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Enregistrement W7062594106

Treatment of Aqueous Arsenic Using Chemically and Electrochemically Modified Biomaterials

2023· dissertation· en· W7062594106 sur OpenAlexfundno aff

Notice bibliographique

RevueUniversity Library (University of Saskatchewan) · 2023
Typedissertation
Langueen
DomaineDecision Sciences
ThématiqueScientific Measurement and Uncertainty Evaluation
Établissements canadiensnon disponible
Organismes subventionnairesNatural Sciences and Engineering Research Council of CanadaMitacs
Mots-clésAdsorptionArsenicSorptionContaminationBiomass (ecology)Water treatmentAqueous solutionHuman decontamination
DOInon disponible

Résumé

récupéré en direct d'OpenAlex

This research hypothesizes that agricultural residues can be transformed into value-added adsorbents with the ability to remove arsenic from water effectively. Modifying these residues is expected to enhance adsorption capacity, providing a promising solution to address the global issue of arsenic contamination in water. \nArsenic (As) contamination in drinking water poses a significant global water health hazard. To address this issue, adsorption has gained increasing attention as a promising technology for As removal, offering improved cost efficiency and simplified treatment operations. The utilization of agricultural biomass residues as As adsorbents has emerged as a promising approach. However, untreated biomasses exhibit limitations such as low sorption capacity, coloration issues in treated waters, increased BOD, COD, and TOC levels due to the release of soluble organic compounds, poor solubility and stability, and their unsuitability for conventional process equipment due to their fragile nature and swelling. It is evident that modification of biomasses is necessary to overcome these drawbacks, enabling their application at commercial and industrial scales. \nMetal oxides, such as iron oxide, have demonstrated high efficacy as As adsorbents. However, due to their small particle size, using them in adsorption systems presents challenges. In the last two decades, the use of the terms engineered- or modified-biomass/biochar has been gaining momentum in the literature. These terms refer to chemically treated biomasses/biochars produced to improve adsorption capacities. Generally, the modification process consists of impregnating the biomass/biochar with a metal agent with a high affinity to the target contaminant (e.g., As). The resulting composite material consists of the original biomass or biochar acting as a support structure for the metal oxide, which serves as the active site for adsorption. This modification process can significantly improve the adsorption capacity, selectivity, and stability of the material, making it a more effective adsorbent for water treatment applications. \n The modification process is typically conducted by mixing the untreated biomass/biochar materials in a chemical solution. However, this process can be time-consuming, is difficult to control product formation, and results in potentially unstable and unreproducible physicochemical properties of the modified materials. Clearly, it would be beneficial to have a better method for this modification process. \nThe electrochemical modification offers a promising and simplified approach to overcome the limitations associated with chemical-based methods for preparing modified biomass/biochar adsorbents. This technique involves a two-electrode system within an electrochemical cell, where a sacrificial anode (such as Fe) eliminates the need for external chemical modifiers. The modification process begins by passing an electric current through the electrodes in an electrolyte solution, while the biomass/biochar materials are continuously stirred within the solution between the electrodes. As the sacrificial anode dissolves, the modifying agent ions (e.g., Fe2+) are released and undergo a series of reactions, resulting in the deposition of the desired modifying agent (e.g., iron oxide) onto the surface of the biomass/biochar. \nThe overall objective of the conducted research over three years was the development of biomass/biochar-based adsorbents with high As adsorption capacities using chemical and electrochemical modification methods. Seven different adsorbents, including chemically iron-loaded biomass (ICS), electrochemically iron-loaded biomass and biochar (OBM and OBC), microwave-assisted and electrochemically iron and manganese-loaded biochar (MnBC and FeMnBC), and microwave-assisted and electrochemically aluminum and zinc-loaded biochar (ZnBC, and AlZnBC) were developed and used for As adsorption. The effects of parameters affecting the As adsorption capacity of the modified adsorbents were investigated, and the modification conditions were optimized. The concept of the shrinking core model was applied to develop a mathematical model to characterize the As adsorption process for OBM and OBC. A diffusional mass transfer model (DMTM) was developed to identify the external mass transfer coefficient (kf), effective pore volume diffusion coefficient (Dp), and surface diffusion coefficient (Ds) in the adsorption of As onto MnBC and FeMnBC. Finally, a model was developed to study temperature distribution inside the biomass during pyrolysis for making ZnBC. \nOverall, the modified adsorbents prepared through the applied modification methods exhibited exceptional performance in removing both As(III) and As(V) from water. However, their adsorption capacities varied depending on the optimization considerations for the modification conditions, resulting in higher efficiency for either As(III) or As(V) removal. The combination of microwave pyrolysis and electrochemical treatment demonstrated significant potential as an alternative to traditional pyrolysis and chemical treatment processes, showcasing its viability for preparing biomass/biochar-based adsorbents. \nMoreover, extensive investigations were conducted to assess the influence of different adsorption conditions on the As adsorption capacity of the modified adsorbents. Parameters such as pH, temperature, initial As concentration, and adsorption time were systematically studied, revealing their significant impact on the adsorption capacity. By analyzing the effects of these adsorption conditions, valuable insights were obtained regarding the underlying mechanisms governing the adsorption process. Notably, chemisorption was found to be the dominant and rate-limiting mechanism in most cases. This understanding of the adsorption mechanisms is crucial for optimizing the adsorption process and designing effective As removal strategies using the modified adsorbents. \nThis research provides a substantial contribution to the field by offering valuable insights into the conversion of agricultural residues into value-added and efficient adsorbents for As removal. By exploring different modification methods and optimizing the adsorption conditions, this study paves the way for the development of enhanced water treatment approaches to address the challenges posed by As contamination. Moreover, the findings have the potential to be extended to the development of adsorbents for other contaminants. By harnessing the potential of biomass-based adsorbents, this research not only expands our knowledge regarding the utilization of agricultural residues but also provides practical solutions for mitigating water pollution issues.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,000
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesMéta-épidémiologie (sens strict)
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Expérimental (laboratoire) · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,472
Score d'incertitude au seuil1,000

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0010,000
Bibliométrie0,0010,001
Études des sciences et des technologies0,0000,000
Communication savante0,0000,001
Science ouverte0,0010,000
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0010,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,080
Tête enseignante GPT0,283
Écart entre enseignants0,202 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.

Devis d'étudeExpérimental (laboratoire)
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2023
Routes d'admission1
Résumé présentoui

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