326 resultados para Iridium


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A biostratigraphically complete Cretaceous/Tertiary boundary was recovered during Ocean Drilling Program Leg 121. The boundary, cored in ODP Hole 752B on Broken Ridge, is the most expanded deep-sea section yet recovered by ODP/DSDP. The initial Danian subzone, CP la, spans nearly 5 m and the underlying uppermost Maestrichtian Nephrolithus frequens Zone extends 50 m below the boundary. The paleolatitude of Broken Ridge at Cretaceous/Tertiary time is estimated at 50°-55°S which includes this site among the latest in a series of complete or near complete high southern latitude Cretaceous/Tertiary boundary sections recovered by ODP (Leg 113 Site 690 and Leg 119 Site 738). The boundary at Site 752 lies at the base of a thick (6-6.5 m) volcanic ash unit composed of multiple ash layers which overlies indurated Maestrichtian chalks. Magnetostratigraphy indicates that the boundary lies within Subchron 29R, which is the case for all other known complete sections for which the polarity has been determined. Anomalous abundances of the trace element iridium are present at the boundary. A second iridium peak, 80 cm above the boundary, corresponds to an increase in redeposited Cretaceous nannofossils. The nannofossil succession is similar to that found at previously studied austral high-latitude ODP drill sites with few differences due to the more northerly location of this site. Individual nannofossil species were counted and placed into three categories. A plot of the percent abundance of Cretaceous, Tertiary, and 'survivor' groups illustrates the rapid replacement of the Cretaceous nannoflora by 'survivor' forms beginning at the boundary and the dominance of this latter group through the initial Danian biozone. This 'survivor' or opportunistic assemblage is then rapidly replaced by newly evolved Tertiary taxa. The assemblage of the uppermost Maestrichtian is biased toward dissolution-resistant forms such as Micula decussata. In those few intervals where preservation is good, the dissolution susceptible species, Prediscosphaera stoveri, is more prevalent and overall diversity of the assemblage is higher. The 'survivor' assemblage is dominated by Zygodiscus sigmoides and Thoracosphaera. The Tertiary assemblage consists of rare Biantholithus sparsus, the first of this group to appear. It is followed several meters upsection by Cruciplacolithus primus. Cruciplacolithus tenuis and small Prinsius spp. dominate the assemblage beginning at about 5 m above the boundary.

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Stable isotopic records across the Cretaceous/Paleogene (K/P) boundary in Maud Rise Holes 689B and 690C indicate that significant climatic changes occurred during the latest Cretaceous, beginning approximately 500 k.y. prior to the mass extinction event and the enrichment of iridium at the K/P boundary (66.4 Ma). An oxygen isotopic decrease of ~0.7 per mil - ~1.0 per mil is recorded in the Late Cretaceous planktonic and benthic foraminifers between 66.9 and 66.6 Ma. The negative isotope excursion was followed by a positive excursion of similar magnitude between 66.6 Ma (latest Cretaceous) and ~66.3 Ma (earliest Paleocene). No other isotopic excursions of this magnitude are recorded in the planktonic and benthic microfossil records 1.0 m.y prior to, and for 2.0 m.y following the mass extinction event at the K/P boundary. The magnitude and duration of these isotopic excursions were similar to those at the Paleocene/Eocene and Eocene/Oligocene boundaries. A major d13C excursion occurred 200 k.y. prior to the boundary, involving a positive shift in planktonic and benthic d13C of ~0.5 per mil - 0.75 per mil. Similar changes observed in other deep-sea sequences indicate that this reflected a global change in d13C of the oceanic total dissolved carbon (TDC) reservoir. The magnitude of this inferred carbon reservoir change and its association with high latitude surface-water temperature changes recorded in the d18O records implies that it was linked to global climate change through feedback loops in the carbon cycle. At the K/P boundary, the surface-to-deep water d13C gradient is reduced by approximately 0.6 per mil - ~0.2 per mil. However, unlike sequences elsewhere, the planktonic-benthic d13C gradient (Delta d13C) was not eliminated in the Antarctic. The surface-to-deep water gradient was re-established gradually during the 400 k.y. following the mass extinction. Full recovery of the Delta d13C occurred by ~60.0 Ma. In addition to the reduced vertical d13C gradient across the K/P boundary, there was a negative excursion in both planktonic and benthic d13C beginning approximately 100 k.y. after the boundary (66.3 Ma). This excursion resulted in benthic d13C values in the early Paleogene that were similar to those in the pre-K/P boundary intervals. This negative shift appears to reflect a change in the d13C of the oceanic TDC reservoir shift that may have resulted from reduced carbon burial and/or increased carbon flux to the oceans. Any model that attempts to explain the demise of the oceanic plankton at the end of the Cretaceous should consider the oceanic environmental changes that were occurring prior to the massive extinction event.

