Relevant bibliographies by topics / Oxygen kinetics

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

Academic literature on the topic 'Oxygen kinetics'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 March 2023

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Journal articles on the topic "Oxygen kinetics"

1

Galotto, M. J., S. A. Anfossi, and A. Guarda. "Oxygen Absorption Kinetics of Sheets and Films Containing a Commercial Iron-based Oxygen Scavenger." Food Science and Technology International 15, no. 2 (April 2009): 159–68. http://dx.doi.org/10.1177/1082013208106207.

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Absorption kinetics of three different forms of the same iron-based oxygen scavenger were studied. Oxygen scavengers were used as pellet, sheet, and film materials. Two scavenger concentrations were used for sheet and film forms. Scavenger samples were analyzed at 75 or 100% relative humidities and stored at 5, 15, and 25°C. Oxygen concentration in the headspace was measured as a function of time. Absorption kinetics was best described by the Chapman-Richards empirical growth model rather than by a first-order reaction. Arrhenius behavior was observed for variations in the final absorption rate with temperature. Absorption capacities, final absorption rates, and activation energies were evaluated and discussed. Scavenger concentration, relative humidity, and temperature effects on kinetic parameters were studied for each experimental condition. Temperature was the most important factor that affected kinetic parameters. At the relative humidity levels studied, any important effect on kinetic parameters was not observed, except on absorption capacities.
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Manns, P. J., C. R. Tomczak, and R. G. Haennel. "OXYGEN UPTAKE KINETICS." Journal of Cardiopulmonary Rehabilitation and Prevention 29, no. 5 (September 2009): 333. http://dx.doi.org/10.1097/01.hcr.0000361192.80278.bb.

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Lyman, John L., and Redus Holland. "Oxygen fluoride chemical kinetics." Journal of Physical Chemistry 92, no. 26 (December 1988): 7232–41. http://dx.doi.org/10.1021/j100337a015.

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Faiia, A., and X. Feng. "Zeolite oxygen exchange kinetics." Chinese Science Bulletin 43, S1 (August 1998): 38. http://dx.doi.org/10.1007/bf02891422.

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de Jesus, Kelly, Ana Sousa, Karla de Jesus, João Ribeiro, Leandro Machado, Ferran Rodríguez, Kari Keskinen, João Paulo Vilas-Boas, and Ricardo J. Fernandes. "The effects of intensity on V̇O2 kinetics during incremental free swimming." Applied Physiology, Nutrition, and Metabolism 40, no. 9 (September 2015): 918–23. http://dx.doi.org/10.1139/apnm-2015-0029.

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Swimming and training are carried out with wide variability in distances and intensities. However, oxygen uptake kinetics for the intensities seen in swimming has not been reported. The purpose of this study was to assess and compare the oxygen uptake kinetics throughout low-moderate to severe intensities during incremental swimming exercise. We hypothesized that the oxygen uptake kinetic parameters would be affected by swimming intensity. Twenty male trained swimmers completed an incremental protocol of seven 200-m crawl swims to exhaustion (0.05 m·s−1 increments and 30-s intervals). Oxygen uptake was continuously measured by a portable gas analyzer connected to a respiratory snorkel and valve system. Oxygen uptake kinetics was assessed using a double exponential regression model that yielded both fast and slow components of the response of oxygen uptake to exercise. From low-moderate to severe swimming intensities changes occurred for the first and second oxygen uptake amplitudes (P ≤ 0.04), time constants (P = 0.01), and time delays (P ≤ 0.02). At the heavy and severe intensities, a notable oxygen uptake slow component (>255 mL·min−1) occurred in all swimmers. Oxygen uptake kinetics whilst swimming at different intensities offers relevant information regarding cardiorespiratory and metabolic stress that might be useful for appropriate performance diagnosis and training prescription.
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Zhang, Yong-Feng, Xiang-Yun Chen, Qian-Cheng Zhang, Chun-Ping Li, and Quan Zhou. "Oxygen-enriched combustion of lignite." Thermal Science 19, no. 4 (2015): 1389–92. http://dx.doi.org/10.2298/tsci1504389z.

