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.     

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.

     

On the association between poly(vinyl alcohol) and sodium dodecyl sulfate and its effect on liquid–liquid interfacial tension: A mathematical model

Association between poly(vinyl alcohol-co-vinyl acetate) copolymer (PVA) and sodium dodecyl sulfate (SDS) was studied experimentally and theoretically. It was found that, for the ethyl acetate-aqueous phase interface in which PVA was previously adsorbed, the interfacial tension (γ) increases abruptly to a maximum and then exhibits a relatively mild decay with the addition of SDS to the aqueous phase. The theoretical results indicate that vinyl acetate (VAc) segments determine γ. However, for relatively low concentrations of SDS (C_SDS), this latter plays a major role because through its association with the VAc segments it modulates the extent to which PVA is adsorbed at the interface, indirectly determining the value of γ. As C_SDS approaches to the CMC value for SDS, its influence on γ decreases because SDS tends to self-assembly rather than associates with VAc. These model predictions are consistent with experimental findings reported in the literature.     

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.

     

An Effective Approach on Attaining Enhanced Silicon Solar Cell Performance Through Sputter Deposited Perovskite Thin Films

Silicon - Antireflection coatings (ARCs) have become one of the key techniques for mass production of Si solar cells. They are generally performed by vacuum processes such as thermal evaporation,...     

Recent Advances in CNT-based FET Transistor Biosensors to Detect Biomarkers of Clinical Significance

Silicon - The development of advanced materials has attracted interest for promising novel applications in biosensing and realm of nanophotonics. This interest in nanoelectronics, and...