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Relevant bibliographies by topics / Peroxides

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Academic literature on the topic 'Peroxides'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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Journal articles on the topic "Peroxides"

1

Zhao, Rong, Denghu Chang, and Lei Shi. "Recent Advances in Cyclic Diacyl Peroxides: Reactivity and Selectivity Enhancement Brought by the Cyclic Structure." Synthesis 49, no. 15 (June 12, 2017): 3357–65. http://dx.doi.org/10.1055/s-0036-1588458.

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Preliminarily studies on cyclic diacyl peroxides have shown novel and superior reactivities compared with their acyclic diacyl peroxide counterparts in many reaction types. After summarizing the methods available for the preparation of cyclic diacyl peroxides and describing their structural features, this review brings together an overview of their reactivities with respect to oxidations and decarboxylations, and demonstrates the advantages of reactions with cyclic diacyl peroxides, which include metal-free, additive-free, milder conditions, higher yields and better selectivities.1 Introductio

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Lubeigt, X., F. Flies, M. J. Bourgeois, E. Montaudon, and B. Maillard. "Déplacements homolytiques intramoléculaires. 19. Stéréochimie de la décomposition induite de peroxydes insaturés conduisant à la formation d'hétérocycles à trois et quatre chaînons." Canadian Journal of Chemistry 69, no. 8 (August 1, 1991): 1320–25. http://dx.doi.org/10.1139/v91-196.

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Homolytic decomposition induced by addition of dichloromethyl radicals to β- and γ-unsaturated peroxides having a substituent on the chain linking the unsaturation and the peroxide function was studied. The stereochemistry of the heterocycles produced was determined by I3C NMR and the stereoselectivity of intramolecular homolytic substitution on the peroxidic bond discussed. Key words: unsaturated peroxides, homolytic intramolecular substitutions, radical additions, oxygenated heterocycles.

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Ajima, A., SG Cao, K. Takahashi, A. Matsushima, Y. Saito, and Y. Inada. "An attempt to determine lipid peroxides with polyethylene glycol‐modified hemin." Biotechnology and Applied Biochemistry 9, no. 1 (February 1987): 53–57. http://dx.doi.org/10.1111/j.1470-8744.1987.tb00462.x.

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Hemin, having two carboxyl groups, was coupled with alpha‐(3‐aminopropyl)‐omega‐methoxypoly(oxyethylene) through the acid‐amide bond formed with carbodiimide. The modified hemin catalyzed the peroxidase reaction in 1,1,1‐trichloroethane using benzoyl peroxide or peroxides in unsaturated fatty acids as the hydrogen acceptor and leuco crystal violet as the hydrogen donor. A basic study on quantitative microanalysis of the lipid peroxides was attempted.

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Veal, Elizabeth A., Lewis E. Tomalin, Brian A. Morgan, and Alison M. Day. "The fission yeast Schizosaccharomyces pombe as a model to understand how peroxiredoxins influence cell responses to hydrogen peroxide." Biochemical Society Transactions 42, no. 4 (August 1, 2014): 909–16. http://dx.doi.org/10.1042/bst20140059.

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As a more selectively reactive oxygen species, H2O2 (hydrogen peroxide) has been co-opted as a signalling molecule, but high levels can still lead to lethal amounts of cell damage. 2-Cys Prxs (peroxiredoxins) are ubiquitous thioredoxin peroxidases which utilize reversibly oxidized catalytic cysteine residues to reduce peroxides. As such, Prxs potentially make an important contribution to the repertoire of cell defences against oxidative damage. Although the abundance of eukaryotic 2-Cys Prxs suggests an important role in maintaining cell redox, the surprising sensitivity of their thioredoxin p

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Missall, Tricia A., Jocie F. Cherry-Harris, and Jennifer K. Lodge. "Two glutathione peroxidases in the fungal pathogen Cryptococcus neoformans are expressed in the presence of specific substrates." Microbiology 151, no. 8 (August 1, 2005): 2573–81. http://dx.doi.org/10.1099/mic.0.28132-0.

