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Food Science and Technology

Print version ISSN 0101-2061

Ciênc. Tecnol. Aliment. vol.30 no.4 Campinas Oct./Dec. 2010

https://doi.org/10.1590/S0101-20612010000400033 

ORIGINAL

 

A method to determine volatile contaminants in polyethylene terephthalate (PET) packages by HDC-GC-FID and its application to post-consumer materials

 

Determinação de contaminantes voláteis em embalagens de polietileno tereftalato (PET) por CDEL-CG-DIC e sua aplicação a materiais pós-consumo

 

 

Samanta FabrisI; Maria Teresa de Alvarenga FreireII,*; Roger WagnerI; Felix Guillermo ReyesI

IDepartamento de Ciência de Alimentos, Faculdade de Engenharia de Alimentos, Universidade Estadual de Campinas - UNICAMP, CEP 13083-970, Campinas - SP, Brasil
IIDepartamento de Engenharia de Alimentos, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo - USP, CEP 13635-900, Pirassununga - SP, Brasil, E-mail: freiremt@usp.br

 

 


ABSTRACT

A simple and low cost method to determine volatile contaminants in post-consumer recycled PET flakes was developed and validated by Headspace Dynamic Concentration and Gas Chromatography-Flame Ionization Detection (HDC-GC-FID). The analytical parameters evaluated by using surrogates include: correlation coefficient, detection limit, quantification limit, accuracy, intra-assay precision, and inter-assay precision. In order to compare the efficiency of the proposed method to recognized automated techniques, post-consumer PET packaging samples collected in Brazil were used. GC-MS was used to confirm the identity of the substances identified in the PET packaging. Some of the identified contaminants were estimated in the post-consumer material at concentrations higher than 220 ng.g-1. The findings in this work corroborate data available in the scientific literature pointing out the suitability of the proposed analytical method.

Keywords: extraction; validation; gas chromatography; PET packaging.


RESUMO

Um método simples e de baixo custo foi desenvolvido e validado para a determinação de contaminantes voláteis em flakes de PET pós-consumo reciclado por Concentração Dinâmica do Espaço Livre e Cromatografia em fase Gasosa com Detecção por Ionização de Chama (CDEL-CG-DIC). Os parâmetros analíticos avaliados pelo uso de substâncias modelo incluíram: coeficiente de correlação, limite de detecção, limite de quantificação, exatidão, precisão intra-ensaio e inter-ensaio. Com o objetivo de comparar a eficiência do método proposto com técnicas automáticas reconhecidas, amostras de embalagens PET pós-consumo coletadas no Brasil foram utilizadas. CG-EMS foi utilizada para a confirmação da identificação das substâncias identificadas no PET. Alguns dos contaminantes identificados foram estimados quantitativamente no material pós-consumo em concentrações superiores a 220 ng.g-1. Os resultados obtidos neste trabalho corroboram os dados disponíveis na literatura científica, evidenciando a adequação do método analítico proposto.

Palavras-chave: extração; validação; cromatografia gasosa; PET.


 

 

1 Introduction

The increase in production of solid urban residue is a worldwide reality, and it depends on the population size and local economic development. In recent years, the concern about the increase in plastic-based residues has received greater attention. As a result, the recycling of plastic materials discarded in urban and residential areas has gained support throughout the world, especially from entities concerned about environmental preservation.

Among the plastic packaging materials available on the consumer market, PET (polyethylene terephthalate) is one of the most widely applied polymers (INTERNATIONAL..., 2000; FREIRE; REYES, 1997).

With regard to the recycling process for subsequent use of the recycled material in food packaging, one must consider not only contamination of the packages by chemical compounds coming from the packaged food, for example, fruit juice aromas, but also substances resulting from the inappropriate use of the package by the consumer before discarding it (BAYER, 2002). The presence of intrinsic contaminants from the recycling process, such as chemical additives and their degradation products, should be equally considered because the conventional recycling processes occur at high temperatures (WIDÉN; LEUFVÉN; NIELSEN, 2004). Thus one must ensure that the recovered material, when destined to come into contact with food, shows the same characteristics presented by the virgin material approved by regulatory agencies (KUZNESOF; VANDERVEER, 1995).

