1983
DOI: 10.2343/geochemj.17.165
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Nitrogen in stone meteorites and terrestrial standards.

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Cited by 7 publications
(3 citation statements)
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“…However, the large range for BCR‐1/2 from 15 to 62 μg g −1 possibly results from the heterogeneous distribution of N in BCR‐1/2 (Murty et al . ), or the inevitable disadvantage inherent in the NAA technique including contamination by atmospheric N 2 (Norris and Schaeffer ) or interfering reactions during neutron irradiation (Shukla et al . ).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…However, the large range for BCR‐1/2 from 15 to 62 μg g −1 possibly results from the heterogeneous distribution of N in BCR‐1/2 (Murty et al . ), or the inevitable disadvantage inherent in the NAA technique including contamination by atmospheric N 2 (Norris and Schaeffer ) or interfering reactions during neutron irradiation (Shukla et al . ).…”
Section: Resultsmentioning
confidence: 99%
“…The nitrogen mass fractions of BCR-2 and BHVO-2 have been determined by neutron activation analysis (NAA) as 34 ± 12 lg g -1 and 22.6 ± 3 lg g -1 , respectively. However, the large range for BCR-1/2 from 15 to 62 lg g -1 possibly results from the heterogeneous distribution of N in BCR-1/2 (Murty et al 1983), or the inevitable disadvantage inherent in the NAA technique including contamination by atmospheric N 2 (Norris and Schaeffer 1982) or interfering reactions during neutron irradiation (Shukla et al 1978).…”
Section: Nitrogen Mass Fractions and Isotopic Compositions Of Bcr-2 Amentioning
confidence: 99%
“…The analytical techniques traditionally employed to determine these elements in geological materials are combustion methods, gravimetric methods and the Kjeldahl method. More recently, analytical techniques such as neutron activation analysis (Shukla et al 1978, Murty et al 1983, infrared absorption spectrometry (Terashima 1979(Terashima , 1988 and automatic elemental analyser (Din and Jones 1978, McGeehan and Naylor 1988, David et al 1989, Artiola 1990, Terashima 1993, Matejovic 1997, Kowalenko 2001) have been used. Coulometric titration (Atkin and Somerfield 1994), flame photometry (Marcó et al 2001), inductively coupled plasma-atomic emission spectrometry (ICP-AES, Okai et al 2001), high-resolution inductively coupled plasma-mass spectrometry (HP-ICP-MS, Makishima and Nakamura 2001), and elemental analyser-continuous flow isotope ratio mass spectrometry (EA-CFIRMS, Studley et al 2002) were reported as methods covering only S determination.…”
mentioning
confidence: 99%