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Glutathione peroxidases catalyse the reduction of peroxides by reduced glutathione. To determine if these enzymes are important for resistance to oxidative stress and evasion of the innate immune system by the fungal pathogen Cryptococcus neoformans, two glutathione peroxidase homologues, which share 38 % identity, were identified and investigated. In this study, these peroxidases, Gpx1 and Gpx2, their localization, their contribution to total glutathione peroxidase activity, and their importance to the oxidative and nitrosative stress resistance of C. neoformans are described. It is shown tha

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Gutowicz, Marzena. "Antioxidant and detoxycative mechanisms in central nervous system." Postępy Higieny i Medycyny Doświadczalnej 74 (February 19, 2020): 1–11. http://dx.doi.org/10.5604/01.3001.0013.8548.

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Since the brain contains a large amount of polyunsaturated fatty acids, consumes up to 20% of oxygen used by the whole body and exhibits low antioxidants activity, it seems to be especially vulnerable to oxidative stress. The most important antioxidant enzymes are superoxide dismutase (SOD), which catalyze the dismutation of superoxide anion to hydrogen peroxide, catalase (CAT), which converts toxic hydrogen peroxide to water and oxygen, and glutathione peroxidase (Se-GSHPx), which reduces hydrogen peroxide and organic peroxides with glutathione as the cofactor. Among other detoxifying enzymes

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Iturbe-Ormaetxe, Iñaki, Manuel A. Matamoros, Maria C. Rubio, David A. Dalton, and Manuel Becana. "The Antioxidants of Legume Nodule Mitochondria." Molecular Plant-Microbe Interactions® 14, no. 10 (October 2001): 1189–96. http://dx.doi.org/10.1094/mpmi.2001.14.10.1189.

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The mitochondria of legume root nodules are critical to sustain the energy-intensive process of nitrogen fixation. They also generate reactive oxygen species at high rates and thus require the protection of antioxidant enzymes and metabolites. We show here that highly purified mitochondria from bean nodules (Phaseolus vulgaris L. cv. Contender × Rhizobium leguminosarum bv. phaseoli strain 3622) contain ascorbate peroxidase primarily in the inner membrane (with lesser amounts detected occasionally in the matrix), guaiacol peroxidases in the outer membrane and matrix, and manganese superoxide di

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Naskar, Kinsuk, and Jacques W. M. Noordermeer. "Dynamically Vulcanized PP/EPDM Blends: Multifunctional Peroxides as Crosslinking Agents — Part I." Rubber Chemistry and Technology 77, no. 5 (November 1, 2004): 955–71. http://dx.doi.org/10.5254/1.3547862.

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Abstract Thermoplastic vulcanizates (TPVs) or dynamic vulcanizates are a special class of thermoplastic elastomers, produced by mixing and crosslinking of a rubber and a thermoplastic polymer simultaneously. In a previous study, it was demonstrated that the use of dicumyl peroxide in combination with triallyl cyanurate as crosslinking agents provides a good overall balance of physical properties of PP/EPDM TPVs. Commonly used peroxides like dicumyl peroxide generally produce volatile decomposition products, which sometimes provide a typical smell or show a blooming effect. In this paper multif

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Brenot, Audrey, Katherine Y. King, Blythe Janowiak, Owen Griffith, and Michael G. Caparon. "Contribution of Glutathione Peroxidase to the Virulence of Streptococcus pyogenes." Infection and Immunity 72, no. 1 (January 2004): 408–13. http://dx.doi.org/10.1128/iai.72.1.408-413.2004.

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ABSTRACT Glutathione peroxidases are widespread among eukaryotic organisms and function as a major defense against hydrogen peroxide and organic peroxides. However, glutathione peroxidases are not well studied among prokaryotic organisms and have not previously been shown to promote bacterial virulence. Recently, a gene with homology to glutathione peroxidase was shown to contribute to the antioxidant defenses of Streptococcus pyogenes (group A streptococcus). Since this bacterium causes numerous suppurative diseases that require it to thrive in highly inflamed tissue, it was of interest to de

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Fleychuk, Roman, Lidiya Vuytsyk, Ananiy Kohut, and Orest Hevus. "Synthesis of Epoxyperoxides and Peroxide Derivatives of -D-Galactopyranose Based Thereon." Chemistry & Chemical Technology 14, no. 4 (December 15, 2020): 439–47. http://dx.doi.org/10.23939/chcht14.04.439.

