Research on Chemical Intermediates - We prepared unique BiVO4/reduce graphene oxide (BiVO4/rGO) nanocomposite with enhanced photocatalytic ability by hydrothermal method applying... 相似文献
Additive manufacturing has established itself as a popular and powerful tool in electrochemistry research and development. In this short review, we focus on the latest results in both 3D printing and electrochemistry communities that could potentially benefit manufacturing in the electrochemical industry. We provide insights from recent and relevant research works and conclude that the likely scenario in the industry is the deployment of a combination of subtractive and additive technologies in order to manufacture high quality and cost-effective electrochemical reactors within reasonable timeframes. 相似文献
In order to improve the membrane lipophilicity and the affinity towards the environment of lipid bilayers, squalene (SQ) could be conjugated to phospholipids in the formation of liposomes. The effect of membrane composition and concentrations on the degradation of liposomes prepared via the extrusion method was investigated. Liposomes were prepared using a mixture of SQ, cholesterol (CH) and Tween80 (TW80). Based on the optimal conditions, liposome batches were prepared in the absence and presence of SQ. Their physicochemical and stability behavior were evaluated as a function of liposome constituent. From the optimization study, the liposomal formulation containing 5% (w/w) mixed soy lecithin (ML), 0.5% (w/w) SQ, 0.3% (w/w) CH and 0.75% (w/w) TW80 had optimal physicochemical properties and displayed a unilamellar structure. Liposome prepared using the optimal formulation had a low particle size (158.31 ± 2.96 nm) and acceptable %increase in the particle size (15.09% ± 3.76%) and %trolox equivalent antioxidant capacity (%TEAC) loss (35.69% ± 0.72%) against UV light treatment (280–320 nm) for 6 h. The interesting outcome of this research was the association of naturally occurring substance SQ for size reduction without the extra input of energy or mechanical procedures, and improvement of vesicle stability and antioxidant activity of ML-based liposome. This study also demonstrated that the presence of SQ in the membrane might increase the acyl chain dynamics and decrease the viscosity of the dispersion, thereby limiting long-term stability of the liposome. 相似文献
In this work, a novel electrochemiluminescent (ECL) pesticide sensor based on zinc oxide nanocrystals decorated nickel foam is proposed for determination of imidacloprid for the first time. The silica film was used as a morphology‐controlling factor for modification of the electrode with zinc oxide nanocrystals. Zinc oxide was selected as luminescent material due to its cheapness, non‐toxicity, high thermal stability and excellent luminescence properties which truly adhered on the surface of nickel foam. The K2S2O8 was used as strong co‐reactant for this purpose. The silica template plays an important role in controlling the size of ZnO nanocrystals. The Physical morphology of the ZnO/Ni‐foam electrode was performed by electrochemical impedance spectroscopy, Brunauer‐Emmett‐Teller (BET), X‐Ray diffraction analysis, field emission scanning electron microscopy, and energy‐dispersive X‐ray analysis. The ultra‐sensitive electrochemiluminescence method was successfully used for ultra‐trace determination of imidacloprid. The linear dynamic range and low detection limit were obtained 3×10?14 ?8×10?8 M and 4.4×10?15 M, respectively. Also, the relative standard deviation for 15 repetitive optical signals was calculated 1.09 %.The present ECL sensor exhibited superior performance toward the accurate determination of imidacloprid with good reproducibility and stability. 相似文献
Structural Chemistry - A new series of 4-oxobenzo[d]1,2,3-triazin-pyridinium-phenylacetamide hybrids 8a–p was designed, synthesized, and screened as the potential cholinesterase inhibitors... 相似文献
Artificially fabricated hydroxyapatite (HAP) shows excellent biocompatibility with various kinds of cells and tissues which makes it an ideal candidate for a bone substitute material. In this study, hydroxyapatite nanoparticles have been prepared by using the wet chemical precipitation method using calcium nitrate tetra-hydrate [Ca(NO3)2.4H2O] and di-ammonium hydrogen phosphate [(NH4)2 HPO4] as precursors. The composite scaffolds have been prepared by a freeze-drying method with hydroxyapatite, chitosan, and gelatin which form a 3D network of interconnected pores. Glutaraldehyde solution has been used in the scaffolds to crosslink the amino groups (|NH2) of gelatin with the aldehyde groups (|CHO) of chitosan. The X-ray diffraction (XRD) performed on different scaffolds indicates that the incorporation of a certain amount of hydroxyapatite has no