樟脑致气孔的氮化石墨碳可见光敏感涂层

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Dominik Schimon , Sylvia Patakyová , Petr Stavárek , Petr Dzik , Tomáš Homola , František Zažímal , Petr Klusoň
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引用次数: 0

摘要

石墨化氮化碳是一种光敏材料,在光催化领域具有重要地位。多次研究表明,光催化氧化还原反应动力学数据的解释不是一件容易的事情。与标准的多相催化不同,发育良好的微孔结构并不总是必要的特征。一个非常精细的多孔结构带来了很大一部分的活性表面。然而,它通常不适用于光子。当接触到表面时,它们会形成活性物质,然后扩散到催化颗粒的深处。然而,该过程更多地受到质量传递的驱动,反应速率的测量不再在动力学范围内进行。这种限制可以通过使用提供充分显影表面的光敏材料来避免,但仅限于入射光子可以直接接触到的程度。在这里,描述了这种类型的薄膜催化剂,并使用致孔樟脑来创建合适的表面形貌和孔隙度。实验验证了樟脑含量和附加等离子体处理的作用。所有的涂层都描述了一系列的技术,重点是它们的结构和形态特性。然后将该涂层用于狭缝型微光反应器中的四环素氧化。然而,将它们的性能与化学结构相同的结构进行了比较,这些结构没有多孔体,和/或额外的等离子体处理。所选择的四环素转化既代表了一个合适的模型反应,又代表了一个与含药物废水净化具有普遍相关性的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visible-light-sensitive coatings of graphitic carbon nitride with inherent porosity induced by camphor
Graphitic carbon nitride is referred to as a light-sensitive material with a prominent position in photocatalysis. It was shown repeatedly that the interpretation of kinetic data in the photocatalytic ox/redox reactions is not an easy task. The well-developed microporous structure, unlike that of standard heterogeneous catalysis, is not always the necessary feature. A very fine porous structure brings a significant part of the active surface. However, it is not usually available for photons. When hit the surface, they form reactive species that then diffuse deeper into the catalytic particle. However, the process becomes more driven by mass transport and the reaction rate measurement no longer takes place in the kinetic regime. This limitation can be avoided by using light-sensitive materials that offer a sufficiently developed surface, but only to the extent that it is directly accessible to the incident photons. Here, such a type of thin-film catalyst is described, and porogenic camphor is used to create a suitable surface morphology and porosity. The roles of camphor content and additional plasma treatment were experimentally verified. All coatings were described with a battery of techniques with a focus on their structural and morphological properties. The coatings were then employed in a tetracycline oxidation in a slit-type micro-photoreactor. Their performance was compared with chemically identical structures, however, obtained without the porogenic body, and/or the additional plasma treatment. The chosen transformation of tetracycline represents both a suitable model reaction and a process of general relevance in the decontamination of wastewater containing pharmaceuticals.
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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