• Core Journal of China
  • DOAJ
  • Scopus
  • Chinese Scientific and Technical Papers and Citations (CSTPC)
  • Chinese Science Citation Database (CSCD)
Wen XU, Jian-wei ZHOU, Cun-fu LIU, Yi-qun GAN, Yun-de LIU, Yan-peng ZHANG. Online Measurement Technique on 15N and 18O Isotopes of Nitrate in Groundwater[J]. Rock and Mineral Analysis, 2013, 32(2): 305-312.
Citation: Wen XU, Jian-wei ZHOU, Cun-fu LIU, Yi-qun GAN, Yun-de LIU, Yan-peng ZHANG. Online Measurement Technique on 15N and 18O Isotopes of Nitrate in Groundwater[J]. Rock and Mineral Analysis, 2013, 32(2): 305-312.

Online Measurement Technique on 15N and 18O Isotopes of Nitrate in Groundwater

More Information
  • Received Date: July 25, 2012
  • Accepted Date: August 20, 2012
  • Published Date: March 31, 2013
  • The studying of 15N and 18O in soil and water can be used to identify the origin, transportation and transformation of the nitrate, which provides reliable evidence for the remediation of the polluted environment. At present, high-temperature pyrolysis is the most widely used method for assessing 15N and 18O. However, NO from the ion source may interfere with the measurement of δ18O, which is efficiently reduced by the He dilution method. In this article, the selection of four international standards (IAEA-No-3, USGS32, USGS34 and USGS35) and one laboratory standard (CUGL-No-1) are documented to verify the practicability of high-temperature pyrolysis. Over the course of eight months, 238 tests were conducted for 100 groundwater samples by using coupled elemental analyser and MAT 253 stable isotope ratio mass spectrometer (EA-IRMS). Three new conclusions were obtained through the study. Firstly, the low cost target sample of KNO3 was convenient for the comparison to the international standards. Secondly, it was concluded that online high-temperature pyrolysis was the best method to study 15N and 18O in nitrate of standards and samples. In this research, the sample amount of KNO3 was only 500 μg. Moreover, the values of δ15N and δ18O were determined simultaneously in one sample input, which took just 720 s and had the added advantages of being rapid and having high efficiency. The accuracies of δ15N and δ18O were 0.25‰ and 0.6‰, respectively, which were close to the corresponding international level. Thirdly, the He dilution method reduced the interference to δ18O without any improvement of the EA-IRMS system.
  • Kendall C, Grim E. Combustion tube method for measurement of nitroge isotope ratios using calcium oxide for total removal of carbon dioxide and water [J]. Analytical Chemistry, 1990,62: 526-529. doi: 10.1021/ac00204a019
    Kendall C, Silva S R, Chang C C Y, Burns D A, Campbell D H, Shanley J B. Use of δ18O and δ15N of Nitrate to Determine Sources of Nitrate in Early Spring Runoff in Forested Catchments[C]//Internation Symposium on Isotope in Water Resources Management. Vienna: International Atomic Energy Agency,1995.
    Silva S R, Kendall C, Wilkison D H, Ziegler A C, Chang C C Y, Avanzino R J. A new method for collection of nitrate from fresh water and the analysis of nitrogen and oxygen isotope ratios [J]. Journal of Hydrology, 2000, 228: 22-36. doi: 10.1016/S0022-1694(99)00205-X
    Wassenaar L I. Evaluation of the origin and fate of nitrate in the Abbotsford aquifer using the isotopes of 18O and 15N in NO3-[J]. Applied Geochemistry, 1995, 10: 391-405. doi: 10.1016/0883-2927(95)00013-A
    Revesz K, Böhlke J K, Yoshinari T. Determination of δ18O and δ15N in nitrate [J]. Analytical Chemistry, 1997, 69: 4375-4380. doi: 10.1021/ac9610523
    蔡鹤生, 刘存富, 周爱国, 杨琰.硝酸盐中15N和18O测试新技术 [J].矿物岩石地球化学通报, 2001,20(4): 421-424.
    Werner R A, Kornexl B E, Roβmann A, Schmidt H L. On-line determination of δ18O values of organic substan-ces [J]. Analytical Chimica Acta, 1996, 319: 159-164. doi: 10.1016/0003-2670(95)00468-8