influence on the chitosan/gelatin network and at the same time, the organic matrix does not affect the crystallinity of hydroxyapatite. Transmission electron microscope (TEM) images show the needle-like crystal structure of hydroxyapatite nanoparticle. Scanning Electron Microscope (SEM) analysis shows an interconnected porous network in the scaffold where HAP nanoparticles are found to be dispersed in the biopolymer matrix. Fourier transforms infrared spectroscopy (FTIR) confirms the presence of hydroxyl group (OH-) , phosphate group (PO3-4) , carbonate group (CO2-3) , imine group (C=N), etc. TGA reveals the thermal stability of the scaffolds. The cytotoxicity of the scaffolds is examined qualitatively by VERO (animal cell) cell and quantitatively by MTTassay. The MTT-assay suggests keeping the weight percentage of glutaraldehyde solution lower than 0.2%. The result found from this study demonstrated that a proper bone replacing scaffold can be made up by controlling the amount of hydroxyapatite, gelatin, and chitosan which will be biocompatible, biodegradable, and biofriendly for any living organism. 相似文献
Pyrolysis is a commonly used method for the recovery of used lubricating oil (ULO), which should be kinetically improved by a catalyst, due to its high level of energy consumption. In this research, the catalytic effects of carbon nanotube (CNT) and graphene nanoplatelets on the pyrolysis of ULO were studied through thermogravimetric analysis. First, the kinetic parameters of ULO pyrolysis including activation energy were calculated to be 170.12 and 167.01 kJ mol?1 by FWO and KAS methods, respectively. Then, the catalytic effects of CNT and graphene nanoplatelets on pyrolysis kinetics were studied. While CNT had a negligible effect on the pyrolysis process, graphene nanoplatelets significantly reduced the temperature of maximum conversion during pyrolysis from 400 to 350 °C, due to high thermal conductivity and homogenous heat transfer in the pyrolysis process. On the other hand, graphene nanoplatelets maximized the rate of conversion of highly volatile components at lower temperatures (<?100 °C), which was mainly due to the high affinity of these components toward graphene nanoplatelets and also the effect of nanoplatelets’ edges which have free tails and can bond with other molecules. Moreover, graphene nanoplatelets decreased the activation energy of the conversion to 154.48 and 152.13 kJ mol?1 by FWO and KAS methods, respectively.
The double crossover junction (DX) is a fundamental building block for generating complex and varied structures from DNA. However, its implementation in functional devices is limited to the inherent properties of DNA itself. Here, we developed design strategies to generate the first metal–DX DNA tiles (DXM) by site‐specifically functionalizing the tile crossovers with tetrahedral binding pockets that coordinate CuI. These DX junctions bind two CuI ions independently at distinct sites, display greater thermal stability than native DX tiles upon metalation, and melt in a cooperative fashion. In addition, the right‐handed helical chirality of DNA is transferred to the metal centers. Our tiles display high metal ion selectivity, such that CuII is spontaneously reduced to CuI in situ. By modifying our design over three generations of tiles, we elucidated the thermodynamic and geometric requirements for the successful assembly of DXM tiles, which have direct applicability in developing robust, stable DNA‐based materials with electroactive, photoactive, and catalytic properties. 相似文献
Using a one‐step synthetic route for block copolymers avoids the repeated addition of monomers to the polymerization mixture, which can easily lead to contamination and, therefore, to the unwanted termination of chain growth. For this purpose, monomers ( M1 – M5 ) with different steric hindrances and different propagation rates are explored. Copolymerization of M1 (propagating rapidly) with M2 (propagating slowly), M1 with M3 (propagating extremely slowly) and M4 (propagating rapidly) with M5 (propagating slowly) yielded diblock‐like copolymers using Grubbs’ first ( G1 ) or third generation catalyst ( G3 ). The monomer consumption was followed by 1H NMR spectroscopy, which revealed vastly different reactivity ratios for M1 and M2 . In the case of M1 and M3 , we observed the highest difference in reactivity ratios (r1=324 and r2=0.003) ever reported for a copolymerization method. A triblock‐like copolymer was also synthesized using G3 by first allowing the consumption of the mixture of M1 and M2 and then adding M1 again. In addition, in order to measure the fast reaction rates of the G3 catalyst with M1 , we report a novel retardation technique based on an unusual reversible G3 Fischer‐carbene to G3 benzylidene/alkylidene transformation. 相似文献