Relevant bibliographies by topics / Hydrazidy

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Hydrazidy'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Hydrazidy"

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Ibrahim, Hassan K., Sayed H. El-Tamany, Reda F. El-Shaarawy, and Ibrahim M. El-Deen. "Synthesis and investigation of mass spectra of some novel benzimidazole derivatives." Macedonian Journal of Chemistry and Chemical Engineering 27, no. 1 (2008): 65. http://dx.doi.org/10.20450/mjcce.2008.248.

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2-Substituted benzimidazoles (3) and (4a-c) were prepared via condensation of ethyl 2-thionyl-pyruvate (1) and hydrazidoyl derivatives (2a-c) with o-phenylene diamine in acetic acid. Acetylation of compound (4a) with acetic anhydride yielded the corresponding N-acetyl derivative (5). Treatment of compound 4b with hydrazine hydrate gave the corresponding hydrazino derivative (6). Reaction of 2-[(2-thionyl)acetyl)] benzimidazole (3) with hydrazine hydrate gave the pyrazolyl derivative (7) and hydrazino derivative (8). Alkylation of compound 3 with alkyl halide gave the corresponding 2,3-disubsti
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Elshaarawy, Reda F. M., and Christoph Janiak. "2-Thiophenecarbohydrazides: A Novel Efficient Method for the Synthesis of 2-Thiophenecarbohydrazide." Zeitschrift für Naturforschung B 66, no. 12 (2011): 1202–8. http://dx.doi.org/10.1515/znb-2011-1202.

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Hydrazinolysis of carboxylic acid esters in alcoholic solutions is the standard method for preparing carbohydrazides (carboxylic hydrazides). Here we report an efficient process, involving the reaction of activated esters or amides with hydrazine, for the preparation of thiophenecarbohydrazides in yields larger than 90% and high purity. With this new method, a series of heteroaryl-, aryl-, or aralkyl- substituted carbohydrazides were synthesized and characterized. The X-ray crystal structure of 2-thiophenecarbohydrazide (thiophene-2-carboxylic hydrazide, 2-thenoyl-hydrazine) has revealed that
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Ananthi, Vadamalai, Kaliyaraj Rajalakshmi, Inbasekaran Muthuvel, and Ganesamoorthy Thirunarayanan. "Solid acidic FeCl3/Bentonite catalyzed solvent-free condensation: Synthesis, spectral studies and antimicrobial activities of some aryl hydrazine Schiff’s bases." Annales Universitatis Mariae Curie-Sklodowska, sectio AA – Chemia 71, no. 2 (2017): 127. http://dx.doi.org/10.17951/aa.2016.71.2.127.

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<p>Some aryl hydrazide derivatives have been synthesized including 1-(3-chloro-4-nitrophenyl)-2-(3-substituted benzylidene) hydrazines by FeCl<sub>3</sub>/Bentonite catalyzed solvent-free condensation of substituted phenyl hydrazine and aldehydes under microwave irradiation. The yields of the hydrazides are more than 70%. The synthesized hydrazides are characterized by the physical constants, micro analysis and spectroscopic data. Effect of catalyst, solvent effect substituent effect and optimization of the catalyst was studied by the percentage of isolated yields. From the c
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Peng, Seng, Xiao Bin Tang, Hao Wang, Yan Wei, and Gang Chen. "Preparation of Poly-Hydrazide and Use as Pour Point Depressor for Heavy Oil." Materials Science Forum 943 (January 2019): 135–40. http://dx.doi.org/10.4028/www.scientific.net/msf.943.135.

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To develop new pour point depressor, in this work, a poly-hydrazide is designed and prepared from vegetable oil, hydrazine hydrate and epichlorohydrin. The effectiveness of the poly-hydrazides on four crude oils was tested as pour point depressants as well as paraffin inhibiters. The results showed that the highest pour point reduction depression was achieved as 9.8°C with 2000ppm PH3O-3 in 2# crude oil. Below the pour point of the crude and processed oils, paraffin crystals will deposit and tend to plug flow lines and filters. The saturated hydrocarbons were separated, and the paraffin crysta
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Abidov, Musa T. "Pharmacological aspects of hydrazides and hydrazide derivatives." Health Promotion & Physical Activity 2, no. 3 (2017): 9–21. http://dx.doi.org/10.5604/01.3001.0010.7718.

