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Abstract: An efficient method for the synthesis of α-aminonitriles via one-pot three-component condensation of ketones, amines and potassium hexacyanoferrate(II) using benzoyl chloride as a promoter and PEG-400 as a reaction medium was described. This protocol has the features of use of eco-friendly cyanide source, green reaction medium, high yield, and simple work-up procedure. [Copyright &y& Elsevier]

A unit cell-based design support system (UCBDSS) for composite structural design is introduced. A unit cell is defined as the smallest representative volumetric element to carry the information of composite constituent materials, heterogeneous structures, homogenized mechanical properties, and appropriate manufacturing processes. The database of various composite unit cells is organized to form a unit cell library (UCL). The UCBDSS can intelligently use the information from the UCL to simplify and automate the composite design process, to increase the design efficiency, and to facilitate the tailored composite structure design. The framework of the UCBDSS, its modules, the development of the UCL, the blackboard architecture for design control, and the UCBDSS working environment for Internet-based design are presented. [Copyright &y& Elsevier]

Development of effective methods for quantificationally characterizing the thermal resistance of the intumescent char layer of fired fire-retardant coating is of interest in many academic researches and industrial applications. In this work, a novel approach is proposed to calculate the thermal resistance of the intumescent char layer produced after the ultra-thin fire-retardant coating exposed to fire. A correlation was established based on the relative thermal resistance of the char layer to that of steel plate and the surface temperature at the back of the coated steel plate under steady-state heat transfer. The thermal resistance of the steel plate was obtained about 0.009 K·m2·W−1 by calculating the heat flux based on the radiation heat exchange involving three-surface enclosure model (flame, steel, and wall). The thermal resistances of the char layers without and with the layered double hydroxide (LDH) were 0.011 K·m2·W−1 and 0.013 K·m2·W−1, respectively. The results show that the external roughness and internal honeycomb structure can increase both the conductivity and the convective thermal resistances of the char layer to protect the steel structures. The porosity of the char layer is between 0.15 and 0.18, and its thermal conductivity is between 0.4 and 0.8 W·m−1·K−1 in the process of fire. Unlabelled Image • A novel method is proposed to calculate thermal resistance of intumescent char layer. • Thermal resistance is used to evaluate heat-shielding performance of char layer. • LDH improves external roughness and internal honeycomb structure of char layer. • Porosity of char layers is obtained to be 0.15–0.18 via SEM images processing. • Thermal conductivity of char layers is 0.4–0.8 W·m−1·K−1 in the process fire. [ABSTRACT FROM AUTHOR]

• A smartphone-assisted fluorescence-colorimetric immunosensing platform was proposed. • NH 2 -UiO-66@PtNPs was exploited to construct a fluorescence-colorimetric signal probe. • The multi-mode immunosensing microarray showed satisfactory results of AMD detection. • The efficient, visual and portable method showed great potential in food analysis. Amantadine (AMD) is an antiviral drug used to treat animal-based infectious diseases such as avian influenza. However, its illegal use in animal-derived food industries endangers human health. Therefore, an efficient, portable, and visual sensor to detect AMD in food is crucial for ensuring food safety. A multifunctional nanocomposite NH 2 -UiO-66@PtNPs was exploited to design a smartphone-assisted fluorescence-colorimetric immunosensing microarray for multidimensional detection of AMD in animal-derived foods. Platinum nanoparticles (NPs) were immobilized on a Zr-based metal–organic framework (NH 2 -UiO-66). Pt NPs exhibited peroxidase-like activity, whereas NH 2 -UiO-66 stabilized Pt NPs and improved the colorimetric signal of the sensor. Moreover, the fluorescence ligand NH 2 -BDC in NH 2 -UiO-66 was released via alkaline hydrolysis, amplifying the fluorescence signal and improving detection sensitivity. The smartphone-assisted color recognition system accurately identified the color changes of the microarray. The immunocompetitive reaction of AMD and the antibody (Ab) in the microarray NH 2 -UiO-66@PtNPs@Ab 2 allowed the quantitative and visual detection of AMD in a wide concentration range (0.1–1000 ng/mL) with high sensitivity [limit of detection = 0.0022 ng/mL (fluorescence), 0.069 ng/mL (colorimetric), and 0.68 ng/mL (smartphone)]. This detection strategy was verified in AMD-spiked food samples with satisfactory recoveries (82.0–103.0%) and stability (RSD: ≤7.1%, n = 3), showing its great potential for visual screening and portable detection of other food contaminants. [ABSTRACT FROM AUTHOR]

