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Absorption and photocatalytic degradation of VOCs by perfluorinated ionomeric coating with TiO2 nanopowders for air purification

机译:用TiO2纳米粉用TiO2纳米粉用于空气净化的对VOC的吸收和光催化降解

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In this work, we propose a transparent multilayered perfluoropolymeric coating as immobilization method for TiO2 nanoparticles, and evaluate its suitability in the gas phase photocatalytic degradation of six different volatile organic compounds. The coating was made of a layer of TiO2-containing perfluorosulfonic acid polymer on a layer of perfluorinated amorphous polymer. The chemical stability of perfluoropolymeric materials to UV radiation and UV-activated TiO2 overcomes the possible degradation of the polymeric immobilization system which is typical of more traditional polymeric coatings. Moreover, the TiO2-containing ionomeric perfluorosulfonic layer worked as selective membrane for pollutants absorption and catalyst preservation, depending on the interactions between the superacidic polar heads of the ionomer and the pollutants, in particular those capable of hydrogen bonding. Gas-phase photocatalytic degradation tests were performed using pentane, methanol, 2-propanol, toluene, dichloromethane and pyridine as reference volatile organic pollutants, thus ranging on different polarity properties. Results indicate performances comparable to other approaches reported in the literature and show a strong influence of both atmospheric conditions (namely, humidity) and pollutant nature - polarity, proticity - on the actual kinetics of photodegradation, also depending on the interactions regulating the affinity between the ionomeric layer of the coating and pollutants. The high potential of the coating in the photodegradation was confirmed by the observed values of the photoabatement rates: all approximatively above 10(-5) s(-1) and maximum for alcohols (1.4x10(-4) and 1.7x10(-4) s(-1) in dry and humid conditions, respectively).
机译:在这项工作中,我们提出了一种透明的多层全氟聚合涂层作为TiO2纳米颗粒的固定化方法,并评估其在六种不同挥发性有机化合物的气相光催化降解中的适用性。在一层全氟化的无定形聚合物层上由含有TiO 2的全氟磺酸聚合物制成的涂层。全氟聚合物材料与UV辐射和UV活化TiO2的化学稳定性克服了典型的更传统的聚合物涂层的聚合物固定体系的可能降解。此外,含TiO 2的离聚物全氟含层作为选择性膜作为污染物吸收和催化剂保存,取决于离聚物的超酸极性头部与污染物之间的相互作用,特别是能够氢键的相互作用。使用戊烷,甲醇,2-丙醇,甲苯,二氯甲烷和吡啶作为参考挥发性有机污染物进行气相光催化降解试验,从而在不同的极性性质上测量。结果表明,与文献中报道的其他方法相当的性能,并显示出大气条件(即湿度)和污染物性质 - 极性,特殊性 - 对光电降解的实际动力学的强烈影响,也取决于调节与之间的亲和力的相互作用涂层和污染物的离子化层。通过观察到的光降低速率的观察值证实光降解中的涂层的高电位:均高于10(-5)S(-1)和醇的最大值(1.4×10(-4)和1.7×10(-4) )S(-1)分别在干燥和潮湿的条件下)。

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