Assessment of cerium adsorption potential of phosphoric acid activated biochar in aqueous system: Modelling and mechanistic insights.

Environ Res

Biochemical and Environmental Engineering Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India. Electronic address:

Published: January 2025

AI Article Synopsis

  • Cerium pollution from industrial waste poses significant environmental risks, necessitating effective treatment methods for contaminated water.
  • This study investigates the use of phosphoric acid-activated biochar (PPMB), derived from palmyra palm male flower, as an efficient adsorbent for removing cerium from water, optimizing key parameters for adsorption efficiency.
  • Findings indicate that PPMB’s superior adsorption capacity (141.35 mg/g) is attributed to its unique surface properties and mechanisms, making it a promising and sustainable solution for cerium pollution remediation.

Article Abstract

Cerium pollution in waterbodies by improper industrial waste disposal is a major concern due to its detrimental impacts on the environment. Therefore, treatment of cerium-contaminated water is inevitable. Hence, this study is focused on the remediation of cerium pollution using phosphoric acid-activated biochar (PPMB) as an adsorbent, synthesized upon pyrolytic activation of palmyra palm male flower-based pristine biochar (PMFB) with HPO at 500 °C. The physico-chemical surface properties of PMFB and PPMB were evaluated through various microscopic and spectroscopic analyses. The key parameters such as biochar dosage, pH, temperature, contact time and initial cerium concentration were optimized as 0.5 g/L, 5.0, 303 K, 180 min and 50 mg/L respectively via batch adsorption. Pseudo-second order kinetic and Toth isotherm are the best-fitted models. The thermodynamic parameters including ΔG (-30.4707 ± 0.7618 kJ/mol at 303 K), ΔH (16.1499 ± 0.78 kJ/mol), and ΔS (153.617 ± 3.8404 J/mol/K) conveying that cerium adsorption onto PPMB was spontaneous, endothermic, and highly disordered at PPMB-bulk adsorption medium interface. Precipitation, electrostatic attraction, and surface complexation are predicted to be the predominant mechanisms for the chosen PPMB-cerium adsorption system. Moreover, cerium phytotoxicity on Vigna radiata explains the real-time applicability and feasibility of cerium adsorption using PPMB. Thus, the key findings of this study specified that the higher adsorption capacity of PPMB (141.3484 ± 6.9856 mg/g) contributed by the incorporated phosphate groups, predominant mesoporosity, SSA of 230.559 m/g and anionic surface at a wider pH range (pH>3.08) make PPMB as efficient, economically feasible and environmentally friendly adsorbent for cerium adsorption in aqueous system.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.envres.2024.120301DOI Listing

Publication Analysis

Top Keywords

cerium adsorption
16
adsorption
8
aqueous system
8
cerium pollution
8
adsorption ppmb
8
cerium
7
ppmb
6
assessment cerium
4
adsorption potential
4
potential phosphoric
4

Similar Publications

This study focuses on the synthesis of a novel Cerium-Magnesium (CeO-MgO) binary oxide nanomaterials by a simple co-precipitation process and used to remove harmful pollutants such as Cr(VI), Cu(II), and F. The morphology, phase, crystallite size, thermal stability, functional groups, surface area, and porosity of the synthesized nanomaterial were determined by using XRD, SEM, FTIR, TGA/DTA, and BET studies. The prepared nanomaterials showed adsorption selectivity of Cu(II) ≈ F> Cr(VI) with a high adsorption capacity of 84.

View Article and Find Full Text PDF

Developing efficient and cost-effective rare earth element-based electrocatalysts for water splitting remains a significant challenge. To address this, interface engineering and charge modulation strategies were employed to create a three-dimensional coral-like CeF/MoO heterostructure electrocatalyst, grown in situ on the multistage porous channels of carbonized sugarcane fiber (CSF). Integrating abundant CeF/MoO heterostructure interfaces and numerous oxygen vacancy defects significantly enhanced the catalyst's active sites and molecular activation capabilities.

View Article and Find Full Text PDF

Electrochemical destruction of PFAS at low oxidation potential enabled by CeO electrodes utilizing adsorption and activation strategies.

J Hazard Mater

December 2024

School of Environmental Science and Engineering, Southern University of Science and Technology, Shenzhen 518055, PR China; Guangdong Provincial Key Laboratory of Soil and Groundwater Pollution Control, Southern University of Science and Technology, Shenzhen 518055, PR China. Electronic address:

The persistence and ecological impact of per- and poly-fluoroalkyl substances (PFAS) in water sources necessitate effective and energy-efficient treatment solutions. This study introduces a novel approach using cerium dioxide (CeO) electrodes enhanced with oxygen vacancy (O) to catalyze the defluorination of PFAS. By leveraging the unique affinity between cerium and fluorine-containing species, our approach enables adsorptive preconcentration and catalytic degradation at low oxidation potentials (1.

View Article and Find Full Text PDF

Hydrogen (H) is a viable alternative as a sustainable energy source, however, new highly efficient electrocatalysts for water splitting are still a research challenge. In this context, metal-organic frameworks (MOFs)-derived nanomaterials are prominent high-performance electrocatalysts for hydrogen production, especially in the oxygen evolution reaction (OER). Here, a new synthesis of two cerium oxide (CeO) electrocatalysts using Ce-succinates MOFs as templates is proposed.

View Article and Find Full Text PDF

Promotional effect and mechanism of Ce-modified VO-WO/TiO catalyst in low-temperature NH-SCR.

Environ Sci Pollut Res Int

January 2025

College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou Gansu, 730070, China.

The enhancement effect of Ce modification on VO-WO/TiO catalysts at low temperatures was investigated for the selective catalytic reduction (SCR) of NO with NH (NH-SCR). By adding 9% CeO to 0.5%VO-3%WO/TiO catalyst, the low-temperature denitrification performance of CeVWTi catalyst after Ce modification was significantly improved, achieving a NO conversion above 90% within a broad temperature range of 200-350℃, with catalytic activity comparable to that of 3% VO-3% WO/TiO.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!