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Intense search for new antimicrobials, including anti-tuberculosis drugs, is dictated by the phenomenon of bacterial multidrug resistance. Hydrazides are considered the key intermediate and valuable starting material for some novel biologically active compounds. Over 70% of recently reported synthetic hydrazide derivatives are evaluated for antimicrobial and/or antifungal activity. The most frequently applied hydrazide is an anti- tuberculosis drug isoniazid/isonicotinic acid hydrazide (NIH). Hydrazide chemicals are sharing a common functional group characterized by a nitrogen- to-nitrogen cov
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Kantlehner, Willi, Jochen Mezger, Rüdiger Stieglitz, et al. "Orthoamide, LXV [1]. Kondensationsreaktionen von Amidinen, Guanidinen, Hydrazin und Hydrazin-Derivaten mit Orthoamiden von Alkincarbonsäuren / Orthoamides,LXV [1]. Condensation Reactions of Amidines, Guanidines, Hydrazine and Hydrazine Derivatives with Orthoamides of Alkyne Carboxylic Acids." Zeitschrift für Naturforschung B 62, no. 8 (2007): 1015–29. http://dx.doi.org/10.1515/znb-2007-0804.

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The orthoamide derivatives 4 react with amidines 10 and guanidines 11 to give 4-dimethylaminopyrimidines 12. The 3-dimethylamino-pyrazoles 13a - c can be prepared from orthoamides 4 and hydrazine. The hydrazine derivative 14, whose constitution was established by crystal structure analysis, is obtained in low yield when hydrazine is added dropwise to a boiling solution of 4d in THF.Methyl- and phenylhydrazine, undergo reaction with the orthoamides 4a, c yielding mixtures of the isomeric pyrazoles 19 and 20. The reaction of 4c with acylhydrazines 21a - e affords the pyrazole 13b. The pyrazole 2
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Afsah, Elsayed M., Saad S. Elmorsy, Soha M. Abdelmageed, and Zaki E. Zaki. "Synthesis of some new hydrazide-hydrazones related to isatin and its Mannich and Schiff bases." Zeitschrift für Naturforschung B 71, no. 11 (2016): 1147–57. http://dx.doi.org/10.1515/znb-2016-0130.

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AbstractThe hydrazide-hydrazones 6a–d and 7a, b were obtained by treating isatin (1) or its Mannich base 2 with hydrazides incorporating piperidine, morpholine, and piperazine units. The reaction of 1 and 2 with hydrazides related to triazenes having piperidine, morpholine, and 1,2,3,4-tetrahydroisoquinoline moieties gave 12a–c and 13a–c. Treatment of 1 and 2 with iminodiacetohydrazide (14) and ethylenediamine tetraacetohydrazide (18) afforded 15–17 and 19a, b, respectively. The Mannich reaction of the Schiff base 20 with formaldehyde and the appropriate hydrazide or bis(hydrazide) gave 21a, b
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Cai, Yan-Hua, and Shun-Jiang Li. "Synthesis and Performance ofN-(Benzoyl) Stearic Acid Hydrazide." E-Journal of Chemistry 9, no. 2 (2012): 545–52. http://dx.doi.org/10.1155/2012/514386.

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N-(benzoyl) stearic acid hydrazide was synthesized from benzoyl hydrazine and stearyl chloride which was deprived from stearic acid via acylation. The structure of the compound had been characterized by FT-IR,1H NMR, at the same time, the structure of N-(benzoyl) stearic acid hydrazide was optimized by the semiempirical method PM3. The influence of the reaction ratio, reaction time and reaction temperature to the yield ofN-(benzoyl) stearic acid hydrazide was investigated by orthogonal experiment, and the optimized reaction condition was molar ratio of benzoyl hydrazine: stearyl chloride 1:1,
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Oinuma, Ken-Ichi, Atsushi Takuwa, Kosuke Taniyama, Yuki Doi, and Naoki Takaya. "Hydrazidase, a Novel Amidase Signature Enzyme That Hydrolyzes Acylhydrazides." Journal of Bacteriology 197, no. 6 (2015): 1115–24. http://dx.doi.org/10.1128/jb.02443-14.

