The adsorption of oxygen on Rh(110) was investigated by thermal desorption spectroscopy (TDS), X-ray photoelectron spectroscopy (XPS) and scanning tunnelling microscopy (STM). The desorption of chemisorbed oxygen was observed at 700 K to 1200 K. Above 1400 K exists another desorption peak which is attributed to subsurface oxygen. The content of subsurface oxygen in Rh(110) influences the chemisorption states on the surface, so that the desorbing character of the surface oxygen species is changed. The subsurface-state needs high preparation temperature and has not any reaction with residual gas or added hydrogen in the chamber, which clarifies its spatial isolation. The XPS result showed that the binding energy of subsurface species is higher than the one of surface oxygen. This confirms the TDS observation. The subsurface-oxygen containing surface showed in STM oxygen induced hillock-like structures.

The chemical adsorption and reaction of methyl fluoride, methyl chloride, methyl bromide, methyl iodide, methyl sulfide, dimethyl sulfide, dimethyl disulfide, and bis(trifluoromethyl) disulfide on clean, polycrystalline nickel surface (at 25°C) were investigated using an X-ray photoelectron spectrometer (XPS) and a thermal desorption system with mass spectrometric analysis (TD). The ion implantation of the methyl halide series on nickel was investigated by XPS. The nickel surface was cleaned by high temperature heating in vacuum or argon ion sputtering. An industrial lubricant, FC-43 (tri-hepta-fluorobutyl amine), was adsorbed on a gold-plated nickel surface at 25°C. Tne FC-43 adsorption system was investigated by TD. The adsorption of the methyl halide series on nickel was predominantly dissociative with several co-existing surface species being observed. The XPS results show that two carbon and two halogen species are formed. The possible structures for carbon are a CH₃-type and a CH₂-type or CH_nX (n = 0-3) adsorbed species. The halogen species appear to be neutral and ionic species. The TO results support the dissociative adsorption process for methyl halides on nickel. The adsorption of methyl fluoride and methyl chloride on nickel studied by TD resulted in the corresponding nickel halide being detected. The adsorption of methyl bromide and methyl iodide on nickel studied by TO resulted in the corresponding hydrogen halide, HX, being detected. The XPS results of the ion implantation of the methyl halides resulted in only one type of carbon that is similar to graphite. A halide type of halogen was also formed upon ion implantation. The XPS results for the adsorption of methyl sulfide, dimethyl sulfide, and dimethyl disulfide on nickel showed that only one carbon and one sulfur were observed. The possible structure for carbon is a CH₃-type of adsorbed specie. lhe sulfur species appears to be a sulfide S⁼-type adsorbed specie. The XPS results for the adsorption of bis(trifluoromethyl) disulfide on nickel showed that only sulfur was observed on the nickel surface. The TD results- for the methyl sulfide adsorption process was shown to be predominantly an associative type. The TO results for the dimethyl sulfide adsorption process were a mixture of dissociative and associative adsorption processes. The dimethyl disulfide adsorption process was determined by TD to be predominantly a dissociative type. The bis(trifluoromethyl} disulfide was determined by TD to be completely dissociative upon adsorption and reacted with nickel to form nickel sulfide. The TD results of FC-43 adsorption on gold-plated nickel showed that the predominant adsorption process was the associative type. / Ph. D.