The application of recycled plastics for contact with food has become possible on account of the development of decontamination technologies. The main processes commonly applied to PET packaging include conventional washing and super washing. Conventional washing involves only selecting, grinding, washing, and drying of the PET flakes. The super washing process involves the conventional process followed by steps of deep cleaning that include washing the bottles with hot chemical agents such as sodium hydroxide and detergents, followed by drying of the material (FRANZ; MAUER; WELLE, 2004; TRIANTAFYLLOU et al., 2002). Some companies even apply an additional cleaning by friction, consisting of a rinsing of the flakes after the hot washing step, in a process in which the material suffers considerable abrasion (flake against flake), eliminating the majority of the contaminants. Modern super washing methods include a final extrusion step followed by Solid State Post-condensation (SSP) that increases the intrinsic viscosity of the polymer and also promotes its decontamination since the material is submitted to high temperatures (ca. 225 ºC) and high vacuum in this step (FRANZ; MAUER; WELLE, 2004; FRANZ; WELLE, 2002). After this last process, the recycled product is comparable to the virgin material, and its application in packaging for direct contact with foods can be considered viable. However, despite the positive results obtained with this technology, in Brazil its application to post-consumer PET bottles has been questioned. This questioning is based on the different characteristics of post-consumer materials in Brazil, where there is no efficient selective collection system, and the majority of the post-consumer material is directed to large-scale municipal rubbish dumps.

Consequently, it is important to evaluate the chemical quality of recycled materials (NIELSEN; DAMANT; CASTLE, 1997; SADLER, 1995), and thus there is a need to develop and apply analytical methods to determine contaminants coming from virgin and recycled packaging in order to help manage consumer health risks.

The techniques for the extraction of the volatile compounds absorbed by the packaging material include the use of solvents, concentration of the extract, and subsequent determination by Gas Chromatography (GC) using a flame ionisation (FID) or Mass Spectrometry (MS) detector (LEBOSSÉ; DUCRUET; FEIGENBAUM, 1997; PAIK, 1992; REYNIER et al., 2004; FREIRE et al., 1998; KALJURAND; SMIT, 1994; WIDÉN; LEUFVÉN; NIELSEN, 2005). Currently, the most used extraction systems involve headspace analysis. There are many variations to this analytical technique such as the direct analysis of the headspace, and static and dynamic concentration of the headspace using traps consisting of porous polymers, especially tenax (FRANZ; MAUER; WELLE, 2004; van WILLIGE et al., 2003; KALJURAND; SMIT, 1994; HAKKARAINEN; GRONING; ALBERTSSON, 2003; SOTO-VALDEZ; GRAMSHAW; VANDENGURG, 1997; WIDÉN; LEUFVÉN; NIELSEN, 2005; NONGONIERMA et al., 2006). Recent advances include automatic systems that allow the coupling of the headspace sampler to the gas chromatograph injector, known as the purge and trap injection system (LEBOSSÉ; DUCRUET; FEIGENBAUM, 1997; WEZL; LANKMAYR, 2002; REYNIER et al., 2004; VILLBERG; VEIJANEN; GUSTAFSSON, 1998; KALJURAND; SMIT, 1994). The solid phase micro-extraction system is a recent modification introduced for the analysis of matrixes such as packaging materials (ZHANG; PAWLISZYN, 1993; EZQUERRO; PONS; TENA, 2003; PAWLISZYN, 1997).

Gas chromatography coupled to a mass spectrometer detector is the approach most often used in the identification of volatile compounds, together with a variety of additional techniques such as the comparison between the retention times of the analyte and the standard, co-chromatography (this consists of adding the standard to the sample and verifying the increase in size of the chromatographic peak or appearance of an additional peak), and retention indexes (e.g. the Kovatz Index), amongst others (LANÇAS, 1993; VALENTE SOARES, 2001).

Considering the limited analytical resources available in developing countries, constraints and barriers faced by those countries should be considered when developing and validating analytical methods, especially when requirements are not practical for their needs. International organizations that provide guidelines related to the validation of analytical methods for food control emphasize the importance of establishing practical and cost effective methods. However, methods of analysis should only be recommended if their reliability and performance has been recognized (FOOD..., 1998).

Considering the importance of packaging recycling in food safety, the aim of this work was to develop and validate a simple and low cost analytical method to determine the volatile contaminants from conventionally cleaned up post-consumer PET packaging collected from landfills. For this purpose, dynamic headspace concentration for the extraction step, and chromatographic techniques (GC-FID and GC-MS) for separation, identification, and quantification steps were used. The method efficiency was evaluated using post-consumer PET flakes obtained from two different washing regimes widely applied in Brazil.

