copper hexacyanoferrate
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2022 ◽  
Vol 216 ◽  
pp. 106367
Author(s):  
Lingdan Zhu ◽  
Deqin Zhu ◽  
Yu Sheng ◽  
Jiajia Xu ◽  
David Harbottle ◽  
...  

Author(s):  
Priya Jain ◽  
Shwetambara Jha ◽  
Pravin Ingole

Development of an efficient non-precious metal-based bi-functional oxygen electro-catalyst for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is crucial for various electrochemical energy conversion and storage devices. Prussian...


Author(s):  
Dinh Trung Nguyen ◽  
Vu Tram Anh Le ◽  
Dong Phuong Truong ◽  
Thi Dan Thy Kieu ◽  
Tran Thuy Hong Nguyen ◽  
...  

Low-cost nanoscale copper hexacyanoferrate (CuHF), a good selective adsorbent for cesium (Cs+) removal, was prepared using the chemical co-precipitation method. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), and high-resolution transmission electron microscopy (HR-TEM) were conducted to determine the CuHF morphology. Copper hexacyanoferrate, Cu13[Fe(CN)6]14.(2K).10H2O, has a cubic structure (space group F-43m) in the range of 10-30 nm and a Brunauer-Emmett-Teller (BET) surface area of 462.42 m2/g. The removal of Cs+ and Sr2+ is dependent on pH; the maximum adsorption capacity (qmax) of CuHF is achieved at a pH = 6. From the Langmuir model, qmax = 143.95 mg/g for Cs+ and 79.26 mg/g for Sr2+, respectively. At high concentrations, Na+, Ca2+, and K+ ions have very little effect on Cs+ removal, and Na+ and K+ ions have a higher affinity for removing Sr2+ than Ca2+ at all concentrations. CuHF has a high affinity for alkaline cations in the order: Cs+ > K+ > Na+ > Ca2+ > Sr2+, as proposed and discussed.


2021 ◽  
Vol 394 ◽  
pp. 139147
Author(s):  
Sukanya Jankhunthod ◽  
Chochanon Moonla ◽  
Athis Watwiangkham ◽  
Suwit Suthirakun ◽  
Theeranun Siritanon ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Chi Ma ◽  
Zhenzhen Jiang ◽  
Senjian Han ◽  
Yafei Guo ◽  
Tianlong Deng

Efficient removal of radioactive cesium from complex wastewater is a challenge. Unlike traditional precipitation and hydrothermal synthesis, a novel vast specific surface area adsorbent of copper hexacyanoferrates named EA-CuHCF was synthesized using a one-pot solvothermal method under the moderate ethanol media characterized by XRD, SEM, EDS, BET, and FTIR. It was found that the maximum adsorption capacity towards Cs+ was 452.5 mg/g, which is far higher than most of the reported Prussian blue analogues so far. Moreover, EA-CuHCF could effectively adsorb Cs+ at a wide pH range and low concentration of Cs+ in geothermal water within 30 minutes, and the removal rate of Cs+ was 92.1%. Finally, the separation factors between Cs+ and other competitive ions were higher than 553, and the distribution coefficient of Cs+ reached up to 2.343 × 104 mL/g. These properties suggest that EA-CuHCF synthesized by the solvothermal method has high capacity and selectivity and can be used as a candidate for Cs+ removal from wastewater.


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