TL;DR: In this paper, the synthesis of mesoporous inorganic solids from calcination of aluminosilicate gels in the presence of surfactants is described, in which the silicate material forms inorganic walls between ordered surfactant micelles.
Abstract: MICROPOROUS and mesoporous inorganic solids (with pore diameters of ≤20 A and ∼20–500 A respectively)1 have found great utility as catalysts and sorption media because of their large internal surface area. Typical microporous materials are the crystalline framework solids, such as zeolites2, but the largest pore dimensions found so far are ∼10–12 A for some metallophosphates3–5 and ∼14 A for the mineral cacoxenite6. Examples of mesoporous solids include silicas7 and modified layered materials8–11, but these are invariably amorphous or paracrystalline, with pores that are irregularly spaced and broadly distributed in size8,12. Pore size can be controlled by intercalation of layered silicates with a surfactant species9,13, but the final product retains, in part, the layered nature of the precursor material. Here we report the synthesis of mesoporous solids from the calcination of aluminosilicate gels in the presence of surfactants. The material14,15 possesses regular arrays of uniform channels, the dimensions of which can be tailored (in the range 16 A to 100 A or more) through the choice of surfactant, auxiliary chemicals and reaction conditions. We propose that the formation of these materials takes place by means of a liquid-crystal 'templating' mechanism, in which the silicate material forms inorganic walls between ordered surfactant micelles.
TL;DR: In this paper, a new application of MCM-41 mesoporous materials has been developed, where two kinds of surfactants, C16TAB and C12TAB, have been employed to get different pore sizes.
Abstract: A new application of MCM-41 mesoporous materials has been developed. Two kinds of surfactants, C16TAB and C12TAB, have been employed to get different pore sizes. The samples were disk-shaped conformed before and after charging with ibuprofen, an anti-inflammatory drug. In all the cases the weight percent ratio of drug/MCM-41 was 30%. The drug release plots show a different behavior depending on the method for charging the drug in the material but not on the employed surfactant.
TL;DR: In this paper, a review of the preparation of ordered mesoporous catalysts is presented, and the essential properties of the resulting materials are described in the first part of this review.
TL;DR: In this article, a mesoporous molecular sieve of MCM-41 type (MCM41-PEI) has been used as a CO2 adsorbent.
Abstract: The objective of the work presented here is to develop a nanoporous solid adsorbent which can serve as a “molecular basket” for CO2 in the condensed form Polyethylenimine (PEI)-modified mesoporous molecular sieve of MCM-41 type (MCM-41-PEI) has been prepared and tested as a CO2 adsorbent The physical properties of the adsorbents were characterized by X-ray powder diffraction (XRD), N2 adsorption/desorption, and thermogravimetric analysis (TGA) The characterizations indicated that the structure of the MCM-41 was preserved after loading the PEI, and the PEI was uniformly dispersed into the channels of the molecular sieve The CO2 adsorption/desorption performance was tested in a flow system using a microbalance to track the weight change The mesoporous molecular sieve had a synergetic effect on the adsorption of CO2 by PEI A CO2 adsorption capacity as high as 215 mg-CO2/g-PEI was obtained with MCM-41-PEI-50 at 75 °C, which is 24 times higher than that of the MCM-41 and is even 2 times that of the pure