scholarly journals Cloud Point Extraction as a Method for Preconcentration of Metal Ions

2020 ◽  
Vol 12 (2) ◽  
Author(s):  
Nusretá Hasic ◽  
Emir Horozic

Cloud point extraction (CPE) is an attractive technique that reduces solvent con- sumption and exposure, disposal costs, and process time. This method has an im- portant practical application and is used to separate and concentrate the analyte as a step before its determination, and after the formation of a poorly water-soluble complex. Use of nonionic surfactants as ”green solvents” which represent an effec- tive alternative to toxic organic solvents (in classical extraction), along with other advantages, such as low cost and low flammability, makes this method attractive and worth further research and optimization. This paper presents a detailed de- scription of the principles, procedure, advantages, disadvantages and application of CPE.

2013 ◽  
Vol 830 ◽  
pp. 345-348
Author(s):  
Lin Gao ◽  
Sheng Jie Chen ◽  
Fang Chen ◽  
Wen Hong Zhou ◽  
Jun Long Yao

A simple, sensitive, green and low cost detection method based on the cloud point extraction (CPE) separation and spectrophotometry was proposed for the determination of lead. In pH=9.0 H3BO3 buffer solution, Pb(II) reacts with 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP) in the presence of Triton X-100 yielding a hydrophobic complex, which then is extracted into micro-volume surfactant-rich phase. The calibration graph was linear in the range of 20-400 µg/L (at 560 nm). Under the optimized conditions, the detection limits of 10.94 µg/L and the relative standard deviations(RSD) of 2.0% (n=5) for Lead(II) were found, respectively. The sensitivity and absorbance of this method are at least five times higher when compared with that of usual 5-Br-PADAP spectrophotometry without CPE, and the proposed method has been applied to the determination of Lead in environment water samples with satisfactory results.


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.


2020 ◽  
Vol 17 (1) ◽  
pp. 0057
Author(s):  
Maha Al-Tameemi

In current article an easy and selective method is proposed for spectrophotometric estimation of metoclopramide (MCP) in pharmaceutical preparations using cloud point extraction (CPE) procedure. The method involved reaction between MCP with 1-Naphthol in alkali conditions using Triton X-114 to form a stable dark purple dye. The Beer’s law limit in the range 0.34-9 μg mL-1 of MCP with r =0.9959 (n=3) after optimization. The relative standard deviation (RSD) and percentage recoveries were 0.89 %, and (96.99–104.11%) respectively. As well, using surfactant cloud point extraction as a method to extract MCP was reinforced the extinction coefficient(ε) to 1.7333×105L/mol.cm in surfactant-rich phase. The small volume of organic solvent (500mL/sample) provides an environmentally friendly and low-cost preconcentration method. The suggested method was utilized for analyzing of MCP in commercial pharmaceutical injections.


2018 ◽  
Vol 156 ◽  
pp. 01011 ◽  
Author(s):  
Orchidea Rachmaniah ◽  
Lailatul Jumiati Fazriyah ◽  
Nurul Hesti Seftiyani ◽  
M. Rachimoellah

Recently Natural Deep Eutectic Solvents (NADES) show their potential as a promising green solvents at 21th century for extraction of natural products. Rutin, a poorly water soluble flavonoid, was reported better solubilized in NADES than in water as well as a paclitaxel and ginkgolide B, a completely water-insoluble compound. In case of curcuminoids, phenolic compounds from powder of Curcuma Zeodaria shown better solubilized in acidic type of NADES such malic acid-sucrose-water (MAS-H2O = 1:1:11, mole ratio) and citric acid-sucrose-water (CAS-H2O = 1:2:15, mole ratio) compare to water and ethanol. Indicating that NADES, a water-based solvent, appropriate for extracting curcuminoids. However, the inherent high viscosity of NADES hamper the process extraction. Lowering the viscosity, water content of NADES is varied, adding a certain amount of water up to 60% of water content. All the varied water content of both CAS-H2O and MAS-H2O were successfully extracted curcuminoids. Yielded 0.06-0.16 mg curcuminoids/g dry weight. However, 60% of water content of both CAS-H2O and MAS-H2O gave more or less similar value of curcuminoids to CAS-H2O (20% of water) and MAS-H2O (30% of water). Curcuminoids is more stable in CAS-H2O compare to MAS-H2O for 96 h of time duration.


2016 ◽  
Vol 8 (30) ◽  
pp. 5984-5993 ◽  
Author(s):  
Guirong Li ◽  
Jiekang Li ◽  
Qian Han

(1) Extracting and purifying uranium in complex samples by dCPE with [UO22+–SA1]. (2) Detecting uranium super sensitively by a photocatalytic RF method with [UO22+–SA2]. (3) Coupling with separation, purification and analysis procedures exhibited a number of advantages, including high selectivity, high sensitivity and low cost.


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

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