NaOH-assisted hydrothermal reduction of graphene oxide.

The influence of the pH of the reaction medium on the structural characteristics of hydrothermally reduced graphene oxide, synthesized by the tour method, has been investigated. Varying the pH of the reaction medium within the range of 8.0, 10.0 and 12.0 (adjusted with NaOH) has revealed distinct effects on the morphology and properties of the resulting reduced graphene oxide. At a pH of 8.0 the hydrothermal treatment yielded reduced graphene oxide comprising of two particle fractions with a thickness equivalent to 4-5 graphitic layers each. In contrast, pH of 10.0 resulted in two particle fractions corresponding to 2-3 and 4 layers, respectively, while pH of 12.0 produced a single fraction with a particle thickness of 0.70 nm, encompassing 3 graphitic layers. Increasing the pH led to a decrease in the average lateral size of reduced graphene oxide particles to about 8 nm. All rGOs had micro- and mesopores with a specific surface area up to 226 m2g-1, showing a proportional increase in mesopores with increasing pH. Analysis of slit-like micropores revealed a minimum fractal dimension (D= 2.18) at pH = 8.0. The obtained results provide valuable insights into tailoring the structural properties of hydrothermally reduced graphene oxide by controlling the pH of the reaction medium, offering potential applications in various fields, including nanotechnology and materials science.

Effect of Thermal Activation on the Structure and Electrochemical Properties of Carbon Material Obtained from Walnut Shells.

A simple activation method has been used to obtain porous carbon material from walnut shells. The effect of the activation duration at 400 °C in an atmosphere with limited air access on the structural, morphological, and electrochemical properties of the porous carbon material obtained from walnut shells has been studied. Moreover, the structure and morphology of the original and activated carbon samples have been characterized by SAXS, low-temperature adsorption porosimetry, SEM, and Raman spectroscopy. Therefore, the results indicate that increasing the duration of activation at a constant temperature results in a reduction in the thickness values of interplanar spacing (d002) in a range of 0.38-0.36 nm and lateral dimensions of the graphite crystallite from 3.79 to 2.52 nm. It has been demonstrated that thermal activation allows for an approximate doubling of the specific SBET surface area of the original carbon material and contributes to the development of its mesoporous structure, with a relative mesopore content of approximately 75-78% and an average pore diameter of about 5 nm. The fractal dimension of the obtained carbon materials was calculated using the Frenkel-Halsey-Hill method; it shows that its values for thermally activated samples (2.52, 2.69) are significantly higher than for the original sample (2.17). Thus, the porous carbon materials obtained were used to fabricate electrodes for electrochemical capacitors. Electrochemical investigations of these cells in a 6 M KOH aqueous electrolyte were conducted by cyclic voltammetry, galvanostatic charge/discharge, and impedance spectroscopy. Consequently, it was established that the carbon material activated at 400 °C for 2 h exhibits a specific capacity of approximately 110-130 F/g at a discharge current density ranging from 4 to 100 mA/g.

Porous Structure and Fractal Dimensions of Activated Carbon Prepared from Waste Coffee Grounds.

The present work reports the results of a systematic study on the evolution of the morphological properties of porous carbons derived from coffee waste using a one-pot potassium-hydroxide-assisted process at temperatures in the range of 400-900 °C. Raw materials and obtained carbons were studied by TG, DTG, SEM and nitrogen adsorption porosimetry. The decomposition temperature ranges for hemicellulose, cellulose and lignin as the main component of the feedstock have been established. It is shown that the proposed method for the thermochemical treatment of coffee waste makes it possible to obtain activated carbon with a controllable pore size distribution and a high specific surface area (up to 1050 m2/g). A comparative study of the evolution of the distribution of pore size, pore area and pore volume has been carried out based on the BJH and NL-DFT (slit-like pores approximation) methods. The fractal dimension of the obtained carbons has been calculated by Frenkel-Halsey-Hill method for single-layer and multilayer adsorptions.

Cobalt ferrite as an electromagnetically boosted metal oxide hetero-Fenton catalyst for water treatment.

The cobalt ferrite Fenton catalysts were obtained by the flow co-precipitation method. FTIR, XRD, and Mössbauer spectroscopy confirmed the spinel structure. The crystallite size of the as-synthesized sample is 12 nm, while the samples annealed at 400 and 600 °C have crystallite sizes of 16 and 18 nm, respectively. The as-synthesized sample has a grain size of 0.1-5.0 µm in size, while the annealed samples have grain sizes of 0.5 µm-15 µm. The degree of structure inversion ranges from 0.87 to 0.97. The catalytic activity of cobalt ferrites has been tested in the decomposition of hydrogen peroxide and the oxidation of caffeine. The annealing of the CoFe2O4 increases its catalytic activity in both model reactions, with the optimal annealing temperature being 400 °C. The reaction order has been found to increase with increasing H2O2 concentration. Electromagnetic heating accelerates the catalytic reaction more than 2 times. As a result, the degree of caffeine decomposition increases from 40% to 85%. The used catalysts have insignificant changes in crystallite size and distribution of cations. Thus, the electromagnetically heated cobalt ferrite can be a controlled catalyst in water purification technology.