scholarly journals Cloud Point Extraction and Determination of Silver Ion in Real Sample using Bis((1H-benzo[d]imidazol-2yl)methyl)sulfane

2011 ◽  
Vol 8 (1) ◽  
pp. 435-442 ◽  
Author(s):  
Farshid Ahmadi ◽  
Khodabakhsh Niknam ◽  
Ebrahim Niknam ◽  
Saeid Delavari ◽  
Azadeh Khanmohammadi

Bis((1H-benzo[d]imidazol-2yl)methyl)sulfane (BHIS) was used as a complexing agent in cloud point extraction for the first time and applied for selective pre-concentration of trace amounts of silver. The method is based on the extraction of silver at pH 8.0 by using non-ionic surfactant T-X114 and bis((1H-benzo[d]imidazol-2yl)methyl)sulfane as a chelating agent. The adopted concentrations for BHIS, Triton X-114 and HNO3, bath temperature, centrifuge rate and time were optimized. Detection limits (3SDb/m) of 1.7 along with enrichment factor of 39 for silver ion was achieved. The high efficiency of cloud point extraction to carry out the determination of analytes in complex matrices was demonstrated. The proposed method was successfully applied to the ultra-trace determination of silver in real samples.

2018 ◽  
Vol 5 (7) ◽  
pp. 180070 ◽  
Author(s):  
H. Z. Hazrina ◽  
M. S. Noorashikin ◽  
S. Y. Beh ◽  
S. H. Loh ◽  
N. N. M. Zain

Cloud point extraction (CPE) is a separation and preconcentration of non-ionic surfactant from one liquid phase to another. In this study, Sylgard 309 and three different types of additives for CPE, namely CPE-Sylgard, CPE-Sylgard-BMIMBr and CPE-Sylgard-GLDA, are investigated to extract methylphenol from water samples. The methylphenols are well separated by reversed-phase high-performance liquid chromatography (HPLC) with isocratic elution of acetonitrile : water; 60 : 40 (v/v) and detection at 260 nm. The optimized parameters for the effect of salt, surfactant, temperature, time of extraction, pH, interference study and the performance of different additives on methylphenol extraction are investigated. CPE-Sylgard-GLDA is chosen because it gives us a high peak and good peak area compared with CPE-Sylgard and CPE-Sylgard-BMIMBr. The recovery extractions of CPE-Sylgard-GLDA are obtained in the range of 80–99% as the percentage of relative standard deviation (RSD) is less than 10. The LOD and LOQ are 0.05 ppm and 0.18 ppm, respectively. The method developed for CPE-Sylgard-GLDA coupled with HPLC is feasible for the determination of methylphenol because it is simple, effective, cheap, and produces a high percentage of recovery.


2020 ◽  
Vol 10 (03) ◽  
pp. 459-464
Author(s):  
Azhar A. Ghali

During the last years, the cloud point extraction was applied for determination, separation, and enrichment of the elements. The current study used cloud point extraction (CPE) for the extraction of Ag(I) ions pre-concentration from watery solutions by a non-ionic surfactant (Triton X-114) and chelating agent a 6-(4-bromo-phenylazo)m-anisidine[6-(4-BrPAA)], then estimation by using the spectrophotometry at 514 nm. Several condition effects on the efficiency of the cloud-point extraction included Triton X-114 concentration, [6-(4-BrPAA)] concentration, pH, time, and incubation temperature. The silver reacts with [6-(4-BrPAA)] to produce complex at a ratio of one to one. 0.009 to 1.5 μg mL-1 is the range of linearity. The detection limit and quantification of Ag(I) ion were 0.0054 and 0.0182 μg mL-1, respectively. The interference of the cations was examined. The cloud-point extraction was used for the evaluation of silver concentration in the water specimen.