 

2 Material and methods

2.1 Chemicals

Toluene (99.9% pure), chlorobenzene (99% pure), benzaldehyde (99% pure), and linalool (98% pure), all from Merck (Germany); and (R) - (+) - limonene (97% pure) from Sigma-Aldrich (USA), n-hexane (HPLC grade, 98% pure) from Merck (Germany).

2.2 Samples

Samples of virgin PET bottles were supplied by Engepack Embalagens S.A., São Paulo - SP, Brazil. Samples of post-consumer PET were supplied by a Brazilian recycling company in the State of São Paulo and consisted of samples submitted to washing with water (Washing Regime 1: samples A, B, and C) and of samples submitted to Washing Regime 1 followed by processing stages that included: washing of the flakes with hot sodium hydroxide and detergents and washing by friction and drying of the material (Washing Regime 2: Samples A1, B1, and C1). All samples were ground in a Marconi model MA580 mill (Brazil) to a granule size below 20 mesh (850 µm).

2.3 Extraction process

The volatile contaminants were extracted using a modification of the dynamic headspace concentration technique described by Franco and Rodriguez (1983). Figure 1 shows the system used to obtain the extracts. Twenty-eight grams of sample, corresponding to the weight of a 510 mL PET bottle, were placed in a 250 mL flask. The trap, containing 100 mg Tenax TA 60/80 mesh (Supelco, USA), was connected to the flask exit and placed in a cooling bath at -10 ± 3 ºC. The analytical conditions were: reduced pressure of 14.6 kPa (11 cmHg), temperature of 155 ºC (± 5 ºC), and 90 minutes of extraction. The volatile substances trapped on the Tenax were eluted using enough n-hexane to reach a volume of 1.5 mL, and then added directly to 2 mL flasks together with 30 µL of 17.4 µg.L-1 linalool (internal standard).

 

 

2.4 Equipment

GC/FID (Gas Chromatograph with Flame Ionisation Detector)

A Varian model 3400 gas chromatograph was used with a model 1075 split/splitless injector, DB-5 (J & W Scientific, USA) 60 m × 0.32 mm i.d. × 0.25 µm column. The operating conditions were as follows: carrier gas (N2) at a constant pressure of 20 psi and flow rate of 1.3 mL/minute (at the oven temperature of 100 ºC); injector temperature of 250 ºC; detector temperature of 300 ºC; and splitless time of 0.75 minutes. The injection volume was 2 µL. The initial oven temperature was 40 ºC, held for 8 minutes, followed by heating to 130 ºC at 3 ºC/ minute, held for 1 minute, then heated from 130 to 250 ºC at 6 ºC/minute, and held for 5 minutes.

GC-MS (Gas Chromatograph coupled to a Mass Spectrometer)

A Shimadzu QP5000 system with a mass-range from 35 to 450 m/z, equipped with a (60 m × 0.32 mm i.d. × 0.25) DB-5 column (J & W Scientific, USA), was used. The GC operational conditions were as follows: carrier gas (He) at a constant pressure of 69.6 kPa and flow rate of 1.3 mL/minute (at the oven temperature of 100 ºC); injector and detector temperatures of 250 ºC; and splitless time of 0.75 minutes. The injection volume was 2 µL. The initial oven temperature was 40 ºC, held for 8 minutes, followed by heating to 130 ºC at 3 ºC/minute, held for 1 minute, then heated from 130 to 250 ºC at 6 ºC/minute, and held for 5 minutes.

2.5 Method validation

The method was in-house validated according to the following criteria: linearity and linear range, sensitivity, selectivity, intra-assay and inter-assay precision, detection and quantification limits, and accuracy (LIN et al., 1997; RIBANI et al., 2004).

The linearity, linear range, sensitivity and detection and quantification limits were established using the analytical curve from triplicate analyses of four model substances (toluene, chlorobenzene, benzaldehyd, and limonene) at five concentrations: 36, 83, 155, 298, and 597 mg.kg-1 for toluene; 34, 80, 148, 285, and 571 mg.kg-1 for chlorobenzene; 16, 32, 76, 140, 270, and 540 mg.kg-1 for benzaldehyde and 17, 35, 81, 150, 289, and 78 mg.kg-1 for limonene. The Limit Of Detection (LOD) and Limit Of Quantification (LOQ) for each model substance were calculated according to Miller and Miller (1993) using the following expressions: LOD=3sy/x/m and LOQ=10 sy/x/m, where sy/x is the standard deviation and m the slope of the analytical curve, respectively.