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The degradation mechanisms of natural and artificial hydrazides have been elucidated. Here we screened and isolated bacteria that utilize the acylhydrazide 4-hydroxybenzoic acid 1-phenylethylidene hydrazide (HBPH) from soils. Physiological and phylogenetic studies identified one bacterium asMicrobacteriumsp. strain HM58-2, from which we purified intracellular hydrazidase, cloned its gene, and prepared recombinant hydrazidase using anEscherichia coliexpression system. TheMicrobacteriumsp. HM58-2 hydrazidase is a 631-amino-acid monomer that was 31% identical to indoleacetamide hydrolase isolated
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Dzhumadullaeva, S. A., A. B. Bayeshov, and A. V. Kolesnikov. "STUDY OF THE CATALYTIC HYDRAZINOLYSIS OF HIGHER FATTY ACIDS." SERIES CHEMISTRY AND TECHNOLOGY 2, no. 440 (2020): 56–61. http://dx.doi.org/10.32014/2020.2518-1491.23.

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In this work, the reaction of hydrazinolysis of higher fatty acid in the presence of an ionite catalyst is considered for the first time. Synthetic commodity anion exchange resin AB-17-8 was used as a catalyst. Before use, the anionite was converted to OH-form and its exchange capacity was determined. The experiments were made in the static conditions in a glass reactor with mixing of the reaction mixture.The reaction of palmitic acid with hydrazine yielded the corresponding hydrazide. The influence of various factors (quantity of hydrazine hydrate, catalyst, butyl alcohol, temperature, reacti
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Dissertations / Theses on the topic "Hydrazidy"

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Selby, Jonathan D. "Synthesis and reactivity of titanium hydrazido(2-) complexes." Thesis, University of Oxford, 2009. http://ora.ox.ac.uk/objects/uuid:afee94b7-7cd7-437c-8c31-1cba8a145720.

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This Thesis describes the synthesis and characterisation of titanium hydrazido(2-) complexes and their reactivity towards unsaturated molecules. Exploration of the bonding in titanium hydrazido(2-) complexes is performed through structural and computational studies. <strong>Chapter 1</strong> introduces current Group 4 hydrazido chemistry and describes its relevance with comparison to Group 4 imido and mid/late metal hydrazido examples. <strong>Chapter 2</strong> describes the synthesis and characterisation of new titanium hydrazido(2-) half-sandwich complexes. A general route to new titanium
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Zerkout, Saïd. "Synthèse d'hydrazino peptides." Vandoeuvre-les-Nancy, INPL, 1994. http://www.theses.fr/1994INPL052N.

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La modification de la liaison amide dans les peptides a plusieurs conséquences potentielles: une biodégradabilité réduite, une possible modulation structurale due aux perturbations du réseau de liaisons hydrogène, et éventuellement, une bio-activité modulée pour l'analogue pseudopeptidique résultant, sans nécessiter de changer les chaines latérales. Nous avons étudie les perturbations structurales induites par la substitution d'une liaison amide par un groupe hydrazide dans diverses séquences mono-, di- et tripeptidiques protégées à leurs deux extrémités par une fonction amide, et contenant l'
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Clavette, Christian. "Synthesis of Beta-Aminocarbonyl Compounds and Hydrazine Derivatives Using Amino- and Imino-Isocyanates." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32004.

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Over the past recent years, β-aminocarbonyls have been of great interest to medicinal chemists. As a practical method to obtain these moieties, alkene aminocarbonylation, accounting for the formation of a C-N and a C-C bond, has been the subject of limited research efforts (very specific intramolecular metal-catalyzed variants have been reported). Direct aminocarbonylation of alkenes constitutes a challenging and an important potential innovation in the synthesis of β-aminocarbonyls such as β-amino acids. The research efforts described in the present thesis have been primarily directed towards
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Hsu, Ivann Hong, Joanna Emerson, Andrew Wong, and Phillip Zinsli. "2-HYDROXYETHYL HYDRAZINE AND HYDRAZINE HYDRATE PLANT DESIGN." Thesis, The University of Arizona, 2009. http://hdl.handle.net/10150/192492.

