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Here, we report a facile approach, by the photochemical reduction technique, for in situ synthesis of Au-reduced graphene oxide (Au-RGO) nanohybrids, which demonstrate excellent adsorption capacities and recyclability for a broad range of dyes. High-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) data confirm the successful synthesis of Au-RGO nanohybrids. The effect of several experimental parameters (temperature and pH) variation can effectively control the dye adsorption capability. Furthermore, kinetic adsorption data reveal that the adsorption process follows a pseudo second-order model. The negative value of Gibbs free energy (ΔG0) confirms spontaneity while the positive enthalpy (ΔH0) indicates the endothermic nature of the adsorption process. Picosecond resolved fluorescence technique unravels the excited state dynamical processes of dye molecules adsorbed on the Au-RGO surface. Time resolved fluorescence quenching of Rh123 after adsorption on Au-RGO nanohybrids indicates efficient energy transfer from Rh123 to Au nanoparticles. A prototype device has been fabricated using Au-RGO nanohybrids on a syringe filter (pore size: 0.220 μm) and the experimental data indicate efficient removal of dyes from waste water with high recyclability. The application of this nanohybrid may lead to the development of an efficient reusable adsorbent in portable water purification.  相似文献   
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A four‐band metamaterial harvester for harvesting 0.9 GHz, 1.8 GHz, 2.6 GHz, and 5.8 GHz signals is proposed by a dual‐layer structure. 0.9 GHz and 1.8 GHz bands are harvested by the resistors in front layer, whereas harvesting of 2.6 GHz is achieved by the resistors in second layer. All resistors in front and back layer contribute to harvesting at 5.8 GHz. Numerical calculations are verified by two different full‐wave electromagnetic solvers based on finite‐integration and finite‐element techniques. Power dissipation ratios at 0.9 GHz, 1.8 GHz, 2.6 GHz and 5.8 GHz frequencies concentrated at the resistors are found as 82.3%, 82.8%, 74.6%, and 83.6%, respectively, by the finite‐integration‐based solver. Besides, the finite‐element method‐based solver results in harvesting efficiencies of 79.6%, 93.4%, 73.7%, and 93.8%. The efficiency of the harvester is investigated for different oblique incidences. The proposed metamaterial harvester can be a good candidate for multi‐band absorption and harvesting applications.  相似文献   
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Summary: Five new crosslinkers for use in dental composites were synthesized. Four are based on TBHMA: 1 via reaction of TBBr and Bisphenol A; 2 by hydrolysis of t‐butyl groups of the first monomer to give a diacid derivative; 3 by conversion of the first monomer to an amide derivative using benzyl amine; 4 by conversion of the first monomer to amide derivative using APTES. The AHM‐based monomer 5 was synthesized from the Michael addition of APTES to AHM. The photopolymerization behaviors of the synthesized monomers with Bis‐GMA, TEGDMA and HEMA were investigated using photodifferential scanning calorimetry at 40 °C using DMPA as photoinitiator. The polymerization rates and degrees of conversion for mixtures of any of the monomers 1 – 4 with Bis‐GMA:TEGDMA were found to be similar to Bis‐GMA:TEGDMA, higher than Bis‐GMA:HEMA, and also higher than mixtures with Bis‐GMA:HEMA. The incorporation of TBHMA‐based monomers into the conventional resin mixture (Bis‐GMA and TEGDMA) reduced the polymerization shrinkages. Monomer 5 and its mixtures polymerized much faster and to higher degrees of conversion than the other investigated systems, however, this system exhibited the largest volume shrinkage.

Structures of some of the new crosslinkers synthesized.  相似文献   

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The corrosion mechanism and microstructural characteristics of yttria (Y2O3) exposed to uranium hexafluoride (UF4) and uranium tetrafluoride gases at temperatures above 900°C were investigated. Processed yttria samples were exposed for times ranging from 5 to 40 min. A weight increase was observed after each test exposure. An outer corrosion scale composed of UO2 and YF3, and an inner corrosion layer of YF3, were observed following the UF6 reaction at nearly 1200 K. During the UF4 exposure, an outer layer containing a liquid mixture of fluoride, oxygen, yttrium, uranium compounds, a secondary reaction layer of UO2 followed by an inner layer composed of a solution of Y2O3 and YF3, possibly in the form of YOF inner layer, were observed. It was found that the corrosion process is controlled by the diffusion which is evidenced by the parabolic growth rate of the secondary layer. After completion of the solidification process, the formation of a eutectic region and dendrites were observed throughout the outer scale. In general, at temperatures above 1173 K, high corrosion rates were observed, and yttria did not appear to be a viable containment material for UF4 and UF6.  相似文献   
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Bulletin of Engineering Geology and the Environment - Understanding the physical and especially mechanical properties of forest soils is very important in forest engineering operations including...  相似文献   
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Diterpenoidal anti-cancer drug andrographolide (AD) was encapsulated into solid lipid nanoparticle (SLN) because of poor aqueous solubility and high lipophilicity. AD-SLNs were prepared by solvent injection method and characterized for droplet size, surface morphology, zeta potential, etc. In vitro drug release was carried out by dialysis-membrane method. A pharmacokinetic study was performed by UPLC/Q-TOF-MS method to determine the maximum plasma concentration (Cmax), area under the curve (AUC), etc. There was an improvement in Cmax and AUC of AD-SLNs when compared with AD, thereby enhancing the bioavailability of AD. The tmax was increased than that of AD suspension, indicating the sustained release pattern of AD-SLNs. The antitumor activity was carried out on Balb/c mice showing better results with AD-SLNs as compared to AD. Thus, the AD-loaded SLNs would be useful for delivering poorly water-soluble AD with enhanced bioavailability and improved antitumor activity.  相似文献   
30.
Atherosclerotic cardiovascular disease is an important cause of mortality and morbidity in hemodialysis patients. Iron accumulation in arterial wall macrophages is increased in atherosclerotic lesions. Hepcidin is a key hepatic hormone regulating iron balance. It inhibits iron release from macrophages and iron absorption from enterocytes by binding and inactivating the cellular iron exporter ferroportin. The aim of this study is to investigate the relation of hepcidin‐25, iron parameters, and atherosclerosis measured by carotid intima media thickness (CIMT) in hemodialysis patients. Eighty‐two hemodialysis patients were enrolled in this cross‐sectional study. Predialysis blood samples were centrifuged at 1500 g and 4°C for 10 minutes and stored at ?80°C for the measurement of hepcidin‐25. DRG hepcidin enzyme‐linked immunosorbent assay kit was used for the measurement of hepcidin‐25. Ultrasonographical B‐mode imaging of bilateral carotid arteries was performed with a high‐resolution real‐time ultrasonography (Mindray DC7). Mean age of the study population was 57.90 ± 16.08 years and 43.9% were men. Total study population was grouped into two according to median value of hepcidin‐25. There was no difference between groups with respect to age, dialysis vintage, and C‐reactive protein. CIMT was found to be statistically significantly higher in low hepcidin‐25 group. In correlation analysis, CIMT was found to be correlated with age (P < 0.01, R = 0.33) and hepcidin‐25 (P < 0.01, R = 0.46). In linear regression analysis, age (β = 0.31) and hepcidin‐25 (β = 0.44) were found to be the determinants of CIMT in hemodialysis patients. Our results implicate that hepcidin may take part in pathophysiology of atherosclerosis and cardiovascular disease in hemodialysis patients.  相似文献   
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