Progress and major BARRIERS of nanocatalyst development in direct methanol fuel cell: A review

Direct methanol fuel cells (DMFC), among the most suited and prospective alternatives for portable electronics, have lately been treated with nanotechnology. DMFCs may be able to remedy the energy security issue by having low operating temperatures, high conversion efficiencies, and minimal emission levels. Though, slow reaction kinetics are a significant restriction of DMFC, lowering efficiency and energy output. Nowadays, research is more focused on fundamental studies that are studying the factors that can improve the capacity and activity of catalysts. In DMFC, among the most widely explored catalysts are platinum and ruthenium which are enhanced in nature by the presence of supporting materials such as nanocarbons and metal oxides. As a result, this research sheds light on nanocatalyst development for DMFCs based on Platinum noble metal. To summarize, this research focuses on the structure of nanocatalysts, as well as support materials for nanocatalysts that can be 3D, 2D, 1D, or 0D. The support material described is made up of CNT, CNF, and CNW, which are the most extensively used because they improve the performance of catalysts in DMFCs. In addition, cost estimations for fuel cell technology are emphasized to show the technology's status and requirements. Finally, challenges to nanocatalyst development have been recognized, as well as future prospects, as recommendations for more innovative future research.     

Studies on influence of hydrogen and carbon monoxide concentration on reduction progression behavior of molybdenum oxide catalyst

Temperature programmed reduction (TPR) analysis was applied to investigate the chemical reduction progression behavior of molybdenum oxide (MoO₃) catalyst. The composition and morphology of the reduced phases were characterized by X-ray diffraction spectroscopy (XRD), X-ray photoelectron spectroscopy (XPS), and field emission scanning electron microscopy (FE-SEM). The reduction progression of MoO₃ catalyst was attained with different reductant types and concentration (10% H₂/N₂, 10% and 20% CO/N₂ (%, v/v)). Two different modes of reduction process were applied. The first approach of reduction involved non-isothermal mode reduction up to 700 °C, while the second approach of reduction involved the isothermal mode reduction for 60 min at 700 °C. Hydrogen temperature programmed reduction (H₂-TPR) results showed the reduction progression of three-stage reduction of MoO₃ (Mo⁶⁺ → Mo⁵⁺ → Mo⁴⁺ → Mo⁰) with Mo⁵⁺ and Mo⁴⁺. XRD analysis confirmed the formation of Mo₄O₁₁ phase as an intermediate phase followed by MoO₂ phase. After 60 min of isothermal reduction, peaks of metallic molybdenum (Mo) appeared. Whereas, FESEM analysis showed porous crater-like structure on the surface cracks of MoO₂ layer which led to the growth of Mo phase. Meanwhile, the reduction of MoO₃ catalyst in 10% carbon monoxide (CO) showed the formation of unstable intermediate phase of Mo₉O₂₆ at the early stage of reduction. Furthermore, by increasing 20% CO led to the carburization of MoO₂ phase, resulted in the formation of Mo₂C rather than the formation of metallic Mo, as confirmed by XPS analysis. Therefore, the presented study shows that hydrogen gave better reducibility due to smaller molecular size, which contributed to high diffusion rate and achieved deeper penetration into the MoO₃ catalyst compared to carbon monoxide reductant. Hence, the reduction of MoO₃ in carbon monoxide atmosphere promoted the formation of Mo₂C which was in agreement with the thermodynamic assessment.     

Improvement of adhesive bonding of grit-blasted steel substrates by using diluted resin as a primer

This study reveals the micro-structural details on the metal substrate surface prepared by grit blasting, and then proposes a simple resin pre-coating method aiming at full wetting of the substrate surface for stronger adhesive bonding. The resin pre-coating solution consisting of around 90% acetone and around 10% resin without hardener is used as a primer, which can be sprayed or blushed onto the grit-blasted metal substrate. The acetone solution can carry resin deep into micro-cavities created by grit blasting and effectively coat and wet micro-debris so that micro-voids or gaps between the adhesive joint and metal substrate can be removed. Since the resin pre-coating does not contain hardener and remains wet, the wettability of the substrate is also improved. The normal epoxy adhesive with hardener can then be applied onto the substrate surface. Despite having the primer-like function, the proposed resin pre-coating method still maintains the simplicity of one epoxy resin system. Based on the current study, a resin and acetone solution without hardener does not seem to have adverse effects on the final bonding strengths of adhesive joints, although acetone is known to have detrimental effects on resin and hardener adhesive systems. Four different surface conditions are examined, each having 14 specimens: (1) Grit-Blasted (GB) surface, (2) GB-surface with ultrasonic cleaning, (3) GB-surface with resin Pre-Coating (PC) only, and (4) GB-surface with both ultrasonic cleaning and PC. 25% improvement in the shear strength has been achieved by the resin pre-coating method, even without ultrasonic cleaning, in comparison with 8% improvement after ultrasonic cleaning. These results show GB-surface with PC is beneficial to adhesive bonding, which can be adopted for structural applications even if thorough substrate surface cleaning on site is not possible. The improved wettability of metal substrates after resin pre-coating contributes to the maximum possible utilization of the contact areas over the roughened substrate surfaces and thus leads to the enhanced adhesive bond strength.     

