Argon Fire Extinguishing Systems - the Simple Solution Wolfgang Koch C/O Minimax Gmbh Industriestr
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Smoke Alarms in US Home Fires Marty Ahrens February 2021
Smoke Alarms in US Home Fires Marty Ahrens February 2021 Copyright © 2021 National Fire Protection Association® (NFPA®) Key Findings Smoke alarms were present in three-quarters (74 percent) of the injuries from fires in homes with smoke alarms occurred in properties reported homei fires in 2014–2018. Almost three out of five home with battery-powered alarms. When present, hardwired smoke alarms fire deathsii were caused by fires in properties with no smoke alarms operated in 94 percent of the fires considered large enough to trigger a (41 percent) or smoke alarms that failed to operate (16 percent). smoke alarm. Battery-powered alarms operated 82 percent of the time. Missing or non-functional power sources, including missing or The death rate per 1,000 home structure fires is 55 percent lower in disconnected batteries, dead batteries, and disconnected hardwired homes with working smoke alarms than in homes with no alarms or alarms or other AC power issues, were the most common factors alarms that fail to operate. when smoke alarms failed to operate. Of the fire fatalities that occurred in homes with working smoke Compared to reported home fires with no smoke alarms or automatic alarms, 22 percent of those killed were alerted by the device but extinguishing systems (AES) present, the death rate per 1,000 reported failed to respond, while 11 percent were not alerted by the operating fires was as follows: alarm. • 35 percent lower when battery-powered smoke alarms were People who were fatally injured in home fires with working smoke present, but AES was not, alarms were more likely to have been in the area of origin and • 51 percent lower when smoke alarms with any power source involved in the ignition, to have a disability, to be at least 65 years were present but AES was not, old, to have acted irrationally, or to have tried to fight the fire themselves. -
And Abiogenesis
Historical Development of the Distinction between Bio- and Abiogenesis. Robert B. Sheldon NASA/MSFC/NSSTC, 320 Sparkman Dr, Huntsville, AL, USA ABSTRACT Early greek philosophers laid the philosophical foundations of the distinction between bio and abiogenesis, when they debated organic and non-organic explanations for natural phenomena. Plato and Aristotle gave organic, or purpose-driven explanations for physical phenomena, whereas the materialist school of Democritus and Epicurus gave non-organic, or materialist explanations. These competing schools have alternated in popularity through history, with the present era dominated by epicurean schools of thought. Present controversies concerning evidence for exobiology and biogenesis have many aspects which reflect this millennial debate. Therefore this paper traces a selected history of this debate with some modern, 20th century developments due to quantum mechanics. It ¯nishes with an application of quantum information theory to several exobiology debates. Keywords: Biogenesis, Abiogenesis, Aristotle, Epicurus, Materialism, Information Theory 1. INTRODUCTION & ANCIENT HISTORY 1.1. Plato and Aristotle Both Plato and Aristotle believed that purpose was an essential ingredient in any scienti¯c explanation, or teleology in philosophical nomenclature. Therefore all explanations, said Aristotle, answer four basic questions: what is it made of, what does it represent, who made it, and why was it made, which have the nomenclature material, formal, e±cient and ¯nal causes.1 This aristotelean framework shaped the terms of the scienti¯c enquiry, invisibly directing greek science for over 500 years. For example, \organic" or \¯nal" causes were often deemed su±cient to explain natural phenomena, so that a rock fell when released from rest because it \desired" its own kind, the earth, over unlike elements such as air, water or ¯re. -
Identification of a Chemical Fingerprint Linking the Undeclared 2017 Release of 106Ru to Advanced Nuclear Fuel Reprocessing
Identification of a chemical fingerprint linking the undeclared 2017 release of 106Ru to advanced nuclear fuel reprocessing Michael W. Cookea,1, Adrian Bottia, Dorian Zokb, Georg Steinhauserb, and Kurt R. Ungara aRadiation Protection Bureau, Health Canada, Ottawa, ON K1A 1C1, Canada; and bInstitute of Radioecology and Radiation Protection, Leibniz Universität Hannover, 30419 Hannover, Germany Edited by Kristin Bowman-James, University of Kansas, Lawrence, KS, and accepted by Editorial Board Member Marcetta Y. Darensbourg May 1, 2020 (received for review February 7, 2020) The undeclared release and subsequent detection of ruthenium- constitutes the identification of unique signatures. From a radiologi- 106 (106Ru) across Europe from late September to early October of cal perspective, there is none. Samples have been shown to be radi- 2017 prompted an international effort to ascertain the circum- opure and to carry the stable ruthenium isotopic signature of civilian stances of the event. While dispersion modeling, corroborated spent nuclear fuel (10), while stable elemental analysis by scanning by ground deposition measurements, has narrowed possible loca- electron microscopy and neutron activation has revealed no detect- tions of origin, there has been a lack of direct empirical evidence to able anomalies compared to aerosol filter media sampled prior to the address the nature of the release. This is due to the absence of advent of the 106Ru contaminant (1, 11). We are, then, left with the radiological and chemical signatures in the sample matrices, con- definition of a limiting case for a nuclear forensic investigation. sidering that such signatures encode the history and circumstances Fortunately, we are concerned with an element that has sig- of the radioactive contaminant. -
