Ti3AlC2 max phase- graphene oxide (GO) nanocomposite for selective solid phase microextraction of palladium in environmental samples and medical appliances prior to its detection with high-resolution continuum source flame atomic absorption spectrometry (HR-CS-FAAS)

石墨烯 纳米复合材料 材料科学 氧化物 固相微萃取 原子吸收光谱法 相(物质) 分析化学(期刊) 吸收(声学) 纳米技术 化学 环境化学 色谱法 物理 气相色谱-质谱法 质谱法 有机化学 复合材料 催化作用 冶金 量子力学
作者
Mansoor Khan,Mustafa Soylak
出处
期刊:Microchemical Journal [Elsevier BV]
卷期号:185: 108200-108200 被引量:23
标识
DOI:10.1016/j.microc.2022.108200
摘要

• Novel material Ti 3 AlC 2 max phase graphene oxide GO nanocomposite has been synthesized. • Solid phase extrication method based Ti 3 AlC 2 max phase GO nanocomposite has been develop for palladium. • All the extrication efficiency effecting parameters of the adsorbent has been optimized. • The method was applied to medical appliances samples. Palladium is an important metal as it has a wide range of applications in different fields but can cause cancer in human beings. Therefore, precise quantification of palladium is important. For this purpose, new material Ti 3 AlC 2 max phase having unique properties like high stability, thermal conductivity and environmental friendly has been synthesized. To increase its surface area of Ti 3 AlC 2 max phase, graphene oxide (GO) has been incorporated to form Ti 3 AlC 2 max phase GO nanocomposite. Ti 3 AlC 2 max phase GO nanocomposite was used as solid phase extracting material for microextraction and preconcentration of Pd(II) in environmental samples and medical appliances. Characterization of the adsorbent was achieved by using fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), x-ray diffraction (XRD), energy dispersive x-ray (EDX) and surface area analyzer (SAA). All the parameters that influence the extraction efficiency of the adsorbent like solution pH, amount of adsorbent, volume of sample, vortex time, desorption condition and interferences effect were determined and optimized. The limit of detection (0.327 µg L -1 ) and limit of quantification (1.09 µg L -1 ) show that the method is highly sensitive. The relative standard deviation was calculated as 5.48 % for five repeated measurements, which shows that the developed method is reproducible. The method is highly efficient with large values of preconcentration factor (20) and enhancement factors (20). The method was validated by applying the method to real water samples, soil samples and medical appliances with satisfied recovery results (94-106 %).
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