scholarly journals Synthesis of Mo2C by Thermal Decomposition of Molybdenum Blue Nanoparticles

Nanomaterials ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 2053 ◽  
Author(s):  
Natalia Gavrilova ◽  
Victor Dyakonov ◽  
Maria Myachina ◽  
Victor Nazarov ◽  
Valery Skudin
Keyword(s):  
Thermal Decomposition ◽  
Pore Size ◽  
Molybdenum Carbide ◽  
Synthesis Method ◽  
Mesoporous Structure ◽  
Inert Atmosphere ◽  
Molar Ratio ◽  
Narrow Pore Size Distribution ◽  
Molybdenum Blue ◽  
Catalytic Application

In recent years, the development of methods for the synthesis of Mo2C for catalytic application has become especially important. In this work a series of Mo2C samples was synthesized by thermal decomposition of molybdenum blue xerogels obtained using ascorbic acid. The influence of the molar ratio reducing agent/Mo [R]/[Mo] on morphology, phase composition and characteristics of the porous structure of Mo2C has been established. The developed synthesis method allows the synthesis to be carried out in an inert atmosphere and does not require a carburization step. The resulting molybdenum carbide has a mesoporous structure with a narrow pore size distribution and a predominant pore size of 4 nm.

scholarly journals Synthesis of Microporous Mo2C-W2C Binary Carbides by Thermal Decomposition of Molybdenum-Tungsten Blues

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2428
Author(s):  
Natalia Gavrilova ◽  
Maria Myachina ◽  
Victor Dyakonov ◽  
Victor Nazarov ◽  
Valery Skudin
Keyword(s):  
Thermal Decomposition ◽  
Porous Structure ◽  
Synthesis Method ◽  
Nitrogen Adsorption ◽  
Inert Atmosphere ◽  
Platinum Group Metals ◽  
Molar Ratio ◽  
Tungsten Carbides ◽  
Catalytic Systems ◽  
And Tungsten

Molybdenum and tungsten carbides are perspective catalytic systems. Their activity in many reactions is comparable to the activity of platinum group metals. The development of the synthesis method for of highly dispersed binary molybdenum and tungsten carbides is an important task. Dispersions of molybdenum-tungsten blue were used as a precursor for synthesis of binary molybdenum and tungsten carbides. The synthesis of carbides was carried out by thermal decomposition of molybdenum-tungsten blue xerogels in an inert atmosphere. The binary carbides were characterized by XRD, TGA, SEM and nitrogen adsorption. The influence of the molar ratio reducing agent/Me [R]/[ΣMe], molar ratio molybdenum/tungsten [Mo]/[W] on phase composition, and morphology and porous structure of binary carbides was investigated. Samples of binary molybdenum and tungsten carbides with a highly developed porous structure and a specific surface area were synthesized.

Dehydrogenation of Propane to Propene over Mesoporous ZrO2-Supported VCrO Catalysts

2014 ◽  
Vol 1008-1009 ◽  
pp. 290-294
Author(s):  
Bao Agula ◽  
Si Qin Dalai ◽  
Yue Chao Wu
Keyword(s):  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Mesoporous Structure ◽  
Molar Ratio ◽  
Impregnation Method ◽  
Size Distributions ◽  
Tem Analysis ◽  
Surfactant Assisted ◽  
Uniform Pore Size

Mesoporous ZrO2with narrow mesopore size distributions has been prepared by the surfactant-assisted method of nanoparticle assembly. A series of VCrO/ZrO2catalysts with different V/Cr molar ratio (0.3, 0.6, 1.0, 1.3 and 1.6) were prepared by the wetness impregnation method and characterized by XRD, N2adsorption and TEM techniques. N2adsorption and TEM analysis revealed that the surfactant-assisted method prepared VCrO/ZrO2catalysts have wormhole-like mesoporous structure with uniform pore size distribution. VCrO/ZrO2catalysts have been applied for direct dehydrogenation of propane to propene. The optimistic catalyst was V/Cr-0.6 with highest yield of 41.7% the corresponding conversion of propane was 44.1% and selectivity to propene was 94.5% at 550 °C.

