Preparation of catalyst as Au doped Mn1Co9Ox/ceramic system for total oxidation of CO

2021 ◽  
Vol 10 (4) ◽  
pp. 39-45
Author(s):  
Phuong Pham Thi Mai ◽  
Hoan Nguyen Quoc ◽  
Quan Do Quoc ◽  
Hung Nguyen Thanh

In this paper, the Au doped Mn1Co9Ox was investigated for total oxidation of CO. The sol-gel method was applied to prepare this catalyst and some modern analysis methods as XRD, EPR, TPx, SEM were utilized to characterize its properties. The XRD patterns showed only Co3O4 phase without any peaks belonging to Mn or Au. However, the presence of Au and Mn was confirmed by EPR and O2-TPD results. With the aim to further apply catalyst in reality, the Au doped Mn1Co9Ox was deposited on ceramic by sol-gel, wet impregnation. The SEM images displayed the successful coating of active phase on substrate. However, the complete catalyst system didn’t have the high activity in total CO oxidation like the catalyst powder because of large agglomerations on coatings.

2017 ◽  
Vol 727 ◽  
pp. 327-334
Author(s):  
Yan Wang ◽  
Jun Wang ◽  
Xiao Fei Zhang ◽  
Ya Qing Liu

La-Nd co-doped barium hexaferrites, Ba0.7(LamNdn)0.3Fe12O19 (D-BaM), were successfully prepared by sol-gel method. PANI / D-BaM composites were synthesized by in-situ polymerization in solution. The structure, morphology and properties of samples have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), four-probe conductivity tester and vector network analyzer. The XRD patterns showed that the crystal structure of all the samples exist as M-type phases. The SEM images revealed that the particles presented a hexagonal platelet-like morphology. The magnetic properties could be improved by substitutions of La and Nd ions. The saturation magnetization (Ms) and coercive force (Hc) increased with the change of La / Nd ratio to the maximum at La / Nd = 3:1. The doped particles have also been embedded in conductive PANI to prepare electromagnetic materials, and the conductivity kept on the order of 10-2. The microwave absorbing properties of composites at 30 MHz-6 GHz improved obviously, the peak value of reflection loss could reach-7.5 dB.


2021 ◽  
Vol 12 (4) ◽  
pp. 2523-2529
Author(s):  
Daniel Sam N ◽  
Anish C I ◽  
Sabeena G ◽  
Rajaduraipandian S ◽  
Manobala ◽  
...  

Sol gel methods were used for the study of the antimicrobial activity of Cd-TiO2 against gram-negative and positive bacteria. These Cd-TiO2 have been characterized by various optical and techniques. They have been exhibited by X-ray diffraction, scanning electron microscopy, ultraviolet spectroscopy, and infrared spectroscopy. The structures of the various XRD patterns indicate that the product has a structure. The particle size of Cd-TiO2 is 35nm. The SEM images confirm the spherical appearance of the sample. The energy X-ray spectra have been confirmed as well and then C, O, Ti, Cd, Pt element are present in Cd-TiO2. The weight percentage of Cadmium is 5.8%, Ti is 51.03%, C is 5.13% and O is 31.75% in Cd-TiO2. BET image shows that the major pore size distribution of Cd-TiO2 is ranged from 2.24 nm. The Cd-TiO2 that the antibacterial activity when tested against the pathogens only gram-negative bacteria such as Pseudomonas. The zone of minimum inhibition concentration was measured in a range of 20mm in 25μl and 30mm in 100μl.


2020 ◽  
Vol 842 ◽  
pp. 182-185
Author(s):  
Sha Sha Wang ◽  
Yue Long Xu ◽  
Li Hui Zhang ◽  
Zhen Fa Liu

Phloroglucinol–resorcinol–formaldehyde (PRF) carbon aerogels were synthesized by sol–gel reaction. The results of condition of shrinkage showed a degree of crosslinking more obvious with the increasing of the carbonization temperature. CA900 displays the highest adsorption amount and the biggest loops, as well as an increase in pore size and volume in comparison to the others samples. The SEM images of carbon aerogels under different carbonization temperature possess closer network structure and excellent connectivity, the holes between the network are abundant. The XRD patterns show that the high carbonization temperature can enhance the graphitization degree of carbon aerogels.