Laser Technology Smoke Detector
APPLICATIONS GUIDE Laser Technology Smoke Detector APPLICATIONS GUIDE Laser Technology Smoke Detector Contents Section 1 Introduction .....................................................................................................................................................................2 Section 2 Benefits ............................................................................................................................................................................2 Section 3 Applications ....................................................................................................................................................................2 Ideal Applications ..........................................................................................................................................................2 Applications to Avoid ....................................................................................................................................................2 Section 4 How it Works ..................................................................................................................................................................3 The Principles of Laser Detection...............................................................................................................................3 Section 5 Performance ...................................................................................................................................................................4 -
Fire Service Features of Buildings and Fire Protection Systems
Fire Service Features of Buildings and Fire Protection Systems OSHA 3256-09R 2015 Occupational Safety and Health Act of 1970 “To assure safe and healthful working conditions for working men and women; by authorizing enforcement of the standards developed under the Act; by assisting and encouraging the States in their efforts to assure safe and healthful working conditions; by providing for research, information, education, and training in the field of occupational safety and health.” This publication provides a general overview of a particular standards- related topic. This publication does not alter or determine compliance responsibilities which are set forth in OSHA standards and the Occupational Safety and Health Act. Moreover, because interpretations and enforcement policy may change over time, for additional guidance on OSHA compliance requirements the reader should consult current administrative interpretations and decisions by the Occupational Safety and Health Review Commission and the courts. Material contained in this publication is in the public domain and may be reproduced, fully or partially, without permission. Source credit is requested but not required. This information will be made available to sensory-impaired individuals upon request. Voice phone: (202) 693-1999; teletypewriter (TTY) number: 1-877-889-5627. This guidance document is not a standard or regulation, and it creates no new legal obligations. It contains recommendations as well as descriptions of mandatory safety and health standards. The recommendations are advisory in nature, informational in content, and are intended to assist employers in providing a safe and healthful workplace. The Occupational Safety and Health Act requires employers to comply with safety and health standards and regulations promulgated by OSHA or by a state with an OSHA-approved state plan. -
Viscosity of Gases References
VISCOSITY OF GASES Marcia L. Huber and Allan H. Harvey The following table gives the viscosity of some common gases generally less than 2% . Uncertainties for the viscosities of gases in as a function of temperature . Unless otherwise noted, the viscosity this table are generally less than 3%; uncertainty information on values refer to a pressure of 100 kPa (1 bar) . The notation P = 0 specific fluids can be found in the references . Viscosity is given in indicates that the low-pressure limiting value is given . The dif- units of μPa s; note that 1 μPa s = 10–5 poise . Substances are listed ference between the viscosity at 100 kPa and the limiting value is in the modified Hill order (see Introduction) . Viscosity in μPa s 100 K 200 K 300 K 400 K 500 K 600 K Ref. Air 7 .1 13 .3 18 .5 23 .1 27 .1 30 .8 1 Ar Argon (P = 0) 8 .1 15 .9 22 .7 28 .6 33 .9 38 .8 2, 3*, 4* BF3 Boron trifluoride 12 .3 17 .1 21 .7 26 .1 30 .2 5 ClH Hydrogen chloride 14 .6 19 .7 24 .3 5 F6S Sulfur hexafluoride (P = 0) 15 .3 19 .7 23 .8 27 .6 6 H2 Normal hydrogen (P = 0) 4 .1 6 .8 8 .9 10 .9 12 .8 14 .5 3*, 7 D2 Deuterium (P = 0) 5 .9 9 .6 12 .6 15 .4 17 .9 20 .3 8 H2O Water (P = 0) 9 .8 13 .4 17 .3 21 .4 9 D2O Deuterium oxide (P = 0) 10 .2 13 .7 17 .8 22 .0 10 H2S Hydrogen sulfide 12 .5 16 .9 21 .2 25 .4 11 H3N Ammonia 10 .2 14 .0 17 .9 21 .7 12 He Helium (P = 0) 9 .6 15 .1 19 .9 24 .3 28 .3 32 .2 13 Kr Krypton (P = 0) 17 .4 25 .5 32 .9 39 .6 45 .8 14 NO Nitric oxide 13 .8 19 .2 23 .8 28 .0 31 .9 5 N2 Nitrogen 7 .0 12 .9 17 .9 22 .2 26 .1 29 .6 1, 15* N2O Nitrous -
