Immobilized cells of Rhodococcus strain UCC 0004 as source of green biocatalyst for decolourization and biodegradation of methyl orange

2018 ◽  
Vol 16 ◽  
pp. 569-578 ◽  
Author(s):  
Maegala Nallapan Maniyam ◽  
Nor Suhaila Yaacob ◽  
Hazeeq Hazwan Azman ◽  
Noor Azmahera Ab Ghaffar ◽  
Hasdianty Abdullah
Keyword(s):  
Methyl Orange ◽  
Immobilized Cells ◽  
Rhodococcus Strain

Removal of Methyl Orange from Aqueous Solutions by Using Zn-Al Layered Double Hydroxide as Photocatalyst

2015 ◽  
Vol 1 (2) ◽  
pp. 36-41
Author(s):  
Laura Cocheci ◽  
◽  
Ancuta-Corina Marcu ◽  
Paul Barvinschi ◽  
Aniela Pop
Keyword(s):  
Methyl Orange ◽  
Aqueous Solutions ◽  
Layered Double Hydroxide ◽  
Double Hydroxide

Preparation and Characterization of Polymer Blend (PVA/PEO) Filled with Methyl Orange Thin Films

2018 ◽  
Vol 14 (2) ◽  
pp. 221-234
Author(s):  
Ahmed Namah Mohamed ◽  
◽  
Jafer Fahdel Odah ◽  
Haider Tawfiq Naeem
Keyword(s):  
Thin Films ◽  
Methyl Orange ◽  
Polymer Blend

Kinetic of oxidation of methyl orange by vanadium(V) under conditions VO2+ and decavanadates coexist: Catalysis by Triton X-100 micellar medium

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Methyl Orange ◽  
Solution Ph ◽  
Vanadium Concentration ◽  
Limiting Behavior ◽  
First Order ◽  
First Order Kinetics ◽  
Ph Range ◽  
Kinetic Pattern ◽  
Triton X ◽  
Kinetics Of

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.

Preparation of (Fe, Ni)-Codoped ZnO and Its Photocatalytic Activity for Deg-radation of Methyl Orange

2010 ◽  
Vol 31 (7) ◽  
pp. 797-802 ◽  
Author(s):  
Tianhua FU ◽  
Qianqian GAO ◽  
Fei LIU ◽  
Huajun DAI ◽  
Xingming KOU
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange

Preparation and Photo-catalytic Activity of Cu-Supported Nano-TiO2

2020 ◽  
Vol 1 (1) ◽  
pp. 38-42
Author(s):  
Jun Yan
Keyword(s):  
Catalytic Activity ◽  
Methyl Orange ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Nano Tio2 ◽  
Hydrolysis Method ◽  
Response Range ◽  
Photo Response ◽  
Forced Hydrolysis ◽  
Visible Photocatalytic Activity

Cu-supported nano-TiO2 catalyst was prepared by forced hydrolysis method under mild condition. The morphology, composition and optical absorption properties of the samples were characterized by means of scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS) and UV-Vis diffuse reflectance spectroscopy (UV-VIS DRS). Visible photocatalytic activity of the samples was investigated by photocatalytic degradation experiment on methyl orange. The results indicated that nano-TiO2 was about 20nm in size with the main form of anatase, and photo response range was significantly broadened after it was loaded on the surface of Cu. The sample possessed high visible light catalytic activity, with the degradation rate of methyl orange reaching 94% under simulated natural light.

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