Cloud point extraction and separation of copper and lanthanoids using Triton X-100 with water-soluble p-sulfonatocalix[4]arene as a chelating agent

2010 ◽  
Vol 169 (3-4) ◽  
pp. 297-301 ◽  
Author(s):  
Yancun Wei ◽  
Yanling Li ◽  
Xinjun Quan ◽  
Wuping Liao
2011 ◽  
Vol 94 (6) ◽  
pp. 1853-1862 ◽  
Author(s):  
Ebru Ates ◽  
Klaus Mittendorf ◽  
Hamide Senyuva

Abstract A cloud point extraction method is reported using LC/MS for the determination of regulated water-soluble food colors (Allura Red, Sunset Yellow, erythrosine, and tartrazine) and banned fat-soluble synthetic azo dyes (Sudan I, II, III, and IV; Red B; 7B; Black B; Red G; Metanil Yellow; and Rhodamine B). The extraction of all 14 colors was carried out with cloud point extraction using the nonionic surfactant Triton X 114. Optimized conditions for cloud point extraction were 3% Triton X 114 (w/v), 0.1 M ammonium acetate, and heating at 50°C for 30 min. This approach proved effective in giving quantitative recoveries from a diverse range of food matrixes, and optimized LC gave baseline chromatographic separation for all colors including Sudan IV and Red B. Single-laboratory validation was performed with spiking into liquid matrixes (wine and homemade wine), semiliquid matrixes (sauce and homemade paprika paste), and solid matrixes (spice and homemade chili powder) using the respective blank matrixes for matrix-matched calibration. The LOQ values for water-soluble colors were in the range of 15–150 mg/kg, and for the fat-soluble colors, 0.1–1.5 mg/kg. The mean recovery values were in the range of 69.6–116.0% (except Allura Red and Sunset Yellow in wine, for which recoveries were lower). The mean RSDs for colors were in the range of 4.0–14.8%. A small survey was conducted of samples of confectionery products, dried fruits, wines, bitter sodas, juices, sauces, pastes, and spices, which demonstrated the applicability of the method to a diverse selection of real food samples. Allura Red was detected in strawberry jelly and Sunset Yellow in artificial saffron.


Talanta ◽  
2006 ◽  
Vol 68 (3) ◽  
pp. 863-868 ◽  
Author(s):  
Asiya Mustafina ◽  
Julia Elistratova ◽  
Alexander Burilov ◽  
Irina Knyazeva ◽  
Rustem Zairov ◽  
...  

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.


2010 ◽  
Vol 8 (1) ◽  
pp. 34-40 ◽  
Author(s):  
Wifky El-Naggar ◽  
Taysseer Lasheen ◽  
El-Said Nouh ◽  
Ahmed Ghonaim

AbstractBrilliant green was used as a complexing agent in cloud point extraction (CPE) and applied for selective preconcentration of trace amounts of gold in geological matrices. The analyte in the initial aqueous solution was acidified with hydrochloric acid (0.1 M) and octylphenoxypolyethoxyethanol (Triton X-114) was added as a surfactant. After phase separation, based on the cloud point separation of the mixture, the surfactant rich phase was diluted with methanol and the analyte determined in the surfactant rich phase by flame atomic absorption spectrometry (FAAS). After optimization of the complexation and extraction conditions, a preconcentration factor of 31 was obtained for only 10 mL of sample. The analytical curve was linear in the range of 3–1000 ng mL−1 and the limit of detection was 1.5 ng mL−1. The proposed method was applied to the determination of gold in geological samples.


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.


RSC Advances ◽  
2016 ◽  
Vol 6 (77) ◽  
pp. 73797-73804
Author(s):  
Alaa S. Amin ◽  
Mohammed A. Kassem ◽  
Sayed M. N. Moalla

Effect of 5.0% Triton X-100 on the complexation of 40 ng mL−1 Sc(iii) with ATAP.


Materials ◽  
2016 ◽  
Vol 9 (5) ◽  
pp. 385 ◽  
Author(s):  
Minh Pham ◽  
Ting-Chun Wen ◽  
Hung-Cheng Li ◽  
Pei-Hsuan Hsieh ◽  
Yet-Ran Chen ◽  
...  

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