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251.
Ultrafine fibers were spun from polyacrylonitrile (PAN) solution in N,N‐dimethylformamide using a homemade electrospinning setup. Fibers with diameter ranging from 80 to 340 nm were obtained. Fiber size and fiber size distribution were investigated for various concentration, applied voltage, and tip‐to‐collector distance using image analysis. The diameters of the electrospun fibers increase when increasing the solution concentration and decrease slightly when increasing the voltage and needle tip‐to‐collector distance. Porosity and air permeability are vital properties in applications of electrospun nanofibrous structures. In this study, effects of process parameters on the porosity and air permeability of electrospun nanoweb were investigated as well. Results of statistical analysis showed that solution concentration and applied voltage have significant influences on pore diameters. It was concluded that nanofiber diameter played an important role on the diameter of pores formed by the intersections of nanofibers. A more realistic understanding of porosity was obtained and a quantitative relationship between nanoweb parameters and its air permeability was established by regression analysis. Two separate models were constructed for predicting air permeability in relation to process parameters. Optimization of electrospinning process for producing nanoweb with desirable air permeability is well achieved by these models. The models presented in this study are of high importance for their ability to predict the air permeability of PAN nanoweb both by process or structure parameters. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
252.
In this study, crosslinked poly(4-vinylpyridine/crotonic acid) [poly(4-VPy/CrA)] and its N-oxide derivative were synthesized
to compare the adsorption of cationic methylene blue (MB) dye on these materials. The adsorptive removal of MB from aqueous
solution onto adsorbents was studied by using column adsorption method. Experimental results showed that MB was removed more
effective by poly(4-VPy/CrA)–N-oxide than poly(4-VPy/CrA) resins. The percentage removal of MB increased with pH, and it was
observed that basic pH was favorable for the adsorption of MB. The adsorption capacity for poly(4-VPy/CrA)–N-oxide resin was
found to 19.96 mg/g. It was found that the adsorption isotherm of the MB-fitted Langmuir-type isotherm. For the adsorption
of MB, the pseudo-second-order chemical reaction kinetics provides the best correlation with the experimental data. Ten adsorption–desorption
cycles demonstrated that the resins were suitable for repeated use without considerable change in adsorption capacity. 相似文献
253.
Ag, Pd and Pt-modified alkaline leached NiCoZn composite coatings were prepared on a copper specimen by electrochemical technique. The chemical composition of layers before and after leaching as well as after noble metal modification was determined by energy dispersive X-ray spectroscopy (EDX). The surface morphologies of the composite coatings were examined with the help of scanning electron microscopy (SEM). The hydrogen evolution activity of the electrodes was studied in 1 M KOH solution. For this purpose, cathodic current-potential curves and electrochemical impedance spectroscopy (EIS) techniques were used. Furthermore, the change of hydrogen evolution activity of the electrodes as a function of operation time in alkaline solution was also investigated. Surface morphologies showed that the composite coatings prepared to have compact and porous surface. EDX analysis confirmed the presence of Ag, Pd and Pt metals over the NiCoZn layer. The co-deposition of nickel, cobalt and zinc on copper surface and subsequently alkaline leaching of zinc rendered cathode material very active in hydrogen evolution. The modification of alkaline leached NiCoZn ternary coating by deposition of small amounts of Ag, Pd and Pt can further enhance the hydrogen evolution performance of this Raney-type electrode when compared to NiCoZn individually. The order of hydrogen evolution activity of catalysts studied is Ni < NiCoZn < NiCoZn-Pd < NiCoZn-Ag < NiCoZn-Pt. The long-term electrolysis tests showed that the Pt-modified electrode has the better time stability than the others. The superiority of Pt-modified catalyst explained by well known intrinsic catalytic activity of Pt. 相似文献
254.
Mahboobeh Attaei Mário Vale Abdul Shakoor Ramazan Kahraman M. Fátima Montemor Ana C. Marques 《应用聚合物科学杂志》2020,137(22):48751
Silica-polyurea/polyuretane hybrid shell microcapsules (MCs) loaded with isophorone diisocyanate (IPDI) with long shelf-life and high thermal and chemical stability are prepared via emulsification followed by interfacial polymerization at the surface of oil droplets of the oil-in-water emulsion. The resultant MCs are aimed at self-healing performance in epoxy coatings. A commercially available, highly reactive polyisocyanate named tris(p-isocyanatophenyl) thiophosphate is successfully employed as shell forming agent, while triethoxyoctylsilane and hexadecyltrimethoxysilane (HDMS) are tested as “latent” active hydrogen sources. The resulting MCs display core–shell morphology, spherical shape with diameter of 5–20 μm, shell thickness ca. 1–2 μm, and an IPDI core fraction of 69 and 65 wt %, when HDMS and triethoxyoctylsilane are employed, respectively. MCs exhibit an increased thermal stability, comparing with pure IPDI, which makes them robust enough to resist the thermal cycles involved in the coating's preparation. Stability of MCs inside specific solvents and chemicals, their chemical composition and shelf-life as well as effect of MCs on the epoxy curing are evaluated by Fourier transformed infrared spectroscopy. MCs, remarkably, show excellent environment stability and a long shelf-life of more than 3.5 months. Their addition to an epoxy formulation is found to heal damaged zones in the epoxy coating, as shown by scanning electron microscopy and electrochemical impedance spectroscopy. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48751. 相似文献