Browsing by Subject "Chemical structural changes"

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    Electrospun BiOI nano/microtectonic plate-like structure synthesis and UV-light assisted photodegradation of ARS dye
    (Royal Society of Chemistry, 2014) Babu, V. J.; Bhavatharini, R. S. R.; Ramakrishna, S.
    BiOI electrospun nanofibers were prepared by using PAN as a supporting polymer. Subsequent annealing at 500 °C for 5 h, with a ramp rate of about 5 °C min-1 in air, breaks the nanofibers down to tectonic plate-like nano/microstructures. The surface physical and chemical structural changes were then further characterized by FE-SEM, TEM, XRD and XPS. The results reveal that the morphology and crystallite size of BiOI vary strongly depending on the precursor concentration used in the synthesis method. These nanostructures were later employed for photocatalytic degradation of a synthetic textile dye, Alizarin Red S (ARS). The photocatalytic efficiencies were found to be about 93.34% after 100 min of UV-light (340 nm) illumination. Photocatalytic activity (PCA) performance depends on morphology and band alignment. All the compositions follow first order pseudo-kinetics, which was found to be 0.1197 min-1 for a doping concentration of 3%. The enhancement in photodegradation could be possibly by photocatalysis and a photosensitization phenomenon. This has been explained based on the band edge position. © the Partner Organisations 2014.
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    Fabrication of cellulose acetate/polybenzoxazine cross-linked electrospun nanofibrous membrane for water treatment
    (Elsevier, 2017-12) Ertaş, Yelda; Uyar, Tamer
    Herein, polybenzoxazine based cross-linked cellulose acetate nanofibrous membrane exhibiting enhanced thermal/mechanical properties and improved adsorption efficiency was successfully produced via electrospinning and thermal curing. Initially, suitable solution composition was determined by varying the amount of the benzoxazine (BA-a) resin, cellulose acetate (CA) and citric acid (CTR) to obtain uniform nanofibrous membrane via electrospinning. Subsequently, thermal curing was performed by step-wise at 150, 175, 200 and 225 °C to obtain cross-linked composite nanofibrous membranes. SEM images and solubility experiments demonstrated that most favorable result was obtained from the 10% (w/v) CA, 5% (w/v) BA-a and 1% (w/v) CTR composition and cross-linked nanofibrous membrane (CA10/PolyBA-a5/CTR1) was obtained after the thermal curing. Chemical structural changes (ring opening) occurred by thermal curing revealed successful cross-linking of BA-a in the composite nanofibrous membrane. Thermal, mechanical and adsorption performance of pristine CA and CA10/PolyBA-a5/CTR1 nanofibrous membranes were studied. Char yield of the pristine CA nanofibrous membrane has increased notably from 12 to 24.7% for composite CA10/PolyBA-a5/CTR1 membrane. When compared to pristine CA membrane, CA10/PolyBA-a5/CTR1 nanofibrous membrane has shown superior mechanical properties having tensile strength and Young's modulus of 8.64 ± 0.63 MPa and 213.87 ± 30.79 MPa, respectively. Finally, adsorption performance of pristine CA and CA10/PolyBA-a5/CTR1 nanofibrous membranes was examined by a model polycyclic aromatic hydrocarbon (PAH) compound (i.e. phenanthrene) in aqueous solution, in which CA10/PolyBA-a5/CTR1 nanofibrous membrane has shown better removal efficiency (98.5%) and adsorption capacity (592 μg/g).