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Saalmann, Thomas. "Umwandlung cyclischer Hydrazine." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=97226888X.

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Vogt, Kirkland W. "Nitridation reactions with hydrazine." Diss., Georgia Institute of Technology, 1994. http://hdl.handle.net/1853/10032.

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Shan, Hui. "New late transition metal oxo and hydrazido complexes /." free to MU campus, to others for purchase, 1998. http://wwwlib.umi.com/cr/mo/fullcit?p9924922.

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Stevenson, Laura. "New reactions of titanium imido and hydrazido complexes." Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:7abf8708-30ca-455f-b53b-a2e1470c3e66.

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This Thesis reports the synthesis and reactions of titanium-nitrogen multiply bonded compounds. Reactions with both acidic and hydridic element-hydrogen bonds are explored along with unsaturated small molecules in general. <b>Chapter One</b> provides a background on imido and hydrazido complexes, starting with the relevance of the hydrazido ligand to nitrogen fixation. Group 4 alkylidene hydrazide and alkoxyimide complexes are also reviewed. The Chapter focuses in particular on the synthesis, structure, and stoichiometric and catalytic reactions of these complexes with unsaturated substrates.
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Tiong, Pei Jen. "Synthesis and reactivity of new titanium hydrazido complexes." Thesis, University of Oxford, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559841.

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This Thesis describes the synthesis and characterisation of titanium hydrazido(2-) and alkylidene hydrazido(2-) complexes and their reactivity towards unsaturated molecules. Exploration of the bonding in titanium hydrazido(2-) and alkylidene hydrazido(2-) complexes is performed through structural and computational studies. Chapter 1 introduces current Group 4 hydrazido chemistry in comparison to Group 4 imido and mid/late metal hydrazido examples. Current Group 4 alkylidene hydrazido chemistry is also described. Chapter 2 describes the synthesis, bonding and the novel reaction chemistry of tit
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REIS, RONALD DA SILVA. "TREATEMENT WASTEWATER EFFLUENTS CONTAINING HYDRAZINE." PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO, 2003. http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=5112@1.

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No Brasil está em larga expansão o uso de geração de eletricidade por termoeléctricas. Na geração de eletricidade por usinas térmicas são utilizados grandes quantidades de água e produtos químicos, que após utilização geram efluentes. A hidrazina é um produto químico usado para controle de corrosão em águas de caldeiras, sistemas de vapor e outros sistemas de usinas térmicas que após utilização acaba incorporada aos efluentes líquidos destas usinas. Com intuito de promover uma sistemática de controle de efluentes produzidos nas usinas, procurou-se, nesta dissertação, estudar efluentes
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Books on the topic "Hydrazidy"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Hidorajin: Hydrazine. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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Patil, K. C., and Tanu Mimani Rattan, eds. Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.

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Schmidt, Eckart W. Hydrazine and its derivatives: Preparation, properties, applications. 2nd ed. Wiley-Interscience, 2001.

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Suzuki, M. Decomposition of hydrazine by high frequency glow electrical discharges. National Aeronautics and Space Administration, 1988.

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Canada, Canada Health. Hydrazine sulphate: An information package. Health Canada, 1996.

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Yade, N. Treatment for hydrazine-containing waste water solution. National Aeronautics and Space Administration, 1986.

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Yade, N. Treatment for hydrazine-containing waste water solution. National Aeronautics and Space Administration, 1986.

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Yade, N. Treatment for hydrazine-containing waste water solution. National Aeronautics and Space Administration, 1986.

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Curran, Francis M. In-situ analysis of hydrazine decomposition products. National Aeronautics and Space Administration, 1987.

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Curran, Francis M. In-situ analysis of hydrazine decomposition products. National Aeronautics and Space Administration, 1987.