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New epoxide-containing peroxides have been synthesized via the interaction between epichlorohydrin and ditertiary -hydroxyalkyl peroxides. The effect of reaction conditions on both the yield and composition of the reaction products has been established. Through the reactions of either the synthesized epoxide-containing peroxides with 1,2;3,4-di-O-isopropylidene--D-galactopyranose or 6-O-glycidyl-1,2;3,4-di-O-isopropylidene--D-galactopyranose with the -hydroxyalkyl peroxides, new peroxide derivatives with ditertiary and primary-tertiary peroxide groups have been synthesized successfully. Th

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Dissertations / Theses on the topic "Peroxides"

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McDonald, Iain M. "Bicyclic peroxides : synthesis, structure and reactions." Thesis, Heriot-Watt University, 1987. http://hdl.handle.net/10399/1047.

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Gray, Norman. "The oxidation of arenethiols by peroxides." Thesis, University of Aberdeen, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328218.

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The oxidation of 4-substituted-benzenethiolate ions by hydrogen peroxide or <i>t</i>-butyl hydroperoxide gave the corresponding disulphide, sulphinic acid and sulphonic acid. With hydrogen peroxide the oxidation was of the second-order with p = -0.71 and showed a small positive salt effect. Benzenethiolate ion gave a small increase in rate with increasing solvent polarity and in 50% v/v dioxan at 25.0°C had ΔH<sup>dag</sup> 54.7 kJ mol<sup>-1</sup>, ΔS^dag -52.2 J mol^-1K^-1 and ΔG<sup>dag</sup> 70.2 kJ mol<sup>-1</sup>. 2-Nitrobenzenethiolate similarlygave ΔH^dag 39.7 kJ mol^-1, ΔS<sup>dag</s

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Dragan, Andrei. "Oxidations with endocyclic peroxides and their derivatives." Thesis, University of Strathclyde, 2016. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=27446.

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This thesis describes two novel transformations (a method to synthesize alkylidene phthalides and a different approach toward the Baeyer-Villiger oxidation) and the development and mechanistic study of a metal-free oxidation of arenes. Chapter 1 introduces the concept of alkene oxyamination. Synthesis of a series of hydroxylamine derivatives of endocyclic peroxides was undertaken, which were then reacted with nitrogen, sulfur and carbon nucleophiles. This led to the discovery of a new reaction that provides access to alkylidene phthalides, a class of compounds which exhibit interesting biologi

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Rawling, Michael J. "Metal-free syn-dihydroxylation of alkenes using malonoyl peroxides." Thesis, University of Strathclyde, 2013. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=25565.

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This thesis describes the successful application of cyclopropyl malonoyl peroxide II in the metal-free syn-dihydroxylation of alkenes I. Chapter 1 outlines the available metal-free methods for achieving syn-1,2- dioxygenation of alkenes. The use of hypervalent iodine, selenium, sulfur and peroxide reagents are discussed in terms of the advantages and limitations of each method. Chapter 2 details a mechanistic investigation into the dihydroxylation reaction using cyclopropyl malonoyl peroxide II. Through kinetic studies, Hammett analysis, multiple isotopic labelling experiments, NMR investigati

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Smith, David P. "Characterisation of peracids." Thesis, University of Cambridge, 1996. https://www.repository.cam.ac.uk/handle/1810/272276.

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Haq, Ahsanul. "The preparation of macrocyclic compounds by thermolysis of cyclic peroxides." Thesis, Heriot-Watt University, 1992. http://hdl.handle.net/10399/1491.

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DiPasquale, Antonio Giovanni. "Peroxide complexes of non-redox active metal centers : models for alternative mechanisms in cytochrome P450 oxidations? /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/11603.

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R, Morris Vernon. "An investigation of transient atmospheric inorganic peroxides : a theoretical and experimental study." Diss., Georgia Institute of Technology, 1991. http://hdl.handle.net/1853/25857.

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Tribelhorn, Michael John. "Reactions of iron- and zinc-fuelled pyrotechnic systems." Thesis, Rhodes University, 1995. http://hdl.handle.net/10962/d1005003.

