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Nanosized low-temperature phases of titanium(IV) oxide with anatase and eta-phase structures: composition, structure, and photocatalytic properties

机译:钛(IV)氧化钛纳米型低温相,具有锐钛矿和ETA相结构:组成,结构和光催化性能

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摘要

Nanosized low-temperature modifications of titanium(IV) oxide with the anatase and eta-phase (TiO2-x center dot mH(2)O) structures were prepared by the sulfate method (pH 3) and for the first time characterized by a complex of methods (X-ray diffractometry, scanning electron microscopy, IR spectroscopy, Raman spectroscopy, differential scanning calorimetry, low-temperature sorption capacity of samples to nitrogen, and differentiating dissolution). The physicochemical properties of the modifications were compared. Differences in compositions of the surface and volumes of the samples, compositions and structures of the phases (structure of eta-phase is superstructure to anatase), and microstructure elements (sizes of crystallites, nanoparticles, and specific surface area; volume of nano- and ultrananopores) were revealed. The region of eta-phase stability was found in the coordinates of temperature (T = 50-95 degrees C) and hydrolysis duration (tau = 10-80 min) and temperature (T = 200 degrees C) and annealing duration (tau6 h). The distinctions in the thermal behavior of the nanosized anatase and eta-phase were studied. The photocatalytic activity (PCA) is determined by the physicochemical characteristics of the samples and phases and also by the composition and structure of the decomposed substrate. In the case of difenoxazole, the PCA is affected by the compositions of the samples, phases, and surface (the presence of OH groups) and specific surface area, whereas the composition of the samples and specific surface area affect the PCA in the case of thiamethoxam.
机译:通过硫酸盐法(pH <3)制备纳米钛(IV)氧化钛(IV)氧化钛(IV)氧化物(TiO2-X中心点MH(2)O)结构的纳米化的低温修饰一种方法复合物(X射线衍射测定,扫描电子显微镜,IR光谱,拉曼光谱,差分扫描量热法,氮气的低温吸附能力和分化溶解)。比较了修饰的物理化学性质。样品的表面和体积的组合物的差异,阶段的组合物和结构(Eta-pace的结构是上层建静的锐钛矿),和微结构元件(微晶,纳米粒子和比表面积的尺寸;纳米体积和ultrananopores)被揭示。在温度(T = 50-95摄氏度)和水解持续时间(Tau = 10-80分钟)和温度(T = 200摄氏度)和退火持续时间(Tau&Lt ; 6小时)。研究了纳米氧化酶和ETA相的热行为中的区别。光催化活性(PCA)由样品和阶段的物理化学特性和分解基材的组成和结构决定。在苯恶唑的情况下,PCA受样品,相和表面(OH基团的存在)和比表面积的组合物的影响,而样品和特定表面积的组成在此情况下影响PCA泰国紫红色。

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