Abstract

The detection and removal of phosphate were advantageous means to predict and mitigate eutrophication of aquatic ecosystems. In this study, a luminescent rod-like terbium-based metal organic frameworks (MOFs) had been synthesized successfully via facile hydrothermal reaction for convenient and efficient detection and adsorption of phosphate. Specifically, the Tb-based MOFs (Tb-BTC) exhibited high selectivity for sensing of phosphate through fluorescence quenching mechanism with the quenching constant values (Ksv) of 1.18 × 104 M−1 and low limit of detection (LOD) of 2.97 μM. Simultaneously, Tb-BTC also possessed superior adsorption ability for phosphate based on Langmuir isotherm model and pseudo-second-order kinetic model determining that the maximum adsorption capacity reached up to 222.2 mg/g with equilibrium time of 30 min. More significantly, Tb-BTC nanoparticle could be stably integrated into polyacrylonitrile (PAN) nanofibers for constructing hierarchically hybrid nanofibrous membrane (PAN/TB) through electrospinning to further improve its operability and recoverability. And the obtained customized membrane maintained selective detection for phosphate with visual LOD of 3 × 10−4 M and good capture of phosphate with the maximum adsorption capacity of 111.3 mg/g, respectively. Therefore, this study provided prospective candidate for detection and removal of phosphate making contribution at a certain level to predict and attenuate water eutrophication.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.