化学
试剂
锌
高效液相色谱法
掩蔽剂
色谱法
检出限
水溶液
硫酸
乙腈
萃取(化学)
微量
无机化学
有机化学
病理
医学
替代医学
作者
Nobuo Uehara,Kazutomo NOMOTO,Tokuo Shimizu
标识
DOI:10.2355/tetsutohagane1955.89.9_914
摘要
A novel method for the determination of trace amounts of zinc in iron and steel has been demonstrated by a reversed-phase HPLC using α, β, γ, δ-tetrakis(4-carboxyphenyl)porphine as a derivatizing reagent. Certified reference materials of iron and steel were used to prepare digestive samples by decomposition followed by 4-methyl-2-pentanone extraction and sulfuric acid fuming. The digested sample solutions were derivatized with Cd(II)-α, β, γ, δ-tetrakis(4-carboxyphenyl)porphine solution in ammonium buffer (pH 9.0) solution, using 5-sulfosalicylate as a masking reagent. Aqueous-acetonitrile (45:55 w/w) containing 7.0 × 10-2 mol kg-1 of lactate buffer (pH 4.15) was used as an eluent and was monitored at 422 nm.A linear calibration was observed in the concentration range from 1 × 10-8 mol dm-3 to 1 × 10-6 mol dm-3. The detection limit (3σ) of Zn(II) was 1.3 × 10-9 mol dm-3, which corresponded to 0.32 ppm in iron and steel samples. The recoveries of zinc added to the digested solution of iron and steel were with in 97 to 107%. The good recovery and high sensitivity indicate that the proposed system is of great promise for the determination of zinc present in iron and steel.
科研通智能强力驱动
Strongly Powered by AbleSci AI