The intra-assay precision of the method, expressed as the relative standard deviation (% RSD) of peak-area measurement (n = 3) was evaluated from the results obtained over one day under the same conditions using the solutions of each model substance at three different concentrations as follows: 1.2xLOQ, 2xLOQ, and 5xLOQ. The inter-assay precision was determined for these same concentrations on 3 different days, also expressed as % RSD.

The selectivity was evaluated comparing the chromatograms of the extracts obtained for the matrix without the substance of interest to those obtained for the matrix for each model substances added. The accuracy of the method was determined from the recovery of the nine extractions from a single concentration on different days for each model substance, expressed as a percentage of recovery.

2.6 Statistical analysis

The SIMCA - P software (v. 11.0, Umetrics, Umea, Sweden) was used for the statistical evaluation of the data at the optimisation step, under the extraction conditions, for the principle component analysis using the Loading Column Plot.

To construct the analytical curves and obtain the data for validation, the programme GraphPad Software, version 2.01 was used.

 

3 Results and discussion

3.1 Choice of the model substances

In the present study, toluene, chlorobenzene, benzaldehyde, and limonene were chosen as the model substances to represent the volatile contaminants. Thus, according to the US-FDA 2006 protocol, toluene and chlorobenzene were selected to represent the non-polar volatile substances, and benzaldehyde and limonene to represent the flavour compounds, which are frequently determined in post-consumer analyses. The presence of benzaldehyde in recycled PET packages has been reported by various authors, and is also considered as a flavour compound (BAYER, 2002; NIELSEN; DAMANT; CASTLE, 1995; NERÍN et al., 2003).

3.2 Optimisation of the chromatographic conditions

Due to the complexity of the samples, the first phase of the present study was based on the determination of the optimal conditions for the chromatographic analysis. In order to develop the chromatographic method, the system suitability parameters [Nº of plates/m (N), retention factor (k), resolution (Rs) and separation factor (α)] were considered and calculated according to Bruce, Minkkinen and Riekkola (1998). The results are shown in Table 1.

Since many different classes of volatile contaminants with different polarities could be present in the post-consumer plastic material, the chromatographic conditions were established to obtain good resolution between toluene, chlorobenzene, benzaldehyde, limonene, and linalool (internal standard).

With respect to the retention (k) and separation (α) factors, all results were within the values recommended in the literature (k > 2 and 1.05 < α <2.0, respectively). On the other hand, for quantification, a minimum resolution of 1 between the two closest peaks is recommended, and all the results were within this value (Rs > 1) (BRUCE; MINKKINEN; RIEKKOLA, 1998). These parameters indicated adequate separation and resolution of the model contaminants under the established conditions.

Figure 2 shows a typical chromatographic profile obtained by GC/FID for the recycled PET flakes.

 

 

3.3 Optimisation of the chromatographic conditions

Preliminary trials for the extraction of the volatiles demonstrated that the use of temperatures above 170 ºC caused colour changes (yellow) in the packaging material, indicating undesirable polymer degradation. Under these conditions, an equal accentuated degradation of limonene was shown, demonstrated by the low recovery levels found.

Based on these results, a temperature of 155 ºC was selected and the extraction time varied to evaluate the recovery levels of the model substances. Figure 3 shows the recovery profiles at 4 different times: 30, 60, 90, and 120 minutes.

 

 

The loading column plot of the data presented in Figure 3 indicated that the best condition for extracting the volatile contaminants was 155 ºC for 90 minutes showing a percent recovery above 89% for all the substances evaluated.

3.4 Validation of the analytical method

Recognised protocols recommend the use of Certified Reference Materials (CRM) for quality control methods in order to obtain reliable recovery results in the validation process (BRUCE; MINKKINEN; RIEKKOLA, 1998). In the case of dynamic headspace extraction methods, the analytes would have to be introduced into the material, e.g., by spiking during the preform production. Nonetheless, such CRM is not available. Considering the lack of an appropriate CRM, the proposed method was carried out spiking the surrogates in the PET flakes. The validation parameters of the method, determined for each of the model substances, are shown in Table 2.