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The study is concerned on the oxygen-enriched combustion kinetics of lignite. Thermogravimetric experiments were carried out in a thermogravimetric analyzer under O2/N2 conditions, and operated at different heating rates ranging from 5?C per minute to 25?C per minute. Flynn-Wall-Ozawa method was used to calculate the kinetic parameter. The value of activation energy increased when the oxygen concentration varied from 21% to 70%.
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Koschate, Jessica, Uwe Drescher, Christian Brinkmann, Klaus Baum, Thorsten Schiffer, Joachim Latsch, Klara Brixius, and Uwe Hoffmann. "Faster heart rate and muscular oxygen uptake kinetics in type 2 diabetes patients following endurance training." Applied Physiology, Nutrition, and Metabolism 41, no. 11 (November 2016): 1146–54. http://dx.doi.org/10.1139/apnm-2016-0001.

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Cardiorespiratory kinetics were analyzed in type 2 diabetes patients before and after a 12-week endurance exercise-training intervention. It was hypothesized that muscular oxygen uptake and heart rate (HR) kinetics would be faster after the training intervention and that this would be detectable using a standardized work rate protocol with pseudo-random binary sequences. The cardiorespiratory kinetics of 13 male sedentary, middle-aged, overweight type 2 diabetes patients (age, 60 ± 8 years; body mass index, 33 ± 4 kg·m−2) were tested before and after the 12-week exercise intervention. Subjects performed endurance training 3 times a week on nonconsecutive days. Pseudo-random binary sequences exercise protocols in combination with time series analysis were used to estimate kinetics. Greater maxima in cross-correlation functions (CCFmax) represent faster kinetics of the respective parameter. CCFmax of muscular oxygen uptake (pre-training: 0.31 ± 0.03; post-training: 0.37 ± 0.1, P = 0.024) and CCFmax of HR (pre-training: 0.25 ± 0.04; post-training: 0.29 ± 0.06, P = 0.007) as well as peak oxygen uptake (pre-training: 24.4 ± 4.7 mL·kg−1·min−1; post-training: 29.3 ± 6.5 mL·kg−1·min−1, P = 0.004) increased significantly over the course of the exercise intervention. In conclusion, kinetic responses to changing work rates in the moderate-intensity range are similar to metabolic demands occurring in everyday habitual activities. Moderate endurance training accelerated the kinetic responses of HR and muscular oxygen uptake. Furthermore, the applicability of the used method to detect these accelerations was demonstrated.
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Trofè, Aurelio, Milena Raffi, David Muehsam, Andrea Meoni, Francesco Campa, Stefania Toselli, and Alessandro Piras. "Effect of PEMF on Muscle Oxygenation during Cycling: A Single-Blind Controlled Pilot Study." Applied Sciences 11, no. 8 (April 17, 2021): 3624. http://dx.doi.org/10.3390/app11083624.

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Pulsed electromagnetic fields (PEMFs) are used as non-invasive tools to enhance microcirculation and tissue oxygenation, with a modulatory influence on the microvasculature. This study aimed to measure the acute effect of PEMF on muscle oxygenation and its influence on pulmonary oxygen kinetics during exercise. Eighteen male cyclists performed, on different days, a constant-load exercise in both active (ON) and inactive (OFF) PEMF stimulations while deoxyhemoglobin and pulmonary oxygen kinetics, total oxygenation index, and blood lactate were collected. PEMF enhanced muscle oxygenation, with higher values of deoxyhemoglobin both at the primary component and at the steady-state level. Moreover, PEMF accelerated deoxyhemoglobin on-transition kinetic, with a shorter time delay, time constant, and mean response time than the OFF condition. Lactate concentration was higher during stimulation. No differences were found for total oxygenation index and pulmonary oxygen kinetics. Local application of a precise PEMF stimulation can increase the rate of the muscle O2 extraction and utilization. These changes were not accompanied by faster oxygen kinetics, reduced oxygen slow component, or reduced blood lactate level. It seems that oxygen consumption is more influenced by exercise involving large muscle mass like cycling, whereas PEMF might only act at the local level.
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Khanh, Le Quoc. "A STUDY ON THE KINETICS OF OXYGEN REDUCTION FOCOAR." Vietnam Journal of Science and Technology 55, no. 5B (March 24, 2018): 111. http://dx.doi.org/10.15625/2525-2518/55/5b/12216.

