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Journal ArticleDOI

Novel synthesis of porous carbons with tunable pore size by surfactant-templated sol-gel process and carbonisation.

04 Nov 2002-Chemical Communications (The Royal Society of Chemistry)-Iss: 22, pp 2722-2723
TL;DR: Surfactant-templated sol-gel polymerisation was explored to synthesize the resorcinol-formaldehyde gels without supercritical drying step, which were further carbonised to obtain porous carbons of a tunable pore size.
About: This article is published in Chemical Communications.The article was published on 2002-11-04 and is currently open access. It has received 77 citations till now. The article focuses on the topics: Supercritical drying.

Summary (1 min read)

T h i s j o u r n a l i s © T h e R o y a l S o c i e t y o f

  • The pore size is primarily determined by the size of gel clusters, which is in turn controlled by the monomer/surfactant concentration.
  • It is thus very likely that, in acidic conditions, the cross-linking between gel clusters becomes more facilitated to produce a more rigid gel network, and the pore collapse or shrinking at both the drying step and subsequent carbonisation step is suppressed.
  • To test this possibility, the sol-gel polymerisation was performed at different pH by varying the R/F ratio in this work (samples C5-C7).
  • When the pore properties are compared for samples C5-C7, there appears a strong correlation between the porosity and pH of the sol-gel medium even if the carbon cluster size is comparable for the three because the monomer/surfactant concentration is the same.
  • Fig. 3(b) shows the pore size distribution of samples C3-C7 as calculated by the Barrett-Joyner-Halenda (BJH) method from the desorption branch of the isotherm.

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Citations
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Journal ArticleDOI
TL;DR: In this paper , polybenzoxazine (PBZ) was synthesized and carbonized at 1173 K for use as a CO2 capture material and a catalytic support for the hydrogenation of CO2 to methanol.

3 citations

Journal ArticleDOI
TL;DR: In this article, mesoporous carbon membranes have been prepared by means of an organic sol-gel method, and the sol formed by resorcinol and formaldehyde was layered on the outer surface of a fly-ash-based microfiltration ceramic membrane, and was then subjected to gelling, drying, and carbonization to form a mesophorous carbon layer.
Abstract: Mesoporous carbon membranes have been prepared by means of an organic sol–gel method. The sol formed by resorcinol and formaldehyde was layered on the outer surface of a fly-ash-based microfiltration ceramic membrane, and was then subjected to gelling, drying, and carbonization to form a mesoporous carbon layer. Several surfactants were used to allow the carbon membranes to dry under ambient pressure. The pore properties of the carbon membranes have been examined by physical adsorption of nitrogen and subsequent pore structure analysis. The surface area, mesopore volume, and average pore diameter have been controlled by changing the surfactant species and concentration, the resorcinol/formaldehyde concentration, and the sol synthesis time. The as-prepared carbon membranes showed high performance with low transport resistance. The pore size/distribution can be tailored for a specific separation process by adjusting the preparation conditions. These carbon membranes can be applied in ultrafiltration...

2 citations

Book ChapterDOI
01 Jan 2008

2 citations

Journal ArticleDOI
TL;DR: In this article, the successful design and preparation of PNSP with a novel type of one-dimensional network unit, i.e., microporous heterogeneous nanowire, is presented.
Abstract: Design and fabrication of the micro/nanostructures of the network units is a critical issue for porous nanonetwork structured materials. Significant progress has been attained in construction of the network units with zero-dimensional spherical shapes. However, owing to the limitations of synthetic methods, construction of porous building blocks in one dimension featuring high aspect ratios for porous nanonetwork structured polymer (PNSP) remains largely unexplored. Here we present the successful design and preparation of PNSP with a novel type of one-dimensional network unit, i.e., microporous heterogeneous nanowire. Well-defined core-shell polymer nanoobjects prepared from a gelable block copolymer, poly(3-(triethoxysilyl)propyl methacrylate)-block-polystyrene are employed as building blocks, and facilely transformed into PNSP via hypercrosslinking of polystyrene shell. The as-prepared PNSP exhibits unique three-dimensional hierarchical nanonetwork morphologies with large surface area. These findings could provide a new avenue for fabrication of unique well-defined PNSP, and thus generate valuable breakthroughs in many applications.

