Surface Properties of Halloysite-Carbon Nanocomposites and Their Application for Adsorption of Paracetamol

Analysis of surface properties of halloysite-carbon nanocomposites and non-modified halloysite was carried out with surface sensitive X-ray photoelectron spectroscopy (XPS) and inverse gas chromatography (IGC). The XPS spectra were measured in a wide range of the electron binding energy (survey spectra) and in the region of C 1s photoelectron peak (narrow scans). The IGC results show the changes of halloysite surface from basic for pure halloysite to acidic for carbon-halloysite nanocomposites. Halloysite-carbon nanocomposites were used as adsorbents of paracetamol from an aqueous solution. The adsorption mechanism was found to follow the pseudo-second-order and intra-particle diffusion models. The Langmuir multi-center adsorption model described well the obtained experimental data. The presence of carbon increased significantly the adsorption ability of halloysite-carbon nanocomposites for paracetamol in comparison to the non-modified halloysite.

in Situ X-ray Photoelectron Spectroscopic and Electrochemical Studies of the Bromide Anions Dissolved in 1-Ethyl-3-Methyl Imidazolium Tetrafluoroborate

Influence of electrode potential on the electrochemical behavior of a 1-ethyl-3-methylimidazolium tetrafluoroborate (EMImBF4) solution containing 5 wt % 1-ethyl-3-methylimidazolium bromide (EMImBr) has been investigated using electrochemical and synchrotron-initiated high-resolution in situ X-ray photoelectron spectroscopy (XPS) methods. Observation of the Br 3d5/2 in situ XPS signal, collected in a 5 wt % EMImBr solution at an EMImBF4–vacuum interface, enabled the detection of the start of the electrooxidation process of the Br- anion to Br3- anion and thereafter to the Br2 at the micro-mesoporous carbon electrode, polarized continuously at the high fixed positive potentials. A new photoelectron peak, corresponding to B–O bond formation in the B 1s in situ XPS spectra at E ≤ –1.17 V, parallel to the start of the electroreduction of the residual water at the micro-mesoporous carbon electrode, was observed and is discussed. The electroreduction of the residual water caused a reduction in the absolute value of binding energy vs. potential plot slope twice to ca. dBE dE-1 = –0.5 eV V-1 at E ≤ –1.17 V for C 1s, N 1s, B 1s, F 1s, and Br 3d5/2 photoelectrons.

Femtosecond dopant-to-solvent energy transfer inside helium nanodroplets

Photoexcitation of atoms solvated inside superfluid helium nanodroplets is investigated with femtosecond photoelectron spectroscopy. Expansion of the solvation shell within about 600 fs is observed as transient photoelectron peak shift. For larger photoexcitation energies within the blue-shifted absorption band, more energy is transferred to the He droplet and the expansion proceeds faster.

THE GAS MONITORING OF THE BESIII DRIFT CHAMBER

Two monitoring proportional counters (MPCs), installed at the inlet and outlet of the gas system of BESIII drift chamber (DC), were used to monitor the operation of the BESIII DC successfully and effectively as reported in this paper. The ratio of G out /G in (full energy photoelectron peak position of 55 Fe 5.9 keV X-ray in inlet MPC as Gin and outlet MPC as Gout ) is used as the main monitoring parameter. The MPC method is very useful for the gas detector system.

Surface chemical states of barium titanate: Influence of sample processing

The composition and chemistry of the near-surface region of BaTiO3 have been studied using x-ray photoelectron spectroscopy (XPS). It is found that the Ba3d photoclectron peak shows two chemical states, one of which is attributed to the bulk perovskite and the other to a special surface state unrelated to contamination. The bulk component is reduced and the surface component increases when the material is annealed at high temperatures (either in reducing or oxidizing atmosphere). Both the components are unaltered if the sample is exposed to air, solvents, or water: processes that lead to adsorption of impurities. The surface peak, therefore, attributed to a relaxation related and not contamination-related state, has been compared with those in other Ba-containing oxides. The oxygen photoelectron peak consists of a normal perovskite peak typical of most titanates and a higher energy component clearly related to surface contamination. Annealing in reducing atmosphere results in drastically different optical and electrical properties, and in chemical reduction of some Ti4+ ions to Ti3+. The overall stoichiometry, however, does not change with annealing atmosphere. These results have been discussed in light of our current understanding of this and other related oxides.