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  • Bergman, FannyLund University, Sweden (författare)

Physicochemical metamorphosis of re-aerosolized urban PM2.5

  • Artikel/kapitelEngelska2024

Förlag, utgivningsår, omfång ...

  • Elsevier Ltd,2024
  • electronicrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:ri-73776
  • https://urn.kb.se/resolve?urn=urn:nbn:se:ri:diva-73776URI
  • https://doi.org/10.1016/j.jaerosci.2024.106416DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:art swepub-publicationtype

Anmärkningar

  • This work was supported by Formas (2019-00320), The Crafoord Foundation (20200673) and AFA (160226)
  • The toxicity of particulate matter (PM) is dependent on particle physical and chemical properties and is commonly studied using in vivo and in vitro approaches. PM to be used for in vivo and in vitro studies is often collected on filters and then extracted from the filter surface using a solvent. During extraction and further PM sample handling, particle properties change, but this is often neglected in toxicology studies, with possible implications for health effect assessment. To address the current lack of knowledge and investigate changes in particle properties further, ambient PM with diameter less than 2.5 μm (PM2.5) was collected on filters at an urban site and extracted using a standard methanol protocol. After extraction, the PM was dried, dispersed in water and subsequently nebulized. The resulting aerosol properties were then compared to those of the ambient PM2.5. The number size distribution for the nebulized aerosol resembled the ambient in terms of the main mode diameter, and >90 % of particle mass in the nebulized size distribution was still in the PM2.5 range. Black carbon made up a similar fraction of PM mass in nebulized as in ambient aerosol. The sulfate content in the nebulized aerosol seemed depleted and the chemical composition of the organic fraction was altered, but it remains unclear to what extent other non-refractory components were affected by the extraction process. Trace elements were not distributed equally across size fractions, neither in ambient nor nebulized PM. Change in chemical form was studied for zinc, copper and iron. The form did not appear to be different between the ambient and nebulized PM for iron and copper, but seemed altered for zinc. Although many of the studied properties were reasonably well preserved, it is clear that the PM2.5 collection and re-aerosolization process affects particles, and thus potentially also their health effects. Because of this, the effect of the particle collection and extraction process must be considered when evaluating cellular and physiological outcomes upon PM2.5 exposure. © 2024 The Authors

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Eriksson, Axel C.Lund University, Sweden (författare)
  • Spanne, MartenCity of Malmö, Sweden (författare)
  • Ohlsson, LenaLund University, Sweden (författare)
  • Mahmutovic Persson, IrmaLund University, Sweden (författare)
  • Uller, LenaLund University, Sweden (författare)
  • Rissler, JennyRISE,Material- och ytdesign,Lund University, Sweden(Swepub:ri)JennyRi@ri.se (författare)
  • Isaxon, ChristinaLund University, Sweden (författare)
  • Lund University, SwedenCity of Malmö, Sweden (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Journal of Aerosol Science: Elsevier Ltd1810021-85021879-1964

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