Lannoy Anthony, Kania Nicolas, Bleta Rudina, Fourmentin Sophie, Machut-Binkowski Cécile, Monflier Eric, Ponchel Anne
Univ. Artois, UMR 8181, Unité de Catalyse et de Chimie du Solide (UCCS), F-62300 Lens, France; CNRS, UMR 8181, Unité de Catalyse et de Chimie du Solide (UCCS), Lille F-59000, France.
Université du Littoral Côte d'Opale, Unité de Chimie Environnementale et Interactions sur le Vivant (UCEIV), F-59140 Dunkerque, France.
J Colloid Interface Sci. 2016 Jan 1;461:317-325. doi: 10.1016/j.jcis.2015.09.022. Epub 2015 Sep 9.
Cyclodextrin-assisted photodegradation of toluene was investigated in water in the presence of a photo-irradiated commercial titanium dioxide photocatalyst. It was expected that cyclodextrins could form water-soluble supramolecular host/guest complexes with the toluene and thus promote the approach of the pollutant on the TiO2 surface and enhance the phototocatalytic oxidation efficiency.
Photodegradation kinetics of toluene were investigated under UV-C and near-visible light radiation in aqueous suspensions of TiO2. Impact of cyclodextrin (CD) on the photocatalytic efficiency of TiO2 was evaluated with different cyclodextrins: α-CD, β-CD, γ-CD and RAME-β-CD. Host-guest association constants were determined by static headspace gas chromatography and affinity of cyclodextrins for the TiO2 surface by isothermal adsorption studies. Issue of the cyclodextrin stability during the degradation process was examined using Total Organic Carbon, NMR and MALDI-TOF analyses.
Toluene could be fully mineralized by TiO2 in water within hours, even if the presence of cyclodextrin caused a delay in the photodegradation process. The chemical nature of cyclodextrins was found to exert a significant influence on the extent of inhibitory effect, which was discussed in terms of balance between solubilization efficiency, substrate protection and coverage of active sites of TiO2 by competitive adsorption. The cyclodextrin degradation was also studied and discussed.
在光辐照的商用二氧化钛光催化剂存在下,研究了环糊精辅助甲苯在水中的光降解。预计环糊精可与甲苯形成水溶性超分子主/客体复合物,从而促进污染物接近二氧化钛表面并提高光催化氧化效率。
在二氧化钛水悬浮液中,研究了紫外-C和近可见光辐射下甲苯的光降解动力学。用不同的环糊精(α-环糊精、β-环糊精、γ-环糊精和随机甲基化-β-环糊精)评估了环糊精(CD)对二氧化钛光催化效率的影响。通过静态顶空气相色谱法测定主客体缔合常数,并通过等温吸附研究测定环糊精对二氧化钛表面的亲和力。使用总有机碳、核磁共振和基质辅助激光解吸电离飞行时间分析研究了降解过程中环糊精的稳定性问题。
即使环糊精的存在导致光降解过程延迟,二氧化钛仍可在数小时内使水中的甲苯完全矿化。发现环糊精的化学性质对抑制作用程度有显著影响,这从增溶效率、底物保护和竞争吸附对二氧化钛活性位点覆盖之间的平衡角度进行了讨论。还对环糊精的降解进行了研究和讨论。