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An ultrasonic thermometer has been developed for high temperature measurement over a wide temperature range. It is particularly suitable for use in measuring nuclear fuel rod centerline temperatures in advanced liquid metal and high flux nuclear reactors. The thermometer which was designed to determine fuel temperature up to the fuel melting point, utilizes the temperature dependence of the ultrasonic propagation velocity (related to the elastic modulus} in a thin rod sensor as the temperature transducing mechanism. A pulse excitation technique has been used, where the mechanical resonator at the remote end of the acoustic·line is madto vibrate. Its natural frequency is proportional to the ultrasonic velocity in the material. This is measured by the electronic instrumentation and enables a frequency­ temperature or period-temperature calibration to be obtained. A completely digital automatic instrument has been designed, constructed and tested to track the resonance frequency of the temperature sensors. It operates smoothly over a frequency range of about 30%, more than the maximum working range of most probe materials. The control uses the basic property of a resonator that the stored energy decays exponentially at the natural frequency of the resonator.The operation of the electronic system is based on a digital multichannel transmitter that is capable of operating with a predefined number of cycles in the burst. this overcomes a basic defect in the previous deslgn where the analogue time-delayed circuits failed to hold synchronization and hence automatic control could be lost. Development of a particular type of temperature probe, that is small enough to fit into a standard 2 mm reactor tube has made the ultrasonic thermometer a practicable device for measuring fuel temperature. The bulkiness of previous probes has been overcome, the new design consists of a tuning fork, integral with a 1mm line, while maintaining a frequency of no more than 100 kHz. A magnetostrictive rod, acoustically matched to the probe is used to launch and receive the acoustic oscillations. This requires a magnetic bias and the previously used bulky magnets have been replaced by a direct current coil. The probe is supported by terminating the launcher with a short heavy isolating rod which can be secured to the reactor structure. This support, the bias and launching coil and the launcher are made up into a single compact unit. On the material side an extensive study of a wide range of refractory materials identified molybdenum, iridium, rhenium and tungsten as satisfactory for a number of applications but mostly exhibiting to some degree a calibration drift with thermal cycling. When attention was directed to ceramic materials, Sapphire (single crystal alumina) was found to have numerous advantages, particularly in respect of stability of calibration which remained with ±2°C after many cycles to 1800oC. Tungsten and thoriated tungsten (W - 2% Tho2) were also found to be quite satisfactory to 1600oC, the specification for a Euratom application.

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Experiments were conducted in annealed iridium using pyramidal and spherical indenters over a wide range of load. For a Berkovich pyramidal indenter, the hardness increased with decreasing depth of penetration. However, for spherical indenters, hardness increased with decreasing sphere radius. Based on the number of geometrically necessary dislocations generated during indentation, a theory that takes into account the work hardening differences between pyramidal and spherical indenters is developed to correlate the indentation size effects measured with the two indenters. The experimental results verify the theoretical correlation.

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Iridium nanoparticles deposited on a variety of surfaces exhibited thermal sintering characteristics that were very strongly correlated with the lability of lattice oxygen in the supporting oxide materials. Specifically, the higher the lability of oxygen ions in the support, the greater the resistance of the nanoparticles to sintering in an oxidative environment. Thus with γ-Al2O3 as the support, rapid and extensive sintering occurred. In striking contrast, when supported on gadolinia-ceria and alumina-ceria-zirconia composite, the Ir nanoparticles underwent negligible sintering. In keeping with this trend, the behavior found with yttria-stabilized zirconia was an intermediate between the two extremes. This resistance, or lack of resistance, to sintering is considered in terms of oxygen spillover from support to nanoparticles and discussed with respect to the alternative mechanisms of Ostwald ripening versus nanoparticle diffusion. Activity towards the decomposition of N2O, a reaction that displays pronounced sensitivity to catalyst particle size (large particles more active than small particles), was used to confirm that catalytic behavior was consistent with the independently measured sintering characteristics. It was found that the nanoparticle active phase was Ir oxide, which is metallic, possibly present as a capping layer. Moreover, observed turnover frequencies indicated that catalyst-support interactions were important in the cases of the sinter-resistant systems, an effect that may itself be linked to the phenomena that gave rise to materials with a strong resistance to nanoparticle sintering.