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A major industrial use of pyrotechnic compositions is as delay fuses in electric detonators. Suitable delay times may be achieved through (i) choice of chemical components (ii) adjustment of composition of the system chosen and, finally, (iii) adjustment of the length of fuse used. This study forms part of a survey of binary fuel/oxidant combinations in an attempt to provide some fundamental information on the first step above: (i) choice of chemical components. The complete survey has included studies of a single fuel in combination with one of a variety of oxidants, and studies of the oxidat

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Leahy, Christopher David. "The oxidation by peroxides of cyanides, cyanide complexes and related species." Thesis, Imperial College London, 1990. http://hdl.handle.net/10044/1/46407.

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Books on the topic "Peroxides"

1

1934-, Andō Wataru, ed. Organic peroxides. Chichester: Wiley, 1992.

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Liebman, Joel F., and Alexander Greer. The chemistry of peroxides. Chichester, West Sussex: John Wiley & Sons Inc., 2014.

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Rappoport, Zvi, ed. The Chemistry of Peroxides. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/0470862769.

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Zvi, Rappoport, ed. The chemistry of peroxides. Chichester: John Wiley & Sons, 2006.

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5

V, Kazakov D., Bubnov I͡U︡ N, and Institut organicheskoĭ khimii (Akademii͡a︡ nauk SSSR. Uralʹskiĭ nauchnyĭ t͡s︡entr), eds. Khimii͡a︡ i khemili͡u︡minest͡s︡ent͡s︡ii͡a︡ dioksiranov. Moskva: "Nauka", 1999.

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Antonovskiĭ, V. L. Fizicheskai︠a︡ khimii︠a︡ organicheskikh peroksidov. Moskva: Akademkniga, 2003.

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Antonovskiĭ, V. L. Progress v khimii organicheskikh peroksidov: Obzornai͡a︡ informat͡s︡ii͡a︡. Moskva: T͡S︡NIITĖneftekhim, 1992.

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Russia) Mezhdunarodnai︠a︡ konferent︠s︡ii︠a︡ po khimii organicheskikh i ėlementoorganicheskikh peroksidov (10th 1998 Moscow. X Mezhdunarodnai︠a︡ konferent︠s︡ii︠a︡ po khimii organicheskikh i ėlementoorganicheskikh peroksidov, 16-18 ii︠u︡ni︠a︡ 1998 g., Moskva: Tezisy. Moscow: s.n., 1998.

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Dri͡uk, V. G. Oksirany - sintez i biologicheskai͡a aktivnostʹ: Mekhanizm, assot͡siativnye i stericheskie ėffekty peroksidnogo ėpoksidirovanii͡a alkenov. Chernogolovka: Bogorodskiĭ pechatnik, 1999.

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Kunio, Yagi, ed. Active oxygens, lipid peroxides and antioxidants. Boca Raton: CRC Press, 1993.

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Book chapters on the topic "Peroxides"

1

Pope, M. T. "From Hydrogen Peroxide and Organic Peroxides." In Inorganic Reactions and Methods, 6–7. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145203.ch6.

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Matyáš, Robert, and Jiří Pachman. "Organic Peroxides." In Primary Explosives, 255–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28436-6_10.

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Böttcher, P. "Of Peroxides." In Inorganic Reactions and Methods, 333–35. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch249.

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Gooch, Jan W. "Organic Peroxides." In Encyclopedic Dictionary of Polymers, 505. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8239.

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Ingraham, Llyod L., and Damon L. Meyer. "Dialkyl Peroxides." In Biochemistry of Dioxygen, 75–89. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2475-1_5.

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Pope, M. T. "From Organic Peroxides." In Inorganic Reactions and Methods, 70. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145203.ch57.

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Bächmann, K., and J. Hauptmann. "Determination of Organic Peroxides." In Mechanisms and Effects of Pollutant-Transfer into Forests, 119–24. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1023-2_13.

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Bächmann, K., and J. Hauptmann. "Determination of Organic Peroxides." In Physico-Chemical Behaviour of Atmospheric Pollutants, 98–102. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0567-2_15.

