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Toward Controlling Disassembly Step within the ADOR Process for the Synthesis of Zeolites

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F21%3A10430159" target="_blank" >RIV/00216208:11310/21:10430159 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=cVkZzV5BRe" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=cVkZzV5BRe</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.chemmater.0c03993" target="_blank" >10.1021/acs.chemmater.0c03993</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Toward Controlling Disassembly Step within the ADOR Process for the Synthesis of Zeolites

  • Original language description

    The application of the Assembly-Disassembly-Organization-Reassembly (ADOR) protocol to the synthesis of germanosilicate zeolites has become a major milestone in material design by enabling the preparation of previously unknown &quot;isoreticular&quot; zeolites with tunable building units (i.e., -d4r-, - s4r-, -O-) connecting crystalline layers. Two processes operating in the disassembly step, deconstructive &quot;deintercalation&quot; and reconstructive &quot;rearrangement&quot;, determine the structure of ADOR-derived zeolites. However, independent management of these key ADOR processes, which would be desirable to regulate the characteristics of the products, has remained elusive thus far. Herein, we report a new method for controlling the primary steps of the ADOR process and present the first example of a &quot;cycled&quot; structural transformation of interlayer units (d4r -&gt; s4r -&gt; d4r) in the germanosilicate UTL zeolite under &quot;slow deintercalation&quot;/&quot;fast rearrangement&quot; conditions. The &quot; slow deintercalation&quot; mode of ADOR enabled us to prepare the previously known OKO, *PCS, IPC-7 zeolites via gradual reduction of interlayer units in UTL (d4r -&gt; d4r/s4r -&gt; s4r -&gt; s4r/-O-), in contrast to conventional rearrangement-driven synthesis (-O-. s4r/-O- -&gt; s4r...). X-ray powder diffraction (XRD), sorption, and solid-state NMR time-resolved studies revealed that the &quot;slow deintercalation/fast rearrangement&quot; modification of ADOR makes it possible to adjust the pore architecture of germanosilicate zeolites toward increasing their micropore size, which has never been achieved before in the classical ADOR mechanism. Therefore, &quot;slow deintercalation&quot; or &quot;slow deintercalation/fast rearrangement&quot; routes provide a tool for controlling the &quot;isoreticular&quot; zeolite structure. Ultimately, the results from this study may facilitate the design of previously predicted but inaccessible members of the ADORable zeolite family.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Chemistry of Materials

  • ISSN

    0897-4756

  • e-ISSN

  • Volume of the periodical

    33

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    1228-1237

  • UT code for WoS article

    000623043600014

  • EID of the result in the Scopus database

    2-s2.0-85100991449