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Book chapters on the topic "Hydrazidy"

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Dilworth, J. R., and S. Morton. "To Form Hydrazine and Hydrazine and Hydrazido Complexes." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch13.

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Gordon, Paul G., Ludwig F. Audrieth, and P. Lensi. "Allophanyl Hydrazide." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132364.ch13.

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Hallenbeck, William H., and Kathleen M. Cunningham-Burns. "Maleic Hydrazide." In Pesticides and Human Health. Springer New York, 1985. http://dx.doi.org/10.1007/978-1-4612-5054-8_51.

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Lane, J. D., C. J. Pickett, and D. R. Stanley. "Hydrazine and Substituted Hydrazine Complexes." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch74.

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Audrieth, L. F., T. T. Nickles, G. Gibson, and R. E. Kirk. "Hydrazine Sulfate." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch31.

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Aruna, Singanahally T., and K. C. Patil. "Hydrazine Salts." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch02.

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Audrieth, L. F., T. T. Nickles, G. Gibson, and R. E. Kirk. "Recovery of Hydrazine Residues as Hydrazine Dihydro Chloride or Hydrazine Sulfate." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch32.

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Chemie, B. G. "Benzene sulphonic acid hydrazide." In Toxicological Evaluations 6. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84992-3_2.

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Rattan, Tanu Mimani, and K. C. Patil. "Hydrazine and Its Inorganic Derivatives." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch01.

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Gajapathy, Dasaratharam, and Tanu Mimani Rattan. "Metal Hydrazines." In Inorganic Hydrazine Derivatives. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch03.

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Conference papers on the topic "Hydrazidy"

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Guo, Hong, Pengdi Ren, Xiaoyu Zhang, Guangxiong Chen, and Yi Ye. "Fretting Wear Behavior of NC30Fe in Distilled Water and Hydrazine Solution." In 2013 21st International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icone21-15879.

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In this study, fretting wear behavior of NC30Fe tubes against 1Cr13 stainless steel cylinder in distilled water and hydrazine solution was investigated at room temperature. Wear scar was analyzed systematically by NanoMap500DLS dual-mode profilometer, SEM, EDX. The results showed that the fretting logs were running in slip regime. The hydrazine solution may lead to corrosion. The friction coefficient in aqueous medium was lowered obviously, but it in distilled water was lower than that in hydrazine solution due to the effect of hydrazine solution. The wear was lightened in aqueous medium signi
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Won, Hui-Jun, Jung-Soon Park, Chong-Hun Jung, Sang-Yoon Park, Wang-Kyu Choi, and Jei-Kwon Moon. "A Reductive Dissolution Study of Magnetite." In ASME 2013 15th International Conference on Environmental Remediation and Radioactive Waste Management. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icem2013-96101.

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Magnetite dissolution tests using a hydrazine base solution were performed at a temperature range of 90 to 150 °C. The dissolution rate of magnetite increased with [N2H4], time, and temperature. The optimum solution pH in the experimental range was 3. The addition of copper ion to the hydrazine base solution greatly increased the magnetite dissolution rate. This was explained by the complex formation between N2H4 and Cu ions, and the reducing power of the hydrazine-Cu complex to the ferric ions of magnetite. The reductive decontamination solution can be applied below 100 °C by the addition of
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Domae, Masafumi, Hirotaka Kawamura, Daisuke Akutagawa, Kenji Hisamune, Yosuke Katsumura, and Yusa Muroya. "Corrosion Test of 304 Stainless Steel in Hydrazine and Methanol Solutions at 320°C Under Gamma-Irradiation and Gamma Radiolysis of Hydrazine and Methanol." In 18th International Conference on Nuclear Engineering. ASMEDC, 2010. http://dx.doi.org/10.1115/icone18-29281.

