scholarly journals One-step synthesis of zinc-encapsulated MCM-41 as H2S adsorbent and optimization of adsorption parameters

2020 ◽  
Vol 3 (02) ◽  
pp. 74-81
Author(s):  
Nastaran Hazrati ◽  
Ali Akbar Miran Beigi ◽  
Majid Abdouss ◽  
Amir Vahid
Keyword(s):  
Pore Diameter ◽  
High Specific Surface Area ◽  
Adsorption Parameters ◽  
N2 Adsorption ◽  
Structure Directing Agent ◽  
Functionalized Mesoporous Silica ◽  
One Step ◽  
Ammonia Aqueous Solution ◽  
Adsorption Desorption ◽  
Mcm 41

The nano-sized structure of well-ordered Zn@MCM-41 adsorbent was synthesized through a direct hydrothermal method using CTAB as a structure-directing agent in an ammonia aqueous solution with different amounts of zinc acetylacetonate which were inserted into the structure-directing agent's loop during the synthesis. The XRD, HRTEM, and N2 adsorption-desorption isotherms were used to characterize the prepared ZnO functionalized mesoporous silica samples. As a result, the presence of ZnO in highly-ordered MCM-41's pore was proved as well as maintenance of the ordered mesostructure of MCM-41. The materials were possessed with a high specific surface area (1114-509 m2.g-1) and a large pore diameter (4.03-3.27 nm). Based on the obtained results from the adsorption of H2S gas in a lab-made setup, the Znx@MCM-41 showed the superior ability to increase of ZnO amount up to 7 hours as a breakthrough point. 

Nanosized Titanium Oxynitride and Molybdenum Oxynitride Particles Assembled in Mesoporous Silica MCM-41

2006 ◽  
Vol 510-511 ◽  
pp. 138-141 ◽  
Author(s):  
Shan Zheng ◽  
Lian Gao
Keyword(s):  
Composite Materials ◽  
Mesoporous Silica ◽  
Mesoporous Materials ◽  
N2 Adsorption ◽  
Xps Spectra ◽  
Desorption Isotherms ◽  
Adsorption Desorption ◽  
Nitridation Temperature ◽  
Mcm 41

Titanium oxynitride and molybdenum oxynitride assembled in the pores of mesoporous materials were achieved by nitriding titania-modified MCM-41 and molybdena-modified MCM-41 at 800°C for 3 hours under flowing NH3 atmosphere. XRD, XPS and N2 adsorption-desorption isotherms were employed to characterize the structure of the composite materials. The results showed that the nanosized TiOxNy and MoOxNy particles were assembled in mesoporous silica MCM-41 with the restrict mesopores. The hexagonal periodicity of the parent MCM-41 materials was maintained upon assembly at the provided nitridation temperature. The exact formation was TiO0.4N0.8 in MCM-TiOxNy, and MoO1.7N0.57 in MCM-MoOxNy, which were calculated from the data in XPS spectra of Ti 2p and Mo 3d.

Comparison of TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 Hybrid Catalysts in Characteristics and Photodegradation of Tetramethylammonium

2010 ◽  
Vol 93-94 ◽  
pp. 22-26 ◽  
Author(s):  
Surachai Artkla ◽  
Won Yong Choi ◽  
Jatuporn Wittayakun
Keyword(s):  
Irradiation Time ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
N2 Adsorption ◽  
X Ray ◽  
Transmission Electron ◽  
Photocatalytic Activities ◽  
Adsorption Desorption ◽  
Two Hybrid ◽  
Mcm 41

This work compared properties and catalytic performance of two hybrid photocatalysts, TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 prepared by loading nanoparticles of TiO2 (10 wt.%) on MCM-41 synthesized with rice husk silica and tetraethyl orthosilicate respectively. The supports and catalysts were characterized by X-ray diffraction, N2 adsorption-desorption, transmission electron microscopy and zeta potential. The photocatalytic activities of the TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 for the degradation of tetramethylammonium (TMA) in aqueous slurry were similar with a complete conversion after irradiation time of 90 min at pH 7.

Catalytic Activity of Dehydrogenation of Methanol to MF over Cu/MCM-41 and Cu-ZnO/MCM-41 Prepared by Impregnation and Grinding

2011 ◽  
Vol 396-398 ◽  
pp. 730-733
Author(s):  
Guo Ru Li ◽  
Gong Li ◽  
Shu Xi Zhou ◽  
Hui Juan Tong
Keyword(s):  
Catalytic Activity ◽  
Atmospheric Pressure ◽  
Molecular Sieves ◽  
Conversion Rate ◽  
Methyl Formate ◽  
Methanol Conversion ◽  
N2 Adsorption ◽  
Flow Microreactor ◽  
Adsorption Desorption ◽  
Mcm 41

Abstract. Using MCM-41 molecular sieves as the support, Cu-ZnO/MCM-41 and Cu/MCM-41 catalysts were prepared by impregnation and grinding. The catalysts were characterized by XRD, N2 adsorption-desorption and TPR methods. The catalytic activity of the dehydrogenation of methanol to methyl formate (MF) was evaluated using the flow microreactor under atmospheric pressure. According to the results, the catalyst prepared by impregnation had a better selectivity for the MF, but a lower methanol conversion rate. However, the product's selectivity could be improved by adding ZnO additive while the methanol conversion rate was reduced. For Cu/MCM-41 prepared by impregnation and grinding, the methanol conversion rate was 20.18% and 24.13% respectively at 250°C and the MF selectivity was 73.75% and 67.35% respectively. Likewise for Cu-ZnO/MCM-41 prepared by impregnation and grinding, the methanol conversion rate was 15.28% and 18.83% respectively at 250°C and the MF selectivity was 81.31% and 75.32% respectively.