Thesis (MSc)--Stellenbosch University, 2004. / ENGLISH ABSTRACT: The choice of the sample preparation technique used in combination with a chromatographic technique in environmental analysis strongly influences the performance of the method as a whole. The main aim of this work was to evaluate methods like: micro liquid-liquid extraction (цLLE)and solid phase micro extraction (SPME) in combination with gas chromatography-electron capture detector (GCECD) and a recently developed technique named stir bar sorptive extraction (SBSE) combined with thermal desorption system-programmable temperature vaporizationgas chromatography-mass spectrometer (TDS-PTV-GC-MS) for the analysis of organochloro-pesticides (OCPs) in natural water and to make a comparison between them. The most suitable method was then selected for the analysis of water samples collected from Eritrea. An additional goal was to develop a sensitive method for the analysis ofOCPs in soil and sediment samples. цLLE-GC-ECD and SPME-GC-ECD methods were evaluated for the analysis of OCPs in water. The former allowed achieving a sensitivity of less than 100 ppt and the latter was able to detect down to the 1 ppt level. Both methods were found to be repeatable with %RSD of3% to 19% and 5% to 12% as well as linear with a range of 1:103 and 1:5x103 respectivey. SBSE-TDS-GC-MS was also investigated for the analysis of OCPs in water samples. With this technique a good sensitivity down to 1 ppt was also obtained. The less sensitive nature of the MS compared to ECD was hereby compensated for by the large amount of polydimethylsiloxane (PDMS) phase on the stir bar. The method was repeatable and linear with a range of 1:5000, which is similar to the one obtained for the SPME-GC-ECD method. All three methods were also tested with real contaminated water samples and a comparison of the three techniques in terms of sensitivity, linearity, repeatability, availability and cost effectiveness was done. As a method of choice in terms of the above criteria, SPMEGC- ECD was applied to the water samples collected from Eritrea. The presence of some oePs such as a-BBC (benzenehexachloride), heptachlor, heptachlor epoxide, endosulfan I, p,p'-DDE (dichlorodiphenylchloroethylene), endosulfan II, p,p'-DDD (dichlorodiphenyldichloroethane), endosu!fan sulfate and p,p'-DDT (dichlorodiphenyltrichloroethane) in some of the Eritrean water samples was demonstrated The SPME-GC-ECD technique for the analysis OCPs in soil and sediment samples was investigated. It was shown to be able to detect down to 1 pg/g (lppt) with good linearity and repeatability. The method was also evaluated for authentic soil samples. Due to a lack of time the method could not be applied for the analysis of the soil and sediment samples collected from Eritrea. / AFRIKAANSE OPSOMMING: Die keuse van 'n gepaste monster-voorbereidingsmetode wat gebruik word tesame met 'n chromatografiese skeidingtegniek in omgewings-analise het 'n beduidende effek op die algehele metode. Die doel van hierdie werk was om metodes soos mikrovloeistof- vloeistof ekstraksie (цLLE) en soliede fase mikro ekstraksie (SPME) in kombinasie met gaschromatografie met elektronvangs deteksie (GC-ECD) te ontwikkel vir die analise van organochloor-pestisiede (OCPs) in natuurlike water. Vervolgens is hierdie metodes vergelyk met die onlangs-ontwikkelde roerstaaf sorptiewe ekstraksie tegniek (SBSE) in kombinasie met termiese desorbsie-GCmassaspektrometriese deteksie (TDS-GC-MSD). Die mees geskikte metode is vervolgens gebruik vir die analise van Eritreaanse watermonsters. Daarbenewens was die doelook om 'n sensitiewe metode te ontwikkel vir die analise van OCPs in gronden sedimentmonsters. Beide цLLE en SPME-GC-ECD metodes is gekarakteriseer deur goeie herhaalbaarheid en lineariteit. Die sensitiwiteit van bogenoemde metodes was minder as 100 dele per triljoen (ppt) en 1 ppt, respektiewelik. Ook met SBSE-TDS-GC-MSD kon 'n deteksielimiet van 1 ppt bereik word. In hierdie geval is vir die verlies van sensitiwiteit van die MSD in vergelyking met die ECD, gekompenseer deur die groter hoeveelheid PDMS op die roerstaaf in vergelyking met 'n SPME apparaat. Die herhaalbaarheid en lineariteit van die metode is vergelykbaar met dié van die SPMEGC- ECD metode. Al drie metodes is vergelyk vir die analise van gekontamineerde watermonsters in terme van sensitiwiteit, liniêre bereik, herhaalbaarheid, toeganklikheid en kosteeffektiwiteit. SPME-GC-ECD is vervolgens gekies as metode van voorkeur vir die analise van Eritreaanse watermonsters. Die teenwoordigheid van sekere OCPs soos a-BHC, heptachloor, heptachloorepoksied, endosulfan I, p,p'-DDE, endosulfan II, p,p' -DDD, endosulfan sulfaat en p,p' -DDT in die monsters is gedemonstreer. Die toepasbaarheid van die SPME-GC-ECD metode vir die analise van OCPs in grond-en sedimentmonsters is ook geëvalueer, en dit was moontlik om so min as 1 pg/g waar te neem. Weens tydbeperkings was dit nie moontlik om Eritreaanse grondmonsters met die ontwikkelde metode te analiseer nie.

