Organometallic precursor induced defect-enriched mesoporous CeO2 with high specific surface area: preparation and catalytic performance

2020 ◽  
Vol 8 (28) ◽  
pp. 14006-14014 ◽  
Author(s):  
Shaowei Yang ◽  
Haidong Shen ◽  
Fang Cheng ◽  
Chen Wu ◽  
Yueling Cao ◽  
...  
Keyword(s):  
Physicochemical Properties ◽  
Specific Surface ◽  
Porous Structure ◽  
Surface Area ◽  
Catalytic Performance ◽  
High Specific Surface Area ◽  
Surface Areas ◽  
Organometallic Precursor ◽  
Specific Surface Areas ◽  
Mesoporous Ceo2

CeO2 with special physicochemical properties including high specific surface areas, suitable porous structure and surface enriched defects has been prepared by an organometallic precursor induced method.

scholarly journals The Effects of Various Parameters of the Microwave-Assisted Solvothermal Synthesis on the Specific Surface Area and Catalytic Performance of MgF2 Nanoparticles

Materials ◽  
2020 ◽  
Vol 13 (16) ◽  
pp. 3566
Author(s):  
Yawen Wang ◽  
Zahra Gohari Bajestani ◽  
Jérôme Lhoste ◽  
Sandy Auguste ◽  
Annie Hémon-Ribaud ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Solvothermal Synthesis ◽  
Catalytic Performance ◽  
High Specific Surface Area ◽  
Microwave Assisted ◽  
Surface Areas ◽  
Specific Surface Areas ◽  
Nanoparticle Sizes

High-specific-surface-area MgF2 was prepared by microwave-assisted solvothermal synthesis. The influences of the solvent and the magnesium precursors, and the calcination atmospheres, on the nanoparticle sizes and specific surface areas, estimated by X-Ray Powder Diffraction, N2 sorption and TEM analyses, were investigated. Nanocrystallized (~7 nm) magnesium partially hydroxylated fluorides (MgF2−x(OH)x) with significant specific surface areas between 290 and 330 m2∙g−1 were obtained. After activation under gaseous HF, MgF2−x(OH)x catalysts underwent a large decrease of both their surface area and their hydroxide, rates as shown by their 19F and 1H solid-state NMR spectra. Expect for MgF2 prepared from the acetate precursor, an activity of 30–32 mmol/h∙g was obtained which was about 40% higher compared with that of MgF2 prepared using Trifluoroacetate method (21.6 mmol/h∙g).

scholarly journals An eco-friendly route for template-free synthesis of high specific surface area mesoporous CeO2 powders and their adsorption for acid orange 7

RSC Advances ◽  
2019 ◽  
Vol 9 (39) ◽  
pp. 22366-22375 ◽  
Author(s):  
Yaohui Xu ◽  
Ruixing Li ◽  
Yang Zhou
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Specific Surface Area ◽  
Acid Orange 7 ◽  
Acid Orange ◽  
Surface Areas ◽  
Template Free ◽  
Specific Surface Areas ◽  
Mesoporous Ceo2

An eco-friendly route for template-free synthesis of mesoporous CeO2 powders with high specific surface areas.

Effect of Different Silicate Supports on the Catalytic Performance of MoVTeO Mixed Oxides in Partial Oxidation of Isobutane

2014 ◽  
Vol 12 (1) ◽  
pp. 623-628
Author(s):  
Jing Hu ◽  
Zhifang Li ◽  
Xiaoyuan Yang ◽  
Wenli Ding ◽  
Jingqi Guan
Keyword(s):  
Catalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Partial Oxidation ◽  
Mixed Oxides ◽  
Supported Catalysts ◽  
Catalytic Performance ◽  
Surface Areas ◽  
Specific Surface Areas ◽  
Mcm 41

Abstract A series of 5% MoV0.3Te0.25 supported on different silicates (i.e. SiO2, HMS, MCM-41, and MCM-48) have been prepared, characterized, and tested as catalysts in the partial oxidation of isobutane to methacrolein. Characterization results showed that the supports almost kept intact structures after supporting 5 wt.% MoV0.3Te0.25 and the supported catalysts had large specific surface areas. Catalytic tests showed that the specific surface area played a key role in the catalytic activity for the supported catalysts.

