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Mesoporous TiO2 encapsulating a visible-light responsive upconversion agent for enhanced sonocatalytic degradation of bisphenol-A

机译:介孔TiO2包封了可见光响应性上转化剂,用于增强双酚-A的单偶催化降解

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Herein, we report the integration of a visible-light active upconversion agent (Er:Y _(2) O _(3) ) with mesoporous TiO _(2) via a modified two-step sol–gel coating method. The resultant material possesses a well-defined core–shell structure with a good upconversion property and exhibits uniform worm-like mesopores (~3.8 nm), a high BET surface area (~151.5 m ~(2) g ~(?1) ) and a large pore volume (~0.23 cm ~(3) g ~(?1) ). The composite was demonstrated as an advanced sonocatalyst, showing a superior degradation performance for bisphenol-A (BPA). The effect of the erbium dopant content on the upconversion property and sonocatalytic performance was evaluated for the production of the best sonocatalyst. We found that the maximum pseudo first-order reaction rate constant in the presence of the composite with an Er ~(3+) content of 3 wt% in Y _(2) O _(3) nanocrystals is calculated to be 0.155 min ~(?1) , which is 2.9 and 2 times larger than that of US alone (0.054 min ~(?1) ) and hollow structured mesoporous TiO _(2) (0.077 min ~(?1) ), respectively. More importantly, the degradation rate is much higher than that of the sonocatalysts reported previously for treatment of BPA (0.09–0.14 min ~(?1) ). The superior catalytic activity can be attributed to an intensified cavitation reaction zone and an enhanced amount of photo-generated charges. Moreover, the recycling test shows that a constant catalytic activity is retained even after 4 cycles. This study paves a promising way for the development of a multi-functional catalyst for sonochemical processes.
机译:在此,我们通过改性的两步溶胶 - 凝胶涂布方法报告可见光活性上转化剂(ER:Y _(2)O _(3))与中孔TiO_(2)的整合。所得材料具有明确定义的核 - 壳结构,具有良好的上转化性能,并且表现出均匀的蠕虫叶片(〜3.8nm),高BET表面积(〜151.5m〜(2)g〜(?1))和大的孔体积(〜0.23cm〜(3)g〜(?1))。复合材料被证明为先进的儿童催留性,显示出对双酚-A(BPA)的优异降解性能。评价铒掺杂剂含量对升级性质和同胞催化性能的影响,用于生产最佳的儿童催留性。我们发现,在Y _(2)O _(3)纳米晶体中的3wt%3wt%的ER〜(3+)含量在复合材料存在下最大的伪第一阶反应速率常数计算为0.155分钟〜 (?1),它们单独的2.9倍和2倍(0.054分钟〜(α1))和中空结构化介孔TiO _(2)(0.077min〜(?1))。更重要的是,降解速率远高于先前用于治疗BPA(0.09-0.14分钟〜(?1))的儿童催化剂。优异的催化活性可归因于强化的空化反应区和增强量的光产生电荷。此外,再循环试验表明甚至在4个循环后均未保留恒定的催化活性。本研究铺平了一种有希望的方式,用于开发多功能催化剂用于多官能催化剂进行多种功能性催化剂。

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