Ethylene Vinyl Alcohol Copolymer ( EVOH ) as a Functional Barrier against Surrogate Components Migrating from Paperboard

Kuraray-Eval Europe NV, Haven 1053 Nieuwe Weg 1, Bus 10, 2070 Zwijndrecht, Belgium Hasselt University, Packaging Technology Center IMO-IMOMEC, Wetenschapspark 27, 3590 Diepenbeek, Belgium Université de Pau et des Pays de l’Adour, École Nationale Supérieure en Génie des Technologies Industrielles, 64000 Pau, France Hasselt University, Applied and Analytical Chemistry IMO-IMOMEC, Agoralaan Building D, 3590 Diepenbeek, Belgium


Introduction
Mineral oil hydrocarbons (MOHs) contamination in food has become a major concern in the past decade when it was brought to light that these substances might be potentially harmful for the human health.Both the German Federal Institute for Risk Assessment (BfR) [1] and the European Food Safety Authority (EFSA) [2] published a scientific opinion on the potential health risks of MOHs present in food due to contamination in the food chain.
In terms of MOHs contamination and toxicology, the EFSA [2] distinguishes two main groups: mineral oilsaturated hydrocarbons (MOSHs), which can be n-alkanes, branched alkanes and cycloalkanes, and mineral oil aromatic hydrocarbons (MOAHs), which are polyaromatic hydrocarbons, mainly alkylated.MOSHs from C 16 to C 35 may accumulate and cause microgranulomas in the lymph nodes, spleen, liver, and other tissues [2].For MOAHs, there are only few toxicological data available; however, MOAHs with 3 or more nonalkylated and minor alkylated aromatic rings are suspected for being mutagenic and carcinogenic and are therefore of concern [2].Due to these findings, the EFSA also recommends that the revision of the acceptable daily intake (ADI) of some food-grade MOSHs is necessary.
Migration from recycled paperboard was found to be one of the main sources for this contamination.Several studies reported severe migration of both MOSHs and MOAHs from paperboard packaging into foodstuff which was not only limited to the primary but also originated from the secondary and even the tertiary packaging [3][4][5][6][7].Lorenzini et al. [7] found that about 60-80% of the <n-C 24 fraction of MOSHs/MOAHs present in the paperboard was transferred to the food inside the package.Vollmer et al. [6] confirmed these findings and also reported that 10-20% of the migrated fraction were MOAHs.
Regulation (EC) No. 1935/2004 [8] states that food contact materials (FCMs) should not transfer any of their constituents to food in quantities that may endanger human health and bring about unacceptable changes in the composition of the food or a deterioration in the organoleptic characteristics thereof.Unfortunately, so far, no harmonised European Regulation for paperboard packaging exists.Recently, Commission Recommendation (EU) 2017/84 [9] has been issued to monitor the presence of MOHs and their sources in 2017 and 2018.e results of this study are expected in 2019.Several countries already took the lead by establishing their own recommendation or regulation; for instance, in Austria, the Federal Ministry of Health states in Recommendation BMG-75210/0018-II/B/13/2012 [10] that if food is packaged in recycled paperboard, it should be protected by a functional barrier.Switzerland has a similar approach in its "Bedarfsgegenständeverordnung" 817.023.21[11], which states that recycled paperboard should not be in contact with food, unless measures are taken, e.g. by means of a barrier layer.