Potential use of Fourier transform infrared spectroscopy for differentiation of bovine and porcine gelatins

In order to classify unknown gelatin into their species of origin, a simple and rapid method for the qualitative determination was developed using Fourier transform infrared (FTIR) in combination with attenuated total reflectance (ATR) and discriminant analysis. The spectra were analysed using a chemometric method, principal component analysis (PCA), to classify and characterise gelatin compounds using regions of the FTIR spectra in the range of 3290–3280 cm^?1 and 1660–1200 cm^?1 as calibration models. Results from PCA, which were subsequently represented by the Cooman’s plot showed a clear distinction between gelatin samples of bovine and porcine origins. This qualitative approach, besides providing a rapid determination of the source of gelatin, may also be established based on a second derivative study of the FTIR spectrum to alleviate any doubt of the gelatin source for applications in the food and pharmaceutical industries.     

Performance Evaluation of Cost-Effective Multicast–Unicast Key Management Method

Group key management is one of the key security issues in multicast networks. The main challenge is to provide a secure group key management method which avoids high key update cost in terms of the number of transmitted keys. In order to achieve low key update cost for group key management, most of the existing methods increase their encryption/decryption cycles which requires a strong cryptographic function. In this paper, a cost-effective key management method is proposed to address the problem of high key update cost without increasing the encryption/decryption cycles. We evaluated our proposed method with existing tree-based methods by using Markov chain and Poisson Arrival Process. Results indicate the efficiency of our proposed method in reducing the key update cost significantly compared to the existing tree-based key management methods.     

Antifungal activity of Lactobacillus fermentum Te007, Pediococcus pentosaceus Te010, Lactobacillus pentosus G004, and L. paracasi D5 on selected foods

In the search for new preservatives from natural resources to replace or to reduce the use of chemical preservatives 4 strains of lactic acid bacteria (LAB) were selected to be evaluated for their antifungal activity on selected foods. The supernatants of the selected strains delayed the growth of fungi for 23 to 40 d at 4 °C and 5 to 6 d at 20 and 30 °C in tomato puree, 19 to 29 d at 4 °C and 6 to 12 d at 20 and 30 °C in processed cheese, and 27 to 30 d at 4 °C and 12 to 24 d at 20 and 30 °C in commercial bread. The shelf life of bread with added LAB cells or their supernatants were longer than normal bread. This study demonstrates that Lactobacillus fermentum Te007, Pediococcus pentosaceus Te010, L. pentosus G004, and L. paracasi D5 either the cells or their supernatants could be used as biopreservative in bakery products and other processed foods. PRACTICAL APPLICATION: The heat stability nature of the antifungal compounds produced by the LAB isolates offers a promising application of L. fermentum Te007, P. pentosaceus Te010, L. pentosus G004, and L. paracasi D5 as biopreservative in bakery products or other processed foods to replace or reduce the use of chemical preservatives.     

Improvement in the measurement of spectrophotometric data in the m-hydroxydiphenyl pectin determination methods

In the pectin analysis of foods by visible spectrophotometry using the m-hydroxydiphenyl (MHDP) as the chromogenic reagent, the evolution of the absorbance at 520 nm of the MHDP/5FF chromophore with respect to the elapsed time from the beginning of the reaction for different d-galacturonic acid concentrations was studied.It was observed that after 45 min, the stability of the readings predicted by the different methods was not reached. This evolution depended on the d-galacturonic acid concentration. The need to analyse the samples in sequence was noted, in such a way that after the addition of MHDP, a protocol was established so that the spectrophotometric data measurements taken at the highest absorbance have high reproducibility.     

