journal article·2025-09Open access

Targeted Selenite Adsorption Using Defective Fe‐BTC: Effective in Acidic and Alkaline Conditions

Asong Byun, Byeoksong Lee, Yujin Jeong, Joongoo Kang, Jinkyu Park, Jinhee Park

Small· Volume 21· Issue 37

Abstract

Abstract Amorphous Fe‐BTC, characterized by entirely defective metal nodes, has been employed for the effective adsorption of toxic selenite anions from aqueous solutions. Remarkably, Fe‐BTC maintains high adsorption efficiency across a broad pH range (2–12), achieving a maximum adsorption capacity of 491 mg g −1 , ranking among the highest recorded for adsorbents, including MOFs. The adsorption process involves distinct chemical interactions depending on pH: weak and variable interactions under acidic conditions (pH 2) and strong, diverse coordination modes under alkaline conditions (pH 11). Notably, the strong coordination ability of selenite ensures high selectivity over selenate and competing anions such as Cl − , NO 2 − , NO 3 − , CO 3 2− , SO 4 2− , and PO 4 3− . The abundance of metal defects endows Fe‐BTC with superior adsorption capacity compared to crystalline Fe‐MOF, MIL‐100(Fe). This study provides a comparative analysis of selenite adsorption on Fe‐BTC under acidic and alkaline conditions, emphasizing pH‐dependent adsorption mechanisms and their implications for designing effective adsorbents for toxic species removal.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Mercury impact and mitigation studies · Arsenic contamination and mitigation · Metal-Organic Frameworks: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Physics and Chemistry Daegu Gyeongbuk Institute of Science and Technology (DGIST) Daegu 42988 Republic of Korea

Department of Plant & Biomaterials Science College of Natural Sciences Gyeongsang National University Jinju 52828 Republic of Korea

Department of Green Bio Science Gyeongsang National University Jinju 52828 Republic of Korea

Funding

Ministry of Science and ICT, South Korea

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