High Catalytic Efficiency of Nanostructured β-CoMoO4 in the Reduction of the Ortho-, Meta- and Para-Nitrophenol Isomers

被引:18
作者
Al-Wadaani, Fahd [1 ]
Omer, Ahmed [1 ]
Abboudi, Mostafa [1 ]
Hassani, Hicham Oudghiri [1 ,2 ]
Rakass, Souad [1 ]
Messali, Mouslim [1 ]
Benaissa, Mohammed [3 ]
机构
[1] Taibah Univ, Chem Dept, Coll Sci, Almadinah 30002, Saudi Arabia
[2] Cegep Drummondville, Dept Sci Nat, 960 Rue St Georges, Drummondville, PQ J2C 6A2, Canada
[3] Univ Mohammed 5, Fac Sci, Dept Phys, LMPHE, BP 1014 RP, Rabat 10000, Morocco
关键词
nanostructures; beta-CoMoO4; nitrophenol reduction; nanoparticles; ELECTROCHEMICAL PROPERTIES; PHOTOCATALYTIC ACTIVITY; THERMAL-DECOMPOSITION; COMOO4; OXALATE; CO; OXIDATION; MOLYBDATE; NANOPARTICLES; TEMPERATURE;
D O I
10.3390/molecules23020364
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nanostructured beta-CoMoO4 catalysts have been prepared via the thermal decomposition of an oxalate precursor. The catalyst was characterized by infrared spectroscopy (FTIR), X-ray diffraction (XRD), Brunauer-Emmett-Teller method (BET), energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The efficiency of these nanoparticles in the reduction of ortho- and meta-nitrophenol isomers (2-NP, 3-NP, and 4-NP) to their corresponding aminophenols was tested using UV-visible spectroscopy measurements. It was found that, with a beta-CoMoO4 catalyst, NaBH4 reduces 3-NP instantaneously, whilst the reduction of 2-NP and 4-NP is slower at 8 min. This difference is thought to arise from the lower acidity of 3-NP, where the negative charge of the phenolate could not be delocalized onto the oxygen atoms of the meta-nitro group.
引用
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页数:10
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共 34 条
[1]   Synthesis of CuO, La2O3, and La2CuO4 by the Thermal-Decomposition of Oxalates Precursors Using a New Method [J].
Abboudi, Mostafa ;
Messali, Mouslim ;
Kadiri, Naima ;
Ben Ali, Abdelouahid ;
Moran, Emilio .
SYNTHESIS AND REACTIVITY IN INORGANIC METAL-ORGANIC AND NANO-METAL CHEMISTRY, 2011, 41 (06) :683-688
[2]   Improving humidity sensing properties of nanoporous TiO2-10 mol% SnO2 thin film by co-doping with La3+ and K+ [J].
Anbia, Mansoor ;
Fard, S. Ebrahim Moosavi .
SENSORS AND ACTUATORS B-CHEMICAL, 2011, 160 (01) :215-221
[3]   Synthesis of nanocrystalline Mn-Zn ferrite powders through thermolysis of mixed oxalates [J].
Angermann, Andre ;
Toepfer, Joerg .
CERAMICS INTERNATIONAL, 2011, 37 (03) :995-1002
[4]   Effect of phase composition of the oxidic precursor on the HDS activity of the sulfided molybdates of Fe(II), Co(II), and Ni(II) [J].
Brito, JL ;
Barbosa, AL .
JOURNAL OF CATALYSIS, 1997, 171 (02) :467-475
[5]   Ultra-small and low crystalline CoMoO4 nanorods for electrochemical capacitors [J].
Duc Tai Dam ;
Huang, Tan ;
Lee, Jong-Min .
SUSTAINABLE ENERGY & FUELS, 2017, 1 (02) :324-335
[6]   Preparation of cobalt molybdate nanoparticles; Taguchi optimization and photocatalytic oxidation of Reactive Black 8 dye [J].
Edrissi, Mohammad ;
Samadanian-Isfahani, Samaneh ;
Soleymani, Meysam .
POWDER TECHNOLOGY, 2013, 249 :378-385
[7]   CoMoO4 as a novel heterogeneous catalyst of peroxymonosulfate activation for the degradation of organic dyes [J].
Fan, Yanan ;
Ma, Wenjie ;
He, Jianglong ;
Du, Yunchen .
RSC ADVANCES, 2017, 7 (57) :36193-36200
[8]   Effect of calcination temperature on Co(II) oxalate dihydrate-iron(II) oxalate dihydrate mixture DTA-TG, XRD, Mossbauer, FT-IR and SEM studies (Part II) [J].
Gabal, MA ;
El-Bellihi, AA ;
Ata-Allah, SS .
MATERIALS CHEMISTRY AND PHYSICS, 2003, 81 (01) :84-92
[9]   Investigation of phase formation temperature of nano-sized solid solution of copper/cobalt molybdate and chromium-phosphate (M1xCr1-xMoxP1-xO4) [M1 = Co, Cu] [J].
Ghorai, TK ;
Dhak, D ;
Azizan, A ;
Pramanik, P .
MATERIALS SCIENCE AND ENGINEERING B-SOLID STATE MATERIALS FOR ADVANCED TECHNOLOGY, 2005, 121 (03) :216-223
[10]   Facile reduction of nitrophenols: Comparative catalytic efficiency of MFe2O4 (M = Ni, Cu, Zn) nano ferrites [J].
Goyal, Ankita ;
Bansal, S. ;
Singhal, Sonal .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2014, 39 (10) :4895-4908