Bimetallic platinum–ruthenium nanoparticles immobilized on reduced graphene oxide-TiO2 (RGO-TiO2) support for ethanol electro oxidation in acidic media

The present work addresses the potentialities of Pt–Ru nanoparticles deposited on a graphene oxide (RGO) and TiO₂ composite support towards electrochemical oxidation of ethanol in acidic media relevant for fuel cell applications. To immobilize platinum–ruthenium bimetallic nanoparticles on to an RGO-TiO₂ nanohybrid support a simple solution-phase chemical reduction method is utilized. An examination using electron microscopy and energy dispersive X-ray spectroscopy (EDS) indicated that Pt–Ru particles of 4–8 nm in diameter are dispersed on RGO-TiO₂ composite support. The corresponding Pt–Ru/RGO-TiO₂ nanocomposite electrocatalyst was studied for the electrochemical oxidation of ethanol in acidic media. Compared to the commercial Pt–Ru/C and Pt/C catalysts, Pt–Ru/RGO-TiO₂ nanocomposite yields higher mass-specific activity of about 1.4 and 3.2 times, respectively towards ethanol oxidation reaction (EOR). The synergistic boosting provided by RGO-TiO₂ composite support and Pt–Ru ensemble together contributed to the observed higher EOR activity and stability to Pt–Ru/RGO-TiO₂ nanocomposite compared with other in-house synthesized Pt–Ru/RGO, Pt/RGO and commercial Pt–Ru/C and Pt/C electrocatalysts. Further optimization of RGO-TiO₂ composite support provides opportunity to deposit many other types of metallic nanoparticles onto it for fuel cell electrocatalysis applications.     

1D sub 10 nm nanofabrication of ultrahydrophobic Ag@TiO2 nanowires and their photocatalytic,UV shielding and antibacterial properties

Here we report the synthesis of 1D TiO₂ sub 10 nm nanowires through one pot hydrothermal method in an alkaline NaOH medium at 95 °C for 36 h. Further, these TiO₂ nanowires were embellished with silver (Ag) using polyvinylpyrrolidone (PVP) and ethylene glycol (EG) based solvothermal route at 160 °C for 4 h. With Ag decoration the photocatalytic activity was enhanced and the complete photooxidation of Methylene Blue (MB) was achieved in 35 min under optimized conditions. Super- and ultra-hydrophobic coating on cotton fabric exhibited a consistent antibacterial activity with enhanced UV-blocking property. Enhanced multifunctional properties observed were primarily attributed to the formation of Ag decorated 1D sub 10 nm TiO₂ nanowires heterojunctions achieved using facile chemical route. Hence, such multiple functionalities make the 1D sub 10 nm TiO₂ nanowires good candidate for industrial and domestic wastewater treatment.     

Thermal transport and chemical conversion in single reacting sorbent particles

The effects of particle size and carbon dioxide concentration on chemical conversion in engineered spherical particles undergoing calcium oxide looping are investigated. Particles are thermochemically cycled in a furnace under different carbon dioxide concentrations. Changes in composition due to chemical reactions are measured using thermogravimetric analysis. Gas composition at the furnace exit is evaluated with mass spectroscopy. A numerical model of thermal transport phenomena developed previously is adapted to match the physical system investigated in the present study. The model is used to elucidate effects of reacting medium characteristics on particle temperature and reaction extent. Experimental and numerical results show that (1) an increase in particle size results in a decrease in carbonation extent, and (2) the carbonation step consists of fast and slow reaction regimes. The reaction rates in the fast and slow carbonation regimes increase with increasing carbon dioxide concentration. The effect of carbon dioxide concentration and the distinction between the fast and slow regimes become more pronounced with increasing particle size.     

Engineering Silver-Enriched Copper Core-Shell Electrocatalysts to Enhance the Production of Ethylene and C2+ Chemicals from Carbon Dioxide at Low Cell Potentials

Copper catalysts are widely studied for the electroreduction of carbon dioxide (CO₂) to value-added hydrocarbon products. Controlling the surface composition of copper nanomaterials may provide the electronic and structural properties necessary for carbon-carbon coupling, thus increasing the Faradaic efficiency (FE) towards ethylene and other multi-carbon (C₂₊) products. Synthesis and catalytic study of silver-coated copper nanoparticles (Cu@Ag NPs) for the reduction of CO₂ are presented. Bimetallic CuAg NPs are typically difficult to produce due to the bulk immiscibility between these two metals. Slow injection of the silver precursor, concentrations of organic capping agents, and gas environment proved critical to control the size and metal distribution of the Cu@Ag NPs. The optimized Cu@Ag electrocatalyst exhibited a very low onset cell potential of −2.25 V for ethylene formation, reaching a FE towards C₂₊ products (FE_C2+) of 43% at −2.50 V, which is 1.0 V lower than a reference Cu catalyst to reach a similar FE_C2+. The high ethylene formation at low potentials is attributed to enhanced C C coupling on the Ag enriched shell of the Cu@Ag electrocatalysts. This study offers a new catalyst design towards increasing the efficiency for the electroreduction of CO₂ to value-added chemicals.     

