Alkaline activation of coals and carbon-base materials

Data on the reactions and processes occurring under the conditions of the alkaline activation of carbon substances—the production of activated carbons by the thermolysis of carbon substances in the presence of alkali metal hydroxides MOH—are summarized. The following most important activation processes were recognized: (1) the interaction of functional groups with MOH and the formation of intermediate structures with the C-O-M group; (2) their conversion into metal-containing compounds (primarily, M₂CO₃ and M₂O) in reactions with carbon, especially, with terminal C atoms on the periphery of graphenes; and (3) the reduction of M₂CO₃ and M₂O to the metal M, which is intercalated into the interlayer spaces of crystallites. The mechanism of alkaline activation was studied in most detail for KOH as an activating agent. The thermally initiated reduction of potassium oxide with carbon and the intercalation of potassium metal are the two most important processes for the development of the microporosity of activated carbon.     

Direct Synthesis of 1-Butanol from Ethanol in a Plug Flow Reactor: Reactor and Reaction Kinetics Modeling

Bio-ethanol is well known for its use as a gasoline additive. However, it can be blended in low portions to traditional gasoline although it has a corrosive nature. By taking advantage of modern continuous reactor technology and heterogeneous alumina catalysts, ethanol can be upgraded to 1-butanol in fixed beds. Butanol has more feasible properties as fuel component in comparison to ethanol. Mathematical modeling of reaction kinetics revealed a simple kinetic model could be used to describe the complex reaction process on a Cu/alumina catalyst. The reaction kinetics model is based on five parallel reactions in which ethanol reacts to 1-butanol, acetealdehyde, ethyl acetate, diethyl ether and diethoxyethane, respectively.

     

Synthesis of hyperbranched conjugated polymers based on 3-hexylthiophene,triphenylamine and benzo [c] [1,2,5] thiadiazole moieties: convenient synthesis through suzuki polymerization and impact of structures on optical properties

Novel 3-hexylthiophene-based hyperbranched conjugated polymers containing triphenylamine and benzo [c] [1, 2, 5] thiadiazole moieties were synthesized by Suzuki coupling polymerization of tris (4-bromophenyl) amine, 2,2′-(3-hexylthiophene-2,5-diyl) bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) and 4,7-dibromobenzo [c] [1, 2, 5] thiadiazole. Organic solvent-soluble polymers with number-average molecular weights of 24,000 and 42,000 g/mol were obtained in 54–57 % yields. Their structures, molecular weights and thermal properties were characterized via proton nuclear magnetic resonance (¹H NMR) and Fourier transform infrared (FT-IR) spectroscopies, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and wide-angle powder X-ray diffraction (XRD) measurements. Optical investigation by UV–vis and fluorescence spectroscopies revealed that the incorporation of the benzo [c] [1, 2, 5] thiadiazole moiety in the hyperbranched polymer structure resulted in a red-shift of the maximum absorption wavelength and an increase in the solution-photoluminescence quantum yield, indicating an extension of the conjugation length. The UV–vis, DSC and XRD results demonstrated that the aggregation of conjugated polymer chains could effectively be reduced by the hyperbranched structures and that conjugation length extension via the introduction of benzo [c] [1, 2, 5] thiadiazole units led to the coexistence of both crystalline and amorphous phases in the solid state and in solution upon addition of a non-solvent.     

Laser Zone Melting and microstructure of waveguide coatings obtained on soda-lime glass

This study presents a Laser Zone Melting method with potential for producing planar waveguides at large scale, based on the surface coupling of two chemically compatible glass layers which exhibit distinct indices of refraction. The method is based on a recent patent, particularly applicable to process glass and ceramics with low thermal shock resistance. Glass coatings containing 76.24% by weight PbO are thus here reported, as obtained by this method on commercial soda-lime planar glass substrates. Their higher indices of refraction (1.58 vs 1.52 for commercial soda-lime glass) result in attractive waveguiding potential, as demonstrated with measurements using focused light from a He-Ne laser beam. Scanning and transmission electron microscopy studies reveal excellent integration and compatibility between the observed coatings and substrates, where diffusion in the proximity of the interface was studied by EDS analysis. Crystalline phases have not been found within the coating, or within the substrate, as concluded from the absence of Bragg-peaks in XRD experiments.     

Copper(I) Bromide‐Dimethyl Sulfide‐Catalyzed Direct Sulfanylation of 4‐Hydroxycoumarins and 4‐Hydroxyquinolinones with Arylsulfonylhydrazides and Selective Fluorescence Switch‐ On Sensing of Cadmium(II) Ion in Water

An efficient protocol for the direct sulfanylation of various 4‐hydroxycoumarins and 4‐hydroxyquinolinones in good yield with arylsulfonylhydrazides as sulfanylating agents was developed via copper(I) bromide⋅dimethyl sulfide‐catalyzed S–O, S–N bond cleavage and C–S cross‐coupling reactions. A highly selective fluorescence turning‐on sensing of cadmium(II) ions in water using the synthesized 3‐sulfanyl‐4‐hydroxycoumarin derivative was also investigated.

