David Dodoo-Arhin

High-performance symmetric electrochemical capacitor based on graphene foam and nanostructured manganese oxide

We have fabricated a symmetric electrochemical capacitor with high energy and power densities based on a composite of graphene foam (GF) with ∼80 wt% of manganese oxide (MnO2) deposited by hydrothermal synthesis. Raman spectroscopy and X-ray diffraction measurements showed the presence of nanocrystalline MnO2 on the GF, while scanning and transmission electron microscopies showed needle-like manganese oxide coated and anchored onto the surface of graphene. Electrochemical measurements of the composite electrode gave a specific capacitance of 240 Fg−1 at a current density of 0.1 Ag−1 for symmetric supercapacitors using a two-electrode configuration. A maximum energy density of 8.3 Whkg−1 was obtained, with power density of 20 kWkg−1 and no capacitance loss after 1000 cycles. GF is an excellent support for pseudo-capacitive oxide materials such as MnO2, and the composite electrode provided a high energy density due to a combination of double-layer and redox capacitance mechanisms.

Microemulsion Synthesis of Copper Oxide Nanorod-Like Structures

Copper oxide (CuO) nanorod-like structures made of spherical nanocrystals were synthesized at moderate temperature (80°C) starting from CuCl2·2H2O crystals in a water/n-heptane microemulsion stabilised by the nonionic Brij-30 surfactant. Whole Powder Pattern Modelling of the X-ray diffraction pattern shows absence of linear and planar defects with crystalline domains in the range of 4–8 nm. A linear correlation between the average size of the particles and the quantity of water in the system was observed: all synthesised specimens show a large blue shift of the energy bandgap (up to 2.7 eV versus 1.2 eV of bulk CuO) resulting from quantum confinement effects. The mechanism of growth of the spherical nanoparticles into nanorod-like structures has been elucidated.

Effect of mechanical activation on mullite formation in an alumina-silica ceramics system at lower temperature

Purpose This work aims to analyze the effect of mechanical activation on structural disordering (amorphization) in an alumina-silica ceramics system and formation of mullite most notably at a lower temperature using X-ray diffraction (XRD). Also, an objective of this work is to focus on a low-temperature fabrication route for the production of mullite powders. Design/methodology/approach A batch composition of kaolin, alumina and silica was manually pre-milled and then mechanically activated in a ball mill for 30 and 60 min. The activated samples were sintered at 1,150°C for a soaking period of 2 h. Mullite formation was characterized by XRD and scanning electron microscopy (SEM). Findings It was determined that the mechanical activation increased the quantity of the mullite phase. SEM results revealed that short milling times only helped in mixing of the precursor powders and caused partial agglomeration, while longer milling times, however, resulted in greater agglomeration. Originality/value It is noted that, a manual pre-milling of approximately 20 min and a ball milling approach of 60 min milling time can be suggested as the optimum milling time for the temperature decrease succeeded for the production of mullite from the specific stoichiometric batch formed.

Preparation and Characterization of Rubber Blends for Industrial Tire Tread Fabrication

The physico-mechanical properties of variable rubber blends including epoxide natural rubber (ENR), polybutadiene rubber (BR), and solution polymerized styrene-butadiene rubber (SBR) filled with silanized silica and carbon black mixtures were explored. The tensile, hardness, resilience, abrasion, and fatigue behavior were investigated. An optimized composition involving 30 phr of ENR and 70 phr SBR filled with mixtures of carbon blacks and silanized silica was proposed to be a suitable composition for the future development of green passenger truck tires, with low rolling resistance (fuel saving ability), high wear resistance, and desired fatigue failure properties.

Catalytic abatement of CO species from incomplete combustion of solid fuels used in domestic cooking

This study reveals a first time approach to catalytic based interventions primarily on indoor air pollution emanating from commercial and household solid fuel burning in a region in Nigeria. An intensive survey of the temperatures at different locations in the common stoves used for cooking was conducted so as to ascertain temperatures suitable for catalyst efficiency and stability. Furthermore, cobalt and iron based catalysts were prepared using ultra stable Y type zeolite as supports. The synthesized catalysts were characterized for its physico-chemical properties. The catalytic efficiency of the supported catalysts was tested using simulated exhaust gases in a fix bed reactor. The study further explored real time testing of the catalyzed ceramic monolith using two different wood species. First, the best catalyst in terms of simulated exhaust testing was selected. Consequently, a small layer of zeolite Y was deposited at 3% of the monolith weight to enhance the subsequent adhesion of the best catalyst powder to the structured monolith. Then to catalyze the zeolite Y wash-coated monolith with the cobalt precursor, the dip coating technique was used. From the results, the average values of temperatures observed from the surveyed cook stoves using wood and plant residue as fuel were confirmed to be in the range of 203–425 °C which is considered suitable for catalysts activity. The Co/ZY catalyst showed approximately 100% CO conversion (T100) at 250 °C for initial CO concentration of 1000 ppm, making it the most effective, while T100 was increased to 275 °C and 325 °C for Fe/ZY and Co-Fe/ZY catalyst respectively at an exhaust residence time of 20000 h−1. The catalytic converter in real time testing for CO abatement performed well for both wood species. Only minor differences have been noticed.