Novel polymer composites of RuO2@nBaTiO3/PVDF with a high dielectric constant

The dielectric properties of a novel polymer dielectric material were investigated. The conductive phase of RuO₂ was synthesized for deposition on the surface of a nanosized BaTiO₃ (nBT). The RuO₂@nBT hybrid particles were incorporated into a poly (vinylidene fluoride) (PVDF) as a three-phase composite (RuO₂@nBT/PVDF). The obtained dielectric constant (ε′) was significantly high (3837.16) for the composite with a volume fraction of $f_{Ru{O}_2@nBT}$ = 0.50. The large interfacial polarization between the RuO₂?nBT and RuO₂?PVDF interfaces considerably increased the value of ε′. Therefore, interfacial polarization is a critical factor in improving the dielectric properties. The dielectric behavior of the RuO₂@nBT/PVDF composites can be described using the effective medium percolation theory model, which indicates the significant contributions of the conductive RuO₂ phase and high-permittivity nBT phase.     

Crystalline phase of TiO2 nanotube arrays on Ti–35Nb–4Zr alloy: Surface roughness,electrochemical behavior and cellular response

An investigation was made into the electrochemical, structural and biological properties of self-organized amorphous and anatase/rutile titanium dioxide (TiO₂) nanotubes deposited on Ti–35Nb–4Zr alloy through anodization-induced surface modification. The surface of as-anodized and heat-treated TiO₂ nanotubes was analyzed by field emission scanning electron microscopy (FE-SEM), revealing morphological parameters such as tube diameter, wall thickness and cross-sectional length. Glancing angle X-ray diffraction (GAXRD) was employed to identify the structural phases of titanium dioxide, while atomic force microscopy (AFM) was used to measure surface roughness associated with cell interaction properties. The electrochemical stability of TiO₂ was examined by electrochemical impedance spectroscopy (EIS) and the results obtained were correlated with the microstructural characterization. The in vitro bioactivity of as-anodized and crystallized TiO₂ nanotubes was also analyzed as a function of the presence of different TiO₂ polymorphic phases. The results indicated that anatase TiO₂ showed higher surface corrosion resistance and greater cell viability than amorphous TiO₂, confirming that TiO₂ nanotube crystallization plays an important role in the material's electrochemical behavior and biocompatibility.     

Exergy analysis and optimisation of waste heat recovery systems for cement plants

In the last decades, heat recovery systems have received much attention due to the increase in fuel cost and the increase in environmental issues. In this study, different heat recovery systems for a cement plant are compared in terms of electricity generation and exergy analysis. The heat sources are available in high temperature (HT) and low temperature (LT). For the HT section a dual pressure Rankine cycle, a simple dual pressure Organic Rankine Cycle (ORC) and a regenerative dual pressure ORC are compared. Also, for the LT section, a simple ORC is compared with transcritical carbon dioxide cycle. To find the best system, an optimisation algorithm is applied to all proposed cycles. The results show that for the HT section, regenerative ORC has the highest exergy efficiency and has the capability of producing nearly 7?MW electricity for a cement factory with the capacity of 3400 ton per day. The main reason for this is introducing the regenerative heat exchanger to the cycle. For the LT section, ORC showed a better performance than the CO₂ cycle. It is worth mentioning that the generated power in this section is far lower than that of the HT section and is equal to nearly 300?kW.     

Effect of high temperature and separated combustion on SO2 release characteristics during coal combustion under O2/CO2 atmosphere

This paper studied the effect of high temperature (up to 1873K) and separated combustion mode (volatile combustion and char combustion are separated) on SO₂ release characteristics during pulverized coal combustion under O₂/CO₂ atmosphere. Coal combustion experiments were conducted at different combustion environment temperatures utilizing a high temperature fixed-bed setup. The results show that as temperature rises, the SO₂ release curve is transformed from a single-peak process to a double-peak process. In separated combustion, temperature has little effect on the volatile-SO₂ (SO₂ released during volatile combustion) but brings about a significant effect on char-SO₂ (SO₂ released during char combustion). Char-SO₂ release amount and the ratio of it to fuel-SO₂ release amount (total SO₂ released during coal combustion) increase with temperature rising. The increase of temperature leads to a dramatic decreasing of sulphur mass fixed in the ash and causes SO₂ release amount to rise when temperature is lower than 1573 K. Separated combustion causes a higher SO₂ release amount than coupled combustion (the same as conventional combustion, volatile combustion and char combustion are simultaneous). Thermochemistry equilibrium composition calculation results show that alkali metals and alkaline-earth metals are significant in sulphur retention. CaSO₄ and Na₂SO₄ are the main sulphates at high temperatures.     

利用电解水替代SO2改进玉米淀粉生产浸泡新工艺研究

采用电解水代替SO_2以改进玉米淀粉生产工艺。以传统工艺(0.2%SO_2)作为对照,通过酸性电解水(Ac EW)与碱性电解水(Al EW)二次浸泡来提取玉米淀粉。结果表明,最佳提取工艺为Ac EW浸泡43 h后再使用Al EW浸泡5 h,此工艺下淀粉收率最高,达到(67.2±1.6)%,并与传统的湿法工艺(SO2浸泡48 h)的淀粉收率(67.4±1.0)%比较,无显著性差异(P0.05)。