检出限
荧光团
铯
膜
荧光
化学
水溶液
萃取(化学)
卤水
选择性
光诱导电子转移
化学工程
纳米技术
无机化学
盐(化学)
选矿
膜透性
分析化学(期刊)
环境友好型
作者
Bibek Chaw pattnayak,Upasana Mohapatro,P. Barik,Malay Kumar Rana,Sasmita Mohapatra
标识
DOI:10.1002/adsu.202501713
摘要
ABSTRACT With rising global cesium (Cs) demand and energy‐intensive ore processing, extraction from salt lakes and brines offers a sustainable alternative. However, selective Cs recovery remains challenging due to extremely low concentrations amid competing ions. Here, we report DTA, a novel anthraquinone‐based fluorophore functionalized with dithiothreitol as a cesium‐selective chelator. DTA exhibits distinctive turn‐on green fluorescence specific to Cs + ions, maintaining high selectivity against oceanic interferents (Mg 2 + , Na + , K + ) in aqueous media with an ultralow detection limit of 2.9 n M . DFT calculations confirm that Cs + binding disrupts hydrogen‐bond‐assisted photoinduced electron transfer (PET), restoring anthraquinone's intrinsic fluorescence. Incorporating DTA into hydrogel matrices yields high‐performance membranes for cesium extraction. The optimized DTAH4 membrane demonstrates 1.8‐fold enhanced water permeability (525.2 L·m − 2 ·h − 1 ·bar − 1 ) compared to pristine DTAH0, while achieving a remarkable 97% Cs extraction efficiency versus only 11% for the control. Importantly, we demonstrate smartphone‐based visual RGB detection, enabling portable, real‐time monitoring of cesium contamination. This integrated approach, combining ultrasensitive fluorescent detection with efficient membrane separation, presents a practical platform for sustainable cesium recovery for technological applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI