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Determination of Trace Amounts of Iodide by an Inhibition Kinetic Spectrophotometric Method

机译:阻抑动力学光度法测定痕量碘化物。

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In this study,the reaction between Co(III)-EDTA and hypophosphite ion.catalyzed by Pd(II),was chosen as the indicator reaction.The inhibition kinetics of this catalytic reaction were investigated in the presence of iodide ion and the possibility of its analytical application was evaluated.Catalyzers other than PdCl_2(Pt,Au and Ni salts)were assayed for the indicator reaction and it was observed that these catalysts have no effect on the reaction.The important variables that affected the reaction rate were investigated and the optimum conditions giving maximum sensitivity were established.The calibration graph,prepared following the inhibition kinetic method,gave a curve exhibiting a linear relationship(r = -0.9878)between the initial rate and iodide concentrations up to 35 ng.mL~(-1)I~-. Iodide was quantitatively be determined in the range 2-35 ng.mL I with a detection limit of 1.2 ng.mL~(-1)I~(-1)(3S_b/m criterion).The RSDs of the method(n = 5)for 7 and 14 ng.mL~(-1)are 1.19 and 0.81%,depending on the iodide concentration,respectively.The reaction was monitored spectrophotometrically by measuring the change in absorbance over time at 540 nm.Iodide in trace amounts had a strong inhibitory effect under optimum conditions.The possibility of the estimation of trace amounts of iodide based on its inhibitory effect was investigated.The method was applied to the determination of iodide in water,urine,table salt and some drug samples,and was compared with the modified Saiidell-Kolthoff method.The determination of the iodide content of biological fluids is important both in malnutrition conditions and in metabolic and epidemiological studies of thyroid diseases.The main advantage of this proposed method for the determination of iodide in urine samples is that it does not necessitate an additional pretreatrnent step.The quantitative method developed,based on inhibition kinetics,is practical,fast and economical.For this reason,it is a technique open to research for the development of application fields(chemistry,biochemistry,environmental,pharmaceutical chemistry etc.).
机译:本研究选择了钯(II)催化的Co(III)-EDTA与次磷酸根离子的反应作为指示剂反应。研究了在碘离子存在下该催化反应的抑制动力学及可能的机理。用PdCl_2(Pt,Au和Ni盐)以外的催化剂进行指示剂反应的分析,发现这些催化剂对反应没有影响。研究了影响反应速率的重要变量并研究了建立了抑制灵敏度最佳条件。按照抑制动力学方法制备的校正曲线在初始速率和碘化物浓度最高至35 ng.mL〜(-1)之间呈线性关系(r = -0.9878)。我~~在2-35 ng.mL I范围内定量测定碘化物,检出限为1.2 ng.mL〜(-1)I〜(-1)(3S_b / m标准)。 5)7和14 ng.mL〜(-1)分别为1.19和0.81%,这取决于碘化物的浓度。通过分光光度法通过测量540 nm处的吸光度随时间的变化来监测反应。研究了基于其抑制作用估算痕量碘化物的可能性。该方法用于水,尿液,食盐和一些药物样品中碘化物的测定,并进行了比较测定营养液状况以及甲状腺疾病的代谢和流行病学研究中,生物液体中碘含量的测定都很重要。该建议方法测定尿液样品中碘化物的主要优点是:它不需要在抑制动力学的基础上开发的定量方法是实用,快速和经济的。因此,这是一个为开发应用领域(化学,生物化学,环境,药物化学等)而研究的技术。 )。

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