Some Generalised Characteristics of the Electro-dynamics of the Plasma Focus in Its Axial Phase: Illustrated by an Application to Independantly Determine the Drive Current Fraction and the Mass Swept-Up Fraction

We describe the axial phase of the Mather plasma focus by two coupled equations of motion and circuit. We non-dimensionalised these equations resulting in two coupled equations which are characterised by only three scaling parameters α, β and δ which are ratios of electrical to transit times, inductances and impedances respectively. The normalised current waveform, trajectory and speed profile are unique for each combination of α, β, δ which are the ratios of characteristic times (electrical discharge vs. axial transit), inductances (tube inductance vs. static inductance) and impedances (stray resistance vs. electrical surge impedance). This leads to important information and insight into various aspects of the axial phase. In the present work we show that in a time-matched plasma focus shot we deduce the value of axial phase current fraction f_c simply by measuring the calibrated voltage waveform and the uncalibrated current waveform. The scaling parameters β and δ are fixed; and by form-fitting the measured current waveform to the normalised current waveform using the value of α of the shot is determined uniquely; from which the peak current and the ratio of peak to average speed [the speed form factor (SFF)] are obtained. The average transit speed is measured by time-of-flight using the voltage upturn as indicator of end of axial phase. Then the SFF yields the peak speed. The measured voltage (back EMF), peak current and peak axial speed (all at the end of axial phase) allows the unambiguous measurement of f_c. The value of the mass swept-up fraction f_m is deduced from α which is the ratio of the characteristic discharge and the characteristic transit times, both deduced during the non-dimensionalisation of the equations. Analysis of a time-matched shot in the INTI PF at 15 kV, 3 Torr D₂ gave f_c = 0.68 and f_m = 0.05.     

Numerical investigation of the first bifurcation for the flow in a rotor–stator cavity of radial aspect ratio 10

The nature of transition to unsteadiness of rotor–stator disk flows of large radial aspect ratio is investigated by means of several numerical tools which consist in computing the base flow even when unstable, performing linearized or non-linear time integrations starting from initial conditions of different amplitudes and computing the spectrum of the Jacobian using the ARPACK library. From these numerical experiments we conclude that, in a cavity of radial aspect ratio 10, the transition to unsteadiness occurs through a subcritical Hopf bifurcation. In addition these calculations show the existence of a large amplitude chaotic branch for values of the Reynolds number far below the linear stability threshold, and onto which the solutions are attracted for large subcritical values due to the strong non-normality of the Jacobian of the evolution operator.     

Effect of strontium and zirconium doped barium cerate on the performance of proton ceramic electrolyser cell for syngas production from carbon dioxide and steam

Syngas has been produced from carbon dioxide (CO₂) and steam using a proton ceramic electrolyser cell. Proton-conducting electrolytes which exhibit high conductivity can suffer from low chemical stability. In this study, to optimize both proton conductivity and chemical stability, barium cerate and doped barium cerate are synthesized using solid state reaction method: BaCeO₃ (BC), Ba_0.6Sr_0.4CeO_3-α (BSC), Ba_0.6Sr_0.4Ce_0.9Y_0.1O_3-α (BSCY), and BaCe_0.6Zr_0.4O_3-α (BCZ). The BC, BSC, and BSCY are calcined at 1100 °C for 2 h and BCZ is calcined at 1300 °C for 12 h, respectively. All samples exhibit 100% perovskite and crystallite sizes equal 37.05, 28.46, 23.65 and 17.46 nm for BC, BSC, BSCY and BCZ, respectively. Proton conductivity during steam electrolysis as well as catalytic activity toward the reverse water gas shift reaction (RWGS) is tested between 400 and 800 °C. The conductivity increases with temperature and the values of activation energy of conduction are 64.69, 100.80, 103.78 and 108.12 kJ mol⁻¹ for BSCY, BC, BSC, and BCZ, respectively. It is found that although BCZ exhibits relatively low conductivity, the material provides the highest CO yield at 550–800 °C, followed by BSCY, BSC, and BC, correlating to the crystallite size and BET surface area of the samples. Catalytic activity toward RWGS of composited Cu and electrolytes is also measured. Additional Cu (60 wt%) significantly increases catalytic activity. The CO yield increases from 3.01% (BCZ) to 43.60% (Cu/BCZ) at 600 °C and CO can be produced at temperature below 400 °C. There is no impurity phase detected in BCZ sample after exposure to CO₂-containing gas mixture (600 °C for 5 h) while CeO₂ phase is detected in BSC and BSCY and both CeO₂ and BaO are observed in BC sample.