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Carbonaceous and Nitrogenous Disinfecion By-Product Formation Potentials of Amino Acids

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dc.creator Shan, Junhong
dc.creator KAPLAN BEKAROĞLU, Şehnaz Şule
dc.creator Karanfil, Tanju
dc.creator Selbes, Merlc
dc.date 2014-12-31T22:00:00Z
dc.date.accessioned 2020-10-06T10:50:51Z
dc.date.available 2020-10-06T10:50:51Z
dc.identifier a1ca181d-c75e-4d18-9cca-0ffccf891cc7
dc.identifier https://avesis.sdu.edu.tr/publication/details/a1ca181d-c75e-4d18-9cca-0ffccf891cc7/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/67990
dc.description Nine amino acids (AAs) were examined under different oxidation conditions to determine their formation potential for regulated carbonaceous DBPs (trihalomethanes (THMs) and haloacetic acids (HAAs)) and selected emerging nitrogenous DBPs (haloacetonitriles (HANs), halonitromethanes (HNMs) and nitrosamines). Aspartic acid and histidine exhibited very high dihalogenated-HANs and HAAs formation during chlorination, but their reactivity significantly decreased after ozonation. Glycine followed by lysine yieled the highest level of HNMs and THMs formation during ozonation-chlorination, but they did not have measurable yields for either classes of DBPs during chlorination. All other AAs showed very low carbonaceous and nitrogenous DBP yields. The nitrosamine yields of all nine AAs were very low or below the minimum reporting levels during chloramination, ozonation, and ozonation-chloramination. These results indicated that the presence of AAs in natural waters can result in some contributions to certain halogenated DBPs depending on the oxidation conditions. However, they do not appear to be an important contributor to nitrosamines formation.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Carbonaceous and Nitrogenous Disinfecion By-Product Formation Potentials of Amino Acids
dc.type info:eu-repo/semantics/conferenceObject


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