Zabielska-Konopka Magda, Zambrzycka-Szelewa Elżbieta, Kowalewska Zofia, Godlewska-Żyłkiewicz Beata
Doctoral School of Exact and Natural Sciences, University of Bialystok, Ciołkowskiego 1K, 15-245, Białystok, Poland.
Department of Analytical and Inorganic Chemistry, Faculty of Chemistry, University of Bialystok, K. Ciołkowskiego 1K, 15-245, Białystok, Poland.
Talanta. 2025 Jan 1;281:126894. doi: 10.1016/j.talanta.2024.126894. Epub 2024 Sep 14.
This work presents a simple and accurate method for the fast sequential determination of Rh, Pd, and Pt in spent automotive catalysts and e-wastes using high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS). Extensive research was carried out in model systems on the impact of potential interfering substances on analyte's signals measured in two types of flame (air-CH and NO-CH). Mutual analyte interactions were also taken into account. Different background corrections offered by the HR-CS AAS spectrometer were tested to obtain interference-free analyte signals and the best detectability. Using an air-CH flame and 1 % La solution as a spectrochemical buffer provided good sensitivity and accurate determinations of Rh, Pd, and Pt using a simple calibration graph. Microwave-assisted leaching of PGE from waste samples with aqua regia at 240 °C for 60 min efficiently leached all target metals, which significantly simplified and shortened the sample preparation step. The detectability of the method (detection limit of 0.4, 0.6, and 5 mg kg for Rh, Pd, and Pt, respectively) and precision (< 7 %) were satisfactory. The accuracy of the method was confirmed by analysis of certified reference materials (spent automotive catalyst (ERM-EB504), electronic scrap (BAM-M505a)), and calculated zeta score values. The recoveries for Rh, Pd, and Pt in ERM-EB504 were 93, 101, and 96 %, respectively, and for Pd in BAM-M505a, 97 %. The developed method can be used to assess the value of secondary raw materials, such as various types of spent catalysts and e-waste containing Rh, Pd, and Pt.
本研究提出了一种简单且准确的方法,利用高分辨率连续光源火焰原子吸收光谱法(HR-CS FAAS)快速连续测定废旧汽车催化剂及电子废弃物中的铑(Rh)、钯(Pd)和铂(Pt)。在模型体系中,针对潜在干扰物质对两种火焰(空气 - 乙炔和氧化亚氮 - 乙炔)中分析物信号的影响展开了广泛研究。同时也考虑了分析物之间的相互作用。对HR-CS AAS光谱仪提供的不同背景校正方法进行了测试,以获得无干扰的分析物信号及最佳检测限。使用空气 - 乙炔火焰和1%的镧溶液作为光谱化学缓冲剂,通过简单的校准曲线即可实现对Rh、Pd和Pt的良好灵敏度和准确测定。采用王水在240℃下对废弃物样品进行60分钟的微波辅助浸出,能有效浸出所有目标金属,显著简化并缩短了样品制备步骤。该方法的检测限(Rh、Pd和Pt分别为0.4、0.6和5 mg/kg)和精密度(<7%)令人满意。通过对有证标准物质(废旧汽车催化剂(ERM-EB504)、电子废料(BAM-M505a))的分析及计算zeta评分值,证实了该方法的准确性。ERM-EB504中Rh、Pd和Pt的回收率分别为93%、101%和96%,BAM-M505a中Pd的回收率为97%。所开发的方法可用于评估各类含Rh、Pd和Pt的废旧催化剂及电子废弃物等二次原材料的价值。