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Bimodal activated carbons derived from resorcinol-formaldehyde cryogels
Andrzej Szczurek1, Gisele Amaral-Labat1, Vanessa Fierro1
1Institut Jean Lamour-UMR CNRS 7198, CNRS-Nancy-Université-UPV-Metz, Département Chimie et Physique des Solides et des Surfaces. ENSTIB, 27 rue Philippe Séguin, BP 1041, 88051 Épinal cedex 9, France.
Science and Technology of Advanced Materials
|November 24, 2016
Summary
Resorcinol-formaldehyde cryogels activated with phosphoric acid yield high-surface-area microporous carbons. Optimization of acid concentration and contact time produced carbons with surface areas nearing 2200 m² g⁻¹.
Area of Science:
- Materials Science
- Porous Materials
- Carbon Materials
Background:
- Resorcinol-formaldehyde (RF) cryogels are precursors for carbon materials.
- Pyrolysis and acid activation are common methods for carbon material synthesis.
- Understanding pore structure development is crucial for optimizing carbon properties.
Purpose of the Study:
- To investigate the pore texture of RF cryogels activated with phosphoric acid.
- To compare these materials with those obtained by pyrolysis.
- To optimize the acid activation process for high-surface-area microporous carbons.
Main Methods:
- RF cryogels were prepared at various dilution ratios.
- Cryogels were activated using phosphoric acid (H3PO4) at 450 °C.
- Control samples were pyrolyzed at 900 °C for comparison.
Main Results:
- Acid-activated cryogels exhibited different pore textures compared to pyrolyzed samples.
- Highly diluted cryogels yielded microporous carbons with high surface areas.
- Optimized activation (2 M H3PO4, optimal contact time) achieved surface areas up to ~2200 m² g⁻¹ and micropore volumes of ~0.7 cm³ g⁻¹.
- Activation at 1.2 M H3PO4 produced bimodal carbons with accessible macroporosity.
Conclusions:
- Phosphoric acid activation of RF cryogels is an effective route to high-surface-area microporous carbons.
- Dilution ratio, acid concentration, and contact time are critical parameters for controlling pore structure.
- Optimized activation offers a viable alternative to pyrolysis for producing advanced carbon materials.

