Bossu, Carla Maíra [UNESP]De Oca Carioni, Vivian MontesNaozuka, JulianaDe Oliveira, Pedro VitorianoNomura, Cassiana Seimi2019-10-062019-10-062019-01-01Ecletica Quimica, v. 44, n. 2, p. 37-44, 2019.1678-46180100-4670http://hdl.handle.net/11449/187700This work describes a simple and rapid screening method for direct speciation of arsenobetaine (AsB) in tuna fish tissue and total As in tuna fish tissue and robalo liver using SLS-GF AAS. All procedures were proposed after careful optimization of pyrolysis and evaluation of chemical modifiers. Best results for total As were acquired using 25 μg Pd + 15 μg Mg + 0.1% w/v Triton X-100 in tuna fish (4.4 ± 0.3 mg kg-1) and 100 μg Pd + 0.1 % w/v Triton X-100 solution in robalo liver (10.3 ± 0.6 mg kg-1) as chemical modifiers. The direct speciation of AsB (3.6 ± 0.4 mg kg-1) in tuna fish was achieved when 5 μg Pd + 3 μg Mg + 0.1% w/v Triton X-100 was used as a chemical modifier. Accuracy was verified using a tuna fish certified reference material (CRM BCR 627), with statistically equivalent concentrations (Student's t-test) for both total As and AsB.37-44eng1. arsenic 2. direct chemical speciation 3. tuna fish 4. robalo liver 5. reference materialDirect determination of arsenobetaine and total As in robalo fish liver and tuna fish candidate reference material by slurry sampling graphite furnace atomic absorption spectrometry (SLS-GF AAS)Artigo10.26850/1678-4618eqj.v44.2.p37-44Acesso restrito2-s2.0-85066250968