Preparation, Characterization and Catalytic Performance of ZnO-SBA-15 Catalysts

2016 ◽  
Vol 690 ◽  
pp. 212-217 ◽  
Author(s):  
Supranee Lao-Ubol ◽  
Rungsinee Khunlad ◽  
Siriporn Larpkiattaworn ◽  
Shih Yuan Chen
Keyword(s):  
Pore Size ◽  
Mesoporous Structure ◽  
Catalytic Performance ◽  
Acid Sites ◽  
Total Acid ◽  
Narrow Pore Size Distribution ◽  
Surface Areas ◽  
Ordered Mesoporous ◽  
Temperature Programmed ◽  
Adsorption Desorption

The series of ZnO-SBA-15 catalysts with 0.9wt% to 8.5wt% ZnO content have been synthesized by solvothermal impregnated of Zn acetate in ethanol on mesoporous silica SBA-15 platelets in order to maximize the methyl ester selectivity in transesterification reaction. The properties of these catalyst were characterized by N2 adsorption-desorption isotherm, NH3 temperature-programmed desorption, SEM, and XRD. The results showed that the ordered mesoporous structure of SBA-15 was remained with specific surface areas above 500 m2/g and a narrow pore size distribution observed with the mean pore size around 60 Å after ZnO modification. The strength of the acid sites and total acid amount of ZnO-SBA-15 catalysts is varied with number of ZnO loadings. The synthesized ZnO-SBA-15 catalyst was tested for catalytic activity in transesterification of crude Jatropha oil. It was found that at 200 °C for 2 h reaction of the ZnO-SBA-15 catalysts with acid capacities of 0.36-1.29 mmol H+/g-catal gave 68-98wt% of FAME yields and 0.4-1.4wt% of FFA yields which are comparable to the pure ZnO.

scholarly journals Simple Synthesis of Molybdenum Carbides from Molybdenum Blue Nanoparticles

Nanomaterials ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 873
Author(s):  
Natalia Gavrilova ◽  
Maria Myachina ◽  
Victor Nazarov ◽  
Valery Skudin
Keyword(s):  
Catalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Molybdenum Carbide ◽  
Synthesis Method ◽  
High Catalytic Activity ◽  
Molybdenum Blue ◽  
Molybdenum Carbides ◽  
Vis Spectroscopy

In recent years, much attention has been paid to the development of a new flexible and variable method for molybdenum carbide (Mo2C) synthesis. This work reports the applicability of nano-size clusters of molybdenum blue to molybdenum carbide production by thermal treatment of molybdenum blue xerogels in an inert atmosphere. The method developed made it possible to vary the type (glucose, hydroquinone) and content of the organic reducing agent (molar ratio R/Mo). The effect of these parameters on the phase composition and specific surface area of molybdenum carbides and their catalytic activity was investigated. TEM, UV–VIS spectroscopy, DTA, SEM, XRD, and nitrogen adsorption were performed to characterize nanoparticles and molybdenum carbide. The results showed that, depending on the synthesis conditions, variants of molybdenum carbide can be formed: α-Mo2C, η-MoC, or γ-MoC. The synthesized samples had a high specific surface area (7.1–203.0 m2/g) and meso- and microporosity. The samples also showed high catalytic activity during the dry reforming of methane. The proposed synthesis method is simple and variable and can be successfully used to obtain both Mo2C-based powder and supports catalysts.

scholarly journals One-step synthesis of nitrogen-grafted copper-gallic acid for enhanced methylene blue removal

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shella Permatasari Santoso ◽  
Vania Bundjaja ◽  
Artik Elisa Angkawijaya ◽  
Chintya Gunarto ◽  
Alchris Woo Go ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Gallic Acid ◽  
Synthesis Method ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
One Step ◽  
Detailed Assessment ◽  
Higher Temperature

