Research on the Detection Method of Emulsified Oil in Condensed Water

2012 ◽  
Vol 573-574 ◽  
pp. 622-626
Author(s):  
Bao Ping Li ◽  
Wang Xuan ◽  
Xiao Long Lu ◽  
Chun Xia Hao

Emulsified oil is one of the main pollutants in condensed water. At present, the difficulties in demulsification of emulsified oil and dephenolization of petroleum ether are the main challenges in quantitative determination of emulsified oil in water by UV spectrophotometry. In this paper, second derivative ultraviolet spectrophotometry and demulsification with NaCl and ultrasonic were adopted to eliminate the disturbance of petroleum ether and avoid dephenolization process. Results show that the linear range of the standard oil is from 0 to 30mg/L, the recovery lies between 90.4%-101.6%, the relative errors are no more than 3%, the coefficient of variation are no more than 1.4%, and the repeatability standard deviation is only 0.1366. These results indicate that the emulsified oil detection method established has such advantages as high sensitivity, little interference, simple determination procedure, and accurate and reliable measuring result.

2011 ◽  
Vol 239-242 ◽  
pp. 368-371
Author(s):  
Fu Qiang Fan ◽  
Jun Feng Dou ◽  
Li Rong Cheng ◽  
Ai Zhong Ding ◽  
Lin Jiang ◽  
...  

A detection method for organophosphorus pesticides using electrochemical sensor based on enzyme inhibition has been developed. Acetylcholine esterase (AChE) was selected to quantify the pesticides concentration in water samples due to its activity was non-competitively inhibited in the presence of pesticides. To detect parathion and dichlorvos, optimized analytical conditions were that the substrate concentration was 3mmol/L, enzyme solution concentration was 18g/L and reaction time was 20min. Under the optimized detection conditons, a detection limit of 1.2ng/mL and 0.004ng/mL for parathion and dichlorvos was obtained, respectively. The approach was rapid, simple, accurate and of high sensitivity when compared with immunoassays or chromatographic methods.


2020 ◽  
Vol 140 (5) ◽  
pp. 409-414
Author(s):  
Masaru Tatemi ◽  
Hisao Inami ◽  
Toshiaki Rokunohe ◽  
Makoto Hirose

2019 ◽  
Vol 85 (2) ◽  
pp. 12-16
Author(s):  
I. V. Saunina ◽  
E. N. Gribanov ◽  
E. R. Oskotskaya

The sorption of Hg (II), Cd (II), and As (III) by natural aluminosilicate is studied. It is shown that the mineral absorbs those toxicants in a rather wide pH range, quantitative extraction of analytes being achieved in a neutral or close to neutral medium (pH values range within 7.0 - 8.0; 6.3 - 7.5; 7.4 - 8.5 for Hg (II), As (III), and Cd (II), respectively). The effect of the time of phase contact on the degree of extraction of elements is shown. The sorption capacity of the mineral in optimal conditions of the medium acidity (0.06 mmol/g for mercury, 0.31 mmol/g for cadmium, and 0.52 mmol/g for arsenic) is determined. The distribution coefficients attain values of aboutnX 103-nX 104. A new combined method for determination of Hg (II), Cd (II), and As (III) in natural and waste water is developed and tested. The method consists in a preliminary group sorption concentration of the analytes by aluminosilicate, desorption of the analytes from the surface of the mineral and their subsequent atomic absorption determination. The correctness of the method is verified in analysis of spiked samples. The method is easy to use and exhibits high sensitivity, reproducibility and accuracy of analyte determination. The relative standard deviation does not exceed 0.13. Economic availability and possibility of using domestic sorption materials are the important advantages of the proposed procedure which can be used in the practice of laboratories monitoring the quality and safety of environmental objects.


Author(s):  
Sirazhudin Dzh. Mekhtikhanov ◽  
◽  
Dzhamilya P. Babaeva ◽  
Kusum M. Magomedova ◽  
Patimat A. Gamzatova ◽  
...  

2020 ◽  
Vol 23 (10) ◽  
pp. 1010-1022
Author(s):  
Emrah Dural

Aim and scope: Due to the serious toxicological risks and their widespread use, quantitative determination of phthalates in cosmetic products have importance for public health. The aim of this study was to develop a validated simple, rapid and reliable high-performance liquid chromatography (HPLC) method for the determination of phthalates which are; dimethyl phthalate (DMP), diethyl phthalate (DEP), benzyl butyl phthalate (BBP), di-n-butyl phthalate (DBP), di(2- ethylhexyl) phthalate (DEHP), in cosmetic products and to investigate these phthalate (PHT) levels in 48 cosmetic products marketing in Sivas, Turkey. Materials and Methods: Separation was achieved by a reverse-phase ACE-5 C18 column (4.6 x 250 mm, 5.0 μm). As the mobile phase, 5 mM KH2PO4 and acetonitrile were used gradiently at 1.5 ml min-1. All PHT esters were detected at 230 nm and the run time was taking 21 minutes. Results: This method showed the high sensitivity value the limit of quantification (LOQ) values for which are below 0.64 μg mL-1 of all phthalates. Method linearity was ≥0.999 (r2). Accuracy and precision values of all phthalates were calculated between (-6.5) and 6.6 (RE%) and ≤6.2 (RSD%), respectively. Average recovery was between 94.8% and 99.6%. Forty-eight samples used for both babies and adults were successfully analyzed by the developed method. Results have shown that, DMP (340.7 μg mL-1 ±323.7), DEP (1852.1 μg mL-1 ± 2192.0), and DBP (691.3 μg mL-1 ± 1378.5) were used highly in nail polish, fragrance and cream products, respectively. Conclusion: Phthalate esters, which are mostly detected in the content of fragrance, cream and nail polish products and our research in general, are DEP (1852.1 μg mL-1 ± 2192.0), DBP (691.3 μg mL-1 ± 1378.5) and DMP (340.7 μg mL-1 ±323.7), respectively. Phthalates were found in the content of all 48 cosmetic products examined, and the most detected phthalates in general average were DEP (581.7 μg mL-1 + 1405.2) with a rate of 79.2%. The unexpectedly high phthalate content in the examined cosmetic products revealed a great risk of these products on human health. The developed method is a simple, sensitive, reliable and economical alternative for the determination of phthalates in the content of cosmetic products, it can be used to identify phthalate esters in different products after some modifications.


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