Souza e Silva Renata, de Carvalho Maria de Fátima Batista, Santelli Ricardo Erthal
Programa de Pós-Graduação em Química, Universidade Federal Fluminense, Outeiro de São João Batista s/n, Centro, Niterói/RJ 24020-150, Brazil.
J Chromatogr A. 2006 Sep 15;1127(1-2):200-6. doi: 10.1016/j.chroma.2006.06.020. Epub 2006 Aug 4.
A separation and determination method for the analysis of cyanometallic complexes of Fe(II), Ni(II) and Co(III) was developed to be applied to the analysis of petroleum refinery streams (sour water). Ion-interaction chromatography was used employing an analytical column IonPac NS1 10 microm and a chromatographic system ICS 2500 equipped with a membrane conductivity suppression ASRS ultra 4mm, both supplied by Dionex Corporation. The mobile phase was composed of 2 mmol l(-1) TBAOH, 1 mmol l(-1) Na(2)CO(3), 0.1 mol l(-1) NaCN and ACN (77:23, v/v), flowing at 0.7 ml min(-1). At the optimized conditions, detection limits estimated by the calibration curve parameters and relative standard deviation were: 0.002 mg CNl(-1) and 3.1% for Fe(CN)(6)(4-); 0.003 mg CNl(-1) and 2.5% for Ni(CN)(4)(2-) and 0.003 mg CNl(-1) and 2.8% for Co(CN)(6)(3-). Sour water samples without any pretreatment (except membrane filtration) from a petroleum refinery in Brazil were analyzed successfully by external calibration method.
开发了一种用于分析Fe(II)、Ni(II)和Co(III)的氰基金属配合物的分离和测定方法,并将其应用于石油炼制物流(酸性水)的分析。采用离子相互作用色谱法,使用Dionex公司提供的IonPac NS1 10微米分析柱和配备4毫米ASRS ultra膜抑制器的ICS 2500色谱系统。流动相由2 mmol l(-1) TBAOH、1 mmol l(-1) Na(2)CO(3)、0.1 mol l(-1) NaCN和乙腈(77:23,v/v)组成,流速为0.7 ml min(-1)。在优化条件下,通过校准曲线参数估计的检测限和相对标准偏差分别为:Fe(CN)(6)(4-)为0.002 mg CNl(-1)和3.1%;Ni(CN)(4)(2-)为0.003 mg CNl(-1)和2.5%;Co(CN)(6)(3-)为0.003 mg CNl(-1)和2.8%。采用外标法成功分析了巴西一家炼油厂未经任何预处理(除膜过滤外)的酸性水样品。