2013 ◽  
Vol 726-731 ◽  
pp. 720-724 ◽  
Author(s):  
Jian Hua Li ◽  
Meng Jie Feng ◽  
Mei Lin Jia

A series of mesoporous TiO2 supports were synthesized by the sol-gel template method by using different surfactant and Au/TiO2 catalysts were prepared by the solution reduction method. The catalytic oxidation of CO was taken as the probe reaction for comparing the catalyst activity. Wide-angle XRD patterns and N2 adsorption–desorption isotherms revealed that the TiO2 with crystallized anatase and mesoporous structure can be synthesized after an optimized sol-gel template method. The results indicated that the pore size of TiO2 plays a key role in the catalyst activity. Among them the activity of Au/TiO2-F1 catalyst synthesized by using the F127 surfactant demonstrated superior activity to other catalysts. CO could be converted at 70 °C.


2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Beyene Tesfaw Ayalew ◽  
P. Vijay Bhaskar Rao

Ce0.5Sr0.5 (Co0.8Fe0.2)1−x ZrxO3−δ (CSCFZ) powders were synthesized by the sol-gel method and characterized to study structural and electrochemical properties. X-ray diffractometer (XRD) patterns of all samples give nanosized particles of a high-degree crystalline cathode having a cubic-type perovskite structure of space group Pm-3m with the existence of oxygen vacancies in the lattices. The results have the perovskite phase with average crystallite sizes of 26.57 nm, 18.14 nm, 18.13 nm, and 18.12 nm with porosities of 9.93%, 9.87%, 9.50%, and 9.08% for x = 0, 0.1, 0.15, and 0.2, respectively. Scanning electron microscope (SEM) micrographs showed the presence of pores on the microstructure. Average grain sizes of prepared samples found from SEM images were in the range of 105.30–183.02 nm. The partial substitution of zirconium at the B-site shows more stable materials than the host without decreasing the porosity that much. The results of electronic conductivity analyzed by the four-probe dc technique show that the conductivity of synthesized materials increases with the increment of both dopant concentration and temperature by the decrement of area specific resistances. The electrical conductivity of CSCFZ steadily increased with the increment of temperature which reached 42.76 Scm−1 at around 450°C.


2013 ◽  
Vol 32 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Sima Alikhanzadeh-Arani ◽  
Masoud Salavati-Niasari ◽  
Fatemeh Davar

AbstractA modified sol-gel synthesis route has been used to prepare the fine homogeneous powder of Sr2CuO3 ceramic using strontium nitrate, copper nitrate, diethylene glycol monobutyl ether and citric acid. XRD patterns showed that the temperature of forming Sr2CuO3 is about 900°C and single phase of Sr2CuO3 with high purity obtains at 950°C. Influence of concentration of citric acid on the structure of prepared materials was investigated by SEM images.


Materials ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 5470
Author(s):  
Jorge Cortez-Elizalde ◽  
Ignacio Cuauhtémoc-López ◽  
Zenaida Guerra-Que ◽  
Alejandra Elvira Espinosa de los Monteros ◽  
Ma. Antonia Lunagómez-Rocha ◽  
...  

