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Kinetics, isotherm, thermodynamic, and adsorption mechanism studies of La(OH)3-modified exfoliated vermiculites as highly efficient phosphate adsorbents

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TLDR
In this paper, a modified exfoliated vermiculite (La5EV) was fabricated, characterized, and investigated for phosphate removal in batch tests for the first time, and the effect of initial phosphate concentration, contact time, temperature, pH, and coexisting ions on the adsorption capacity of La5EV was investigated in detail.
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This article is published in Chemical Engineering Journal.The article was published on 2014-01-15 and is currently open access. It has received 255 citations till now. The article focuses on the topics: Adsorption & Langmuir adsorption model.

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Journal ArticleDOI

Enhanced Phosphate Removal by Nanosized Hydrated La(III) Oxide Confined in Cross-linked Polystyrene Networks

TL;DR: A new nanocomposite adsorbent La-201 of extremely high capacity and specific affinity toward phosphate was fabricated and well characterized, and the formation of LaPO4·xH2O is verified to be the dominant pathway for selective phosphate adsorption by the immobilized nano-HLO.
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Highly Efficient and Selective Phosphate Removal from Wastewater by Magnetically Recoverable La(OH) 3 /Fe 3 O 4 Nanocomposites

TL;DR: The developed La(OH)3/Fe3O4 (4:1) nanocomposite has an excellent magnetic separation efficiency, fast sorption kinetics of 30 min, high sorption capacity of 83.5 mg P/g, and strong selectivity for phosphate in presence of competing ions.
Journal ArticleDOI

Critical of linear and nonlinear equations of pseudo-first order and pseudo-second order kinetic models

TL;DR: The experimental adsorption equilibrium of Cd(II) onto chitosan (CdII)/CS and methyl orange onto bentonite (MO/Bt) were studied in batch adsorsorption experiments at room temperature for an initial concentration of 236.5mg/L for Cd (II) (pH = 5) and 33mg/l for MO (pHO = 3).
Journal ArticleDOI

Adsorption as a technology to achieve ultra-low concentrations of phosphate: Research gaps and economic analysis.

TL;DR: The main parameters that affect the economics of phosphate adsorption are discussed, a scenario and sensitivity analysis shows the importance of adsorbent regeneration and reuse and the research gaps are highlighted.
References
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Pseudo-second order model for sorption processes

TL;DR: In this paper, a literature review of the use of sorbents and biosorbents to treat polluted aqueous effluents containing dyes:organics or metal ions has been conducted.
Journal ArticleDOI

Kinetics of Adsorption on Carbon from Solution

TL;DR: In this paper, it was shown that the rate of adsorption of persistent organic compounds on granular carbon is quite low and the rate is partially a function of the pore size distribution of the adsorbent, of the molecular size and configuration of the solute, and of the relative electrokinetic properties of adsorbate and adsorbents.
Related Papers (5)
Frequently Asked Questions (19)
Q1. What are the contributions in this paper?

Li et al. this paper used an exfoliated vermiculite ( EV ) as an adsorbent for removing contaminants from water. 

The third part is the final equilibrium stage in which the intra-particle diffusion slows down ascribed to the low concentration of residual phosphate in the solution [48, 49]. 

In their study, three important thermodynamic parameters, ∆G°, ∆H° and ∆S°, are taken into account to determine the spontaneous nature of the processes. 

the phosphate uptake capacities increase from La0.63EV to La10EV; which is attributed to the greater La loadings in the resulting adsorbents by increasing La/EV ratios in the initial synthetic solution. 

8.0 g of EV was firstly dispersed in 200.0 mL of DI water under continuously stirring for 2 h to obtain a uniform EV aqueous mixture. 

For instance, in Yuan’s work, the phosphate adsorption ratios of fourteen types of LaCl3-modified clays, including argil, pumice, attapulgite, kaolinite, etc., ranged from 93 % to 99 %, which were around 6 % – 37 % greater than those of unmodified clays [18]. 

200.0 mL of isopropanol solution consisting of a certain amount of La(NO3)3·6H2O (Tianjin Daomao reagent factory) was slowly added into the prepared EV aqueous mixture. 

the deposition of La(OH)3 nanorods on the surfaces of EV may contribute to the evident increase of external superficial area in La5EV. 

To study the effect of coexisting anions on the phosphate removal capacities, 0.050 g of the adsorbent was added into the phosphate solution containing 0.01 M and 0.10 M coexisting ions, which were prepared by dissolving sodium salt forms of F−, Cl−, NO3 −, SO4 2−, and CO3 2− into 20 mg P/L phosphate solution. 

As seen, the phosphate adsorption capacity strongly depends on the initial P concentration of solution; that the adsorption capacity of La5EV recorded at 48 h increases from 20.7 mg P/g in 20 mg P /L solution to 70.3 mg P/g in 80 mg P/L solution. 

The SAED pattern of La(OH)3 (the inset of Fig. 3d) indicates the ring pattern, which is due to the polycrystalline nature of La(OH)3 nanorods formed on EV. 

The other possible mechanism to explain the high phosphate adsorption at a low pH value is that the presence of a large number of H+ ions in the solution may induce the formation of protonated vermiculite20surfaces, favoring the electrostatic attraction to the phosphate species H2PO4 −; herein an example of reaction is shown. 

Adsorption kinetic experiments were conducted as follows: 0.20 g of the adsorbent was added in 200.0 mL of phosphate solution with initial concentrations of 20, 50 and 80 mg P/L, respectively. 

After adding La5EV, the pH value gradually increases to 10.23 after 12 h, when the equilibrium is reached in the solution with an initial phosphate concentration of 20 mg P/L according to the finding in their kinetic study (Fig. 4a); and maintains at 10.23 for another 36 h. 

By taking into account of ~ 88.5 % desorption ratio of spent La5EV within 24 h (Fig. S3), the decreasing adsorption capability observed in the adsorption-desorption cycle studies may be attributed to the incomplete desorption of adsorbed phosphate during regeneration. 

There is a negligible effect on qe of La5EV by adding 0.01 M coexisting anions in the solution, suggesting that La5EV possess a high selective adsorption capacity to phosphate anions. 

the unmodified EV exhibits the phosphate adsorption capacity of approximately 2.15 mg P/g after 12 h in the solution with an initial concentration of 20 mg P/L. 

Li and co-workers reported that the adsorption capacity of the vesuvianite modified with a La/Ves mass ratio of 0.16 (1.30 mg P/g) was around 3.6 times greater than that of undoped vesuvianite (0.28 mg P/g) [17]. 

The phosphate removal performance of adsorbent in synthetic secondary treated wastewater was also studied, which was prepared according to the reference [35], with the respective carbon (as COD), nitrogen (N), and phosphate (P) concentrations of 100 mg/L, 12 mg/L, and 2 mg/L, respectively.