Evidence map›Paper›PMID 38239454›Full record

ArticleRSC advances2024

An integrated experimental and theoretical approach to probe Cr(vi) uptake using decorated halloysite nanotubes for efficient water treatment.

Syed Nadeem Ahmad Shah, Sonia Zulfiqar, Fernando Ruipérez, Muhammad Rafique, Mudassir Iqbal, Michael J Forrester, Muhammad Ilyas Sarwar Late, Eric W Cochran

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Article in RSC advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Syed Nadeem Ahmad ShahDepartment of Chemistry, School of Natural Sciences, National University of Sciences and Technology H-12 Islamabad 44000 Pakistan.ORCID https://orcid.org/0009-0006-1241-9695
Sonia ZulfiqarDepartment of Chemistry, Faculty of Science, University of Ostrava 30. Dubna 22 Ostrava 701 03 Czech Republic sonia.zulfiqar@osu.cz zulfiqar@iastate.edu.ORCID https://orcid.org/0000-0002-5692-6334
Fernando RuipérezPOLYMAT, Physical Chemistry Department, Faculty of Pharmacy, University of the Basque Country UPV/EHU 01006 Vitoria-Gasteiz Spain.
Muhammad RafiqueDepartment of Chemistry, Quaid-i-Azam University Islamabad 45320 Pakistan.
Mudassir IqbalDepartment of Chemistry, School of Natural Sciences, National University of Sciences and Technology H-12 Islamabad 44000 Pakistan.ORCID https://orcid.org/0000-0002-9830-8235
Michael J ForresterDepartment of Chemical and Biological Engineering, Iowa State University Sweeney Hall, 618 Bissell Road, Ames Iowa 50011 USA ecochran@iastate.edu.ORCID https://orcid.org/0000-0003-3063-9975
Muhammad Ilyas Sarwar LateDepartment of Chemistry, Quaid-i-Azam University Islamabad 45320 Pakistan.
Eric W CochranDepartment of Chemical and Biological Engineering, Iowa State University Sweeney Hall, 618 Bissell Road, Ames Iowa 50011 USA ecochran@iastate.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Halloysite nanotubes (HNTs) were surface functionalized using four distinct chemical moieties (amidoxime, hydrazone, ethylenediamine (EDA), and diethylenetriamine (DETA)), producing modified HNTs (H1-H4) capable of binding with Cr(vi) ions. Advanced techniques like FTIR, XRD, SEM, and EDX provided evidence of the successful functionalization of these HNTs. Notably, the functionalization occurred on the surface of HNTs, rather than within the interlayer or lumen. These decorated HNTs were effective in capturing Cr(vi) ions at optimized sorption parameters, with adsorption rates ranging between 58-94%, as confirmed by atomic absorption spectroscopy (AAS). The mechanism of adsorption was further scrutinized through the Freundlich and Langmuir isotherms. Langmuir isotherms revealed the nearest fit to the data suggesting the monolayer adsorption of Cr(vi) ions onto the nanotubes, indicating a favorable adsorption process. It was hypothesized that Cr(vi) ions are primarily attracted to the amine groups on the modified nanotubes. Quantum chemical calculations further revealed that HNTs functionalized with hydrazone structures (H2) demonstrated a higher affinity (interaction energy -26.33 kcal mol

Identifiers

PMID38239454
PMCPMC10794904

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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.