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Böttcher, P. "Of Peroxides and Superoxides." In Inorganic Reactions and Methods, 325–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch241.

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Li, Yiming. "Overall Safety of Peroxides." In Tooth Whitening, 35–44. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-38849-6_3.

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Conference papers on the topic "Peroxides"

1

Heikes, Brian G., William L. Miller, and Meehye Lee. "Hydrogen peroxide and organic peroxides in the marine environment." In Optics, Electro-Optics, and Laser Applications in Science and Engineering, edited by Harold I. Schiff. SPIE, 1991. http://dx.doi.org/10.1117/12.46169.

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Milata, Viktor, Daniel Végh, Ladislav Štibrányi, and Jozefína Žúžiová. "Peroxides Like Home Made Explosives." In Annual International Conference on Forensic Sciences & Criminalistics Research. Global Science & Technology Forum (GSTF), 2014. http://dx.doi.org/10.5176/2382-5642_fscr14.14.

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Jian, Wang, Lu Yungcai, Zhen Erzhen, Guo Zhaozheng, and Shi Fang. "EFFECT OF LIPID PEROXIDES ON PROSTACYCLIN AND THROMBOXANE GENERATION IN HYPERCHOLESTEROLEMIC RABBITS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643375.

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Rabbits feeding on atherogenic diet for 60 days resulted in high level of plasma lipid peroxides as well as extreme hypercholesterolemia. Both of them kept at high level until 35 days after atherogenic diet stopped. At the same time, as compared with the control group, plasma PGI2 level was remarkably decreased while TXA2 and platelet aggregability were increased. Atherosclerotic vessel walls contain high levels of lipid peroxides associated with decreased PGI2 and increased TXA2 generation. Atherosclerotic plaques had the highest level of lipid peroxides and TXA2 while PGI production was the

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Osmont, Antoine, Marc Genetier, and Gerard Baudin. "Ability of thermochemical calculation to treat organic peroxides." In SHOCK COMPRESSION OF CONDENSED MATTER - 2017: Proceedings of the Conference of the American Physical Society Topical Group on Shock Compression of Condensed Matter. Author(s), 2018. http://dx.doi.org/10.1063/1.5044986.

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KIMURA, M., G. LU, H. IGA, and H. NISHIKAWA. "LOPHINE PEROXIDES AS AN EFFICIENT ORGANIC SOURCE OF SINGLET OXYGEN." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0071.

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Naegeli, David W. "The Role of Sulfur in the Thermal Stability of Jet Fuel." In ASME 1999 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/99-gt-298.

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The autoxidation of Jet A, dodecane, and a dodecane-15%-cumene blend doped with sulfur compounds were studied at 433 K. Oxygen, hydro peroxide and soluble gum were monitored during the autoxidation. Dodecane, cumene, and the dodecane-15%-cumene blend autoxidized rapidly, while Jet A had an induction period followed by a relatively slow post autoxidation. The results suggest that an inhibitor formed early in the post autoxidation of Jet A. Gum formed in the autoxidation of Jet A, whereas none was detected in dodecane, cumene, or dodecane-15% cumene. However, gum was detected in dodecane and dod

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Jonsson, Malin, Kajsa Larsson, Jesper Borggren, Marcus Aldén, and Joakim Bood. "Investigation of ps-PFLIF for detection of hydrogen peroxides in laminar flames." In Laser Applications to Chemical, Security and Environmental Analysis. Washington, D.C.: OSA, 2014. http://dx.doi.org/10.1364/lacsea.2014.lm2d.3.

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Gebarski, Benjamin, and Udo Becker. "Quantum Mechanical Models to Electrochemistry: Understanding the Redox Properties of Uranyl Peroxides." In Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.811.

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Bordet, J. C., M. Guichardant, and M. Lagarde. "PEROXIDE STIMULATION OF PGI3 AND DIHOMO-PGI2 IN ENDOTHELIUM." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643366.

