Determination of lead and beryllium in boron samples using 4-sulfamoylphenyl dithiocarbamate salt by ICP-OES

被引:0
|
作者
Dundar, Mustafa S. [1 ]
Gucunlu, Hatice [1 ]
Caner, Celal [1 ]
Altundag, Huseyin [1 ,2 ]
Gulec, Ozcan [1 ]
Arslan, Mustafa [1 ]
机构
[1] Sakarya Univ, Fac Sci, Dept Chem, TR-54187 Serdivan, Sakarya, Turkiye
[2] Sakarya Univ, Biomed Magnet & Semicond Mat Res Ctr BIMAS RC, TR-54187 Serdivan, Sakarya, Turkiye
来源
JOURNAL OF CHEMICAL METROLOGY | 2024年 / 18卷 / 01期
关键词
Boron waste; boron ore; processed boron ore; 4-sulfamoylphenyl dithiocarbamate salt; ICP-OES; cloud point extraction; CLOUD POINT EXTRACTION; TRACE AMOUNTS; HEAVY-METALS; WATER; PRECONCENTRATION; SPECTROMETRY; SEPARATION; PROGRESS; FOOD;
D O I
10.25135/jcm.110.2404.3183
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Today, high amounts of boron waste are generated due to the widespread use of boron and boron compounds. Boron waste in boron-producing enterprises in T & uuml;rkiye reaches six hundred thousand tons annually. The utilization of boron wastes includes various stages, such as storage of refuse in appropriate places, recovery of boron from boron wastes, and utilization in proper sectors. In this study, the amounts of lead (Pb) and beryllium (Be) in three different boron samples (boron waste, boron ore, and processed boron ore) obtained from K & uuml;tahyaEmet region were determined by ICP-OES spectroscopic technique by cloud point extraction (CPE) method using 4-sulfamoylphenyl dithiocarbamate salt complexing agent. Colemanite was used as a boron ore in the study. According to the results, the optimum conditions for the recovery of lead and beryllium ions from aqueous media were found as pH=9, 0.12% (w/w) ligand, and 0.1% (w/w) surfactant concentration, 45 oC incubation temperature and 60 min incubation time. The RSD % of the method under the optimum conditions found were 2 and 2.5 for Pb2+ and Be2+, respectively. The procedure was successfully applied to boron waste samples, and Pb2+ and Be2+ recoveries between 96-105% were obtained.
引用
收藏
页码:71 / 82
页数:12
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