Effects of ozonation and ultraviolet irradiation on biodegradability of oil shale wastewater organic solutes
Ozonation and u.v. irradiation were evaluated for their abilities to (1) mineralize organic solutes that remained in a biooxidized oil shale process wastewater and (2) effect sufficient structural modification of the remaining biorefractory organic solutes to promote secondary biooxidation. Full-spe...
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Veröffentlicht in: | Water research (Oxford) 1985, Vol.19 (11), p.1421-1428 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Ozonation and u.v. irradiation were evaluated for their abilities to (1) mineralize organic solutes that remained in a biooxidized oil shale process wastewater and (2) effect sufficient structural modification of the remaining biorefractory organic solutes to promote secondary biooxidation. Full-spectrum u.v. radiation (5 h, total dose of 10.2 × 10
6 J l
−1) failed to mineralize or effect the biooxidation of any of the biorefractory carbon. Although ozonation (5 h, total dose of 1.6 g O
3 l
−1) directly mineralized only 8% of the biorefractory carbon, it enhanced secondary biooxidation; 26% of the refractory carbon was mineralized by an acclimated microbial inoculum. When u.v. irradiation and ozonation were combined simultaneously, a synergistic effect was observed; 3 h of combined treatment (5.9 × 10
6 J l
−1 and 0.83 g O
3 l
−1) was as effective a pretreatment for secondary biooxidation as was 5 h of ozonation. Sequential application of primary biooxidation, 6 h of combined u.v./ozonation, and secondary biooxidation removed only 59% of the dissolved organic carbon; total reduction of 87% was achieved by using a culture in the secondary biooxidation step that was specifically adapted to this oxidized water. Each time-course sample was analyzed for the distribution of polar and nonpolar organic solutes. In general, ozonation and combined u.v./ozonation mineralized carbon from the nonpolar fraction; biooxidation of formerly refractory carbon was promoted by oxidation of nonpolar carbon to yield more polar or lower-molecular-weight species. |
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ISSN: | 0043-1354 1879-2448 |
DOI: | 10.1016/0043-1354(85)90309-4 |