{"title":"密度比光谱一阶导数法同时测定环境样品中硝基酚异构体","authors":"F. Bagheban-Shahri, A. Niazi, A. Akrami","doi":"10.22034/JCHR.2018.544009","DOIUrl":null,"url":null,"abstract":"A new spectrophotometric method was developed for the simultaneous of ternary mixtures of nitrophenol isomers, without prior separation steps. This method is called the first derivative of the density ratio spectra. All factors affecting on the sensitivity were optimized and the linear dynamic range for determination of nitrophenol isomers was found. The method made use of a derivative of the double-divisor- ratio spectra of optical density. In this case, the linear determination ranges are 1.0-25.0 g mL -1 for m- nitrophenol, 1.0-25.0 g mL -1 for o-nitrophenol and 1.0-15.0 g mL -1 for p-nitrophenol. The RMSEP for m- nitrophenol, o-nitrophenol and p-nitrophenol by proposed method was 0.4907, 0.4779 and 0.2068, respectively. The method developed in this paper was rapid, easy to apply, not expensive and it was suitable for analyzing to overlapping signals of compounds in their mixtures without any chemical pre-treatment and also, the proposed method was satisfactorily applied to the rapid simultaneous determination of m-nitrophenol, o-nitrophenol and p-nitrophenol in synthetic and water samples. i , , , , , ,","PeriodicalId":15347,"journal":{"name":"Journal of Chemical Health Risks","volume":"2 1","pages":"21-28"},"PeriodicalIF":0.0000,"publicationDate":"2012-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"SIMULTANEOUS SPECTROPHOTOMETRIC DETERMINATION OF NITROPHENOL ISOMERS IN ENVIRONMENTAL SAMPLES USING FIRST DERIVATIVE OF THE DENSITY RATIO SPECTRA\",\"authors\":\"F. Bagheban-Shahri, A. Niazi, A. Akrami\",\"doi\":\"10.22034/JCHR.2018.544009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A new spectrophotometric method was developed for the simultaneous of ternary mixtures of nitrophenol isomers, without prior separation steps. This method is called the first derivative of the density ratio spectra. All factors affecting on the sensitivity were optimized and the linear dynamic range for determination of nitrophenol isomers was found. The method made use of a derivative of the double-divisor- ratio spectra of optical density. In this case, the linear determination ranges are 1.0-25.0 g mL -1 for m- nitrophenol, 1.0-25.0 g mL -1 for o-nitrophenol and 1.0-15.0 g mL -1 for p-nitrophenol. The RMSEP for m- nitrophenol, o-nitrophenol and p-nitrophenol by proposed method was 0.4907, 0.4779 and 0.2068, respectively. The method developed in this paper was rapid, easy to apply, not expensive and it was suitable for analyzing to overlapping signals of compounds in their mixtures without any chemical pre-treatment and also, the proposed method was satisfactorily applied to the rapid simultaneous determination of m-nitrophenol, o-nitrophenol and p-nitrophenol in synthetic and water samples. i , , , , , ,\",\"PeriodicalId\":15347,\"journal\":{\"name\":\"Journal of Chemical Health Risks\",\"volume\":\"2 1\",\"pages\":\"21-28\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Health Risks\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22034/JCHR.2018.544009\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Health Risks","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22034/JCHR.2018.544009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 9
摘要
建立了一种新的分光光度法,可同时测定硝基酚同分异构体的三元混合物,无需预先分离。这种方法称为密度比谱的一阶导数。对影响灵敏度的各因素进行了优化,确定了测定硝基酚异构体的线性动态范围。该方法利用了光密度的双因子比谱的导数。在这种情况下,对硝基苯酚的线性测定范围为1.0-25.0g mL -1,邻硝基苯酚的线性测定范围为1.0-25.0g mL -1,对硝基苯酚的线性测定范围为1.0-15.0g mL -1。该方法对间硝基酚、邻硝基酚和对硝基酚的RMSEP分别为0.4907、0.4779和0.2068。该方法快速、简便、成本低,适用于化合物混合物中重叠信号的分析,无需任何化学预处理,可用于合成样品和水样中间硝基酚、邻硝基酚和对硝基酚的快速同时测定。一、整机整机整机,,,,,,
SIMULTANEOUS SPECTROPHOTOMETRIC DETERMINATION OF NITROPHENOL ISOMERS IN ENVIRONMENTAL SAMPLES USING FIRST DERIVATIVE OF THE DENSITY RATIO SPECTRA
A new spectrophotometric method was developed for the simultaneous of ternary mixtures of nitrophenol isomers, without prior separation steps. This method is called the first derivative of the density ratio spectra. All factors affecting on the sensitivity were optimized and the linear dynamic range for determination of nitrophenol isomers was found. The method made use of a derivative of the double-divisor- ratio spectra of optical density. In this case, the linear determination ranges are 1.0-25.0 g mL -1 for m- nitrophenol, 1.0-25.0 g mL -1 for o-nitrophenol and 1.0-15.0 g mL -1 for p-nitrophenol. The RMSEP for m- nitrophenol, o-nitrophenol and p-nitrophenol by proposed method was 0.4907, 0.4779 and 0.2068, respectively. The method developed in this paper was rapid, easy to apply, not expensive and it was suitable for analyzing to overlapping signals of compounds in their mixtures without any chemical pre-treatment and also, the proposed method was satisfactorily applied to the rapid simultaneous determination of m-nitrophenol, o-nitrophenol and p-nitrophenol in synthetic and water samples. i , , , , , ,