The Rising Cost of Wildfire Protection
A Research Paper by The Rising Cost of Wildfire Protection Ross Gorte, Ph.D. Retired Senior Policy Analyst, Congressional Research Service Affiliate Research Professor, Earth Systems Research Center of the Earth, Oceans, and Space Institute, University of New Hampshire June 2013 The Rising Cost of Wildfire Protection June 2013 PUBLISHED ONLINE: http://headwaterseconomics.org/wildfire/fire-costs-background/ ABOUT THIS REPORT Headwaters Economics produced this report to better understand and address why wildfires are becoming more severe and expensive. The report also describes how the protection of homes in the Wildland-Urban Interface has added to these costs and concludes with a brief discussion of solutions that may help control escalating costs. Headwaters Economics is making a long-term commitment to better understanding these issues. For additional resources, see: http://headwaterseconomics.org/wildfire. ABOUT HEADWATERS ECONOMICS Headwaters Economics is an independent, nonprofit research group whose mission is to improve community development and land management decisions in the West. CONTACT INFORMATION Ray Rasker, Ph.D. Executive Director, Headwaters Economics [email protected] 406 570-7044 Ross Gorte, Ph.D.: http://www.eos.unh.edu/Faculty/rosswgorte P.O. Box 7059 Bozeman, MT 59771 http://headwaterseconomics.org Cover image “Firewise” by Monte Dolack used by permission, Monty Dolack Gallery, Missoula Montana. TABLE OF CONTENTS SUMMARY ................................................................................................................................................. -
Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Ions
J. Phys. Chem. A 2000, 104, 3655-3669 3655 Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Ions. 5. PAHs Incorporating a Cyclopentadienyl Ring† D. M. Hudgins,* C. W. Bauschlicher, Jr., and L. J. Allamandola NASA Ames Research Center, MS 245-6, Moffett Field, California 94035 J. C. Fetzer CheVron Research Company, Richmond, California 94802 ReceiVed: NoVember 5, 1999; In Final Form: February 9, 2000 The matrix-isolation technique has been employed to measure the mid-infrared spectra of the ions of several polycyclic aromatic hydrocarbons whose structures incorporate a cyclopentadienyl ring. These include the cations of fluoranthene (C16H10), benzo[a]fluoranthene, benzo[b]fluoranthene, benzo[j]fluoranthene, and benzo- [k]fluoranthene (all C20H12 isomers), as well as the anions of benzo[a]fluoranthene and benzo[j]fluoranthene. With the exception of fluoranthene, which presented significant theoretical difficulties, the experimental data are compared to theoretically calculated values obtained using density functional theory (DFT) at the B3LYP/ 4-31G level. In general, there is good overall agreement between the two data sets, with the positional agreement between the experimentally measured and theoretically predicted bands somewhat better than that associated with their intensities. The results are also consistent with previous experimental studies of polycyclic aromatic hydrocarbon ions. Specifically, in both the cationic and anionic species the strongest ion bands typically cluster in the 1450 to 1300 cm-1 range, reflecting an order-of-magnitude enhancement in the CC stretching and CH in-plane bending modes between 1600 and 1100 cm-1 in these species. The aromatic CH out-of- plane bending modes, on the other hand, are usually modestly suppressed (e 2x - 5x) in the cations relative to those of the neutral species, with the nonadjacent CH modes most strongly affected. -
Measurement of Cp/Cv for Argon, Nitrogen, Carbon Dioxide and an Argon + Nitrogen Mixture
Measurement of Cp/Cv for Argon, Nitrogen, Carbon Dioxide and an Argon + Nitrogen Mixture Stephen Lucas 05/11/10 Measurement of Cp/Cv for Argon, Nitrogen, Carbon Dioxide and an Argon + Nitrogen Mixture Stephen Lucas With laboratory partner: Christopher Richards University College London 5th November 2010 Abstract: The ratio of specific heats, γ, at constant pressure, Cp and constant volume, Cv, have been determined by measuring the oscillation frequency when a ball bearing undergoes simple harmonic motion due to the gravitational and pressure forces acting upon it. The γ value is an important gas property as it relates the microscopic properties of the molecules on a macroscopic scale. In this experiment values of γ were determined for input gases: CO2, Ar, N2, and an Ar + N2 mixture in the ratio 0.51:0.49. These were found to be: 1.1652 ± 0.0003, 1.4353 ± 0.0003, 1.2377 ± 0.0001and 1.3587 ± 0.0002 respectively. The small uncertainties in γ suggest a precise procedure while the discrepancy between experimental and accepted values indicates inaccuracy. Systematic errors are suggested; however it was noted that an average discrepancy of 0.18 between accepted and experimental values occurred. If this difference is accounted for, it can be seen that we measure lower vibrational contributions to γ at room temperature than those predicted by the equipartition principle. It can be therefore deduced that the classical idea of all modes contributing to γ is incorrect and there is actually a „freezing out‟ of vibrational modes at lower temperatures. I. Introduction II. Method The primary objective of this experiment was to determine the ratio of specific heats, γ, for gaseous Ar, N2, CO2 and an Ar + N2 mixture. -
