The magnetic-poly(divinylbenzene-1-vinylimidazole) [m-poly(DVB-VIM)] microbeads (average diameter 53–212 μm) were synthesized and characterized; their use as adsorbent in removal of Cr(VI) ions from aqueous solutions was investigated. The m-poly(DVB-VIM) microbeads were prepared by copolymerizing of divinylbenzene (DVB) with 1-vinylimidazole (VIM). The m-poly(DVB-VIM) microbeads were characterized by N2 adsorption/desorption isotherms, ESR, elemental analysis, scanning electron microscope (SEM) and swelling studies. At fixed solid/solution ratio the various factors affecting adsorption of Cr(VI) ions from aqueous solutions such as pH, initial concentration, contact time and temperature were analyzed. Langmuir, Freundlich and Dubinin–Radushkvich isotherms were used as the model adsorption equilibrium data. Langmuir isotherm model was the most adequate. The pseudo-first-order, pseudo-second-order, Ritch-second-order and intraparticle diffusion models were used to describe the adsorption kinetics. The apparent activation energy was found to be 5.024 kJ mol−1, which is characteristic of a chemically controlled reaction. The experimental data fitted to pseudo-second-order kinetic. The study of temperature effect was quantified by calculating various thermodynamic parameters such as Gibbs free energy, enthalpy and entropy changes. The thermodynamic parameters obtained indicated the endothermic nature of adsorption of Cr(VI) ions. Morever, after the use in adsorption, the m-poly(DVB-VIM) microbeads with paramagnetic property were separeted via the applied magnetic force. The magnetic beads could be desorbed up to about 97% by treating with 1.0 M NaOH. These features make the m-poly(DVB-VIM) microbeads a potential candidate for support of Cr(VI) ions removal under magnetic field.
ABSTRACT:We prepared poly(ethylene glycol dimethacrylate-1-vinyl-1,2,4-triazole) [poly(EGDMA-VTAZ)] beads (average diameter ¼ 150-200 mm) by copolymerizing ethylene glycol dimethacrylate (EGDMA) with 1-vinyl-1,2,4-triazole (VTAZ). The copolymer composition was characterized by elemental analysis and found to contain five EGDMA monomer units for each VTAZ monomer unit. The poly(EGDMA-VTAZ) beads had a specific surface area of 65.8 m 2 /g. Poly(EGDMA-VTAZ) beads were characterized by Fourier transform infrared spectroscopy, elemental analysis, surface area measurements, swelling studies, and scanning electron microscopy. Poly(EGDMA-VTAZ) beads with a swelling ratio of 84% were used for the heavy-metal removal studies. The adsorption capacities of the beads for Cd(II), Hg(II), and Pb(II) were investigated in aqueous media containing different amounts of these ions (5-750 mg/L) and at different pH values (3.0-7.0). The maximum adsorption capacities of the poly(EGDMA-VTAZ) beads were 85.7 mg/g (0.76 mmol/g) for Cd(II), 134.9 mg/g (0.65 mmol/g) for Pb(II), and 186.5 mg/g (0.93 mmol/g) for Hg(II). The affinity order toward triazole groups on a molar basis was observed as follows: Hg(II) > Cd(II) > Pb(II). pH significantly affected the adsorption capacity of the VTAZ-incorporated beads. The equilibrium data were well fitted to the Redlich-Peterson isotherm. Consideration of the kinetic data suggested that chemisorption processes could have been the rate-limiting step in the adsorption process. Regeneration of the chelatingbeads was easily performed with 0.1M HNO 3 .
Graphical abstractElectric chatacterization of organic field effect transistors with PVT dielectric layer: Pentacene is used as active layer in p-channel device; Fullerene is the active layer in n-channel device. Channel length is 2mm, channel width is 0.06mm. Research highlights► PVT shows low leakage current and high breakdown voltage. ► Both n-channel and p-channel OFET devices give low threshold voltage and are lack of hysteresis. ► Excellent film formation property of PVT allows for fabricating low voltage operation OFET devices. ► All solution processed polymer ambipolar OFET device is realized via layer by layer coating.
a b s t r a c tThe quasi-static and dynamic crushing response and the energy absorption characteristics of combined geometry shells composed of a hemispherical cap and a cylindrical segment were investigated both experimentally and numerically. The inelastic deformation of the shells initiated with the inversion of the hemisphere cap and followed by the axisymmetric or diamond folding of the cylindrical segment depending on the loading rate and dimensions. The fracture of the thinner specimens in dynamic tests was ascribed to the rise of the flow stress to the fracture stress with increasing strain rate. The hemisphere cap absorbed more energy at dynamic rates than at quasi-static rates, while it exhibited lower strain rate and inertia sensitivities than the cylinder segment. For both the hemisphere cap and the cylinder segment, the inertial effect was shown to be more pronounced than strain rate effect at increasing impact velocities.
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