Université du Québec à Montréal, Chemistry Department, PO Box 8888, succ. Centre-Ville, Montréal, Québec H3C 3P8, Canada; Institut de recherche Robert-Sauvé en santé et en sécurité du travail, 505, De Maisonneuve Blvd West., Montréal, Québec H3A 3C2, Canada.
Institut de recherche Robert-Sauvé en santé et en sécurité du travail, 505, De Maisonneuve Blvd West., Montréal, Québec H3A 3C2, Canada.
J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Apr 1;1142:122027. doi: 10.1016/j.jchromb.2020.122027. Epub 2020 Feb 27.
The US Environmental protection agency (EPA) has published guidance that includes test procedures for evaluating indoor exposure to chemicals from products. One of the test procedures represents the migration test for evaluating potential dermal exposure from home furniture. Such an evaluation involves the chemical measurement of the sweat which is currently unavailable in the literature. The objective of this project was to develop and validate an analytical method for quantification of migration of 4,4'-methylenediphenyl diisocyanate (MDI), 2,6-toluene diisocyanate (2,6-TDI) and 2,4-toluene diisocyanate (2,4-TDI) from a polyurethane (PU) flexible foam to artificial sweat that meets the recommendations of the EPA test protocol. Following the EPA protocol, six synthetic sweat solutions were prepared and used in evaluation of isocyanate recovery performance. The migration tests were conducted using five foam types that were chosen and supplied by PU foam manufacturers to represent the types most commonly found in commercial products, and with formulations anticipated to have the highest potential residual TDI or MDI. Migration tests were conducted using glass fiber filters (GFF) coated with 1-(2-methoxyphenyl)piperazine (1,2-MP) and analyzed using HPLC equipped with a UV detector for quantification and a MS detector to qualify peaks. The detection limits of the method were 0.002 µg/mL for 2,6-TDI, 0.011 µg/mL for 2,4-TDI, and 0.003 µg/mL for MDI. Quantification limits were 0.006 µg/mL, 0.037 µg/mL, and 0.010 µg/mL, respectively. The recovery tests on a Teflon surface for 5 of the 6 EPA-recommended synthetic sweat solutions indicate the recovery percentage was approximately 80% for diisocyanates. Recovery for the sixth sweat solution was low, approximately 30%. TDI and MDI migration was not observed when testing was conducted on foam samples.
美国环保署 (EPA) 发布了一份指南,其中包括评估产品中化学物质的室内暴露的测试程序。其中一种测试程序代表了评估家用家具潜在皮肤接触的迁移测试。这种评估涉及到汗液的化学测量,而目前文献中尚未提供这种测量。本项目的目的是开发和验证一种分析方法,用于量化从聚氨酯 (PU) 柔性泡沫中迁移 4,4'-亚甲基二苯基二异氰酸酯 (MDI)、2,6-甲苯二异氰酸酯 (2,6-TDI) 和 2,4-甲苯二异氰酸酯 (2,4-TDI) 到符合 EPA 测试方案建议的人工汗水中的迁移率。按照 EPA 协议,制备了六种合成汗液溶液,并用于评估异氰酸酯的回收性能。迁移测试使用由 PU 泡沫制造商选择和供应的五种泡沫类型进行,这些泡沫类型代表了商业产品中最常见的类型,并且预计具有最高的潜在残留 TDI 或 MDI 含量。使用涂有 1-(2-甲氧基苯基)哌嗪 (1,2-MP) 的玻璃纤维过滤器 (GFF) 进行迁移测试,并使用配备 UV 检测器进行定量和 MS 检测器进行定性的 HPLC 进行分析。该方法的检测限为 2,6-TDI 为 0.002 µg/mL,2,4-TDI 为 0.011 µg/mL,MDI 为 0.003 µg/mL。定量限分别为 0.006 µg/mL、0.037 µg/mL 和 0.010 µg/mL。对 EPA 推荐的 6 种合成汗液溶液中的 5 种在特氟龙表面上的回收测试表明,异氰酸酯的回收率约为 80%。第六种汗液溶液的回收率较低,约为 30%。在对泡沫样品进行测试时,没有观察到 TDI 和 MDI 的迁移。