Browsing by Subject "Chemical composition"
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Item Evidence from high-temporal-resolution strain rates for strain softening due to episodic fluid influx at Passo del Sole, Central Swiss Alps(2012-12) Stacy, Sarah Jean; Carlson, William, 1952-; Cloos, Mark; Ketcham, Richard ABerg (2007) determined hand-sample-scale high-temporal-resolution strain rates from rotated garnet for two samples of quartzose pelitic gneiss at Passo del Sole, Central Swiss Alps, documenting a correlation between dramatic increases in strain rate and compositionally anomalous garnet growth zones. Considering additional evidence that these anomalous zones resulted from externally derived ephemeral fluid flow, he concluded that increased strain rates at Passo del Sole are the result of strain softening caused by fluid influx. This study tests Berg's interpretation by calculating new hand-sample-scale high-temporal-resolution strain rates for two additional samples of the same gneiss: a control sample (Sample PDS 03-30) that shows no unusual zoning patterns, implying that it was unaffected by fluids; and another (Sample PDS 03-2) that features a prominent Ca spike, suggesting that it has been affected by fluid influx. Unique features of garnet from this locality--contemporaneity of chemical zones, near-simultaneous nucleation, size-proportional growth, and rock-wide chemical equilibrium--were exploited to calculate strain rates of unprecedentedly high temporal resolution. Thermodynamically modeled temperatures for several growth-zone boundaries in each garnet crystal were combined with a regional heating rate of 11.5 ± 3.5 °C/Myr (presumed constant) and measured deflections of inclusion trails in each zone to calculate strain rates for several discrete time increments during garnet growth. Sample PDS 03-2 displays a 2- to 16-fold increase in strain rate that correlates with growth of the high-Ca zone; strain rates are 0.4 x 10⁻¹⁴ s⁻¹ to 4.1 x 10⁻¹⁴ s⁻¹ for zones with normal Ca concentration and 9.1 x 10⁻¹⁴ s⁻¹ to 17.9 x 10⁻¹⁴ s⁻¹ for the high-Ca zone. Distinct amongst all analyzed samples from Passo del Sole, Sample PDS 03-30--which has not been affected by fluid influx--shows no fluctuations in strain rates, which remain low and similar (0.2 x 10⁻¹⁴ s⁻¹ to 2.6 x 10⁻¹⁴ s⁻¹) across all zones. Results from this study therefore further substantiate the correlation of high strain rates with compositionally anomalous zones, strengthening the interpretation that elevated strain rates at Passo del Sole result from strain softening caused by episodic, externally controlled flow of fluids through the system during synkinematic garnet growth.Item Natural Organic Matter (NOM) in Aquatic Systems: Interactions with Radionuclides (234Th (IV), 129 I) and Biofilms(2011-10-21) Zhang, SaijinA series of laboratory and field investigations were carried out to elucidate the importance of natural organic matter in aquatic systems, i.e., trace element scavenging (e.g., 234Th) by exopolymeric substances (EPS), formation of biofilms, as well as interactions with 129I. A method involving cross flow ultrafiltration, followed by a three-step cartridge soaking and stirred-cell diafiltration, was developed for isolating EPS from phytoplankton cultures, especially in seawater media. EPS isolated from a marine diatom, Amphora sp. was then subjected to semi-quantitative (e.g., carbohydrate, proteins) and quantitative analysis (e.g., neutral sugars, acidic sugars, sulfate). It appeared that Th (IV) binding by EPS was dominated by the acidic polysaccharides of fraction. For EPS of biofilms collected from polluted streams, hydrophobic proteins were the most abundant components in EPS, followed by more hydrophilic carbohydrates. However, chemical composition of carbohydrates or proteins, i.e., monosaccharides and amino acids, respectively, varied with environmental conditions and substrata applied, which suggests that the formation of biofilms on different substrates is regulated by specific properties of microorganisms, environmental conditions and nature of substratum. No correlation between relative hydrophobicity of substratum and development of biofilm was found in this study. A sensitive and rapid GC-MS method was developed to enable the determination of isotopic ratios (129I/127I) of speciated iodine in natural waters. At the F-area of the Savannah River Site (SRS), iodine species in the groundwater consisted of 48.8 percent iodide, 27.3 percent iodate and 23.9 percent organo-iodine. Each of these iodine species exhibited vastly different transport behavior in the column experiments using surface soil from the SRS. Results demonstrated that mobility of iodine species depended greatly on the iodine concentration, mostly due to the limited sorptive capacity for anions of the soil. EPS, especially enzymes (e.g., haloperoxidases) could facilitate the incorporation of iodide to natural organic carbon. At high input concentrations of iodate (78.7 ?M), iodate was found to be completely reduced and subsequently followed the transport behavior of iodide. The marked reduction of iodate was probably associated with natural organic carbon and facilitated by bacteria, besides inorganic reductants (e.g., Fe2 ) in sediments and pore water.Item Tensile strength of asphalt binder and influence of chemical composition on binder rheology and strength(2014-08) Sultana, Sharmin; Bhasin, Amit; Liechti, Kenneth M.; Prozzi, Jorge A.; Zhang, Zhanmin; Fowler , David W.Asphalt mixtures or asphalt concrete are used to pave about 93% of about 2.6 million miles paved roads and highways in the US. Asphalt concrete is a composite of aggregates and asphalt binder; asphalt binder works as a glue to bind the aggregate particles. The mechanical response of the asphalt binder is dependent on the time/rate of loading, temperature and age. An asphalt concrete mixture inherits most of these characteristics from the asphalt binder. Also the asphalt binder plays a critical role in providing the asphalt concrete the ability to resist tensile stresses and relaxing thermally induced stresses that can lead to fatigue and low temperature cracking, respectively. Hence, it is very important (but not sufficient) to ensure that asphalt binders used in the production of asphalt concrete are inherently resistant to cracking, rutting and other distresses that a pavement may undergo. Current binder specification (AASHTO M-320) to evaluate its fatigue cracking is based on the stiffness of the binder and not on its tensile strength. Also, measurements following current specifications are made on test specimens subjected to a uniaxial mode of loading that does not produce the same stress state in the binder as in the case of asphalt concrete. Another challenge in being able to produce binders with inherently superior performing characteristics is the fact that the asphalt binders produced in a refinery do not have a consistent chemical composition. The chemical composition of asphalt binder depends on the source and refining process of crude oil. There is a need to better quantify the tensile strength of asphalt binder and understand the relationship between the chemical composition of asphalt binders and its mechanical properties. The knowledge from this study can be used to engineer asphalt binders that have superior performance characteristics. The objective of this research was to quantify the tensile strength of asphalt binder, develop a metric for the tensile strength and identify the relationship between chemical composition and mechanical properties of asphalt binder. Laboratory tests were performed on binders of different grades using a poker chip geometry to simulate confined state by varying the film thickness, rate of loading and modes of loading. The chemical properties of asphalt binder were studied based on SARA fractionation. The findings from this research showed that the modified correspondence principles can unify and explain the rate and mode dependency of asphalt binder. This study also quantified the relationship between chemical composition, and rheological and mechanical properties of asphalt binder. Finally, a composite model was developed based on the individual properties of chemical fractions which could predict the dynamic modulus of the asphaltenes doped and resins doped binder.