首页> 美国卫生研究院文献>Molecules >Towards a Non-Biased Formaldehyde Quantification in Leather: New Derivatization Conditions before HPLC Analysis of 24-Dinitrophenylhydrazine Derivatives
【2h】

Towards a Non-Biased Formaldehyde Quantification in Leather: New Derivatization Conditions before HPLC Analysis of 24-Dinitrophenylhydrazine Derivatives

机译:朝着皮革中的非偏见甲醛定量:HPLC分析24-二硝基苯基肼衍生物的新衍生条件

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In leathers, formaldehyde is currently analyzed according to EN ISO 17226-1 standard, by reversed phase liquid chromatography after off-line precolumn derivatization with 2,4 dinitrophenylhydrazine (DNPH) in strong acidic conditions. We first demonstrate that this standard is not adapted to leather retanned with resins likely to release formaldehyde by hydrolysis. Indeed, formaldehyde content may be largely overestimated due to concomitant resin hydrolysis (in harsh acidic conditions) that releases formaldehyde during the derivatization step and during the waiting time on autosampler before analysis. Therefore, we thoroughly studied the derivatization step in order to propose new derivatization conditions. Replacing orthophosphoric acid by less acidic buffer solutions is not enough to avoid hydrolysis. A derivatization without adding acid is realized by solubilizing DNPH in acetonitrile instead of orthophosphoric acid. These conditions lead to a complete derivatization of formaldehyde in 3 h at 50 °C (in a water bath) while avoiding the hydrolysis of co-extracted dicyandiamide and melamine resins. The as-obtained leather extracts are stable over time. Formaldehyde contents found with this method agree with the formaldehyde content measured immediately at the end of derivatization reaction in standard conditions or with formaldehyde content measured by a home-designed flow injection analysis with acetylacetone online derivatization and UV detection.
机译:在皮带中,目前根据EN ISO 17226-1标准进行甲醛,通过在强酸性条件下用2,4二硝基苯基肼(DNPH)离线预先突出衍生物后反相液相色谱法。我们首先证明该标准不适用于通过水解释放甲醛的树脂重刺的皮革。实际上,由于在衍生化步骤中释放甲醛的伴随的树脂水解(在苛刻的酸性条件下)并且在分析之前,在自动进样器的等待时间期间,甲醛含量可能很大估计。因此,我们彻底研究了衍生化步骤,以提出新的衍生条件。通过较少的酸性缓冲溶液替换正磷酸是不足以避免水解的。通过在乙腈代替正磷酸中溶解DNPH来实现不添加酸的衍生化。这些条件导致在50℃(水浴中)在3小时内完全衍生甲醛,同时避免共萃取的双氰胺和三聚氰胺树脂的水解。随着时间的推移,所获得的皮革提取物是稳定的。用该方法发现的甲醛含量与在标准条件下衍生化反应结束时立即测量的甲醛含量,或者通过用乙酰丙酮在线衍生化和UV检测测量甲醛含量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号