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dc.contributor.authorZhao, Shizhen
dc.contributor.authorBreivik, Knut
dc.contributor.authorLiu, Guorui
dc.contributor.authorZheng, Minghui
dc.contributor.authorJones, Kevin C
dc.contributor.authorSweetman, Andrew J
dc.date.accessioned2017-12-04T11:03:47Z
dc.date.available2017-12-04T11:03:47Z
dc.date.created2017-01-28T12:01:45Z
dc.date.issued2017
dc.identifier.citationZhao, S., Breivik, K., Liu, G., Zheng, M., Jones, K.C., & Sweetman, A.J. (2017). Long-term temporal trends of polychlorinated biphenyls and their controlling sources in China. Environmental Science & Technology, 51, 2838-2845. doi:10.1021/acs.est.6b05341nb_NO
dc.identifier.issn0013-936X
dc.identifier.urihttp://hdl.handle.net/11250/2468978
dc.description.abstractPolychlorinated biphenyls (PCBs) are industrial organic contaminants identified as persistent, bioaccumulative, toxic (PBT) and subject to long-range transport (LRT) with global scale significance. This study focuses on a reconstruction and prediction for China of long-term emission trends of intentionally and unintentionally produced (UP) Σ7PCBs (UP-PCBs, from the manufacture of steel, cement and sinter iron) and their re-emissions from secondary sources (e.g., soils and vegetation), using a dynamic fate model (BETR-Global). Contemporary emission estimates combined with predictions from the multimedia fate model suggest that primary sources still dominate, although unintentional sources are predicted to become a main contributor from 2035 for PCB-28. Imported e-waste is predicted to play an increasing role until 2020-2030 on a national scale due to the decline of IP emissions. Hypothetical emission scenarios suggest that China could become a potential source to neighbouring regions with a net output of ~0.4 t year-1 in the case of 7 PCBs around 2050. However, future emission scenarios and hence model results will be dictated by the efficiency of control measures.nb_NO
dc.language.isoengnb_NO
dc.titleLong-Term Temporal Trends of Polychlorinated Biphenyls and Their Controlling Sources in Chinanb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.rights.holderCopyright © 2017 American Chemical Societynb_NO
dc.source.pagenumber2838-2845nb_NO
dc.source.volume51nb_NO
dc.source.journalEnvironmental Science and Technologynb_NO
dc.source.issue5nb_NO
dc.identifier.doi10.1021/acs.est.6b05341
dc.identifier.cristin1439865
dc.relation.projectNorges forskningsråd: 213577nb_NO
cristin.unitcode7460,57,0,0
cristin.unitnameAtmosfære og klima
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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