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1.
Chemosphere ; 263: 128068, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33297072

RESUMEN

Several years after decommissioning, a magnesium dross and mixed waste heap at a former industrial facility is still reactive, as evidenced by the emission of heat, Volatile Organic Carbon (VOCs), acetylene (C2H2), cyanide (HCN) and ammonia (NH3) from deep, discordant, epigenetic fissures. To evaluate the longer-term stability of the waste heap material, four cores were collected to evaluate vertical variations in temperature, moisture, gas composition, geochemistry, and mineralogy. Temperature increased with depth and peaked at around 8 m, reaching in excess of 90 °C. The waste heap was a mixture of unreacted materials (mainly MgO and CaO) and a variety of hydrated secondary reaction products. Formation of the latter could account for the generation of heat and creation of the fissures via thermal and secondary mineral volumetric expansion. With a large inventory of unreacted CaO and MgO and substantial in situ water present, the waste heap will probably remain reactive in the foreseeable future. Importantly, the CaO/MgO ratio of solid materials in the waste heap provides a useful proxy for down hole temperature, pH, and fugitive gas concentrations. Fugitive gases emitted by the waste heap are related to the reaction of co-existing minerals in the heap based on an historical analysis of site waste disposal. These waste materials include calcium carbide (CaC2), magnesium nitride (Mg3N2) and calcium cyanamide (CaCN2). Capping to limit the ingress of additional meteoric water and targeted venting to facilitate cooling and the controlled release and dispersion of gases are recommended to manage the environmental risk.


Asunto(s)
Gases , Eliminación de Residuos , Carbono , Minerales , Residuos
2.
J Contam Hydrol ; 127(1-4): 15-29, 2012 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-21600670

RESUMEN

Many intervention activities in the terrestrial subsurface involve the need to recover/emplace distributions of scalar quantities (e.g. dissolved phase concentrations or heat) from/in volumes of saturated porous media. These scalars can be targeted by pump-and-treat methods or by amendment technologies. Application examples include in-situ leaching for metals, recovery of dissolved contaminant plumes, or utilizing heat energy in geothermal reservoirs. While conventional pumping methods work reasonably well, costs associated with maintaining pumping schedules are high and improvements in efficiency would be welcome. In this paper we discuss how transient switching of the pressure at different wells can intimately control subsurface flow, generating a range of "programmed" flows with various beneficial characteristics. Some programs produce chaotic flows which accelerate mixing, while others create encapsulating flows which can isolate fluid zones for lengthy periods. In a simplified model of an aquifer subject to balanced pumping, chaotic flow topologies have been predicted theoretically and verified experimentally using Hele-Shaw cells. Here, a survey of the key characteristics of chaotic advection is presented. Mathematical methods are used to show how these characteristics may translate into practical situations involving regional flows and heterogeneity. The results are robust to perturbations, and withstand significant aquifer heterogeneity. It is proposed that chaotic advection may form the basis of new efficient technologies for groundwater interventions.


Asunto(s)
Agua Subterránea/química , Movimientos del Agua , Purificación del Agua/métodos , Restauración y Remediación Ambiental , Modelos Teóricos , Dinámicas no Lineales
5.
Chemosphere ; 52(6): 975-87, 2003 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12781231

RESUMEN

Although petroleum contamination has been identified at many Antarctic research stations, and is recognized as posing a significant threat to the Antarctic environment, full-scale in situ remediation has not yet been used in Antarctica. This is partly because it has been assumed that temperatures are too low for effective biodegradation. To test this, the effects of temperature on the hydrocarbon mineralisation rate in Antarctic terrestrial sediments were quantified. 14C-labelled octadecane was added to nutrient amended microcosms that were incubated over a range of temperatures between -2 and 42 degrees C. We found a positive correlation between temperature and mineralisation rate, with the fastest rates occurring in samples incubated at the highest temperatures. At temperatures below or near the freezing point of water there was a virtual absence of mineralisation. High temperatures (37 and 42 degrees C) and the temperatures just above the freezing point of water (4 degrees C) showed an initial mineralisation lag period, then a sharp increase in the mineralisation rate before a protracted plateau phase. Mineralisation at temperatures between 10 and 28 degrees C had no initial lag phase. The high rate of mineralisation at 37 and 42 degrees C was surprising, as most continental Antarctic microorganisms described thus far have an optimal temperature for growth of between 20 and 30 degrees C and a maximal growth temperature <37 degrees C. The main implications for bioremediation in Antarctica from this study are that a high-temperature treatment would yield the most rapid biodegradation of the contaminant. However, in situ biodegradation using nutrients and other amendments is still possible at soil temperatures that occur naturally in summer at the Antarctic site we studies (Casey Station 66 degrees 17(') S, 110 degrees 32(') E), although treatment times could be excessively long.


Asunto(s)
Sedimentos Geológicos/análisis , Petróleo/análisis , Contaminantes Químicos del Agua/análisis , Alcanos/química , Alcanos/metabolismo , Regiones Antárticas , Biodegradación Ambiental , Dióxido de Carbono/análisis , Radioisótopos de Carbono , Cromatografía de Gases , Monitoreo del Ambiente , Sedimentos Geológicos/química , Sedimentos Geológicos/microbiología , Cinética , Petróleo/metabolismo , Análisis de Regresión , Temperatura , Contaminantes Químicos del Agua/metabolismo
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