{"title":"分散液相微萃取-石墨炉原子吸收光谱法分离测定高盐度采出水中CdII","authors":"Nicolle F. Robaina, G. Cruz, R. Cassella","doi":"10.21577/0103-5053.20230007","DOIUrl":null,"url":null,"abstract":"In this study, we propose a microextraction method for the determination of CdII in produced waters. The process is based on the conversion of CdII ions into a hydrophobic diethyldithiocarbamate (DDTC) complex with its subsequent dispersive liquid phase microextraction (DLPME) from the aqueous medium with chloroform. The organic phase was then diluted with ethanol and Cd absorbance was measured by graphite furnace atomic absorption spectrometry (GF AAS). The experimental conditions related to the DLPME process were investigated, and the best microextraction conditions were achieved at pH = 6.0 (acetate buffer), 7.5 × 10-6 mol L-1 of DDTC, and when using 200 µL of chloroform as the extracting solvent. No dispersing solvent was needed, which allowed the recovery of approximately 140 µL of chloroform extract. Pyrolysis and atomization temperatures of the GF AAS program were determined through the construction of the respective curves. The estimated limits of detection (LOD) and quantification (LOQ) were 5 and 17 ng L-1, respectively, whereas the enrichment factor for the method was 17. Six samples of seawater and five samples of produced waters with salinities between 30 and 270‰ were analyzed as well as two certified reference materials of saline waters.","PeriodicalId":17257,"journal":{"name":"Journal of the Brazilian Chemical Society","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2023-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dispersive Liquid Phase Microextraction (DLPME) as a Strategy for CdII Separation and Determination in High-Salinity Produced Waters by Graphite Furnace Atomic Absorption Spectrometry\",\"authors\":\"Nicolle F. Robaina, G. Cruz, R. Cassella\",\"doi\":\"10.21577/0103-5053.20230007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, we propose a microextraction method for the determination of CdII in produced waters. The process is based on the conversion of CdII ions into a hydrophobic diethyldithiocarbamate (DDTC) complex with its subsequent dispersive liquid phase microextraction (DLPME) from the aqueous medium with chloroform. The organic phase was then diluted with ethanol and Cd absorbance was measured by graphite furnace atomic absorption spectrometry (GF AAS). The experimental conditions related to the DLPME process were investigated, and the best microextraction conditions were achieved at pH = 6.0 (acetate buffer), 7.5 × 10-6 mol L-1 of DDTC, and when using 200 µL of chloroform as the extracting solvent. No dispersing solvent was needed, which allowed the recovery of approximately 140 µL of chloroform extract. Pyrolysis and atomization temperatures of the GF AAS program were determined through the construction of the respective curves. The estimated limits of detection (LOD) and quantification (LOQ) were 5 and 17 ng L-1, respectively, whereas the enrichment factor for the method was 17. Six samples of seawater and five samples of produced waters with salinities between 30 and 270‰ were analyzed as well as two certified reference materials of saline waters.\",\"PeriodicalId\":17257,\"journal\":{\"name\":\"Journal of the Brazilian Chemical Society\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-06-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Brazilian Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.21577/0103-5053.20230007\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Brazilian Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.21577/0103-5053.20230007","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Dispersive Liquid Phase Microextraction (DLPME) as a Strategy for CdII Separation and Determination in High-Salinity Produced Waters by Graphite Furnace Atomic Absorption Spectrometry
In this study, we propose a microextraction method for the determination of CdII in produced waters. The process is based on the conversion of CdII ions into a hydrophobic diethyldithiocarbamate (DDTC) complex with its subsequent dispersive liquid phase microextraction (DLPME) from the aqueous medium with chloroform. The organic phase was then diluted with ethanol and Cd absorbance was measured by graphite furnace atomic absorption spectrometry (GF AAS). The experimental conditions related to the DLPME process were investigated, and the best microextraction conditions were achieved at pH = 6.0 (acetate buffer), 7.5 × 10-6 mol L-1 of DDTC, and when using 200 µL of chloroform as the extracting solvent. No dispersing solvent was needed, which allowed the recovery of approximately 140 µL of chloroform extract. Pyrolysis and atomization temperatures of the GF AAS program were determined through the construction of the respective curves. The estimated limits of detection (LOD) and quantification (LOQ) were 5 and 17 ng L-1, respectively, whereas the enrichment factor for the method was 17. Six samples of seawater and five samples of produced waters with salinities between 30 and 270‰ were analyzed as well as two certified reference materials of saline waters.
期刊介绍:
The Journal of the Brazilian Chemical Society embraces all aspects of chemistry except education, philosophy and history of chemistry. It is a medium for reporting selected original and significant contributions to new chemical knowledge.