Making Oxygen and Carbon Dioxide Airspace Aeronautics Research Mission Directorate
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Understanding Pigments: the Third Step to Higher Quality And
Understanding Pigments: The Third Mark Harber October, 2000 Step to Higher Quality and Consistency Putting great color in your product is part of the pigments. However, they are less opaque and systems approach for resolving issues of sub- would have to be used at higher loading levels to standard properties and appearance. achieve similar whiteness and opacity. This article on pigments is the third in a four-part Titanium Dioxide is used in the majority of the series about the interrelationship of the material products made by the cast polymer industry. Tita- components used in marble and solid surface nium Dioxide-based colors include most whites, manufacturing. These AOC-authored articles re- pastels, earth tones and off-whites such as bone, spond to the challenge that the cast polymer in- ivory, beige or biscuit. As noted in Table 1, non- dustries aspire to higher standards of quality and white synthetic oxides are combined with Titani- consistency. Because resolving cast polymer is- um Dioxide to create pastels and earth tones for sues requires a systems approach, other articles cultured marble and solid surface applications. in this series address resins, gel coats and pro- cessing. All articles begin with background infor- Phthalocyanine pigments, or "Phthalos," impart mation on the main subject matter, followed by deep colors such as the automotive "Hunter ten related issues and guidelines. Green" of a sport utility vehicle or the high strength Blue used in ballpoint pens. Because A BACKGROUND ON COLORANTS they are so deep when used by themselves, In their natural state, cast polymer resins meet a Phthalo Blue and Phthalo Green are normally variety of performance requirements but are lack- blended with other pigments, many times Titani- ing in the color that draws the customer to the um Dioxide. -
The Decomposition Kinetics of Peracetic Acid and Hydrogen Peroxide in Municipal Wastewaters
Disinfection Forum No 10, October 2015 The Decomposition Kinetics of Peracetic Acid and Hydrogen Peroxide in Municipal Wastewaters INTRODUCTION Efficient control of microbial populations in municipal wastewater using peracetic acid (PAA) requires an understanding of the PAA decomposition kinetics. This knowledge is critical to ensure the proper dosing of PAA needed to achieve an adequate concentration within the contact time of the disinfection chamber. In addition, the impact of PAA on the environment, post-discharge into the receiving water body, also is dependent upon the longevity of the PAA in the environment, before decomposing to acetic acid, oxygen and water. As a result, the decomposition kinetics of PAA may have a significant impact on aquatic and environmental toxicity. PAA is not manufactured as a pure compound. The solution exists as an equilibrium mixture of PAA, hydrogen peroxide, acetic acid, and water: ↔ + + Acetic Acid Hydrogen Peroxide Peracetic Acid Water PeroxyChem’s VigorOx® WWT II Wastewater Disinfection Technology contains 15% peracetic acid by weight and 23% hydrogen peroxide as delivered. Although hydrogen peroxide is present in the formulation, peracetic acid is considered to be the active component for disinfection1 in wastewater. There have been several published studies investigating the decomposition kinetics of PAA in different water matrices, including municipal wastewater2-7. Yuan7 states that PAA may be consumed in the following three competitive reactions: 1. Spontaneous decomposition 2 CH3CO3H à 2 CH3CO2H + O2 Eq (1) 2. Hydrolysis CH3CO3H + H2O à CH3CO2H + H2O2 Eq (2) 3. Transition metal catalyzed decomposition + CH3CO3H + M à CH3CO2H + O2 + other products Eq (3) At neutral pH’s, both peracetic acid and hydrogen peroxide can be rapidly consumed by these reactions7 (hydrogen peroxide will decompose to water and oxygen via 2H2O2 à 2H2O + O2). -
This Ubiquitous Carbon…
Engineering Physics Department Presents Dr. Cristian Contescu Senior Research Staff, Materials Science and Technology Division Oak Ridge National Laboratory This ubiquitous carbon… Abstract: After Stone Age, Bronze Age, and Iron Age, and after the Silicon Age of the informational revolution, the technologies of 21st century are marked by the ubiquitous presence of various forms of carbon allotropes. For a very long time, diamond and graphite were the only known carbon allotropes, but that has changed with the serendipitous discovery of fullerenes, carbon nanotubes, and graphene. Every ten or fifteen years scientists unveil new forms of carbons with new and perplexing properties, while computations suggest that the carbon’s family still has members unknown to us today. At a dramatically accelerated pace, new carbon forms find their place at the leading edge of scientific and technological innovations. At the same time traditional forms of carbon are being used in new and exciting applications that make our life safer, healthier, and more enjoyable. The 21st century may soon be recognized as the Age of Carbon forms. This educational talk will show how carbon, the fourth most abundant element in the Galaxy and the basis of life on Earth, was the engine of most important technological developments throughout the history of civilization. It will emphasize the ability of carbon atoms to generate a variety of mutual combinations and with many other chemical elements. These properties have placed carbon at the core of numerous inventions that define our civilization, while emerging new technologies open a rich path for value-added products in today’s market. -
Properties of Carbon the Atomic Element Carbon Has Very Diverse
Properties of Carbon The atomic element carbon has very diverse physical and chemical properties due to the nature of its bonding and atomic arrangement. fig. 1 Allotropes of Carbon Some allotropes of carbon: (a) diamond, (b) graphite, (c) lonsdaleite, (d–f) fullerenes (C60, C540, C70), (g) amorphous carbon, and (h) carbon nanotube. Carbon has several allotropes, or different forms in which it can exist. These allotropes include graphite and diamond, whose properties span a range of extremes. Despite carbon's ability to make 4 bonds and its presence in many compounds, it is highly unreactive under normal conditions. Carbon exists in 2 main isotopes: 12C and 13C. There are many other known isotopes, but they tend to be short-lived and have extremely short half-lives. Allotropes The different forms of a chemical element. Cabon is the chemical element with the symbol C and atomic number 6. As a member of group 14 on the periodic table, it is nonmetallic and tetravalent—making four electrons available to form covalent chemical bonds. Carbon has 6 protons and 6 Source URL: https://www.boundless.com/chemistry/nonmetallic-elements/carbon/properties-carbon/ Saylor URL: http://www.saylor.org/courses/chem102#6.1 Attributed to: Boundless www.saylor.org Page 1 of 2 neutrons, and has a standard atomic weight of 12.0107 amu. Its electron configuration is denoted as 1s22s22p2. It is a solid, and sublimes at 3,642 °C. It's oxidation state ranges from 4 to -4, and it has an electronegativity rating of 2.55 on the Pauling scale. Carbon has several allotropes, or different forms in which it exists. -
University of Groningen Discovery of a Eugenol Oxidase From
University of Groningen Discovery of a eugenol oxidase from Rhodococcus sp strain RHA1 Jin, J.F.; Mazon, H.; van den Heuvel, R.H.H.; Janssen, D.B.; Fraaije, M.W. Published in: Febs Journal DOI: 10.1111/j.1742-4658.2007.05767.x IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below. Document Version Publisher's PDF, also known as Version of record Publication date: 2007 Link to publication in University of Groningen/UMCG research database Citation for published version (APA): Jin, J. F., Mazon, H., van den Heuvel, R. H. H., Janssen, D. B., & Fraaije, M. W. (2007). Discovery of a eugenol oxidase from Rhodococcus sp strain RHA1. Febs Journal, 274(9), 2311 - 2321. https://doi.org/10.1111/j.1742-4658.2007.05767.x Copyright Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons). Take-down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum. Download date: 23-09-2021 Discovery of a eugenol oxidase from Rhodococcus sp. -
The Sociology of Music and Social Distinctions: P!NK's Career As an Example of Social Linkage
