DocumentCode
3331549
Title
Notice of Retraction
Online Automatic Monitoring of Trace Amounts of Zinc in Environmental Water
Author
Liang Wei ; Xin-shen Zhang
Author_Institution
Coll. of Environ. & Resource, Southwest Univ. of Sci. & Technol., Mianyang, China
fYear
2011
fDate
10-12 May 2011
Firstpage
1
Lastpage
4
Abstract
Notice of Retraction
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
It is found that in pH 9.3 buffer solutions, zinc (II) reacts with 1-(2-pyridineazo)-2-naphtho to form a water-soluble complex of Zn (II)-1-(2-pyridineazo)-2-naphtho at the presence of Tween-80. Based on this, a simple and sensitive flow injection spectrophotometric method was proposed for online automatic monitoring of trace amounts of zinc in environmental water. Beer´s law was obeyed in the concentration range of 2.0 μg/L ~ 360.0 μg/L for zinc (II) and the detection limit calculated from three times of background noise was 0.42 μg/L. The relative standard deviation was 3.6% and 2.1% for 5.0 μg/L and 50.0 μg/L of zinc standard solution, respectively (n=8). The proposed method had good selectivity (No ions interfered with the determination of zinc (II) except the ions of Ni2+, Cd2+, Mn2+, Pb2+, Fe2+ and Cu2+, which interference was eliminated by adding sodium hexametaphosphate, o-phenanthroline, and sodium diethyldithiocarbamate as appropriate masking reagents). The method had been successfully applied to online automatic monitoring of trace amounts of zinc in environmental water and the analytical results were satisfactory.
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
It is found that in pH 9.3 buffer solutions, zinc (II) reacts with 1-(2-pyridineazo)-2-naphtho to form a water-soluble complex of Zn (II)-1-(2-pyridineazo)-2-naphtho at the presence of Tween-80. Based on this, a simple and sensitive flow injection spectrophotometric method was proposed for online automatic monitoring of trace amounts of zinc in environmental water. Beer´s law was obeyed in the concentration range of 2.0 μg/L ~ 360.0 μg/L for zinc (II) and the detection limit calculated from three times of background noise was 0.42 μg/L. The relative standard deviation was 3.6% and 2.1% for 5.0 μg/L and 50.0 μg/L of zinc standard solution, respectively (n=8). The proposed method had good selectivity (No ions interfered with the determination of zinc (II) except the ions of Ni2+, Cd2+, Mn2+, Pb2+, Fe2+ and Cu2+, which interference was eliminated by adding sodium hexametaphosphate, o-phenanthroline, and sodium diethyldithiocarbamate as appropriate masking reagents). The method had been successfully applied to online automatic monitoring of trace amounts of zinc in environmental water and the analytical results were satisfactory.
Keywords
computerised monitoring; geochemistry; organic compounds; pH; spectrophotometry; water quality; zinc; Beer law; environmental water; online automatic monitoring; pH 9.3 buffer solution; sensitive flow injection spectrophotometric method; standard deviation; trace amounts; zinc standard solution; Absorption; Copper; Ions; Monitoring; Sensitivity; Spectroscopy; Zinc;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedical Engineering, (iCBBE) 2011 5th International Conference on
Conference_Location
Wuhan
ISSN
2151-7614
Print_ISBN
978-1-4244-5088-6
Type
conf
DOI
10.1109/icbbe.2011.5780757
Filename
5780757
Link To Document