Evidence map›Paper›PMID 35574041›Full record

ArticleJACS Au2021

Correlating the Morphological Evolution of Individual Catalyst Particles to the Kinetic Behavior of Metallocene-Based Ethylene Polymerization Catalysts.

Maximilian J Werny, Jelena Zarupski, Iris C Ten Have, Alessandro Piovano, Coen Hendriksen, Nicolaas H Friederichs, Florian Meirer, Elena Groppo, Bert M Weckhuysen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in JACS Au, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Maximilian J WernyInorganic Chemistry and Catalysis group, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.ORCID https://orcid.org/0000-0002-5714-3446
Jelena ZarupskiDepartment of Chemistry, INSTM and NIS Centre, University of Torino, Via G. Quarello 15A, 10135 Torino, Italy.
Iris C Ten HaveInorganic Chemistry and Catalysis group, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.
Alessandro PiovanoDepartment of Chemistry, INSTM and NIS Centre, University of Torino, Via G. Quarello 15A, 10135 Torino, Italy.ORCID https://orcid.org/0000-0002-5784-6897
Coen HendriksenSABIC Technology Center, Urmonderbaan 22, 6167 RD Geleen, The Netherlands.
Nicolaas H FriederichsSABIC Technology Center, Urmonderbaan 22, 6167 RD Geleen, The Netherlands.
Florian MeirerInorganic Chemistry and Catalysis group, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.ORCID https://orcid.org/0000-0001-5581-5790
Elena GroppoDepartment of Chemistry, INSTM and NIS Centre, University of Torino, Via G. Quarello 15A, 10135 Torino, Italy.ORCID https://orcid.org/0000-0003-4153-5709
Bert M WeckhuysenInorganic Chemistry and Catalysis group, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.ORCID https://orcid.org/0000-0001-5245-1426
Utrecht University · NLDutch Polymer Institute · NLSaudi Arabia Basic Industries (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kinetics-based differences in the early stage fragmentation of two structurally analogous silica-supported hafnocene- and zirconocene-based catalysts were observed during gas-phase ethylene polymerization at low pressures. A combination of focused ion beam-scanning electron microscopy (FIB-SEM) and nanoscale infrared photoinduced force microscopy (IR PiFM) revealed notable differences in the distribution of the support, polymer, and composite phases between the two catalyst materials. By means of time-resolved probe molecule infrared spectroscopy, correlations between this divergence in morphology and the kinetic behavior of the catalysts' active sites were established. The rate of polymer formation, a property that is inherently related to a catalyst's kinetics and the applied reaction conditions, ultimately governs mass transfer and thus the degree of homogeneity achieved during support fragmentation. In the absence of strong mass transfer limitations, a layer-by-layer mechanism dominates at the level of the individual catalyst support domains under the given experimental conditions.

Identifiers

PMID35574041
PMCPMC8611720
OpenAlexW3206521020

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.