Anti-competitive adsorption of gaseous benzene on hydrophilic microporous carbon in humid conditions.

The adsorption capture of ambient volatile organic compounds (VOCs) is of practical importance for air quality management. Herein, unique anti-competitive adsorption behavior of benzene on a hydrophilic activated carbon (Procarb-900 (P900)) is evidenced in the presence of competing components (e.g., formaldehyde (FA) and/or moisture). Contrary to general expectations, the adsorption capacity of 10 Pa benzene (QB) onto P900 (30 mg) at the 99 % breakthrough level improves from 144.8 to 187 mg g-1 as the relative humidity (RH) increases from 0 to 25 %. Such pattern is maintained at 183.9 mg g-1 even at the relatively high RH of 50 %. Furthermore, QB exhibits a remarkable increase of 56.1 % (to 226.0 mg g-1) in the binary phase (100 ppm benzene plus 50 ppm FA) relative to its single phase (144.8 mg g-1). The kinetic studies confirm the occurrence of anti-competitive adsorption of benzene under humid conditions with the unusual decrease in rate constants at the elevated RHs (i.e., 25 and 50 %). The thermodynamic studies suggest the exothermic nature of benzene adsorption onto P900. The hydrophilicity of P900's outer surface promotes the preferential adsorption of polar FA and water vapor over non-polar benzene, which deforms the activated carbon texture and lowers the pore size distribution (PSD). The narrow PSD enhances benzene uptake in the complex systems due to the confinement effect. Overall, this study offers insights into the unique anti-competitive adsorption of non-polar VOCs (e.g., benzene) on hydrophilic microporous adsorbents in the presence of potential interferences such as polar water vapor and FA. These findings offer a guideline for the practical implementation of adsorption techniques for gaseous VOCs in humid conditions.

Influence of counter ions on structure, morphology, thermal stability of lanthanide complexes containing dipicolinic acid ligand.

Two kinds of lanthanide coordination polymers formed by dipicolinic acid with lanthanide ions were synthesized by varying the counter ions. And their crystal structures, morphology and thermal stabilities were measured and compared. X-ray single-crystal diffraction analysis reveals that Na3[Ln(DPA)3] (Ln = Tb or Eu) stretches to a rigid network by means of bridging Na+ ion. Moreover, Na3[Ln(DPA)]3 exhibits good thermal stability and luminescent properties, and its optical properties can be remained even after heating at 200 °C more than 3 days. However, when Na+ in Na3[Ln(DPA)3] was replaced with NH4+, i.e., (NH4)3[Ln(DPA)3] with a supramolecular structure based on π-π stacking and other weak interactions, shows relatively poor thermal stability which leads to deterioration of their luminescence properties after heating treatment. This result confirms that the rigid frame structure of Na3[Ln(DPA)]3 plays a crucial role in improving its thermal stability and keeping its highly luminescent quantum efficiency.