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电感耦合等离子体质谱法测定食品营养强化剂中5种痕量有害金属元素 被引量:9

ICP-MS Determination of Trace Amounts of 5 Harmful Metal Elements in Food Nutrition Fortifier
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摘要 食品营养强化剂样品经硝酸(2+98)溶液溶解,用电感耦合等离子体质谱法测定其中重金属元素铅、砷、镉、汞、铜等的含量。选择钇(测铜及砷)、铑(测铅及镉)及金(测汞)作为内标元素可减小样品的基体效应。测定维生素C样品中汞量时,需加入硫脲作络合剂,使回收率达到正常值。方法的检出限(3S/N)在0.006~0.064μg·L^(-1)之间,各元素的相对标准偏差(n=11)在2.9%~5.9%之间。应用此法测定7种食品营养强化剂中的5种痕量重金属元素,加标回收率在92.0%~105%之间。 The sample of food nutrition fortifier was dissolved in HNOa (2+98) solution and the contents of Pb, As, Cd, Hg and Cu in the sample solution were determined by ICP-MS. Yttrium (for det'n, of Cu and As), rhodium (for Pb and Cd) and gold (for Hg) were selected as internal standards to decrease the matrix effects. In analyzing sample of vitamin C for its Hg-content, thiourea should be added as complexing agent to obtain normal recovery. Values of detection limit (3S/N) found were in the range of 0. 006-0. 064μg ·L-1 , and values of RSD's (n=ll) found were in the range of 2. 9%-5.9%. The proposed method was applied to the determination of trace amount of the 5 metal elements in 7 samples of nutrition fortifier, and values of recovery found by standard addition method were in the range of 92. 0%-105 %.
出处 《理化检验(化学分册)》 CAS CSCD 北大核心 2013年第9期1058-1060,1064,共4页 Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
关键词 电感耦合等离子体质谱法 食品营养强化剂 金属元素 ICP-MS Food nutrition fortifier Metal elements
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  • 1NILSON A, PIZA J. Food fortification: a tool for fighting hidden hunger[J]. Food Nutr Bull, 1998,19 49-60.
  • 2ZIMMERMANN M B, HURRELI, R F, HURRELL R F. Nutritional iron deficiency[J]. Lancet, 2007,370 (9586) : 511-520.
  • 3CLARKSON T W, MACK)S L. The toxicology of mercury and its chemical compounds, critical reviews in toxicology[J]. Crit Rev Toxicol, 2006,36.. 609-662.
  • 4LOCKITCH G. Perspectives on lead toxicity, clinical biochemistry[J]. Clin Biochem, 1993,26 (5) .. 371-381.
  • 5黄广民,姚伯元.高钙强化剂中痕量汞的测定[J].食品科学,2003,24(8):112-114. 被引量:6
  • 6MATTOS J C P, NUNES A M, MARTINS A F, etal. Influence of citric acid as chemical modifier for lead determination in dietary calcium supplement samples by graphite furnace atomic absorption spectrometry [J]. Spectrochim Acta, 2005,60B..687-692.
  • 7TYSON J F, ELLIS R I, CARNRICK G, et al. Flow injection hydride generation electrothermal atomic ab- sorption spectrometry with in-atomizer trapping for the determination of lead in calcium supplements[J]. Ta- lanta, 2000,52(3) .. 403-410.
  • 8BRINDLE I D, CMLAUGHLIN R, TANGREAM- JITMUN N. Determination of lead in calcium carbon- ate by flow-injection hydride generation with de plasma atomic emission detection [J]. Spectrochim Acta, 1998,53B: 1121-1129.
  • 9KIRBY J K, LYONS G H, KARKKAINEN M P. Se- lenium speciation and bioavailability in hiofortified products using species-unspecific isotope dilution and reverse phase ion pairing-inductively coupled plasma- mass spectrometry[J]. J Agric Food Chem, 2008,56 (5) :1772-1779.
  • 10FANG J, LIU L W, YAN X P. Minimization of mass interferences in quadrupole inductively coupled plasma mass spectrometric (ICP-MS) determination of palla- dium using a flow injection on-line displacement solid- phase extraction protocol[J] Spectrochim Acta, 2006,61B: 864-869.

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