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Feasibility Study on the Use of Recycled Polymers for Malathion Adsorption: Isotherms and Kinetic Modeling.

ABSTRACT: In this study, the use of Polyvinylchloride (PVC) and High Density Polystyrene (HDPS) was demonstrated as an alternative for the adsorption of Malathion. Adsorption kinetics and isotherms were used to compare three different adsorbent materials: PVC, HDPS, and activated carbon. The adsorption capacity of PVC was three times higher than activated carbon, and a theoretical value of 96.15 mg of Malathion could be adsorbed when using only 1 g of PVC. A pseudo first-order rate constant of 1.98 (1/h) was achieved according to Lagergren kinetic model. The adsorption rate and capacity values obtained in the present study are very promising since with very little adsorbent material it is possible to obtain high removal efficiencies. Phosphorous and sulfur elements were identified through Energy Dispersive X-ray (EDX) analysis and evidenced the malathion adsorption on PVC. The characteristic spectrum of malathion was identified by the Fourier Transform Infrared (FTIR) Spectroscopy analysis. The Thermogravimetric and Differential Thermal Analysis (TG/DTA) suggested that the adsorption of malathion on the surface of the polymers was mainly determined by hydrogen bonds.

SUBMITTER: Hermosillo-Nevarez JJ

PROVIDER: S-EPMC7215715 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Feasibility Study on the Use of Recycled Polymers for Malathion Adsorption: Isotherms and Kinetic Modeling.

Hermosillo-Nevárez Jhonatan J JJ Bustos-Terrones Victoria V Bustos-Terrones Yaneth A YA Uriarte-Aceves Perla Marysol PM Rangel-Peraza Jesus Gabriel JG

Materials (Basel, Switzerland) 20200412 8

In this study, the use of Polyvinylchloride (PVC) and High Density Polystyrene (HDPS) was demonstrated as an alternative for the adsorption of Malathion. Adsorption kinetics and isotherms were used to compare three different adsorbent materials: PVC, HDPS, and activated carbon. The adsorption capacity of PVC was three times higher than activated carbon, and a theoretical value of 96.15 mg of Malathion could be adsorbed when using only 1 g of PVC. A pseudo first-order rate constant of 1.98 (1/h) ...[more]

PMID: 32290629

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Project description:A scaling theory is developed for selective adsorption of polymers induced by the strong binding between specific monomers and complementary surface adsorption sites. By "selective" we mean specific attraction between a subset of all monomers, called "sticky", and a subset of surface sites, called "adsorption sites". We demonstrate that, in addition to the expected dependence on the polymer volume fraction ϕbulk in the bulk solution, selective adsorption strongly depends on the ratio between two characteristic length scales, the root-mean-square distance l between neighboring sticky monomers along the polymer, and the average distance d between neighboring surface adsorption sites. The role of the ratio l/d arises from the fact that a polymer needs to deform to enable the spatial commensurability between its sticky monomers and the surface adsorption sites for selective adsorption. We study strong selective adsorption of both telechelic polymers with two end monomers being sticky and multisticker polymers with many sticky monomers between sticky ends. For telechelic polymers, we identify four adsorption regimes at l/d < 1 that are characterized by the fraction of occupied adsorption sites and whether the dominant conformation of adsorbed chains is a single-end-adsorbed "mushroom" or double-end-adsorbed loop. For l/d > 1, we expect that the adsorption layer at exponentially low ϕbulk consists of separated unstretched loops, while as ϕbulk increases the layer crosses over to a brush of extended loops with a second layer of weakly overlapping tails. For multisticker chains, in the limit of exponentially low ϕbulk, adsorbed polymers are well separated from each other. As l/d increases, the conformation of an individual polymer changes from a single-end-adsorbed "mushroom" to a random walk of loops. For high ϕbulk, adsorbed polymers at small l/d are mushrooms that cover all the adsorption sites. At sufficiently large l/d, adsorbed multisticker polymers strongly overlap. We anticipate the formation of a self-similar carpet and with increasing l/d a two-layer structure with a brush of loops covered by a self-similar carpet. As l/d exceeds the threshold determined by the adsorption energy, the brush of loops under the carpet reaches a saturated state, resulting in a l/d-independent brush-under-carpet structure, which can also be applied to describe adsorbed multisticker polymers in nonselective adsorption where a sticker can strongly bind to any place on the adsorption surface. We examine the adsorbed amount Γ of multisticker polymers in different regimes for selective adsorption. If the adsorbed multisticker polymers are nonoverlapping mushrooms, the adsorbed amount Γ increases linearly with the surface density of adsorption sites Σ ≈ 1/d2. In the self-similar carpet regime, Γ increases sublinearly as Σ0.15 in a good solvent, while only logarithmically in a theta solvent. Formation of a brush layer under the carpet contributes an additional adsorbed amount. This additional amount increases linearly with Σ and eventually dominates the overall adsorbed amount Γ before saturating at a plateau value controlled by the adsorption energy.

Dataset Information

Feasibility Study on the Use of Recycled Polymers for Malathion Adsorption: Isotherms and Kinetic Modeling.

Publications

Feasibility Study on the Use of Recycled Polymers for Malathion Adsorption: Isotherms and Kinetic Modeling.

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