2017
DOI: 10.1016/j.molliq.2017.04.066
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Ligandless switchable solvent based liquid phase microextraction of nickel from food and cigarette samples prior to its micro-sampling flame atomic absorption spectrometric determination

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Cited by 53 publications
(8 citation statements)
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“…The kinetics of the photocatalytic degradation rate of the probe molecules was evaluated according to the Langmuir–Hinshelwood kinetic model as given below. 8 equivalent Hinshelwood kinetic model: The photocatalytic degradation efficiency of g-C 3 N 4 @TiO 2 @Fe 3 O 4 NPs for the trimethoprim and isoniazid drug active species was analyzed according to the Langmuir–Hinshelwood kinetic model. The results obtained showed that ∼100% of trimethoprim and isoniazid were photocatalytically degraded in ∼120 and 100 min, respectively ( Figure 7 A).…”
Section: Results and Discussionmentioning
confidence: 99%
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“…The kinetics of the photocatalytic degradation rate of the probe molecules was evaluated according to the Langmuir–Hinshelwood kinetic model as given below. 8 equivalent Hinshelwood kinetic model: The photocatalytic degradation efficiency of g-C 3 N 4 @TiO 2 @Fe 3 O 4 NPs for the trimethoprim and isoniazid drug active species was analyzed according to the Langmuir–Hinshelwood kinetic model. The results obtained showed that ∼100% of trimethoprim and isoniazid were photocatalytically degraded in ∼120 and 100 min, respectively ( Figure 7 A).…”
Section: Results and Discussionmentioning
confidence: 99%
“…Analysis techniques for drug active ingredients include high-performance liquid chromatography (HPLC), gas chromatography–mass spectroscopy (GC–MS), liquid chromatography–mass spectroscopy (LC–MS), and high-performance thin-layer chromatography (HPTLC) . However, direct analysis is not always possible due to complications such as the lowest analyte concentration that these devices can measure, higher than the amounts found in the samples studied, and/or the matrix effects of foreign species present in the sample environment. , Therefore, for the accurate and sensitive analysis of drug active ingredients in the instrumental detection system, a sample preparation method is required to separate drug active ingredients from the matrix environment and bring their concentration to a measurable level …”
Section: Introductionmentioning
confidence: 99%
“…Despite all the above, SHSs have not attracted the interest compared with other alternative solvents used in liquidphase microextraction techniques. First of all, in spite of employing CO 2 for the solubilization step, the subsequent pH change is normally performed with strong acids [14][15][16] or strong bases [17,18]. Second, about their safety, some SHSs (especially, those formed from secondary amines) are expected to be safer than traditional solvents in some terms like flammability or smog formation [19].…”
Section: Switchable Hydrophilicity Solventsmentioning
confidence: 99%
“…A negligible amount of organic solvent is used for the extraction and pre-concentration of the sample before analysis [62][63][64][65][66][67][68][69][70]. Microextraction has different modes such as vortex-assisted liquid-liquid microextraction [71, 72], solid-phase microextraction (SPME) [73][74][75][76][77][78][79][80][81][82][83][84][85][86] and liquid-phase microextraction (LPME) [75,77,79,[87][88][89][90][91][92][93], Dispersive liquid-liquid microextraction (DLLME) [75,94], cloud point extraction, (CPE) [95][96][97][98][99], single-drop microextraction (SDME) [100], ionic liquid-based dispersive liquid-liquid microextraction (IL-DLLME) [101,102] dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO) [103]. However, the recent trends involve the miniaturization of the conventional liquid-liquid extraction principle.…”
Section: Suprass-based Lpmementioning
confidence: 99%