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首页> 外文期刊>Analytical methods >Determination of ascorbic acid via luminescence quenching of LaF3:Ce,Tb nanoparticles synthesized through a microwave-assisted solvothermal method
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Determination of ascorbic acid via luminescence quenching of LaF3:Ce,Tb nanoparticles synthesized through a microwave-assisted solvothermal method

机译:微波溶剂热法合成LaF3:Ce,Tb纳米粒子的发光猝灭法测定抗坏血酸

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摘要

A novel approach for the rapid determination of ascorbic acid was developed based on the direct luminescence quenching of LaF3:Ce,Tb nanoparticles. The LaF3:Ce,Tb nanoparticles were synthesized via a microwave-assisted method with ionic liquids (BmimBF4) as the fluorine source. The as-prepared nanoparticles were uniformly ellipsoidal with an average size of about 12 nm. They are water soluble and highly fluorescent under 249 nm excitation. A new method for the rapid determination of ascorbic acid was established based on the large degree of overlap between the excitation spectrum of LaF3:Ce,Tb nanoparticles and the absorption spectrum of ascorbic acid. Ascorbic acid exhibits a broad band from 200 to 300 nm with the maximum absorption at 260 nm, which can absorb the excitation light of LaF3:Ce,Tb nanoparticles, consequently resulting in the luminescence quenching. The results showed a good inverse linear relationship between the luminescent intensity 6f LaF3:Ce,Tb nanoparticles and the concentration of ascorbic acid in the range 8.0 × 10~(-6) to 1.0 × 10~(-4) mol L~(-1) (R = 0.9995), with the detection limit of 2.4 × 10~(-5) mol L~(-1) and a RSD of 0.5% (5.33 × 10~(-5) mol L~(-1) n = 11). Compared with the standard redox titration method, our new method is effective for the determination of ascorbic acid.
机译:基于LaF3:Ce,Tb纳米粒子的直接发光猝灭,开发了一种快速测定抗坏血酸的新方法。通过微波辅助法,以离子液体(BmimBF4)为氟源,合成了LaF3:Ce,Tb纳米粒子。所制备的纳米颗粒是均匀的椭圆形,平均尺寸为约12nm。它们是水溶性的,在249 nm激发下具有很高的荧光性。 LaF3:Ce,Tb纳米粒子的激发光谱与抗坏血酸的吸收光谱之间存在较大的重叠度,从而建立了一种快速测定抗坏血酸的新方法。抗坏血酸表现出200至300 nm的宽带,在260 nm处具有最大吸收,可吸收LaF3:Ce,Tb纳米粒子的激发光,从而导致发光猝灭。结果表明,发光强度6f LaF3:Ce,Tb纳米颗粒与抗坏血酸浓度在8.0×10〜(-6)至1.0×10〜(-4)mol L〜(-)之间具有良好的反线性关系。 1)(R = 0.9995),检出限为2.4×10〜(-5)mol L〜(-1),RSD为0.5%(5.33×10〜(-5)mol L〜(-1) n = 11)。与标准的氧化还原滴定法相比,我们的新方法可有效测定抗坏血酸。

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