Adsorption of bisulfate on the Ru(0001) single crystal electrode surface

Adsorption of anions from sulfuric acid solutions has been studied on Ru(0001) single crystal and polycrystalline surfaces by electrochemical techniques and in-situ Fourier transform infrared spectroscopy. Infrared spectroscopy shows that bisulfate is the anion adsorbed on the Ru(0001) surface. The bisulfate adsorption is detected at the H₂ evolution potential and extends into the potential region where the Ru surface is oxidized. A method for extracting unipolar bands from bipolar bands has been presented. The tuning rate of adsorbed bisulfate in the double layer potential region of Ru(0001) was found to be significantly smaller than those observed for other platinum metals. This has been ascribed to a small change in bisulfate coverage on Ru(0001) in this potential range. Bisulfate vibration frequencies are higher on this surface than at any face-centered cubic metal with the (111) orientation. Oxidation of the Ru(0001) surface is limited to one electron per Ru atom, distinctly different from the high degree of oxidation seen in polycrystalline surfaces. For oxidized polycrystalline Ru, only solution phase sulfates and bisulfates are observed in the IR spectra.     

Combined Raman spectrometer/laser-induced breakdown spectrometer for the next ESA mission to Mars

Among the different instruments that have been pre-selected to be on-board the Pasteur payload on ExoMars is the Raman/laser induced breakdown spectroscopy (LIBS) instrument. Raman spectroscopy and LIBS will be integrated into a single instrument sharing many hardware commonalities. An international team under the lead of TNO has been gathered to produce a design concept for a combined Raman spectrometer/LIBS elegant bread-board (EBB). The instrument is based on a specially designed, extremely compact, spectrometer with high resolution over a large wavelength range, suitable for both Raman spectroscopy and LIBS measurements. Low mass, size and power consumption are the main drivers of the instrument's design concept. In this paper, science objectives for the combined instrument are detailed. Background information on Raman spectroscopy and LIBS are presented, focussing on the synergy of these two techniques. In the last section, the instrument concept resulting from the assessment of the feasibility of the combined Raman/LIBS EBB is presented.     

Spectroscopy of Fluid Phases—The Study of Chemical Reactions and Equilibria up to High Pressures

The properties of fluid phases can be altered considerably by the external conditions. Phase equilibria and chemical equilibria can be greatly affected, and it is possible to carry out chemical reactions by exploiting the special properties of compressed fluid phases. The use of high pressure in chemical reactions is of considerable diagnostic and preparative value. Applied research is directed towards elucidating the details of existing technical high pressure processes and to the development of novel fluid phase reactions where the application of high pressure is able to induce selectivity. In order to pursue these lines of research, and to study structure and dynamics throughout the entire range from gaseous to liquidlike states, it is important to have spectroscopic methods for characterizing systems at high pressures and temperatures. This article is concerned with quantitative absorption spectroscopy in the infrared to the ultraviolet spectral region at pressures up to about 7 kbar and temperatures up to 900 K.     

Sun Exposure at School

There is strong evidence that sun exposure during childhood and adolescence plays an important role in the etiology of skin cancer, in particular cutaneous melanoma. Between the age of 6 and 18, most children and adolescents will spend around 200 days per year at school and may receive a substantial fraction of their daily total solar ultraviolet radiation (UVR) exposure while at school. This study estimated the average daily erythemally effective dose of 70 grade 8 students from a high school in Townsville during 5 school days in July 1998. Through UV measurements of shade locations at the school and a combination of frequency counts and a questionnaire of grade 8 students, it was possible to determine the fraction of solar UVR reaching under the shade structures during lunch breaks and routine outdoor activities. Also, a routinely operating UV-Biometer provided the annual variation of the daily dose that was used to calculate exposure levels for the 70 students. Our results suggest that up to 47% of the daily total dose fell within the time periods where students were outdoors during school hours. For students not seeking shade structures during the breaks (which usually was the case when involved in sport activities such as basketball or soccer), the average daily dose could have been as high as 14 SED (standard erythemal dose). Using results from the questionnaire of 70 grade 8 students, their average annual dose while at school was 414 SED or 2 SED per school day. However, the distribution of average daily erythemal effective dose per grade 8 student over the whole year showed that on 31% of all school days in 1998, this dose was exceeded. Because most previous attempts to change arguably poor sun-protective behavior of young Australian children and adolescents at school showed little success, one way of decreasing the amount of harmful UVR reaching unprotected skin is the more careful design of shade structures at schools.     