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In poor oxygenated environments the oxidation and growth of the living organisms are slowed or stopped, so that food is better preserved. The most appropriate method for oxygen depletion in the air-tight minienvironment is oxygen reduction with iron-based reducing agent, which can reduce the air oxygen concentration to about 0 %, and maintain this low oxygen concentration long during storage. This paper studies the kinetics of oxygen reduction by reducing agent FOCOAR in an airtight minienvironment under isobaric conditions. The kinetics of the reduction process calculated according to the relation vav = [21 % - (end) ] / tend, in which vav is average reduction rate, (end) is oxygen concentration at the end of the experiment, tend is total time needed for the oxygen reduction experiment. Instantaneous reduction rate vred was calculated according to equation vred = ∆/△t, in which ∆is oxygen concentration reduced in time △t, and △t = ti+1 - ti is time interval for oxygen reduction. It is found that vav depends on the quantity of reducing agent FOCOAR, and in certain time interval varies as linear function of reduction time, corresponding to constant vred. The kinetic result allows an estimating the amount of the reducing agent FOCOAR needed for a preserve minienvironment.
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Kutlugil’dina, Galiya G. "Kinetic scheme of apple pectin oxidative transformations under the action of the ozone-oxygen mixture." Butlerov Communications 61, no. 2 (February 29, 2020): 79–89. http://dx.doi.org/10.37952/roi-jbc-01/20-61-2-79.

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Mathematical modeling of apple pectin oxidative transformations (AP) under the action of the ozone-oxygen mixture in aqueous solutions (the reaction system "AP + O3 + O2 + H2O") has been carried out. The kinetic scheme of the oxidation process was compiled basing on the well-known ideas of liquid-phase oxidation mechanisms of organic compounds (taking into account the currently known experimental results on AP oxidation). Using the "KhimKinOptima" software package for the proposed scheme, the inverse and direct chemical kinetics problems were solved. The well-known literature data on the rate constants of elementary stages were used. The rate constants of the oxidation key stages have been determined after solving the chemical kinetics inverse problem with the index method of the observed and calculated kinetic data global optimization. It turned out that the rate constants of the individual stages obtained by calculation are in good agreement with the values of the rate constants taken from literary sources. The chemical kinetics direct problem has been solved with the found rate constants and allowed obtaining kinetic curves of all participants in the apple pectin ozonized oxidation. It was found that the kinetic curve of the accumulation of carboxyl groups, obtained experimentally, completely coincided with the theoretical dependence. It has been also shown that the proposed apple pectin oxidative conversion scheme in the "AP + O3 + O2 + H2O" reaction system allows one to explain all the currently available experimental results. The apple pectin ozonized oxidation under another initiator (Н2О2 + FeSO4) has been studied to confirm the kinetic scheme. To do this, 3 new stages has been introduced into the scheme proposed, characterizing the catalytic decomposition of hydrogen peroxide under a transition metal (Fe2+). By solving the chemical kinetics direct problem, the accumulation kinetic curves of the final reaction products were obtained. It has been found that the carboxyl groups accumulation kinetics in the reaction system "AP + O3 + O2 + H2O2 + FeSO4 + H2O" after the supplementary experiment coincided with the theoretical kinetic curve. Thereby, the accuracy of the apple pectin proposed oxidative conversion scheme is confirmed.
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Dissertations / Theses on the topic "Oxygen kinetics"

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Olinde, Lindsay. "Sediment Oxygen Demand Kinetics." Thesis, Virginia Tech, 2007. http://hdl.handle.net/10919/42437.

