RESUMEN
The nanostructural design of heterogeneous catalysts has often been demanded for assessing synergetic effects, which should be developed further by using high-surface-area porous metal oxide supports. However, such opportunities have been undermined by the poor stability of ordered mesoporous structures. Herein, rational design is demonstrated to obtain nanocomposite catalysts showing improved NOx storage properties owing to the presence of Ba species over a well-designed mesoporous alumina (Al2 O3 ) support. It is found that Ba species are impregnated successfully only after the stabilization of the mesoporous structure by full crystallization of Al2 O3 frameworks to the γ-phase, with the formation of Pt nanoparticles coinciding with complete removal of organic components. All the insights during this synthetic procedure are essential for designing high-performance catalysts to purify and recover NOx molecules, and are applied for designing a variety of cutting-edge mesoporous nanocomposite catalysts.
RESUMEN
Mesoporous metal organophosphonates having embedded organic functions are a promising platform to hybridize organics and non-siliceous inorganic frameworks in their molecular scale. However, the reactivity between a bisphosphonate and a metal source is dramatically different for their combination and then hampers to construct ordered mesoporous structures even when using amphiphilic organic molecules. By proposing an advanced method to adjust such reactivity, we recently succeeded in fabricating ordered mesoporous aluminum organophosphonate (AOP) films with chemically designable benzene units inside their hybrid frameworks. The reactivity of the organically bridged bisphosphonates has been controlled by utilizing dissimilar reactivities of acid-base pairs like P-OH and P-OEt groups to AlCl3 . Here, we further prove our reactivity-control concept through the introduction of organic groups, such as those having symmetric thiophene, asymmetric amide, and hydrophilic ether units. Liquid-state 31 Pâ NMR measurements further clarified the usefulness of the control of the -OH/ -OEt ratio in the same bisphosphonate molecules for obtaining highly ordered mesostructured AOP films.
RESUMEN
The concept of protecting groups and leaving groups in organic synthesis was applied to the synthesis of siloxane-based molecules. Alkoxy-functionalized siloxane oligomers composed of SiO4 , RSiO3 , or R2 SiO2 units were chosen as targets (R: functional groups, such as Me and Ph). Herein we describe a novel synthesis of alkoxysiloxane oligomers based on the substitution reaction of trimethylsilyl (TMS) groups with alkoxysilyl groups. Oligosiloxanes possessing TMS groups were reacted with alkoxychlorosilane in the presence of BiCl3 as a catalyst. TMS groups were substituted with alkoxysilyl groups, leading to the synthesis of alkoxysiloxane oligomers. Siloxane oligomers composed of RSiO3 and R2 SiO2 units were synthesized more efficiently than those composed of SiO4 units, suggesting that the steric hindrance around the TMS groups of the oligosiloxanes makes a difference in the degree of substitution. This reaction uses TMS groups as both protecting and leaving groups for SiOH/SiO- groups.
RESUMEN
A solvent extraction method was improved using organic bases such as triethylamine (Et3N) that neutralize HCl effectively and stabilize sol-gel derivative alumina frameworks as insoluble species, thereby achieving removal of EOnPOmEOn at a rate higher than 90% to obtain high-quality mesoporous alumina.
RESUMEN
Surfactant-assisted synthesis is a promising technique for the tailor-made design of highly porous metal oxide based nanomaterials. There has been a demand for the comprehensive design of their morphology, porous structure and crystallinity to extend potential applications using metal oxide based materials such as titania (TiO2). However, the porous structure is often deformed and/or destroyed during the process of crystallizing metal oxide frameworks. Herein, the aerosol-assisted synthesis of mesoporous TiO2 powders was conducted in the presence of high-molecular-weight poly(styrene)-block-poly(ethylene oxide) (PS-b-PEO), which improved the stability of the derivative mesoporous structure with an increase in the thickness of the TiO2 frameworks. To propose a rational synthetic route for stable and porous metal oxides, the resultant mesoporous structure and the textural morphology of the mesoporous TiO2 powders were surveyed using PS-b-PEO with different lengths of PS and PEO chains. By a judicious choice of the molecular structure of PS-b-PEO, the morphological design of the fully crystallized anatase phase of TiO2 from spherical to fibrous ones was achieved with control over the mesopore diameter.
RESUMEN
Aqueous colloidal mesoporous nanoparticles with ethenylene-bridged silsesquioxane frameworks with a uniform diameter of â¼20 nm were prepared from bis(triethoxysilyl)ethenylene in a basic aqueous solution containing cationic surfactants. The nanoparticles, which had higher hydrolysis resistance under aqueous conditions, showed lower hemolytic activity toward bovine red blood cells than colloidal mesoporous silica nanoparticles.
