scholarly journals Silvlated MCM-41 Synthesized from RiceHusk

2006 ◽  
Vol 6 (2) ◽  
pp. 91
Author(s):  
N. Ketcome ◽  
N. Grisdanurak

Mesoporous material, MCM-41, synthesized from rice husk (RH-MCM-41) was modified by loading silylating agent (either Trimethylchlorosilane (TMCS), Dimethyl- dichlorosilane (DMCS) or Phenyl-trichlorosilane (PTCS)) in different concentration (1-9 %wt), and aging time, varied from I, 6, 9 and 24 hr. Properties of samples were characterized by XRD, Nz adsorption, FfIR, and TPD and adsorption of water, hexane, and toluene. Chemical modification resulted smaller pore size average and less surface area of RH-MCM-41, from 2.9 to 2.2 nm and from 900 to 500 mZ/g, respectively. PTCS could affect RH-MCM-41 surface structure more than other two. Adsorption behavior of modified RH-MCM-41 was also reflected to comparatively higher hydrophobicity.

2019 ◽  
Vol 964 ◽  
pp. 88-96
Author(s):  
Hariyati Purwaningsih ◽  
Slamet Raharjo ◽  
Vania Mitha Pratiwi ◽  
Diah Susanti ◽  
Agung Purniawan

Rice became the main product of agriculture in agrarian countries including Indonesia. Rice husk is a waste of rice as one of the largest silica producers. Silica from rice husks can be used as a source of silica in the manufacture of sodium silicate as an alternative to the formation of mesoporous silica at a low price. In this research, the characterization of mesoporous silica nanoparticle (MSN) MCM-41 from rice husk (rice husk) with sol-gel method followed by hydrothermal treatment. Silica extraction was performed by titrating sodium silica using HCl method until the gel was formed. The mesoporous synthesis was performed with the addition of CTAB. The titration is then carried out using a solution of acetic acid. XRD shows silica with an amorphous structure. The FTIR results show that extraction silica and MSN MCM-41 contain pure silica displayed with Si-O-Si functional groups in the sample. The SEM results show MSN MCM-41 images such as a coral-like structure of agglomerated silica and the higher temperature hydrothermal treatment then it would be the more large size of particles. The material has a hexagonal pore structure such as a honeycomb as characteristic of MCM-41 with a pore size of 2.535 nm which includes mesoporous material. The result of nitrogen adsorption-desorption isotherms shows lower hydrothermal temperature will increase the specific surface area and decrease average pore size, where the best result with surface area value is 825.365 m2/gr and average pore size is 6.10426 nm obtained from process hydrothermal at 85°C.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Guotao Zhao ◽  
Zhenxiao Zhao ◽  
Junliang Wu ◽  
Daiqi Ye

Fluorine-containing hydrophobic mesoporous material (MFS) with high surface area is successfully synthesized with hydrothermal synthesis method by using a perfluorinated surfactant SURFLON S-386 template. The adsorption properties of water vapor on the synthesized MFS are also investigated by using gravimetric method. Results show that SEM image of the MFS depicted roundish morphology with the average crystal size of 1-2 μm. The BET surface area and total pore volume of the MFS are 865.4 m2 g−1and 0.74 cm3 g−1with a narrow pore size distribution at 4.9 nm. The amount of water vapor on the MFS is about 0.41 mmol g−1at 303 K, which is only 52.6% and 55.4% of MCM-41 and SBA-15 under the similar conditions, separately. The isosteric adsorption heat of water on the MFS is gradually about 27.0–19.8 kJ mol−1, which decreases as the absorbed water vapor amount increases. The value is much smaller than that on MCM-41 and SBA-15. Therefore, the MFS shows more hydrophobic surface properties than the MCM-41 and SBA-15. It may be a kind of good candidate for adsorption of large molecule and catalyst carrier with high moisture resistance.


2008 ◽  
Vol 8 (2) ◽  
pp. 549-556 ◽  
Author(s):  
Asli Nalbant ◽  
Timur Dogu ◽  
Suna Balci

Nickel and copper incorporated MCM-41-like mesoporous nanocomposite materials prepared by the direct hydrothermal synthesis and the impregnation procedures showed highly attractive pore structure and surface area results for catalytic applications. The XRD patterns showed that characteristic MCM-41 structure was preserved for the materials synthesized following an impregnation procedure before the calcination step. The surface area of the Cu impregnated material with a quite high Cu/Si atomic ratio (0.19) was 631 m2/g. Very narrow pore size distributions with an average pore diameter of about 2.7 nm were obtained as a result of plugging of some of the smaller pores by Cu nanoballs. For lower metal to Si ratios (for instance for Ni/Si = 0.06) much higher surface area values (1130 m2/g) were obtained. In the case of nanocomposite materials synthesized by the direct hydrothermal route, MCM-41 structure was not destroyed for samples containing metal to Si atomic ratios as high as 0.12. In the case of materials containing Cu/Si and Ni/Si ratios over 0.2 wider pore size distributions and some decrease of surface area were observed.