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Hypolimnetic oxygen diffusers increase sediment oxygen demand (SOD) and, if not accounted for in design, can further exacerbate anoxic conditions. A study using extracted sediment cores, that included both field and laboratory experiments, was performed to investigate SOD kinetics in Carvinâ s Cove Reservoir, a eutrophic water supply reservoir for Roanoke, Virginia. A bubble-plume diffuser is used in Carvinâ s Cove to replenish oxygen consumed while the reservoir is thermally stratified. The applicability of zero-order, first-order, and Monod kinetics to describe transient and steady state SOD was modeled using analytical and numerical techniques. Field and laboratory experiments suggested that first-order kinetics characterize Carvinâ s Cove SOD. SOD calculated from field experiments reflected diffuser flow changes. Laboratory experiments using mini-diffusers to vary dissolved oxygen concentration and turbulence were conducted at 4°C and 20°C. Similar to field observations, the laboratory results followed changes in mini-diffuser flow. Kinetic-temperature relationships were also observed in the laboratory experiments. A definitive conclusion could not be made on the broad applicability of first-order kinetics to Carvinâ s Cove SOD due to variability within field experiments. However, in situ experiments are underway that should assist in the overall understanding of the reservoirâ s SOD kinetics.
Master of Science
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Fawkner, Samantha Gieva. "Oxygen uptake kinetics in children." Thesis, University of Exeter, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393144.

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Violette, Steven M. "Oxygen Delignification Kinetics and Selectivity Improvement." Fogler Library, University of Maine, 2003. http://www.library.umaine.edu/theses/pdf/VioletteSM2003.pdf.

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Ji, Yun. "Kinetics and Mechanism of Oxygen Delignification." Fogler Library, University of Maine, 2007. http://www.library.umaine.edu/theses/pdf/JiY2007.pdf.

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Dogan, Ismail. "Mass Transfer And Kinetics In Oxygen Delignification." Phd thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605562/index.pdf.

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In this study, the kinetic analysis of oxygen delignification of Turkish southern hardwood Kraft pulp was carried out. Kraft pulp was obtained from Mopak Dalaman pulp and paper mill. The kinetic rate data were collected in a 1 L high pressure batch reactor. The delignification experiments were carried out under a wide range of industrially significant conditions of temperature (90, 100 and 110 oC), alkali charge (1, 3, 5% on oven dry pulp), and oxygen partial pressure (0.5, 3.5, 6.5 bar). In order to achieve this objective, the study is separated into different stages. In the first stage of the work, the mass transfer effects were examined for different pulp consistencies. It was seen that the inter-fiber mass transfer resistances become negligible at the consistencies below 1%. Therefore, the experiments were performed at 0.5% consistency. In the following stage, the kinetics of oxygen delignification was studied and the governing rate equations were derived. Then, the kinetics of the carbohydrate degradation was analyzed in order to determine the extent of delignification without the reduction in the pulp strength. The delignification and the carbohydrate degredation rate during oxygen delignification increase with increasing in alkali concentration, oxygen partial pressure and temperature. However, the most effective parameters are the alkali concentration and temperature. The dimensionless terms for Kappa number, intrinsic viscosity and reaction time were used in order to generalize the results and to make them independent of the initial Kappa number, the intrinsic viscosity, experimental conditions and pulping conditions prior to oxygen delignification. These dimensionless parameters were fitted to nonlinear equations from which the control of the oxygen delignification towers can be done with a simple equation. The same approach was also used for the reported studies in the literature which allowed the comparison with the results of this study. In the final stage of the study, the simulation of the oxygen delignification unit preceding the CEHDED bleach plant is performed, in order to see the effect of oxygen delignification on the amount of total wastes coming out from the bleach plant. When an oxygen delignification unit is added to the existing CEHDED bleach plant, the amount of pollutants are decreased by 17.96% with output brightness of 92.95. When the overall process parameter optimization of the CEHDED bleach plant is done with oxygen delignification unit, the total amount of dissolved solids coming out from the six washers are decreased by 25.97% with output brightness of 89.5. In order to reduce the pollution load and chemical consumption in Mopak Dalaman pulp and paper mill, management has decided to install an oxygen delignification unit to the plant. Therefore, the rate equations obtained from this study can form a basis for the design and optimization of oxygen reactor in the mill.
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Bell, Christopher. "Control and modelling of oxygen uptake kinetics." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ42497.pdf.

