Degradation of azo dye methyl red by alkaliphilic, halotolerant Nesterenkonia lacusekhoensis EMLA3: application in alkaline and salt-rich dyeing effluent treatment

Extremophiles ◽  
2017 ◽  
Vol 21 (3) ◽  
pp. 479-490 ◽  
Author(s):  
Amrik Bhattacharya ◽  
Nidhi Goyal ◽  
Anshu Gupta
2017 ◽  
Vol 125 ◽  
pp. 62-72 ◽  
Author(s):  
Simin Vatandoostarani ◽  
Tayebe Bagheri Lotfabad ◽  
Amir Heidarinasab ◽  
Soheila Yaghmaei

Desalination ◽  
2011 ◽  
Vol 274 (1-3) ◽  
pp. 272-277 ◽  
Author(s):  
Lamia Ayed ◽  
Abdelkarim Mahdhi ◽  
Abdelkarim Cheref ◽  
Amina Bakhrouf

2014 ◽  
Vol 31 (10) ◽  
pp. 541-547 ◽  
Author(s):  
Yan Liu ◽  
Xi-Kui Wang ◽  
Bing Chen ◽  
Chen Wang ◽  
Ting-Ting Shen

2011 ◽  
Vol 181-182 ◽  
pp. 257-260
Author(s):  
David Statman ◽  
Andrew Jockers ◽  
Daniel Brennan

Chiral nematic liquid crystals prepared with Grandjean texture demonstrate a photonic bandgap whose central wavelength is proportional to the pitch length, P, of the liquid crystal and whose width is given by (ne – no)P. We show that methyl red doped chiral nematics undergo a shift in the photonic bandgap upon photo-isomerization. This shift is a result of (1) photo-induced change in anchoring energy on the nematic surface, and (2) change in the natural pitch length from the photo-isomerization of the azo dye.


2014 ◽  
Vol 1010-1012 ◽  
pp. 928-933
Author(s):  
Ju Chi Kuang ◽  
Xiao Gang Chen ◽  
Min Hua Chen

The principle and methodology of effluent treatment by iron-carbon micro electrolysis were introduced in the paper. Then design of the orthogonal experiments for dyeing effluent treatment was formulated. Discussion of influences of related factors on effluent treatment followed. Results were got after the detailed analysis. Therefore, we deduced the mechanism that the cations of Transition Metal (TM) and rare earth (RE) assist of zero-valent irons catalyzing degradation of dyeing effluent. The mechanism is formed based on the following explanation. Cations of manganese and cobalt easily penetrate Fe0lattices, while Ce4+cations do it difficultly because of their larger radius. Thus Ce4+is weaker than both of Mn2+and Co2+for helping zero-valent irons to improve their activity. Furthermore, because the valence electron structure of Mn2+is more stable than that of Co2+, Mn2+is better for assisting zero-valent iron catalysis of degradation of dyeing effluent than Co2+. Therefore, ranking of influence for zero-valent iron catalysis activity from greatest to smallest is Mn2+, Co2+and Ce4+.


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