2 citations

Journal ArticleDOI
TL;DR: In this paper, the amount of CTAB, water and catalyst had a significant impact on the morphology and size of spherical carbon nanoparticles and the difference in the pore size of 1.5 nm to 3.0 nm probably contributed to the difference of capacitance.
Abstract: Spherical carbon nanoparticles were synthesized by sol-gel polymerization of resorcinol and formaldehyde in the presence of CTAB(cetyltrimethylammonium bromide) and subsequent carbonization at 900°C. It is found that the amount of CTAB, water and catalyst showed a significant impact on the morphology and size of carbon nanoparticles. According to the BET surface area and capacitance, the nanoparticles were divided into two groups. The carbon nanoparticles with surface area of 725-758 m2/g showed capacitance between 120-140 F/g, while those with surface area of 596-649 m2/g showed capacitance only 60-80 F/g. Difference in the pore size of 1.5 nm to 3.0 nm probably contributed to the difference of capacitance.

2 citations

References
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Journal ArticleDOI
TL;DR: In this paper, the polycondensation of resorcinol with formaldehyde under alkaline conditions results in the formation of surface functionalized polymer "clusters" which are processed under supercritical conditions to obtain low density, organic aerogels.
Abstract: The polycondensation of resorcinol with formaldehyde under alkaline conditions results in the formation of surface functionalized polymer “clusters”. The covalent crosslinking of these “clusters” produces gels which are processed under supercritical conditions to obtain low density, organic aerogels ( ⩽ 0.1 g cm−3). The aerogels are transparent, dark red in colour, and consist of interconnected colloidal-like particles with diameters of approximately 10 nm. The polymerization mechanism, structure and properties of the resorcinol-formaldehyde aerogels are similar to the sol-gel processing of silica.

1,603 citations

Journal ArticleDOI
TL;DR: Ordered mesoporous carbons have been synthesized using ordered mesopore silica templates as discussed by the authors, where the template needs to exhibit three-dimensional pore structure in order to be suitable for the ordered mesophorous carbon synthesis, otherwise disordered microporous carbon is formed.
Abstract: Ordered mesoporous carbons have recently been synthesized using ordered mesoporous silica templates. The synthesis procedure involves infiltration of the pores of the template with appropriate carbon precursor, its carbonization, and subsequent template removal. The template needs to exhibit three-dimensional pore structure in order to be suitable for the ordered mesoporous carbon synthesis, otherwise disordered microporous carbon is formed. MCM-48, SBA-1, and SBA-15 silicas were successfully used to synthesize carbons with cubic or hexagonal frameworks, narrow mesopore size distributions, high nitrogen Brunauer–Emmett–Teller (BET) specific surface areas (up to 1800 m2 g–1), and large pore volumes. Ordered mesoporous carbons are promising in many applications, including adsorption of large molecules, chromatography, and manufacturing of electrochemical double-layer capacitors.

1,467 citations

Journal ArticleDOI
TL;DR: In this paper, the authors reviewed the mechanisms of gel formation in silicate systems derived from metal alkoxides and proposed that the resulting polysilicate species formed prior to gelation is not a dense colloidal particle of anhydrous silica but instead a solvated polymeric chain or cluster.
Abstract: The mechanisms of gel formation in silicate systems derived from metal alkoxides were reviewed. There is compelling experimental evidence proving, that under many conditions employed in silica gel preparation, the resulting polysilicate species formed prior to gelation is not a dense colloidal particle of anhydrous silica but instead a solvated polymeric chain or cluster. The skeletal gel phase which results during desiccation is, therefore, expected to be less highly crosslinked than the corresponding melted glass, and perhaps to contain additional excess free volume. It is proposed that, during gel densification, the desiccated gel will change to become more highly crosslinked while reducing its surface area and free volume. Thus, it is necessary to consider both the macroscopic physical structure and the local chemical structure of gels in order to explain the gel to glass conversion.

511 citations

Journal ArticleDOI
01 Jan 1997-Carbon
TL;DR: In this article, mesoporous carbon xerogels were prepared from the sol-gel polymerization of resorcinol with formaldehyde (RF) followed by carbonization.

346 citations

Journal ArticleDOI
01 Jan 1999-Carbon
TL;DR: In this paper, a solgel polycondensation of resorcinol with formaldehyde and freeze drying with t -butanol was used to obtain mesoporous materials with high surface areas and large mesopore volumes.

278 citations

Frequently Asked Questions (1)
Q1. What have the authors contributed in "Novel synthesis of porous carbons with tunable pore size by surfactant-templated sol–gel process and carbonisation" ?

Here, the authors report another low-cost preparation method for RF xerogels, where a normal drying is still applicable because the pore collapse can be minimized during the water evaporation. The microto nanosized spherical gel clusters are formed within the micelles, which are further three-dimensionally connected via a crosslinking reaction. The resulting RF gels are dried at 85 °C and further heat-treated at 1000 °C for 3 h under argon atmosphere to obtain porous carbons in monolithic shape.