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Bauer, Timothy Alan. "Oxygen uptake kinetics in peripheral arterial disease." Diss., Manhattan, Kan. : Kansas State University, 2005. http://hdl.handle.net/2097/125.

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Walker, Forest P. "Kinetics of Arsenopyrite Oxidative Dissolution by Oxygen." Thesis, Virginia Tech, 2004. http://hdl.handle.net/10919/9881.

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The objective of this study is to use a mixed flow reactor system to determine the dissolution rate and infer potential mechanisms of arsenopyrite (FeAsS) oxidation by dissolved oxygen at 25°C and circumneutral pH. Release rates for iron, arsenic and sulfur are calculated for a variety of initial dissolved oxygen (DO) concentrations. Results indicate that the rate of arsenopyrite oxidation, represented by the rate law r = A(6.76 x 10-11) where the rate, r, is in mol/s and surface area, A, is in m2, is not significantly dependent on DO concentration. Arsenic and sulfur are released in a 1:1 molar ratio while iron is released more slowly due to precipitation of iron oxyhydroxides. Our results suggest that the rate determining step in arsenopyrite oxidation is determined by the attachment of oxygen at the anodic site in the mineral, and not the transfer of electrons from the cathodic site to oxygen, as is suggested for other sulfide minerals such as pyrite. Previous work on FeAsS oxidation has been limited to low pH conditions with ferric iron as the oxidant. However, not all arsenopyrite weathering occurs exclusively in acidic environments. For example, at an abandoned arsenopyrite mine in Virginia, the pH of ground and surface waters is consistently between 4 and 7. Results of this study provide important insight to arsenic mobilization processes and rates, at field-relevant conditions, consequently aiding in the effort to understand arsenic release and retention in the environment.
Master of Science
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Blumoff, Sonja. "Oxygen Uptake Kinetics in Severe Intensity Exercise." Thesis, University of North Texas, 2000. https://digital.library.unt.edu/ark:/67531/metadc2539/.

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The purpose of this study was to describe mathematically the oxygen uptake kinetics during cycle ergometry, and to examine the effect of intensity on the kinetic responses within the severe domain. Sixteen volunteers performed a series of exercise tests at a range of intensities selected to elicit fatigue in ~3 to 10 min. A simple mono-exponential model effectively described the response across all intensities. There was a positive correlation between the response time and the time to fatigue, demonstrating that the maximal oxygen uptake was achieved faster at higher intensities within the severe domain. Models incorporating two components effectively described the responses only in tests lasting 8 min or more. It was concluded that there is a second, slow component in the oxygen uptake response only at the lower intensities within the severe domain.
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Wilkerson, Daryl P. "Oxygen uptake kinetics during supra-maximal intensity exercise." Thesis, Manchester Metropolitan University, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424750.

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Books on the topic "Oxygen kinetics"

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Arnold, Graham S. Kinetics of oxygen interaction with materials. New York: American Institute of Aeronautics and Astronautics, 1985.

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Ingham, Stephen A. Oxygen uptake kinetics and performance in rowing. Roehampton: University of Surrey Roehampton, 2003.

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Behrens, Robert George. Vaporization kinetics and thermodynamics in the arsenic-oxygen and antimony-oxygen systems. Ann Arbor, MI: University Microfilms International, 1989.

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1970-, Jones Andrew M., and Poole David C. 1959-, eds. Oxygen uptake kinetics in sport, exercise and medicine. London: Routledge, 2005.

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Joos, Nathaniel Ian. Surface oxygen exchange kinetics and oxygen diffusion rates in YSZ single crystals and mixed conducting oxides. Ottawa: National Library of Canada, 1999.

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Halbig, Michael C. Oxygen diffusion and reaction kinetics in continuous fiber ceramic matrix composites. [Cleveland, Ohio]: National Aeronautics and Space Administration, Lewis Research Center, 1999.

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Jones, Andrew M. Oxygen uptake kinetics in sport, exercise and medicine: A practical handbook. New York: Routledge, 2004.