NiWAu trimetallic nanoparticles (NPs) on the surface of support Al2O3-CeO2-TiO2 were synthesized by a three-step synthetic method in which Au NPs were incorporated into presynthesized NiW/Al2O3-CeO2-TiO2. The recharge method, also known as the redox method, was used to add 2.5 wt% gold. The Al2O3-CeO2-TiO2 support was made by a sol–gel method with two different compositions, and then two metals were simultaneously loaded (5 wt% nickel and 2.5 wt% tungsten) by two different methods, incipient wet impregnation and ultrasound impregnation method. In this paper, we study the effect of Au addition using the recharge method on NiW nanomaterials supported on mixed oxides on the physicochemical properties of synthesized nanomaterials. The prepared nanomaterials were characterized by scanning electron microscopy, BET specific surface area, X-ray diffraction, diffuse reflectance spectroscopy in the UV–visible range and temperature-programmed desorption of hydrogen. The experimental results showed that after loading of gold, the dispersion was higher (46% and 50%) with the trimetallic nanomaterials synthesized by incipient wet impregnation plus recharge method than with impregnation plus ultrasound recharge method, indicating a greater number of active trimetallic (NiWAu) sites in these materials. Small-sized Au from NiWAu/ACTU1 trimetallic nanostructures was enlarged for NiWAu/ACT1. The strong metal NPs–support interaction shown for the formation of NiAl2O4, Ni-W-O and Ni-Au-O species simultaneously present in the surface of trimetallic nanomaterial probably plays an important role in the degree of dispersion of the gold active phase.


2007 ◽  
pp. 69-74 ◽  
Author(s):  
Marijana Kovacevic ◽  
Erne Kis ◽  
Goran Boskovic

Mesoporous nanocristalline SnO2 supports were synthesized by a modified sol-gel method starting from SnCl2?2H2O and citric acid at pH 2.0 and 9.5. Noble metal was introduced via wet impregnation using PdCl2 as active phase precursor. Catalysts activities in water denitration were correlated with their textural, structural and morphological properties using LTNA (BET), XRD and SEM/EDS analysis. Lower pH value during the catalyst synthesis resulted in a final material characterized with more developed porosity and higher surface area. Although both catalysts turned out to be tailored from nanoscale crystallites, higher pore fraction of mesopores resulting from the synthesis in acidic conditions, was found to be responsible for superior catalytic behavior.


2014 ◽  
Vol 979 ◽  
pp. 208-211 ◽  
Author(s):  
Apichaya Worawong ◽  
Tula Jutarosaga ◽  
Wandee Onreabroy

Magnetite (Fe3O4) nanoparticles were successfully synthesized by the sol-gel method from ferric nitrate-EG (EG=ethylene glycol) gel. The precursors were calcined in argon under an atmospheric pressure at the temperatures varied from 400°C to 500°C. The synthesized magnetic nanoparticles were characterized by X-ray diffractrometer (XRD), field emission scanning electron microscope (FE-SEM) and vibrating sample magnetometer (VSM). The XRD patterns of powder calcined temperature at 400๐C showed clearer Fe3O4phase than those calcined at other temperatures. The particle size and morphology of magnetic nanoparticles were studied using FE-SEM. The FE-SEM images showed that the particle sizes varied from 30-108 nm. The particle sizes increased with the increase of calcination temperature. VSM measurements indicated that the Fe3O4nanoparticles were soft ferrite with the maximum magnetization (Mm) and coercivity (Hc) of 35 emu/g and 17 Oe, respectively.


2011 ◽  
Vol 675-677 ◽  
pp. 375-378
Author(s):  
Peng Song ◽  
Qi Wang

In this paper, perovskite LaFeO3 nanoparticles were synthesised by a sol-gel method. Then, polypyrrole (PPy)/LaFeO3 nanocomposites were prepared by a simple in situ chemical polymerization method. By means of X-ray diffraction (XRD), Fourier transform infrared (FTIR) and scanning electron microscopy (SEM), the microstructure of PPy/LaFeO3 nanocomposites was characterized. The XRD patterns indicated that LaFeO3 nanoparticles have a perovskite phase with orthorhombic structure, and incorporation of PPy did not change the crystalline structure of LaFeO3. The PPy was evenly dispersed on the surface of LaFeO3 particles, which was endorsed by FTIR spectral analyses. And SEM images indicate that the PPy was evenly dispersed on the surface of LaFeO3 particles without apparent agglomeration. And we found that the nanocomposites exhibited a higher response to CO gas.


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