Ultrasonic spray pyrolysis synthesis of TiO2/Al2O3 microspheres with enhanced removal efficiency towards toxic industrial dyes

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Developing low-cost and highly effective adsorbent materials to decolorate wastewater is still challenging in the industry. In this study, TiO2-modified Al2O3 microspheres with different TiO2 contents were produced by spray pyrolysis, which is rapid and easy to scale up. Results reveal that the modification of γ-Al2O3 with TiO2 reduced the crystallite size of Al2O3 and generated more active sites in the composite sample. The as-synthesized Al2O3-TiO2 microspheres were applied to remove anionic methyl orange (MO) and cationic rhodamine B (RB) dyes in an aqueous solution using batch and continuous flow column sorption processes. Results show that the Al2O3 microspheres modified with 15 wt% of TiO2 exhibited the maximum adsorbing capacity of ∼41.15 mg g-1 and ∼32.28 mg g-1 for MO and RB, respectively, exceeding the bare γ-Al2O3 and TiO2. The impact of environmental complexities on the material's reactivity for the organic pollutants was further delineated by adjusting the pH and adding coexisting ions. At pH ∼5.5, the TiO2/Al2O3 microspheres showed higher sorption selectivity towards MO. In the continuous flow column removal, the TiO2/Al2O3 microspheres achieved sorption capacities of ∼31 mg g-1 and ∼19 mg g-1 until the breakthrough point for MO and RB, respectively. The findings reveal that TiO2-modified Al2O3 microspheres were rapidly prepared by spray pyrolysis, and they effectively treated organic dyes in water in batch and continuous flow removal processes.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

RSC advances - 13(2023), 9 vom: 14. Feb., Seite 5859-5868

Sprache:

Englisch

Beteiligte Personen:

Nguyen, Thi Hong Anh [VerfasserIn]
Quang, Duong Tuan [VerfasserIn]
Tan, Le Van [VerfasserIn]
Vo, The Ky [VerfasserIn]

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Journal Article

Anmerkungen:

Date Revised 24.02.2023

published: Electronic-eCollection

Citation Status PubMed-not-MEDLINE

doi:

10.1039/d3ra00024a

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM353223484