Mesoporous carbons were synthesized via both soft and hard template methods and compared to a commercial powder activated carbon (PAC) for the adsorption ability of bisphenol-A (BPA) from an aqueous solution. The commercial PAC had a BET-surface of 1027 m²/g with fine pores of 3 nm and less. The hard templated carbon (CMK-3) material had an even higher BET-surface of 1420 m²/g with an average pore size of 4 nm. The soft templated carbon (SMC) reached a BET-surface of 476 m²/g and a pore size of 7 nm. The maximum observed adsorption capacity (q_max) of CMK-3 was the highest with 474 mg/g, compared to 290 mg/g for PAC and 154 mg/g for SMC. The difference in adsorption capacities was attributed to the specific surface area and hydrophobicity of the adsorbent. The microporous PAC showed the slowest adsorption, while the ordered mesopores of SMC and CMK-3 enhanced the BPA diffusion into the adsorbent. This difference in adsorption kinetics is caused by the increase in pore diameter. However, CMK-3 with an open geometry consisting of interlinked nanorods allows for even faster intraparticle diffusion.

High-performance supported palladium nanoparticle (Pd-NP) catalysts help to address the growing demand for ‘green’ chemical production processes. At present, literature information on how the NP characteristics, NP–support and support–reactant/product interactions affect the catalytic performance, is scattered. As a result, the present review aims to bring together and critically analyze the relevant literature reports on the catalytic performance of supported Pd-NP catalysts in various liquid-phase reactions such as (de-)hydrogenation, alcohol (electro-)oxidation and cross-coupling reactions. The five main NP support classes, i.e., metal oxides, zeolites, carbon structures, polymers and ordered porous materials, are discussed in detail. A thorough understanding about the catalytic behaviour of supported Pd-NP catalysts via the NP characteristics, NP–support and support–reactant/product interactions give useful insights to optimize current or even create novel NP catalysts for a specific liquid-phase reaction.

In different regions across the globe, elevated arsenic contents in the groundwater constitute a major health problem. In this work, a biopolymer chitosan has been blended with volcanic rocks (red scoria and pumice) for arsenic (V) removal. The effect of three blending ratios of chitosan and volcanic rocks (1:2, 1:5 and 1:10) on arsenic removal has been studied. The optimal blending ratio was 1:5 (chitosan: volcanic rocks) with maximum adsorption capacity of 0.72 mg/g and 0.71 mg/g for chitosan: red scoria (Ch–Rs) and chitosan: pumice (Ch–Pu), respectively. The experimental adsorption data fitted well a Langmuir isotherm (R² > 0.99) and followed pseudo-second-order kinetics. The high stability of the materials and their high arsenic (V) removal efficiency (~93%) in a wide pH range (4 to 10) are useful for real field applications. Moreover, the blends could be regenerated using 0.05 M NaOH and used for several cycles without losing their original arsenic removal efficiency. The results of the study demonstrate that chitosan-volcanic rock blends should be further explored as a potential sustainable solution for removal of arsenic (V) from water.