CO 2 capture and utilisation (CCU) is a promising strategy to effectively mitigate the adverse greenhouse effects caused by CO 2 emissions at an industrial scale. Through a process intensification strategy known as integrated CO 2 capture and utilisation (ICCU), CO 2 capture and catalytic CO 2 conversion can be achieved in a single process with the use of dual function materials (DFMs), which are both CO 2 sorbents and CO 2 conversion catalysts. Given the significantly different operating conditions of ICCU from conventional catalytic CO 2 hydrogenation, the catalytic mechanism of DFMs, especially during CO 2 hydrogenation, needs to be thoroughly investigated. In this study, the relationship between the nature of the Ni/carbonate interfaces and the performance of Ni-based DFMs over ICCU cycles is systematically investigated. A series of Ni/alkaline earth carbonate DFMs were synthesised with varying Ca:Mg ratios to simulate different metal-carbonate model interfaces. At 400 °C, CH 4 formation with nearly 100% CH 4 selectivity was achieved on Ni/CaCO 3 over 15 ICCU cycles. In general, Ni/CaCO 3 interfaces correspond to higher CO 2 conversion and higher CH 4 selectivity than Ni/MgCO 3 interfaces. Such trend may be attributed to the higher surface basicity of CaO and the higher thermal stability of CaCO 3. As a consequence, the hydrogenation of the Ni/CaCO 3 interface proceed via the formate pathway, in which carbonates are consecutively converted to surface formates, methoxyl, methyl species and eventually desorb as methane. This reaction model is applicable to the hydrogenation of both surface carbonate and bulk carbonates, although the former proceeds with much faster kinetics. On the weakly alkaline Ni/MgCO 3 interface, MgCO 3 preferentially decomposes to form gaseous CO 2 , which is subsequently hydrogenated via the reverse-water-gas-shift pathway, with CO as the key reaction intermediate. Interestingly, in situ infrared spectroscopy shows similar surface significant species during the direct hydrogenation of DFMs and during the conventional catalytic hydrogenation of molecular CO 2 , suggesting that the catalytic mechanisms during the two operating regimes are highly correlated. [Display omitted] • Novel Ni/carbonate dual function materials for CO 2 capture and hydrogenation. • Different hydrogenation behaviour and pathway on Ni/CaCO 3 and Ni/MgCO 3 interfaces. • Two reaction regimes proposed during hydrogenation of Ni/CaCO 3. • Suitable basic sites and metal-support interaction favours the hydrogenation. • Correlation between ICCU cycles and those of conventional CO 2 hydrogenation. [ABSTRACT FROM AUTHOR]

Abstract: A novel biosensor is developed based on immobilization of proteins on nanoflake-like SnS2 modified glass carbon electrode (GCE). With glucose oxidase (GOD) as a model, direct electrochemistry of the GOD/nanoflake-like SnS2 is studied. The prepared SnS2 has large surface area and can offer favorable microenvironment for facilitating the electron transfer between protein and electrode surface. The properties of GOD/SnS2 are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV–vis spectroscopy, Fourier transform infrared spectroscopy (FTIR) and cyclic voltammetry (CV), respectively. The immobilized enzyme on nanoflake-like SnS2 retains its native structure and bioactivity and exhibits a surface-controlled, reversible two-proton and two-electron transfer reaction with the apparent electron transfer rate constant (k s) of 3.68s−1. The proposed biosensor shows fast amperometric response (8s) to glucose with a wide linear range from 2.5×10−5 M to 1.1×10−3 M, a low detection limit of 1.0×10−5 M at signal-to-noise of 3 and good sensitivity (7.6±0.5mAM−1 cm−2). The resulting biosensor has acceptable operational stability, good reproducibility and excellent selectivity and can be successfully applied in the reagentless glucose sensing at −0.45V. It should be worthwhile noting that it opens a new avenue for fabricating excellent electrochemical biosensor. [Copyright &y& Elsevier]