Solid oxide fuel cell bi-layer anode with gadolinia-doped ceria for utilization of solid carbon fuel

Pyrolytic carbon was used as fuel in a solid oxide fuel cell (SOFC) with a yttria-stabilized zirconia (YSZ) electrolyte and a bi-layer anode composed of nickel oxide gadolinia-doped ceria (NiO-GDC) and NiO-YSZ. The common problems of bulk shrinkage and emergent porosity in the YSZ layer adjacent to the GDC/YSZ interface were avoided by using an interlayer of porous NiO-YSZ as a buffer anode layer between the electrolyte and the NiO-GDC primary anode. Cells were fabricated from commercially available component powders so that unconventional production methods suggested in the literature were avoided, that is, the necessity of glycine-nitrate combustion synthesis, specialty multicomponent oxide powders, sputtering, or chemical vapor deposition. The easily-fabricated cell was successfully utilized with hydrogen and propane fuels as well as carbon deposited on the anode during the cyclic operation with the propane. A cell of similar construction could be used in the exhaust stream of a diesel engine to capture and utilize soot for secondary power generation and decreased particulate pollution without the need for filter regeneration.     

Solar energy-economic growth nexus in top 10 countries with the highest installed capacity

ABSTRACT

This paper investigates the relationship between solar energy production and economic growth for top 10 countries with the highest installed solar energy production capacity as of 2017 (China, the USA, Japan, Germany, Italy, India, the UK, France, Australia, and Spain, respectively) using data over the period 1999–2015. For this purpose, the paper employs panel cointegration and causality methods that are robust to cross-sectional dependence. The findings imply that the coefficient of solar energy is insignificant in the empirical model and that there is no causality between solar energy and GDP, indicating the neutrality hypothesis prevails for solar energy. Theoretical and practical implications are also discussed.     

Impact of H.I. Schlesinger's discoveries upon the course of modern chemistry on B−(N−)H hydrogen carriers

Representatives of B?(N?)H hydrogen carriers are alkali borohydrides (e.g. LiBH₄ and NaBH₄) and amine boranes (e.g. NH₃BH₃ and NaNH₂BH₃). These are old compounds; they were discovered in the first half of the 20th century. One of the main contributors to their development is Prof. Hermann I. Schlesinger (1882–1960). In the recent years, there has been new interest in these old compounds as novel chemical H storage materials. Sodium borohydride NaBH₄ is a typical example. It was discovered by Schlesinger and collaborators in the 1950s. At that time it was found to be an attractive H₂ generator; owing to this property it reemerged in the early 2000s for on-board H₂ generation. Today, Schlesinger is commonly considered as the pioneer of NaBH₄ as hydrogen carrier but the impact of Schlesinger and collaborators' discoveries upon the course of modern chemistry on B?(N?)H hydrogen carriers is far more extensive … This is highlighted herein.     

Towards more active and stable PdAgCr electrocatalysts for formic acid electrooxidation: The role of optimization via response surface methodology