[pt] O presente trabalho avaliou a eficácia da dessorção térmica in situ em remediar materiais contaminados por hidrocarbonetos de petróleo em refinarias. Paralelamente, foi projetado e construído um novo sistema modular para ser empregado sob dutovias para remediação de britas contaminadas. Os resultados do programa experimental revelaram ser possível a remediação de pavimentos de concreto contaminados por óleo combustível. A aplicação de calor na superfície do pavimento reduziu em até 65 por cento a sua resistência, porém propiciou a restauração de sua cor original. Verificou-se que os resíduos do processo, após análises mineralógicas por difração de raios X e químicas por espectroscopia de fluorescência, apresentavam uma composição muito semelhante ao solo empregado como material de construção dos aterros da refinaria, sugerindo que o resíduo possa ser advindo de transporte eólico. O sistema desenvolvido no presente trabalho apresentou um desempenho satisfatório. Verificou-se a necessidade de aeração do material remediado para eliminar a produção de coque. Adicionalmente, observou-se a importância de um bom isolamento térmico para minimizar o consumo energético e impedir a propagação de calor e das emissões para a atmosfera. As emissões geradas pelo aquecimento consistiam de olefinas e parafinas que podem ser devidamente tratadas pelo oxidador térmico. / [en] This dissertation assessed the adequacy of in situ thermal desorption (istd) in cleaning oil contaminated debris from Refineries. A new modulated istd system was designed and built in order to remediate oiled cobbles under pipeways. The experimental results revealed the possibility of cleaning concrete pavements contaminated by heavy oil. The thermal desorption process restored their original color but reduced their resistance up to 65 percent. It was observed that the resulting debris, after mineralogical analyses by X-ray diffraction and chemical analysis by X-Ray fluorescence, have a similar composition to the soil employed in the fills throughout the Refinery, indicating that the debris could well have been transported by the wind. The system devised here had a satisfactory performance. It was observed the necessity of aeration during the treatment in order to avoid the production of coke. Additionally, it was also observed the importance of a good thermal insulation in order to minimize power consumption and the propagation of heat and gas emissions to the atmosphere. The gases emissions consisted mainly of olefins and paraffins that had been reasonably been treated by the thermal oxidizer devised herein.