Vanadium Doped Sol-Gel TiO2 Coatings

A study of the experimental conditions required to obtain vanadium doped sol-gel TiO2 coatings is presented. Tetraethyl orthotitanate was employed as the TiO2 source and VCl3, VOSO4 · H2O and VOSO4 dissolved H2SO4 where employed as vanadium sources.Dip coating has been used to produce coatings on silicon wafers, spectral carbon electrodes and titanium electrodes. Both supported and unsupported films have been studied by UV-Vis spectra, IR spectroscopy and X-ray diffraction (XRD). The measurements have been made on samples as prepared and treated thermally at temperatures between 100°C and 300°C. The thermal treatment temperatures have been established from DTA/TGA measurements.The vanadium doped sol-gel TiO2 coatings have been tested as sensors for redox potential measurements in electrochemical processes. The influence of both the thickness of films and the nature of substrate has been investigated.     

Recent developments in oriented polymers for biomedical and engineering applications

A review is presented of recent research at Leeds University which has been directed at devising novel methods for the production of oriented polymer structures. First, the new hot compaction process for oriented fibre and tapes is described, together with its applications to polyethylene and polypropylene where there are a number of practical developments. Secondly, there is the use of hydrostatic extrusion to make load bearing oriented products from hydroxyapatite filled polyethylenes. The production routes include the application of high pressure annealing prior to hydrostatic extrusion and the preparation of high modulus polyethylene fibre/hydroxyapatite billets as the starting point. Finally, recent progress on die-drawing as a means to producing oriented monofilaments and biaxially oriented tubes is described, where the applications include polymer ropes, pipes for gas and water distribution and transparent cans for packaging.     

Preliminary synchrotron radiation characterization of first multilayer mirrors for the soft X-ray water window

The development of high-reflectivity devices for soft X-rays at quasi-normal incidence is a challenging research for the development of synchrotron radiation optics, particularly for soft X-ray microscopy and X-ray microprobe spectroscopy. Here we present data concerning the deposition of the first Ni/Ti and Ni/TiO₂ multilayers grown at the INFN Legnaro Laboratories (LNL). These multilayers have a lattice spacing in the order of 14 Å and more than 100 of bilayers. Experimental tests on these multilayers have been performed by a vacuum compatible θ–2θ reflectometer, set up at the INFN Frascati Laboratories (LNF), where their characterization has been accomplished by means of synchrotron radiation.The first multilayer mirrors tailored in order to work at quasi-normal geometry have been measured in the lower X-ray energy domain using both white-beam and monochromatic radiation at about 1 keV.     

Gamma-ray production cross section from energetic neutron inelastic scattering for methodical improvements in planetary gamma-ray spectroscopy

Planetary gamma-ray spectroscopy can be used to chemically analyze the top soil from planets in future planetary missions. The production from inelastic neutron interaction plays an effective role in the determination on the C and H at the surface. The gamma-ray production cross section from the strongest lines excited in the neutron bombardment of Fe have been measured by the use of a time analyzed quasi-mono-energetic neutron beam and a high purity germanium detector. The results from En=6.5, 32, 43, and 65 MeV are presented.     

The asilomar conference on ion spectroscopy,October 16–20, 2009

The ASMS conference on ion spectroscopy brought together at Asilomar on October 16–20, 2009 a large group of mass spectrometrists working in the area of ion spectroscopy. In this introduction to the field, we provide a brief history, its current state, and where it is going. Ion spectroscopy of intermediate size molecules began with photoelectron spectroscopy in the 1960s, while electronic spectroscopy of ions using the photodissociation “action spectroscopic” mode became active in the next decade. These approaches remained for many years the main source of information about ionization energies, electronic states, and electronic transitions of ions. In recent years, high-resolution laser techniques coupled with pulsed field ionization and sample cooling in molecular beams have provided high precision ionization energies and vibrational frequencies of small to intermediate sized molecules, including a number of radicals. More recently, optical parametric oscillator (OPO) IR lasers and free electron lasers have been developed and employed to record the IR spectra of molecular ions in either molecular beams or ion traps. These results, in combination with theoretical ab initio molecular orbital (MO) methods, are providing unprecedented structural and energetic information about gas-phase ions.     