    Koziet J. Isotope ratio mass spectrometric method for the on-line determination of oxygen-18 in organic matter [J]. Mass Spectrometry, 1997, 32: 103. doi: 10.1002/(ISSN)1096-9888
    Farquhar G D, Henry B K, Styles J M. A rapid on-line technique for determination of oxygen isotope composition of nitrogen-containing organic matter and water [J]. Rapid Communications in Mass Spectrometry, 1997, 11: 1554. doi: 10.1002/(ISSN)1097-0231
    Brand W A, Tegtmeyer A R, Hilkert A. Compound-specific isotope analysis: Extending toward 15N/14N and 18O/16O [J]. Organic Geochemistry, 1994, 21: 585-594. doi: 10.1016/0146-6380(94)90004-3
    Begley I S, Scrimgeour C M. High-precision δ2H and δ18O measurement for water and volatile organic compounds by continuous-flow pyrolysis isotope ratio mass spectrometry [J]. Analytical Chemistry, 1997, 69: 1530. doi: 10.1021/ac960935r
    Kornexl B E, Gehre M, Höfling R, Werner R A. On-line δ18O measurement of organic and inorganic substances [J]. Rapid Communications in Mass Spectrometry, 1999, 13: 1685-1693. doi: 10.1002/(ISSN)1097-0231
    Böhlke J K, Mroczkowski S J, Coplen T B. Oxygen isotopes in nitrate: New reference materials for 18O : 17O : 16O measurements and observations on nitrate-water equilibration [J]. Rapid Communications in Mass Spectrometry, 2003, 17: 1835-1846. doi: 10.1002/rcm.v17:16
    Gehre M, Strauch G. High-temperature element analysis and pyrolysis techniques for stable isotope analysis [J]. Rapid Communications in Mass Spectrometry, 2003, 17: 1497-1503. doi: 10.1002/(ISSN)1097-0231
    Werner R A. The online 18O/16O analysis: Development and application [J]. Isotopes in Environmental and Health Studies, 2003, 39: 85-104. doi: 10.1080/1025601031000108642
    Accoe F, Berglund M, Geypens β, Taylor P. Method to reduce interference effect in thermal conversion elemental analyzer/continuous flow isotope ratio mass spectrometry δ18O measurements of nitrogen-containing compounds [J]. Rapid Communications in Mass Spectrometry, 2008, 22: 2280-2286. doi: 10.1002/rcm.3609
    Brand W A, Coplen T B, Aerts-Bijma A T, Böhlke J K, Gehre M, Geilmann H, Gröning M, Jansen H G, Meijer H A J, Mroczkowski S J, Qi H P, Soergel K, Stuart-Williams H S, Weisl S M, Werner R A. Comprehensive inter-laboratory calibration of reference materials for δ18O versus VSMOW using various on-line high-temperature conversion techniques [J]. Rapid Communications in Mass Spectrometry, 2009, 23: 999-1019. doi: 10.1002/rcm.v23:7
    Hunsinger G B, Hagopian W M, Jahren A H. Offline oxygen isotope analysis of organic compounds with high N : O [J]. Rapid Communications in Mass Spectrometry, 2010, 24: 3182-3186. doi: 10.1002/rcm.4752
    Huber B, Bernasconi S M, Luster J, Pannatier E G. A new isolation procedure of nitrate from freshwater for nitrogen and oxygen isotope analysis [J]. Rapid Communication in Mass Spectrometry, 2011, 25: 3056-3062. doi: 10.1002/rcm.5199
    Li S L, Liu C Q, Lan Y C, Zhao Z Q, Zhou Z H. Tracing the sources of nitrate in karstic groundwater in Zunyi, Southwest China: A combined nitrogen isotope and water chemistry approach [J]. Environmental Earth Sciences, 2010, DOI10(100)/s12665-009-0277-0. doi: 10(100)/s12665-009-0277-0
    Li S L, Liu C Q, Li J, Liu X L, Chetelat B, Wang B L, Wang F S. Assessment of the source of nitrate in the Changjiang River, China: Using a nitrogen and oxygen isotopic approach [J]. Environmental Science & Technology, 2010, 44: 1573-1578.
    马传明, 刘存富, 蔡鹤生, 岳向冰, 王嫣然.微量水硝酸盐和亚硝酸盐在线测试新技术——两阶段化学转化法[M]//同位素水文学新技术学习方法.武汉: 中国地质大学出版社, 2010: 182-193.

Catalog

    Article views (1171) PDF downloads (8) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return