光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
SPECTROSCOPY AND SPECTRAL ANALYSIS
2009年
12期
3416-3419
,共4页
叶艳青%吴娜%杨丽娟%念晓%张代云%高云涛
葉豔青%吳娜%楊麗娟%唸曉%張代雲%高雲濤
협염청%오나%양려연%념효%장대운%고운도
灯台叶%金属元素%火焰原子吸收光谱法%形态分析
燈檯葉%金屬元素%火燄原子吸收光譜法%形態分析
등태협%금속원소%화염원자흡수광보법%형태분석
Alstonia scholaris%Metal element%Flame atomic absorption spectrometry%Speciation analysis
照传统煎煮法对中药灯台叶中铜、锌、铁、镁、钙、铬、锰和镉8种元素进行提取;用微孔滤膜分离提取液中的可溶态与悬浮态,利用大孔吸附树脂柱对可溶态中的有机态与无机态进行分离;采用火焰原子吸收光谱法对各种形态中的8种元素进行测定.结果显示,灯台叶中8种元素的总提取率为9.84%~89.07%,浸留比为10.96%~903.4%,悬浮态颗粒吸附率为3.44%~23.37%.该法对各元素的加标回收率为94.5%~111.6%;相对标准偏差在0.29%~2.47%之间,测定结果的精密度和准确度令人满意.
照傳統煎煮法對中藥燈檯葉中銅、鋅、鐵、鎂、鈣、鉻、錳和鎘8種元素進行提取;用微孔濾膜分離提取液中的可溶態與懸浮態,利用大孔吸附樹脂柱對可溶態中的有機態與無機態進行分離;採用火燄原子吸收光譜法對各種形態中的8種元素進行測定.結果顯示,燈檯葉中8種元素的總提取率為9.84%~89.07%,浸留比為10.96%~903.4%,懸浮態顆粒吸附率為3.44%~23.37%.該法對各元素的加標迴收率為94.5%~111.6%;相對標準偏差在0.29%~2.47%之間,測定結果的精密度和準確度令人滿意.
조전통전자법대중약등태협중동、자、철、미、개、락、맹화력8충원소진행제취;용미공려막분리제취액중적가용태여현부태,이용대공흡부수지주대가용태중적유궤태여무궤태진행분리;채용화염원자흡수광보법대각충형태중적8충원소진행측정.결과현시,등태협중8충원소적총제취솔위9.84%~89.07%,침류비위10.96%~903.4%,현부태과립흡부솔위3.44%~23.37%.해법대각원소적가표회수솔위94.5%~111.6%;상대표준편차재0.29%~2.47%지간,측정결과적정밀도화준학도령인만의.
The eight elements, Cu, Zn, Fe, Mg, Ca, Cr, Mn and Cd, in the leaves of Alstonia scholaris were extracted based on traditional analytical flowchart program and separated into water-soluble state and suspension state by micro porous filtering film. The water-soluble state was divided into organic state and inorganic state based on macro porous adsorption resin. The ele-ments were detected by flame atomic adsorption spectrometry (FAAS). The results show that the extractive rates of the ele-ments were in the range of 9. 84%-89.07%, and the immersion-residue ratio in the range of 10. 96%-903.4%. Adsorption ration of suspension state was in the range of 3.44%-23.37 %. The recovery ratios by standard addition were in the range of 94. 5%-111.6%, and the relative standard deviations (RSD) were in the range of 0. 29%-2. 47%. The precision and accuracy of deter-mining results are satisfactory.