Controllable synthesis of Ni nanotube arrays and their structure-dependent catalytic activity toward dye degradation

CrystEngComm ◽  
2014 ◽  
Vol 16 (21) ◽  
pp. 4406-4413 ◽  
Author(s):  
Xiang-Zi Li ◽  
Kong-Lin Wu ◽  
Yin Ye ◽  
Xian-Wen Wei

Ni nanotube (nanorod) arrays are controllably fabricated by a one-step approach, the GDDATG and DDCG growth mechanisms are introduced. The Ni nanostructures present higher catalytic activities for dye degradation, the relationship between structures and catalytic properties is also studied.

2014 ◽  
Vol 1033-1034 ◽  
pp. 95-98
Author(s):  
Peng Yang ◽  
Shi Yu Zhou ◽  
Jia Heng Lei

Mesoporous ceria catalysts were prepared by nanocasting of a mesoporous carbon and KIT-6. The prepared mesoporous ceria catalysts were used to catalyze CO oxidation. The various characterization techniques were employed to study the relationship between catalyst nature and catalytic properties. The results indicate that ceria prepared by using mesoporous carbon as template possess an ordered mesoporous architecture and exhibit much better catalytic activity compared with those prepared by using KIT-6 as template. The residual SiO2from KIT-6 was demonstrated to be the main reason for the much worse catalytic activities by the characterization results of X-ray Fluorescence Spectrometer and FTIR spectra.


2010 ◽  
Vol 24 (25n26) ◽  
pp. 5128-5138 ◽  
Author(s):  
SILVIA GONZALEZ ◽  
CARMEN SOUSA ◽  
FRANCESC ILLAS

The study of bimetallic catalysts has scientific and technologic importance because of special catalytic activity towards several reactions. RhCu is an interesting bimetallic system due to combination of the very different catalytic activities of Rh and Cu. The catalytic activity of this bimetallic does not result from simple interpolation of the constituents. In fact, at low Cu content, the catalytic activity of RhCu is superior to that of Rh but when the Cu content is higher the activity decays. This is a curious trend which theoretical works had attempted to explain. This paper reports an overview of the most recent research works about this bimetallic system with emphasis in its especial characteristics.


Materials ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 142
Author(s):  
Bartłomiej Rogalewicz ◽  
Tomasz Maniecki ◽  
Radosław Ciesielski ◽  
Agnieszka Czylkowska

In one of our previously published articles, we reported the synthesis, spectroscopic, thermal, and catalytic properties of four new M(II) acetate (where M = Co, Ni, Cu, Zn) complexes with imidazole. Presented compounds exhibited activity in the reaction on catalytic oxidation of styrene. In this study we have synthesized and investigated properties of analogous compounds, however using formates or propionates of mentioned metal cations instead of acetates. Such an approach allowed us to draw valuable conclusions concerning the relationship between the carbon chain length and catalytic activity, which is an important factor for catalyst modeling. Synthesized compounds have been thoroughly investigated using appropriate analytic techniques: AAS (Atomic Absorption Spectrometry), FTIR (Fourier-Transform Infrared Spectroscopy), and TGA (Thermogravimetric Analysis). Catalytic properties have been studied under the same previous conditions, using GC-FID (GC-chromatograph equipped with FID detector).


1995 ◽  
Vol 12 (2) ◽  
pp. 119-128 ◽  
Author(s):  
G.A. El-Shobaky ◽  
A.M. Ghozza ◽  
S. Hammad

Manganese/aluminium mixed oxide solids having the formula 0.2MnCO3/Al2O3 were prepared by mechanical mixing of a known weight of finely powdered manganese carbonate and aluminium hydroxide. The solids obtained were treated with NaNO3 (0.75–6 mol%) solution and dried at 110°C, then calcined in air at 500°C and 800°C for 6 h. The phases produced were identified by XRD analysis. The surface properties (SBET, Vp and r̄) of the pure and doped solids were studied by using N2 adsorption at – 196°C and their catalytic activities were determined by studying the oxidation of CO by O2at 125–300°C. The results obtained reveal that pure and doped mixed solids preheated in air at 500°C and 800°C consist of Mn2O3 (partridgite) and a poorly crystalline γ-alumina. Doping with sodium oxide at 500°C and 800°C resulted in a small decrease (14–19%) in the SBET value of the treated solids. However, this treatment brought about a significant modification in the catalytic activity of the doped solids. Doping with 0.75% Na2O at 500°C led to an increase of about 30–50% in the specific catalytic activity which was found to decrease on increasing the percentage of Na2O above this limit, falling to values smaller than that measured for the undoped catalyst. Doping at 800°C led to a progressive decrease in the activity of the treated solid to an extent proportional to the amount of dopant present. The doping process at 500°C and 800°C did not modify the mechanism of the catalytic reaction but altered the number of catalytically-active sites contributing in the catalysis of CO oxidation by O2 without changing their energetic nature.


