Evidence map›Paper›PMID 38370278›Full record

ArticleChemistry of materials : a publication of the American Chemical Society2024

Building Semipermeable Films One Monomer at a Time: Structural Advantages via Molecular Layer Deposition vs Interfacial Polymerization.

Brian C Welch, Emma N Antonio, Thomas P Chaney, Olivia M McIntee, Joseph Strzalka, Victor M Bright, Alan R Greenberg, Tamar Segal-Peretz, Michael Toney, Steven M George

Open access · hybridAbstract read
In one paragraph

Article in Chemistry of materials : a publication of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.8field-weighted citation impact, top 17% of its field
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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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

10 authors at 3 institutions in 2 countries.

Brian C WelchIsrael Institute of Technology, Haifa 3200003, Israel.ORCID https://orcid.org/0000-0002-9747-045X
Emma N AntonioUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.
Thomas P ChaneyUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.ORCID https://orcid.org/0000-0002-8123-7215
Olivia M McInteeUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.
Joseph StrzalkaArgonne National Laboratory, Lemont, Illinois 60439, United States.ORCID https://orcid.org/0000-0003-4619-8932
Victor M BrightUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.
Alan R GreenbergUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.ORCID https://orcid.org/0000-0003-1785-9439
Tamar Segal-PeretzIsrael Institute of Technology, Haifa 3200003, Israel.ORCID https://orcid.org/0000-0003-3222-6429
Michael ToneyUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.ORCID https://orcid.org/0000-0002-7513-1166
Steven M GeorgeUniversity of Colorado Boulder, Boulder, Colorado 80309, United States.ORCID https://orcid.org/0000-0003-0253-9184
University of Colorado Boulder · USTechnion – Israel Institute of Technology · ILArgonne National Laboratory · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular layer deposition (MLD) provides the opportunity to perform condensation polymerization one vaporized monomer at a time for the creation of precise, selective nanofilms for desalination membranes. Here, we compare the structure, chemistry, and morphology of two types of commercial interfacial polymerzation (IP) membranes with lab-made MLD films. M-phenylenediamine (MPD) and trimesoyl chloride (TMC) produced a cross-linked, aromatic polyamide often used in reverse osmosis membranes at MLD growth rates of 2.9 Å/cycle at 115 °C. Likewise, piperazine (PIP) and TMC formed polypiperazine amide, a common selective layer in nanofiltration membranes, with MLD growth rates of 1.5 Å/cycle at 115 °C. Ellipsometry and X-ray reflectivity results suggest that the surface of the MLD films is comprised of polymer segments roughly two monomers in length, which are connected at one end to the cross-linked bulk layer. As a result of this structure as well as the triple-functionality of TMC, MPD-TMC had a temperature window of stable growth rate from 115 to 150 °C, which is unlike any non-cross-linked MLD chemistries reported in the literature. Compared to IP films, corresponding MLD films were denser and morphologically conformal, which suggests a reduction in void volumes; this explains the high degree of salt rejection and reduced flux previously observed for exceptionally thin MPD-TMC MLD membranes. Using X-ray photoelectron spectroscopy and infrared spectroscopy, MLD PIP-TMC films evidenced a completely cross-linked internal structure, which lacked amine and carboxyl groups, pointing to a hydrophobic bulk structure, ideal for optimized water flux. Grazing-incidence wide-angle X-ray scattering showed broad features in each polyamide with

Identifiers

PMID38370278
PMCPMC10870709
OpenAlexW4390972587

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.