Digital Commons @ Assumption University Honors Theses Honors Program 2019 The Sociology of Music and Social Distinctions: P!NK's Career as an Example of Social Linkage David Cifarelli Assumption College Follow this and additional works at: https://digitalcommons.assumption.edu/honorstheses Part of the Music Commons, and the Social and Behavioral Sciences Commons Recommended Citation Cifarelli, David, "The Sociology of Music and Social Distinctions: P!NK's Career as an Example of Social Linkage" (2019). Honors Theses. 49. https://digitalcommons.assumption.edu/honorstheses/49 This Honors Thesis is brought to you for free and open access by the Honors Program at Digital Commons @ Assumption University. It has been accepted for inclusion in Honors Theses by an authorized administrator of Digital Commons @ Assumption University. For more information, please contact [email protected]. The Sociology of Music and Social Distinctions: P!NK’s Career as an Example of Social Linkage David Cifarelli Faculty Supervisor: Christopher Gilbert, Ph. D Department of English A Thesis Submitted to Fulfill the Requirements of the Honors Program at Assumption College Spring 2019 Cifarelli 1 Introduction Music is extremely social. It is one of the most expressive art forms our society holds. Due this expressive nature, the art of making music can hold many social connotations and directly involve or relate itself to social occurrences, movements and ideals. This intertwined relationship thus allows music to be a conductor of social change by existing and working within these various social constructs. In addition, those involved with the music-making business are, by association, also potential conductors of social change. -
Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 11
This PDF is available from The National Academies Press at http://www.nap.edu/catalog.php?record_id=13374 Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 11 ISBN Committee on Acute Exposure Guideline Levels; Committee on 978-0-309-25481-6 Toxicology; National Research Council 356 pages 6 x 9 PAPERBACK (2012) Visit the National Academies Press online and register for... Instant access to free PDF downloads of titles from the NATIONAL ACADEMY OF SCIENCES NATIONAL ACADEMY OF ENGINEERING INSTITUTE OF MEDICINE NATIONAL RESEARCH COUNCIL 10% off print titles Custom notification of new releases in your field of interest Special offers and discounts Distribution, posting, or copying of this PDF is strictly prohibited without written permission of the National Academies Press. Unless otherwise indicated, all materials in this PDF are copyrighted by the National Academy of Sciences. Request reprint permission for this book Copyright © National Academy of Sciences. All rights reserved. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 11 Committee on Acute Exposure Guideline Levels Committee on Toxicology Board on Environmental Studies and Toxicology Division on Earth and Life Studies Copyright © National Academy of Sciences. All rights reserved. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 11 THE NATIONAL ACADEMIES PRESS 500 FIFTH STREET, NW WASHINGTON, DC 20001 NOTICE: The project that is the subject of this report was approved by the Governing Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, the National Academy of Engineering, and the Insti- tute of Medicine. The members of the committee responsible for the report were chosen for their special competences and with regard for appropriate balance. -
Sp Carbon Chain Interaction with Silver Nanoparticles Probed by Surface Enhanced Raman Scattering
