A review on microbial potential of toxic azo dyes bioremediation in aquatic system

2022 ◽  
pp. 241-261
Author(s):  
Raya Majumdar ◽  
Wasim Akram Shaikh ◽  
Sukalyan Chakraborty ◽  
Santanu Chowdhury
2018 ◽  
Vol 21 (2) ◽  
pp. 59-63
Author(s):  
Muhamad Abduh Hasibuan ◽  
Didik Setiyo Widodo ◽  
Retno Ariadi Lusiana

Study on decolourization of remazol black B (RBB) solution has been performed in a scale up reactor. As an artificial waste, the dye sample that contains azo groups is difficult to decompose under ordinary environmental conditions so it requires further treatment before discharging to open aquatic system. Many efforts have been reported and further developed toward other azo dyes. One of an outstanding approach is Fenton method. This study modified the method with PbO2 rather than Fe2+. In this modification, the dyestuff was degraded by radical •OH resulting from reaction between H2O2 and Pb2+ ion generated from PbO2. In Preliminary works, decolourization was performed and optimized in lab-scaled. Analysis were conducted and the best condition was applied to decolorize the sample in a scale-up size. Characteristics of the reactor was also determined. Results showed that at optimum condition, 100 mL of 50 ppm remazol black B was decolorized up to 98.82 % within 15 minutes. On scale up to 1 L-sized reactor, within the time highest percentages of remazol black B decolourization was reached 82.02 % by addition of 10 % H2O2 and COD decrease to 98.96 %. In the 1 L reactor, RBB sample with concentration of 50 ppm, PbO2 1 gram and H2O2 10 % obey the proposed decolourization equation of D = -0,0011x2 + 0.5705x – 0.6788 with x = volume peroxide (in mL), D = percent of decolourization.


2019 ◽  
Vol 9 (02) ◽  
Author(s):  
Zena G. Alrecabi ◽  
Zainab Amer ◽  
Naeemah Al-Lami

This study including prepared new colored esters containing heterocyclic with high molecular weights. In the first part of work we synthesized azo dyes [1,2] from the reaction p-toluidine with β-naphthol and o-nitro phenol, thin we synthesized Schiff bases [3,4] by the reaction anthranilic acid with benzaldehyde and dimethyl benzaldehyde. The reaction azo dyes (contain OH group) with Schiff base (contain COOH group) these led to produce the new colored esters [A1-A4]. The second part of work was modification the (C=N-) group in esters to heterocyclic compounds by reacting with phenyl iso cyanide to produce new β-lactam [B1-B4] and with anthranilic acid to get new hydroquinazoline [C1-C4]. All these compounds were characterized by physical properties and spectral methods FTIR, 1H-NMR and 13C-NMR.


2000 ◽  
Vol 42 (5-6) ◽  
pp. 329-336 ◽  
Author(s):  
M. Quezada ◽  
I. Linares ◽  
G. Buitrón

The degradation of azo dyes in an aerobic biofilter operated in an SBR system was studied. The azo dyes studied were Acid Red 151 and a textile effluent containing basic dyes (Basic Blue 41, Basic Red 46 and 16 and Basic Yellow 28 and 19). In the case of Acid Red 151 a maximal substrate degradation rate of 288 mg AR 151/lliquid·d was obtained and degradation efficiencies were between 60 and 99%. Mineralization studies showed that 73% (as carbon) of the initial azo dye was transformed to CO2 by the consortia. The textile effluent was efficiently biodegraded by the reactor. A maximal removal rate of 2.3 kg COD/lliquid·d was obtained with removal efficiencies (as COD) varying from 76 to 97%. In all the cycles the system presented 80% of colour removal.


2015 ◽  
Vol 11 (2) ◽  
pp. 147-152
Author(s):  
Wafaa Lemerini ◽  
Zoheir Arrar ◽  
Kajima Joseph ◽  
Zoheir Dahmani ◽  
Wassila Drici ◽  
...  

1994 ◽  
Vol 59 (3) ◽  
pp. 575-581 ◽  
Author(s):  
Zdeněk Skaličan ◽  
Zbyněk Kobliha ◽  
Emil Halámek

Ion-associates of N,N-diethyllysergamide with the sulfophthaleins: Bromoxylenol Blue, Eriochrome Cyanine R, Xylenol Blue, and Cresol Red, and the azo dyes: Acid Black I and Orange-I were studied by extraction spectrophotometry. The extraction recoveries, distribution ratios, conditional extraction constants and limits of detection and determination were calculated.


1989 ◽  
Vol 54 (7) ◽  
pp. 2021-2026
Author(s):  
Marie Stiborová ◽  
Befekadu Asfaw ◽  
Pavel Anzenbacher

Ce(IV) ions in acidic medium convert a carcinogenic non-aminoazo dye, 1-phenylazo-2-hydroxy-naphthalene (Sudan I) into an ultimate carcinogen, which binds to calf thymus DNA. The principal product of Sudan I oxidation by the Ce(IV) system is the benzenediazonium ion. A minor product is the dihydroxyderivative of Sudan I, 1-(4-hydroxyphenylazo)-2,6-dihydroxynaphthalene. Other minor coloured products (yellow and brown) were not identified. The principal product (the benzenediazonium ion) is responsible for the carcinogenicity of Sudan I, as it covalently binds to DNA. Ce(IV) ions in acidic medium represent a suitable model system, which imitates the activation route of carcinogenic azo dyes.


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