scholarly journals Mesoporous Materials: From Synthesis to Applications

2019 ◽  
Vol 20 (13) ◽  
pp. 3213 ◽  
Author(s):  
Juan Antonio Cecilia ◽  
Ramón Moreno Tost ◽  
María Retuerto Millán

Mesoporous silica are inorganic materials, which are formed by the condensation of sodium silicate or silicon alkoxides around an ordered surfactant used as template [...]

2003 ◽  
Vol 775 ◽  
Author(s):  
G.V.Rama Rao ◽  
Qiang Fu ◽  
Linnea K. Ista ◽  
Huifang Xu ◽  
S. Balamurugan ◽  
...  

AbstractThis study details development of hybrid mesoporous materials in which molecular transport through mesopores can be precisely controlled and reversibly modulated. Mesoporous silica materials formed by surfactant templating were modified by surface initiated atom transfer radical polymerization of poly(N-isopropyl acrylamide) (PNIPAAm) a stimuli responsive polymer (SRP) within the porous network. Thermo gravimetric analysis and FTIR spectroscopy were used to confirm the presence of PNIPAAm on the silica surface. Nitrogen porosimetry, transmission electron microscopy and X-ray diffraction analyses confirmed that polymerization occurred uniformly within the porous network. Uptake and release of fluorescent dyes from the particles was monitored by spectrofluorimetry and scanning laser confocal microscopy. Results suggest that the presence of PNIPAAm, a SRP, in the porous network can be used to modulate the transport of aqueous solutes. At low temperature, (e.g., room temperature) the PNIPAAm is hydrated and extended and inhibits transport of analytes; at higher temperatures (e.g., 50°C) it is hydrophobic and is collapsed within the pore network, thus allowing solute diffusion into or out of the mesoporous silica. The transition form hydrophilic to hydrophobic state on polymer grafted mesoporous membranes was determined by contact angle measurements. This work has implications for the development of materials for the selective control of transport of molecular solutes in a variety of applications.


1990 ◽  
Vol 180 ◽  
Author(s):  
G. Teowee ◽  
J.M. Boulton ◽  
H.H. Fox ◽  
A. Koussa ◽  
T. Gudgel ◽  
...  

ABSTRACTPolycerams are an emergent class of hybrid, multifunctional materials which combine the properties of organic and inorganic materials. Films have been prepared from silicon alkoxides and reactive, functionalized polymers such as triethoxysilyl modified polybutadiene (MPBD), (N-triethoxysilylpropyl)O polyethylene oxide urethane (MPEOU) and trimethoxysilylpropyl substituted polyethyleneimine (MPEI). Characterization of dielectric constant and tan δ of the films has been carried out over a range of frequency from 500 Hz to 100 kHz; and the results are used to consider the potential of Polycerams as dielectric materials.


2021 ◽  
Author(s):  
Ahmed Wasel Alsmaeil ◽  
Mohamed Amen Hammami ◽  
Amr Ismail Abdel-Fattah ◽  
Mazin Yousef Kanj ◽  
Emmanuel P Giannelis

Abstract Developing nanocarriers deliver molecules to targeted locations has received widespread attention in different fields ranging from biomedical to oil and gas industries. Mesoporous Silica Nanoparticles (MSNs), where the pore size diameter ranges from 2-50 nm, have become attractive in many fields including biomedicine. One advantage is the ability to control the size, morphology of the particles, and the internal and external surfaces properties which enable encapsulating molecules of different size and charges. Moreover, it is possible to functionalize the pores and the surface of the MSNs, which make them suitable to host different molecules and release them in situ in a controlled manner. Despite the numerous studies of MSNs, little has been devoted to subsurface applications. This review will highlight some of the interesting characteristics of MSNs that make them promising carriers of molecules for slow and/or stimuli-responsive delivery for oil field applications. For example, they could be utilized for the controlled release of surfactants for enhanced oil recovery applications to minimize surfactant losses near the well-bore area. The mesoporous materials can be designed to harvest the ions normally present in oil field water, and the high temperatures encountered when travelling deep in the reservoir to release the surfactant. The ion exchange process makes it possible to engineer the MSNs to release their cargo for efficient and stimuli responsive delivery applications. The ion-responsive release was analyzed by the interfacial tension behavior between crude oil and high salinity water (HSW). It is concluded that the interfacial tension could be reduced up to 0.0045 mN/m when the mesoporous silica particles are suspended in HSW in comparison to 0.9 mN/m when suspended in DI water.


Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 348 ◽  
Author(s):  
Marina Santana Vega ◽  
Andrés Guerrero Martínez ◽  
Fabio Cucinotta

Hybrid materials prepared by encapsulation of plasmonic nanoparticles in porous silica systems are of increasing interest due to their high chemical stability and applications in optics, catalysis and biological sensing. Particularly promising is the possibility of obtaining gold@silica nanoparticles (Au@SiO2 NPs) with Janus morphology, as the induced anisotropy can be further exploited to achieve selectivity and directionality in physical interactions and chemical reactivity. However, current methods to realise such systems rely on the use of complex procedures based on binary solvent mixtures and varying concentrations of precursors and reaction conditions, with reproducibility limited to specific Au@SiO2 NP types. Here, we report a simple one-pot protocol leading to controlled crystallinity, pore order, monodispersity, and position of gold nanoparticles (AuNPs) within mesoporous silica by the simple addition of a small amount of sodium silicate. Using a fully water-based strategy and constant content of synthetic precursors, cetyl trimethylammonium bromide (CTAB) and tetraethyl orthosilicate (TEOS), we prepared a series of four silica systems: (A) without added silicate, (B) with added silicate, (C) with AuNPs and without added silicate, and (D) with AuNPs and with added silicate. The obtained samples were characterised by transmission electron microscopy (TEM), small angle X-ray scattering (SAXS), and UV-visible spectroscopy, and kinetic studies were carried out by monitoring the growth of the silica samples at different stages of the reaction: 1, 10, 15, 30 and 120 min. The analysis shows that the addition of sodium silicate in system B induces slower MCM-41 nanoparticle (MCM-41 NP) growth, with consequent higher crystallinity and better-defined hexagonal columnar porosity than those in system A. When the synthesis was carried out in the presence of CTAB-capped AuNPs, two different outcomes were obtained: without added silicate, isotropic mesoporous silica with AuNPs located at the centre and radial pore order (C), whereas the addition of silicate produced Janus-type Au@SiO2 NPs (D) in the form of MCM-41 and AuNPs positioned at the silica–water interface. Our method was nicely reproducible with gold nanospheres of different sizes (10, 30, and 68 nm diameter) and gold nanorods (55 × 19 nm), proving to be the simplest and most versatile method to date for the realisation of Janus-type systems based on MCM-41-coated plasmonic nanoparticles.


2006 ◽  
Vol 510-511 ◽  
pp. 138-141 ◽  
Author(s):  
Shan Zheng ◽  
Lian Gao

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.


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