{"title":"六氰铁酸盐(II)与吡嗪之间配体取代反应的动力学催化及光度法测定汞(II","authors":"Radhey Mohan Naik, Pradeep Kumar Singh, Richa Rastogi, Ruchi Singh, Abhinav Agarwal","doi":"10.1002/adic.200790103","DOIUrl":null,"url":null,"abstract":"<p>A sensitive, simple and rapid spectrophotometric method for the determination of mercury (II) based on its catalytic effect on the abstraction of coordinated cyanide from hexacyanoferrate (II) by pyrazine has been developed using fixed time procedure. The extent of the reaction is monitored spectrophotometrically by measuring the increase in absorbance at λ<sub>max</sub>=440 nm of the yellow colored complex, [Fe(CN)<sub>5</sub>Pz]<sup>3−</sup> under the reaction conditions; [Fe(CN)<sub>6</sub>]<sup>4−</sup>=7.2×10<sup>−3</sup> mol L<sup>−1</sup>, [P<sub>z</sub>]=3.75×10<sup>−4</sup> mol L<sup>−1</sup>, temperature=25.0±0.1 °C, pH= 2.50±0.02 and I=0.1 mol L<sup>−1</sup>(KNO<sub>3</sub>). The experimental rate data under the conditions used in the present study exhibited a linear dependence between absorbance and [Hg<sup>2+</sup>] catalyst in the range 5.065–50.15 ng mL<sup>−1</sup>. The detection limit is found to be 4.01 ng mL<sup>−1</sup>. The maximum relative standard deviations and percentage errors for mercury(II) determination are found to be 2.2 and 3 % respectively. The percentage recoveries are found to be in the range of 99–102 %. Analytical data fordetermination of mercury(II) is presented together with the application of proposed method in water spiked synthetic mixtures. The validity of the proposed method is tested by comparing the results obtained by present method with atomic absorption spectrometry.</p>","PeriodicalId":8193,"journal":{"name":"Annali di chimica","volume":"97 11-12","pages":"1169-1179"},"PeriodicalIF":0.0000,"publicationDate":"2007-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/adic.200790103","citationCount":"7","resultStr":"{\"title\":\"Kinetic-Catalytic and Spectrophotometric Determination of Hg(II) Using its Catalytic Effect on Ligand Substitution Reaction between Hexacyanoferrate(II) and Pyrazine\",\"authors\":\"Radhey Mohan Naik, Pradeep Kumar Singh, Richa Rastogi, Ruchi Singh, Abhinav Agarwal\",\"doi\":\"10.1002/adic.200790103\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A sensitive, simple and rapid spectrophotometric method for the determination of mercury (II) based on its catalytic effect on the abstraction of coordinated cyanide from hexacyanoferrate (II) by pyrazine has been developed using fixed time procedure. The extent of the reaction is monitored spectrophotometrically by measuring the increase in absorbance at λ<sub>max</sub>=440 nm of the yellow colored complex, [Fe(CN)<sub>5</sub>Pz]<sup>3−</sup> under the reaction conditions; [Fe(CN)<sub>6</sub>]<sup>4−</sup>=7.2×10<sup>−3</sup> mol L<sup>−1</sup>, [P<sub>z</sub>]=3.75×10<sup>−4</sup> mol L<sup>−1</sup>, temperature=25.0±0.1 °C, pH= 2.50±0.02 and I=0.1 mol L<sup>−1</sup>(KNO<sub>3</sub>). The experimental rate data under the conditions used in the present study exhibited a linear dependence between absorbance and [Hg<sup>2+</sup>] catalyst in the range 5.065–50.15 ng mL<sup>−1</sup>. The detection limit is found to be 4.01 ng mL<sup>−1</sup>. The maximum relative standard deviations and percentage errors for mercury(II) determination are found to be 2.2 and 3 % respectively. The percentage recoveries are found to be in the range of 99–102 %. Analytical data fordetermination of mercury(II) is presented together with the application of proposed method in water spiked synthetic mixtures. The validity of the proposed method is tested by comparing the results obtained by present method with atomic absorption spectrometry.</p>\",\"PeriodicalId\":8193,\"journal\":{\"name\":\"Annali di chimica\",\"volume\":\"97 11-12\",\"pages\":\"1169-1179\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/adic.200790103\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annali di chimica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/adic.200790103\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annali di chimica","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adic.200790103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
摘要
利用汞(II)对吡嗪萃取六氰高铁酸盐(II)中配位氰化物的催化作用,建立了一种灵敏、简便、快速的固定时间光度法测定汞(II)的方法。通过测定在反应条件下黄色配合物[Fe(CN)5Pz]3−在λmax=440 nm处吸光度的增加,分光光度法监测了反应的程度;[Fe(CN)6]4−=7.2×10−3 mol L−1,[Pz]=3.75×10−4 mol L−1,温度=25.0±0.1℃,pH= 2.50±0.02,I=0.1 mol L−1(KNO3)。在本研究条件下的实验速率数据显示,吸光度与[Hg2+]催化剂在5.065 ~ 50.15 ng mL−1范围内呈线性关系。检测限为4.01 ng mL−1。汞(II)测定的最大相对标准偏差和百分比误差分别为2.2%和3%。加样回收率为99 ~ 102%。给出了测定汞(II)的分析数据,并介绍了该方法在加水合成混合物中的应用。通过与原子吸收光谱法测定结果的比较,验证了方法的有效性。
Kinetic-Catalytic and Spectrophotometric Determination of Hg(II) Using its Catalytic Effect on Ligand Substitution Reaction between Hexacyanoferrate(II) and Pyrazine
A sensitive, simple and rapid spectrophotometric method for the determination of mercury (II) based on its catalytic effect on the abstraction of coordinated cyanide from hexacyanoferrate (II) by pyrazine has been developed using fixed time procedure. The extent of the reaction is monitored spectrophotometrically by measuring the increase in absorbance at λmax=440 nm of the yellow colored complex, [Fe(CN)5Pz]3− under the reaction conditions; [Fe(CN)6]4−=7.2×10−3 mol L−1, [Pz]=3.75×10−4 mol L−1, temperature=25.0±0.1 °C, pH= 2.50±0.02 and I=0.1 mol L−1(KNO3). The experimental rate data under the conditions used in the present study exhibited a linear dependence between absorbance and [Hg2+] catalyst in the range 5.065–50.15 ng mL−1. The detection limit is found to be 4.01 ng mL−1. The maximum relative standard deviations and percentage errors for mercury(II) determination are found to be 2.2 and 3 % respectively. The percentage recoveries are found to be in the range of 99–102 %. Analytical data fordetermination of mercury(II) is presented together with the application of proposed method in water spiked synthetic mixtures. The validity of the proposed method is tested by comparing the results obtained by present method with atomic absorption spectrometry.