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United States. National Aeronautics and Space Administration., ed. Computation of kinetics for the hydrogen/oxygen system using the thermodynamic method. [Washington, D.C: National Aeronautics and Space Administration, 1996.

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M, Capitelli, ed. Plasma kinetics in atmospheric gases. Berlin: Springer, 2000.

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Goodwin, Ashley. Oxygen Uptake Kinetics in Skeletal Muscle Using Near-Infrared Spectroscopy (NIRS): Evaluating Healthy Responses of Muscle Deoxygenation. [New York, N.Y.?]: [publisher not identified], 2021.

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Book chapters on the topic "Oxygen kinetics"

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van Holde, K. E., and Karen I. Miller. "Kinetics and Equilibria of Octopus Hemocyanin Association." In Invertebrate Oxygen Carriers, 245–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71481-8_43.

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Wilkins, Ralph G. "Kinetics of Formation of Biological Oxygen Carriers." In Oxygen Complexes and Oxygen Activation by Transition Metals, 49–60. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0955-0_5.

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Paterson, Donald H., David A. Cunningham, and Mark A. Babcock. "Oxygen Kinetics in the Elderly." In Respiratory Control, 171–78. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0529-3_19.

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Basak, Arup K., and Arthur E. Martell. "Kinetics and Mechanisms of Degradation of Binuclear Cobalt Dioxygen Complexes." In Oxygen Complexes and Oxygen Activation by Transition Metals, 307. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0955-0_22.

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Bassingthwaighte, James B., Richard B. King, John E. Sambrook, and Brett van Steenwyk. "Fractal Analysis of Blood-Tissue Exchange Kinetics." In Oxygen Transport to Tissue X, 15–23. New York, NY: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-9510-6_2.

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Cochrane, J. E., R. L. Hughson, and P. C. Murphy. "On Modelling Alveolar Oxygen Uptake Kinetics." In Respiratory Control, 147–53. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0529-3_16.

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Coley, Kenneth S., Elaine Chen, and Michael Pomeroy. "Kinetics of Reaction Important in Oxygen Steelmaking." In Celebrating the Megascale, 289–302. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-48234-7_26.

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Coley, Kenneth S., Elaine Chen, and Michael Pomeroy. "Kinetics of Reaction Important in Oxygen Steelmaking." In Celebrating the Megascale, 289–302. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118889657.ch26.

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Swenson, E. R. "Kinetics of Oxygen and Carbon Dioxide Exchange." In Vertebrate Gas Exchange, 163–210. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75380-0_6.

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Thompson, Ambler, W. H. Biggley, and Howard H. Seliger. "Luciferase Reverse Micellar Bioluminescence: Kinetics and Emission Spectra." In Oxygen Radicals in Biology and Medicine, 229–32. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5568-7_35.

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Conference papers on the topic "Oxygen kinetics"

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Hobbs, Keith R., Boris V. Zhdanov, Thomas L. Henshaw, and David K. Neumann. "Singlet delta oxygen kinetics in optically excited liquid oxygen." In Lasers and Applications in Science and Engineering, edited by Steven J. Davis and Michael C. Heaven. SPIE, 2004. http://dx.doi.org/10.1117/12.537752.

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Torbin, A. P., P. A. Mikheyev, M. C. Heaven, and V. N. Azyazov. "Vibrational kinetics of molecular singlet oxygen." In 2016 International Conference Laser Optics (LO). IEEE, 2016. http://dx.doi.org/10.1109/lo.2016.7549694.

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ARNOLD, G., and D. PEPLINSKI. "Kinetics of oxygen interaction with materials." In 23rd Aerospace Sciences Meeting. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1985. http://dx.doi.org/10.2514/6.1985-472.

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Torbin, A. P., M. C. Heaven, V. N. Azyazov, A. A. Pershin, and A. M. Mebel. "O2(a1∆) vibrational kinetics in oxygen-iodine laser." In Saratov Fall Meeting 2017: Fifth International Symposium on Optics and Biophotonics: Laser Physics and Photonics XIX; Computational Biophysics and Analysis of Biomedical Data IV, edited by Vladimir L. Derbov and Dmitry E. Postnov. SPIE, 2018. http://dx.doi.org/10.1117/12.2317881.

