Surface chemistry, thermal stability and structural properties of graphene oxide/12-tungstophosphoric acid nanocomposite

In recent years the nanocomposites of graphene oxide (GO) and different inorganic and organic compounds have shown great potential for charge storage applications. In present work we have investigated the influence of 12-tungstophosphoric acid (WPA) on surface chemistry of graphene oxide and thermal stability of nanocomposite. For this purpose nanocomposites with different mass ratios of GO and WPA were prepared. The thermal stability of nanocomposites was investigated by thermogravimetric and differential thermal analysis (TGA-DTA) while changes in surface chemistry of GO and structural properties of WPA were investigated by Fourier transform infrared spectroscopy (FTIR) and temperature programmed desorption (TPD) method. The TGA-DTA measurements of composites have shown that the major mass loss, due to carbon combustion, is shifted to higher temperatures (~500 °C vs. 380 °C of pure GO). Furthermore, when the amount of WPA is higher than 25 mass percent the nanocomposites start to act like individual components, which was also confirmed by FTIR analysis. The amount of surface oxygen groups, monitored by both TPD and FTIR methods, showed ˝V˝ shaped dependence from the quantity of WPA with minimum at about 12 mass percent of WPA. At the same time, the FTIR spectra revealed the structural changes of WPA, displayed as shifting and splitting of characteristic bands of Keggin anion structure

Surface chemistry, thermal stability and structural properties of graphene oxide/12-tungstophosphoric acid nanocomposite

In recent years the nanocomposites of graphene oxide (GO) and different inorganic and organic compounds have shown great potential for charge storage applications. In present work we have investigated the influence of 12-tungstophosphoric acid (WPA) on surface chemistry of graphene oxide and thermal stability of nanocomposite. For this purpose nanocomposites with different mass ratios of GO and WPA were prepared. The thermal stability of nanocomposites was investigated by thermogravimetric and differential thermal analysis (TGA-DTA) while changes in surface chemistry of GO and structural properties of WPA were investigated by Fourier transform infrared spectroscopy (FTIR) and temperature programmed desorption (TPD) method. The TGA-DTA measurements of composites have shown that the major mass loss, due to carbon combustion, is shifted to higher temperatures (~500 °C vs. 380 °C of pure GO). Furthermore, when the amount of WPA is higher than 25 mass percent the nanocomposites start to act like individual components, which was also confirmed by FTIR analysis. The amount of surface oxygen groups, monitored by both TPD and FTIR methods, showed ˝V˝ shaped dependence from the quantity of WPA with minimum at about 12 mass percent of WPA. At the same time, the FTIR spectra revealed the structural changes of WPA, displayed as shifting and splitting of characteristic bands of Keggin anion structure

Surface chemistry, thermal stability and structural properties of graphene oxide/12-tungstophosphoric acid nanocomposite

In recent years the nanocomposites of graphene oxide (GO) and different inorganic and organic compounds have shown great potential for charge storage applications. In present work we have investigated the influence of 12-tungstophosphoric acid (WPA) on surface chemistry of graphene oxide and thermal stability of nanocomposite. For this purpose nanocomposites with different mass ratios of GO and WPA were prepared. The thermal stability of nanocomposites was investigated by thermogravimetric and differential thermal analysis (TGA-DTA) while changes in surface chemistry of GO and structural properties of WPA were investigated by Fourier transform infrared spectroscopy (FTIR) and temperature programmed desorption (TPD) method. The TGA-DTA measurements of composites have shown that the major mass loss, due to carbon combustion, is shifted to higher temperatures (~500 °C vs. 380 °C of pure GO). Furthermore, when the amount of WPA is higher than 25 mass percent the nanocomposites start to act like individual components, which was also confirmed by FTIR analysis. The amount of surface oxygen groups, monitored by both TPD and FTIR methods, showed ˝V˝ shaped dependence from the quantity of WPA with minimum at about 12 mass percent of WPA. At the same time, the FTIR spectra revealed the structural changes of WPA, displayed as shifting and splitting of characteristic bands of Keggin anion structure

Surface chemistry and structural properties of proton-beam irradiated graphene oxide paper

Graphene oxide (GO) is a promising material for the futuregraphene-based electronics where the surface chemistry and structural properties of GO may play an important role. One of the unique methods with great potentialfor controllable modification of materials’ properties is the ion beam irradiation. In the present study, GO paper was irradiated with 15 keV proton- beam to a fluences from 5×10 16 to 2×1017 ionscm-2 , while Fourier-transform infrared spectroscopy (ATR-FTIR), X-ray photoelectronspectroscopy (XPS) and Raman spectroscopy (RS)were used for the examination of surface chemistry and structural properties of the irradiated material. It was shown that proton beam irradiation leads to a partial reduction of GOwith the preferential removal of the alkoxy and epoxy groups. With the increasing fluence, the oxygen content from the XPS method and the intensity ratioof D and G Raman bandsboth showed decreasing trends. When oxygen content was compared to relative areas of specific functional groups and parameters of Raman peaks an interesting correlation was found that suggest optimal fluences for tuning the surface chemistry and structural properties of GO. The observed effects on surface chemistry and structural propertiescan be ascribed to physical and chemical effectsof ion beam irradiation. The interaction of functional groups with H-atom was investigated using DFT andsemi-empirical (SE) approach. SE calculations revealed that the reduction of the epoxy group appears at H-atom energies below 1.5 eV. This work identifies ion beam irradiation as a preferable technique for selective removal of surface oxygen groups and structural modification of GO where the applied fluence can be used for tuning the degree of change.IX Serbian Ceramic Society Conference - Advanced Ceramics and Application : new frontiers in multifunctional material science and processing : program and the book of abstracts; September 20-21, 2021; Belgrad

