Determination of trihalomethanes in drinking water by GC-ICP-MS using compound independent calibration with internal standard

2007 ◽  
Vol 22 (9) ◽  
pp. 1138 ◽  
Author(s):  
Adriana González-Gago ◽  
Juan Manuel Marchante-Gayón ◽  
José Ignacio García Alonso
2021 ◽  
Vol 245 ◽  
pp. 03004
Author(s):  
Yanxia Zeng ◽  
Xiashi Zhu

A subject for the rapid determination of iodine content in drinking water by isopropyl sensitization and ICP-MS was established. The samples were dissolved in 1% ammonia solution, 127I was selected as the mass number to be measured and 159Tb as an internal standard. At the same time, 4% (V/V) isopropanol was used to enhance aerosol gasification efficiency, 2% NH3·H2O was used to effectively eliminate memory effects of iodine by cleaning sample for 180 seconds. The results show that, the detection limits of iodine in this method are 0.007 mg·kg-1 and it is superior to other literature. The standard curve has a good linear relationship and the recovery rates of testing rusults range are from 96.00% to 112.3%. The content of iodine in standard substance water samples was determined by ICP-MS method. The iodine content in water samples from seven drinking water sources in Lianyungang area was analyzed between 14~21 μg·L-1. It was in line with the allowable value of 10~300 μg·L-1 of the sanitary standard for drinking water, suggesting that the iodine content of drinking water resources in Lianyungang area was in a safe range.


Metals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 851 ◽  
Author(s):  
Manh Chu ◽  
Lan Nguyen ◽  
Xuan Mai ◽  
Doan Thuan ◽  
Long Bach ◽  
...  

High purity Zirconium (Zr) materials are essential in many components of nuclear reactors, especially fuel cladding tubes. Due to the matrix influence, determination of impurities in the Zr materials requires separation from the Zr matrix. Among extraction methods, solvent extraction is common and suitable for large-scale production. In this study, extraction capability of Zr(IV) by 2-ethylhexyl phosphonic acid mono 2-ethylhexyl ester (PC88A) was examined by FT-IR and UV of ZrO(NO3)2 salt, PC88A-toluene solvent, and Zr-PC88A-toluene complex. ZrO2 (obtained from Institute for Technology of Radioactive and Rare Elements—ITRRE), after being separated from the Zr matrix, was determined for impurities using internal standard (indium, In) by 50% of PC88A dissolved in toluene. Separation of impurities from the Zr matrix underwent two stages. First, one cycle of extraction of the Zr matrix and impurities in 3 M HNO3 using 50% PC88A/toluene was conducted. Second, impurities were scrubbed by 4 M HNO3 in two cycles. Results revealed that approximately 74% of Zr(IV) was separated to the organic phase and 26% remained in the aqueous phase. Determination of impurities after separation from the Zr matrix by ICP-MS using internal standard in revealed that the recovery of impurities achieved 95–100%. With the mentioned amount of Zr, the effect of the Zr matrix on the determination of elements by ICP-MS is negligible. Levels of impurities have relative standard deviations (RSD) of less than 6.9% and recovery of 88.6–98.8%. Therefore, the determination of impurities has high reliability and accuracy. The back-extraction of Zr(IV) in organic phase by 1 M H2SO4 has stripped about 99.5% of the Zr matrix back to the aqueous phase. Following this, NH3 was added to the solution containing Zr after back-extraction to form Zr(OH)4 which was then desiccated to produce ZrO2. X-ray Diffraction (XRD), Scanning and Transmission Electron Microscopy (SEM and TEM) images showed that the new ZrO2 product has spherical nanostructure with diameters of less than 25 nm, which is suitable for applications for the treatment of colorants, metal ions in wastewater sources and manufacture of anti-corrosion steel. In addition, the energy dispersive X-ray (EDX) of the new ZrO2 product showed that it has high purity.


2016 ◽  
Vol 31 (10) ◽  
pp. 2060-2068 ◽  
Author(s):  
Runsheng Yin ◽  
David P. Krabbenhoft ◽  
Bridget A. Bergquist ◽  
Wang Zheng ◽  
Ryan F. Lepak ◽  
...  

Thallium (Tl) has been widely used as an internal standard for mass bias correction during high precision mercury (Hg) isotope ratio measurements using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS).


1998 ◽  
Vol 47 (1) ◽  
pp. 59-62 ◽  
Author(s):  
Manabu OKAZAKI ◽  
Hideji TANAKA ◽  
Tohru ETO ◽  
Michio MATSUBARA ◽  
Kensaku OKAMOTO

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Adriana Dehelean ◽  
Dana Alina Magdas

The presence of potentially toxic elements and compounds in foodstuffs is of intense public interest and thus requires rapid and accurate methods to determine the levels of these contaminants. Inductively coupled plasma mass spectrometry is a powerful tool for the determination of metals and nonmetals in fruit juices. In this study, 21 commercial fruit juices (apple, peach, apricot, orange, kiwi, pear, pineapple, and multifruit) present on Romanian market were investigated from the heavy metals and mineral content point of view by ICP-MS. Our obtained results were compared with those reported in literature and also with the maximum admissible limit in drinking water by USEPA and WHO. For Mn the obtained values exceeded the limits imposed by these international organizations. Co, Cu, Zn, As, and Cd concentrations were below the acceptable limit for drinking water for all samples while the concentrations of Ni and Pb exceeded the limits imposed by USEPA and WHO for some fruit juices. The results obtained in this study are comparable to those found in the literature.


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