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Sulfonation of nanoporous activated carbon (NAC) was performed in the different ways available within the synthetic organic chemistry armory for preparing solid acid catalysts of isopropyl alcohol ...

In this study, we considered changes in the surface chemistry after introducing fluorine into the surface layer of nanoporous activated carbon (BAU) produced from the birch wood. Here, we examined the BAU treated with 1,1,1,2-tetrafluoroethane at the selected temperature in the range of 400–800 °C. Diverse methods, including chemical analysis, nitrogen adsorption–desorption, SEM–EDS, XPS, and 19F solid-state NMR, were used for the characterization of the prepared materials. It was found that one can introduce from 0.17 to 0.42 mmol of F per gram of BAU using fluoroalkylation at 400–500 °C. Increasing the temperature to 600 °C increases the fluorination efficiency, and the relatively high fluorine content of 1.86 mmol of F per gram of BAU can be reached. At least three group types, namely, C–F, CF2, and CF3 groups, were found by XPS and 19F solid-state NMR after such treatment. The content of “semi-ionic” fluorine drastically increases in the surface layer after high-temperature fluoroalkylation at 700 °C and 800 °C. This “semi-ionic” fluorine, in the form of C–F and CF2 groups, is directly conjugated with the π-electron system of the carbon matrix.

Nanoporous activated carbon (NAC) beads that prepared by carbonization of microporous polymer 2,6-di-tert-butyl pyridine beads were subjected to bromination followed by amination to synthesize the ...

Because of the low content of chelating groups onto carbon fibers (CFs), their adsorptive parameters are poor, and this has negative effects on their applications as lightweight sorbents. In this work, we established a modification method to incorporate amine groups into carbon fiber surfaces by bromination followed by ammonolysis to create an interfacial layer which can adsorb heavy metal ions from solutions. The changed chemical composition, surface morphology, and thermal stability were investigated. Thermoprogrammed desorption mass-spectrometry and thermal analysis showed thermal transformation and interplay between forms of the grafted bromine groups of 0.5 mmol/g and the resulting amino groups of 0.44–0.56 mmol/g. After grafting, the surface chemistry parameters were improved due to the covalent bonding and grafting of the amine groups as interface modifier. Scanning electron microscopy observation also confirmed that the surface morphology maintains the same, without impairment of fiber properties. This work is therefore a beneficial approach towards enhancing the adsorption parameters by controlling the interface layer of CFs.

The surface of microporous Norit® GAC 830 W carbon was fluoroalkylated by heating in 1,1,1,2-tetrafluoroethane and 1,1,1,2,2-pentafluoroethane at 400 and 500 °C. Elemental analysis, FTIR ATR spectroscopy, and TG studies showed the presence of ∼0.1–0.7 mmol g−1 of the fluorine-containing groups. Nitrogen adsorption measurements and quenched solid density functional theory simulations proved an increase in the mesoporosity. By combining the results of solid-state 19F NMR and XPS analyses, we determined the functionalization of the carbon surface with CF, CF3, and CF2 fluorine-containing groups. Supercapacitor electrodes prepared from these materials were subjected to the charge-discharge tests and electrical impedance measurements. During galvanostatic cycling in the aqueous 30% KOH, they showed an enhanced charge capacitance compared to the parent (830 W) and the reference (Supra 30) carbons. These observations suggest that the fluoroalkylated surface and the modified microporous structure have an additive effect on capacitance parameters of carbon electrodes studied in symmetric, negative and positive modes. The fluoroalkylation caused an increase in the surface capacitance up to 38%. Herein, we demonstrate the fluoroalkylation is a simple way to increase a capacitance of carbon electrodes.

International audience; A novel sensing system was designed for pH measurements based on the enhanced and quenched photoluminescence (PL) and UV–Vis absorption of the diluted water solutions of F-, O-, and N-containing carbon nanoparticles (FON-CNPs). These FON-CNPs were solvothermally synthesized, dissolved, ultra-filtrated, and separated by thin-layer chromatography. The total fluorine content in them was found to be 1.2–1.5 mmol per gram. Their TGA showed a total weight loss of 52.7% because of the thermal decomposition and detachment of the surface groups and the partial burning of the functionalized shell on the carbon core at temperatures below 1200 °C. TEM and Raman data confirmed the presence of graphitic structures in the carbon core. From the results of ATR FTIR and UV–Vis spectroscopies, we showed that a carbon shell incorporates different functional groups covering the carbon core. The surface groups of the carbon shell include carboxyl, phenolic, and carbonyl groups. Heterocyclic N-containing and amino groups and trifluoromethyl groups supporting the hydrophobicity were also found. We suggested the possible reasons for the pH responses obtained with the sensing system considering them dependent on the de-protonation of functional groups with pH change.

