Evidence map›Paper›PMID 39720224›Full record

ArticleACS earth & space chemistry2024

Chemical Differences in Environmental Films Collected on Surfaces with Different Hydrophilicity.

Jessica L DeYoung, Uchechukwu Grace Akporere, Zezhen Cheng, Swarup China, Gregory W Vandergrift, Christopher R Anderton, Yadong Zhou, Zihua Zhu, Scott K Shaw

Abstract read
In one paragraph

Article in ACS earth & space chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Jessica L DeYoungUniversity of Iowa, Iowa City, Iowa state 52242, United States.
Uchechukwu Grace AkporereUniversity of Iowa, Iowa City, Iowa state 52242, United States.
Zezhen ChengEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States.ORCID https://orcid.org/0000-0001-6320-4519
Swarup ChinaEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States.ORCID https://orcid.org/0000-0001-7670-335X
Gregory W VandergriftEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States.ORCID https://orcid.org/0000-0002-8962-9897
Christopher R AndertonEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States.ORCID https://orcid.org/0000-0002-6170-1033
Yadong ZhouEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States.ORCID https://orcid.org/0000-0002-9012-7536
Zihua ZhuEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, United States.ORCID https://orcid.org/0000-0001-5770-8462
Scott K ShawUniversity of Iowa, Iowa City, Iowa state 52242, United States.ORCID https://orcid.org/0000-0003-3767-3236

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Environmental films form when airborne particles and molecular species adsorb on solid surfaces. Recent studies have characterized these films but overlook how collection methods and host-surface character (orientation, chemical functionality, or height) change the deposition process. In this work, environmental films are collected at a rural location on gold and silicon surfaces (water contact angles of ca. 57° and <1°, respectively) to determine how the different substrate changes the properties of the accumulated environmental film. Results show that gold surfaces have a homogeneous distribution of film mass across the surface, while silicon surfaces collect films with irregular patchy domains. The two surfaces also develop different surface coverages and particle number densities, and the particles' packing arrangements are quantified by analyzing nearest-neighbor distances. Computer-controlled scanning electron microscopy with energy-dispersive X-ray spectroscopy suggests that, despite morphological differences, larger (>5 μm) particles have similar elemental compositions. Minor variations are observed at smaller particle sizes (∼5 μm), which include carbon-rich particles primarily attributed to pollen or biotic activity. Chemical analysis shows the presence of nitrate and sulfate, as well as heterogeneous cation pools on the surfaces.

Identifiers

PMID39720224
PMCPMC11664647

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.