Efficient Removal of Cd2+ by the Mesoporous Silica Functionalized by APTES

2013 ◽  
Vol 726-731 ◽  
pp. 2409-2412
Author(s):  
Xiao Feng Cai ◽  
Kang Wei Ji ◽  
Wan Hao Wu ◽  
Jie Hou ◽  
Shi You Hao
Keyword(s):  
Aqueous Solution ◽  
Mesoporous Silica ◽  
Ph Value ◽  
High Surface ◽  
High Surface Area ◽  
Efficient Removal ◽  
Structure Directing Agent ◽  
Functionalized Mesoporous Silica ◽  
Adsorption Desorption ◽  
Large Pore Size

Amino-functionalized mesoporous silica (AFMS) with high amino loading, high surface area, and large pore size was synthesized using the anionic surfactant N-lauroylsarcosine sodium (Sar-Na) as template and 3-aminopropyltriethoxysilane (APTES) as co-structure directing agent (CSDA). The synthesized AFMS was characterized by N2adsorption-desorption, TEM and elemental analyzer. The results of the removal of Cd2+from aqueous solution showed that the pH value of aqueous solution affected the removal efficiency of Cd2+greatly, and that unary adsorption isotherm of Cd2+on the AFMS was well described by the Sips isotherm model, in which the adsorption capacity was 2.43 mmol/g for Cd2+, much higher than the literature data.

scholarly journals Hydrogenation of 1-octene by Co-Mo/MCM-41 catalysts

2012 ◽  
Vol 23 (2) ◽  
pp. 133-136
Author(s):  
Chol Ryong Jang ◽  
Vasile Matei ◽  
Anca Borcea ◽  
Viorel Voicu ◽  
Raluca Proscanu ◽  
...  
Keyword(s):  
Detection Limit ◽  
Metal Species ◽  
Synthesis And Characterization ◽  
N2 Adsorption ◽  
Hydrogenation Activity ◽  
Bet Specific Surface Area ◽  
Xrd Patterns ◽  
Adsorption Desorption ◽  
Mcm 41

AbstractThe synthesis and characterization of MCM-41 supported Co-Mo catalysts and catalytic hydrogenation of 1-octene to n-octane were discussed. BET specific surface area of MCM-41, calculated from N2 adsorption/desorption isotherm, was 1690 m2/g. The XRD patterns of the Co-Mo/MCM-41 catalysts show that metal species are finely dispersed and the size of CoO and MoO3 particles is below the detection limit by XRD. The 1-octene hydrogenation activity of the catalysts decreased with increasing the Co content up to 9 wt.% for the Co-promoted Co-Mo/MCM-41 catalysts with a MoO3 content of 12 wt.%. All the catalysts show increased hydrogenation activity with increasing reaction temperature in the temperature range from 200 to 350°C.

scholarly journals Synthesis and characterization of mesoporous materials with SBA and MCM structure types

Cerâmica ◽  
2019 ◽  
Vol 65 (376) ◽  
pp. 585-591
Author(s):  
R. A. Sacramento ◽  
O. M. S. Cysneiros ◽  
B. J. B. Silva ◽  
A. O. S. Silva
Keyword(s):  
Surface Area ◽  
Mesoporous Materials ◽  
High Surface ◽  
High Surface Area ◽  
Textural Properties ◽  
N2 Adsorption ◽  
Structure Directing Agent ◽  
Type Iv ◽  
Xrd Patterns ◽  
Adsorption Desorption

Abstract Mesoporous materials are promising structures for application in catalysis and adsorption due to high surface area and large pore size. Mesoporous materials were synthesized by the hydrothermal method with novel surfactants, distinct from those observed in the literature, in order to carry out a study of its structure and to obtain materials with better textural properties. The structures synthesized with the surfactants Igepal CO630 and Brij O20 presented the best results of specific surface area, 1074 and 1075 m2.g-1, respectively. The obtained materials were characterized by XRD, TG/DTG, N2 adsorption-desorption, and FTIR techniques. XRD patterns indicated that the highly ordered mesoporous silica structures, such as MCM-41 and MCM-48, using CTMABr as the structure-directing agent and the SBA-15, SBA-16 and other SBA structures using different block copolymers were obtained. Through N2 adsorption-desorption isotherms, it was observed type IV isotherms, attributed to mesoporous materials. The FTIR spectra presented similar behaviors with characteristic vibrational bands of MCM and SBA type materials.

