Synthesis mesoporous carbon

Zhu S, Zhou H, Hibino M, Honma I, Ichihara M (2005) Synthesis of Mn02 nanoparticles confined in ordered mesoporous carbon using a sonochemical method. Adv Funct Mater 15 381-386... 

Fuertes A.B. Template synthesis of mesoporous carbons with a controlled particle size, J. Mater. Chem. 2003 13 3085-8. 

Recent reports describe the use of various porous carbon materials for protein adsorption. For example, Hyeon and coworkers summarized the recent development of porous carbon materials in their review [163], where the successful use of mesoporous carbons as adsorbents for bulky pollutants, as electrodes for supercapacitors and fuel cells, and as hosts for protein immobilization are described. Gogotsi and coworkers synthesized novel mesoporous carbon materials using ternary MAX-phase carbides that can be optimized for efficient adsorption of large inflammatory proteins [164]. The synthesized carbons possess tunable pore size with a large volume of slit-shaped mesopores. They demonstrated that not only micropores (0.4—2 nm) but also mesopores (2-50 nm) can be tuned in a controlled way by extraction of metals from carbides, providing a mechanism for the optimization of adsorption systems for selective adsorption of a large variety of biomolecules. Furthermore, Vinu and coworkers have successfully developed the synthesis of... 

The aluminum is incorporated in a tetrahedral way into the mesoporous structure, given place to Bronsted acidic sites which are corroborated by FTIR using pyridine as probe molecule. The presence of aluminum reduces the quantity of amorphous carbon produced in the synthesis of carbon nanotubes which does not happen for mesoporous silica impregnated only with iron. It was observed a decrease in thermal stability of MWCNTs due to the presence of more metal particles which help to their earlier oxidation process. 

Keywords Microwave synthesis Mesoporous zeolite Carbon template Sn-MFI Baeyer-Villiger Oxidation... 

Nowadays synthesis of mesoporous materials with zeolite character has been suggested to overcome the problems of week catalytic activity and poor hydrothermal stability of highly silicious materials. So different approaches for the synthesis of this new generation of bimodal porous materials have been described in the literature like dealumination [4] or desilication [5], use of various carbon forms as templates like carbon black, carbon aerosols, mesoporous carbon or carbon replicas [6] have been applied. These mesoporous zeolites potentially improve the efficiency of zeolitic catalysis via increase in external surface area, accessibility of large molecules due to the mesoporosity and hydrothermal stability due to zeolitic crystalline walls. During past few years various research groups emphasized the importance of the synthesis of siliceous materials with micro- and mesoporosity [7-9]. Microwave synthesis had... 

The synthesis of carbon templated mesoporous tin MFI catalysts with different Si/Sn was carried out using microwave and in typical synthesis methodology TEOS, TPAOH, [Sn(C5H70)2]2]Cl2, ethanol and water were employed where the molar composition of the reaction mixture was 0.06 TPAOH 0.67 H20 0.028 TEOS 1.3 g EtOH X mg of tin precursor (X = 85, 63, 42, 21 mg). This synthesis mixture was stirred for 90 min at room temperature and then Black pearl 2000 carbon (10% wt. of TEOS) was added and again stirred for 4 h vigorously. The crystallization of C-meso-Sn-Silicalite was performed in a Teflon cup placed in a microwave oven (MARS-5, CEM, maximum power of 1200 W). 

Despite the advantages offered by CNTs and CNFs, there are still many obstacles (cost, synthesis methods) to overcome to allow large-scale production. Another type of catalyst support material is mesoporous carbon that provides high surface area and conductivity [100, 141]. It can be classified into ordered (OMC) and disordered (DOMC) mesoporous carbon [100], OMCs have been extensively used as catalyst support materials for fuel cells [140,142-146], The large surface area and 3D connected monodis-persed mesospheres facilitate diffusion of the reactants, making them very attractive materials as catalyst supports [100]. 

Dash RK, Yushin G, Gogotsi Y et al (2005) Synthesis, structure and porosity analysis of microporous and mesoporous carbon derived from zirconium carbide. Micropor Mesopor Mater 86(l-3) 50-57... 

Gu, Z., Deng, B. and Yang, J. (2007) Synthesis and evaluation of iron-containing ordered mesoporous carbon (FeOMC) for arsenic adsorption. Microporous and Mesoporous Materials, 102(1-3), 265-73. 

Figure 2.15 General concept of the syntheses of mesoporous materials (a) mesoporous silica synthesis with soft template (b) mesoporous carbon synthesis with hard template.

Tanaka, S., Nishiyama, N., Egashira, Y., and Ueyama, K. Synthesis of ordered mesoporous carbons with channel structure from an organic-organic nanocomposite. Chem. Commun. 2005 2125-2127. 

Urbonaite, S., Juarez-Galan, J.M., Leis, J., Rodriguez-Reinoso, F., and Svensson, G. Porosity development along the synthesis of carbons from metal carbides. Micropor. Mesopor. Mat., 113(1-3), 2008 14-21. DOI 10.1016/j. micromeso.2007.10.046. 

Titirici MM, Thomas A, Yu SH, Antonietti M. A direct synthesis of mesoporous carbon with bicontinuous pore morphology from crude plant material by hydrothermal carbonization. Chem Mater. 2007 19 4205-12. 

Recently, there has been an increasing interest in the synthesis of ordered mesoporous carbons, since such materials are very promising as adsorbents, catalyst supports, and electrochemical double-layer capacitors. Ordered mesoporous silicas have been shown as suitable templates to prepare periodic mesoporous carbons with various pore shapes and connectivity. The synthesis procedure involves impregnation of the mesoporous silica with an appropriate carbon precursor, carbonization of carbon source, and subsequent removal of silica using an aqueous solution of HF or NaOH. ... 

For the accurate characterization of the adsorption phenomena, it is necessary to obtain accurate information on pore stmctures. However, most of ordinary microporous carbons and mesoporous carbons are obtained with amorphous stmctures that are characterized by irregular arrangements of non-uniform pores. X-ray (or electron) diffraction (XRD) techniques are not useful for such carbons because there are no well-defined stmctural factors to correlate with the adsorption behavior. Moreover, porous carbons exhibit wide varieties of the surface functional groups and the thickness of the pore walls, depending on the details of the synthesis conditions. The lack of distinct XRD lines makes it difficult to distinguish stmctural differences between samples which causes many works to depend empirically on specific samples. 

CMK-5 is the first example of the ordered tube-type mesoporous carbons that can be characterized with well-defined Bragg diffractions by ordinary XRD instrument [6]. The XRD pattern of the CMK-5 carbon is distinguished from that of CMK-3 by the much lower intensity of the (100) diffraction. The structure of CMK-5 may be described by the substitution of the carbon nanorods in CMK-3 with nanopipes. The CMK-5 carbon is synthesized using SBA-IS, similar to CMK-3, but the carbon source and synthesis condition are somewhat different from those for CMK-3. The synthesis method for the tube-type carbon can be extended to the SBA-16 mesoporous template. The resultant CMK-7 carbon has a bicontinuous mesoporous structure [15]. 

The methods developed for the synthesis of ordered mesoporous carbons are simple and cost-efricient, and the pore size can be tailored. The synthesis process can be scaled up for production in bulk quantities. Recent works on the synthesis of mesoporous silicas brought about much improvement in the cost-efficient and custom-tailored synthesis of the templates [18]. The discovery of new mesoporous silicas is also expected to provide additional promising templates for the synthesis of new mesoporous carbons. The resulting high-surface-area materials with uniform pores promise to be suitable as... 

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