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dc.contributor.authorZhi, Cao
dc.contributor.authorTaihong, Yan
dc.contributor.authorXiaoyan, Bian
dc.contributor.authorChuanbo, Li
dc.contributor.authorChen, Zuo
dc.contributor.authorWeifang, Zheng
dc.date.accessioned2019-06-08T09:29:04Z
dc.date.available2019-06-08T09:29:04Z
dc.date.copyright3/15/2019 12:00:00 AM
dc.date.issued2019
dc.identifier.issn2332-8983
dc.identifier.otherners_005_02_020914.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4257665
dc.description.abstractThe thermal stability of N, N-dimethylhydroxylamine (DMHAN) in the HNO3 solution was studied using microcalorimeter. The influence of concentration of HNO3, DMHAN, methylhydrazine (MH), atmosphere (air and nitrogen), and metals was investigated. The kinetic parameters and self-accelerating decomposition temperature (SADT) of the feed in process (stripping reagents 1BX, scouring agent 2DS, stripping reagents 2BX, and waste aqueous phase 2DW) were calculated by Advanced Kinetics and Technology Solutions (akts) thermokinetics software. The molar enthalpy of the reaction of NaNO2 with DMHAN and MH was also determined. The results show that the initial reaction temperature (T0) of DMHAN/HNO3 (HNO3: 1.5–3.0 mol/L, DMHAN: 0.05–0.8 mol/L) is increased as the acidity is reduced or the concentration of DMHAN is increased. Holding reductant MH made the induction period of the autocatalytic reaction longer. The air, nitrogen atmosphere, Fe, and the fission products (Zr, Ru) do not affect the decomposition of DMHAN, but the stainless steel made the T0 of DMHAN/HNO3 become lower. The SADT of 1BX/2DS, 2BX, and 2DW is 56 °C, 52 °C and 47 °C, respectively. The molar enthalpies of formation of the reaction of NaNO2 with DMHAN and MH are −411.3 kJ/mol, −246.0 kJ/mol, respectively.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleMicro-Calorimetric Study on the Thermal Stability of N, N-Dimethylhydroxylamine in the APOR Process
dc.typeJournal Paper
dc.journal.volume5
dc.journal.issue2
dc.journal.titleJournal of Nuclear Engineering and Radiation Science
dc.identifier.doi10.1115/1.4042499
dc.journal.fristpage20914
dc.journal.lastpage020914-7
dc.treeJournal of Nuclear Engineering and Radiation Science:;2019:;volume( 005 ):;issue: 002
dc.contenttypeFulltext


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