AbstractNitrogen-grafting through the addition of glycine (Gly) was performed on a metal- phenolic network (MPN) of copper (Cu2+) and gallic acid (GA) to increase its adsorption capacity. Herein, we reported a one-step synthesis method of MPN, which was developed according to the metal–ligand complexation principle. The nitrogen grafted CuGA (Ng-CuGA) MPN was obtained by reacting Cu2+, GA, and Gly in an aqueous solution at a molar ratio of 1:1:1 and a pH of 8. Several physicochemical measurements, such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), N2 sorption, X-ray diffraction (XRD), and thermal gravimetry analysis (TGA), were done on Ng-CuGA to elucidate its characteristics. The analysis revealed that the Ng-CuGA has non-uniform spherical shaped morphology with a pore volume of 0.56 cc/g, a pore size of 23.25 nm, and thermal stability up to 205 °C. The applicational potential of the Ng-CuGA was determined based on its adsorption capacity against methylene blue (MB). The Ng-CuGA was able to adsorb 190.81 mg MB per g adsorbent at a pH of 6 and temperature of 30 °C, which is 1.53 times higher than the non-grafted CuGA. Detailed assessment of Ng-CuGA adsorption properties revealed their pH- and temperature-dependent nature. The adsorption capacity and affinity were found to decrease at a higher temperature, demonstrating the exothermic adsorption behavior.

Effect of the Synthesis Method on the Properties of Ultrafine YAG Powder

2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Hydrothermal Reaction ◽  
Synthesis Method ◽  
Particle Morphology ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Synthesis Process ◽  
Powder Materials ◽  
Co Precipitation

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.

On the dimorphism of Pr6Mo10O39

2017 ◽  
Vol 72 (11) ◽  
pp. 765-774
Author(s):  
Daniel Rudolph ◽  
Sonja Laufer ◽  
Ingo Hartenbach
Keyword(s):  
Crystal Structure ◽  
Thermal Decomposition ◽  
Single Crystals ◽  
Main Product ◽  
Molar Ratio ◽  
Coordination Environment ◽  
Space Group ◽  
Coordination Numbers ◽  
Dense Modification

AbstractAttempts to synthesize Pr4Mo7O27 using Pr, Pr6O11 and MoO3 in a molar ratio of 8:6:77 led to a main product of scheelite-type Pr0.667[MoO4] and few single crystals of the triclinic A-type Pr6Mo10O39. The latter crystallizes in space group P1̅ (a=945.25(1), b=1058.49(2), c=1815.16(3) pm; α=104.149(1), β=95.220(1), γ=102.617(1)°, Z=2). Its crystal structure comprises six crystallographically independent Pr3+ cations, eight tetrahedral [MoO4]2− units, and one [Mo2O7]2− entity. The cations display coordination numbers of seven (1×) and eight (5×), while the [MoO4]2− tetrahedra are surrounded by five Pr3+ cations each. The [Mo2O7]2− anions exhibit a coordination environment of seven Pr3+ cations. The attempt to synthesize PrF[MoO4] using PrOF (from in situ thermal decomposition of PrF[CO3]) as reagent did not lead to the desired product but to monoclinic B-type Pr6Mo10O39. This slightly less dense modification compared to its triclinic analogue crystallizes in space group C2/c (a=1247.93(3), b=1989.68(6), c=1392.52 (4) pm, β=100.505(2)°, Z=4) with three crystallographically independent Pr3+ cations, four [MoO4]2− tetrahedra, and again one [Mo2O7]2− unit in the crystal structure. Thus, both Pr6Mo10O39 modifications are better described with the structured formula Pr6[MoO4]8[Mo2O7]. The coordination numbers around the Pr3+ cations are seven (1×) and eight (2×) while all four [MoO4]2− anions are again surrounded by five Pr3+ cations each. Six of the latter represent the coordination environment around the [Mo2O7]2− entities. Besides the thorough comparison of the crystal structures single crystal Raman spectra were recorded for both Pr6Mo10O39 phases.

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