scholarly journals Preparation and characterization of high specific surface area Mn3O4 from electrolytic manganese residue

2010 ◽  
Vol 8 (5) ◽  
pp. 1059-1068 ◽  
Author(s):  
Tiefeng Peng ◽  
Longjun Xu ◽  
Hongchong Chen
Keyword(s):  
Particle Size ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Magnetic Measurements ◽  
High Specific Surface Area ◽  
Surface Areas ◽  
Electrolytic Manganese ◽  
Electrolytic Manganese Residue ◽  
Specific Surface Areas

AbstractMn3O4 powders have been produced from Electrolytic Manganese Residue (EMR). After leaching of EMR in sulfuric acid, MnSO4 solution containing various ions was obtained. Purifying the solution obtained and then adding aqueous alkali to the purified MnSO4 solution, Mn(OH)2 was prepared. Two methods were employed to produce Mn3O4. One way was oxidation of Mn(OH)2 in aqueous phase under atmosphere pressure to obtain Mn3O4. The other way was roasting Mn(OH)2 precursors in the range of 500°C to 700°C. The prepared samples were investigated by using several techniques including X-ray powder diffraction (XRD), Fourier Transformation Infra-Red (FTIR) spectra, and Brunauer-Emmett-Teller (BET) specific surface area instrument. Particle distribution and magnetic measurements were carried out on laser particle size analyzer, vibrating sample magnetometer (VSM). Through XRD, FTIR and determination of total Mn content (TMC), the products prepared were confirmed to be a single phase Mn3O4. BET specific surface areas can reach to 32 m2 g−1. The results indicated that products synthesized by aqueous solution oxidation method had higher specific surface areas and smaller particle size than those prepared by means of roasting. However the products prepared using the above two methods showed no obvious differences in magnetic property.

Fabrication of an N-doped mesoporous bio-carbon electrocatalyst efficient in Zn–air batteries by an in situ gas-foaming strategy

2019 ◽  
Vol 55 (100) ◽  
pp. 15117-15120 ◽  
Author(s):  
Hong Wang ◽  
Wei Li ◽  
Zhiwei Zhu ◽  
Yijuan Wang ◽  
Pan Li ◽  
...  
Keyword(s):  
Specific Surface ◽  
Porous Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
Electrocatalytic Activity ◽  
High Specific Surface Area ◽  
Carbon Catalyst ◽  
Gas Foaming

An N-doped bio-carbon catalyst with a hierarchical interconnected macro/meso-porous structure and high specific surface area exhibited significantly enhanced electrocatalytic activity.

Hierarchically porous carbons from an emulsion-templated, urea-based deep eutectic

2017 ◽  
Vol 5 (31) ◽  
pp. 16376-16385 ◽  
Author(s):  
Katya Kapilov-Buchman ◽  
Lotan Portal ◽  
Youjia Zhang ◽  
Nina Fechler ◽  
Markus Antonietti ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Specific Surface ◽  
Porous Structure ◽  
Surface Area ◽  
Porous Carbon ◽  
High Specific Surface Area ◽  
Hierarchically Porous ◽  
Carbon Monolith ◽  
A Chain ◽  
Micrometer Scale

A hierarchically porous carbon monolith (97% porosity) was generated through the carbonization of an emulsion-templated monolith formed from a chain extended, urea-based, deep-eutectic polymer. The highly interconnected micrometer-scale porous structure had a high specific surface area (812 m2 g−1, largely microporous) and exhibited promising results for aqueous solution sorption applications.

A Comparison of Methods for Determining Surface Areas of Carbon Black

1973 ◽  
Vol 46 (1) ◽  
pp. 192-203 ◽  
Author(s):  
R. A. Klyne ◽  
B. D. Simpson ◽  
M. L. Studebaker
Keyword(s):  
Carbon Black ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Surface Areas ◽  
Furnace Black ◽  
Area Increase ◽  
Experimental Errors ◽  
Specific Surface Areas ◽  
Surface Area Increase

