scholarly journals Decolorization of Orange-G Aqueous Solutions over C60/MCM-41 Photocatalysts

2019 ◽  
Vol 9 (9) ◽  
pp. 1958 ◽  
Author(s):  
John Kyriakopoulos ◽  
Eleana Kordouli ◽  
Kyriakos Bourikas ◽  
Christos Kordulis ◽  
Alexis Lycourghiotis

The majority of the photocatalysts studied for azo-dye degradation are based on semiconductor materials. Studies reported on non-semiconducting materials are very scarce. In the present work, we studied the fullerene (C60) ability to accelerate photodegradation of the dye’s azo bond in the presence of ascorbic acid. A series of C60 supported on ordered mesoporous silica (MCM-41) catalysts, containing 1, 3, 6, 9, and 12 wt % of fullerene C60, was studied using Orange G (OG) as representative azo-dye. This study showed that partial decolorization is achieved in the dark by simple adsorption of the dye on the bare surface of the carrier. The extent of decolorization increases with the irradiation of the suspension due to photocatalytic degradation of the azo-bond. This is maximized over the sample containing 3 wt % of C60 and it has been attributed to the best combination of the extent of the dye adsorption with the high intrinsic photocatalytic activity of small C60 clusters predominated in this sample. This catalyst proved to be quite stable upon five subsequent photocatalytic cycles, losing less than 5% of its initial activity. No degradation of OG takes place in the absence of ascorbic acid.

2016 ◽  
Vol 18 (26) ◽  
pp. 17237-17243 ◽  
Author(s):  
Marta Falkowska ◽  
Sarayute Chansai ◽  
Haresh G. Manyar ◽  
Lynn F. Gladden ◽  
Daniel T. Bowron ◽  
...  

Total neutron scattering has been used to follow the hydrogenation of toluene-d8 to methylcyclohexane-d14 over 3 wt% platinum supported on highly ordered mesoporous silica (MCM-41) at 298 K and under 150–250 mbar D2 pressure.


2021 ◽  
Vol 21 (5) ◽  
pp. 2847-2854
Author(s):  
Alessandra Scano ◽  
Federico Ebau ◽  
Valentina Cabras ◽  
Franca Sini ◽  
Guido Ennas

In this work, the influence of the use of alternative inexpensive silica sources on the structural, morphological and textural properties of MCM-41 like mesoporous materials to be used for biomedical applications has been investigated. The Liquid Crystal Template Method has been used to prepare the ordered mesoporous structured materials according to a novel composition starting from fumed silica or granular silica gel as alternative silica sources. The obtained materials have been characterized by X-ray Powder Diffraction, Transmission and Scanning Electron Microscopy, and nitrogen sorption, which showed for both samples the formation of the ordered hexagonal pore arrangement typical of a MCM-41 material. However, when using fumed silica, higher long-range hexagonal pore ordering as well as higher surface area have been obtained (1030 vs. 763 m2/g). For comparison, the features of a commercial silica mesostructured MCM-41 type have been investigated as well. Again, the silica fumed based sample has showed higher long-range hexagonal pore ordering, higher surface area and wall thickness. Preliminary stability studies on the fumed silica based material showed a decrease in the pore ordering at the end of the third year after the synthesis.


2019 ◽  
Vol 55 (38) ◽  
pp. 5507-5510 ◽  
Author(s):  
Aleksandr Glotov ◽  
Nikolay Levshakov ◽  
Anna Stavitskaya ◽  
Maria Artemova ◽  
Pavel Gushchin ◽  
...  

Self-assembly of ordered silica arrays on clay nanotubes resulted in mesoporous MCM-41 type materials with enhanced catalytic properties.


2015 ◽  
Vol 7 (23) ◽  
pp. 10052-10060 ◽  
Author(s):  
Bingqian Han ◽  
Nan Chen ◽  
Dongyang Deng ◽  
Shaojuan Deng ◽  
Igor Djerdj ◽  
...  

A series of ordered mesoporous silica loaded with samarium oxide (Sm-MCM-41) were synthesized by a facile one-step sol–gel route using CTAB as the template, TEOS as the silica source, and hexahydrated samarium chloride as the precursor.


2012 ◽  
Vol 133 (2-3) ◽  
pp. 850-856 ◽  
Author(s):  
P.B. Lihitkar ◽  
Samuel Violet ◽  
Mandar Shirolkar ◽  
Jai Singh ◽  
O.N. Srivastava ◽  
...  

2010 ◽  
Vol 636-637 ◽  
pp. 54-59 ◽  
Author(s):  
F. Sezões ◽  
Manuela M.L. Ribeiro Carrott ◽  
Paulo A.M. Mourão ◽  
P.A. Russo ◽  
Peter J.M. Carrott

Lysozyme and BSA were used, as model proteins of considerably different dimensions, in order to evaluate the influence of the distinct pore structural characteristics of three types of ordered mesoporous silica materials (MCF, SBA-15 and MCM-41) on protein adsorption. Characterisation by X ray diffraction and nitrogen adsorption at 77K revealed the typical pore structural features of each type of material. The maximum of the pore size distributions indicated that the width of the windows of MCF (2) (mesitylene/P123 of 2) was larger than the pore diameter of the unidirectional tubular pores of SBA-15. All the materials presented similar small external surface areas but high pore volumes, with that of MCF (2) being the highest. The adsorption of lysozyme at pH=8 increased in the order MCM-41<< SBA-15< MCF (2), and the uptakes were well above those of BSA at pH=5. Although BSA is not completely excluded from the mesopores of SBA-15 and MCF (2), as happens with MCM-41, the adsorption occurs to a very limited extent. The overall behaviour of these SBA-15 and MCF (2) samples was not significantly different and both revealed potential for the separation of these proteins.


Author(s):  
Xin Zhang ◽  
Yingzhi Qin ◽  
Weiting Zhang ◽  
Yali Zhang ◽  
Guang-En Yuan

Abstract Orange G (OG), a typical azo dye in textile wastewaters, has been the subject of intense investigations. This study investigated oxidative degradation of OG in aqueous solution by persulfate (PS) activated with pyrite. A complete destruction of OG was achieved within 60 min in the pyrite/PS system. Lower solution pH, smaller pyrite particles and higher pyrite dosage was beneficial for OG degradation. Higher PS concentration was also in favour of OG degradation, but excess PS would decrease the removal efficiency of OG. The addition of HCO3− and H2PO4− but Cl− had inhibitory effects on the destruction of OG. The results of quenching experiments and electron paramagnetic resonance tests proved that SO4•− and •OH were the dominant reactive species responsible for OG degradation in the pyrite/PS system. The azo bond, naphthalene ring and benzene ring of OG were all destroyed by the generated reactive species. The mineralization rate of OG reached 34.4% after 60 min of reaction. This work will provide information for understanding azo dye degradation by pyrite activated PS.


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