Migration of Bisphenol A (BPA) from Epoxy Can Coatings to Jalapeño Peppers and an Acid Food Simulant

2002 ◽  
Vol 50 (25) ◽  
pp. 7299-7302 ◽  
Author(s):  
Elvia M. Munguia-Lopez ◽  
Elizabeth Peralta ◽  
Alberto Gonzalez-Leon ◽  
Claudia Vargas-Requena ◽  
Herlinda Soto-Valdez
Keyword(s):  
2004 ◽  
Vol 22 (SI - Chem. Reactions in Foods V) ◽  
pp. S272-S275
Author(s):  
I. Poustková ◽  
J. Dobiáš ◽  
J. Poustka ◽  
M. Voldřich

Varnishes used as the inner coatings of food cans are often based on epoxy resins or vinylic organosols. The epoxy resins can be produced from bisphenol A (BPA) and bisphenol F (BPF) and they also contain bisphenol A diglycidyl ether (BADGE) of bisphenol F diglycidyl ether (BFDGE) as stabilising components. These compounds may break down during storage and also by influence of food simulants. The stability of BADGE and BFDGE was studied using reverse-phase gradient high performance liquid chromatography (RP-HPLC) with fluorescence detection (FLD). Four experiments were compared: (i) BPA solution at the concentration 3 μg/ml of each food simulant, (ii) BADGE solution at the concentration 3 μg/ml of each food simulant, (iii) BFDGE solution at the concentration 3 μg/ml of each food simulant and (iv) mixture of all bisphenols solution at the concentration 3 μg/ml of each food simulant. Distilled water, 10% ethanol, 95% ethanol and 3% acetic acid were used as food simulants. It was observed that BPA, BADGE and BFDGE were most stabile in 95% ethanol and least stabile in 3% acetic acid. Creation of hydroxy and chlorohydroxy derivatives was in each food simulant different so it cannot be predicted.


2005 ◽  
Vol 22 (9) ◽  
pp. 892-898 ◽  
Author(s):  
E. M. Munguía-López ◽  
S. Gerardo-Lugo ◽  
E. Peralta ◽  
S. Bolumen ◽  
H. Soto-Valdez

2014 ◽  
Vol 240 (2) ◽  
pp. 335-343 ◽  
Author(s):  
A. Torres ◽  
C. Ramirez ◽  
J. Romero ◽  
G. Guerrero ◽  
X. Valenzuela ◽  
...  

Beverages ◽  
2019 ◽  
Vol 5 (1) ◽  
pp. 3 ◽  
Author(s):  
Carina Stärker ◽  
Frank Welle

Beverage cans are used for energy drinks, soft-drinks, sparkling waters, and beer. Bisphenol A is still part of the formulation of epoxy coatings of beverage cans. Due to concerns that bisphenol A acts as an endocrine-active substance, the migration of bisphenol A is restricted. Typically, the migration from beverage cans is tested at elevated temperatures into food simulants, like 20% ethanol in water. However, comparison tests of the migration of bisphenol A at the end of shelf life, with the migration into ethanolic food simulants, are not available in the scientific literature. The aim of the study was to determine the migration of the migration of bisphenol A into real beverages, compared to routine migration tests into the European official food simulant of 20% ethanol at 40 °C and 60 °C after storage for 10 days. As a result, bisphenol A-containing coatings show a considerably higher migration when tested at 60 °C in comparison to 40 °C. On the other hand, migration into energy drinks and coke, from the same coatings at the end of shelf life when stored at room temperature, was below the detection limit in either case. As expected, migration values of bisphenol A below the analytical detection limits were observed for any test conditions from the coating labeled bisphenol A-free. Spiking tests show that bisphenol A is stable in real beverages. Therefore, it can be concluded that the accelerated migration tests with 20% ethanol at the test conditions 10 d at 40 °C and 10 d at 60 °C significantly overestimate the real migration into beverages at the end of shelf life. This overestimation of the migration of bisphenol A is due to swelling of the epoxy can coating by the ethanolic food simulant. These findings were supported by migration modeling based on diffusion coefficients predicted for polyethylene terephthalate.


Author(s):  
E. G. Rightor ◽  
G. P. Young

Investigation of neat polymers by TEM is often thwarted by their sensitivity to the incident electron beam, which also limits the usefulness of chemical and spectroscopic information available by electron energy loss spectroscopy (EELS) for these materials. However, parallel-detection EELS systems allow reduced radiation damage, due to their far greater efficiency, thereby promoting their use to obtain this information for polymers. This is evident in qualitative identification of beam sensitive components in polymer blends and detailed investigations of near-edge features of homopolymers.Spectra were obtained for a poly(bisphenol-A carbonate) (BPAC) blend containing poly(tetrafluoroethylene) (PTFE) using a parallel-EELS and a serial-EELS (Gatan 666, 607) for comparison. A series of homopolymers was also examined using parallel-EELS on a JEOL 2000FX TEM employing a LaB6 filament at 100 kV. Pure homopolymers were obtained from Scientific Polymer Products. The PTFE sample was commercial grade. Polymers were microtomed on a Reichert-Jung Ultracut E and placed on holey carbon grids.


2011 ◽  
pp. 053111130856
Author(s):  
Stephen Ritter
Keyword(s):  

2011 ◽  
pp. 062311292128
Author(s):  
Erika Gebel
Keyword(s):  

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