Although the metallurgical industry has made great strides in the reduction of unwanted emissions to the atmosphere as a result of production processes, significant challenges still exist. From a global perspective, even large reductions in emissions per produced ton become immaterial when considering that the total world production of metals continues to increase. Two such particularly hazardous emissions are sulfur dioxide, primarily from copper ore roasting, and mercury, which has had increasing emissions from the steel industry in recent years. Both pollutants have severe consequences for the environment and also for human health. The primary motivations of this work have hence been: (1). to study sulfate formation on soot from sulfur dioxide emissions reacting with ozone and H2O in the vapor phase and (2). to study factors involving the behavior of mercury adsorption on metal surfaces involved in steelmaking, in order to further the understanding of select emissions from scrap-based steelmaking. Gas phase experiments were conducted to examine the heterogeneous oxidation of sulfur dioxide on soot in the presence of ozone and water vapor. The sulfur dioxide oxidation into sulfate was quantified using a particle-into-liquid sampler coupled with ion chromatography to measure the sulfate formation at atmospheric pressure. Water vapor, ozone and sulfur dioxide concentrations were controlled. Due to the ozone oxidation, multilayer adsorption of sulfur dioxide on soot, as well as sulfate formation and physisorption on secondary surface layer sites were observed. The exposure also caused the soot to become hydrophilic, due to the sulfur dioxide adsorption and also likely the formation of carboxyl groups on the surface. No significant increase in sulfate formation was observed at ozone concentrations above 1000 ppm. The effects of common surface contaminants such as oxygen and chlorine were examined on the metal surfaces, as well as the impact of changes in temperature, with controlled conditions using thermal desorption auger electron spectroscopy. It was established that low temperatures (82 K through 111 K) were conducive to mercury adsorption, wherein physisorption and subsequent lateral mercury interactions in mercury adlayers occurred. Chlorine appeared to favor mercury uptake, as determined by the increased mercury coverage at low temperatures on polycrystalline iron, copper and zinc. Oxygen, however, was found to be an inhibitor of mercury, most notably at room temperature. It was surprising to establish that no mercury adsorbed on zinc surfaces at room temperature and only on polycrystalline samples at low temperature. The mercury signal intensity increased up to the limit of the melting temperature for iron systems, on the oxidized copper surface and the polycrystalline zinc surfaces, prior to desorption from the surfaces. It is suggested that this is due to a rearrangement of mercury atoms on the surface at increasing temperatures, whereas at 85 K, mercury adhered to its initial adsorption position. In other words, mercury wet these surfaces on annealing, transitioning from an islanded surface at low temperature to a smooth layer before desorption. Based on these results, it was concluded that the mercury bond to the oxidized surface was weakened compared to clean copper. Furthermore, it is proposed that a surface phase transition occurred on polycrystalline zinc prior to desorption. No such transition was observed on iron. Activation energies of desorption were calculated for the relevant metal surfaces. It was established that clean iron had the highest activation energy of desorption. The large bond strength between mercury and iron may account for the highest desorption temperature of the iron systems. Zinc and copper had similar activation energies and desorption temperatures, which were respectively lower than that of iron. X-Ray Photoelectron and Auger Electron Spectroscopy were used to ascertain common surface contamination, i.e. chlorine, oxygen and sulfur, which affected mercury adsorption. Laser Ablation Inductively Coupled Plasma Time of Flight Mass Spectrometry was used to determine the depth of mercury adsorption on the samples. The technique also showed that the samples contained mercury in the surface layers. Accompanied by the rising demand for metals is the increase in emissions from metals manufacturing. Moreover, it is critical to minimize sulfur dioxide emissions as particulates from soot continue to be released in the atmosphere. For scrap-based steelmaking, monolayer mercury adsorption on clean iron and copper at room temperature are significant results. With the rising use of electronic devices in vehicles, the sorting of scrap becomes increasingly important. Mercury not adsorbing on zinc at room temperature is also of relevance as it disproves the theory of increased mercury adsorption with the increased use of galvanized scrap in summer conditions. However, the low temperature studies showed multilayer adsorption of mercury on iron, zinc and copper, which has relevance for the reported temporal variations of mercury deposition in arctic regions. Keywords: mercury, iron, zinc, sulfur dioxide, adsorption, pollution, thermal desorption, polycrystalline, surfaces, spectroscopy / QC 20120326

Demands for zero greenhouse-gas emission vehicles have sharpened with today’s increased focus on global warming. Hydrogen storage is a key technology for the implementation of hydrogen powered vehicles. Metal hydrides can claim higher energy densities than alternative hydrogen storage materials, but a remaining challenge is to find a metal hydride which satisfies all current demands on practical usability. Several metals store large amounts of hydrogen by forming a metal hydride, e.g., Mg, Ti and Al. The main problems are the weight of the material and the reaction energy between the metal and hydrogen. Magnesium has a high storage capacity (7.6 wt.% hydrogen) in forming MgH2; this is a slow reaction, but can be accelerated either by minimizing the diffusion length within the hydride or by changing the diffusion properties. Light-metal hydrides have been studied in this thesis with the goal of finding new hydrogen storage compounds and of gaining a better understanding of the parameters which determine their storage properties. Various magnesium-containing compounds have been investigated. These systems represent different ways to address the problems which arise in exploiting magnesium based materials. The compounds were synthesized in sealed tantalum tubes, and investigated by in situ synchrotron radiation X-ray powder diffraction, neutron powder diffraction, isothermal measurements, thermal desorption spectroscopy and electron microscopy. It is demonstrated that hydrogen storage properties can be improved by alloying magnesium with yttrium or scandium. Mg-Y-compounds decompose in hydrogen to form MgH2 nano-structures. Hydrogen desorption kinetics are improved compared to pure MgH2. The influence of adding a third element, gallium or zinc has also been studied; it is shown that gallium improves hydrogen desorption from YH2. ScAl1-xMgx is presented here for the first time as a hydrogen storage material. It absorbs hydrogen by forming ScH2 and Al(Mg) in a fully reversible reaction. It is shown that the hydrogen desorption temperature of ScH2 is reduced by more than 400 °C by alloying with aluminium and magnesium.