In this study, multiwall carbon nanotube (MCNT)‐supported Pd (Pd/MWCNT) catalysts are prepared by using NaBH₄ reduction method. In order to maximize the oxidation and reduction of H₂SO₄, synthesis conditions (Pd ratio, molar ratio of NaBH₄/K₂PdCl₄, volume of deionized water, and duration of agitation) are optimized by using response surface methodology (RSM). The optimum synthesis conditions are determined as 58.2% of Pd by weight, 154.6 molar ratio of NaBH₄ to K₂PdCl₄, 19.48 mL of deionized water, and 186.16 min of agitation duration. The effect of electrochemical measurement conditions on the oxidation kinetics of Pd/MWCNT is also investigated by RSM. The optimum electrochemical measurement conditions are found as 10 μL of catalyst mixture, 90°C of H₂SO₄ solution, and 5.5 M H₂SO₄. The Pd/MWCNT, Pd₅₀Ag₅₀/MWCNT, and Pd_65.6Ag_33.6Cr_0.80/MWCNT catalysts prepared under optimized conditions are characterized by using X‐ray diffraction, transmission electron microscopy, N₂ adsorption‐desorption, and inductively coupled plasma mass spectrometry. The crystallite sizes of these catalysts are found as 4.85, 5.66, and 5.26 nm for Pd/MWCNT, Pd₅₀Ag₅₀/MWCNT, and Pd_65.6Ag_33.6Cr_0.80/MWCNT catalysts, respectively. Isotherms of all these catalysts are found to be similar to Type V isotherms with H3 hysteresis loop. The average particle size of Pd₅₀Ag₅₀/MWCNT and Pd_65.6Ag_33.6Cr_0.80/MWCNT catalysts are determined as 5.2 and 9.2 nm, respectively. Electrochemical performance of as‐prepared catalysts is evaluated by using cyclic voltammetry and chronoamperometry. The formic acid electrooxidation (FAEO) activities are found as 18.9, 27.8, and 51.6 mA/cm² for Pd/MWCNT, Pd₅₀Ag₅₀/MWCNT, and Pd_65.6Ag_33.6Cr_0.80/MWCNT, respectively. Pd_65.6Ag_33.6Cr_0.80/MWCNT shows the highest activity and stability. Optimization of synthesis conditions and electrochemical measurement parameters allow us to obtain very good electrochemical activity and stability for FAEO reaction compared with anode catalysts in the literature.     

Biometric identification using fingertip electrocardiogram signals

In this research work, we present a newly fingertip electrocardiogram (ECG) data acquisition device capable of recording the lead-1 ECG signal through the right- and left-hand thumb fingers. The proposed device is high-sensitive, dry-contact, portable, user-friendly, inexpensive, and does not require using conventional components which are cumbersome and irritating such as wet adhesive Ag/AgCl electrodes. One of the other advantages of this device is to make it possible to record and use the lead-1 ECG signal easily in any condition and anywhere incorporating with any platform to use for advanced applications such as biometric recognition and clinical diagnostics. Furthermore, we proposed a biometric identification method based on combining autocorrelation and discrete cosine transform-based features, cepstral features, and QRS beat information. The proposed method was evaluated on three fingertip ECG signal databases recorded by utilizing the proposed device. The experimental results demonstrate that the proposed biometric identification method achieves person recognition rate values of 100% (30 out of 30), 100\(\%\) (45 out of 45), and 98.33\(\%\) (59 out of 60) for 30, 45, and 60 subjects, respectively.     

Micelle Crosslinked Polyacrylic Acid Hydrogels with Resilience and Self-Recovery Properties

Micelle crosslinking method is one of the several techniques to fabricate hydrogels with good mechanical performance. Micelle crosslinked hydrogels reported so far are fabricated using a multistep preparation process due to the functionalization of block copolymers or surfactants with acrylate, aldehyde, azo, or reversible addition-fragmentation chain transfer groups to create a polymer network. Herein, a simple one-step approach is introduced to produce resilient hydrogels prepared by bulk polymerization of acrylic acid and esterification with Triton X-100 (TX-100) in the presence of catalyst sulfuric acid (H₂SO₄). The advantage of this study is that TX-100 surfactants self-assembling into micelles are directly bonded onto polymer chains through an ester bond without any further modification. The obtained hydrogels exhibit tensile strengths up to 135 ± 8 kPa and compressive strengths up to 16 ± 1 MPa over 94% strains as well as complete self-recovery and high resilience abilities (≈86% at strains up to 400%) originating from hydrophobic associations in the core of micelles acting as dynamic cross-linkers along with hydrogen bonds and entanglements between polymer chains acting as additional crosslink points. The overall results show that the hydrogels can be good candidate as elastic materials in many fields.     

