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contributor authorM. Anheden
contributor authorG. Svedberg
contributor authorD. Y. Goswami
date accessioned2017-05-08T23:51:32Z
date available2017-05-08T23:51:32Z
date copyrightFebruary, 1996
date issued1996
identifier issn0199-6231
identifier otherJSEEDO-28262#2_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/117627
description abstractThis paper presents some of the experimental results from a study conducted to demonstrate the potential use of photocatalytic oxidation for decolorization and COD reduction of wastewater from 5–fluorouracil manufacturing. A series of batch experiments, were carried out using diluted solutions of the wastewater with 0.1 percent w/v TiO2 . Low pressure mercury lamps were used to simulate the UV part of sunlight. The experiments showed that a complete decolorization and a substantial reduction of COD was achieved within 20 hours with a 20 percent solution. During the reaction period, the pH was noted to decrease considerably, indicating formation of acids. Adding hydrogen peroxide to the solution was found to significantly increase the reaction rates. Adding 2400 ppm of H2 O2 gave an 80 percent decrease in color in one hour and a 70-80 percent decrease in COD in 20 hours. The influence of UV-light intensity was also examined. This experiment showed that with a UV-intensity of 15 W/m2, i.e., a cloudy day, the decolorization rate was still considerable, while the COD reduction rate was very low.
publisherThe American Society of Mechanical Engineers (ASME)
titlePhotocatalytic Treatment of Wastewater From 5–Fluorouracil Manufacturing
typeJournal Paper
journal volume118
journal issue1
journal titleJournal of Solar Energy Engineering
identifier doi10.1115/1.2847912
journal fristpage2
journal lastpage8
identifier eissn1528-8986
keywordsManufacturing
keywordsWastewater treatment
keywordsUltraviolet radiation
keywordsSewage
keywordsMercury lamps
keywordsChemical kinetics
keywordsHydrogen
keywordsoxidation
keywordsSunlight AND Pressure
treeJournal of Solar Energy Engineering:;1996:;volume( 118 ):;issue: 001
contenttypeFulltext


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