Influence of boron doping on characteristics of glucose based hydrothermal carbons

In this study, the influence of boron doping on structural and surface properties of carbon material synthesized by hydrothermal method was investigated, and the obtained results were compared with the previously published influence that boron has on characteristics of carbonized boron-doped hydrothermal carbons (CHTCB). Hydrothermal carbons doped with boron (HTCB), were obtained by hydrothermal synthesis of glucose solution with the different nominal concentrations of boric acid. It was found that glucose based hydrothermal carbon does not have developed porosity, and the presence of boron in their structure has insignificant influence on it. On the contrary, additional carbonization increases the specific surface area of the undoped sample, while the increase in boron content drastically decreases specific surface area. Boron doping leads to a decrease in the amount of surface oxygen groups, for both, hydrothermally synthesized and additionally carbonized material. Raman analysis showed that boron content does not affect the structural arrangement of HTCB samples, and Raman structural parameters show higher degree of disorder, compared to the CHTCB samples. Comparison of structural and surface characteristics of hydrothermal carbons and carbonized materials contributes to the study of the so far, insufficiently clarified influence that boron incorporation has on the material characteristics.

Ударное разрушение кристаллического, аморфизованного имплантацией Ar-=SUP=-+-=/SUP=- и аморфного диоксида кремния

The mechanical fracture of silicon dioxide initiates the mechanoluminescence (ML) lighting due to multiple breakage of interatomic bonds with producing non-bridged oxygen groups of [Si–O–]. The detected ML signals consisted of series of pulses, the energy of which is proportional to the number of photons irradiated from the broken bonds. The comparative analysis of the energy distributions in ML series induced by the impact damage of the surface of crystalline and vitreous SiO2 before and after the Ar+-ion implantation was conducted. The interplay between random and correlated accumulation of broken bonds under the impact loading was found and discussed.

Effect of Microwave Treatment in a High Pressure Microwave Reactor on Graphene Oxide Reduction Process—TEM, XRD, Raman, IR and Surface Electron Spectroscopic Studies

Reduced graphene oxide (rGO) was prepared by chemical reduction of graphene oxide (GO) (with a modified Hummers method) in aqueous solutions of hydrazine (N2H4), formaldehyde (CH2O), formic acid (HCO2H) accompanied by a microwave treatment at 250 °C (MWT) by a high pressure microwave reactor (HPMWR) at 55 bar. The substrates and received products were investigated by TEM, XRD, Raman and IR spectroscopies, XPS, XAES and REELS. MWT assisted reduction using different agents resulted in rGOs of a large number of vacancy defects, smaller than at GO surface C sp3 defects, oxygen groups and interstitial water, interlayer distance and diameter of stacking nanostructures (flakes). The average number of flake layers obtained from XRD and REELS was consistent, being the smallest for CH2O and then increasing for HCO2H and N2H4. The number of layers in rGOs increases with decreasing content of vacancy, C sp3 defects, oxygen groups, water and flake diameter. MWT conditions facilitate formation of vacancies and additional hydroxyl, carbonyl and carboxyl groups at these vacancies, provide no remarkable modification of flake diameter, what results in more competitive penetration of reducing agent between the interstitial sites than via vacancies. MWT reduction of GO using a weak reducing agent (CH2O) provided rGO of 8 layers thickness.

Graphene Oxide Synthesis, Properties and Characterization Techniques: A Comprehensive Review

The unique properties of graphene oxide (GO) have attracted the attention of the research community and cost-effective routes for its production are studied. The type and percentage of the oxygen groups that decorate a GO sheet are dependent on the synthesis path, and this path specifies the carbon content of the sheet. The chemical reduction of GO results in reduced graphene oxide (rGO) while the removal of the oxygen groups is also achievable with thermal processes (tpGO). This review article introduces the reader to the carbon allotropes, provides information about graphene which is the backbone of GO and focuses on GO synthesis and properties. The last part covers some characterization techniques of GO (XRD, FTIR, AFM, SEM-EDS, N2 porosimetry and UV-Vis) with a view to the fundamental principles of each technique. Some critical aspects arise for GO synthesized and characterized from our group.

Effects of Chromic Treatment on the Surface Properties of Polypropylene (PP) Wood Composites

The moisture sensitivity of wood–polymer composites (WPCs) is mainly related to their hydrophilic wood components. Coatings are among the alternatives that improve the dimensional stability of these composites. However, the adhesion of most coatings to the WPC surface is generally poor. Thus, chemical and/or mechanical treatments should be applied to the WPC surface to improve the coating adhesion. Therefore, the main objective of this study was to improve the adhesion coating of polypropylene (PP) WPCs through a chromic treatment. PP was reinforced by three different pulp fibers (kraft, thermomechanical (TMP), and chemothermomechanical (CTMP)) at three fiber contents (50, 60, and 70% w/w). A chromic treatment was applied to the PP-based WPCs to activate the surface of the composites and alter their roughness parameters, creating a higher interfacial zone that improved the bonding of the epoxy coating to the surface of the PP composites. The chromic treatment increased the roughness of the surface. An increase in profile and surface parameters was observed after treatment. This treatment modified the chemical composition of the surface by creating polar carbon–oxygen groups and increasing the carbonyl and hydroxyl indexes.

Toxicity and Antioxidant Activity of Fullerenol C60,70 with Low Number of Oxygen Substituents

Fullerene is a nanosized carbon structure with potential drug delivery applications. We studied the bioeffects of a water-soluble fullerene derivative, fullerenol, with 10-12 oxygen groups (F10-12); its structure was characterized by IR and XPS spectroscopy. A bioluminescent enzyme system was used to study toxic and antioxidant effects of F10-12 at the enzymatic level. Antioxidant characteristics of F10-12 were revealed in model solutions of organic and inorganic oxidizers. Low-concentration activation of bioluminescence was validated statistically in oxidizer solutions. Toxic and antioxidant characteristics of F10-12 were compared to those of homologous fullerenols with a higher number of oxygen groups:F24-28 and F40-42. No simple dependency was found between the toxic/antioxidant characteristics and the number of oxygen groups on the fullerene’s carbon cage. Lower toxicity and higher antioxidant activity of F24-28 were identified and presumptively attributed to its higher solubility. An active role of reactive oxygen species (ROS) in the bioeffects of F10-12 was demonstrated. Correlations between toxic/antioxidant characteristics of F10-12 and ROS content were evaluated. Toxic and antioxidant effects were related to the decrease in ROS content in the enzyme solutions. Our results reveal a complexity of ROS effects in the enzymatic assay system.

Laser Patterning of Aligned Carbon Nanotubes Arrays: Morphology, Surface Structure, and Interaction with Terahertz Radiation

The patterning of arrays of aligned multi-walled carbon nanotubes (MWCNTs) allows creating metastructures for terahertz (THz) applications. Here, the strips and columns from MWCNTs vertically grown on silicon substrates are prepared using CO2 laser treatment. The tops of the patterned arrays are flat when the laser power is between 15 and 22 W, and craters appear there with increasing power. Laser treatment does not destroy the alignment of MWCNTs while removing their poorly ordered external layers. The products of oxidative destruction of these layers deposit on the surfaces of newly produced arrays. The oxygen groups resulting from the CO2 laser treatment improve the wettability of nanotube arrays with an epoxy resin. We show that the patterned MWCNT arrays absorb the THz radiation more strongly than the as-synthesized arrays. Moreover, the pattern influences the frequency behavior of the absorbance.