Redox activity of lignite and its accelerating effects on the chemical reduction of azo dye by sulfide

RSC Advances ◽  
2016 ◽  
Vol 6 (71) ◽  
pp. 66930-66937 ◽  
Author(s):  
Juanjuan Li ◽  
Guangfei Liu ◽  
Jiti Zhou ◽  
Aijie Wang ◽  
Jing Wang ◽  
...  

Redox active lignite can act as a mediator to accelerate azo dye decolorization through enhancing electron transfer from sulfide to the azo dye.

RSC Advances ◽  
2017 ◽  
Vol 7 (27) ◽  
pp. 16542-16552 ◽  
Author(s):  
Zhou Fang ◽  
Sichao Cheng ◽  
Hui Wang ◽  
Xian Cao ◽  
Xianning Li

Microbial fuel cells (MFCs) were embedded into constructed wetlands to form microbial fuel cell coupled constructed wetlands (CW-MFCs) and were used for simultaneous azo dye wastewater treatment and bioelectricity generation.


2015 ◽  
Vol 8 (10) ◽  
pp. 950 ◽  
Author(s):  
Farhana Parvin ◽  
Muhammed Mizanur Rahman ◽  
Md. Mahmudul Islam ◽  
Naoshin Jahan ◽  
Md. Pallob Ebna Shaekh ◽  
...  

2010 ◽  
Vol 101 (12) ◽  
pp. 4737-4741 ◽  
Author(s):  
Bor-Yann Chen ◽  
Meng-Meng Zhang ◽  
Chang-Tang Chang ◽  
Yongtao Ding ◽  
Kae-Long Lin ◽  
...  

2018 ◽  
Vol 35 (12) ◽  
pp. 1322-1328
Author(s):  
Luis Enrique Lemus-Gómez ◽  
Maria Aurora Martínez-Trujillo ◽  
Isabel Membrillo-Venegas ◽  
Mayola García-Rivero

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 607 ◽  
Author(s):  
Kamila Malecka ◽  
Shalini Menon ◽  
Gopal Palla ◽  
Krishnapillai Girish Kumar ◽  
Mathias Daniels ◽  
...  

The background: The monolayers self-assembled on the gold electrode incorporated transition metal complexes can act both as receptor (“host” molecules) immobilization sites, as well as transducer for interface recognitions of “guest” molecules present in the aqueous solutions. Their electrochemical parameters influencing the sensing properties strongly depend on the transition metal complex structures. The objectives: The electrochemical characterization of the symmetric terpyridine–M2+–terpyridine and asymmetric dipyrromethene–M2+–terpyridine complexes modified with ssDNA probe covalently attached to the gold electrodes and exploring their ssDNA sensing ability were the main aims of the research presented. The methods: Two transition metal cations have been selected: Cu2+ and Co2+ for creation of redox-active monolayers. The electron transfer coefficients indicating the reversibility and electron transfer rate constant measuring kinetic of redox reactions have been determined for all SAMs studied using: Cyclic Voltammetry, Osteryoung Square-Wave Voltammetry, and Differential Pulse Voltammetry. All redox-active platforms have been applied for immobilization of ssDNA probe. Next, their sensing properties towards complementary DNA target have been explored electrochemically. The results: All SAMs studied were stable displaying quasi-reversible redox activity. The linear relationships between cathodic and anodic current vs. san rate were obtained for both symmetric and asymmetric SAMs incorporating Co2+ and Cu2+, indicating that oxidized and reduced redox sites are adsorbed on the electrode surface. The ssDNA sensing ability were observed in the fM concentration range. The low responses towards non-complementary ssDNA sequences provided evidences for sensors good selectivity. The conclusions: All redox-active SAMs modified with a ssDNA probe were suitable for sensing of ssDNA target, with very good sensitivity in fM range and very good selectivity. The detection limits obtained for SAMs incorporating Cu2+, both symmetric and asymmetric, were better in comparison to SAMs incorporating Co2+. Thus, selection of the right transition metal cation has stronger influence on ssDNA sensing ability, than complex structures.


Chemosphere ◽  
2020 ◽  
Vol 244 ◽  
pp. 125510 ◽  
Author(s):  
Guang Guo ◽  
Xiaohua Li ◽  
Fang Tian ◽  
Tingfeng Liu ◽  
Feng Yang ◽  
...  

2012 ◽  
Vol 43 (5) ◽  
pp. 760-766 ◽  
Author(s):  
Qian Zhang ◽  
You Hai Jing ◽  
Angus Shiue ◽  
Chang-Tang Chang ◽  
Bor-Yann Chen ◽  
...  

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