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It has been pointed out that dissolved hydrogen is one of the key factors of PWSCC (primary water stress corrosion cracking) in the primary systems of pressurized water reactors. The authors consider that application of alternative reductant for hydrogen may mitigate PWSCC. The corrosion tests of 304 stainless steels in 2 mmol dm−3 methanol solution and 2 mmol dm−3 hydrazine solution at 320 °C were carried out under γ-ray irradiation, and the corrosion environment was evaluated. Electrochemical corrosion potential (ECP) of the stainless steels was measured during the immersion tests. The ECP v
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ARNHOLD, J., and J. GEYER. "IRON-MEDIATED HYDROXYLATION OF PHTHALIC HYDRAZIDE." In Bioluminescence and Chemiluminescence - Progress and Current Applications - 12th International Symposium on Bioluminescence (BL) and Chemiluminescence (CL). WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776624_0029.

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Blaja, Svetlana, Kaleria Kuchkova, Lidia Lungu, Vasile Lozovan, and Aculina Aricu. "Synthesis of hydrazide containing trinorlabdane derivatives." In New frontiers in natural product chemistry, scientific seminar with international participation. Institute of Chemistry, 2021. http://dx.doi.org/10.19261/nfnpc.2021.ab15.

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Chapman, K., G. Mihaylov, B. Nurney, and K. Kirollos. "70. Selective, Direct-Read Monitoring System for Parts-Per-Billion Levels of Hydrazine, Monomethyl Hydrazine (MMH), and 1,1-Dimethyl Hydrazine (UDMH)." In AIHce 2003. AIHA, 2003. http://dx.doi.org/10.3320/1.2757969.

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WHITEHEAD, JOHN, DON SWINK, JR., GERALD BREWSTER, JEFFREY MAYBEE, and HANS TOEWS. "Pumped hydrazine miniaturized propulsion system." In 25th Joint Propulsion Conference. American Institute of Aeronautics and Astronautics, 1989. http://dx.doi.org/10.2514/6.1989-2958.

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Garcia, Benjamin O., and David J. Chavez. "Shock compression of liquid hydrazine." In Proceedings of the conference of the American Physical Society topical group on shock compression of condensed matter. AIP, 1996. http://dx.doi.org/10.1063/1.50612.

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Paim, Gisele R., Helio G. Bonacorso, Liliane M. F. Porte, Everton P. Pittaluga, Nilo Zanatta, and Marcos A. P. Martins. "Chemoselective Reactivity Study of 6-Hydrazinonicotinic Acid Hydrazide." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0145-2.

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GRAY, C., and R. WOOD. "Development of a 500N bipropellant apogee engine capable of using hydrazine and monomethyl hydrazine." In 25th Joint Propulsion Conference. American Institute of Aeronautics and Astronautics, 1989. http://dx.doi.org/10.2514/6.1989-2735.

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Reports on the topic "Hydrazidy"

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Garcia, B., and D. Chavez. Shock compression of liquid hydrazine. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/105881.

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Karraker, D. G. The Oxidation of Hydrazine by Nitric Acid. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/784248.

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Thiem, Terry L., Jason Brown, Johnathan Kiel, Eric Holwitt, and Gerald J. O'Brien. The Chemical and Biochemical Degradation of Hydrazine. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada333221.

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Karraker, D. G. Cu(II) - Catalyzed Hydrazine Reduction of Ferrous Nitrate. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/787806.

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HARDING LAWSON ASSOCIATES NOVATO CA. Hydrazine Blending and Storage Facility, Interim Response Action. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada273439.

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Karraker, D. G. The Iron-Catalyzed Oxidation of Hydrazine by Nitric Acid. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/783929.

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7

Zube, Dieter M., and Dan Fye. Low Bus Voltage Hydrazine Arcjet System for Geostationary Satellites. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada408186.

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Bertrand, Guy. Ammonia and hydrazine. Transition-metal-catalyzed hydroamination and metal-free catalyzed functionalization. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1253630.

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HARDING LAWSON ASSOCIATES NOVATO CA. Hydrazine Blending and Storage Facility, Interim Response Action Implementation. Final Safety Plan. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada271897.

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EBASCO SERVICES INC NEW YORK. Hydrazine Blending and Storage Facility Wastewater Treatment and Decommissioning Assessment. Version 3.1. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada272092.

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