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Characterization of CaCO_3 Nanoparticles Synthesized by Reverse Microemulsion Technique in Different Concentrations of Surfactants

机译:反向微乳液技术在不同浓度的表面活性剂上合成的CaCO_3纳米粒子的表征

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Calcium carbonate nano-particles were synthesized by a reverse micro-emulsion method at room temperature with Tween~® 80 and Span~® 80 as co-surfactants. The nano-particles synthesized were surface modified by stearic acid. An important operating variable in the Span 80-Tween 80/tolueneAvater reverse micro-emulsion system, the co-value (water/surfactant molar ratio) was investigated. The material was characterized by SEM, TEM, X-Ray Diffraction (XRD), FT-IR UV-VIS and TGA/DTA techniques. The size of the nano-particles was determined by TEM as well as XRD data for various concentrations of surfactants. The results showed that the size of the nano-particles was influenced by the concentration of the surfactants in the micro-emulsion system. The XRD analysis at room temperature showed single phase formation of calcite. FT-IR confirmed the formation of calcite with characteristic absorption bands observed at 712, 881 and 1460 cm~(-1), corresponding to v_(4), v_2 and v_3 modes of CO _3~(-2) absorption bands of calcite. The results of the UV-VIS spectrophotometric analysis indicated that thecalcite (CaCO_3) is an indirect gap material [(5.60 eV(30 wt.% surfactant), 5.40 eV (36 wt.% surfactant) and 5.36 eV (42 wt. % surfactant)] at room temperature.
机译:碳酸钙纳米粒子是通过反相微乳液法在室温下以80和80作为助表面活性剂合成的。合成的纳米粒子通过硬脂酸表面改性。在Span 80-Tween 80 / tolueneAvater反相微乳液系统中,重要的操作变量是co-value(水/表面活性剂的摩尔比)。该材料通过SEM,TEM,X射线衍射(XRD),FT-IR UV-VIS和TGA / DTA技术进行了表征。通过TEM以及各种浓度的表面活性剂的XRD数据确定纳米颗粒的尺寸。结果表明,纳米颗粒的大小受微乳液体系中表面活性剂浓度的影响。室温下的XRD分析显示方解石的单相形成。 FT-IR证实方解石的形成具有在712、881和1460 cm〜(-1)处观察到的特征吸收带,对应于方解石CO_3〜(-2)吸收带的v_(4),v_2和v_3模式。 UV-VIS分光光度分析的结果表明,方解石(CaCO_3)是一种间接间隙材料[(5.60 eV(30 wt。%表面活性剂),5.40 eV(36 wt。%表面活性剂)和5.36 eV(42 wt。%表面活性剂) )] 在室温下。

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