High-temperature migration of antioxidants from polyolefins

Migration rates of radiolabelled antioxidants, Irganox-1010 (I-1010) and Irganox-1076 (I-1076), were measured from low- and high-density polyethylenes (LDPE, HDPE) and polypropylene (PP) at temperatures up to 135 degrees C. Water, 8 and 95 per cent aqueous ethanol and corn oil were employed as food simulating liquids (FSL). The experiments were conducted in a high-pressure cell in a manner that allowed contact between the polyolefin plaque and the FSL only during the test period and not while being heated. The migrations of the antioxidants varied with the square root of time, and the Fickian diffusion coefficients could be correlated with temperature in an Arrhenius fashion. Under comparable test conditions, antioxidant migrations were largest from PP for aqueous simulants, but for non-aqueous simulants the highest losses were from LDPE. In both instances lowest losses were from HDPE. In most instances there was little difference between the migration behaviour of I-1010 and I-1076. A few tests were conducted to measure the antioxidant migrations to foods. The losses were usually larger than those to water but below those to corn oil.     

Time‐ and temperature‐dependent migration studies of Irganox 1076 from plastics into foods and food simulants

The study provides an exhaustive set of migration data for octadecyl 3‐(3,5‐di‐tert‐butyl‐4‐hydroxyphenyl)propionate (Irganox 1076) from low‐density polyethylene (LDPE) in several food matrices. Irganox 1076 was used as a model migrant because it represents one of the typical substances used as an antioxidant in food packaging polymers. Kinetic (time‐dependent) migration studies of Irganox 1076 were performed for selected foodstuffs chosen with different physical–chemical properties and in relation to the actual European food consumption market. The effect of fat content and of the temperature of storage on the migration from plastic packaging was evaluated. The results show that migration increased with fat content and storage temperature. All data obtained from real foods were also compared with data obtained from simulants tested in the same conditions. In all studied cases, the kinetics in simulants were higher than those in foodstuffs. The work provides data valuable for the extension of the validation of migration model developed on simulants to foodstuffs themselves.     

Feasibility study for the development of certified reference materials for specific migration testing. Part 1: Initial migrant concentration and specific migration

The paper describes a project with the main objective of developing the know how to produce certified reference materials (CRMs) for specific migration testing. Certification parameters discussed are the initial concentration of the migrant in the polymer (C_P,0) and the specific migration into a food simulant under certain temperature/time conditions. Sixteen preliminary candidate CRMs were defined and produced. The most important polymers (low- and high-density polyethylene (LDPE and HDPE), polypropylene (PP), polystyrene (PS), polyethylene terephtalate (PET), plasticized polyvinyl chloride (PVC), rigid PVC, polyamides (PA)) and additives as well as monomers representing different physicochemical properties as target substances for migration were chosen. The stability and homogeneity of the migrants in the materials were tested and methods for the determination of the certification parameters were developed and validated. From the 16 materials produced, the six most suitable CRM candidates (LDPE//Irganox 1076/Irgafos 168, LDPE//1,4-diphenyl-1,3-butadiene (DPBD), HDPE//Chimassorb 81/Uvitex OB, PP homo//Irganox 1076/Irgafos 168, HIPS, 1% mineral oil//styrene, PA 6//caprolactam) were selected. The feasibility of CRM production for the six candidate materials was demonstrated and a trial certification exercise was performed with participation of all four partner laboratories. All six materials showed suitable properties for future production as certified reference materials.     

Time- and temperature-dependent migration studies of Irganox 1076 from plastics into foods and food simulants

The study provides an exhaustive set of migration data for octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate (Irganox 1076) from low-density polyethylene (LDPE) in several food matrices. Irganox 1076 was used as a model migrant because it represents one of the typical substances used as an antioxidant in food packaging polymers. Kinetic (time-dependent) migration studies of Irganox 1076 were performed for selected foodstuffs chosen with different physical-chemical properties and in relation to the actual European food consumption market. The effect of fat content and of the temperature of storage on the migration from plastic packaging was evaluated. The results show that migration increased with fat content and storage temperature. All data obtained from real foods were also compared with data obtained from simulants tested in the same conditions. In all studied cases, the kinetics in simulants were higher than those in foodstuffs. The work provides data valuable for the extension of the validation of migration model developed on simulants to foodstuffs themselves.     