sp carbon chain interaction with silver nanoparticles probed by Surface Enhanced Raman Scattering A. Lucotti1, C. S. Casari2, M. Tommasini1, A. Li Bassi2, D. Fazzi1, V. Russo2, M. Del Zoppo1, C. Castiglioni1, F. Cataldo3, C. E. Bottani2, G. Zerbi1 1 Dipartimento di Chimica, Materiali e Ingegneria Chimica ‘G. Natta’ and NEMAS - Center for NanoEngineered MAterials and Surfaces, Politecnico di Milano, Piazza Leonardo da Vinci 32, I-20133 Milano, Italy 2 Dipartimento di Energia and NEMAS - Center for NanoEngineered MAterials and Surfaces, Politecnico di Milano, via Ponzio 34/3, I-20133 Milano, Italy 3 Actinium Chemical Research srl, via Casilina 1626/A, 00133 Roma, Italy and INAF – Osservatorio Astrofisico di Catania, Via S. Sofia 78, 95123 Catania, Italy Abstract Surface Enhanced Raman Spectroscopy (SERS) is exploited here to investigate the interaction of isolated sp carbon chains (polyynes) in a methanol solution with silver nanoparticles. Hydrogen-terminated polyynes show a strong interaction with silver colloids used as the SERS active medium revealing a chemical SERS effect. SERS spectra after mixing polyynes with silver colloids show a noticeable time evolution. Experimental results, supported by density functional theory (DFT) calculations of the Raman modes, allow us to investigate the behaviour and stability of polyynes of different lengths and the overall sp conversion towards sp2 phase. 1 2 1. Introduction Linear carbon chains with sp hybridization represent one of the simplest one dimensional systems and have therefore attracted a great interest for many years [1, 2]. sp chains can display two types of carbon-carbon bonding: polyynes, chains with single-triple alternating bonds (…-C≡C- C≡C-…) and polycumulenes, chains with all double bonds (…=C=C=C=…). -
Agricultural Soil Carbon Credits: Making Sense of Protocols for Carbon Sequestration and Net Greenhouse Gas Removals
Agricultural Soil Carbon Credits: Making sense of protocols for carbon sequestration and net greenhouse gas removals NATURAL CLIMATE SOLUTIONS About this report This synthesis is for federal and state We contacted each carbon registry and policymakers looking to shape public marketplace to ensure that details investments in climate mitigation presented in this report and through agricultural soil carbon credits, accompanying appendix are accurate. protocol developers, project developers This report does not address carbon and aggregators, buyers of credits and accounting outside of published others interested in learning about the protocols meant to generate verified landscape of soil carbon and net carbon credits. greenhouse gas measurement, reporting While not a focus of the report, we and verification protocols. We use the remain concerned that any end-use of term MRV broadly to encompass the carbon credits as an offset, without range of quantification activities, robust local pollution regulations, will structural considerations and perpetuate the historic and ongoing requirements intended to ensure the negative impacts of carbon trading on integrity of quantified credits. disadvantaged communities and Black, This report is based on careful review Indigenous and other communities of and synthesis of publicly available soil color. Carbon markets have enormous organic carbon MRV protocols published potential to incentivize and reward by nonprofit carbon registries and by climate progress, but markets must be private carbon crediting marketplaces. paired with a strong regulatory backing. Acknowledgements This report was supported through a gift Conservation Cropping Protocol; Miguel to Environmental Defense Fund from the Taboada who provided feedback on the High Meadows Foundation for post- FAO GSOC protocol; Radhika Moolgavkar doctoral fellowships and through the at Nori; Robin Rather, Jim Blackburn, Bezos Earth Fund. -
Unique Properties of Water!
Name: _______ANSWER KEY_______________ Class: _____ Date: _______________ Unique Properties of Water! Word Bank: Adhesion Evaporation Polar Surface tension Cohesion Freezing Positive Universal solvent Condensation Melting Sublimation Dissolve Negative 1. The electrons are not shared equally between the hydrogen and oxygen atoms of water creating a Polar molecule. 2. The polarity of water allows it to dissolve most substances. Because of this it is referred to as the universal solvent 3. Water molecules stick to other water molecules. This property is called cohesion. 4. Hydrogen bonds form between adjacent water molecules because the positive charged hydrogen end of one water molecule attracts the negative charged oxygen end of another water molecule. 5. Water molecules stick to other materials due to its polar nature. This property is called adhesion. 