Recent developments in the high-resolution gas chromatography of polychlorinated biphenyls.

The capillary gas chromatography of polychlorinated biphenyls (PCBs) is reviewed. Focus is on the most recent developments in the separation and detection of PCBs rather than sample preparation methods. Included are a comprehensive look at stationary phases that have been used to separate PCBs and the relatively new work on chiral separations of PCBs. Mass spectrometry and atomic emission are presented as selective detection techniques. Suggestions for additional research are proposed where appropriate.     

Photon-trap spectroscopy of mass-selected ions in an ion trap: optical absorption and magneto-optical effects

A novel experimental technique has been developed to observe a trace of optical absorption of free mass-selected ions. The technique combines a linear radio-frequency ion trap with a high-finesse optical cavity to perform cavity ring-down spectroscopy (photon-trap spectroscopy for generality), where the storage lifetime of photons in the cavity provides a sensitivity high enough to probe the trapped ions. Absorption spectra of the manganese ion Mn(+) are presented, showing hyperfine structures for the (7)P(2,3,4)<--(7)S(3) transitions in the ultraviolet range. Implementation of a solenoidal magnet allows us to observe the Zeeman splitting and the Faraday rotation as well.     

Ion spectroscopy: Where did it come from; where is it now; and where is it going?

The ASMS conference on ion spectroscopy brought together at Asilomar on October 16–20, 2009 a large group of mass spectrometrists working in the area of ion spectroscopy. In this introduction to the field, we provide a brief history, its current state, and where it is going. Ion spectroscopy of intermediate size molecules began with photoelectron spectroscopy in the 1960s, while electronic spectroscopy of ions using the photodissociation “action spectroscopic” mode became active in the next decade. These approaches remained for many years the main source of information about ionization energies, electronic states, and electronic transitions of ions. In recent years, high-resolution laser techniques coupled with pulsed field ionization and sample cooling in molecular beams have provided high precision ionization energies and vibrational frequencies of small to intermediate sized molecules, including a number of radicals. More recently, optical parametric oscillator (OPO) IR lasers and free electron lasers have been developed and employed to record the IR spectra of molecular ions in either molecular beams or ion traps. These results, in combination with theoretical ab initio molecular orbital (MO) methods, are providing unprecedented structural and energetic information about gas-phase ions.     

Semi-empirical studies of torsional potentials in halonitrosomethanes

Semi-empirical molecular electronic structure calculations have been performed on a number of species of the general formulae CX₃NO and CX₂YNO, where X, Y = Cl, F and H. Potential energy curves for the internal rotation (torsion) of the nitroso functional group and geometric parameters of the molecules have been obtained. These calculations have employed the public domain AMPAC package, using both the MNDO and AM1 models available within that package. Graphical results are presented and compared with previous ab initio calculations and experimental determinations, where they exist. The results of these calculations should prove valuable as an aid in the analysis of the spectroscopy of these species.     

Trace element speciation using solid phase microextraction

An initial review of research targeting applications of solid phase microextraction for organometallic speciation, published in 2001, encompassed literature from the early days of solid phase microextraction up to June 2000. In this article, the reader will find a compilation and discussion of relevant literature published from June 2000 to December 2004. Because of the maturity of the technique, only a brief overview of the measurement principles is presented. The major thrust of the article highlights applications of solid phase microextraction to the fields of elemental and organometallic analyses. In contrast to the earlier review, applications related to the determination of phosphorus-, sulfur-, bromine-, chlorine- and iodine-containing compounds have also been included for those cases where the target of the determination is the element or a specific molecule containing the element for which atomic spectroscopy has been advocated as a detection technique. Additionally, other microextraction techniques are also considered, including stirbar sorptive extraction and single droplet microextraction.     