纳米银-聚乙烯复合包装中银对2 种抗氧化剂向食品模拟物迁移的影响

探究纳米银-聚乙烯复合包装中纳米银成分的存在对2 种抗氧化剂（Irganox1076和Irgafos168）向食品模拟物迁移规律的影响。将含有抗氧化剂的聚乙烯包装膜和同时含有抗氧化剂与纳米银的复合包装膜裁成正方形若干,分别浸泡于正己烷和体积分数95%乙醇溶液2 种食品模拟物中,密封后在20、40 ℃以及70 ℃条件下进行迁移实验。食品模拟物中2 种抗氧化剂的加标回收率在79.3%～108.0%之间,相对标准偏差在0.7%～5.3%之间。2 种抗氧化剂的迁移会随着迁移温度的升高以及迁移时间的延长而增加直至达到迁移平衡,且其在正己烷模拟物中的迁移量大于在体积分数95%乙醇模拟物中的迁移量;含纳米银聚乙烯塑料比不含纳米银聚乙烯塑料中的抗氧化剂向食品模拟物中的迁移量小,表明纳米银成分的存在可以抑制包装中的抗氧化剂向食品模拟物中的迁移。     

The use of mechanical analyses,scanning electron microscopy and ultrasonic imaging to study the effects of high‐pressure processing on multilayer films

The effects of high‐pressure processing (HPP) on the mechanical and physical characteristics of eight high‐barrier multilayer films were investigated. These films were PET/SiO_x/LDPE, PET/Al₂O₃/LDPE, PET/PVDC/nylon/HDPE/PP, PE/nylon/EVOH/PE, PE/nylon/PE, metallised PET/EVA/LLDPE, PP/nylon/PP and PET/PVDC/EVA. In addition, PP was evaluated as a monolayer film for comparison purposes. Pouches made from these films were filled with distilled water, sealed, then pressure processed at 600 and 800 MPa for 5, 10 and 20 min at a process temperature of 45 °C. Pouches kept at atmospheric pressure were used as controls. Prior to and after HPP, all films were tested for tensile strength, percentage elongation and modulus of elasticity (at 50 cm min^?1) and imaged by scanning electron microscopy (SEM) and C‐mode scanning acoustic microscopy (C‐SAM). Results showed no significant changes in tensile strength, elongation and modulus of elasticity of all films after HPP. However, significant physical damage to metallised PET (MET‐PET) was identified by SEM and C‐SAM. Thus it could be concluded that MET‐PET is not suitable for batch‐type high‐pressure‐processed food packaging. It can also be concluded that the other materials investigated during this study are suitable for batch‐type high‐pressure‐processed food packaging. Copyright © 2003 Society of Chemical Industry     

Antioxidants and their migration into food simulants on irradiated LLDPE film

Effects of γ-irradiation on residual and migration levels of antioxidants, tris-(2,4-di-tert-butylphenyl) phosphite (Irgafos 168) and octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate (Irganox 1076), and their radiolysis products were investigated in the linear low density polyethylene (LLDPE) packaging samples treated at doses from 0 to 200 kGy. The content of Irgafos 168 was not detected in 5 kGy treated samples and the content of Irganox 1076 decreased by 34.9% from the initial level in 10 kGy treated samples. The radiolysis products, 2,4-di-tert-butylphenol (2,4-DTBP), 1,3-di-tert-butylbenzene (1,3-DTBB), and toluene were identified and their concentrations gradually increased as the irradiation dose increased. Migration of Irgafos 168 from the LLDPE pouch into food simulants, distilled water, acetic acid (4 ml/100 ml distilled water) or ethanol (20 ml/100 ml distilled water), was not detected at dose levels up to 200 kGy while that of the Irganox 1076 was detected in a decreasing mode with increasing dose.     

模拟液的极性对聚丙烯中抗氧化剂迁移的影响

研究了4种抗氧化剂BHA、BHT、Irganox1076、Irgafos168从聚丙烯塑料迁移至6种不同极性的模拟液时,模拟液极性对抗氧化剂迁移规律的影响。结果表明,抗氧化剂与聚丙烯塑料相溶性越差,与模拟液相溶性越好,迁移平衡分配系数越大;同时,模拟液极性越接近聚丙烯时,迁移扩散系数越高,扩散系数受分子量影响越小,反之,则迁移扩散系数受分子量影响较大,扩散系数随分子量的增大而减小;无水乙醇模拟液中,抗氧化剂分子量越大,平衡分配系数受温度影响越大,迁移焓变随分子量增大而增大,而正己烷模拟液中变化正好与之相反。     

Influence of solvent absorption on the migration of Irganox 1076 from LDPE

The effect of solvent absorption on additive migration was studied by relating the diffusion coefficient ( D ) of Irganox 1076 to the maximum solvent absorption of different solvents in low-density polyethylene (LDPE) film. Solvents tested were ethanol, isopropanol, isooctane, ethylacetate, cyclohexane, tributyrin, tricaprylin and olive oil. Diffusion and partition coefficients were determined by fitting the migration curves, i.e. the concentration of Irganox 1076 in solvent as a function of time, with Fick's diffusion equation. The results for the low molecular weight solvents show that with increasing maximum solvent absorption, D of Irganox 1076 is increasing as well. This trend is not observed for the two triglycerides and olive oil. In spite of absorption, no increase in D was observed. The obtained result is the basis of an extended predictive migration model that, besides migrant and polymer properties, is also based on the maximum solvent absorption in the polymer.     