RSC Advances ◽  
2015 ◽  
Vol 5 (96) ◽  
pp. 78457-78467 ◽  
Author(s):  
Lei Zhang ◽  
Jin-Song Hu ◽  
Cheng-Ling Pan ◽  
Xin-Hua Huang ◽  
Chang-Min Hou

Novel Bi25VO40 microcubes were successfully prepared via a facile hydrothermal synthesis route and they exhibited excellent optical and catalytic properties.


2015 ◽  
Vol 778 ◽  
pp. 144-147
Author(s):  
Si Qin Deligen ◽  
Bao Agula

The mesoporous CeO2were prepared via a surfactant-assisted method of nanoparticle assembly, CTAB was used as surfactant. The mesoporous CeO2were used as the supports for preparingxAu/CeO2catalysts by the chemical reduction method, and the catalytic activities of the total oxidation of propane were studied. The prepared catalysts were characterized by XRD, TEM and N2adsorption techniques. The content of Au can affect the catalytic properties of thexAu/CeO2catalysts. 4Au/CeO2exhibited the highest catalytic activity in propane complete oxidation with theT100of 420 °C.


Nanomaterials ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 197 ◽  
Author(s):  
Min Yang ◽  
Genli Shen ◽  
Mi Liu ◽  
Yunfa Chen ◽  
Zhen Wang ◽  
...  

The catalytic activities of CeO2-MnOx composite oxides synthesized through oxalate method were researched. The results exhibited that the catalytic properties of CeO2-MnOx composite oxides were higher than pure CeO2 or MnOx. When the Ceat/Mnat ratio was 3:7, the catalytic activity reached the best. In addition, the activities of CeO2-MnOx synthesized through different routes over benzene oxidation were also comparative researched. The result indicated that the catalytic property of sample prepared by oxalate method was better than others, which maybe closely related with their meso-structures. Meanwhile, the effects of synergistic interaction and oxygen species in the samples on the catalytic ability can’t be ignored.


2009 ◽  
Vol 66 ◽  
pp. 57-60 ◽  
Author(s):  
Xue Hui Huang ◽  
Hao Chen ◽  
Ting Ting Wu

A series of perovskite-like catalusts La4BaCu5-xNixO13+δ (x=0,1,2,3,4,5) were prepared by the citrate method, the structures, forms, properties, and defect structures were studied by means of XRD, SEM, BET and TPD measurements. Meanwhile, their catalytic activities were evaluated by the studying of CO, CH4 oxidation. La4BaCu2Ni3O13+δ shows the highest catalytic activity.


Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 408 ◽  
Author(s):  
Chao Wang ◽  
Wenchao Hua ◽  
Guangtao Chai ◽  
Chuanhui Zhang ◽  
Yanglong Guo

Co3O4 catalysts of cube and sphere shapes were prepared by one-step hydrothermal synthesis with different controlled amounts of Co(NO3)2·6H2O and NaOH. The morphological effects on both physicochemical properties and catalytic activities of vinyl chloride oxidation were investigated by material characterization and performance evaluation. The obtained results showed that the morphology, resulting in the exposure difference of crystal planes, significantly affected the catalytic property. The catalytic activity for vinyl chloride oxidation followed a descending order of Co3O4 cube (Co3O4-c) > Co3O4 sphere (Co3O4-s) > Co3O4 commercial (Co3O4-com). The cube-shaped Co3O4 presented higher catalytic activity and stability than Co3O4 spheres despite their similar crystallographic structures as well as physicochemical and redox properties. Accordingly, the different catalytic behaviors should be attributed to a morphological effect. The Co3O4 cube with a preferential exposure of (001) plane presented higher abundance of surface Co2+ cations and adsorbed oxygen species, which acted as the active sites responsible for the improvement of its catalytic activity.


1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka

The catalytic properties of two-component catalyst nickel oxide-cadmium oxide with the proportions of the components covering the whole composition region 0-100% were examined by studying the decomposition of hydrogen peroxide in aqueous solution on it. In the range 0-25 mol.% CdO, cadmium oxide is found to affect infavourably the ability of nickel oxide to chemisorb oxygen. The amount of the chemisorbed oxygen increases several times on gamma irradiation of the samples. The effect of cadmium oxide on the catalytic activity of the system shows up in fresh samples only indirectly via the changed amount of the oxygen chemisorbed. In older samples the initial catalytic activity of the system is changed, which can be explained based on the concept of bivalent catalytic centres in terms of the co-action of the catalytic centres of the two oxides, which are in equilibrium. The irradiation of the system under study speeds up the processes leading to the establishing of this equilibrium which is thermally very stable, and results in a substantial increase of the catalytic activity of the samples investigated.


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