Preparation of Cu–Al layered double hydroxide intercalated with ethylenediaminetetraacetate by coprecipitation and its uptake of rare earth ions from aqueous solution

2013 ◽  
Vol 17 ◽  
pp. 28-34 ◽  
Author(s):  
Tomohito Kameda ◽  
Kazuaki Hoshi ◽  
Toshiaki Yoshioka
2021 ◽  
pp. 116774
Author(s):  
Fataneh Vasheghani Farahani ◽  
Mohammad Hassan Amini ◽  
Seyed Hamid Ahmadi ◽  
Seyed Amirabbas Zakaria

2018 ◽  
Vol 47 (48) ◽  
pp. 17342-17348 ◽  
Author(s):  
Euiyoung Jung ◽  
Jae Kyeom Kim ◽  
Hyungsuk Choi ◽  
Min Hyung Lee ◽  
Taekyung Yu

Transition metal LDH nanoplates were synthesized by heating an aqueous solution containing a metal salt, PEG, and octylamine. The LDH nanoplates showed comparable electrochemical catalytic performance for the oxygen evolution reaction.


2010 ◽  
Vol 20 (22) ◽  
pp. 4684 ◽  
Author(s):  
Yunfeng Xu ◽  
Yingchun Dai ◽  
Jizhi Zhou ◽  
Zhi Ping Xu ◽  
Guangren Qian ◽  
...  

2020 ◽  
Vol 49 (3) ◽  
pp. 316-331 ◽  
Author(s):  
Wolfram W. Rudolph ◽  
Gert Irmer

Crystals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 342 ◽  
Author(s):  
Kwanjira Panplado ◽  
Maliwan Subsadsana ◽  
Supalax Srijaranai ◽  
Sira Sansuk

This work demonstrates a simple approach for the efficient removal of tetracycline (TC) antibiotic from an aqueous solution. The in situ-adsorption removal method involved instant precipitation formation of mixed metal hydroxides (MMHs), which could immediately act as a sorbent for capturing TC from an aqueous solution, by employing layered double hydroxide (LDH) components including magnesium and aluminum ions in alkaline conditions. By using this approach, 100% removal of TC can be accomplished within 4 min under optimized conditions. The fast removal possibly resulted from an instantaneous adsorption of TC molecules onto the charged surface of MMHs via hydrogen bonding and electrostatically induced attraction. The results revealed that our removal technique was superior to the use of LDH as a sorbent in terms of both removal kinetics and efficiency. Moreover, the recovery of captured TC was tested under the influence of various common anions. It was found that 98% recovery could be simply achieved by using phosphate, possibly due to its highly charged density. Furthermore, this method was successful for efficient removal of TC in real environmental water samples.


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