An efficient approach for treating composition-dependent diffusion within organic particles

O'Meara, Simon; Topping, David O.; Zaveri, Rahul A.; McFiggans, Gordon

doi:https://doi.org/10.5194/acp-17-10477-2017

Articles | Volume 17, issue 17

https://doi.org/10.5194/acp-17-10477-2017

© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.

https://doi.org/10.5194/acp-17-10477-2017

© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.

Articles | Volume 17, issue 17

Research article

|

07 Sep 2017

Research article |

| 07 Sep 2017

An efficient approach for treating composition-dependent diffusion within organic particles

Simon O'Meara, David O. Topping, Rahul A. Zaveri, and Gordon McFiggans

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Final revised paper (published on 07 Sep 2017)
Preprint (discussion started on 12 Jan 2017)

Interactive discussion

Status: closed

AC: Author comment | RC: Referee comment | SC: Short comment | EC: Editor comment

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- Supplement

RC1: 'Reviewer's comments', Anonymous Referee #2, 08 Feb 2017
RC2: 'Referee comment', Anonymous Referee #1, 23 Feb 2017
AC1: 'Authors' Response', Simon O'Meara, 19 Apr 2017

Peer-review completion

AR: Author's response | RR: Referee report | ED: Editor decision

AR by Simon O'Meara on behalf of the Authors (19 Apr 2017) Author's response Manuscript

ED: Referee Nomination & Report Request started (16 May 2017) by Kari Lehtinen

RR by Anonymous Referee #2 (02 Jun 2017)

RR by Anonymous Referee #1 (05 Jun 2017)

ED: Reconsider after minor revisions (Editor review) (05 Jul 2017) by Kari Lehtinen

AR by Simon O'Meara on behalf of the Authors (07 Jul 2017) Author's response Manuscript

ED: Publish as is (18 Jul 2017) by Kari Lehtinen

Short summary

To simulate particle-phase diffusion, an analytical expression is desired because it takes less calculation time than a differential equation. Here a correction is found for the analytical solution for when diffusivity is dependent on composition, thereby making it more widely applicable than before. Consequently, we are able to more realistically evaluate the rate limitation (if any) imposed by particle-phase diffusion on component partitioning between the gas and particle phase.