scholarly journals Synthesis of micro-mesopores flowerlike γ-Al2O3 nano-architectures

2014 ◽  
Vol 79 (8) ◽  
pp. 1007-1017 ◽  
Author(s):  
Mozaffar Abdollahifar ◽  
Reza Zamani ◽  
Ehsan Beiygie ◽  
Hosain Nekouei
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Total Pore Volume ◽  
High Specific Surface Area ◽  
X Ray Diffraction ◽  
N2 Adsorption ◽  
X Ray ◽  
Adsorption Desorption

The micro-mesopores flowerlike ?-Al2O3 nano-architectures have been synthesized by thermal decomposition method using the synthesized AlOOH (boehmite) as precursor. After calcination at 500?C for 5 h, the obtained flowerlike ?-Al2O3 has similar structure like the AlOOH precursor. X-ray diffraction (XRD), FTIR, TG, FESEM and TEM techniques were used to characterize morphology and structure of the synthesized samples. The specific surface area (BET), pore volume and pore-size distribution of the products were determined by N2 adsorption-desorption measurements. The flowerlike ?-Al2O3 showed BET high specific surface area 148 m2 g-1 with total pore volume 0.59 cm3 g-1.

scholarly journals Synthesis, Characterization and Textural Analysis of Functionalized Mesoporous Silica Using Sodium Silicate as Precursor and Silicone Surfactant as Template

2014 ◽  
Vol 11 (2) ◽  
pp. 419-428
Author(s):  
Baghdad Science Journal
Keyword(s):  
Mesoporous Silica ◽  
Sodium Silicate ◽  
Nitrogen Adsorption ◽  
Average Diameter ◽  
Functionalized Silica ◽  
Average Pore ◽  
Force Microscopy ◽  
Functionalized Mesoporous Silica ◽  
One Step ◽  
Adsorption Desorption

Three mesoporous silica with different functional group were prepared by one-step synthesis based on the simultaneous hydrolysis and condensation of sodium silicate with organo - silane in the presence of template surfactant polydimethylsiloxane - polyethyleneoxide (PDMS - PEO). The prepared materials were characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), atomic force microscopy (AFM) and nitrogen adsorption/desorption experiments. The results indicate that the preparation of methyl and phenyl functionalized silica were successful and the mass of methyl and phenyl groups bonded to the silica structure are 15, 38 mmol per gram silica. The average diameter of the silica particles are 103.51, 167.25 , and 86.41 nm while the average pore diameter are 6.7, 16.4, and 2.7 nm for unfunctionalized, methyl, and phenyl functionalized silica respectively.

Molecular design of the amphiphilic AB diblock copolymer toward one-step synthesis of amino-group functionalized large pore mesoporous silica

RSC Advances ◽  
2014 ◽  
Vol 4 (81) ◽  
pp. 43047-43051 ◽  
Author(s):  
Dongpo Xu ◽  
Yuan Yao ◽  
Lu Han ◽  
Shunai Che
Keyword(s):  
Acrylic Acid ◽  
Mesoporous Silica ◽  
Pore Size ◽  
Diblock Copolymer ◽  
Molecular Design ◽  
Amino Group ◽  
Structure Directing Agent ◽  
Functionalized Mesoporous Silica ◽  
One Step ◽  
Loading Amount

A functionalized mesoporous silica with an amino group loading amount of 3.1 mmol g−1 and a pore size of 27.5 nm was achieved by the co-structure directing agent (CSDA) method using poly(styrene)-b-poly(acrylic acid) (PS-b-PAA) as the template.

scholarly journals A one-step self-sustained low temperature carbonization of coconut shell biomass produced a high specific surface area biochar-derived nano-adsorbent

2019 ◽  
Vol 37 (5) ◽  
pp. 551-555 ◽  
Author(s):  
Mohd Hafif Samsudin ◽  
Mohd Ali Hassan ◽  
Juferi Idris ◽  
Norhayati Ramli ◽  
Mohd Zulkhairi Mohd Yusoff ◽  
...  
Keyword(s):  
Low Temperature ◽  
Surface Area ◽  
Pore Diameter ◽  
Total Pore Volume ◽  
High Specific Surface Area ◽  
Coconut Shell ◽  
Activation Process ◽  
One Step ◽  
Separate Activation ◽  
Nano Adsorbent

A one-step self-sustained carbonization of coconut shell biomass, carried out in a brick reactor at a relatively low temperature of 300–500°C, successfully produced a biochar-derived adsorbent with 308 m2/g surface area, 2 nm pore diameter, and 0.15 cm3/g total pore volume. The coconut shell biochar qualifies as a nano-adsorbent, supported by scanning electron microscope images, which showed well-developed nano-pores on the surface of the biochar structure, even though there was no separate activation process. This is the first report whereby coconut shell can be converted to biochar-derived nano-adsorbent at a low carbonization temperature, without the need of the activation process. This is superior to previous reports on biochar produced from oil palm empty fruit bunch.

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