Tea-Waste-Mediated Magnetic Oxide Nanoparticles as a Potential Low-Cost Adsorbent for Phosphate (PO43−) Anion Remediation

Author:

Shah Khizar Hussain1,Fareed Misbah2,Waseem Muhammad1ORCID,Shahida Shabnam3,Hatshan Mohammad Rafe4ORCID,Sarfraz Sadaf5,Batool Aneeqa2,Fahad Muhammad6ORCID,Ahmad Tauqeer7,Shah Noor S.8,Ha Kyungeun9ORCID,Han Changseok910ORCID

Affiliation:

1. Department of Chemistry, COMSATS University Islamabad (Islamabad Campus), Islamabad 45000, Pakistan

2. Department of Chemistry, COMSATS University Islamabad (Abbottabad Campus), Abbottabad 22060, Pakistan

3. Department of Chemistry, Faculty of Applied and Basic Sciences, University of Poonch, Rawalakot 12350, Pakistan

4. Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

5. Department of Chemistry, Lahore Garrison University, Lahore 54000, Pakistan

6. Department of Electrical and Computer Engineering, COMSATS University Islamabad (Abbottabad Campus), Abbottabad 22060, Pakistan

7. Department of Chemistry, University of Mianwali, Mianwali 42200, Pakistan

8. Department of Environmental Sciences, COMSATS University Islamabad (Vehari Campus), Vehari 61100, Pakistan

9. Program in Environmental & Polymer Engineering, Graduate School, INHA University, Incheon 22212, Republic of Korea

10. Department of Environmental Engineering, INHA University, Incheon 22212, Republic of Korea

Abstract

In the current study, magnetic oxide nanoparticle-impregnated tea waste (TW-Fe3O4) is employed as an adsorbent to remove phosphate ions (PO43−) from an aqueous solution. By utilizing a variety of analytical methods, the TW-Fe3O4 nano-adsorbent was characterized by FE-SEM, TEM, EDX, BET, FTIR and XRD. The FE-SEM of TW-Fe3O4 demonstrated the adsorbent’s granular morphology with a variety of magnetic nanoparticle sizes and shapes. The XRD of TW-Fe3O4 showed two diffraction peaks at 2θ values 30.9° and 35.4°, which are in correspondence with the diffraction pattern of magnetite. The synthesis of a TW-Fe3O4 adsorbent with a greater surface area and porosity was demonstrated by BET analysis. Numerous adsorption factors like initial concentration of PO43− ion, pH of the medium, contact time, temperature and adsorbent dose were optimized for phosphate removal. The maximum removal of 92% was achieved by using the adsorbent dose of 1.2 g at 323 K (pH 5). Pseudo-second-order and intra-particle diffusion models were fitted to the sorption kinetic, whereas adsorption isotherm data were found well fitted to Freundlich and Dubinin–Radushkevich (D-R) models. The highest adsorption capacity of TW-Fe3O4 towards phosphate ions was 226.8 mg/g, which is significantly higher than other reported bio-adsorbents. According to thermodynamic data, phosphate adsorption at the solid–liquid interface was of an endothermic and spontaneous nature and characterized by enhanced inevitability.

Funder

HEC, Pakistan through NRPU

King Saud University Riyadh, Saudi Arabia

National Research Foundation of Korea

Publisher

MDPI AG

Subject

Water Science and Technology,Aquatic Science,Geography, Planning and Development,Biochemistry

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