All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Kinetic adsorption mechanism of cobalt(II) ions and Congo red on pristine and Schiff base-surface-modified MIL-101(Fe)-NH2

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F25%3A00616794" target="_blank" >RIV/61389013:_____/25:00616794 - isvavai.cz</a>

  • Alternative codes found

    RIV/61988987:17310/25:A2603ANS

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S1387181125000071?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1387181125000071?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.micromeso.2025.113493" target="_blank" >10.1016/j.micromeso.2025.113493</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Kinetic adsorption mechanism of cobalt(II) ions and Congo red on pristine and Schiff base-surface-modified MIL-101(Fe)-NH2

  • Original language description

    This study investigates the adsorption kinetics of heavy metal ions (Co(II)) and azo dye (Congo red) using surface-modified MIL-101(Fe)-NH2. The material's large surface area and dual pore structure enhance adsorption performance, making it suitable for environmental applications. The MIL-101(Fe)-NH2 material was synthesized and further modified with 2-pyridinecarboxaldehyde to create MIL-101(Fe)-Pyr with the aim of enhancing the adsorption properties. Characterization techniques, including FTIR, TG/DTA, ss-NMR, XPS, N2 adsorption/desorption measurements, and PXRD, confirmed the structural integrity and functionalization of the materials. Kinetic studies revealed that MIL-101(Fe)-Pyr demonstrated superior adsorption capacity and faster kinetics for Co(II) ions compared to pristine MIL-101(Fe)-NH2. The adsorption mechanisms were analyzed using pseudo-first-order, pseudo-second-order, and Elovich models. The pseudo-second-order model provided the best fit for both Co(II) and Congo red adsorption. Boyd's diffusion model indicated that external diffusion is a significant rate-controlling step. The adsorption isotherms were fitted with the Freudlich and Langmuir models, and the thermodynamics of the adsorption processes were also studied. The adsorption mechanism of the selected pollutants was proposed, and the stability and reusability of the materials were investigated. The study concludes that surface modifications enhance the material's adsorption properties, making MIL-101(Fe)-Pyr a promising adsorbent for removing pollutants from aqueous environments.

  • 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

    10404 - Polymer science

Result continuities

  • Project

    <a href="/en/project/LUASK22049" target="_blank" >LUASK22049: Monolithic, hierarchically porous MOF-carbon composites for environmental applications</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Microporous and Mesoporous Materials

  • ISSN

    1387-1811

  • e-ISSN

    1873-3093

  • Volume of the periodical

    386

  • Issue of the periodical within the volume

    15 March

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    18

  • Pages from-to

    113493

  • UT code for WoS article

    001401504700001

  • EID of the result in the Scopus database

    2-s2.0-85214958508