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Hydrothermal synthesis and characterization of CaSO_4 pseudomicrorods

机译:CaSO_4假微棒的水热合成与表征

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Calcium sulphate (CaSO_4) pseudomicrorods have been synthesized by a low-temperature hydrothermal method using CaSO_4 powder as a precursor and hexadecylamine as a surfactant at 180°C for at different intervals of time. The powder X-ray diffraction pattern indicates that the as-formed pseudomicrorods are of orthorhombic phase with lattice parameters a = 7.0023(4) A, b = 6.9939(5) A and c = 6.2434(4) A. Scanning electron microscopy images show that the pseudomicrorods have diameters of about 0.2-2.5 mu m and lengths of about 2-10 mu m. Fourier transform infrared spectroscopy shows a strong doublet near 609 and 681 cm~(-1) arising from v_4 (SO_4~(2-)) bending vibrations. The strongest band observed at 1132 cm~(-1) is associated with v_3 (SO_4~(2-)) stretching vibrations. The band near 420-450 cm~(-1) is attributed to V_2 (SO_4~(2-)) bending vibrations. The Raman spectrum exhibits an intense peak at 1008 cm~(-1) associated with the SO_4~(2-) mode. The photoluminescence spectrum exhibits UV bands (330, 350 nm), strong green bands (402, 436 nm) and weak blue bands (503 nm). A widening of the optical band gap was observed as the particle size decreased.
机译:硫酸钙(CaSO_4)假微棒已通过低温水热法合成,使用CaSO_4粉末作为前体,十六烷基胺作为表面活性剂在180°C下进行不同时间间隔的合成。粉末X射线衍射图表明形成的伪微棒为正交晶相,晶格参数为a = 7.0023(4)A,b = 6.9939(5)A和c = 6.2434(4)A。扫描电子显微镜图像显示假微棒的直径约为0.2-2.5μm,长度约为2-10μm。傅立叶变换红外光谱表明,由于v_4(SO_4〜(2-))弯曲振动,在609和681 cm〜(-1)附近出现了强双峰。在1132 cm〜(-1)处观察到的最强带与v_3(SO_4〜(2-))拉伸振动有关。 420-450 cm〜(-1)附近的波段归因于V_2(SO_4〜(2-))弯曲振动。拉曼光谱在与SO_4〜(2-)模式相关的1008 cm〜(-1)处出现一个强烈的峰值。光致发光光谱显示出UV带(330,350 nm),强绿色带(402,436 nm)和弱蓝色带(503 nm)。随着粒径减小,观察到光学带隙变宽。

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