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Komissarov, Anatoly V., Vasily Goncharov, and Michael C. Heaven. "Chemical oxygen-iodine laser (COIL) kinetics and mechanisms." In XIII International Symposium on Gas Flow and Chemical Lasers and High-Power Laser Conference. SPIE, 2001. http://dx.doi.org/10.1117/12.414032.

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Azyazov, Valeriy N., Md Humayun Kabir, Ivan O. Antonov, and Michael C. Heaven. "Chemical kinetics of discharge-driven oxygen-iodine lasers." In XVI International Symposium on Gas Flow, Chemical Lasers, and High-Power Lasers. SPIE, 2006. http://dx.doi.org/10.1117/12.737190.

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Pitz, Greg A., Matthew A. Lange, and Glen P. Perram. "Singlet oxygen kinetics in a double microwave discharge." In High-Power Laser Ablation 2004, edited by Claude R. Phipps. SPIE, 2004. http://dx.doi.org/10.1117/12.548707.

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Melnikov, Igor, Nikita Muravyev, Ilya Kuchurov, Alla Pivkina, and Vitaly Kiselev. "KINETICS AND MECHANISM PRIMARY DECOMPOSITION CHANNELS OF BCHMX FROM HIGH ACCURACY QUANTUM CHEMISTRY CALCULATIONS." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m770.aks-2019/275-278.

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Barnault, B., D. David, and D. Pigache. "Gas Mixing And Chemical Kinetics In Oxygen-Iodine Lasers." In 7th Intl Symp on Gas Flow and Chemical Lasers, edited by Dieter Schuoecker. SPIE, 1989. http://dx.doi.org/10.1117/12.950542.

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Rawlins, W., S. Lee, W. Kessler, L. Piper, and S. Davis. "Advanced Diagnostics and Kinetics of Oxygen-Iodine Laser Systems." In 36th AIAA Plasmadynamics and Lasers Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2005. http://dx.doi.org/10.2514/6.2005-5299.

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Reports on the topic "Oxygen kinetics"

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Adzic, R. Recent advances in the kinetics of oxygen reduction. Office of Scientific and Technical Information (OSTI), July 1996. http://dx.doi.org/10.2172/259357.

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NA. KINETICS OF CATHODIC REDUCTION OF OXYGEN ON NI-CR-MO-W ALLOY. Office of Scientific and Technical Information (OSTI), April 2006. http://dx.doi.org/10.2172/886552.

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Dr. William Casey. The Kinetics of Dissociations of Aluminum - Oxygen Bonds in Aqueous Complexes - An NMR Study. Office of Scientific and Technical Information (OSTI), September 2003. http://dx.doi.org/10.2172/814687.

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Kelley, D. Kinetics and mechanisms of the reactions of alkyl radicals with oxygen and with complexes of Co(III), Ru(III), and Ni(III). Office of Scientific and Technical Information (OSTI), October 1990. http://dx.doi.org/10.2172/6454295.

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Zauche, Timothy. Kinetics and mechanisms of the oxidation of alcohols and hydroxylamines by hydrogen peroxide, catalyzed by methyltrioxorhenium, MTO, and the oxygen binding properties of cobalt Schiff base complexes. Office of Scientific and Technical Information (OSTI), February 1999. http://dx.doi.org/10.2172/770652.

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Virkar, Anil. Thermodynamic, Kinetic and Electrochemical Studies on Mixed Proton, Oxygen Ion and Electron (Hole) Conductors. Office of Scientific and Technical Information (OSTI), April 2022. http://dx.doi.org/10.2172/1864586.

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Hoffbauer, M. A., J. B. Cross, and F. A. Archuleta. High temperature materials synthesis without heat: Oxide layer growth on electronic materials using high-kinetic-energy atomic oxygen. Office of Scientific and Technical Information (OSTI), April 1996. http://dx.doi.org/10.2172/212548.

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