Even though there is no specific regulatory obligation on the European level, it is now generally recommended to minimise the transfer of MOHs and other harmful components migrating from paperboard packaging [1,2,12,13].e most widely accepted solution is the integration of a functional barrier in the primary packaging concept, where it can limit the migration from primary, secondary, and tertiary packaging as well as the cross-contamination from other products and the environment [5].A functional barrier can either limit the maximum migration into food to a quantity below the specific migration limit (SML) or can prolong the time of breakthrough when migrated components are first detected, to a time beyond the shelf life [14].
Ethylene vinyl alcohol copolymer (EVOH) (see the structure in Figure 1) is a key material of interest due to its outstanding barrier properties as reported by Maes et al. [15].e random copolymer consists of ethylene units, which contribute to processability and flexibility, and vinyl alcohol units, which are responsible for the high barrier properties.EVOH has one of the lowest oxygen permeability rates (P O 2 ) amongst polymers, and it shows excellent barrier properties against other gases, such as nitrogen and carbon dioxide.In addition, it also prevents the scalping of aromas and flavours in food packaging [16][17][18].EVOH also offers a good barrier against fuels and other chemicals, such as benzene, toluene, ethylbenzene and xylene isomers (BTEX), agrochemicals including fumigants, and others.In the automotive sector, EVOH is already widely used in applications like fuel tanks [15].Maes et al. [19] already demonstrated that EVOH offers good protection against mineral oil migration.e breakthrough time of a mineral oil mixture (Gravex 913) was determined for two EVAL ™ EVOH grades, E105B and F171B, using the method developed by Fiselier and Grob [14].e multilayer films containing 5.2 and 4.4 µm EVOH, respectively, showed breakthrough times of, respectively, >7.1 and >10.6 years [19].
More recent studies are focussing on the use of surrogate substances instead of a mineral oil mixture to assess the functional barrier against mineral oil and other contaminants originating from recycled paperboard [20,21]. is approach allows careful evaluation of known components with different polarity and boiling points instead of total migration.Based on these studies, the Schweizerisches Verpackungsinstitut (SVI) published a guideline for the evaluation of the barrier efficiency of internal bags for food packaging in recycled paperboard [22].Because the shelf life of most dry foods is several years, a test at regular storage conditions (25 °C) would take too long; however, the test can be accelerated by increasing the temperature.e acceleration factor can be calculated using the Arrhenius equation (Equation 1) as described in Commission Regulation (EU) No. 10/2011 [9], which suggests an activation energy (E a ) of 80 kJ/mol as a worst-case scenario.A test performed at 60 °C would be accelerated by factor 30 compared to a test at 25 °C, reducing the test time for a shelf time of two years to 25 days: In this paper, EVOH was evaluated as a functional barrier against 5 surrogate substances simulating a MOSH, two MOAHs, a plasticiser, and a printing ink component, migrating from recycled paperboard.
For this study, five different film samples were evaluated.Four of these films were multilayer structures which were  1.Both structures of PA 6/6.6 and PET are given in Figure 2.
e paperboard used as a donor was of virgin grade (290 g/m 2 ) which was provided by Smurfit Kappa Van Mierlo Offset Packaging (Turnhout, Belgium).e receptor material was obtained from BGB Analytik AG (Boeckten, Switzerland) and was made of copy paper (115 g/m 2 ) soaked in 20% polydimethylsiloxane (PDMS), which was cured and cleaned for 8 h at 130 °C and 0.1 bar.

