperovskite oxides, Ba_0.2Sr_0.8Co_0.8Fe_0.2O_3?δ (BSCF), were synthesized via the co-precipitation method using Ba, Sr, Co, and Fe nitrates as precursors. Next, half cells were fabricated by painting BSCF thin film on Sm_0.2Ce_0.8O_x (samarium doped ceria, SDC) electrolyte pellets. X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical impedance spectroscopy (EIS) measurements were carried out on the BSCF powders and pellets obtained after sintering at 900 °C. Investigations revealed that single-phase perovskites with cubic structure was obtained in this study. The impedance spectra for BSCF/SDC/BSCF cells were measured to obtain the interfacial area specific resistances (ASR) at several operating temperatures. The lowest values of ASR were found to be 0.19 Ω cm², 0.14 Ω cm² 0.10 cm², 0.09 Ω cm² and 0.07 Ω cm² at operating temperatures of 600 °C, 650 °C, 700 °C, 750 °C and 800 °C, respectively. The highest conductivity was found for cells sintered at 900 °C with an electrical conductivity of 153 S cm^?1 in air at operating temperature of 700 °C.     

Estimating the scattering distribution of the received signals in multipath fading channels

This paper presents a novel approach for estimating the distribution of the incoming waves at the mobile unit antenna, i.e. the scattering distribution, in a typical micro-cellular system. This estimate is vital in determining many system parameters of interest as well as designing unbiased estimators for the velocity of mobile units in micro-cellular systems. The proposed approach deploys the zero-crossing rates of the quadrature components and the instantaneous frequency of the received signal at the mobile unit to estimate the scattering distribution. We also propose a new model for simulating multipath fading channels with non-isotropic scattering. We use the channel simulator to evaluate the performance of the proposed estimator for the scattering distribution. Simulation results show that proposed estimator exhibits small bias and root mean square error.     

Investigating correlations between crack width,corrosion level and anchorage capacity

In assessing existing structures, inspection results need to be linked to the effects on load-carrying capacity; to provide such information, this study has investigated the correlation between splitting crack width, corrosion level and anchorage capacity. The study was based on 13 reinforced concrete beams that had been exposed to natural corrosion for 32 years, 11 beams with splitting cracks and 2 without. The crack pattern and widths were documented before undergoing structural testing of anchorage capacity. Thereafter, the reinforcement bars were extracted and their corrosion levels measured using two methods, gravimetric weight loss and 3D scanning. The corrosion level from the weight loss method was approximately twice as large; possible reasons are horizontal or subsurface corrosion pits, and the cleaning method. Further, for the same corrosion level, the specimens in this study had much larger crack widths and slightly lower bond capacity than the artificially corroded tests in the literature; a possible reason is that these specimens had been subjected to combined corrosion and freezing. However, the corrosion level and reduction in bond capacity related to crack width were both lower in the present than in previous studies in the literature. Thus, by formulating a damage indicator from the damage visible in the form of crack widths from artificial test data, the structural capacity is estimated to be on the safe side.     

Design,Construction, and Installation of Movable Electrode Biasing System on Tokamak

The first results of the movable electrode biasing experiments performed on the IR-T1 tokamak are presented. For this purpose, a movable electrode biasing system was designed, constructed, and installed on the IR-T1 tokamak, and then the positive voltage applied to an electrode inserted inside the tokamak limiter and the plasma current, poloidal and radial components of the magnetic fields, loop voltage, and diamagnetic flux in the absence and presence of the biased electrode were measured. Results compared and discussed.     

Zinc oxide nanoparticles: solvent-free synthesis,characterization and application as heterogeneous nanocatalyst for photodegradation of dye from aqueous phase

In present study, for the first time, ZnO nanoparticles have been synthesized via a simple, novel, solvent and template free solid-state thermal decomposition of the mixed Zn(NO₃)·6H₂O and cochineal powders as a novel starting reagent at 600?°C for 3 h. The as-prepared product was analyzed by XRD, EDS, SEM, TEM, FT-IR and DRS. Besides, the effect of cochineal powder on the morphology and particle size of ZnO nanoparticles was investigated. The results exhibited that cochineal powder prevents the sintering of nanoparticles and leads to formation of uniform particles. Moreover, the efficiency of ZnO nanoparticles as a photocatalyst for the decolorization of methylene orange (MO) has been evaluated and 90% degradation of MO was obtained after 120 min.     

Hydrogen production using methane: Techno-economics of decarbonizing fuels and chemicals

In the near-to-medium future, hydrogen production will continue to rely on reforming of widely available and relatively low-cost fossil resources. A techno-economic framework is described that compares the current best practice steam methane reforming (SMR) with potential pathways for low-CO₂ hydrogen production; (i) Electrolysis coupled to sustainable renewable electricity sources; (ii) Reforming of hydrocarbons coupled with carbon capture and sequestration (CCS) and; (iii) Thermal dissociation of hydrocarbons into hydrogen and carbon (pyrolysis). For methane pyrolysis, a process based on a catalytic molten Ni-Bi alloy is described and used for comparative cost estimates. In the absence of a price on carbon, SMR has the lowest cost of hydrogen production. For low-CO₂ hydrogen production, methane pyrolysis is significantly more economical than electrochemical-based processes using commercial renewable power sources. At a carbon price exceeding $21 t^?1 CO₂ equivalent, pyrolysis may represent the most cost-effective means of producing low-CO₂ hydrogen and competes favorably to SMR with carbon capture and sequestration. The current cost disparity between renewable and fossil-based hydrogen production suggests that if hydrogen is to fulfil an expanding role in a low CO₂ future, then large-scale production of hydrogen from methane pyrolysis is the most cost-effective means during the transition period while infrastructure and end-use applications are deployed.     

Preparation and functional properties of fish gelatin–chitosan blend edible films

With the goal of improving the physico-chemical performance of fish gelatin-based films, composite films were prepared with increasing concentrations of chitosan (Ch) (100G:0Ch, 80G:20Ch, 70G:30Ch, 60G:40Ch and 0G:100Ch, gelatin:Ch), and some of their main physical and functional properties were characterised. The results indicated that the addition of Ch caused significant increase (p < 0.05) in the tensile strength (TS) and elastic modulus, leading to stronger films as compared with gelatin film, but significantly (p < 0.05) decreased the elongation at break. Ch drastically reduced the water vapour permeability (WVP) and solubility of gelatin films, as this decline for the blend film with a 60:40 ratio has been of about 50% (p < 0.05). The light barrier measurements present low values of transparency at 600 nm of the gelatin–chitosan films, indicating that films are very transparent while they have excellent barrier properties against UV light. The structural properties investigated by FTIR and DSC showed a clear interaction between fish gelatin and Ch, forming a new material with enhanced mechanical properties.