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      An Effective Sol-Gel-Functionalized Polyurethane Foams Solid Platform Packed Minicolumns for Complete Extraction of Chromium (VI) from Water: Kinetic, Sorption Isotherms, Thermodynamic Study, and Analytical Utility

      research-article
      International Journal of Analytical Chemistry
      Wiley

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          Abstract

          In the modern era, sol-gel plays a key role in the progress of a new generation of dispersive solid-phase microextractors (d– µ SPMEs) for the removal of organic and inorganic pollutants in complex matrices. Thus, the current study reports the use of sol-gel-functionalized polyurethane foams (PUFs) as a novel solid platform for complete extraction of chromium (VI) species from aqueous media. The planned protocol was based upon the complete extraction of the formed binary complex ion associates between the protonated ether and/or urethane groups of PUFs and chlorochromate anion [CrO 3Cl] aq in aqueous HCl (≥1M) medium in addition to H-bonding and the electrostatic ππ interaction that resulted between the CrO 3Cl and the silanol group (Si/ZrO 2, Si–O–Zr) and siloxane (Si–O–Si) groups of the sol-gel. The impact of the analytical parameters (solution pH, natural mineral acids, shaking time, temperature, and chromium (VI) concentrations) was critically studied. At the optimal conditions, the uptake capacity of the established extractor (9.9 mg·g −1) was in agreement with the Langmuir adsorption capacity (12.08 mg·g −1) of the monolayer. The sorption data fitted well with the pseudo first-order kinetic model ( R 2 = 0.9961) with an overall rate constant ( k 1) of 0.081 min −1 and an equilibrium capacity ( q e ) of 8.6 mg·g −1, which is in a good agreement with the experimental value (9.9 mg·g −1). The sorption of the oxyion [CrO 3Cl] aq onto the solid sorbent is an endothermic and spontaneous process as reflected from the values of ΔH (6.99 kJ·mol −1) and Δ G (−8.14 kJ·mol −1 at 293 K), respectively. The Δ S value (15.13 kJ·mol −1·K −1) reflects that the [CrO 3Cl] aq retention onto the sol-gel-treated PUFs sorbent proceeded in a more unplanned fashion. Sol-gel-treated PUFs sorbent-packed minicolumns were successfully used for the complete removal of trace levels of chromium (VI) species from water samples. Sorbed chromium (VI) species were recovered with NaOH (0.5 M) and analysed by spectrophotometry, which supports the utility of the sol-gel-treated PUFs as a low-cost solid extractor for water treatment.

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          Pseudo-second order model for sorption processes

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            Determination of organic compounds in water using dispersive liquid-liquid microextraction.

            A new microextraction technique termed dispersive liquid-liquid microextraction (DLLME) was developed. DLLME is a very simple and rapid method for extraction and preconcentration of organic compounds from water samples. In this method, the appropriate mixture of extraction solvent (8.0 microL C2Cl4) and disperser solvent (1.00 mL acetone) are injected into the aqueous sample (5.00 mL) by syringe, rapidly. Therefore, cloudy solution is formed. In fact, it is consisted of fine particles of extraction solvent which is dispersed entirely into aqueous phase. After centrifuging, the fine particles of extraction solvent are sedimented in the bottom of the conical test tube (5.0 +/- 0.2 microL). The performance of DLLME is illustrated with the determination of polycyclic aromatic hydrocarbons (PAHs) in water samples by using gas chromatography-flame ionization detection (GC-FID). Some important parameters, such as kind of extraction and disperser solvent and volume of them, and extraction time were investigated. Under the optimum conditions the enrichment factor ranged from 603 to 1113 and the recovery ranged from 60.3 to 111.3%. The linear range was 0.02-200 microg/L (four orders of magnitude) and limit of detection was 0.007-0.030 microg/L for most of analytes. The relative standard deviations (RSDs) for 2 microg/L of PAHs in water by using internal standard were in the range 1.4-10.2% (n = 5). The recoveries of PAHs from surface water at spiking level of 5.0 microg/L were 82.0-111.0%. The ability of DLLME technique in the extraction of other organic compounds such as organochlorine pesticides, organophosphorus pesticides and substituted benzene compounds (benzene, toluene, ethyl benzene, and xylenes) from water samples were studied. The advantages of DLLME method are simplicity of operation, rapidity, low cost, high recovery, and enrichment factor.
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              About the theory of so-called adsorption of soluble substances.

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                Author and article information

                Contributors
                Journal
                Int J Anal Chem
                Int J Anal Chem
                ijac
                International Journal of Analytical Chemistry
                Wiley
                1687-8760
                1687-8779
                2024
                6 August 2024
                : 2024
                : 3152894
                Affiliations
                Department of Chemistry, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia
                Author notes

                Academic Editor: Daipayan Roy

                Author information
                https://orcid.org/0000-0003-2502-0916
                Article
                10.1155/2024/3152894
                11458274
                39376696
                8632f918-8667-4902-a3a5-2845dc7473a7
                Copyright © 2024 Effat A. Bahaidarah.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 29 December 2023
                : 6 June 2024
                : 15 July 2024
                Funding
                Funded by: King Abdulaziz University
                Award ID: 801-247-1441
                Categories
                Research Article

                Analytical chemistry
                Analytical chemistry

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