In situ formed 1-hexyl-3-methylimidazolium hexafluorophosphate for dispersive liquid-liquid microextraction of Pd(II) prior to electrothermal AAS and spectrophotometry

1-Hexyl-3-methylimidazolium hexafluorophosphate was prepared in situ and used as extractant in dispersive liquid-liquid microextraction. Ultra-trace amounts of Pd(II) could be accurately determined by electrothermal atomic absorption spectrometry (ETAAS) and spectrophotometry after extraction by the formed micro-droplets of the ionic liquid phase. 1-(2-Pyridylazo)-2-naphthol was used to produce a hydrophobic palladium complex prior to extraction. The effects of concentrations of reagents, reaction and extraction times, and the other parameters were investigated and optimized. Beer's law was obeyed in the ranges of 0.015-0.900 and 1.50-63.0 ng mL-1 Pd(II) by ETAAS and spectrophotometry, respectively. Under the optimized conditions, the limit of detection (LOD) by ETAAS was 3 ng L-1 with an enrichment factor of 460. The RSD percent was in the range of 1.3%-4.8% for various standard concentrations of Pd(II) in the range of 0.050-40.0 ng mL-1. Most ions did not interfere. The method was successfully applied to the determination of Pd(II) in some water and alloy samples, jewels, and palladium catalysts.

In situ formed 1-hexyl-3-methylimidazolium hexafluorophosphate for dispersive liquid-liquid microextraction of Pd(II) prior to electrothermal AAS and spectrophotometry

1-Hexyl-3-methylimidazolium hexafluorophosphate was prepared in situ and used as extractant in dispersive liquid-liquid microextraction. Ultra-trace amounts of Pd(II) could be accurately determined by electrothermal atomic absorption spectrometry (ETAAS) and spectrophotometry after extraction by the formed micro-droplets of the ionic liquid phase. 1-(2-Pyridylazo)-2-naphthol was used to produce a hydrophobic palladium complex prior to extraction. The effects of concentrations of reagents, reaction and extraction times, and the other parameters were investigated and optimized. Beer's law was obeyed in the ranges of 0.015-0.900 and 1.50-63.0 ng mL-1 Pd(II) by ETAAS and spectrophotometry, respectively. Under the optimized conditions, the limit of detection (LOD) by ETAAS was 3 ng L-1 with an enrichment factor of 460. The RSD percent was in the range of 1.3%-4.8% for various standard concentrations of Pd(II) in the range of 0.050-40.0 ng mL-1. Most ions did not interfere. The method was successfully applied to the determination of Pd(II) in some water and alloy samples, jewels, and palladium catalysts.

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Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

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Design, synthesis, and biological evaluation of indole-based 1,4-disubstituted piperazines as cytotoxic agents

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Symmetric, twinned, and double-decker phthalocyanines substituted by trialkylated pentaerythritol

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Determination of lidocaine based on electrocatalysis of a chemically modified electrode

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Synthesis and structural characterization of novel square pyramidal oxovanadium(IV) complexes with ligands having N and O donor atoms

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A new absorption based CO2 sensor based on Schiff base doped ethyl cellulose

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Titrimetric determination of anionic surfactant content in anionic/nonionic surfactant mixture solution by anionic surfactant selective electrode

Junwei WANG, Zhiping DU, Wanxu WANG, Wei XUE

Three-component Passerini-Smiles coupling reaction of aldehydes and isocyanides with tropolone catalyzed by silica nanoparticles

Abdolhossain MASSOUDI, Issa AMINI, Ali RAMAZANI And

Facile and rapid synthesis of some novel polysubstituted imidazoles by employing magnetic $Fe_3O_4$ nanoparticles as a high efficient catalyst

Khalil ESKANDARI, Abdolmohammad GHASEMI, Bahador KARAMI

Simultaneous determination of dopamine, uric acid, and tryptophan using an MWCNT modified carbon paste electrode by square wave voltammetry

Hadi BEITOLLAHI, Alireza MOHADESI, Saeedeh KHALILIZADEH MAHANI