Spiking of the Donors.
e spike solution was prepared using n-heptadecane (C17), 4-methylbenzophenone (MBP), and di-n-propyl phthalate (DPP) as surrogate components and Sudan red II for visual control of equal distribution in the paperboard as listed by Biedermann-Brem et al. [21] and in the guideline provided by the SVI [22].As shown in Table 2, C17, MBP, and DPP, respectively, represent an MOSH, photoinitiator, and plasticiser, respectively.Yet MOAH components are of the greatest concern; therefore, anthracene (ANT) and perylene (PER) were added to simulate MOAH components (Table 2).All components were dissolved in MTBE at a concentration of 250 mg/L.e donor paperboard (A5) was soaked in this solution until it was completely saturated; afterwards, it was dried by holding it in a vertical position underneath the fume hood to allow the MTBE to evaporate.Several boards were then tightly wrapped together in aluminium foil and placed in an oven at 40 °C for 2 weeks for conditioning.is condition was chosen based on experiments of Biedermann-Brem et al. to allow the polar components to penetrate the paperboard more deeply.
is allowed a more gradual release of the components from the paperboard mimicking a more realistic migration scenario [21,23].

Preparation of the Test Packs.
After conditioning, the donor paperboard was sampled for the determination of the initial concentrations by removing a piece of 9 cm × 2 cm for extraction and subsequent analysis by gas chromatography using a quadrupole mass spectrometer (GC-MS) as detector.
e remaining donor was then covered in aluminium foil on the top side and folded around the border with approximately 1 cm overlap on all edges of the bottom side. is resulting donor pack was then taped on top of the test film sample, which had larger dimensions.To ensure the donor was wrapped tightly, the excess of the film sample was folded around the donor pack and taped on top.Finally, the receptor (A5) was secured on the other side of the film sample (Figure 3).Afterwards, the test pack was completely covered in aluminium foil.To ensure the receptor was free of possible contaminations, it was first heat-treated at 150 °C for 30 minutes prior to using it in the test pack.
All test packs were put in the oven simultaneously and loaded with a heavy object (e.g. a glass plate) to decrease the air exchange between the packs.e test packs were kept in the oven for 25 days at 60 °C, which covers a period of 2 years of shelf life at 25 °C, using an acceleration factor of 30 as calculated by the Arrhenius equation.
e receptor was sampled at regular intervals by cutting a piece of 9 cm × 2 cm keeping a distance of 1 cm from the border and the previous sampling to avoid the effect of sideways migration due to the absence of the receptor material in the vicinity area.Even though this effect was not found to be considerable, it was found to be a best practice [21].Each film sample was tested in duplicate.

Extraction and GC-MS Analysis.
e samples were extracted using a MTBE/MeOH (95/5 v/v) solution.e 9 cm × 2 m samples of the donor and receptor were cut into smaller pieces and then extracted with, respectively, 10 and 2 mL of the extraction solution.To each of these extracts, 10 µL of the internal standard solution was added, prepared by dissolving 100 mg CyCy in 10 mL MTBE of which 300 μL was then diluted in 10 mL MTBE.e film samples were extracted in the same way as the receptor to check whether there were possible interferences with the analysis of the surrogate substances.e vials containing the samples with extraction solution were put in an oven overnight at 40 °C to facilitate the extraction process after the addition of CyCy as the internal standard.Biedermann-Brem et al. found that the extraction was most challenging for the most polar component (MPB) after it has penetrated the board deeply.However, after a night at 40 °C, the extraction was virtually complete [23].
e extracts were analysed by injecting 1 µL into a Trace Ultra 1310 GC coupled to an ISQ LT Quadrupole MS in a splitless mode at a constant helium flow of 1.2 mL/min.e column used was a 30 m × 0.25 mm i.d.× 0.25 µm film thickness DB5-MS capillary column.e oven temperature was first kept at 30 °C for 5 minutes after injection.en, at a 10 °C/min ramp, the temperature was raised till 330 °C, which was maintained for 2 minutes.6 calibration solutions were prepared to which 10 µL of the internal standard was added to determine the exact amount of the surrogate components in the sample extracts.For each test pack, the amount of migration for each of the 5 substances that passed through the barrier into the receptor was determined. is amount was expressed as a percentage breakthrough value of the initial concentration that was found in the donor paperboard.

O 2 GTR Measurements.
e oxygen transmission rate (O 2 GTR) of all five film samples was determined using a MOCON OX-TRAN ® 2/21 at 20 °C and 65% RH in ac- cordance with ASTM F1927.For the PET and PA 6/6.6 film, the use of a mask was necessary to reduce the test surface area from the standard 50 cm 2 to 5 cm 2 to remain within the detection range of the coulometric detector.