We proposed the brominated carbon cloth that made of polyacrylonitrile-based activated carbon fibers (PAN-ACFs) as a precursor to chemically and uniformly graft SO3H groups to prepare the solid acid catalyst. The thermal and catalytic properties of the sulfonated PAN-ACFs were examined by IR controlled catalytic measurements and thermal analysis. The catalytic test results showed that the sulfonated surface remarkably improved the operating efficiency in isopropanol dehydration by decreasing the reaction temperature. All PAN-ACFs with grafted SO3H groups prepared through brominated precursors can converse 100% of isopropanol into propylene at moderate temperature. They showed the highest catalytic activity compared to PAN-ACFs sulfonated with oleum and chlorosulfonic acid, which conversed only 40% and 70% of isopropanol into propylene and deactivated at the higher temperatures in the reaction medium.

Oxidation of activated carbon (AC) with nitric acid was carried out, and the resulting AC/HNO 3 showed high capacity when used as supercapacitor electrode material operated in the KOH electrolyte. Oxidation caused different structural changes in the AC, reducing the specific surface area and the total pore volume. After oxidation, the content of all types of oxygen-containing groups and, especially, carboxyl groups showed a significant increase. Despite the significant reduction of the specific surface area, the specific capacitance of the oxidized AC in symmetric supercapacitor electrodes is 1.4 times larger than that for the pristine AC.

Bromination and oxidation are concurrent reactions that passed on the surface of carbon solids and carbon nanomaterials. In this study, their products were modeled for a hexagonal carbon network that forming a honeycomb 2D planar structure made of sp2-hybridized bonded carbon. Two types of active centers, namely, HC=CH and C-H groups linked to peripheral zigzag carbon atoms, were considered during the DFT simulations. The oxidation process is more advantageous than bromination. Free active centers, even that on the oxidized surface, maintain their ability to the bromine addition reaction. However, the probability of their existence on the oxidized surface is very low. The active centers of the surface can be renewed by the removal of oxygen-containing groups at thermal treatment in an inert atmosphere.

Mixed barium‑strontium Nd:phosphate glasses of composition: 58P2O5–13K2O–8Al2O3–4B2O3–2.5La2O3–2SiO2–0.5Nd2O3–12(Ba1–xO/SrxO) with a different degree of molar substitution x were prepared. Optical properties of these glasses were examined by UV–Vis-IR and photoluminescence (PL) spectroscopies. Considering IR spectra, it was suggested a certain contribution of oxygen defects in the optical properties of glasses. UV–Vis absorbance and PL emission spectra owing to the internal f–f electron transitions of Nd3+ ions were shown a complex character of electronic processes. The result of a comprehensive analysis of the optical scattering indicatrices has revealed non-monotonic variations of the scattering efficiency against the ratio of Sr to Ba that is correlated with the suggested content of the oxygen defects in the mixed glasses. A cubic nonlinear optical (NLO) response under the pulsed laser radiation self-action at 1064 nm shows that the self-defocusing effect increases with the molar fraction of Ba. For a continuous wave laser excitation at 1064 nm, the most efficient NLO refractive response with Re(χ(3)) = 2.9 × 10−3 esu was obtained in the pure strontium Nd:phosphate glass, being classified as a promising for NLO applications.

Here we disclosed the substantial effect of the local medium in the vicinity of the excited Nd3+ions on the optical properties and the laser characteristics of glasses. The UV-Vis absorption of the...

In this study, we report soft and solvothermal methods for synthesis of zinc oxide nanoparticles (ZnO NPs). Both methods involve a precursor and are carried out at the middle low-temperature regime. The effect of different solvents on the ZnO NPs properties was studied. The nonlinear optical (NLO) response of the NPs was analyzed by the self-action of picosecond laser pulses at 1064 nm and by second harmonic generation (SHG) of a femtosecond laser pulses pump at 800 nm. The luminescence was studied within UV-visible ranges. It was shown that the NLO response efficiency significantly depends on the solvent. The obtained SHG efficiency of small (~2 nm) ZnO NPs is comparable to the one obtained for large (~150 nm) commercial ZnO NPs. The observed results are important for the application of the ZnO NPs in biolabeling. Electronic supplementary material The online version of this article (doi:10.1186/s11671-017-1934-y) contains supplementary material, which is available to authorized users.

The present study is objected to develop an analytical remote optical diagnostics of the functionalized carbons surface. Carbon composites with up to 1 mmol g−1 of irreversibly adsorbed bromine were produced by the room temperature plasma treatment of an activated carbon fabric (ACF) derived from polyacrylonitrile textile. The brominated ACF (BrACF) was studied by elastic optical scattering indicatrix analysis at wavelength 532 nm. The obtained data were interpreted within results of the thermogravimetric analysis, X-ray photoelectron spectroscopy and temperature programmed desorption mass spectrometry. The bromination dramatically reduces the microporosity producing practically non-porous material, while the incorporated into the micropores bromine induces the dielectric and structural impact on surface polarizability and conductivity due to the charging effect. We have found that the elastic optical scattering in proper solid angles in the forward and the backward hemispheres is sensitive to the kind of the bromine bonding, e.g., physical adsorption or chemisorption, and the bromination level, respectively, that can be utilized for the express remote fabrication control of the nanoscale carbons with given interfaces. Electronic supplementary material The online version of this article (doi:10.1186/s11671-017-1873-7) contains supplementary material, which is available to authorized users.