Synthetic carbons activated with phosphoric acid III.: Carbons prepared in air

Synthetic activated carbons were prepared by phosphoric acid activation of a styrene-divinylbenzene copolymer in an air atmosphere at various temperatures in the 400-900 degreesC interval. The carbons were characterized by elemental analysis, cation-exchange capacity measurement, infrared spectroscopy, potentiometric titration, copper adsorption from solution and physical adsorption of N-2 at - 196 degreesC and CO2 at 0 degreesC. It was shown that, similarly to synthetic phosphoric acid activated carbons obtained in argon, the synthetic carbons activated with phosphoric acid in air possess an acidic character and show considerable cation-exchange properties. The contribution of oxygen-containing surface groups along with phosphorus-containing groups to CEC is higher for carbons obtained in air. Three types of surface groups were identified on carbons prepared at temperatures up to 600 degreesC, and four types on carbons prepared at higher temperatures. These groups were assigned to 'super-acidic' (pK<0), phosphorus-containing (pK= 1.1-1.2), carboxylic (pK=4.7-6.0) and phenolic (pK=8.1-9.4) groups. The cation-exchange capacity was at a maximum for the carbon prepared at 800 degreesC. Copper adsorption by synthetic phosphoric acid activated carbons obtained in air at temperatures lower than 800 degreesC is higher than for similar carbons obtained in argon. The increase is due to additional formation of oxygen-containing surface groups. Calculated copper binding constants revealed the importance of phosphorus-containing and carboxylic groups for adsorption of copper from aqueous solution. All carbons show a multimodal pore size distribution including simultaneously micropores and mesopores, but the porous texture is not a prime factor in determining the cation-exchange capacities of these carbons. Synthetic phosphoric acid activated carbons show a greater development of porosity when obtained in air as compared to carbons carbonized in argon. (C) 2003 Elsevier Science Ltd. All rights reserved.