The method covers a large range for the analytical curve of the model compounds used in this study and, consequently, allowed estimation of the concentrations of the contaminants in the samples evaluated. The results show a reliable proportionality between the analyte concentration and the corresponding areas of the chromatographic peaks in the concentration range evaluated.

Selectivity was evaluated for each model substance by comparing the chromatographic signal at the retention time of each analyte for an extract from the matrix of a virgin bottle to an extract of a matrix containing the contaminant. No interfering substance eluted at the same retention time of any model substances. Good resolution was obtained between the peaks for the entire chromatogram (Figure 2).

The maximum level of residual contaminants considered negligible by the US-FDA (2008) for recycled PET for use in contact with foods is 220 µg.kg-1. The method developed proved suitably sensitive because the quantification limits for the model substances were an order of magnitude lower than FDA's acceptable contamination limit (Table 2).

In general, both the intra and inter-assay precisions were below 15% (Table 2). According to Huber (1998), in analytical methods for trace substances and impurities, RSD values of up to 20% are acceptable, depending on the sample complexity.

The accuracy of the method was evaluated using recovery tests for the model substances. Acceptable recovery intervals for the analysis of residues are generally between 70 and 120% with RSD values of up to ± 20% (HUBER, 1998). Thus, the recovery values obtained for toluene (90-119%), chlorobenzene (80-105%), benzaldehyde (108-115%) and limonene (96-112%) demonstrated adequate accuracy of the method.

3.5 Analysis of the market samples - identification

The samples tested were post-consumer PET flakes submitted to two washing regimes: Washing Regime 1 (samples A, B, and C) and Washing Regime 2 (samples A1, B1, C1).

In all samples analysed by GC-MS, 47 volatile compounds with molecular masses from 86 to 282 daltons were tentatively identified. These compounds were mainly aldehydes and hydrocarbons (alkanes). Table 3 presents the volatile compounds identified in the post-consumer PET packaging submitted to the two washing regimes. To corroborate the identity of each of the compounds identified by GC-MS, the experimental Kovats Index values and those obtained by other authors and reported in the National Institute of Standards and Technology Chemistry Webbook (NATIONAL..., 2005) are also included in Table 2.

As reported by Dzieciol and Trzeszczynski (2000), PET is subjected to temperatures in the range from 200 to 300 ºC under vacuum, nitrogen, or air in the production, processing, and recycling steps. These conditions result in degradation reactions that generate changes in the properties of the polymers (for example, reduction in the molecular mass and intrinsic viscosity and yellowing) and the emission of volatile substances. These substances, produced during the heat degradation of PET, include carbon monoxide, aldehydes (acetaldehyde, formaldehyde, and benzaldehyde), C1 - C4 aliphatic hydrocarbons, aromatic hydrocarbons (benzene, toluene, ethylbenzene, and styrene), esters (vinyl benzene, methyl acetate), acetophenone, methanol and 2-methyl-1,3-dioxolane. At low temperatures, the main degradation products are acetaldehyde, formaldehyde, and carbon monoxide, and the concentrations of carbon monoxide, aromatic and aliphatic hydrocarbons, and methyl acetate increase with temperature (DZIECIOL; ZIECIOL; TRZESZCZYNSKI, 1998). Thus, some of the compounds identified in the present study could have been formed during PET degradation reactions.

Other sources of contamination should also be considered. Recently and Widén, Leufvén and Nielsen (2005) identified substances they believe came from recycled packaging material. The authors suggested three possible sources of contamination: 1) misuse of the package by the consumer, 2) food products (fermented and fortified alcoholic beverages), and 3) non-food products (petroleum products, detergents, and cleaning products, compounds containing ethers, and unknown products), apart from other compounds resulting from the deterioration of the original product and storage in an inappropriate place.

Limonene is frequently found in post-consumer PET and originates from prolonged contact with soft drinks or fruit juices (FRANZ, 2002; NERÍN et al., 2003). Limonene is a volatile compound considered to be a precursor of off-flavours in foods, and thus its determination in PET could be used in some instances to guarantee that post-consumer recycled material is free of contaminants (GARCIA et al., 2006; CAVA et al., 2005).