2014 ◽  
Vol 1025-1026 ◽  
pp. 574-579 ◽  
Author(s):  
Nuchanaporn Pijarn ◽  
Pichit Galajak

Silica gel is the chemical substance that has many good advantages such as absorbed moisture, porosity, small diameter, high surface area, and lightweight. It was synthesized by using rice husk ash via sol – gel heating in the microwave technique. The objectives in this work compose of synthesis silica gel by using the microwave technique before characterizatization. This raw material was archived from rice husk ash, obtained from agricultural waste. The silica gel, synthesized by conventional method (CVM) and commercial silica gel (COM), was also studied for comparison purposes. The results showed that successfully synthesized the silica gel by sol - gel technique using microwave. The XRD pattern of silica gel enhanced from this method was not sinificantly different as compared with CVM and COM methods. And the physical properties of this technique could be debated. The particle size of silca gel was determined by zetasizer and it was approxmately 50-70 nm. The pore size diameter, pore volume, and specific surface area of silica gel were calculated by Flowsorb II and a Quantachrome Autosorp-1. The pore size diameter, pore volume, and specific surface area of silica gel are 10-30 nm, 0.7-1.0 cm3/g, and 400-700 m2/g, respectively. Consequently, this work is considered to be the waste to make useful, and a great way to save energy and time in the silica gel synthesis.


2017 ◽  
Vol 126 (1C) ◽  
pp. 37
Author(s):  
Hoàng Văn Đức

<p>In the present paper, a synthesis of MCM-41 mesoporous material with the sodium silicate solution prepared from the rice husk ash as a silica source by the hydrothermal process was demonstrated. The influence of synthesized conditions such as CTAB concentration, SiO<sub>2</sub>/CTAB molar ratio, stirring time and hydrothermal time were investigated. The samples were characterized by XRD, FT–IR and N<sub>2</sub> adsorption–desorption measurement. The obtained results showed that the samples possessed highly ordered hexagonal mesostructure with uniform mesopore size distribution in a large range of CTAB concentration (1,98-4,81% mass) and the SiO<sub>2</sub>/CTAB molar ratio (4-15). The sample had a high surface area (1071 m<sup>2</sup>/g) and large pore diameter (33,5 Å) with the molar ratio of CTAB: SiO<sub>2</sub>: H<sub>2</sub>O = 1: 6: 1000.</p><p>Keywords: MCM-41, sodium silicate solution, rice husk ash</p>


2019 ◽  
Vol 4 (2) ◽  
pp. 61
Author(s):  
Soenandar Milian Tompunu Tengker ◽  
Jenny Kumajas

Mesoporous material MCM-41 cannot be used directly as a catalyst, so need to be added metals or nonmetals to create an acidic site. Nickel is a Lewis acid metal because it is able to accept lone pairs of electrons from ligands to form complex compounds. The purpose of this study was to produce mesoporous material Ni/MCM-41 and to see the effect of the addition Nickel metal to the acidity level of mesoporous material Ni/MCM-41.Tthe ion exchange method is used to produce Ni/MCM-41 and the gravimetric method to test the acidity of the material. The MCM-41 used for Ni/MCM-41 synthesis has an x-ray diffraction pattern with a hexagonal structure that is identical with the MOC researchers results. BET results is showed the type IV of the Langmuir adsorption isotherm with a surface area of ​​Ni/MCM-41 material 775.9 m2/g, pore volume 0.81 cc/g and pore radius 15.2 Å. TEM characterization shows the morphological shape of Ni/MCM-41 in the form of hexagonal structure. The acidity test results of Ni/MCM-41 material have a higher acidity level compared to MCM-41. Based on the research data, it can be concluded that Ni/MCM-41 has a morphological form with a hexagonal structure, has a large surface area and has a pore size classified as mesoporous material and has a higher acidity level than the MCM-41 synthesized.


2014 ◽  
Vol 925 ◽  
pp. 23-27
Author(s):  
Nurhadijah Zainalabidin ◽  
Noor Hasyierah Mohd Salleh ◽  
Dachyar Arbain

Mesoporous materials are favorable for enzyme immobilization due to their unique properties of large surface area, uniform pore system and functionalizable surfaces. Immobilization on these materials enhances enzyme stability, activity and resistance towards harsh environmental conditions such as temperature and pH. The present study deals with synthesis of mesoporous materials namely MCM-41. For that purpose, the MCM-41 was synthesized using cetyltrimethylammonium bromide (CTAB) as a template and extractable silica from rice husk ash as a silica source. The synthesis was performed under alkaline conditions to produce white fine solid particles, followed by grafting with 3-aminopropyltriethoxysilane and activation with carbodiimide before it was immobilized with lipase. Characterization of those fine particles using Nitrogen physisorption gives BET surface area, as BET, and the pore diameterto be 1184 m²/g and 2.58 nm respectively. Fourier Transform Infrared spectra show peak of SiO2, NH2 and COOH functional group which confirms the existence of those compounds in covalent bonding formation between amine-grafted MCM-41 and lipase enzyme. Immobilized enzyme shows an increase in pH stability when compared to free enzyme at fixed temperature of 20°C in time range from 30 to 180 minutes.


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