Hydroxylamine nitrate self-catalytic kinetics study with adiabatic calorimetry.

J Hazard Mater

Mary Kay O'Connor Process Safety Center, Artie McFerrin Department of Chemical Engineering, Texas A&M University System, College Station, TX 77843-3122, USA.

Published: March 2009

Hydroxylamine nitrate (HAN) is an important member of the hydroxylamine compound family with applications that include equipment decontamination in the nuclear industry and aqueous or solid propellants. Due to its instability and autocatalytic behavior, HAN has been involved in several incidents at the Hanford and Savannah River Site (SRS) [Technical Report on Hydroxylamine Nitrate, US Department of Energy, 1998]. Much research has been conducted on HAN in different areas, such as combustion mechanism, decomposition mechanism, and runaway behavior. However, the autocatalytic decomposition behavior of HAN at runaway stage has not been fully addressed due to its highly exothermic and rapid decomposition behavior. This work is focused on extracting HAN autocatalytic kinetics and analyzing HAN critical behavior from adiabatic calorimetry measurements. A lumped autocatalytic kinetic model for HAN and associated model parameters are determined. Also the storage and handling critical conditions of diluted HAN solution without metal presence are quantified.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jhazmat.2008.06.009DOI Listing

Publication Analysis

Top Keywords

hydroxylamine nitrate
12
adiabatic calorimetry
8
han
8
behavior han
8
decomposition behavior
8
behavior
5
hydroxylamine
4
nitrate self-catalytic
4
self-catalytic kinetics
4
kinetics study
4

Similar Publications

Crystalline γ-FeO(OH) dominantly possessing ─OH terminals (𝛾-FeO(OH)), polycrystalline γ-FeO(OH) containing multiple ─O, ─OH, and Fe terminals (𝛾-FeO(OH)), and α-FeO majorly containing ─O surface terminals are used as electrocatalysts to study the effect of surface terminals on electrocatalytic nitrate reduction reaction (eNORR) selectivity and stabilization of reaction intermediates. Brunauer-Emmett-Teller analysis and electrochemically determined surface area suggest a high active surface area of 117.79 m g (ECSA: 0.

View Article and Find Full Text PDF

The formation of a stable alkyl At-C bond occurs during the shipment of At on a 3-octanone-impregnated column and the reactivity of At stripped from columns has been studied. The At could not be recovered from the 3-octanone organic phase using nitric acid or sodium hydroxide, even up to 10 and 15.7 M, respectively.

View Article and Find Full Text PDF

Enrichment of a heterotrophic nitrifying and aerobic denitrifying bacterial consortium: Microbial community succession and nitrogen removal characteristics and mechanisms.

Bioresour Technol

December 2024

Department of Ecology, College of Life Science and Technology, Jinan University, Guangzhou 510632, Guangdong, China. Electronic address:

This study cultivated a bacterial consortium (S60) from landfill leachate that exhibited effective heterotrophic nitrification and aerobic denitrification (HN-AD) properties. Under aerobic conditions, the removal of NH-N reached 100 % when the S60 consortium utilised NH-N either as the sole nitrogen source or in combination with NO-N and NO-N. Optimal HN-AD performance was achieved with sodium acetate as a carbon source and a pH of 7.

View Article and Find Full Text PDF

A Novel System for Simultaneous Real-Time Determination of N-Enriched Ammonia, Hydroxylamine, Nitrite, and Nitrate.

Anal Chem

December 2024

Institute of Carbon Neutrality, Sino-French Institute for Earth System Science, College of Urban and Environmental Sciences, Peking University, Beijing 100091, China.

Ammonium (NH), hydroxylamine (NHOH), nitrite (NO), and nitrate (NO) account for the most important reactive nitrogen (N) species in the N cycle, playing a key role in N elimination and N retention, as well as the production of nitrogenous trace gases. However, it is still challenging to fulfill simultaneous real-time determination of all four N compounds enriched in N. This study successfully established a novel system by coupling an utomatic imultaneous ample reparation unit to a embrane nlet ass pectrometer (4n-ASSP-MIMS) for rapid online N fraction analysis of all four key compounds in the N cycle.

View Article and Find Full Text PDF

Highly Efficient Synthesis of α-Amino Acids via Electrocatalytic C-N Coupling Reaction Over an Atomically Dispersed Iron Loaded Defective TiO.

Adv Mater

December 2024

State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, P. R. China.

The synthesis of α-amino acids via the electrocatalytic C-N coupling attracted extensive attention owing to the mild reaction conditions, controllable reaction parameters, and atom economy. However, the α-amino acid yield remains unsatisfying. Herein, the efficient electrocatalytic synthesis of α-amino acids is achieved with an atomically dispersed Fe loaded defective TiO monolithic electrocatalyst (Fe-TiO/Ti).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!