Although some authors have concluded that the absorption of limonene by the package causes no relevant sensory changes in orange juice (van WILLIGE et al., 2003), a study of the transport mechanisms of limonene is important. The presence of limonene could affect the properties of the container and facilitate the loss of other volatile compounds of greater relevance to the shelf life of the product because of its plasticizing effect on the structure of the package wall (FAYOUX; SEUVRE; VOILLEY, 1997).

Fayoux, Seuvre and Voilley (1997) showed that the majority of the terpenes absorbed by PET were not removed even after the most severe washing treatments, and thus the off-flavours could appear in the next product introduced into the intended package.

It is worth mentioning that the majority of the contaminants identified in the samples analysed in the present study have already been identified in recycled PET by other authors (NERÍN et al., 2003; WIDÉN; LEUFVÉN; NIELSEN, 2005; NIELSEN; DAMANT; CASTLE, 1997; FRANZ; WELLE, 2002; REYNIER et al., 2004; KONKOL et al., 2003), confirming the suitability of the method proposed in this article.

3.6 Analysis of the market samples - quantification

The contamination levels of the substances identified by GC-MS and the Kovats Indexes, and present in the samples after being submitted to the two washing regimes, were estimated using analytical curves for the model substances (toluene, chlorobenzene, benzaldehyde, and limonene). The results are shown in Table 4.

A comparison of the results obtained for material from the suppliers who applied Washing Regime 1 showed that hexanal, 2-methyl phenol, toluene, p-xylene, m-xylene, styrene, cumene, hemelitol, benzaldehyde, limonene, and myrcene were present in all samples. Octanal, 3-methyl phenol and 4-ethyl-o-xylene were present in only a few samples. Octanoic acid, durene and naphthalene, despite having been identified by GC-MS (Table 3), could not be quantified by GC/FID (Table 4). The presence of elevated levels of some contaminants can be attributed to the misuse of post-consumer PET packaging material and lack of control in the collection of the material. After Washing Regime 2, few of these contaminants were completely removed.

According to the US-FDA's model for assessing the efficiency of a recycling process, the maximum acceptable level of a residual contaminant in a polymer that corresponds to an estimated daily rate of 1.5 µg/person/day, depends on the density of the polymer, its thickness, and the consumption factor. Based on this, a maximum value for residues of 220 µg.kg-1 was proposed for recycled PET (with a density of 1.4 g.cm-3) assuming the conservative supposition that all types of foods use packages made with this polymer and that the final item consisted of 100% recycled PET.

Even though the recycled PET evaluated in this study is not intended to food contact, it was used to evaluate the suitability of the proposed validated method in an expected low-level contaminated matrix. The results obtained show that even after the Washing Regime 2, toluene, p-xylene, m-xylene, styrene, hemelitol, limonene, and myrcene presented values above the limit of 220 µg.kg-1. Octanoic acid, durene, and naphthalene were only quantified in samples obtained from Washing Regime 2. This could have occurred due to recontamination in the recycling system or even by external contamination.

It should be emphasized that the most recent investigation on determining the volatile compounds in recycled PET considers fully automated techniques aiming at the reduction of sample preparation time and allowance of higher sample throughput. In spite of these advantages, these techniques are of high cost and need more experienced personnel in order to achieve reliable results. In addition, up to 2007, the Brazilian regulation allowed solely the use of PET functional barrier to food contact application (BRASIL, 1999). Nonetheless, in 2008, the regulation concerning food grade recycled post consumer PET intended to food contact application was published (BRASIL, 2008). The criteria for food safety and the approval of food grade recycled post consumer PET require, among other procedures, the use of reliable validated methods to assure the compliance with the concentration limit for surrogates of 220 µg.kg-1 in the polymer. The method proposed in this study proved reliable, simple, and low cost. Besides, it has never been previously applied, neither for PET material nor for quantification purposes.

 

4 Conclusions

The proposed analytical method, using dynamic headspace concentration as extraction technique and gas chromatography with flame ionization detector, was reliable, simple, practica,l and of low cost. The method presents adequate selectivity and quantification capability to determine the volatile contaminants in post-consumer PET. The method can easily be used in the quality control of the production of recycled PET, as well as by food surveillance governmental agencies.

 

Acknowledgements

The authors gratefully thank CNPq and CAPES for financial support.

 

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Recebido para publicação em 19/12/2008
Aceito para publicação em 16/5/2009 (004002)

 

 

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