     

Core–Shell Nanoarchitectonics of CoFe2O4 Encapsulated La2Fe2O6 Nanoparticles for Their Use in Various Applications

It would be helpful to achieve appropriate synthetic routes to attain larger-scale production at industrial levels of nanocomposites at low costs. In the present work, diphasic composites with core–shell nanostructures formed by La₂Fe₂O₆/CoFe₂O₄ are investigated. The core–shell structure is fabricated via different preparation methods. The advantages and the demerits of the synthesis techniques are discussed. The presence of both the spinel CoFe₂O₄ nano ferrite and orthorhombic La₂Fe₂O₆ perovskite phases is revealed by X-ray diffraction. XPS spectroscopy is utilized to investigate the chemical composition of the prepared samples. The hysteresis loops of the prepared samples exhibit a smooth loop that is resulted from the existence of two homogeneous magnetic phases. For the first time, it has been found that the preparation conditions have the advantage of reducing the switching field distribution value for the core–shell nanoparticles. Exchange coupled core–shell nanoparticles present a high potential to regulate the magnetic properties for numerous applications such as heavy metal removal and/or data storage devices. The maximum adsorption capacity (qm) of Cr III on the core–shell (S3) is higher compared to other adsorbents previously testified in the literature. The cost-effective and eco-friendly prepared core–shell samples with good metal removal capacity have great potential for commercialization.

     

Untangling decision tree and real options analyses: a public infrastructure case study dealing with political decisions,structural integrity and price uncertainty

Managerial flexibility in infrastructure investment and replacement decisions adds value. Real options analysis (ROA) captures this value under uncertain market prices. The concept of ROA is that future unfavourable payoffs can be deferred as soon as more information about market prices becomes available. The popularity of ROA is seen in a growing number of case studies on real assets. Despite its increasing popularity, ROA has not gained a foothold in public infrastructure decision making. One of the difficulties in the application of ROA is the required estimation of market variables. To avoid this, a simplified but not correct version of ROA is easily applied, referred to as a Decision Tree Approach (DTA) to ROA. Another difficulty is that infrastructure assets are subject to other types of uncertainties, defined here as asset uncertainties. This study investigates the value of managerial flexibility in a public infrastructure replacement decision. The uncertainty drivers are the strength of a bridge, political decisions regarding traffic flow and the price development of construction costs. Three valuation approaches are compared: DTA, ROA and the DT approach to ROA. Although it is complex, ROA certainly adds value in public infrastructure decision making when market price uncertainty is prevalent. However, in the absence of reasonable estimates of market variables, the DT approach to ROA is the best alternative. In the absence of market price uncertainties, ROA should be avoided DTA is to be preferred.     

Experimental investigation of lift enhancement by suction-assisted delayed separation of the boundary layer on NACA 0012 airfoil

In the aerodynamic industry, one of the major problems of interest is the lift enhancement without any increase in the drag. In this paper, an attempt is made to increase the lift coefficient by delayed boundary layer separation using suction at various points, also the study is carried out to identify the optimum location for suction which provides maximum lift augmentation. The experiment is conducted with selected suction pressures of 60, 70, 80, 90?kN/m² at different locations in the range of 40–75% of the chord length of the airfoil. Among the selected pressures, the lowest one at the 70% length provides maximum performance. The critical Reynolds number occurs at around 95% of the length instead of 45% of the length when the same experiment is conducted without suction. The suction also assists in the heat transfer enhancement over the airfoil surface.     

A CCD-based reader combined with CdS quantum dot-labeled lateral flow strips for ultrasensitive quantitative detection of CagA

Immunochromatographic assays are widely used to detect many analytes. CagA is proved to be associated closely with initiation of gastric carcinoma. Here, we reported that a charge-coupled device (CCD)-based test strip reader combined with CdS quantum dot-labeled lateral flow strips for quantitative detection of CagA was developed, which used 365-nm ultraviolet LED as the excitation light source, and captured the test strip images through an acquisition module. Then, the captured image was transferred to the computer and was processed by a software system. A revised weighted threshold histogram equalization (WTHE) image processing algorithm was applied to analyze the result. CdS quantum dot-labeled lateral flow strips for detection of CagA were prepared. One hundred sera samples from clinical patients with gastric cancer and healthy people were prepared for detection, which demonstrated that the device could realize rapid, stable, and point-of-care detection, with a sensitivity of 20 pg/mL.