石墨烯/低密度聚乙烯复合包装膜中2种抗氧化剂向食品模拟物异辛烷的迁移

建立高效液相色谱法检测石墨烯/低密度聚乙烯复合食品包装薄膜中2种抗氧化剂(Irganox1076、Irgafos168)的方法。考察时间、温度以及石墨烯和石墨烯微片的存在对2种抗氧化剂向脂肪类食品模拟物异辛烷迁移的影响,同时分析2种不同抗氧化剂在迁移中的相互作用。结果表明,2种抗氧化剂的迁移会随着迁移温度的升高以及迁移时间的延长而增加直至达到迁移平衡;2种抗氧化剂之间存在协同作用,在迁移过程中会相互影响;石墨烯及石墨烯微片纳米粒子的团聚现象和吸附作用抑制了食品包装中的Irganox1076、Irgafos168两种抗氧化剂向异辛烷中的迁移。     

Evaluation of some of the physical properties of atmospheric plasma treated polypropylene fabric

In this study, atmospheric pressure plasma (APP) treatment was applied to polypropylene (PP) fabric with non‐polymerizing gases, such as air, argon, and nitrogen. Properties of the APP‐treated samples including low‐stress mechanical behavior, air permeability, water vapor permeability, and thermal characteristics were evaluated. Tensile and friction coefficient of the specimens were also measured. The changes in these properties are believed to be closely related to the inter‐fiber and inter‐yarn frictional force induced by the APP. The decrease in the air permeability of the APP‐treated PP fabric was probably because of the plasma action effect on change in fabric surface morphology, which was confirmed by scanning electron microscopy micrographs. The change in the thermal properties of the APP‐treated PP fabric was in good agreement with the earlier findings and can be attributed to the amount of air trapped between the yarns and fibers. This study suggests that the APP treatment can influence the final properties of the PP fabric, and also provides information for developing APP‐treated PP fabric for industrial use.     

热力学数学模型对塑料中化学物向食品模拟液中迁移平衡时分配系数的预测研究

目的分配系数能够直接反映出塑料包装材料中有害化学物向食品迁移的水平,研究分配系数与塑料包装材料、迁移物及食品(模拟物)三者之间的关系有重要意义。方法以Scatchard-Hildebrand统计热力学理论为基础,从热力学平衡角度分析了化学物在包装材料/食品体系中的迁移和分配过程,建立了一个预测化学物迁移平衡时分配系数的热力学数学模型。通过所建立的初级数学模型对聚乙烯薄膜中四种抗氧化剂,即2,6-二叔丁基-4-甲基苯酚(BHT)、二丁基羟基茴香醚(BHA)、Irganox1010和Irganox1076向脂肪类食品模拟物异辛烷迁移平衡时状态进行模拟计算,并与已公开发表的实验数据进行了对比。结果聚乙烯薄膜中四种抗氧剂向异辛烷中迁移平衡的分配系数模拟值与实验值随温度变化趋势一致。结论该热力学模型符合迁移理论,对PE/抗氧剂/脂肪类食品体系分配系数的预测有一定的适用性。     

高强聚丙烯纺粘针刺土工布的耐久性能

为研究高强聚丙烯纺粘针刺土工布（HPP）的耐老化性能和耐化学腐蚀性能,采用热氧老化、酸与碱腐蚀液和纯水浸泡等实验,研究了不同温度和不同化学环境对其耐久性的影响,将其与普通聚丙烯土工布（PP）耐久性进行对比。结果表明：当样品在热氧化温度为110、120、130 ℃条件下处理25d 时,HPP 土工布质量保留率分别为 99.06%、98.85% 和 98.10%; PP 土工布质量保留率分别为98.89%、98.78% 和 97.78%;HPP 土工布纵向断裂强度保留率分别为75.00%、67.25% 和 64.71%,PP 土工布纵向断裂强度保留率分别为 72.15%、65.56% 和 54.00%。在 3 种不同液体处理下HPP 土工布的强度损失率均未超过5.00%,表明 HPP 土工布具有良好的耐腐蚀和耐水浸泡性。通过Arrhenius 定理拟合出 HPP 土工布热氧反应速率表达式,预测出 HPP 土工布使用 50a 后的强度保留率为27.30%。     