Breakthrough of Surrogate Components.
In Figure 4, the breakthrough values of the five surrogate components are given in percent of the initial concentration found in the spiked donor for all films after 25 days at 60 °C, which translates into a shelf life of 2 years at 25 °C.e guideline provided by the Swiss Packaging Institute states that the barrier is good when the values remain below 1% of the initial concentration at the end of the shelf life [22].is criterion was based on GC analysis of recycled paperboard extracts initiated by the German Federal Ministry of Food, Agriculture and Consumer Protection (BMELV) and its outcome that no nonevaluated substances in the critical volatility range (C 14 -C 25 ) exceeded 10 mg/kg paperboard.
e BMELV specified a threshold of toxicological relevance of 0.01 mg/kg in food, which corresponds to the detection limit that is widely applied by the EU [24].Taking into account the typical mass ratio of food to paperboard of 10, this leads to the threshold value of 1% of the substances initially found in the paperboard [23].
e results in the graph clearly show that the multilayer films with the two different EVAL ™ grades, 5 and 3 µm F171 and 3 µm L171, are sufficient and can easily compete with a monolayer 12 µm PET film.For the EVAL ™ and PET films, C17 shows the highest migration potential, which is likely due to its low boiling point (302 °C) and selectivity of the polymer matrix.Biedermann-Brem and Grob found that polyvinyl alcohol had a higher selectivity for C17 than for MBP and DPP, making it less resistant to C17, resulting in a higher breakthrough percentage than the other two components [20].e multilayer film containing 3 µm of PA 6/6.6, however, shows higher values for MBP and DPP compared to the other films, but these values are still below the 1% threshold value.It is likely that these components might have caused a plasticising effect on the PA 6/6.6 matrix, which could be less present in PET and EVOH due to stronger inter-and intramolecular bonds caused by the presence of more functional groups [25,26].PA 6/6.6 has longer polar chains and is therefore to be expected that the free space between the chains allows larger molecules to pass through.C17 did not show higher breakthrough values than the other two materials, which indicates a strong change in selectivity as was shown by Biedermann-Brem and Grob [20].ANT is an apolar molecule that shows breakthrough values of nearly 2% after 25 days at 60 °C.e threshold value of 1% for ANT was reached after only 5 days at 60 °C in the PA 6/6.6 film, which is approximately 150 days at 25 °C, indicating that 3 µm PA 6/6.6 does not provide sufficient protection against low-weight MOAH components for products that require a shelf life over 150 days.
is effect was possibly strengthened by the plasticising effect of the polar components or interaction between the components DPP, MBP, and ANT such as copermeation.Zhou et al. reported this effect for limonene and ethyl butyrate, where the presence of ethyl butyrate increased the permeation of limonene through a high-density polyethylene (HDPE) film [27].But further research is needed to confirm these findings.e component PER did not break through in any of the films, which is most likely due to its higher boiling point of 494 °C opposed to C17 (302 °C), MBP (326 °C), DPP (340 °C), and ANT (340 °C), making it less susceptible for migration from the cardboard, as transport of the molecules occurs in the gas phase and requires a minimum vapour pressure [7,14].

Relationship Breakthrough Values and O 2 GTR.
e O 2 GTR values are given in Table 1 as well as the P O 2 normalised to a barrier thickness of 1 μm.e films containing EVOH have very low O 2 GTR values, which are two orders of magnitude lower than the PET film, which is also still considered as a good barrier.e PA 6/6.6 has an O 2 GTR value significantly higher than that of the other two materials, and this was also reflected in the breakthrough values of   MBP, DPP, and ANT.However, a clear correlation between O 2 GTR and the migration of the surrogate components was not visible, as the PA 6/6.6 had similar breakthrough values for C17 as PETand EVOH, which both outperformed the PA 6/6.6 as an oxygen barrier.

Conclusion
e results show that both EVAL ™ F171B (3 and 5 μm) and L171B (3 μm) have good barrier properties against the surrogate components migrating from recycled paperboard.ey can easily compete with PET (12 μm), while clearly outperforming PA 6/6.6 at the same thickness.
When applying the 1% threshold value for breakthrough, both EVOH grades can comfortably protect the food for a shelf life of over 2 years at 25 °C against mineral oil migration.Additionally, EVOH also offers good barrier properties against oxygen, nitrogen, carbon dioxide, odours, aroma, flavours, and others, making it a multifunctional solution.
Dr. Collin 5-layer blown film line by the TS Department of EVAL Europe N.V., and one was a monolayer polyethylene terephthalate (PET) film (12 µm) obtained through the EVAL R&D Department of Kuraray Co. Ltd. in Japan.e general structure of the multilayer films was LDPE/tie/barrier/tie/LDPE. e barrier layer was either

Table 1 :
Film samples and their characteristics.

Table 2 :
Components used in the spike solution and their physical and chemical properties.For each substance, the structure, CAS Registry Number, polarity, partition coefficient for octanol/water (log P o/w ), molar weight (Mw), boiling point (Bp), and simulant group are given.
Figure 3: Test pack before being enclosed in aluminium foil.