CO2 Capture technologies: Current status and new directions using supported ionic liquid phase (SILP) absorbers

Current state-of-the-art techniques for CO2 capture are presented and discussed. Post-combustion capture of CO2 by absorption is the technology most easily retrofitted to existing installations, but at present this is not economically viable to install and run. Using ionic liquids instead of aqueous amine solutions overcomes the major thermodynamic issues. By applying SILP technology further advances, in terms of ease of handling and sorption dynamics, are obtained. Initial experimental studies showed that ionic liquids such as tetrahexylammonium prolinate, [N6666][Pro], provide a good candidate for CO2 absorption using SILP technology. Thus a solid SILP absorber comprised of 40 wt% [N6666][Pro] loaded on precalcined silica quantitatively takes up about 1.2 mole CO2 per mole of ionic liquid in consecutive absorption-desorption cycles in a flow-experiment performed with 0.09 bar of CO2 (9% CO2 in He).     

Reversible formation of a PdC(x) phase in Pd nanoparticles upon CO and O2 exposure

The structure and chemical composition of Pd nanoparticles exposed to pure CO and mixtures of CO and O(2) at elevated temperatures have been studied in situ by a combination of X-ray Diffraction and X-ray Photoelectron Spectroscopy in pressures ranging from ultra high vacuum to 10 mbar and from room temperature to a few hundred degrees celsius. Our investigation shows that under CO exposure, above a certain temperature, carbon dissolves into the Pd particles forming a carbide phase. Upon exposure to CO and O(2) mixtures, the carbide phase forms and disappears reversibly, switching at the stoichiometric ratio for CO oxidation. This finding opens new scenarios for the understanding of catalytic oxidation of C-based molecules.     

Probing the active sites for CO dissociation on ruthenium nanoparticles

The active sites for CO dissociation were probed on mass-selected Ru nanoparticles on a HOPG support by temperature programmed desorption spectroscopy using isotopically labelled CO. Combined with transmission electron microscopy we gain insight on how the size and morphology of the nanoparticles affect the CO dissociation activity. The Ru nanoparticles were synthesized in a UHV chamber by gas-aggregation magnetron sputtering in the size range from 3 to 15 nm and the morphology was investigated in situ by scanning tunneling microscopy and ex situ by high resolution transmission electron microscopy. Surprisingly, it was found that larger particles were more active per surface area for CO dissociation. It is suggested that this is due to larger particles exposing a more rough surface than the smaller particles, giving rise to a higher relative amount of under-coordinated adsorption sites on the larger particles. The induced surface roughness is proposed to be a consequence of the growth processes in the gas-aggregation chamber.     

Electronic structures of methylated azaferrocenes and their borane adducts: photoelectron spectroscopy and electronic structure calculations

The preparation and crystal structure of a new 2,5-dimethylazaferrocene (DMAF) adduct of borane (DMAF-BH(3)) are reported. The electronic structures of 1,2,3,4,5-pentamethylazaferrocene (PMAF), its borane adduct 1,2,3,4,5-pentamethylazaferrocene-BH(3) (PMAF-BH(3)) and of DMAF-BH(3) have been studied by HeI-HeII UV photoelectron spectroscopy (UPS) and high-level DFT methods. UPS data reveal the influence of borane and methyl substitution on the electronic structures of azaferrocenes, which have been rationalized by inductive and hyperconjugative effects. UPS data also allow for the estimation of azaferrocene lone-pair stabilization upon coordination to borane, and suggest that pyridine is a slightly stronger sigma donor toward BH(3) than either azaferrocene studied. UV-Vis spectroscopic data for the radical cation of PMAF were also obtained and compared with the UPS data.     

On the Cl···N halogen bond: a rotational study of CF3Cl···NH3

The rotational spectra of six isotopologues (CF(3)(35)Cl···(14)NH(3), CF(3)(37)Cl···(14)NH(3), CF(3)(35)Cl···(15)NH(3), CF(3)(37)Cl···(15)NH(3), CF(3)(35)Cl···(14)ND(3) and CF(3)(37)Cl···(14)ND(3)) of the CF(3)Cl···NH(3) adduct have been investigated and analyzed by pulsed jet Fourier transform microwave spectroscopy. Rotational, centrifugal distortion and quadrupole ((35)Cl, (37)Cl, (14)N) coupling constants have been precisely obtained. The two subunits of the complex are held together via a Cl···N halogen bond interaction. Information on the internal dynamics and on the dissociation energy of the complex is provided.     