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Human umbilical endothelial cell (EC) monolayers incubated with eicosapentaenoic acid (EPA) produce small amounts of prostaglandin E3 (PGI3). We have previously shown that this metabolite is markedly enhanced in EC supernatant by co-incubating EPA with arachidonic acid (AA) (BBRC 135, 403, 1986). Moreover we found that PGF3a and PGE3 were similarly enhanced, and we concluded that such a stimulation occured at the cyclooxygenase rather than at the prostacyclin synthase level. It is generally assumed that cyclooxygenase is a peroxide-dependent enzyme and the present study shows that the potentia

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ISOBE, H., S. YAMANAKA, M. OKUMURA, and K. YAMAGUCHI. "THEORETICAL CONSIDERATIONS ON THE ROLES OF HYDROGEN BONDING IN THERMAL DECOMPOSITION OF PEROXIDES." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0027.

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Reports on the topic "Peroxides"

1

Weinstein-Lloyd, J. Atmospheric peroxides. Technical progress report. Office of Scientific and Technical Information (OSTI), August 1994. http://dx.doi.org/10.2172/10106399.

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Weinstein-Lloyd, Judith. Atmospheric peroxy radicals and peroxides. Final report. Office of Scientific and Technical Information (OSTI), May 1999. http://dx.doi.org/10.2172/761097.

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Handa, Avtar K., Yuval Eshdat, Avichai Perl, Bruce A. Watkins, Doron Holland, and David Levy. Enhancing Quality Attributes of Potato and Tomato by Modifying and Controlling their Oxidative Stress Outcome. United States Department of Agriculture, May 2004. http://dx.doi.org/10.32747/2004.7586532.bard.

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General The final goal and overall objective of the current research has been to modify lipid hydroperoxidation in order to create desirable phenotypes in two important crops, potato and tomato, which normally are exposed to abiotic stress associated with such oxidation. The specific original objectives were: (i) the roles of lipoxygenase (LOX) and phospholipids hydroperoxide glutathione peroxidase (PHGPx) in regulating endogenous levels of lipid peroxidation in plant tissues; (ii) the effect of modified lipid peroxidation on fruit ripening, tuber quality, crop productivity and abiotic stress

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Conner, W. V. Hydrogen peroxide safety issues. Office of Scientific and Technical Information (OSTI), April 1993. http://dx.doi.org/10.2172/10158827.

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Sears, Jeremiah, Timothy Boyle, and Christopher Dean. Safe handling of potential peroxide forming compounds and their corresponding peroxide yielded derivatives. Office of Scientific and Technical Information (OSTI), June 2013. http://dx.doi.org/10.2172/1089980.

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Kanner, Joseph, Mark Richards, Ron Kohen, and Reed Jess. Improvement of quality and nutritional value of muscle foods. United States Department of Agriculture, December 2008. http://dx.doi.org/10.32747/2008.7591735.bard.

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Food is an essential to our existence but under certain conditions it could become the origin to the accumulative health damages. Technological processes as heating, chopping, mincing, grounding, promote the lipid oxidation process in muscle tissues and meat foodstuffs. Lipid oxidation occurred rapidly in turkey muscle, intermediate in duck, and slowest in chicken during frozen storage. Depletion of tocopherol during frozen storage was more rapid in turkey and duck compared to chicken. These processes developed from lipid peroxides produce many cytotoxic compounds including malondialdehyde (MD

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Melof, Brian Matthew, David L. Keese, Brian V. Ingram, Mark Charles Grubelich, Judith Alison Ruffner, and William Rusty Escapule. Hydrogen peroxide-based propulsion and power systems. Office of Scientific and Technical Information (OSTI), April 2004. http://dx.doi.org/10.2172/903157.

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Walsh, Raymond F., and Alan M. Sutton. Pressure Effects on Hydrogen Peroxide Decomposition Temperature. Fort Belvoir, VA: Defense Technical Information Center, August 2002. http://dx.doi.org/10.21236/ada405753.

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HALGREN DL. EFFLUENT TREATMENT FACILITY PEROXIDE DESTRUCTION CATALYST TESTING. Office of Scientific and Technical Information (OSTI), July 2008. http://dx.doi.org/10.2172/935398.

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Hurst, D. H., K. G. Robinson, and R. L. Siegrist. Hydrogen peroxide treatment of TCE contaminated soil. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10182572.

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