Thesis (Ph.D.)--Ohio University, March, 2005. / Includes bibliographical references (p. 163-176)

Thesis (Ph.D.)--Ohio University, March, 2005. / Title from PDF t.p. Includes bibliographical references (p. 163-176)

The research presented in this thesis started with the idea to study alcohols as modifiers and dopants in differential ion mobility spectrometry (d-IMS) to produce complicated chemical signatures to explore a concept of chemical labels for product security application. D-IMS is a gas phase atmospheric pressure separation and detection technique which distinguishes compounds based on differences in their ions mobility as their travel under a low and high electric field. The hypothesis was that alcohols will form typical d-IMS products such as protonated monomers and proton bound cluster ions. However, the very first experiments revealed unexpected phenomena which included changes in the mobility of ions over a narrow range of concentrations that could not be explained by existing theory. Another observation was the apparent regeneration of reactant ions. It became evident that the observed phenomena had not been described in the open literature and that addressing the research-questions that were being raised would be essential for the determination of alcohols by d-IMS and its use in medical applications for toxicity screening and monitoring of alcohols. The above discovery shifted the research objective towards a fundamental and comprehensive study on the behaviour of alcohols in d-IMS. This thesis describes designed experiments and constructed systems allowing the efficient study of effect of concentration, electric field and temperature on the d-IMS responses of alcohols. The results of those studies demonstate: extensive fragmentation of alcohols, including previously undescribed fragmentation patterns with regeneration of the hydrated proton; new phenomena of adduct ion formation within the d-IMS drift tube, observed in the case of methanol within a narrow range of concentration; and self-modification of the alpha function of alcohols. This knowledge was exploited by developing an non-invasive analytical method for recovery, separation and detection of toxins from human saliva (including alcohols, diols and GHB) using TD-GC-d-IMS (thermal desorption - gas chromatography d-IMS) within a full range of toxicological concentration levels.

[pt] O presente trabalho descreve o desenvolvimento de um sistema de dessorção térmica aplicável a remediação de solos contaminados por compostos orgânicos. O sistema consiste de um bastonete térmico capaz de aquecer o solo através de um fluxo radial e de um oxidador térmico destinado ao tratamento das emissões gasosas. Fazem parte do sistema, como equipamentos acessórios, controladores de temperatura do tipo rampa patamar, isolantes térmicos de fibra cerâmica, membranas plásticas e amostradores de água e de gases. Estes últimos são utilizados para averiguar a eficiência do oxidador térmico. O sistema desenvolvido atingiu aos objetivos de projeto. O bastonete térmico foi capaz de aplicar temperaturas de até 600 ºC seguindo trajetórias de temperatura programadas. O mesmo pode-se afirmar do sistema de tratamento das emissões gasosas. O programa experimental realizado em um solo residual de gnaisse, obtido de um talude rodoviário da Rodovia Washington Luís, contaminado por óleo queimado, revelou que o sistema desenvolvido é capaz de reduzir a concentração de compostos orgânicos a um valor mínimo, bem abaixo dos limites estabelecido pelos órgãos ambientais nacionais e estrangeiros. O programa expôs a importância da aeração da matriz porosa durante o tratamento para impedir a formação de coque. As determinações analíticas revelaram que as emissões gasosas resultantes do aquecimento do solo residual contaminado com óleo queimado tratam-se de parafinas de olefinas. A duração do ensaio bem como o projeto do arranjo espacial da distribuição dos bastonetes em um sistema in situ de remediação pode ser determinada através do emprego da formulação de propagação de calor formulada por Stegemeier (1998). / [en] This dissertation refers to the development of an in situ system devised to remediate soils contaminated with organic compounds. The system consists basically of a thermal probe capable of heating the soil matrix through radial flow and a thermal oxidizer that treats the resulting gases emissions. The system clearly reached the design aims. The thermal probe consistently programed temperatures up to 6000C to the soil matrix following applied thermal paths. The thermal oxidizer was capable to heat gases emissions up to 9000C under prolonged exposure. The experimental program was carried out using a residual soil from gnaiss taken from a slope at Washington Luiz Roadway. This soil was contaminated with used oil and submitted to a series of tests in order to assess the efficiency of the system developed herein. The results suggest that thermal desorption was able to reduce the degree of contamination to levels well below the limits established by National and International Environmental Agencies. The results also revealed the importance of aeration during the process to avoid the formation of coke. Fingerprinting tests carried out on gases emissions revealed that they were composed mainly by olefins and paraffins. The design of an in situ system as well as the termination criteria for in situ thermal desorption treatment might well be accomplished using the heat propagation theory developed by Stegemeier (1998).