Determination of Gold in Various Environment Samples by Flame Atomic Absorption Spectrometry Using Dispersive Liquid–Liquid Microextraction Sampling

Saçmacı, Şerife; Kartal, Şenol; Kalkan, Gülçin

doi:10.5562/cca2412

Croat. Chem. Acta

2015

DOI: 10.5562/cca2412

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Determination of Gold in Various Environment Samples by Flame Atomic Absorption Spectrometry Using Dispersive Liquid–Liquid Microextraction Sampling

Şerife Saçmacı¹,

Şenol Kartal²,

Gülçin Kalkan³

Abstract: Abstract.A new dispersive liquid-liquid microextraction separation/preconcentration procedure as a rapid sample-preparation technique is proposed for detection of ultra trace amounts of Au(III) in various media by flame atomic absorption spectrometry using 1,5-diphenyl-1,3,5-pentanetrione as chelating agent. Carbon tetrachloride and methanol were used as extraction and dispersive solvents, respectively. Various parameters that affect the extraction efficiency such as pH, centrifugation rate and time, chelating… Show more

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Cited by 6 publications

References 26 publications

(27 reference statements)

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A new procedure for determination of nickel in some fake jewelry and cosmetics samples after dispersive liquid–liquid microextraction by FAAS

Saçmacı

2017

Applied Organom Chemis

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A new, simple and cheap dispersive liquid–liquid microextraction (DLLME) procedure was optimized for the preconcentration of trace amounts of Ni(II) as a prior step to its determination by flame atomic absorption spectrometry (FAAS). It is based on the microextraction of nickel, where appropriate amounts of the extraction solvent (CHCl3), disperser solvent (ethanol) and chelating agent, name 5‐[(Z)‐isoxazol‐3‐yl‐diazenyl]‐2‐methyl‐quinolin‐8‐ol (MMD), were firstly synthesized/characterized and used. Various parameters that affect the extraction procedure such as pH, centrifugation rate and time, the chelating agent (MMD) concentration and sampling volume on the recovery of Ni(II) were investigated. The preconcentration of a 20 ml sample solution was thus enhanced by a factor of 80. The resulting calibration graph was linear in the range of 0.24–10 mg L−1 with a correlation coefficient of 0.9998. The limit of detection (3 s/b) obtained under optimal conditions was 1.00 μg L−1. The relative standard deviation for certified reference material determinations was 1.2%. The accuracy of the method was verified by the determination of Ni(II) in the certified reference material of wastewater (Waste water CWW TMD). The proposed procedure was successfully applied to the determination of Ni(II) in some fake jewelry and cosmetics samples.

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A new procedure for determination of nickel in some fake jewelry and cosmetics samples after dispersive liquid–liquid microextraction by FAAS

Saçmacı

2017

Applied Organom Chemis

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A tandem ionic liquid‐based dispersive microextraction method using in‐syringe air‐assisted vesicle system for rapid determination of lead and cadmium in artificial sweat extract of facial cosmetic products

Akhtar

Kazi

Afridi

et al. 2020

Applied Organom Chemis

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In the present study an innovative tandem ionic liquid‐based dispersive microextraction method using an in‐syringe air‐assisted vesicle system was developed to determine the ultra‐trace levels of lead (PbII) and cadmium (CdII) ions in synthetic sweat extract of branded and nonbranded facial cosmetic products. This method is based on injecting 2‐amino‐3‐sulfhydrylpropanoic acid (l‐cysteine) (as an eco‐friendly chelating agent), hexafluorophosphate ion [PF6−] (as an ion pair agent) and 1‐hexyl‐3‐methylimidazolium hexafluorophosphate [HMIM] [PF6] (as an acceptor phase) into the synthetic sweat extract of facial cosmetic products (branded and nonbranded). The acceleration of the dispersion process was carried out by rapid pressure in the syringe through the back‐and‐forth movement of plunger. The sediment phase was removed following centrifugation, and then hydrophobic complexes of analyte were back‐extracted into HNO3 and finally injected into a flame atomic absorption spectrometer. Several factors were systematically optimized. The validity of the methodology was tested by analyzing spiked known standards of both metals in a real sample. The proposed method was applied to the artificial sweat extracts of face makeup products, indicating how much toxic metals from different cosmetics are directly absorbed into skin.

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An ion-imprinted thiocyanato-functionalized mesoporous silica for preconcentration of gold(III) prior to its quantitation by slurry sampling graphite furnace AAS

et al. 2018

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A gold(III)-imprinted thiocyanato-functionalized silica network of type SBA-15 was prepared by co-condensation of tetraethoxysilane (TEOS) with thiocyanatopropyltriethoxysilane (TCTES) in the presence of Pluronic123 and Au(III) ions. Compared to the non-imprinted material, the imprint has a higher selectivity and adsorption capacity for Au(III). The maximum static adsorption capacity for Au(III) is 475 mg·g−1 for the ion-imprinted, and 62 mg·g−1 for the non-imprinted sorbent. The imprint was applied to the sorption of Au(III) from digested geological samples prior to its determination by graphite furnace atomic absorption spectrometry. Adsorption is fast and does not substantially prolong the analytical procedure. Under optimum conditions, the detection limit for Au(III) is 2 ng·g−1. The method was validated by analyzing certified reference materials, and results were in good agreement with certified values. The procedure was successfully applied to the separation and determination of gold in complex geological samples. Graphical abstractSchematic presentation of the preparation of ion-imprinted thiocyanato-functionalized mesoporous silica and its application for the preconcentration of gold from digested soils before its determination by slurry sampling graphite furnace atomic absorption spectrometry (GF AAS). Electronic supplementary materialThe online version of this article (10.1007/s00604-018-3106-x) contains supplementary material, which is available to authorized users.

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Determination of Gold in Various Environment Samples by Flame Atomic Absorption Spectrometry Using Dispersive Liquid–Liquid Microextraction Sampling

Cited by 6 publications

References 26 publications

A new procedure for determination of nickel in some fake jewelry and cosmetics samples after dispersive liquid–liquid microextraction by FAAS

A new procedure for determination of nickel in some fake jewelry and cosmetics samples after dispersive liquid–liquid microextraction by FAAS

A tandem ionic liquid‐based dispersive microextraction method using in‐syringe air‐assisted vesicle system for rapid determination of lead and cadmium in artificial sweat extract of facial cosmetic products

An ion-imprinted thiocyanato-functionalized mesoporous silica for preconcentration of gold(III) prior to its quantitation by slurry sampling graphite furnace AAS

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