Search NASASearch

DOE OSTI · 3684009

High Pressure X-ray Diffraction and Equation of State of Hydrazine

Ripani, Roma [University of Illinois, Chicago, IL (United States)] (ORCID:0000000289366011)·Lamichhane, Anmol [University of Illinois, Chicago, IL (United States)]·Safari, Fatemeh [University of Illinois, Chicago, IL (United States)] (ORCID:000000024584339X)·Gramsch, Stephen A. [University of Illinois, Chicago, IL (United States)]·Ahart, Muhtar [University of Illinois, Chicago, IL (United States)]·Manayil Marathamkottil, Abdul Haseeb [University of Illinois, Chicago, IL (United States)]·Farraj, Husam [University of Illinois, Chicago, IL (United States)] (ORCID:0000000166697937)·Giordano, Nico [Deutsches Elektronen-Synchrotron (DESY), Hamburg (Germany)] (ORCID:0000000195181251)·Glazyrin, Konstantin [Deutsches Elektronen-Synchrotron (DESY), Hamburg (Germany)]·Smith, Jesse [Argonne National Laboratory (ANL), Argonne, IL (United States). High Pressure Collaborative Access Team (HPCAT)]·Parra, Samuel Gallego [European Synchrotron Research Facility (ESRF), Grenoble (France)] (ORCID:0000000165164303)·Mondal, Anshuman [European Synchrotron Research Facility (ESRF), Grenoble (France); National Institute of Technology, Agartala (India)]·Garbarino, Gaston [European Synchrotron Research Facility (ESRF), Grenoble (France)]·Dattelbaum, Dana M. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)]·Chaudhuri, Santanu [University of Illinois, Chicago, IL (United States)] (ORCID:0000000243282947)·Miyagi, Lowell M. [University of Utah, Salt Lake City, UT (United States)]·Hemley, Russell J. [University of Illinois, Chicago, IL (United States)] (ORCID:0000000173988521)

Abstract

Synchrotron X-ray diffraction has been used to investigate the structure and equation of state (EOS) of hydrazine (N 2 H 4 ) up to 54.3 GPa at 298 K. The diffraction patterns could be fit to a monoclinic unit-cell structure and put strong constraints on previously reported phase transitions documented by vibrational spectroscopy over this pressure range. Pressure–volume ( P–V ) data were fit using a Vinet EOS, yielding parameters: V 0 = 45.2 Å 3 /molecule (fixed), K 0 = 11.8(7) GPa, and K 0 ′ = 6.5(2). Previously measured high-pressure vibrational frequency shifts were used to estimate the vibrational free energy and model P–V–T isotherms from 0 to 1200 K. The results of the P–V–T isotherms are compared to existing shock Hugoniot data on hydrazine and 298 K isotherms for assemblages of possible decomposition products. This comparison suggests dissociation at high density under shock loading. Good correspondence was found between the static lattice EOS as calculated by the model and the previously reported EOS as calculated by density functional theory. Finally, these results resolve existing uncertainties about the EOS and crystal symmetry of hydrazine at high pressure and provide valuable baseline information on this important energetic material.

Explore related subjects

Keep this discovery

BibTeXRIS

Ripani, Roma [University of Illinois, Chicago, IL (United States)] (ORCID:0000000289366011), Lamichhane, Anmol [University of Illinois, Chicago, IL (United States)], Safari, Fatemeh [University of Illinois, Chicago, IL (United States)] (ORCID:000000024584339X), Gramsch, Stephen A. [University of Illinois, Chicago, IL (United States)], Ahart, Muhtar [University of Illinois, Chicago, IL (United States)], Manayil Marathamkottil, Abdul Haseeb [University of Illinois, Chicago, IL (United States)], Farraj, Husam [University of Illinois, Chicago, IL (United States)] (ORCID:0000000166697937), Giordano, Nico [Deutsches Elektronen-Synchrotron (DESY), Hamburg (Germany)] (ORCID:0000000195181251), Glazyrin, Konstantin [Deutsches Elektronen-Synchrotron (DESY), Hamburg (Germany)], Smith, Jesse [Argonne National Laboratory (ANL), Argonne, IL (United States). High Pressure Collaborative Access Team (HPCAT)], Parra, Samuel Gallego [European Synchrotron Research Facility (ESRF), Grenoble (France)] (ORCID:0000000165164303), Mondal, Anshuman [European Synchrotron Research Facility (ESRF), Grenoble (France); National Institute of Technology, Agartala (India)], Garbarino, Gaston [European Synchrotron Research Facility (ESRF), Grenoble (France)], Dattelbaum, Dana M. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)], Chaudhuri, Santanu [University of Illinois, Chicago, IL (United States)] (ORCID:0000000243282947), Miyagi, Lowell M. [University of Utah, Salt Lake City, UT (United States)], Hemley, Russell J. [University of Illinois, Chicago, IL (United States)] (ORCID:0000000173988521). 2026-03-13. High Pressure X-ray Diffraction and Equation of State of Hydrazine. https://doi.org/10.1021/acs.jpcc.5c06806

