In this study, a manganese oxide, Mn3O4 was used to remove chromium(III) and chromium(VI) from aqueous solutions. The Mn3O4 nanomaterial was synthesized through a precipitation method, and was characterized using XRD, which confirmed the material had a crystal structure similar to hausmannite. In addition, using Scherrer’s equation it was determined that the nanomaterial had an average grain size of 19.5 ± 1.10 nm. A study of the effects of pH on the binding of chromium(III) and chromium(VI) showed that the optimum binding pH was 4 and 3 respectively. Batch isotherm studies were performed to determine the binding capacity of chromium(III), which was determined to be 18.7 mg/g, 41.7 mg/g, and 54.4 mg/g respectively for 4°C, 21°C, and 45°C. Chromium(VI) on the other hand had lower binding capacities of 2.5 mg/g, 4.3 mg/g, and 5.8 mg/g for 4°C, 21°C, 45°C, respectively. Thermodynamic studies performed indicated the sorption process was for the most part controlled by physisorption. The ΔG for the sorption of chromium(III) and Chromium(VI) ranged from −0.9 to −13 kJ/mol, indicating a spontaneous reaction was occurring. The enthalpy indicated a endothermic reaction was occurring during the binding and show ΔH values of 70.6 and 19.1 kJ.mol for chromium(III) and Chromium(VI), respectively. In addition, ΔS for the reaction had positive values of 267 and 73 J/mol for chromium(III) and chromium(VI) which indicate a spontaneous reaction. In addition, the sorption process was found to follow pseudo second order kinetic and the activation energy studies indicated the binding process occurred through chemisorption.

The development of alternative anode materials out of flexible composite nanofibers has seen a growing interest. In this paper, binary carbon nanofiber electrodes of SnO 2 /NiO and Sn nanoparticles are produced using a scalable technique, Forcespinning (FS), and subsequent thermal treatment (carbonization). The Sn/C composite nanofibers were porous and flexible, while the SnO 2 /NiO composite nanofibers had "hairy-like" particles and pores on the fiber strands. The nanofiber preparation process involved the FS of Sn/PAN and SnO 2 /NiO/PAN solution precursors into nanofibers and subsequent stabilization in air at 280°C and calcination at 800 o C under an inert atmosphere. The flexible composite nanofibers were directly used as working electrodes in lithium-ion batteries without a current collector, conducting additives, or binder. The electrochemical performance of the SnO 2 /NiO/C and Sn/C composite fiber anodes showed a comparable cycle performance of about 675 mAhg -1 after 100 cycles. However, the SnO 2 /NiO/C electrode exhibited a better rate performance than the Sn/C composite anode and was able to recover its capacity after charging with a higher current density. A postmortem analysis of the composite nanofiber electrode after the aging process revealed a heavily passivated electrode from the electrolyte decomposition by-products. The synthesis and

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In the present work, the effect of temperature and additives on the ionic conductivity of mixed organic/ionic liquid electrolytes (MOILEs) was investigated by conducting galvanostatic charge/discharge and ionic conductivity experiments. The mixed electrolyte is based on the ionic liquid (IL) (EMI/TFSI/LiTFSI) and organic solvents EC/DMC (1:1 v/v). The effect of electrolyte type on the electrochemical performance of a LiCoO2 cathode and a SnO2/C composite anode in lithium anode (or cathode) half-cells was also investigated. The results demonstrated that the addition of 5 wt.% succinonitrile (SN) resulted in enhanced ionic conductivity of a 60% EMI-TFSI 40% EC/DMC MOILE from ~14 mS·cm−1 to ~26 mS·cm−1 at room temperature. Additionally, at a temperature of 100 °C, an increase in ionic conductivity from ~38 to ~69 mS·cm−1 was observed for the MOILE with 5 wt% SN. The improvement in the ionic conductivity is attributed to the high polarity of SN and its ability to dissolve various types of salts such as LiTFSI. The galvanostatic charge/discharge results showed that the LiCoO2 cathode with the MOILE (without SN) exhibited a 39% specific capacity loss at the 50th cycle while the LiCoO2 cathode in the MOILE with 5 wt.% SN showed a decrease in specific capacity of only 14%. The addition of 5 wt.% SN to the MOILE with a SnO2/C composite-fiber anode resulted in improved cycling performance and rate capability of the SnO2/C composite-membrane anode in lithium anode half-cells. Based on the results reported in this work, a new avenue and promising outcome for the future use of MOILEs with SN in lithium-ion batteries (LIBs) can be opened.

Fine polyacrylonitrile (PAN) fibers were produced through a scalable centrifugal spinning process. Sodium chloride (NaCl) was added to the PAN‐dimethylformamide solution to decrease the surface tension and consequently promote a decrease in fiber diameter while increasing the fiber output. The fiber preparation process involved the centrifugal spinning of the PAN‐based solution; developed fibers were stabilized in air at 240°C followed by carbonization at 800°C under a Nitrogen atmosphere. The addition of sodium chloride to the PAN solution led to a 37% decrease in the carbon fiber diameter. The carbon fibers were analyzed by scanning electron microcopy, transmission electron microscopy (TEM), X‐ray diffraction, X‐ray photoelectron spectroscopy (XPS) and electrochemical experiments. The TEM results revealed improved graphitization with the addition of sodium chloride. The XPS analysis showed increased functionality (e.g. O2) on the surface of carbon fibers obtained from PAN/NaCl precursor fibers. A significant improvement was achieved in the electrochemical performance of carbon fibers made from PAN/NaCl precursor fibers compared to those made from pure PAN precursor fibers. POLYM. ENG. SCI., 58:2047–2054, 2018. © 2018 Society of Plastics Engineers