Determination of Iodate in Food, Environmental, and Biological Samples after Solid-Phase Extraction with Ni-Al-Zr Ternary Layered Double Hydroxide as a Nanosorbent

被引:32
作者
Abdolmohammad-Zadeh, Hossein [1 ]
Tavarid, Keyvan [1 ]
Talleb, Zeynab [1 ]
机构
[1] Azarbaijan Univ Tarbiat Moallem, Fac Sci, Dept Chem, Tabriz 5375171379, Iran
关键词
KINETIC-SPECTROPHOTOMETRIC DETERMINATION; CHROMATOGRAPHY-MASS SPECTROMETRY; CAPILLARY ZONE ELECTROPHORESIS; GLASSY-CARBON ELECTRODE; FLOW-INJECTION; ION CHROMATOGRAPHY; TABLE SALT; AMPEROMETRIC DETECTION; WATER SAMPLES; IODIDE;
D O I
10.1100/2012/145482
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Nanostructured nickel-aluminum-zirconium ternary layered double hydroxide was successfully applied as a solid-phase extraction sorbent for the separation and pre-concentration of trace levels of iodate in food, environmental and biological samples. An indirect method was used for monitoring of the extracted iodate ions. The method is based on the reaction of the iodate with iodide in acidic solution to produce iodine, which can be spectrophotometrically monitored at 352 nm. The absorbance is directly proportional to the concentration of iodate in the sample. The effect of several parameters such as pH, sample flow rate, amount of nanosorbent, elution conditions, sample volume, and coexisting ions on the recovery was investigated. In the optimum experimental conditions, the limit of detection (3s) and enrichment factor were 0.12 mu g mL(-1) and 20, respectively. The calibration graph using the preconcentration system was linear in the range of 0.2-2.8 mu g mL(-1) with a correlation coefficient of 0.998. In order to validate the presented method, a certified reference material, NIST SRM 1549, was also analyzed.
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页数:8
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