纳米银-聚乙烯复合包装中助剂对银向食品模拟物迁移的影响

为探究纳米银-聚乙烯复合包装中添加剂对纳米银颗粒向食品模拟物迁移的影响,在20、40 ℃和70 ℃条件下分别将空白纳米银聚乙烯复合包装和含有助剂（抗氧化剂1076、抗氧化剂168、光稳定剂622和光稳定剂944）的纳米银聚乙烯复合包装在3 g/100 mL乙酸溶液和体积分数50%乙醇溶液两种食品模拟物中浸泡1～30 h,然后蒸干定容并用电感耦合等离子体质谱测定银的含量。结果表明：食品模拟物中银的加标回收率在84.19%～115.69%之间,相对标准偏差在3.21%～8.75%之间;在8 h内塑料中的添加剂会促进银向两种食品模拟物的迁移;同时银的迁移率会随着迁移温度的升高和迁移时间的增加而增大直至平衡;平衡时,塑料中的添加剂反而阻碍银向这两种食品模拟物的迁移;银在酸性模拟物中的迁移率大于在酒精类模拟物中的迁移率。     

Effect of high‐pressure processing on immunoreactivity,microbial and physicochemical properties of hazelnut milk

This study investigated the effects of high‐pressure processing (HPP) and thermal processing (TP) on the overall quality attributes of hazelnut milk. HPP achieved the same microbial safety as TP, and the pH, °Brix and sugar contents were maintained at the levels of fresh hazelnut milk. Although HPP caused colour changes, the ?E was smaller than that of the TP sample. Increasing pressure significantly decreased the immunoreactivity of the hazelnut milk by 70%, while simultaneously reducing the levels of essential and non‐essential amino acids and chemical score (CS) and the essential amino acid index (EAAI) values. However, neither HPP nor TP significantly affected the fatty acid composition of hazelnut milk. HPP retained higher total phenolic and flavonoid levels of the hazelnut milk, with a better antioxidant capacity than TP samples. Thus, the HPP maintained microbial safety during cold storage, and physicochemical properties of the treated hazelnut milk were not significantly different from those of the fresh hazelnut milk.     

Effectiveness of polypropylene film as a barrier to migration from recycled paperboard packaging to fatty and high-moisture food.

The capability of a polypropylene (PP) film barrier to prevent migration of residual contaminants from recycled paperboard into food simulants was studied. Anthracene, benzophenone, methyl stearate and pentachlorophenol were chosen as chemical surrogates to represent classes of contaminants likely to be found in recycled paper/paperboard. Each surrogate was spiked into a test specimen made of seven thin virgin paper layers at concentrations of 1-50 mg kg(-1). Test specimen were dried, stacked and sandwiched with PP films, laminated with PP film and then subjected to migration experiments using a compression cell maintained at 100 degrees C for 2 h. The concentration of the surrogates in the test specimen and in 95% ethanol, isopropanol and 10% ethanol food-simulating solvents was determined by gas chromatography with flame ionization and electron capture detection. The results show that although the concentrations of the surrogates in the food simulants decreased with an increase in PP film thickness, they were still high and generally resulted in dietary concentrations >0.5 microg kg(-1), the level that US Food and Drug Administration would equate with negligible risk for a contaminant migrating from food packaging. Only at the lowest spiking level (1 mg kg(-1) benzophenone) did migration from the paperboard through a 0.127-mm PP film result in a dietary concentration of 相似文献   

Copper release from nano‑copper/polypropylene composite films to food and the forms of copper in food simulants

The influences of temperature, exposure time, different types of polypropylene (PP), (3-Aminopropyl) triethoxysilane (KH550) used as coupling agent, sterilizing conditions on copper migration from nano‑copper/PP composite films into food/ food simulants were explored. Results showed that copper migrated more easily from polypropylene (PPH) films with a maximum rate of 34.51%, compared to those from copolymer polypropylene (PPR) and block copolymer polypropylene (PPB) to 3% acetic acid (w/v). Gamma (γ) irradiation could significantly increase the copper migration (P < 0.05). Different forms of copper were found in different simulants. Copper crystals were found in 10% ethyl alcohol and identified by scanning electron microscopy and energy dispersed analysis of X-rays (SEM-EDX). The hydroxylation (%) of nano‑copper/PP films was less than 100%. These films had certain antioxidant and antimicrobial properties which could extend the shelf life of packaged food. The migration amount of copper into rice vinegar was the largest, with a maximum of 0.65 mg/ kg.Industrial relevanceAlthough nanomaterials are potentially beneficial for food packaging, migration of nanoparticles to the packaged food can be harmful to the human body. Therefore, it is very important to determine the presence and characterize the morphology of nanoparticles in food. In this paper, we have developed a new and effective packaging material containing nanoparticles and have explored the migration form and morphology in food simulants. In conjunction with the results of current study, nano‑copper/PP packaging material can be suggested for maintaining the product quality and has commercial potential.     

