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三聚氰胺从热固化氨基交联罐头涂料迁移至乙醇水溶液食品模拟物中的情况:水解、相对反应活性及迁移的相关方面

Migration of melamine from thermally cured, amino cross-linked can coatings into an aqueous ethanol food simulant: aspects of hydrolysis, relative reactivity and migration.

作者信息

Magami Saminu M, Oldring Peter K T, Castle Laurence, Guthrie James T

机构信息

a Polymer Science Division, Department of Colour Science, School of Chemistry , University of Leeds , Leeds , UK.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2015;32(3):403-9. doi: 10.1080/19440049.2014.1003150. Epub 2015 Jan 30.

Abstract

Aspects of melamine migration from epoxy-based coatings into a food simulant were studied. Four commercial amino-based cross linkers were incorporated into an epoxy anhydride coating system and into an epoxy phenolic coating system. The epoxy-based coatings were formulated, applied, cured and tested for migration by retorting in contact with the food simulant, 10% ethanol, at 131°C. The commercial melamino-based cross linkers used and the model coatings that were prepared using these cross linkers contained very low or non-detectable levels of free melamine. However, during retorting, the migration of melamine from the coatings increased as the retorting time was increased. This migration process is not the more classical diffusional process but rather the result of chemical attack (hydrolysis) of the coating. For these model can coatings, a substantial fraction of the melamino cross linker was hydrolysed although, curiously, the essential functional properties of the coating are retained. In all cases, for these model systems the migration of melamine was rather low because the cross linkers are used commercially in only small amounts - typically 1-2% of the dry film weight of the coatings. For the standard retorting conditions of 1 h, migration of melamine was up to 0.4 mg kg(-1), depending on the cross linker used. The cross linker that contained the methylol functionality (-CH₂OH group) gave rise to less melamine than did the alkylated cross linkers (methylated and butylated, -OCHv and -O(CH₂)₃CH₃, respectively). This observation could prove useful in formulating coatings with even lower melamine release characteristics.

摘要

研究了三聚氰胺从环氧基涂料迁移到食品模拟物中的情况。将四种商用氨基交联剂分别加入到环氧酸酐涂料体系和环氧酚醛涂料体系中。制备环氧基涂料,涂覆、固化后,通过在131°C下与食品模拟物10%乙醇接触蒸煮来测试迁移情况。所使用的商用蜜胺基交联剂以及使用这些交联剂制备的模型涂料中游离三聚氰胺含量极低或检测不到。然而,在蒸煮过程中,三聚氰胺从涂料中的迁移量随着蒸煮时间的增加而增加。这种迁移过程并非更典型的扩散过程,而是涂料化学侵蚀(水解)的结果。对于这些模型罐头涂料,相当一部分蜜胺交联剂被水解,不过奇怪的是,涂料的基本功能特性得以保留。在所有情况下,对于这些模型体系,三聚氰胺的迁移量相当低,因为交联剂在商业上的用量很少——通常为涂料干膜重量的1 - 2%。在1小时的标准蒸煮条件下,三聚氰胺的迁移量高达0.4 mg kg⁻¹,具体取决于所使用的交联剂。含有羟甲基官能团(-CH₂OH基团)的交联剂产生的三聚氰胺比烷基化交联剂(分别为甲基化和丁基化,-OCH₃和-O(CH₂)₃CH₃)少。这一观察结果可能有助于配制具有更低三聚氰胺释放特性的涂料。

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