6. Hydrogen bonds hold water molecules closely together which causes water to have high surface tension. This is why water tends to clump together to form drops rather than spread out into a thin film. 7. Condensation is when water changes from a gas to a liquid. 8. Sublimation is when water changes from a solid directly to a gas. 9. Freezing is when water changes from a liquid to a solid. 10. Melting is when water changes from a solid to a liquid. 11. Evaporation is when water changes from a liquid to a gas. 12. Why does ice float? Water expands as it freezes, so it is LESS DENSE AS A SOLID. 13. What property refers to water molecules resembling magnets? How are these alike? Polar bonds create positive and negative ends of the molecule. -
Algorithmic Analysis of Chemical Dynamics of the Autoignition of NH3–H2O2/Air Mixtures
energies Article Algorithmic Analysis of Chemical Dynamics of the Autoignition of NH3–H2O2/Air Mixtures Ahmed T. Khalil 1,2, Dimitris M. Manias 3, Efstathios-Al. Tingas 4, Dimitrios C. Kyritsis 1,2,* and Dimitris A. Goussis 1,2 1 Department of Mechanical Engineering, Khalifa University of Science and Technology, Abu Dhabi 127788, UAE; [email protected] (A.T.K.); [email protected] (D.A.G.) 2 Research and Innovation Center on CO2 and H2 (RICH), Khalifa University of Science and Technology, P.O. Box 127788, Abu Dhabi, UAE 3 Department of Mechanics, School of Applied Mathematics and Physical Sciences, National Technical University of Athens, 157 73 Athens, Greece; [email protected] 4 Perth College, University of the Highlands and Islands, (UHI), Perth PH1 2NX, UK; [email protected] * Correspondence: [email protected] Received: 8 September 2019; Accepted: 7 October 2019; Published: 21 November 2019 Abstract: The dynamics of a homogeneous adiabatic autoignition of an ammonia/air mixture at constant volume was studied, using the algorithmic tools of Computational Singular Perturbation. Since ammonia combustion is characterized by both unrealistically long ignition delays and elevated NOx emissions, the time frame of action of the modes that are responsible for ignition was analyzed by calculating the developing time scales throughout the process and by studying their possible relation to NOx emissions. The reactions that support or oppose the explosive time scale were identified, along with the variables that are related the most to the dynamics that drive the system to an explosion. -
Interaction of Ozone and Hydrogen Peroxide in Water Implications For
UC Irvine Faculty Publications Title Interaction of ozone and hydrogen peroxide in water: Implications for analysis of H 2 O 2 in air Permalink https://escholarship.org/uc/item/7j7454z7 Journal Geophysical Research Letters, 9(3) ISSN 00948276 Authors Zika, R. G Saltzman, E. S Publication Date 1982-03-01 DOI 10.1029/GL009i003p00231 License https://creativecommons.org/licenses/by/4.0/ 4.0 Peer reviewed eScholarship.org Powered by the California Digital Library University of California GEOPHYSICLARESEARCH LETTERS, VOL. 9, NO. 3, PAGES231-234 , MARCH1982 INTERACTION OF OZONE AND HYDROGEN PEROXIDE IN WATER: IMPLICATIONSFORANALYSIS oFH20 2 IN AIR R.G. Zika and E.S. Saltzman Division of Marine and Atmospheric Chemistry, University of Miami, Miami, Florida 331#9 Abstract. We have attempted to measure gaseous Analytical Methods H202 in air usingan aqueoustrapping method. With continuousbubbling, H 20 2 levels in the traps reacheda a. Hydrogen Peroxide. Hydrogen peroxide in aqueous plateau, indicating that a state of dynamic equilibrium solution was measured using a modified fluorescence involving H202 destrbction was established. We decay technique [Perschke and Broda, 1976; Zika and attribute this behavior to the interaction of ozone and its Zelmer, 1982]. The method involved the addition of a decompositionproducts (OH, O[) withH 20 2 inacld:•ous known amot•at of scopoletin (6-methyl-7-hydroxyl-i,2- solution. This hypothesis was investigated by replacing benzopyrone)to a pH 7.0 phosphatebuffered. sample. the air stream with a mixture of N2, 02 and 0 3. The The sample was prepared bY diluting an aliquot of the results Of this experiment show that H O was both reaction solution to 20 mls with low contaminant producedand destroyedin the traps.