Abstract 1. The various tint tests correlate with each other—it does not make much difference which of the three procedures is used. The discrimination between similar blacks is comparable. Specific surface areas obtained by the three methods are comparable and differences appear to be due to experimental errors. (Compare Figures 5–7). 2. Surface areas larger than some 90 to 100 m2/g cannot be reliably determined from tint strength measurements alone. 3. Structure exerts a pronounced effect on tint strength of furnace blacks, especially above 90 to 100 m2/g. Porosity and/or composition are apparently also variables which affect tinting strength. 4. Densichron reflectance on the dry carbon black can be used to estimate specific surface areas up to about 140 m2/g; but, since theabsoluteerrorincreases as the specific surface area increases, this method loses some of its reliability at values above about 110 m2/g. The relative error in reflectance determinations does not vary greatly over the furnace-black range. Densichron reflectance is influenced by composition, evidently due to composition-related differences in optical properties of the carbons. 5. In CTAB adsorption measurements, titration errors and handling errors tend to be rather constant for blacks of different surface area. Hence, CTAB permits better discrimination among blacks of small particle size. 6. The errors in Densichron reflectance surface area increase with specific surface area. Hence, the deviations between CTAB and reflectance surface area which are due to experimental error increase with the surface area of the sample.

Experimental Studies of Carbon Electrodes With Various Surface Area for Li–O2 Batteries

2019 ◽  
Vol 16 (4) ◽  
Author(s):  
Fangzhou Wang ◽  
P. K. Kahol ◽  
Ram Gupta ◽  
Xianglin Li
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Discharge Capacity ◽  
Carbon Materials ◽  
High Specific Surface Area ◽  
Acetylene Black ◽  
Carbon Electrodes ◽  
Tea Leaves ◽  
Surface Areas

Li−O2 batteries with carbon electrodes made from three commercial carbons and carbon made from waste tea leaves are investigated in this study. The waste tea leaves are recycled from household tea leaves and activated using KOH. The carbon materials have various specific surface areas, and porous structures are characterized by the N2 adsorption/desorption. Vulcan XC 72 carbon shows a higher specific surface area (264.1 m2/g) than the acetylene black (76.5 m2/g) and Super P (60.9 m2/g). The activated tea leaves have an extremely high specific surface area of 2868.4 m2/g. First, we find that the commercial carbons achieve similar discharge capacities of ∼2.50 Ah/g at 0.5 mA/cm2. The micropores in carbon materials result in a high specific surface area but cannot help to achieve higher discharge capacity because it cannot accommodate the solid discharge product (Li2O2). Mixing the acetylene black and the Vulcan XC 72 improves the discharge capacity due to the optimized porous structure. The discharge capacity increases by 42% (from 2.73 ± 0.46 to 3.88 ± 0.22 Ah/g) at 0.5 mA/cm2 when the mass fraction of Vulcan XC 72 changes from 0 to 0.3. Second, the electrode made from activated tea leaves is demonstrated for the first time in Li−O2 batteries. Mixtures of activated tea leaves and acetylene black confirm that mixtures of carbon material with different specific surface areas can increase the discharge capacity. Moreover, carbon made from recycled tea leaves can reduce the cost of the electrode, making electrodes more economically achievable. This study practically enhances the discharge capacity of Li−O2 batteries using mixed carbons and provides a method for fabricating carbon electrodes with lower cost and better environmental friendliness.

Micro/Nanostructured α-Fe2O3 with Structural Enhanced Removal Capacity of Cr(VI) Ions

2012 ◽  
Vol 518-523 ◽  
pp. 1753-1756 ◽  
Author(s):  
Gang Liu ◽  
Quan Deng ◽  
Yong Yang ◽  
Hui Min Wang ◽  
Guo Zhong Wang
Keyword(s):  
Specific Surface ◽  
Porous Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
Average Diameter ◽  
High Specific Surface Area ◽  
Removal Capacity

We have succeeded in preparing micro/nanostructured α-Fe2O3 spheres (MNFSs). The resulted MNFSs have an average diameter of about 5 µm, and are constructed by subunits of interlinked and elongated particles with a diameter of 20~60 nm. MNFSs show an obviously structural enhanced Cr(VI) removal capacity (5.88 mg/g) compared with nanoscaled (0.81 mg/g) and microscaled α-Fe2O3 (0.1 mg/g) due to its high specific surface area together with the special porous structure. Moreover, MNFSs show good availability of reusing to remove Cr(VI) ions.

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