2015 ◽  
Vol 98 (1) ◽  
pp. 201-205 ◽  
Author(s):  
Sayed Zia Mohammadi ◽  
Mohsen Mohammadnezhad

Abstract In this study, the phase-separation phenomenon ofnon-ionic surfactants was used for separation and preconcentration of Pd(II). The cloud point extraction(CPE) method is based on the formation of PdI2 which is then entrapped in the non-ionic surfactant Triton X-114. Ethanol acidified with 0.5 M HNO3 was added to the surfactant-rich phase prior to its analysis by flame atomic absorption spectrometry. The main factors affecting CPE efficiency, such as sample solution pH, concentration of iodide ion and Triton X-114, equilibration temperature and time, were all investigated and optimized. At optimum conditions, a calibration curve was constructed for the determination of palladium according to the ligandless CPE procedure. Linearity was maintained between 1.0 to 500.0 ng/mL. The LOD based on three times the SD of the blank divided by the slope of analytical curve, (3Sb/m) was 0.3 ng/mL. Seven replicatedeterminations of a solution containing of 4.0 μg palladium gave a mean absorbance of 0.359 with RSD ±1.85%. The high efficiency of CPE to carry out the determination of palladium in complex matrixes was demonstrated. The proposed method has beenapplied to the determination of trace amounts of palladium in a platinum-iridium alloy, water, and dust samples, with satisfactory results.


RSC Advances ◽  
2015 ◽  
Vol 5 (80) ◽  
pp. 65321-65327 ◽  
Author(s):  
Chunlei Fan ◽  
Shengxu Luo ◽  
Rong Liu

BTF is exists with spirolactone species with adding Cu2+, which leads to the absorbance intensity is decreased gradually and the decrease of the absorbance value is linear for Cu2+.


2021 ◽  
pp. 174751982110273
Author(s):  
Quan Han ◽  
Yanyan Huo ◽  
Xiaohui Yang ◽  
Xing Yao

A highly sensitive method for the determination of ultra-trace levels of palladium in water samples by cloud point extraction and graphite furnace atomic absorption spectrometry is developed. The procedure is based on complexation of palladium with a laboratory-prepared novel chelating agent, 2-(5-bromo-4-methyl-2-pyridylazo)-5-dimethylaminoaniline (5-Br-4-CH3-PADMA) and subsequent micelle-mediated extraction of the product using the non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114) as an extracting agent. Analytical parameters affecting the separation and detection process, such as pH, concentration of the chelating agent and surfactant, equilibration temperature, and time are investigated. The optimized conditions are as follows: pH 6.0 HAc–NaAc buffer solution, 1 × 10−5 mol L−1 5-Br-4-CH3-PADMA, and 0.1% (w/v) Triton X-114. Under the optimized conditions, the calibration graph is linear in the range of 0.1–12 ng/mL, the detection limit is 0.05 ng/mL for palladium, and the relative standard deviation is 2.9% ( c = 1.0 ng/mL, n = 10). The enrichment factor, defined as the ratio of the aqueous solution volume to that of the surfactant-rich phase volume after dilution with HNO3–methanol solution, is 200. The proposed method is applied to the determination of palladium in water samples with satisfactory results.


Author(s):  
Ambreen Shah ◽  
Fayyaz Ahmed Keerio ◽  
Saima Qayyum Memon ◽  
Ghulam Zuhra Memon

A new method of cloud point extraction was determined for preconcentration and determination of different metal ions like copper(II), nickel(II) and cobalt(II) ions. The complexation has been done by bis(2-acetyl pyridine 4-phenyl 3-thiosemicarbazone) (APPT) using sodium dodecyl sulphate (SDS) as surfactant. Metal ions are extracted into the phase rich in SDS after centrifugation. Initially, micellar phase was dissolved in 10 mL of deionized water then acidified with 0.5 mol/L HNO3, enhanced the surfactant- rich phase and analyzed by flame atomic absorption spectrometry (FAAS). The effects of pH, the concen- trations of metal ions and chelating agent (APPT), volume of surfactant (SDS), equilibration temperature and time were studied on CPE. The preconcentration factor obtained was 25 and the limits of detection(DL) obtained for cobalt(II), nickel(II) and copper(II) were 1.5, 1.7 and 2.4 ng/mL, respectively. This method of preconcentration was effectively useful for the determination of cobalt(II), nickel(II) and copper(II) in water samples.


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