Modified halloysite nanoclay as a vehicle for sustained drug delivery

This paper presents the effect of modified halloysite nanotubes on the sustained drug release mechanisms of sodium salicylate. Acid treatment and composite polymer-halloysite modification techniques were adopted in this study. After each modification, sodium salicylate drug was loaded, and in vitro release properties were evaluated and compared with the raw unmodified halloysite nanotubes. The results obtained from SEM, TEM and FTIR analyses indicate that both acid treatment and composite formation have no effect on the tubular structure and morphology of halloysite. However, modification of the halloysite nanotubes did influence the drug release rate. In the acid treatment modification, there was an improved loading of sodium salicylate drug which resulted in the sustain release of large amount of the sodium salicylate. In the polymer/halloysite composite formation, a consistent layer of polymer was formed around the halloysite during the composite formation and thus delayed release providing sustained release of sodium salicylate drug over a longer period of time as compared to the acid treated and unmodified halloysite. The results from the invitro release were best fitted with the Higuchi and the Koresymer-Peppas models.

H 2 O 2 rejuvenation-mediated synthesis of stable mixed-morphology Ag 3 PO 4 photocatalysts

Ag3PO4 photocatalyst has attracted interest of the scientific community in recent times due to its reported high efficiency for water oxidation and dye degradation. However, Ag3PO4 photo-corrodes if electron accepter such as AgNO3 is not used as scavenger. Synthesis of efficient Ag3PO4 followed by a simple protocol for regeneration of the photocatalyst is therefore a prerequisite for practical application. Herein, we present a facile method for the synthesis of a highly efficient Ag3PO4, whose photocatalytic efficiency was demonstrated using 3 different organic dyes: Methylene Blue (MB), Methyl orange (MO) and Rhodamine B (RhB) organic dyes for degradation tests. Approximately, 19 % of Ag3PO4 is converted to Ag0 after 4.30 hours of continuous UV-Vis irradiation in presence of MB organic dye. We have shown that the Ag/Ag3PO4 composite can be rejuvenated by a simple chemical oxidation step after several cycles of photocatalysis tests. At an optimal pH of 6.5, a mixture of cubic, rhombic dodecahedron, nanosphere and nanocrystals morphologies of the photocatalyst was formed. H2O2 served as the chemical oxidant to re-insert the surface metallic Ag into the Ag3PO4 photocatalyst but also as the agent that can control morphology of the regenerated as-prepared photocatalyst without the need for any other morphology controlling Agent (MCA). Surprisingly, the as- regenerated Ag3PO4 was found to have higher photocatalytic reactivity than the freshly made material and superior at least 17 times in comparison with the conventional Degussa TiO2, and some of TiO2 composites tested in this work.

Dataset on the comparison of synthesized and commercial zeolites for potential solar adsorption refrigerating system

The purpose of this dataset is to provide a comparison between synthesized and commercial 4A and 13X type zeolites. Metakaolin produced from the calcination of beneficiated kaolin at 750 °C for 4 h was dealuminated using sulphuric acid to get the required silica to alumina ratio for the zeolite synthesis. Zeolite 4A and 13X samples were characterized along-side with the commercial variants using X-ray fluorescence (XRF), X-ray diffraction (XRD), Brunauer, Emmett and Teller (BET) and scanning electron microscopy (SEM) techniques. These analyses revealed that, the zeolites synthesized are of comparatively acceptable quality. The pore size of 120.859 nm, pore volume of 0.0065 cm3/g and surface area of 22 m2/g were obtained from BET analyses for zeolite 4A synthesized from kaolin, while the commercial zeolite 4A used as control gave pore size of 58.143 nm, pore volume of 0.2462 cm3/g and surface area of 559.13 m2/g. In the same vein, the pore size of 10.5059 nm, pore volume of 0.135847 cm3/g and surface area of 324.584 m2/g were obtained from BET analyses for zeolite 13X synthesized from kaolin, while the commercial zeolite 13X gave pore size of 7.2752 nm, pore volume of 0.135951 cm3/g and surface area of 310.0906 m2/g.

Graphene-based inkjet-printable electrodes for dye-sensitized solar cells

We present a stable inkjet printable graphene ink, formulated in isopropyl alcohol via liquid phase exfoliation of chemically pristine graphite with a polymer stabilizer. The rheology and low deposition temperature of the ink allow uniform printing. We use the graphene ink to fabricate counter electrodes (CE) for natural and ruthenium-based dye-sensitized solar cells (DSSCs). The repeatability of the printing process for the CEs is demonstrated through an array of inkjet-printed graphene electrodes, with ~5% standard deviation in the sheet resistance. As photosensitizers, we investigate natural tropical dye extracts from Pennisetum glaucum, Hibiscus sabdariffa and Caesalpinia pulcherrima. Among the three natural dyes, we nd extracts from C. pulcherrima exhibit the best performance, with ~0.9% conversion efciency using a printed graphene CE and a comparable ~1.1% efciency using a platinum (Pt) CE. When used with N719 dye, the inkjet-printed graphene CE shows a ~3.0% conversion efciency, compared to ~4.4% obtained using Pt CEs. Our results show that inkjet printable graphene inks, without any chemical functionalization, offers a exible and scalable fabrication route, with a material cost of only ~2.7% of the equivalent solution processed Pt-based electrodes.

On the modelling of diffraction line profiles from nanocrystalline materials

Recent advances in Line Profile Analysis of powder diffraction patterns must be paralleled by increasing attention to the quality and quantity of experimental data. The analysis of simulated data with different noise levels demonstrates the importance of statistical quality to reveal fine details of interest in the analysis of nanocrystalline materials, like the crystallite shape. It is also shown how synchrotron radiation diffraction can improve data quality with respect to laboratory measurements, both in terms of statistical quality and in terms of accessible information.