Nitrogen distribution and nitrogen isotope fractionation in synthetic 2:1 phyllosilicates under hydrothermal conditions at 200 °C and saturated vapor pressure

This study investigates nitrogen distribution and isotope fractionation within synthetic 2:1 phyllosilicates, simulating submarine hydrothermal environments at 200 °C and saturated vapor pressure. XRD and EDS results revealed the potential coexistence of multiple cations in the interlayer of synthetic 2:1 phyllosilicate, concurrently suggesting cation substitution in the tetrahedral and/or octahedral sheets. Meanwhile, the iron-enriched 25-5 sample exhibited restricted interlayer expansibility. NH 4 + absorptions were identified in the NH 4 -stretching (3200–2800 cm −1 ) and NH 4 -bending (1450–1400 cm −1 ) regions, with wavenumber shifts indicating the influence of interlayer water removal. At pH 10.56, over 95% of nitrogen was released into the gas phase, while at pH 8.88, nitrogen proportions in the liquid and gas phases were comparable (average 48–49%). Experiments with iron at pH ∼8.80 showed that the nitrogen proportion in the gas phase (average 28%) was more than twofold lower than that in the liquid phase (average 68%). Equilibrium isotope fractionation factors indicated discernible preference for heavier nitrogen isotopes in the solid phase ( α solid-liquid = 1.009–1.021 and α solid-gas = 1.011–1.027). The α liquid-gas range for sample 25–2 was 1.001–1.008, while that for the iron-enriched composite 25–5 was 0.997–1.010. Our experimental studies have confirmed that, in the absence of exchange interactions with external substances possessing different nitrogen isotope ratios, nitrogen isotope fractionation between ammonium and ammonia, controlled by variations in temperature and pH during mineralization, plays a crucial role in the variation of nitrogen isotope ratios. Additionally, we confirmed that metal-amines influence nitrogen isotope fractionation by modulating ammonia gas emission. These findings enhance our understanding of nitrogen cycling across the gas, liquid, and solid phases in submarine hydrothermal systems. • The study elaborates on nitrogen dynamics in hydrothermal environments. •PH had strong effect on nitrogen release in gas phase from synthetic 2:1 phyllosilicates. •Presence of iron in starting material strongly affected nitrogen partitioning.

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Publication Details

Journal
Applied Geochemistry
Published
2025-04-29
DOI
https://doi.org/10.1016/j.apgeochem.2025.106403
Primary Topic
Clay minerals and soil interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Nitrogen distribution and nitrogen isotope fractionation in synthetic 2:1 phyllosilicates under hydrothermal conditions at 200 °C and saturated vapor pressure

Hitoshi Chiba, Toshiro Yamanaka, Isao Kadota, Bum Han Lee et al.
Applied Geochemistry
Clay minerals and soil interactions
article

Nitrogen distribution and nitrogen isotope fractionation in synthetic 2:1 phyllosilicates under hydrothermal conditions at 200 °C and saturated vapor pressure

Hitoshi Chiba, Toshiro Yamanaka, Isao Kadota, Bum Han Lee, JiMin Jo, Youko Miyoshi, Masaya Suzuki, Yoshihiro Kuwahara
article en

Abstract

This study investigates nitrogen distribution and isotope fractionation within synthetic 2:1 phyllosilicates, simulating submarine hydrothermal environments at 200 °C and saturated vapor pressure. XRD and EDS results revealed the potential coexistence of multiple cations in the interlayer of synthetic 2:1 phyllosilicate, concurrently suggesting cation substitution in the tetrahedral and/or octahedral sheets. Meanwhile, the iron-enriched 25-5 sample exhibited restricted interlayer expansibility. NH 4 + absorptions were identified in the NH 4 -stretching (3200–2800 cm −1 ) and NH 4 -bending (1450–1400 cm −1 ) regions, with wavenumber shifts indicating the influence of interlayer water removal. At pH 10.56, over 95% of nitrogen was released into the gas phase, while at pH 8.88, nitrogen proportions in the liquid and gas phases were comparable (average 48–49%). Experiments with iron at pH ∼8.80 showed that the nitrogen proportion in the gas phase (average 28%) was more than twofold lower than that in the liquid phase (average 68%). Equilibrium isotope fractionation factors indicated discernible preference for heavier nitrogen isotopes in the solid phase ( α solid-liquid = 1.009–1.021 and α solid-gas = 1.011–1.027). The α liquid-gas range for sample 25–2 was 1.001–1.008, while that for the iron-enriched composite 25–5 was 0.997–1.010. Our experimental studies have confirmed that, in the absence of exchange interactions with external substances possessing different nitrogen isotope ratios, nitrogen isotope fractionation between ammonium and ammonia, controlled by variations in temperature and pH during mineralization, plays a crucial role in the variation of nitrogen isotope ratios. Additionally, we confirmed that metal-amines influence nitrogen isotope fractionation by modulating ammonia gas emission. These findings enhance our understanding of nitrogen cycling across the gas, liquid, and solid phases in submarine hydrothermal systems. • The study elaborates on nitrogen dynamics in hydrothermal environments. •PH had strong effect on nitrogen release in gas phase from synthetic 2:1 phyllosilicates. •Presence of iron in starting material strongly affected nitrogen partitioning.

Applied GeochemistryVol. 187
Kyushu University (JP), Okayama University (JP), Geological Survey of Japan (JP), National Institute of Advanced Industrial Science and Technology (JP)
Ministry of Education, Culture, Sports, Science and Technology, Ministry of Science and ICT, South Korea, Japan Science and Technology Agency, Core Research for Evolutional Science and Technology
Clean water and sanitation
Openalex Percentile: Top 95%
Clay minerals and soil interactions
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