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Ocean Drilling Program (ODP) Leg 207, on the Demerara Rise in the western tropical North Atlantic, recovered multiple Cretaceous-Paleogene boundary sections containing an ejecta layer. Sedimentological, geochemical, and paleontological changes across the boundary closely match patterns expected for a mass extinction caused by a single impact. A normally graded, ~2-cm-thick bed of spherules that is interpreted as a primary air-fall deposit of impact ejecta occurs between sediments of the highest Cretaceous Plummerita hantkeninoides foraminiferal zone and the lowest Paleogene P0 foraminiferal zone. There are no other spherule layers in the section. In addition to extinction of Cretaceous taxa, foraminiferal abundance drops from abundant to rare across the boundary. Ir concentrations reach a maximum of ~1.5 ppb at the top of the spherule bed, and the Ir anomaly is associated with enrichment in other siderophile elements. We attribute the unusually well-preserved and relatively simple stratigraphy to the fact that Demerara Rise was close enough (~4500 km) to the Chicxulub impact site to receive ~2 cm of ejecta, yet was far enough away (and perhaps sheltered by the curve of northern South America) to have been relatively unaffected by impact-induced waves.

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Hole 841B was drilled in the forearc region of the Lau Basin at a water depth of 4810 m. The hole penetrated a roughly 500-m-thick series of Miocene volcanic sediments with a number of basaltic to andesitic units (sills?) varying in thickness between 7 cm and 17 m. The volcanics are slightly to moderately altered and contain analcite, chabazite, natrolite-thompsonite, heulandite (?), prehnite, and quartz as secondary phases. In addition, thaumasite [Ca3Si(OH)6 * 12H2O](SO4)(CO3) was identified in the altered sequence. Sulfur isotope data of two thaumasite separates (+23.5 per mil and +21.1 per mil d34S) indicate a seawater origin of the sulfate sulfur. It is suggested that thaumasite is a product of low-temperature (<60 °C), seawater-derived CaCl2-rich fluids that were almost identical in composition to those presently circulating in the sub-seafloor.

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An autonomous vessel, the Offshore Sensing Sailbuoy, was used for wave measurements near the Ekofisk oil platform complex in the North Sea (56.5 N, 3.2 E, operated by ConocoPhilllips) from 6 to 20 November 2015. Being 100% wind propelled, the Sailbuoy has two-way communication via the Iridium network and has the capability for missions of six months or more. It has previously been deployed in the Arctic, Norwegian Sea and the Gulf of Mexico, but this was the first real test for wave measurements. During the campaign it held position about 20km northeast of Ekofisk (on the lee side) during rough conditions. Mean wind speed measured at Ekofisk during the campaign was near 9.8m/s, with a maximum of 20.4m/s, with wind mostly from south and south west. A Datawell MOSE G1000 GPS based 2Hz wave sensor was mounted on the Sailbuoy. Mean significant wave height (Hs 1hr) measured was 3m, whereas maximum Hs was 6m. Mean wave period was 7.7s, while maximum wave height, Hmax, was 12.6m. These measurements have been compared with non-directional Waverider observations at the Ekofisk complex. Mean Hs at Ekofisk was 3.1m, while maximum Hs was 6.5m. Nevertheless, the correlation between the two measurements was high (97%). Spectra comparison was also good, except for low Hs (~1m), where the motion of the vessel seemed to influence the measurements. Nevertheless, the Sailbuoy performed well during this campaign, and results suggests that it is a suitable platform for wave measurements in rather rough sea conditions.

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Metal–organic frameworks, or MOFs, have emerged as a new class of porous materials made by linking metal and organic units. The easy preparation, structural and functional tunability, ultrahigh porosity, and enormous surface areas of MOFs have led to them becoming one of the fastest growing fields in chemistry. MOFs have potential applications in numerous areas such as clean energy, adsorption and separation processes, biomedicine, and sensing. One of the most promising areas of research with MOFs is heterogeneous catalysis. This thesis describes the design and synthesis of new, carboxylate-based MOFs for use as catalysts. These materials have been characterized using diffraction, spectroscopy, adsorption, and imaging techniques. The thesis has focused on preparing highly-stable MOFs for catalysis, using post-synthetic methods to modify the properties of these crystals, and applying a combination of characterization techniques to probe these complex materials. In the first part of this thesis, several new vanadium MOFs have been presented. The synthesis of MIL-88B(V), MIL-101(V), and MIL-47 were studied using ex situ techniques to gain insight into the synthesis–structure relationships. The properties of these materials have also been studied. In the second part, the use of MOFs as supports for metallic nanoparticles has been investigated. These materials, Pd@MIL-101–NH2(Cr) and Pd@MIL-88B–NH2(Cr), were used as catalysts for Suzuki–Miyaura and oxidation reactions, respectively. The effect of the base on the catalytic activity, crystallinity, porosity, and palladium distribution of Pd@MIL-101–NH2(Cr) was studied. In the final part, the introduction of transition-metal complexes into MOFs through different synthesis routes has been described. A ruthenium complex was grafted onto an aluminium MOF, MOF-253, and an iridium metallolinker was introduced into a zirconium MOF, UiO-68–2CH3. These materials were used as catalysts for alcohol oxidation and allylic alcohol isomerization, respectively.