摘要
利用微波消解-氢化发生原子荧光光谱法测定水产食品中微量砷的含量,实验考察了对测量影响较大的仪器工作参数(如灯电流、负高压等)和氢化发生条件(如载气流速、酸介质、硼氢化钾浓度、预还原剂等)。在优化实验条件下测定了几种水产食品中微量砷的含量及紫菜中无机砷的测定,平均加标回收率为96.3%,具有较高的测量稳定性(RSD<5.9%),样品空白测定方法的检出限(3σ)为0.021μg/kg。结果表明方法具有较高的测量灵敏度,稳定可靠,可应用于水产食品中微量及痕量砷及砷形态的检测。
The trace arsenic in aquatic foods was measured by microwave digestion coupled with the hydride generation-atomic fluorescence spectrometry (HG-AFS). The instrumental parameters and analytical conditions, including lamp (As-HCI) current, carrier gas flow, atomization stove temperature, acid medium, KBH4 concentrations and reducing agents, were investigated and optimized. Under optimum conditions linear response ranged from 0 to 80μg/Lwith R2≥ 0.999. The average recovery tested with adding standards was 96.3%, and the detection limit estimated with 3-fold standard deviation was 0.021μg/kg. The established method, with the advantages of simple operation, high sensitivity, and high efficiency, was successfully used for the determination of As in some aquatic foods.
出处
《食品科学》
EI
CAS
CSCD
北大核心
2006年第10期484-487,共4页
Food Science
基金
厦门市科技项目(3502Z20055025)
校博士科研启动基金课题(C60501)
集美大学中青年创新团队专项基金(2006A003)
关键词
氢化物发生原子荧光光谱法
砷
水产食品
微波消解
hydride generation-atomic fluorescence spectrometry (HG-AFS)
arsenic
aquatic foods
microwave digestion