Linewidth of a quantum-cascade laser assessed from its frequency noise spectrum and impact of the current driver

We report on the measurement of the frequency noise properties of a 4.6-??m distributed-feedback quantum-cascade laser (QCL) operating in continuous wave near room temperature using a spectroscopic set-up. The flank of the R(14) ro-vibrational absorption line of carbon monoxide at 2196.6?cm^?1 is used to convert the frequency fluctuations of the laser into intensity fluctuations that are spectrally analyzed. We evaluate the influence of the laser driver on the observed QCL frequency noise and show how only a low-noise driver with a current noise density below ${\approx} 1~\mbox{nA/}\sqrt{}\mbox{Hz}$ allows observing the frequency noise of the laser itself, without any degradation induced by the current source. We also show how the laser FWHM linewidth, extracted from the frequency noise spectrum using a simple formula, can be drastically broadened at a rate of ${\approx} 1.6~\mbox{MHz/}(\mbox{nA/}\sqrt{}\mbox{Hz})$ for higher current noise densities of the driver. The current noise of commercial QCL drivers can reach several $\mbox{nA/}\sqrt{}\mbox{Hz}$ , leading to a broadening of the linewidth of our QCL of up to several megahertz. To remedy this limitation, we present a low-noise QCL driver with only $350~\mbox{pA/}\sqrt{}\mbox{Hz}$ current noise, which is suitable to observe the ??550?kHz linewidth of our QCL.     

On the polymerization of hexavalent uranium. An electrospray mass spectrometry study

Polymerization in hexavalent uranium solutions was measured by electrospray ionization time-of-flight mass spectrometry in three different acidic media at pH values from 3 to 5.3 in order to detect all hydrolysis species present in solution. The aqueous solutions were directly measured without further dilution in organic solvents. At high uranyl concentrations ([U(VI)]?=?10(-?3) M) artifacts were observed due to the presence of more than one solution species per formed microdroplet. Those artifacts were composed of ions and neutral species being present in the same droplet. However, by analyzing the detected species carefully, the origin of the artifacts could be traced back to the physically meaningful species. Still, only general trends of the hydrolysis behavior can be deduced from the measurements at [U(VI)]?=?1???10(-?3) M. The solutions at [U(VI)]?=?5???10(-?5) M did not show any comparable artifact formation. The detected species distributions resemble the expected trends calculated from the equilibrium constants published in the Nuclear Energy Agency Thermodynamic Database (NEA-TDB). The neutral (UO(2))(CO(3))(0) species present in solution causes, if located in the same microdroplet as a charged species, the apparent formation of dimeric and trimeric ternary hydroxo carbonate complexes at pH 5.3. As the uncharged species is not repelled from the ionic species, it might remain in the same droplet during the droplet fission process. By dividing those detected species into the uncharged (UO(2))(CO(3))(0) and a second ionic species, the relative abundances of the solution species can be corrected, leading to a good agreement with the predictions of the published equilibrium constants. In addition to the well-known trimer, we report the direct mass spectrometric detection of the dimeric (UO(2))(2)(OH)(2)(2+) species.     

Saltwater intrusion modeling: Verification and application to an agricultural coastal arid region in Oman

This paper deals with numerical modeling of density-dependent flow of saltwater intrusion in coastal groundwater systems. We present the implementation of an approach to solve a moving boundary problem for a dynamic water table within an invariant finite element mesh. The model is successfully validated against laboratory experiment data for an unconfined, density-dependent benchmark. The validated software is applied to a regional-scale study area and sufficiently calibrated for a steady state of pre-development conditions. Transient mass transport scenario simulations show good concordance with salinity measurements satisfyingly supporting the model setup.