Evidence map›Paper›PMID 29895798›Full record

ArticleMolecules (Basel, Switzerland)2018

A General Aqueous Silanization Protocol to Introduce Vinyl, Mercapto or Azido Functionalities onto Cellulose Fibers and Nanocelluloses.

Marco Beaumont, Markus Bacher, Martina Opietnik, Wolfgang Gindl-Altmutter, Antje Potthast, Thomas Rosenau

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 70 citations in OpenAlex.

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  20. A Direct Silanization Protocol for Dialdehyde Cellulose.Molecules (Basel, Switzerland) · 2020
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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

6 authors at 3 institutions in 2 countries.

Marco BeaumontDepartment of Chemistry, Division of Chemistry of Renewable Resources, University of Natural Resources and Life Sciences Vienna (BOKU), Konrad-Lorenz-Straße 24, A-3430 Tulln, Austria. markus.bacher@boku.ac.at.ORCID 0000-0002-2571-497X
Markus BacherDepartment of Chemistry, Division of Chemistry of Renewable Resources, University of Natural Resources and Life Sciences Vienna (BOKU), Konrad-Lorenz-Straße 24, A-3430 Tulln, Austria. markus.bacher@boku.ac.at.
Martina OpietnikLenzing AG, 4860 Lenzing, Austria. m.opietnik@lenzing.com.
Wolfgang Gindl-AltmutterDepartment of Materials Science and Process Engineering, Institute of Wood Technology and Renewable Materials, University of Natural Resources and Life Sciences Vienna (BOKU), A-3430 Tulln, Austria. wolfgang.gindl-altmutter@boku.ac.at.
Antje PotthastDepartment of Chemistry, Division of Chemistry of Renewable Resources, University of Natural Resources and Life Sciences Vienna (BOKU), Konrad-Lorenz-Straße 24, A-3430 Tulln, Austria. antje.potthast@boku.ac.at.
Thomas RosenauDepartment of Chemistry, Division of Chemistry of Renewable Resources, University of Natural Resources and Life Sciences Vienna (BOKU), Konrad-Lorenz-Straße 24, A-3430 Tulln, Austria. marcobeaumont1@gmail.com.ORCID 0000-0002-6636-9260
BOKU University · ATÅbo Akademi University · FILenzing (Austria) · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effective and straight-forward modification of nanostructured celluloses under aqueous conditions or as “never-dried” materials is challenging. We report a silanization protocol in water using catalytic amounts of hydrogen chloride and then sodium hydroxide in a two-step protocol. The acidic step hydrolyzes the alkoxysilane to obtain water-soluble silanols and the subsequent addition of catalytic amounts of NaOH induces a covalent reaction between cellulose surficial hydroxyl groups and the respective silanols. The developed protocol enables the incorporation of vinyl, thiol, and azido groups onto cellulose fibers and cellulose nanofibrils. In contrast to conventional methods, no curing or solvent-exchange is necessary, thereby the functionalized celluloses remain never-dried, and no agglomeration or hornification occurs in the process. The successful modification was proven by solid state NMR, ATR-IR, and EDX spectroscopy. In addition, the covalent nature of this bonding was shown by gel permeation chromatography of polyethylene glycol grafted nanofibrils. By varying the amount of silane agents or the reaction time, the silane loading could be tuned up to an amount of 1.2 mmol/g. Multifunctional materials were obtained either by prior carboxymethylation and subsequent silanization; or by simultaneously incorporating both vinyl and azido groups. The protocol reported here is an easy, general, and straight-forward avenue for introduction of anchor groups onto the surface of never-dried celluloses, ready for click chemistry post-modification, to obtain multifunctional cellulose substrates for high-value applications.

Indexed as

CatalysisCelluloseClick ChemistryHydrochloric AcidNanofibersSilanesSodium HydroxideSulfhydryl CompoundsSurface PropertiesVinyl CompoundsWaterCelluloseHydrochloric AcidSilanessilanolSodium HydroxideSulfhydryl CompoundsVinyl CompoundsvinylsilaneWateraqueous silanizationcellulose II gelcellulose modificationcellulose nanofibrilsclick chemistrygreen chemistrynanocellulose

Identifiers

PMID29895798
PMCPMC6100551
OpenAlexW2807712062

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.