ABSTRACT
Zwitterionic betaine polymers are promising adsorbents for the removal of heavy metal ions from industrial effluents. Although the presence of both negative and positively charged groups imparts them the ability to simultaneously remove cations and anions, intra- and/or inter-chain interactions can significantly reduce their adsorption efficiencies. Therefore, in this study, novel gels based on crosslinked co-polymers of thermosensitive N-isopropylacrylamide (NIPAAM) and zwitterionic sulfobetaine N,N-dimethylacrylamido propyl ammonium propane sulfonate (DMAAPS) were synthesized, characterized, and evaluated for ion removal. Fourier-transform infrared (FTIR) and proton nuclear magnetic resonance (1H NMR) analyses confirmed the success of the co-polymerization of NIPAAM and DMAAPS to form poly(NIPAAM-co-DMAAPS). The phase transition temperature of the co-polymer increased with increasing DMAAPS content in the co-polymer, indicating temperature-dependent amphiphilic behavior, as evidenced by contact angle measurements. The ion adsorption analyses of the poly(NIPAAM-co-DMAAPS) gels indicated that co-polymerization increased the molecular distance and weakened the interaction between the DMAAPS-charged groups (SO3- and N+), thereby increasing the ion adsorption. The results confirmed that, with a low concentration of DMAAPS in the co-polymer gels (~10%), the maximum amount of Cr3+ ions adsorbed onto the gel was ~58.49% of the sulfonate content in the gel.
ABSTRACT
Several ZrO2 -supported ruthenium catalysts were prepared and utilized in the oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) under base-free conditions. Full conversion of HMF and almost perfect selectivity towards FDCA (97 %) were achieved after 16â h by using pure O2 as an oxidant and water as a solvent. The catalytic tests show that the size of the Ru particles is crucial for the catalytic performance and that the utilization of high-surface-area ZrO2 leads to formation of very small Ru particles. Superior activity was obtained for catalysts based on ZrO2 that had been synthesized by a surface-casting method and has high surface areas up to 256â m2 g-1 . In addition to good activity and selectivity, these catalysts show also high stability and constant activity upon recycling, confirming the suitability of Ru/ZrO2 in the base-free oxidation of HMF.
ABSTRACT
A series of choline (Ch)-exchanged heteropoly acids (HOCH2 CH2 N(CH3 )3 )x H(6-x) P2 W18 O62 [abbreviated as Chx H(6-x) P2 W18 O62 , x=1-6] was synthesized and used as catalysts for the reaction of α-angelica lactone (alpha-AL) with n-butanol to form butyl levulinate (BL). The solubility of Chx H(6-x) P2 W18 O62 in the reaction mixture was temperature dependent: The catalysts were soluble under the reaction conditions and precipitated upon cooling of the reaction mixture. This facilitated recovery of the catalysts from the liquid phase. Importantly, an increase of the Ch content caused a decrease of the catalyst solubility. Catalytic activity of Chx H(6-x) P2 W18 O62 for the reaction with n-butanol appeared to be in good agreement with the concentration of Brønsted-acidic sites. The results suggest that the reaction proceeded through formation of pseudo-butyl levulinate as intermediate. Ch2 H4 P2 W18 O62 exhibited the best balance between catalytic activity and temperature-dependent solubility. The yield of BL reached 79.4 % at full conversion of alpha-AL at a moderate temperature of 75 °C in an open system. Chx H(6-x) P2 W18 O62 could be successfully reused five times without significant loss of activity.