Electrochemical tuning of capacitive response of graphene oxide

Increasing energy demands of modern society requires deep understanding of the properties of energy storage materials as well as their performance tuning. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, combined with cyclic voltammetry measurement and Raman spectroscopy, have shown that upon the reduction GO is irreversibly deoxygenated which is further accompanied with structural ordering and increasing of electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and de-oxygenation leads to the gradual loss of the capacitance. The observed trend is independent on the preparation route and on the exact chemical and structural properties of GO. It is proposed that an improvement of capacitive properties of any GO can be achieved by optimization of its reduction conditions.Comment: 23 pages, 7 figures, 59 reference

Viscose-Derived Activated Carbons Fibers as Highly Efficient Adsorbents for Dimethoate Removal from Water

Extensive use of pesticides resulting in their accumulation in the environment presents a hazard for their non-target species, including humans. Hence, efficient remediation strategies are needed, and, in this sense, adsorption is seen as the most straightforward approach. We have studied activated carbon fibers (ACFs) derived from viscose fibers impregnated with diammonium hydrogen phosphate (DAHP). By changing the amount of DAHP in the impregnation step, the chemical composition and textural properties of ACFs are effectively tuned, affecting their performance for dimethoate removal from water. The prepared ACFs effectively reduced the toxicity of treated water samples, both deionized water solutions and spiked tap water samples, under batch conditions and in dynamic filtration experiments. Using the results of physicochemical characterization and dimethoate adsorption measurements, multiple linear regression models were made to reliably predict performance towards dimethoate removal from water. These models can be used to quickly screen among larger sets of possible adsorbents and guide the development of novel, highly efficient adsorbents for dimethoate removal from water. © 2022 by the authors. Licensee MDPI, Basel, Switzerland

Influence of heteropoly acids on rat synaptic plasma membrane atp -ase activity

The in vitro influence of 12-tungstosilicic acid (WSiA) and 12-tungstophosporic acid (WPA) on Na+/K+_ATPase activity, using rat synaptic plasma membrane (SPM) as a model system was investigated. The half-maximum inhibition (IC50) of the enzyme activity was achieved with 5.80⋅ 10-5mol/L of WPA and 1.17⋅10-4 mol/L of WSiA. The both examined compounds showed a dose-dependent inhibitory effect on the enzyme activity in the concentration higher than 1 μmol/L

Electrochemical tuning of capacitive response of graphene oxide

The increasing energy demands of modern society require a deep understanding of the properties of energy storage materials, as well as the tuning of their performance. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, in combination with cyclic voltammetry measurements and Raman spectroscopy, have shown that upon reduction GO is irreversibly deoxygenated, which is further accompanied by structural ordering and an increase in electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and deoxygenation leads to a gradual loss of capacitance. The observed trend is independent of the preparation route and the exact chemical and structural properties of GO. It is proposed that an improvement in the capacitive properties of any GO can be achieved by optimization of its reduction conditions.This is the peer-reviewed version of the following article: Gutić, Sanjin J., Dževad Kozlica, Fehim Korać, Danica Bajuk-Bogdanović, Miodrag Mitrić, Vladimir M. Mirsky, Slavko V. Mentus, and Igor A. Pašti. "Electrochemical tuning of capacitive response of graphene oxide." (2018). [https://doi.org/10.1039/C8CP03631D]Published version available at: [http://vinar.vin.bg.ac.rs/handle/123456789/7877

How Well Do Our Adsorbents Actually Perform?—The Case of Dimethoate Removal Using Viscose Fiber-Derived Carbons

Growing pollution is making it necessary to find new strategies and materials for the removal of undesired compounds from the environment. Adsorption is still one of the simplest and most efficient routes for the remediation of air, soil, and water. However, the choice of adsorbent for a given application ultimately depends on its performance assessment results. Here, we show that the uptake of and capacity for dimethoate adsorption by different viscose-derived (activated) carbons strongly depend on the adsorbent dose applied in the adsorption measurements. The specific surface areas of the investigated materials varied across a wide range from 264 m2 g−1 to 2833 m2 g−1. For a dimethoate concentration of 5 × 10−4 mol L−1 and a high adsorbent dose of 10 mg mL−1, the adsorption capacities were all below 15 mg g−1. In the case of high-surface-area activated carbons, the uptakes were almost 100% under identical conditions. However, when the adsorbent dose was reduced to 0.01 mg mL−1, uptake was significantly reduced, but adsorption capacities as high as 1280 mg g−1 were obtained. Further, adsorption capacities were linked to adsorbents’ physical and chemical properties (specific surface area, pore size distribution, chemical composition), and thermodynamic parameters for the adsorption process were evaluated. Based on the Gibbs free energy of the adsorption process, it can be suggested that physisorption was operative for all studied adsorbents. Finally, we suggest that a proper comparison of different adsorbents requires standardization of the protocols used to evaluate pollutant uptakes and adsorption capacities

Physicochemical characterization of mineral mud from spa Vrujci

Mineralogical and physicochemical analysis of healing mud from spa Vrujci was performed by ICP-OES analysis and FTIR and micro-Raman spectroscopy. The therapeutic effect of mud was improved by plant extracts implementation