Microwave-assisted alkaline digestion combined with microwave-assisted distillation for the determination of iodide and total iodine in edible seaweed by catalytic spectrophotometry

被引:46
作者
Gamallo-Lorenzo, D [1 ]
Barciela-Alonso, MD [1 ]
Moreda-Piñeiro, A [1 ]
Bermejo-Barrera, A [1 ]
Bermejo-Barrera, P [1 ]
机构
[1] Univ Santiago de Compostela, Fac Chem, Dept Analyt Chem Nutr & Bromatol, Santiago De Compostela 15782, Spain
关键词
iodide; total iodine; microwave-assisted distillation; edible seaweed; catalytic spectrophotometry;
D O I
10.1016/j.aca.2005.04.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Microwave energy has been novelty applied to speed up a tetramethylammonium hydroxide (TMAH) alkaline digestion of seaweed samples and to assist distillation of iodine from seaweed alkaline digests. Iodide in the alkaline digests from seaweed and distilled iodine, reduced back to iodine in a hydroxylamine hydrochloride solution, was determined by a catalytic spectrophotometric method based on the catalytic effect of iodide on the oxidation of As(III) by Ce(IV) in H2SO4/HCl medium (Sandell-Kolthoff reaction). The determination of iodide was directly performed in the alkaline digests, while total iodine was assessed by analyzing the hydroxylamine hydrochloride solution after the distillation process. Microwave-assisted alkaline digestion was performed using 7.5 mL of TMAH and irradiating samples at 670 W for two 5.5 min steps. Microwave-assisted distillation was carried out using 4.0 mL of the alkaline digest and 3 mL of a 2.2 M hydrochloric acid and 0.05 % (m/v) sodium nitrite solution, with a microwave power at 670 W for two 90 s steps. The distillate (iodine vapor) was bubbled in 10 mL of a 500 mu g mL(-1) hydroxylamine hydrochloride solution (accepting solution). The linear calibration ranges were 0.30-20.0 and 0.40-20.0 mu g L-1 for iodide determination and total iodine determination, respectively. The limit of detection was 9.2 mu g g(-1) for iodide and 28.5 mu g g(-1) for total iodine. Repeatability of the overall procedures, expressed as R.S.D. for 11 determinations, was 2.6 % for 196.3 mu g g(-1) iodide measured after microwave-assisted alkaline digestion, and 5.8 % for 954.3 mu g g(-1) of total iodine by microwave-assisted alkaline digestion followed by microwave-assisted distillation. Finally, accuracy of the methods was assessed by analyzing the NIST-09 (Sargasso) certified reference material and the methods were applied to the determination of iodide and total iodine in different Atlantic edible seaweed samples with satisfactory results. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:287 / 295
页数:9
相关论文
共 27 条
[1]  
[Anonymous], 1993, INT J FOOD SCI NUTR
[2]  
Aquaron R, 2002, CELL MOL BIOL, V48, P563
[3]   Microwave-assisted distillation of iodine for the indirect atomic absorption spectrometric determination of iodide in milk samples [J].
Bermejo-Barrera, P ;
Aboal-Somoza, M ;
Bermejo-Barrera, A ;
Cervera, ML ;
de la Guardia, M .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2001, 16 (04) :382-389
[4]  
Chapman V.J., 1980, SEA VEGETABLES ALGAE
[5]   Use of pseudo-first order kinetics in flow injection for determination of trace inorganic iodine [J].
Choengchan, N ;
Lukkanakul, K ;
Ratanawimarnwong, N ;
Waiyawat, W ;
Wilairata, P ;
Nacapricha, D .
ANALYTICA CHIMICA ACTA, 2003, 499 (1-2) :115-122
[6]  
Department of Health, 1991, DIET REF VAL FOOD EN
[7]   Determination of iodine in food samples by inductively coupled plasma mass spectrometry after alkaline extraction [J].
Fecher, PA ;
Goldmann, I ;
Nagengast, A .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1998, 13 (09) :977-982
[8]  
FERNANDEZSAA C, 2002, ALGAS GALICIA ALIMEN
[9]  
FERNANDEZSANCHE.LM, 1999, J ANAL ATOM SPECTROM, V14, P41
[10]  
FISHER KD, 1985, AM J CLIN NUTR, V42, P1318