Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry

碩士 === 靜宜大學 === 應用化學研究所 === 91 === In this research,graphite furnace and flow-injection atomic absorption spectrometry for the determination of selenium in pig liver and pig kidney from market were established. The bovine liver SRM 1577b were determinated to identify the accuracy. T-test were used t...

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Main Authors: Yat-Sen Sun, 蘇庭瑤
Other Authors: none
Format: Others
Language:zh-TW
Published: 2003
Online Access:http://ndltd.ncl.edu.tw/handle/34717747767544406678
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spelling ndltd-TW-091PU0055000362016-06-08T04:13:19Z http://ndltd.ncl.edu.tw/handle/34717747767544406678 Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry 石墨爐及氫化物原子吸收光譜法測定豬肝及豬腎中硒含量 Yat-Sen Sun 蘇庭瑤 碩士 靜宜大學 應用化學研究所 91 In this research,graphite furnace and flow-injection atomic absorption spectrometry for the determination of selenium in pig liver and pig kidney from market were established. The bovine liver SRM 1577b were determinated to identify the accuracy. T-test were used to confirm the system errors between GFAAS and FIAS-HGAAS methods. When GFAAS was used to determine selenium in samples. Selenium has low pyrolysis temperature (<500℃) and biological samples content a lot of proteins matrix. When proteins heating,the carbide was residued in graphite tube and cause high background absorption. After used ascorbic acid and Pd(NO3)2 mixture modifiers not only increased pyrolysis temperature to 1000℃ but also improved the selenium absorption and reduced background absorption. The established method to determine bovine liver SRM 1577b can also have good accuracy. When selenium in samples was determinated by FIAS-HGAAS. HNO3 was used as digestion solution. Simultaneous content Se (VI) and Se (IV) and had different hydride effect. Thus,the pre-reduced Se(VI) to Se(IV) process was applied to the determination with good accuracy results. In this research,the analytical results were closed and good enough to certified value. The recovery were in 92~105%. The D.L. was 27.6pg in GFAAS and 0.144ppb in FIAS-HGAAS. The linear range was 0.1~2ng with GFAAS and 3~20ppb with FIAS-HGAAS. The content of Se in pig liver was 2.42 ±0.15 (g / g) and 2.21 ±0.16(μg / g),respectively. The content of Se in pig kidney was 8.03 ± 0.55 (μg / g) and 8.41 ± 0.44(μg / g),respectively. There were without certified values. Thus t-test was used to compared with two methods,and the results of t values < 4.6(N=5)were obtained. In this research,there were no system errors between two methods,and good accuracy and precision were obtained. none 蔡素珍 2003 學位論文 ; thesis 89 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 靜宜大學 === 應用化學研究所 === 91 === In this research,graphite furnace and flow-injection atomic absorption spectrometry for the determination of selenium in pig liver and pig kidney from market were established. The bovine liver SRM 1577b were determinated to identify the accuracy. T-test were used to confirm the system errors between GFAAS and FIAS-HGAAS methods. When GFAAS was used to determine selenium in samples. Selenium has low pyrolysis temperature (<500℃) and biological samples content a lot of proteins matrix. When proteins heating,the carbide was residued in graphite tube and cause high background absorption. After used ascorbic acid and Pd(NO3)2 mixture modifiers not only increased pyrolysis temperature to 1000℃ but also improved the selenium absorption and reduced background absorption. The established method to determine bovine liver SRM 1577b can also have good accuracy. When selenium in samples was determinated by FIAS-HGAAS. HNO3 was used as digestion solution. Simultaneous content Se (VI) and Se (IV) and had different hydride effect. Thus,the pre-reduced Se(VI) to Se(IV) process was applied to the determination with good accuracy results. In this research,the analytical results were closed and good enough to certified value. The recovery were in 92~105%. The D.L. was 27.6pg in GFAAS and 0.144ppb in FIAS-HGAAS. The linear range was 0.1~2ng with GFAAS and 3~20ppb with FIAS-HGAAS. The content of Se in pig liver was 2.42 ±0.15 (g / g) and 2.21 ±0.16(μg / g),respectively. The content of Se in pig kidney was 8.03 ± 0.55 (μg / g) and 8.41 ± 0.44(μg / g),respectively. There were without certified values. Thus t-test was used to compared with two methods,and the results of t values < 4.6(N=5)were obtained. In this research,there were no system errors between two methods,and good accuracy and precision were obtained.
author2 none
author_facet none
Yat-Sen Sun
蘇庭瑤
author Yat-Sen Sun
蘇庭瑤
spellingShingle Yat-Sen Sun
蘇庭瑤
Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry
author_sort Yat-Sen Sun
title Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry
title_short Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry
title_full Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry
title_fullStr Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry
title_full_unstemmed Determination of Selenium in Pig Liver and Pig Kidney by Electrothermal and Flow Injection Hydride Generation Atomic Absorption Spectrometry
title_sort determination of selenium in pig liver and pig kidney by electrothermal and flow injection hydride generation atomic absorption spectrometry
publishDate 2003
url http://ndltd.ncl.edu.tw/handle/34717747767544406678
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