Cite the original work for its findings. Save a collection to share your selection of sources.

Discover connections

Connections use source metadata and explicit phrase matches, not verified experimental comparisons.

KEEP EXPLORING

Related discoveries

Anomalous lattice expansion of bcc Ta in helium-loaded diamond anvil cells

Anomalous lattice expansion of bcc Ta is observed in helium-loaded diamond anvil cell (DAC) experiments near 6 GPa and above 400 K, while co-loaded W, Mo, and Au exhibit normal thermal expansion. The Ta volume expansion increases with temperature, reaching ~14% near 650 K before plateauing, and is largely retained after recovery to ambient conditions. Time-resolved measurements at 500 K reveal progressive expansion over several hours, consistent with gradual, thermally activated He incorporation. The largely retained expansion during subsequent cooling and holding at 400 K indicates that the incorporated He is predominantly kinetically trapped. The data reveal two distinct regimes: below ~550 K, modest and spatially uniform expansion consistent with interstitial He trapping at isolated, randomly distributed vacancies; above ~550 K, He-vacancy cluster growth producing dramatically larger expansion, peak broadening, and a core–shell microstructure revealed by micron-resolution X-ray diffraction mapping. These results demonstrate that He is not always a passive pressure medium in DAC experiments and reveal a previously unrecognized regime of He-mediated lattice modification in Ta, complementing conventional ion-implantation studies relevant to nuclear and fusion structural materials.

Diamond anvil cell

Probing the atomic dynamics of ultrafast melting with femtosecond electron diffraction

Melting is an every-day phase transition that is determined by thermodynamic parameters like temperature and pressure. In contrast, ultra-fast melting is governed by the microscopic response to a rapid energy input and, thus, can reveal the strength and dynamics of atomic bonds as well as the energy flow rate to the lattice. Accurately describing these processes remains challenging and requires detailed insights into transient states encountered. Here, we present data from femtosecond electron diffraction measurements that capture the structural evolution of copper during the ultrafast solid-to-liquid phase transformations. At absorbed energy densities 2-4 times the melting threshold, melting begins at the surface slightly below the nominal melting point followed by rapid homogeneous melting throughout the volume. Molecular dynamics simulations reproduce these observations and reveal a weak electron-lattice energy transfer rate for the given experimental conditions. Both simulations and experiments show no indications of rapid lattice collapse when its temperature surpasses proposed limits of superheating, providing evidence that the inherent dynamics limits the speed of disordering in ultrafast melting of metals.

FOS: Physical sciences

Thermal Cycling and Isothermal Deformation Response of Polycrystalline NiTi: Simulations vs. Experiment

A recent microstructure-based FEM model that couples crystal-based plasticity, the B2<-> MB190 phase transformation and anisotropic elasticity at the grain scale is calibrated to recent data for polycrystalline NiTi (49.9 at.% Ni). Inputs include anisotropic elastic properties, texture and differential scanning calorimetry data, as well as a subset of recent isothermal deformation and load-biased thermal cycling data. The model is assessed against additional experimental data. Several experimental trends are captured - in particular, the transformation strain during thermal cycling monotonically increases and reaches a peak with increasing bias stress. This is achieved, in part, by modifying the martensite hardening matrix proposed by Patoor et al. [Patoor E, Eberhardt A, Berveiller M. J Phys IV 1996;6:277]. Some experimental trends are underestimated - in particular, the ratcheting of macrostrain during thermal cycling. This may reflect a model limitation that transformation-plasticity coupling is captured on a coarse (grain) scale but not on a fine (martensitic plate) scale.

Phase Transformations