Intensified-Fenton process for the treatment of phenol aqueous solutions

2014 ◽  
Vol 71 (3) ◽  
pp. 359-365 ◽  
Author(s):  
M. Isabel Pariente ◽  
Raúl Molina ◽  
Juan Antonio Melero ◽  
Juan Ángel Botas ◽  
Fernando Martínez

An intensified-Fenton process for the treatment of phenol aqueous solutions has been studied as a continuous catalytic wet hydrogen peroxide oxidation system. This process consists of coupling the catalytic activity of a heterogeneous Fenton-like catalyst with the homogeneous contribution of its dissolved iron species. Agglomerated mesoporous SBA-15 silica-supported iron oxide (Fe2O3/SBA-15) material was used as heterogeneous catalyst. The influence of the reaction temperature and the initial hydrogen peroxide dosages was studied in order to minimize the operation cost of the process. The catalytic performance of the process was assessed in terms of total organic carbon (TOC) and hydrogen peroxide conversions. Likewise, the stability of the solid Fenton-like catalyst was also evaluated in terms of the dissolved iron species. The increase of the reaction temperature enhanced the TOC conversion and reduced the iron leaching from the heterogeneous catalyst. These results were related to the degradation of oxalic acid as responsible for iron extraction by formation of soluble stable iron complexes into the aqueous medium. Finally, the use of a moderate hydrogen peroxide concentration (2.6 g/L) and milder temperatures (80–120 °C) has led to remarkable results of TOC and phenol reductions as well as oxidant efficiency through the intensified-Fenton process.

2017 ◽  
Vol 53 (3) ◽  
pp. 407-412
Author(s):  
M. Dimitrijevic ◽  
D. Urosevic ◽  
S. Milic ◽  
M. Sokic ◽  
R. Markovic

Leaching of copper smelting slag in chloride media was studied. The lixiviants used were aqueous solutions of hydrochloric acid (0.5-2.0 M HCl) as well as hydrogen peroxide and hydrochloric acid (0.5-3.0 M H2O2, 1.0 M HCl). The maximum final copper extraction from the slag of 73% was attained with 3 M H2O2, at room temperature after 120 minutes of reaction. At the same time, 55% of the iron from the slag was also dissolved. The copper extraction increased during the first 60 minutes of reaction and essentially ceased thereafter. Because of a rapid catalytic decomposition of hydrogen peroxide, it should be added contiuously to the leach suspension rather than at once at the begining of the experiment. In fact, it appears that almost complete dissolution of copper from the slag is achievable after about 4 hours of leaching by implementing the method of continuous lixiviant addition. Also, it seems that the final iron extraction could be limitied to as low as 20% by using this method.


2010 ◽  
Vol 9 (3) ◽  
pp. 351-360 ◽  
Author(s):  
Abdelnaser Omran ◽  
Hamidi Abdul Aziz ◽  
Marniyanti Mamat Noor

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 283
Author(s):  
Oxana Kholdeeva ◽  
Nataliya Maksimchuk

In recent years, metal–organic frameworks (MOFs) have received increasing attention as selective oxidation catalysts and supports for their construction. In this short review paper, we survey recent findings concerning use of MOFs in heterogeneous liquid-phase selective oxidation catalysis with the green oxidant–aqueous hydrogen peroxide. MOFs having outstanding thermal and chemical stability, such as Cr(III)-based MIL-101, Ti(IV)-based MIL-125, Zr(IV)-based UiO-66(67), Zn(II)-based ZIF-8, and some others, will be in the main focus of this work. The effects of the metal nature and MOF structure on catalytic activity and oxidation selectivity are analyzed and the mechanisms of hydrogen peroxide activation are discussed. In some cases, we also make an attempt to analyze relationships between liquid-phase adsorption properties of MOFs and peculiarities of their catalytic performance. Attempts of using MOFs as supports for construction of single-site catalysts through their modification with heterometals will be also addressed in relation to the use of such catalysts for activation of H2O2. Special attention is given to the critical issues of catalyst stability and reusability. The scope and limitations of MOF catalysts in H2O2-based selective oxidation are discussed.


1970 ◽  
Vol 48 (18) ◽  
pp. 2948-2948
Author(s):  
C. E. Burchill ◽  
I. S. Ginns

not available


1979 ◽  
Vol 18 (7) ◽  
pp. 1971-1973 ◽  
Author(s):  
Mark M. Morrison ◽  
Julian L Roberts ◽  
Donald T. Sawyer

1955 ◽  
Vol 3 (4) ◽  
pp. 379 ◽  
Author(s):  
W. V. Mayneord ◽  
W. Anderson ◽  
H. D. Evans ◽  
D. Rosen

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