Effect of Electron Beam and Gamma Radiation on the Migration of Plasticizers from Flexible Food Packaging Materials into Foods and Food Simulants

Author(s):  
Antonios E. Goulas ◽  
Kyriakos A. Riganakos ◽  
Michael G. Kontominas
Author(s):  
Jazmín Osorio ◽  
Margarita Aznar ◽  
Cristina Nerín ◽  
Christopher Elliott ◽  
Olivier Chevallier

Abstract Biopolymers based on polylactic acid (PLA) and starch have numerous advantages, such as coming from renewable sources or being compostable, though they can have deficiencies in mechanical properties, and for this reason, polyester resins are occasionally added to them in order to improve their properties. In this work, migration from a PLA sample and from another starch-based biopolymer to three different food simulants was studied. Attention was focused on the determination of oligomers. The analysis was first performed by ultraperformance liquid chromatography quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF–MS), which allowed the identification of the oligomers present in migration. Then, the samples were analyzed by two ambient desorption/ionization techniques directly coupled to mass spectrometry (ADI), direct analysis in real-time coupled to standardized voltage and pressure (DART-MS) and atmospheric pressure solids analysis probe (ASAP-MS). These methodologies were able to detect simultaneously the main oligomers migrants and their adducts in a very rapid and effective way. Nineteen different polyester oligomers, fourteen linear and five cyclic, composed of different combinations of adipic acid [AA], propylene glycol [PG], dipropylene glycol [DPG], 2,2-dibutyl-1,3-propanediol [DBPG], or isobutanol [i-BuOH] were detected in migration samples from PLA. In migration samples from starch-based biopolymer, fourteen oligomers from poly(butylene adipate co-terephthalate) polyester (PBAT) were identified, twelve cyclic and two linear. The results from ADI techniques showed that they are a very promising alternative tool to assess the safety and legal compliance of food packaging materials. Graphical abstract


2009 ◽  
Vol 57 (20) ◽  
pp. 9516-9523 ◽  
Author(s):  
Ana Sanches-Silva ◽  
Catarina Andre ◽  
Isabel Castanheira ◽  
José Manuel Cruz ◽  
Sarah Pastorelli ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Zhanhua Dong ◽  
Lixin Lu ◽  
Zhigang Liu ◽  
Yali Tang ◽  
Jun Wang

Long-term extraction experiments were carried out on glazed tile specimens with 4 and 10% (v/v) acetic acid, 1% (w/v) citric acid, and 1% (v/v) lactic acid solution in three temperature conditions (20, 40, and 60°C) to investigate the effect of temperature and pH value on extraction of lead, cobalt, nickel, and zinc from ceramic food packaging materials and to study the extraction kinetics of toxic metals. Results showed that except at 60°C the amount of extraction of lead, cobalt, nickel, and zinc had linear dependence on time at longer times and removal of these toxic metals under other conditions increased linearly with the square root of the time, indicating a diffusion-controlled process. The amount of these toxic metals leached out from ceramic food packaging materials into the leachate, and the leaching rate increased with temperature and decreased with pH value of the food simulants. In addition, among these four toxic metals lead was the least leachable element, and nickel was the most leachable one. Disagreement between the ratios of the oxide of lead, cobalt, nickel, and zinc in the glaze and their release in the leachate suggested that extraction of these toxic metals was an incongruent dissolution process.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1544
Author(s):  
Jet Yin Boey ◽  
Lydia Mohamad ◽  
Yong Sen Khok ◽  
Guan Seng Tay ◽  
Siti Baidurah

Overconsumption of plastic goods and improper handling of petroleum-derived plastic waste have brought a plethora of negative impacts to the environment, ecosystem and human health due to its recalcitrance to degradation. These drawbacks become the main driving force behind finding biopolymers with the degradable properties. With the advancement in biopolymer research, polyhydroxyalkanoate (PHA) and poly(lacyic acid) (PLA) and its composites have been alluded to as a potential alternative to replace the petrochemical counterpart. This review highlights the current synthesis process and application of PHAs and PLA and its composites for food packaging materials and coatings. These biopolymers can be further ameliorated to enhance their applicability and are discussed by including the current commercially available packaging products. Factors influencing biodegradation are outlined in the latter part of this review. The main aim of this review article is to organize the scattered available information on various aspects of PHAs and PLA, and its composites for packaging application purposes. It is evident from a literature survey of about 140 recently published papers from the past 15 years that PLA and PHA show excellent physical properties as potential food packaging materials.


2021 ◽  
pp. 467-494
Author(s):  
R.A Ilyas ◽  
S.M Sapuan ◽  
L.N. Megashah ◽  
Rushdan. Ibrahim ◽  
M.S.N. Atikah ◽  
...  

Author(s):  
Susana Guzmán‐Puyol ◽  
Antonio Heredia ◽  
José A. Heredia‐Guerrero ◽  
José J. Benítez

2019 ◽  
Vol 102 (1) ◽  
pp. 255-261 ◽  
Author(s):  
Ji-cai Fan ◽  
Quan Jin ◽  
Hua-li He ◽  
Ren Ren ◽  
Shu-ting Wang

Abstract Background: Phthalate esters (PAEs) are a group of chemical compounds widely used as plasticizers to increase the flexibility of plastics that are used in the manufacturing of kitchen utensils and food containers. Objective: In this study, a simple, rapid, and sensitive method for the determination of 20 PAEs in different kinds of food packaging materials has been developed. Methods: Samples injected with five internal standards were extracted with acetonitrile saturated with n-hexane and then detected by GC-MS/MS without a purification step. Results: The standard calibration curves were linear for all analytes over the concentration range of 5–500 μg/L, and the correlation coefficients ranged from 0.9913 to 0.9999. The LODs and LOQs were in the ranges of 1.7–62.5 and 5.5–208.3 μg/kg, respectively. The accuracy of this method was evaluated by measuring the recovery from spiked samples. The recoveries of all 20 phthalates from samples spiked at three different concentrations were measured, and the recovery was in the range of 82.1–110.8% and the relative standard deviation range of recovery result (n = 6) was 0.3–9.7%. Conclusions: The method presented here is simple, rapid, and sensitive and can be applied to large-scale detection of PAEs in plastic materials. Highlights: Instead of only one solvent, acetonitrile saturated with n-hexane was used as the extraction solvent. Samples were pretreated without a purification step. Five internal standards were used for quantitative determination.


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