Recent progress in atomic and chemical group effective potentials

Recent progress on atomic and chemical group effective potentials is presented. The reviewed effective potentials follow a shape-consistent extraction technique from ab initio data, within a scalar relativistic approximation. Two types of averaged relativistic effective core potentials are considered: the correlated ones where a part of the correlation energy is included in the effective potential, and the polarized ones for which only the core polarization effects are taken into account. In addition spin-orbit polarized pseudopotentials have been extracted, and the effects of the core polarization are tested on the atomic spectroscopy of iodine. Finally a very recent chemical group effective methodology is presented, reducing the number of both electrons and nuclei explicitly treated. Chemical transferability is investigated, and test calculations on a cyclopentadienyl effective group potential are presented.     

Nanostructures in Physical Materials Chemistry: An Exploratory Laboratory

The blend of nanotechnology and material science is often beyond the scope of undergraduate laboratories. Through undergraduate research, graphite-intercalated compounds have been incorporated in the production of carbon-based nanostructures. Based on this work a series of exploratory exercises were designed for the undergraduate physical chemistry laboratory emphasizing nanostructure material science. This rapidly expanding area of science and technology can be introduced at an undergraduate level using a high temperature oven to produce nanostructure samples that are analyzed by Raman spectroscopy, scanning electron microscopy, and transmission electron microscopy at research university laboratories, infrared spectroscopy, and a bomb calorimeter. In these experiments we use samples of pure graphite, fluorinated graphite, and lanthanum oxide to induce the formation of nanostructures. An overview of fullerenes, nanotubes, boron nitride and Si nanostructures, other carbon forms, graphite-intercalated compounds, and the storage of hydrogen in nanotubes are provided in an appendix. Several extensions of the laboratory are proposed.     

Monitoring Fibre Surfaces with XPS in Papermaking Processes

 Recent instrumental advances have vastly improved the analysis power of X-ray photoelectron spectroscopy (XPS), which has been widely used in applied surface research for decades. In this presentation a set of XPS analysis methods well suited for problems and analytical needs encountered in papermaking technology is presented. The emphasis will be on analysis of pulps and non-coated papers. Examples given describe the use of XPS in quantification of surface lignin and extractives; an alternative approach for evaluating elemental surface distributions via the Tougaard background analysis is also presented. The experimental work and interpretations presented are based on more than two thousand XPS analyses performed at Helsinki University of Technology during 1996–2000. With strictly standardised experimental setup, state-of-the-art instrumentation and a proper combination of analysis methods XPS can yield valuable and consistent information on surface properties of natural fibers.     

Phase measurement in nondegenerate three-wave mixing spectroscopy

A detailed model is presented that describes the temporal and spectral interference patterns resulting from phase-recovery infrared-visible sum-frequency spectroscopy. Included in this model are the effects of dispersive elements other than the phase shifting unit placed between the sample and local oscillator signals. This inclusion is critical when considering the interference patterns arising from studies of buried interfaces. Furthermore, in the midinfrared where it is difficult to have high visibility of the fringes, it is demonstrated that local field corrections have a significant effect on the shape of the interference pattern. By collecting and subsequently fitting a two-dimensional interference pattern displaying both temporal and spectral fringes, a complete characterization of all these effects is possible.     

Ultrasound-assisted polyol method for the preparation of SBA-15-supported ruthenium nanoparticles and the study of their catalytic activity on the partial oxidation of methane

Metallic Ru nanoparticles have been successfully produced and incorporated into the pores of SBA-15 in situ employing a simple ultrasound-assisted polyol method. The product has been confirmed by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy, where ultrasound provides both the energy for the reduction of the Ru(III) ion and the driving force for the loading of the Ru(0) nanoparticles into the SBA-15 pores. An ultrasound-assisted insertion mechanism has been proposed based on the microjets and shake-wave effect of the collapsed bubbles. The catalytic properties of the SBA-15-supported Ru nanoparticles have been tested by the partial oxidization of methane and show very high activity and high CO selectivity.