Asunto(s)
Coloides/química , Eritrocitos/efectos de los fármacos , Nanopartículas , Compuestos de Organosilicio/síntesis química , Animales , Bovinos , Hemólisis/efectos de los fármacos , Compuestos de Organosilicio/farmacologíaRESUMEN
The crystallinity of inorganic solids like metal oxides after the porosity design is the crucial factor that should be investigated for enhancing their physicochemical properties. In most cases, metal oxide frameworks around mesopores, that are designed through the supramolecular mediated approach, are resulted to be amorphous. Accordingly, a rational guideline has been required for enhancing the crystallinity of frameworks at such concave surfaces. We have so far surveyed a crystallization behavior of alumina (Al2O3) frameworks to its γ-phase around spherical mesopores (â¼40 nm) and discussed further transition to the α-phase around much larger pores (â¼200 nm). In this paper, we prepared new and helpful Al2O3 powders having PS-b-PEO templated pores (â¼25 nm and â¼75 nm) smaller than those of our previous case. After careful discussion of the pore size variation by considering the molecular structure of PS-b-PEO, we explained the crystallization behavior of the Al2O3 frameworks to enhance its γ-crystallinity. This knowledge is quite beneficial for designing highly porous Al2O3 powders with abundant crystallinity for use as catalyst supports, which is very useful for assessing synthetic procedures of other mesoporous metal oxides having high crystallinity.
RESUMEN
Typical syntheses for the mesostructural design were performed with strategic deviations, being substantially powerful for changing the molecular structure of frameworks, from the synthetic conditions optimized for the preparation of lamellar and 2-d hexagonal mesostructured materials where the frameworks were constructed by aluminophosphate (AlPO) like units with and without organic groups in the molecular scale. A series of the materials such as mesostructured aluminum organophosphonate (AOP) and AlPO type ones were investigated according to the molecular structure and crystallinity of inorganic-organic hybrid and non-hybrid inorganic frameworks. Considering a uniqueness of AlPO based frameworks, a rational insight on strength of interactions between crystalline/amorphous AlPO based units and cationic surfactant molecules was surveyed as one of the most significant factors for understanding the mesostructural variation.
RESUMEN
The regulation of automobile exhaust gas, especially that concerning hazardous nitrogen oxide (called as NOx) becomes stricter year-by-year, which should be urgently corresponded for cleaning the NOx containing emission. According to surface affinity of γ-alumina to metal catalysts and its thermal stability, crystalline γ-alumina has been frequently utilized as catalyst supports showing relatively high specific surface area. From the viewpoint, we consider that highly porous alumina powders prepared using amphiphilic organic molecules are potential as such a catalyst support for improving NOx removing property. In this study, we report surface property of the mesoporous alumina powders against NOx molecules after crystallizing to its γ-phase and NOx storage property after impregnation of barium (Ba) acetate in the mesopores. Adsorption of NO with O2 on mesoporous γ-alumina powders without Ba species were more likely to be bridging bidentate than chelating bidentate nitrates (NO3-) with comparing to commercially available γ-alumina powders. After impregnating the Ba species, admitted NO molecules were oxidized with enough O2 and stored very strongly as ionic nitrate (NO3-) onto the Ba species even after heating at 500 °C. This preliminary study is helpful for designing mesoporous deNOx catalysts combined with unique storage/adsorption property.
RESUMEN
Siloxane formation reactions of both the nonhydrolytic sol-gel process and Piers-Rubinsztajn reaction can be integrated as Lewis acid promoted siloxane syntheses without involving silanol groups. The former was developed in the field of inorganic materials chemistry and the latter was initiated in polymer chemistry. We have realized both reactions are quite similar, in terms of 1)â the nonhydrolytic reaction, 2)â the use of alkoxysilanes, 3)â the group-exchange reactions competing with the siloxane formation, and 4)â the proposed reaction mechanisms. This Minireview focuses on the above two reactions. The evolution of both reactions should realize a more sophisticated molecular design of siloxane compounds, which surely contributes to the development of advanced functional materials.
RESUMEN
Mesoporous silica containing a large amount of isolated Ti was prepared from an alkoxytitanosiloxane precursor through a hard template method. Isopropoxytris(tris-tert-butoxysiloxy)titanium (((i)PrO)Ti[OSi(O(t)Bu)(3)](3), TS3) was synthesized and TS3 was mixed with mesoporous carbon (CMK-3), a hard template. The mixture was pyrolyzed at 180 °C to form a composite consisting of titanosilica and the hard template. After calcination at 600 °C for the removal of the carbon template, the titanium species were not transformed to anatase TiO(2), proved by DR-UV-Vis, FTIR, XPS, and XRD, while the ESR results indicated the presence of isolated Ti. The mesoporous structure was verified by SEM, TEM, and N(2) adsorption. The Si/Ti ratio of the product was consistent with that of the precursor. All the results show that the material prepared from the precursor is ordered mesoporous silica containing a large amount of isolated Ti in the frameworks. The use of well-defined alkoxytitanosiloxane precursor leads to the formation of mesoporous silica with exactly controlled composition of titanium with neither loss of Ti nor transformation to anatase.