Quantitative Scrolling into Microporous Nanotubes of the Hydrous Layered Silicate Ilerite

Author:

Uhlig Felix1,Pietsch Ingmar1,Stich Alexander1,Mansfeld Ulrich2ORCID,Rosenfeldt Sabine3,Senker Jürgen4ORCID,Breu Josef1ORCID

Affiliation:

1. Faculty of Biology, Chemistry & Earth Sciences Chair of Inorganic Colloids for Electrochemical Energy Storage University of Bayreuth 95440 Bayreuth Germany

2. Bavarian Polymer Institute Physical Chemistry I University of Bayreuth 95440 Bayreuth Germany

3. Faculty of Biology, Chemistry & Earth Sciences Physical Chemistry I University of Bayreuth 95440 Bayreuth Germany

4. Faculty of Biology, Chemistry & Earth Sciences Chair of Inorganic Chemistry III University of Bayreuth 95440 Bayreuth Germany

Abstract

AbstractThe synthetic hydrous layered silicate ilerite was quantitatively converted into microporous nanoscrolls (NS). Delamination of ilerite that was ion‐exchanged for N‐Methyl‐D‐glucaminium (Meg+), through one‐dimensional (1D) dissolution initially yields lamellar liquid crystalline (nematic) suspensions. Subsequent protonation with acetic acid of tangling Si‐O to silanol groups reduces the pH‐dependent charge of the basal surfaces. Complete NS formation is then triggered by diluting the nematic suspension below 0.05 wt%. As scrolling commonly has been attributed to hydrophobic interaction of organic counterions, Meg+ was replaced by lithium ions but this showed no detrimental effect on the scrolling efficiency. The resulting NS have a typical length of 2–4 μm that corresponds well with typical diameters of the parent nanosheets. Ar‐physisorption isotherms showed a bimodal micropore size with maxima around 0.8 and 1.9 nm. We attribute the first to the tubular hollow inner diameter of the NS and the latter to wedgelike interparticle porosity. The material showed a large specific surface area of 226 m2 g−1.

Funder

National Science Foundation

Publisher

Wiley

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