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| 气相色谱法测试土壤中分段石油烃的标准化定量方法初探 | |
| 引用本文： | 刘玉龙,黄燕高,刘菲.气相色谱法测试土壤中分段石油烃的标准化定量方法初探[J].岩矿测试,2019,38(1):102-111. |
| 作者姓名： | 刘玉龙 黄燕高 刘菲 |
| 作者单位： | 石油石化污染物控制与处理国家重点实验室, 北京 102206;中国石油集团安全环保技术研究院有限公司, 北京 102206;中国地质大学(北京)北京市水资源与环境工程重点实验室, 北京 100083,湖北省地质局第八地质大队, 湖北 襄阳 441000,中国地质大学(北京)北京市水资源与环境工程重点实验室, 北京 100083 |
| 基金项目： | 中国地质调查局地质调查项目（DD20160312） |
| 摘 要： | 目前土壤样品中分段石油烃的分析方法中石油烃包括的碳原子数范围和采用的校准物质不统一,造成不同实验室的量值不具有可比性。为保证不同实验室之间结果的可比性,本文尝试建立一种石油烃相邻碳原子数标准化定量方法。该方法主要包括:(1)规定了石油烃包括的碳原子数范围为气相色谱峰中正己烷和正四十碳烷之间所有的烃(含正己烷);(2)总石油烃(TPH)分为挥发性石油烃(VPH)和半挥发性石油烃(SPH),分别选取碳原子数为6～10的5个正构烷烃作为VPH校准物质,选取碳原子数为10～40的31个正构烷烃作为SPH校准物质。采用平均响应因子法或一次线性回归法,建立校准物质的峰面积-浓度的校准关系;(3)采用相邻峰标准化校准方法,逐一定量所有的目标色谱峰;(4)计算正构烷烃含量、总石油烃含量和任意分段的石油烃含量。该方法为环境样品中石油烃分析方法的标准化建设提供了数据基础。 |
| 关 键 词： | 石油烃 分段 气相色谱法 标准化方法 |
| 收稿时间： | 2017/9/4 0:00:00 |
| 修稿时间： | 2018/7/22 0:00:00 |
Analysis of Total Petroleum Hydrocarbon Fractions in Soils by Gas Chromatography: Standardized Calibration and Quantitation Method |
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| LIU Yu-long,HUANG Yan-gao and LIU Fei.Analysis of Total Petroleum Hydrocarbon Fractions in Soils by Gas Chromatography: Standardized Calibration and Quantitation Method[J].Rock and Mineral Analysis,2019,38(1):102-111. | |
| Authors: | LIU Yu-long HUANG Yan-gao and LIU Fei |
| Institution: | State Key Laboratory of Petroleum Pollution Control, Beijing 102206, China;Research Institute of Safety and Environment Technology, China National Petroleum Corporation, Beijing 102206, China;Beijing Key Laboratory of Water Resources and Environmental Engineering, China University of Geosciences(Beijing), Beijing 100083, China,The Eighth Geological Brigade of Hubei Geological Bureau, Xiangyang 441000, China and Beijing Key Laboratory of Water Resources and Environmental Engineering, China University of Geosciences(Beijing), Beijing 100083, China |
| Abstract: | BACKGROUND: Inter-laboratory measurement results of total petroleum hydrocarbons (TPH) in soils determined by current Gas Chromatography-Flame Ionization Detector, are not comparable due to specified TPH ranges of alkanes and/or different calibration standards between laboratories. OBJECTIVES: To establish a standardized calibration and quantitation method of TPH and to develop the adjacent-peak calibration and quantitation method (APCQM). METHODS: The APCQM mainly includes:(1) defining TPH range as all compounds eluting between n-hexane and n-tetracontane; (2) division of TPHs into volatile petroleum hydrocarbons (VPH) and semivolatile petroleum hydrocarbons (SPH). Specify and calibrate procedure of TPH. Reference materials (RM) for VPH are 5 n-alkanes, from n-hexane to n-decane, whereas SPH RMs are 31 n-alkanes, from n-decane to n-tetracontane. Calibration equations of peak area and concentration of n-alkanes can be constructed by average response factor or linear regression methods; (3) quantitative concentrations of all target chromatographic peaks acquired by adjacent standard peak calibration; (4) calculation of the contents of n-alkanes, TPH and optional TPH fractions. RESULTS: Using the normal calibration and quantitation method, TPH recoveries of laboratory fortified blanks and laboratory fortified sample matrices could be underestimated or overestimated by 10%. By using the APCQM the paradox in quality control processes was resolved, and thus reliable measurement results of TPH were obtained in laboratories. CONCLUSIONS: The APCQM is applicable to standardization analysis of TPH fractions in environmental samples. |
| Keywords: | total petroleum hydrocarbon fraction Gas Chromatography standardization |
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