Determination of the mass transport properties of chemical additives in polypropylene material/simulated food system

The mass transport process (migration) of five additives from three different types of polypropylene (PP) films into selected food simulants was studied. The migration tests were carried out at different time-temperature conditions, and the concentration of additives in polymer matrix and food simulants were analysed by high-performance liquid chromatography (HPLC). With all data, the mass transport properties for migration kinetics (partition and diffusion coefficients) were determined. Results showed that the partition coefficient was affected significantly by the temperature and simulants’ properties, whereas little affected by the types of PP film and molecular weight of substance. The polarity, structure and shape of substances can also have an influence in their partition between the polymer matrix and food simulants. Additionally, comparison results between the experimental diffusion coefficients and the calculated values by Piringer model suggested that the current migration model with the default modelling parameters for PP does not describe realistically the diffusion coefficients of additives. The calculated diffusion coefficients were greater than the experimental values, as a consequence, the migration of chemical additives will be overestimated. For more realistic migration calculations, more accurate modelling parameters in Piringer model should be established and the effect of food on migration should be high interest in future work.     

Diffusion behaviour of additives in polypropylene in correlation with polymer properties

The migration behaviour of polymer additives in 17 polypropylene (PP) samples is described. These samples cover the major types of PP used in food packaging. The diffusion coefficients of additives with relatively small molecular masses, M _r = 136 (limonene), as well as the migration of typical antioxidants used in PP up to M _r = 1178 (IRGANOX 1010), were measured at different temperatures. In addition, the diffusion data and percentages of xylene-soluble fractions were correlated. This enables a prediction of the migration behaviour of a PP sample by testing its ‘isotactic index’ with xylene. The results clearly indicate that PP can be subdivided, from the migration point of view, into the monophasic homopolymer (h-PP), the monophasic random copolymer (r-PP), and the heterophasic copolymer (heco-PP). The diffusion coefficients for r-PP are at least one order of magnitude higher than those of h-PP and comparable with the values for heco-PP. Upper limits for the diffusion values can be calculated based on the safety margin required by consumer protection laws.     

Development and application of a non-targeted extraction method for the analysis of migrating compounds from plastic baby bottles by GC-MS

In 2011, the European Union prohibited the production of polycarbonate (PC) baby bottles due to the toxic effects of the PC monomer bisphenol-A. Therefore, baby bottles made of alternative materials, e.g. polypropylene (PP) or polyethersulphone (PES), are currently marketed. The principal aim of the study was the identification of major compounds migrating from baby bottles using a liquid–liquid extraction followed by GC/MS analysis. A 50% EtOH in water solution was selected as a simulant for milk. After sterilisation of the bottle, three migration experiments were performed during 2 h at 70°C. A non-targeted liquid–liquid extraction with ethyl acetate–n-hexane (1:1) was performed on the simulant samples. Identification of migrants from 24 baby bottles was done using commercially available WILEY and NIST mass spectra libraries. Differences in the migrating compounds and their intensities were observed between the different types of plastics, but also between the same polymer from a different producer. Differences in the migration patterns were perceived as well between the sterilisation and the migrations and within the different migrations. Silicone, Tritan? and PP exhibited a wide variety of migrating compounds, whereas PES and polyamide (PA) showed a lower amount of migrants, though sometimes in relatively large concentrations (azacyclotridecan-2-one up to 250 µg kg^?1). Alkanes (especially in PP bottles), phthalates (dibutylphthalate in one PP bottle (±40 µg kg^?1) and one silicone bottle (±25 µg kg^?1); diisobutylphthalate in one PP (±10 µg kg^?1), silicone (up to ±80 µg kg^?1); and Tritan? bottle (±30 µg kg^?1)), antioxidants (Irgafos 168, degradation products of Irganox 1010 and Irganox 1076), etc. were detected for PP, silicone and Tritan? bottles. Although the concentrations were relatively low, some compounds not authorised by European Union Regulation No. 10/2011, such as 2,4-di-tert-butylphenol (10–100 µg kg^?1) or 2-butoxyethyl acetate (about 300 µg kg^?1) were detected. Migrating chemicals were identified as confirmed (using a standard) or as tentative (further confirmation required).