Green in situ synthesis of sandwich-like W-bridged siligraphene (g-SiC@WC@g-SiC) heterostructure from Saccharum Ravennae gum for ultrahigh-rate photodegradation of acetaminophen.

Herein, the sandwich-like W-bridged siligraphene (W/g-SiC) as a heterojunction of WC and siligraphene nanosheets have been first accomplished via a simple green synthesis using Saccharum Ravennae gum as a natural Si and W sources and gelatin as a natural C and N sources. In a magnesiothermic process, Si and C atoms bond together and form a graphene-like structure where half of the C atoms are replaced by Si atoms. The presence of W in the natural precursor creates a W-doped siligraphene structure. Tungsten in the form of carbide (WC) creates a heterojunction with g-SiC, which reduces the bandgap. According to the experimental and computational data, the proposed structure of W/g-SiC was predicted by replacing the W atoms with Si atoms and bonding with C atoms in the siligraphene structure. The W-C bond in this structure is elongated and the W atom comes out of the siligraphene sheet and is placed between two siligraphene layers to interact with three carbons from the next layer. Under visible light irradiation, holes are generated on the g-SiC layers and electrons in the WC interlayer, which makes it a highly efficient photocatalyst with ultrafast charge separation and active surface for the removal of Acetaminophen.

Green synthesis of nonprecious metal-doped copper hydroxide nanoparticles for construction of a dopamine sensor.

Background: Copper oxide nanoparticles doped with nonprecious metal species (Ni and Mn) were synthesized. Method: A glassy carbon electrode (GCE) was modified by drop-casting of nanostructure suspensions, constructing Ni:Cu(OH)2/GCE, Mn:Cu(OH)2/GCE and Cu(OH)2/GCE. Results: The voltammetric oxidation of dopamine (DA) by the constructed electrodes confirmed that the electrocatalytic oxidation of DA is a reversible, pH-dependent, diffusion-controlled process; the best response was obtained by Mn:Cu(OH)2/GCE. A sensitive calibration graph (0.664 µA/µM) was produced for DA in the concentration range of 0.3-10.0 µM, with a detection limit of 79 nM using Mn:Cu(OH)2/GCE. Conclusion: The Mn:Cu(OH)2/GCE possessed an accurate response toward DA with an acceptable selectivity, stability and antifouling effect, revealing the applicability of the Mn:Cu(OH)2/GCE for DA analysis in biological samples.

Highly sensitive tin oxide hollow microspheres and nanosheets to ethanol gas prepared by hydrothermal method.

In this study, we synthesized tetragonal-phase SnO2 with a variety of well-crystallized morphologies as solid microspheres, hollow microspheres and mixture of hollow microspheres and nanosheets via the hydrothermal method. The synthesized samples were characterized with XRD, SEM, and BET. SnO2 hollow microsphere structures have been hydrothermally synthesized by using urea and SnCl2 as raw materials. With the addition of cetyltrimethylammonium bromide (CTAB), nanostructures with morphologies of hollow microspheres and nanosheets were obtained. Also, when CTAB was added in the reaction solution without urea, SnO2 microsphere with a solid interior composed of nanoparticles were obtained. A possible formation mechanism of these samples was briefly discussed. The gas sensing properties of sensors based on these samples were investigated. The result revealed that sample with morphology of hollow microsphere and nanosheet calcined at 600 degrees C showed the highest sensitivity to ethanol due to the special morphology and absence of SnO phase.

Fabrication and highly sensitive gas sensors based on h-MoO3/SnO2 hollow nanostructures operated at low temperatures.

Simulated by the synthesis of one dimensional hollow nanostructures with significant sensing, electrical, and optical properties, we have successfully synthesized 1D hollow nanostructures of h-MoO3/SnO2 with well-defined multi-side walls. These hollow nanostructured materials synthesized via a hydrothermal method with SnCl2.2H2O as the precursor and h-MoO3 as the template. SnO2 nanoparticles grew on the surface of h-MoO3 with preferential direction [001]. The morphological change was observed with variation of the growth conditions, such as HNO3, and h-MoO3 concentration. 1D hollow nanostructures of h-MoO3/SnO2 were studied and their growth mechanism was discussed. The result revealed that the existence of h-MoO3 caused to increase the sensor response to ethanol gas and downshift the sensor operating temperature at low temperatures.

Anticholinesterase activity of some major intermediates in carbacylamidophosphate synthesis: preparation, spectral characterization and inhibitory potency determination.

Carbacylamidophosphates with the general formula RC(O)NHP(O)R1R2 constitute organophosphorus compounds that are used as insecticides, pesticides and ureas inhibitors. In this work, we studied the inhibition potency of CCl3-C(O)NHP(O)Cl21, CHCl2C(O)NHP(O)Cl(2)2, CH2ClC(O)NHP(O)Cl23 and CF3C(O)NHP(O)Cl(2)4, which are the major intermediates for carbacylamidophosphates synthesis towards human erythrocyte acetylcholinesterase (hAChe) activity using Ellman's modified kinetic method. Unexpectedly, it was observed that they were not only hydrolytically unstable but also inhibited hAChE in a similar manner to that produced by organophosphorus insecticides. Enzymatic data, bimolecular inhibition rate constants (ki) and IC50 values for inhibition of hAChE demonstrated that they are irreversible inhibitors and the inhibition potency of compound 2 (IC50 = 88 microM) was the greatest in comparison with compounds 1, 3 and 4. Also the electropositivity of the phosphorus atom and the hydrophobicity of the compounds demonstrated that these two factors play an additional effect and different role in the inhibitory activity of these compounds. Hydrolytic stability of the compounds was determined by 31P NMR monitoring of the loss of the parent molecules with D2O as a function of time. This study considers antiacetylcholinesterase activity according to the structural and the electronic aspects of compounds 1-4, according to IR, 1H, 13C and 31P NMR spectral data.