化学分析计量
化學分析計量
화학분석계량
CHEMICAL ANALYSIS AND METERAGE
2013年
4期
44-48
,共5页
薛慧%董宾%宫博%姚梦楠
薛慧%董賓%宮博%姚夢楠
설혜%동빈%궁박%요몽남
氢化物发生-原子荧光法%食品%食品添加剂%砷%汞%铅
氫化物髮生-原子熒光法%食品%食品添加劑%砷%汞%鉛
경화물발생-원자형광법%식품%식품첨가제%신%홍%연
hydrogenation-atomic fluorescent spectrometry%food%food additive%arsenic%mercury%lead
建立氢化物发生-原子荧光光度法测定食品和食品添加剂中砷、汞和铅元素的方法。对茶叶、方便面、精料与二氧化硅样品的前处理方法进行了研究,讨论了酸介质与酸度、还原剂浓度、铁氰化钾与草酸浓度等因素对样品测定的影响。当还原剂质量浓度为20g/L、载流酸度为5%、铁氰化钾和草酸质量浓度分别为4g/L和2g/L时,砷、汞和铅的方法检出限分别为0.024,0.008,0.066μg/L,方法的回收率为85%~105%,测量结果的相对标准偏差分别为0.7%,0.7%,1.8%。该方法简便、快速、结果准确可靠,能满足食品和食品添加剂中砷、汞、铅的测定。
建立氫化物髮生-原子熒光光度法測定食品和食品添加劑中砷、汞和鉛元素的方法。對茶葉、方便麵、精料與二氧化硅樣品的前處理方法進行瞭研究,討論瞭痠介質與痠度、還原劑濃度、鐵氰化鉀與草痠濃度等因素對樣品測定的影響。噹還原劑質量濃度為20g/L、載流痠度為5%、鐵氰化鉀和草痠質量濃度分彆為4g/L和2g/L時,砷、汞和鉛的方法檢齣限分彆為0.024,0.008,0.066μg/L,方法的迴收率為85%~105%,測量結果的相對標準偏差分彆為0.7%,0.7%,1.8%。該方法簡便、快速、結果準確可靠,能滿足食品和食品添加劑中砷、汞、鉛的測定。
건립경화물발생-원자형광광도법측정식품화식품첨가제중신、홍화연원소적방법。대다협、방편면、정료여이양화규양품적전처리방법진행료연구,토론료산개질여산도、환원제농도、철청화갑여초산농도등인소대양품측정적영향。당환원제질량농도위20g/L、재류산도위5%、철청화갑화초산질량농도분별위4g/L화2g/L시,신、홍화연적방법검출한분별위0.024,0.008,0.066μg/L,방법적회수솔위85%~105%,측량결과적상대표준편차분별위0.7%,0.7%,1.8%。해방법간편、쾌속、결과준학가고,능만족식품화식품첨가제중신、홍、연적측정。
The method for determination of arsenic,mercury and lead in food and food additive by using hydrogenation atomic fluorescent spectrometry was established. Tea,instant noodle,concentrate and silicon dioxide were chosen as objects to explore the measurement influence factors such as pretreatment method,acid medium,acidity, reducer concentration,concentration of patassium ferricyanide and oxalic acid. The detection limit of arsenic,mercury and lead were 0.024,0.008,0.066μg/L respectively as the reducer concentration was 20 g/L,carrier acidity was 5%,and concentration of patassium ferricyanidesh and oxalic acid were 4, 2 g/L respectively. The recovery was 85%-105%,and the relative standard deviations of arsenic,mercury and lead were 0.7%,0.7%,1.8%,respectively. The proposed method is convenient,rapid,accurate and reliable,which can meet the measurement requirement of arsenic,mercury and lead in food and food additive.