4.6 Article

Al and Zr Porous Clay Heterostructures as Removal Agents of Basic Blue-41 Dye from an Artificially Polluted Solution: Regeneration Properties and Batch Design

Journal

MATERIALS
Volume 14, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/ma14102528

Keywords

intercalated clays; porous clay heterostructures; Basic Blue-41; removal; regeneration; batch design

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The study successfully removed dye molecules using two doped porous clay heterostructures, with Zr-PCH showing higher efficiency and better regeneration performance compared to Al-PCH, which exhibited lower removal efficiency and significant reduction in efficiency after regeneration.
The removal of Basic Blue-41 dye molecules was carried out by using two doped porous clay heterostructures by aluminum (Al) or zirconium (Zr) species. The proposed method of synthesis showed its efficiency, starting from Al or Zr intercalated hydrolyzed species, prior to its reaction with dodecylamine (C-12 amine) and tetraethyl orthosilicate (TEOS) as a silica source. The intercalated precursors and their porous clay heterostructures (PCH) derivatives were characterized by different techniques. Solid NMR technique proved the presence of Al species into the intercalated silica between the clay sheets, and in addition to Si in different environments within the PCH materials. The Zr-PCH material exhibited a higher surface area and pore volume compared to its Al-PCH counterpart, with a mesoporous character for both materials. A maximum removed amount of 279 and 332 mg/g was achieved and deduced from the Langmuir equation. The regeneration tests revealed that the removal efficiency of Zr-PCH was retained after five regeneration runs, with a loss of 15% of the original value; meanwhile, the Al-PCH lost 45% of its efficiency after only three cycles. A single-stage batch design was proposed based on the Langmuir isotherm parameters. The increase of the removal capacity of Zr-PCH led to the reduction of the required amounts for the target removal of BB-41 dye compared to Al-PCH.

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