Role of lanthanide elements on the catalytic behavior of supported Pd catalysts in the reduction of NO with methane

In this study, the role of lanthanide elements (Ce, Gd, La, and Yb) on Pd/TiO₂ catalysts in the catalytic reduction of NO with methane was investigated. Steady-state reaction experiments in the presence of oxygen showed that the addition of lanthanide elements increases the oxygen resistance of the catalyst. The post-reaction XPS characterization results revealed that majority of the Pd sites remained in the zero oxidation state in the presence of Ce or Gd. The effect of SO₂ (145 ppm) and H₂O (0–6.6%) in NO–CH₄–O₂ reaction over supported Pd and Gd–Pd catalysts was also investigated. Over the Gd–Pd catalyst with the presence of SO₂, more than 70% NO conversion was obtained for over 6 h while the Pd only catalyst showed a sharper drop in NO conversion. Over the Gd–Pd catalyst, the presence of H₂O showed no effect on NO conversion activity (>99% conversion) during the 18 h the catalyst was kept on stream. Among the lanthanide elements tested, Gd is the most effective, allowing the use of above stoichiometric oxygen concentration.     

Olivine catalysts for methane- and tar-steam reforming

The removal of tar and lower hydrocarbons is a vital technological barrier hindering the development of biomass gasification. The present work evaluates four olivine catalysts (three untreated of different origin and one calcined) for lowering the amount of these compounds in biomass derived syngas by reforming model compounds (naphthalene, toluene, and methane). Treatments prior to reaction were shown to largely impact the catalytic activity and physiochemical properties of the olivine catalysts depending on its origin. The formation of free Fe phases following decomposition of a Fe-bearing serpentine phase ((Mg,Fe)₃Si₂O₅(OH)₄) near the surface of untreated olivine catalysts proved most important for facilitating higher activity compared to olivine catalysts with little or no serpentine phase initially. The most active catalyst was efficient at naphthalene removal (90% conversion at 800 °C), but more active catalysts are needed for applications where methane removal is required. Additionally, carbon deposition during naphthalene-steam reforming as well as Fe clustering during naphthalene-steam reforming and exposure to reducing conditions suggested stability may be a liability.     

Investigating Some Physicochemical Properties and Fatty Acid Composition of Native Black Mulberry (<Emphasis Type=Italic>Morus nigra</Emphasis> L.) Seed Oil

The physicochemical properties of seed and seed oil obtained from the native black mulberry (Morus nigra L.) were investigated in 2008 and 2009. The results showed that the seed consisted of 27.5–33% crude oil, 20.2–22.5% crude protein, 3.5–6% ash, 42.4–46.6% carbohydrate and 112.2–152.0 mg total phenolics/100 g. Twenty different fatty acids were determined, with the percentages varying from 0.02% myristic acid (C14:0) to 78.7% linoleic acid (C18:2). According to the GC analysis of fatty acid methyl esters, linoleic acid (C18:2), followed by palmitic acid (C16:0), oleic acid (C18:1) and stearic acid (C18:0) were the major fatty acids, which together comprised approximately 97% of the total identified fatty acids. High C18:2 content (average 73.7%) proved that the black mulberry seed oil is a good source of the essential fatty acid, linoleic acid. Linolenic acid (C18:3) was also found in a relatively lower amount (0.3–0.5%). The α-tocopherol content was found to be between 0.17 and 0.20 mg in 100 g seed oil. The main sterols in the mulberry seed oil were β-sitosterol, Δ5-avenasterol, Δ5, 23-stigmastadienol, clerosterol, sitosterol and Δ5, 24-stigmastadienol. The present study stated that the native black mulberry seed oil can be used as a nutritional dietary substance and has great usage potential.     

Determination of FA composition and total trans FA of Turkish margarines by capillary GLC

In this research, FA composition and total trans FA contents of 16 different brands of margarine (8 hard-type and 8 soft-type) sold in Turkey were determined by capillary GLC method. According to the results, the contents of saturated FA, monounsaturated FA, and PUFA were within the ranges of 23.9–32.3, 44.0–61.9, and 14.2–24.1%, respectively, in hard-type margarines, and 27.0–39.9, 21.0–40.9, and 32.0–53.7%, respectively, in soft-type margarines. Hard-type margarines contained total trans FA concentrations of 20.1–34.3%, whereas soft-type margarines contained less than 8.9% total trans FA. C_18∶1 trans acid content was within the range of 18.5–29.8% in hard-type margarines, and it was significantly higher than the range in soft margarines (0.7–8.1%). C_18∶1 trans acid was the major trans FA in all margarines, and C_18∶3 trans acid concentrations were less than 0.2%.