The complex processing of titanomagnetite concentrates of the Gremyakha-vyrmes deposit with extraction of vanadium and titanium

Titanomagnetites are a complex raw material with a high content of valuable components: iron (35–65 %), vanadium (0.5–1.5 %) and titanium (2–14 %). Today, titanium–magnetite concentrates are processed in two ways: blast furnace (Russia, China) and using electric smelting (South Africa). The blast–furnace method is applicable only for low–titanium titanomagnetites. In the case of using titanomagnetite concentrates with a titanium dioxide content of more than 4 %, the method of electric smelting with preliminary reduction is applicable. Both technologies aim to recover the two components iron and vanadium, while titanium is not recovered. In this regard, the development of a complex technology for processing titanomagnetite concentrate to obtain iron in granular form, vanadium pentoxide and titanium is urgent.

Atomic-Scale Investigation of the Reversible alpha to omega-Phase Lithium Ion Charge – Discharge Characteristics of Electrodeposited Vanadium Pentoxide Nanobelts

Using an electrochemical potential pulse methodology in a mixed solvent system, electrochemical deposition of amorphous vanadium pentoxide (V2O5) nanobelts is possible. Crystallisation of the material is achieved using in air annealing with the temperature of crystallisation identified using in-situ heating transmission electron microscopy (TEM). The resulting alpha-phase V2O5 nanobelts have typical thicknesses of 10-20 nm, widths and lengths in the range 5-37 nm (mean 9 nm) and 15 - 221 nm (mean 134 nm), respectively. One-cycle reversibility studies for lithium intercalation (discharge) and de-intercalation (discharge) reveal a maximum specific capacity associated with three lithium ions incorporated per unit cell, indicative of omega-Li3V2O5 formation. Aberration corrected scanning TEM confirm the formation of omega-Li3V2O5 across the entirety of a nanobelt during discharge and also the reversible formation of the alpha-V2O5 phase upon full charge. Preliminary second cycle studies reveal reformation of the omega-Li3V2O5, accompanied with a morphological change in the nanobelt dimensions. Achieving alpha-V2O5 to omega-Li3V2O5 phase reversibility is extremely challenging given the large structural rearrangements required. This phenomenon has only been seen before in a very limited number of studies also employing nanosized V2O5 materials and never before with electrodeposited nanocrystals.

Recent Development in Vanadium Pentoxide and Carbon Hybrid Active Materials for Energy Storage Devices

With the increasing energy demand for portable electronics, electric vehicles, and green energy storage solutions, the development of high-performance supercapacitors has been at the forefront of energy storage and conversion research. In the past decade, many scientific publications have been dedicated to designing hybrid electrode materials composed of vanadium pentoxide (V2O5) and carbon nanomaterials to bridge the gap in energy and power of traditional batteries and capacitors. V2O5 is a promising electrode material owing to its natural abundance, nontoxicity, and high capacitive potential. However, bulk V2O5 is limited by poor conductivity, low porosity, and dissolution during charge/discharge cycles. To overcome the limitations of V2O5, many researchers have incorporated common carbon nanostructures such as reduced graphene oxides, carbon nanotubes, carbon nanofibers, and other carbon moieties into V2O5. The carbon components facilitate electron mobility and act as porous templates for V2O5 nucleation with an enhanced surface area as well as interconnected surface morphology and structural stability. This review discusses the development of various V2O5/carbon hybrid materials, focusing on the effects of different synthesis methods, V2O5/carbon compositions, and physical treatment strategies on the structure and electrochemical performance of the composite material as promising supercapacitor electrodes.

Cylindrical model of electrochromic colouration of hydrated vanadium pentoxide thin films with point contacts

This article analyses experiments on the kinetics of the internal electrochromism of thin (micron) films of hydrated vanadium pentoxide xerogel with point contacts. It describes a cylindrical model of electrochromic colouration, which was used to evaluate the concentration of the colour centres in the initial film and after additional hydrogenation of this film by plasmaimmersion ion implantation.When we compared the calculated values of the concentration of colour centres with the equilibrium concentration of protons in the xerogel, we saw that the mobility of the protons migrating from the depth of the film to the cathode region, which are involved in the electrochemical reaction, was not a determinant of the electrochromism kinetics.The rate of electrochromic colouration could be increased by the formation of layered film structures based on hydrated vanadium pentoxide, which have increased overall electron conductivity and, as a consequence, low faradaic resistance of the electrochromic cathodic reaction.

Single-layered assembly of vanadium pentoxide nanowires on graphene for nanowire-based lithography technique

Graphene nanoribbon (GNR)-based materials are a promising device material because of their potential high carrier mobility and atomically thin structure. Various approaches have been reported for preparing the GNR-based materials, from bottom-up chemical synthetic procedures to top-down fabrication techniques using lithography of graphene. However, it is still difficult to prepare a large-scale GNR-based material. Here, we develop a procedure to prepare a large-scale GNR network using networked single-layer inorganic nanowires. Vanadium pentoxide (V2O5) nanowires were assembled on graphene with an interfacial layer of a cationic polymer via the electrostatic interaction. A large-scale nanowire network can be prepared on graphene and is stable enough for applying an oxygen plasma. Using plasma etching, a networked graphene structure can be generated. Removing the nanowires results in a networked flat structure whose both surface morphology and Raman spectrum indicate a GNR networked structure. The field-effect device indicates the semiconducting character of the GNR networked structure. This work would be useful for fabricating a large-scale GNR-based material as a platform for GNR junctions for physics and electronic circuits.