Biodegradation of bisphenol A in the aquatic environment

2000 ◽  
Vol 42 (7-8) ◽  
pp. 31-38 ◽  
Author(s):  
M. Ike ◽  
C. S. Jin ◽  
M. Fujita

Biodegradation potential of bisphenol A (BPA) in the aquatic environments was investigated using 3 activated sludge and 44 river water microcosms. The biodegradation potential was exhibited by most of the tested microcosms; 3 activated sludge and 40 river water microcosms. However, only 6 river water microcosms could completely mineralize BPA, and the others showed accumulation of common metabolites which were detected as 2 peaks according to a high-pressure liquid chromatograph. In total 19 BPA-degrading bacteria were isolated from activated sludge and river water samples, and their BPA degradation property was also investigated. Although all the BPA-degrading bacteria could grow on BPA and remove about 70–80% of TOC derived from BPA, they accumulated 2 common metabolites, and they could not be removed by the prolonged cultivation up to more than 1 month. These 2 metabolites were identified as 2,3-bis(4-hydroxyphenyl)-1,2-propanediol and p-hydroxyphenacyl alcohol in the culture of a typical BPA-degrading bacterium. The experimental results suggested that BPA-degrading bacteria ubiquitously exist in the aquatic environments, but that they cannot completely degrade BPA, leading to the accumulation of more recalcitrant metabolites. For complete BPA degradation, the presence of microbes which can degrade the metabolites seems necessary together with BPA-degrading bacteria.

1979 ◽  
Vol 62 (6) ◽  
pp. 1355-1357
Author(s):  
William O Landen

Abstract The use of a collection valve specifically designed for high pressure liquid chromatography is described. Application of the valve to high pressure gel permeation chromatographic (GPC) separation of oil from the vitamin A active fraction of margarine resulted in efficient oil removal after one pass through 2 μStyragel (100A) columns connected in series. Using the normal collection mode of the high pressure liquid chromatograph, 2 passes through the GPC columns were required to adequately resolve the fractions.


2020 ◽  
Vol 114 ◽  
pp. 110989 ◽  
Author(s):  
Marina Baccarin ◽  
Mariani A. Ciciliati ◽  
Osvaldo N. Oliveira ◽  
Eder T.G. Cavalheiro ◽  
Paulo A. Raymundo-Pereira

1980 ◽  
Vol 63 (5) ◽  
pp. 981-984
Author(s):  
Virginia A Thorpe

Abstract Medicated feeds (pelleted or mash) containing guarantees of carbadox, furazolidone, nitrofurazone, and ethopabate are pretreated with water, extracted with 95% dimethylformamide overnight at room temperature, cleaned up on a column of alumina, and injected into a high pressure liquid chromatograph for quantitative measurement. Carbadox, nitrofurazone, and furazolidone can be separated; chromatograms show excellent baseline resolution, and results are in good agreement with colorimetric methods. The same extraction and cleanup can be used to improve colorimetric methods for furazolidone and nitrofurazone.


1978 ◽  
Vol 61 (3) ◽  
pp. 590-592
Author(s):  
Michael E Stack ◽  
Nathan L Brown ◽  
Robert M Eppley

Abstract A method is described for the detection and quantitative analysis of xanthomegnin in corn samples. Initial extraction with CHCI3 in the presence of 0.5M H3PO4 is followed by additional purification using silica gel column chromatography. A high pressure liquid chromatograph equipped with a microparticle silica gel column and a 405 nm absorbance detector is used for detection and quantitation of the xanthomegnin. The identity of xanthomegnin is confirmed by thin layer chromatography on silica gel plates developed with benzenemethanol- acetic acid (90-(-5+5). The recovery of xanthomegnin added to corn samples at levels of 0.75–9.6 mg/kg averaged 41% with a coefficient of variation of 25%.


2018 ◽  
Vol 10 (44) ◽  
pp. 5313-5320 ◽  
Author(s):  
Wei Sheng ◽  
Wenxia Duan ◽  
Yingjie Shi ◽  
Qing Chang ◽  
Yan Zhang ◽  
...  

NaYF4:Yb/Tm upconversion nanoparticles-based fluorescence immunoassay in combination with magnetic separation for detecting bisphenol A in drinking and river water samples.


2017 ◽  
Vol 14 (2) ◽  
pp. 115 ◽  
Author(s):  
Xiaoying Wang ◽  
Yijie Wang ◽  
Meng Jiang ◽  
Yanqun Shan ◽  
Xiaobing Wang

Environmental contextBisphenol A is an endocrine disruptor, which may migrate and transfer to the environment where it presents a potential risk to the health of humans and animals. Herein, we demonstrate that electrospun nanofibers could be used to develop a highly efficient solid-state quenching sensor for on-site determination of bisphenol A in river water samples. The strategy has great potential for routine environmental analyses. AbstractA novel solid-state electrochemiluminescence (ECL) quenching sensor based on luminescent composite nanofibres for detection of bisphenol A (BPA) has been designed. Luminescent composite nanofibres of ruthenium(ii) tris(bipyridine) (Ru(bpy)32+)-doped core–shell Cu@Au alloy nanoparticles (Ru/Cu@Au) mixed with nylon 6 (PA6)–amino-functionalised multi-walled carbon nanotubes (MWCNTs), Ru/Cu@Au-MWCNTs-PA6, were successfully fabricated by a one-step electrospinning technique. The Ru/Cu@Au-MWCNTs-PA6 nanofibres, with a unique 3D nanostructure, large specific surface area and double Ru(bpy)32+-ECL signal amplification, exhibited excellent ECL photoelectric behaviours on a glassy carbon electrode. As a solid-state ECL sensor, the Ru/Cu@Au-MWCNTs-PA6 nanofibres can sensitively detect low concentrations of BPA by monitoring the BPA-dependent ECL intensity change. The detection limit for BPA is 10 pM, which is comparable or better than that in the reported assays. The sensor was successfully applied to on-site determination of BPA in river water samples obtained from eight different sampling sites with good recovery, ranging from 97.8 to 103.4%. The solid-state ECL sensor displayed wide-range linearity, high sensitivity and good stability, and has great potential in the field of environmental analyses.


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