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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Degradation of Naphthenic Acids in Athabasca Oil Sands Process-Affected Water Using Ozone

Hongjing , Fu Unknown Date
No description available.
2

Degradation of Naphthenic Acids in Athabasca Oil Sands Process-Affected Water Using Ozone

Hongjing , Fu 06 1900 (has links)
In order to determine the degradation of Naphthenic Acids (NAs) in oil sands process-affected water (OSPW), a series of semi-batch ozonation experiments have been conducted resulting in a maximum reduction of NAs greater than 99%. Compared to the high NAs removal, the reduction of both COD and DOC was much lower under the same conditions. Following ozone treatments of approx. 80 mg/L, the cBOD5 and cBOD5/COD tripled as compared to original OSPW measurements, suggesting ozone-treated OSPW has a higher biodegradability. The ozone treatments also detoxified the OSPW; with an ozone treatment of approx. 100 mg/L, the treated OSPW showed no toxicity using the Mircotox® bioassay. Additionally, the coke-treated OSPW, treated using a coke/water slurry process, was found to be non-toxic with an ozone treatment of approx. 20 mg/L. The results obtained during this study shows the great potential ozonation may offer as a possible water treatment application for oil sands water management. / Environmental Engineering
3

Adsorption of Single-ring Model Naphthenic Acid from Oil Sands Tailings Pond Water Using Petroleum Coke-derived Activated Carbon

Sarkar, Bithun 17 July 2013 (has links)
Petroleum coke-derived activated carbons were prepared and used for the adsorptive removal of a single-ring naphthenic acid (NA) from synthetic oil sands tailings pond water (TPW). The overall adsorption process was found to be intra-particle diffusion-controlled. The Weber-Morris intra-particle diffusion rate constants decreased from 7.43 to 1.23 mg/g min0.5 after activated carbon was post-oxidized with oxygen, suggesting a hindering effect of oxygen surface groups. The Freundlich model fit of the equilibrium adsorption isotherms and the small negative ΔHo pointed to a physisorption-dominated process and the importance of specific surface area. It was estimated that about 2.7 g/L of basic CO2-activated carbon is needed to reduce NA concentration from 120 mg/L to 2.5 mg/L (~98% removal) in synthetic TPW. However, equilibrium adsorption capacity was found to vary significantly after oxygen or nitrogen groups were introduced onto the surface. Therefore, there is a potential for enhanced adsorption by chemical functionalization of carbon.
4

Adsorption of Single-ring Model Naphthenic Acid from Oil Sands Tailings Pond Water Using Petroleum Coke-derived Activated Carbon

Sarkar, Bithun 17 July 2013 (has links)
Petroleum coke-derived activated carbons were prepared and used for the adsorptive removal of a single-ring naphthenic acid (NA) from synthetic oil sands tailings pond water (TPW). The overall adsorption process was found to be intra-particle diffusion-controlled. The Weber-Morris intra-particle diffusion rate constants decreased from 7.43 to 1.23 mg/g min0.5 after activated carbon was post-oxidized with oxygen, suggesting a hindering effect of oxygen surface groups. The Freundlich model fit of the equilibrium adsorption isotherms and the small negative ΔHo pointed to a physisorption-dominated process and the importance of specific surface area. It was estimated that about 2.7 g/L of basic CO2-activated carbon is needed to reduce NA concentration from 120 mg/L to 2.5 mg/L (~98% removal) in synthetic TPW. However, equilibrium adsorption capacity was found to vary significantly after oxygen or nitrogen groups were introduced onto the surface. Therefore, there is a potential for enhanced adsorption by chemical functionalization of carbon.

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