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Article
Peer-Review Record

Carbonyl Composition and Electrophilicity in Vaping Emissions of Flavored and Unflavored E-Liquids

Toxics 2021, 9(12), 345; https://doi.org/10.3390/toxics9120345
by Jin Y. Chen 1,†, Alexa Canchola 1 and Ying-Hsuan Lin 1,2,*
Reviewer 1: Anonymous
Toxics 2021, 9(12), 345; https://doi.org/10.3390/toxics9120345
Submission received: 27 October 2021 / Revised: 13 November 2021 / Accepted: 6 December 2021 / Published: 9 December 2021
(This article belongs to the Section Toxicology)

Round 1

Reviewer 1 Report

The review has been included in a file.

Comments for author File: Comments.pdf

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

In this manuscript, the authors have investigated the effect of vaping e-liquid constitution on the emitted carbonyls. They have used GC-MS and LC-MS for the characterization and determination of these carbonyls. The results found are interesting; however, the results need more discussion and clarifications. Hence, there are some points needed to be addressed prior to the consideration of the publication of this manuscript.

  • Why have the authors omitted nicotine from vaping e-liquid in their study?
  • In section 2.3., it is difficult to imagine the trapping process from the text. Please draw a diagram for the trapping device.
  • In table 1, why in case of benzyl alcohol flavored e-liquid propionaldehyde, acrolein, and dimethyl glyoxal were not detected. Does benzyl alcohol act as an antioxidant, and the oxidation reaction was directed only to the formation of benzaldehyde? Also, why in the case of menthol-flavored e-liquid propionaldehyde and acrolein are not detected.
  • In table 1 also, what is the possible pathway of formation of trans-2-hexenal in menthol and linalool flavored e-liquids.
  • In Fig. 2, why the presence of alcohol flavoring liquids decreases the formation of formaldehyde, acetaldehyde, and acrolein?
  • In Fig. 2 also, why the presence of trans-2-hexenol largely increased the formation of butyraldehyde. What is the possible oxidation pathway for this butyraldehyde formation from trans-2-hexenol?
  • In your study, menthone and linalool-8-aldehyde were not detected; thus, there is no any importance for the computational study of their reactivity. Hence they should be removed from the computational study in section 3.4.
  • Do not use abbreviations (such as PG-VG) in keywords.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Round 2

Reviewer 2 Report

The authors have adequately addressed all my comments and the discussion of the results on the manuscript becomes acceptable. The paper could be accepted in its current form.   

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