Liquid Argon
Safetygram 8 Liquid argon Liquid argon is tasteless, colorless, odorless, noncorrosive, nonflammable, and extremely cold. Belonging to the family of rare gases, argon is the most plentiful, making up approximately 1% of the earth’s atmosphere. It is monatomic and extremely inert, forming no known chemical compounds. Since argon is inert, special materials of construction are not required. However, materials of construction must be selected to withstand the low temperature of liquid argon. Vessels and piping should be designed to American Society of Mechanical Engineers (ASME) specifications or the Department of Transportation (DOT) codes for the pressures and temperatures involved. Although used more commonly in the gaseous state, argon is commonly stored and transported as a liquid, affording a more cost-effective way of providing product supply. Liquid argon is a cryogenic liquid. Cryogenic liquids are liquefied gases that have a normal boiling point below –130°F (–90°C). Liquid argon has a boiling point of –303°F (–186°C). The temperature difference between the product and the surrounding environment, even in winter, is substantial. Keeping this surrounding heat from the product requires special equipment to store and handle cryogenic liquids. A typical system consists of the following components: a cryogenic storage tank, one or more vaporizers, a pressure control system, and all of the piping required for fill, vaporization. The cryogenic tank is constructed, in principle, like a vacuum bottle. It is designed to keep heat away from the liquid that is contained in the inner vessel. Vaporizers convert the liquid argon to its gaseous state. A pressure control manifold controls the pressure at which the gas is fed to the process. -
Insight Gaseous Fire Suppression System
Insight Balanced Risk Engineering Solutions Gaseous Fire Suppression System All businesses are reliant on computer technology in order to survive today. What if there was a fire in the main computer room. Would it put you out of business? Would it impact on sales & profits? If the answer is yes then you need to evaluate computer room and other critical area fire protection measures in order to ensure that they are adequate. What are the consequences to business survival and employee security? We are all too aware of businesses which have had fires and have failed to restart. All commercial premises now use computers and other high tech electronic systems in order to record sales, purchases, financial information, control production, allow communication and facilitate email correspondence - the modern way of conducting business. Gaseous fire suppression systems are particularly applicable for high value risks where a minor fire within a critical area could have serious financial repercussions for the business far beyond the cost of physical damage and lost production. System Operation Types of Gaseous Fire Suppression Systems Gaseous fire suppression system activation can be There are two main types of gaseous fire suppression manual, automatic or auto/manual. Gas is discharged systems comprising inert gas and chemical agents. The through a pipe network system and enters the protected main agents that are encountered today include: environment through appropriately designed spray nozzles. • Inergen • Argonite Gaseous fire suppression systems when designed and • FM 200 installed correctly should ensure that high value assets are protected from fire and the effects of fire fighting. -
Periodic Trends in the Main Group Elements
Chemistry of The Main Group Elements 1. Hydrogen Hydrogen is the most abundant element in the universe, but it accounts for less than 1% (by mass) in the Earth’s crust. It is the third most abundant element in the living system. There are three naturally occurring isotopes of hydrogen: hydrogen (1H) - the most abundant isotope, deuterium (2H), and tritium 3 ( H) which is radioactive. Most of hydrogen occurs as H2O, hydrocarbon, and biological compounds. Hydrogen is a colorless gas with m.p. = -259oC (14 K) and b.p. = -253oC (20 K). Hydrogen is placed in Group 1A (1), together with alkali metals, because of its single electron in the valence shell and its common oxidation state of +1. However, it is physically and chemically different from any of the alkali metals. Hydrogen reacts with reactive metals (such as those of Group 1A and 2A) to for metal hydrides, where hydrogen is the anion with a “-1” charge. Because of this hydrogen may also be placed in Group 7A (17) together with the halogens. Like other nonmetals, hydrogen has a relatively high ionization energy (I.E. = 1311 kJ/mol), and its electronegativity is 2.1 (twice as high as those of alkali metals). Reactions of Hydrogen with Reactive Metals to form Salt like Hydrides Hydrogen reacts with reactive metals to form ionic (salt like) hydrides: 2Li(s) + H2(g) 2LiH(s); Ca(s) + H2(g) CaH2(s); The hydrides are very reactive and act as a strong base. It reacts violently with water to produce hydrogen gas: NaH(s) + H2O(l) NaOH(aq) + H2(g); It is also a strong reducing agent and is used to reduce TiCl4 to titanium metal: TiCl4(l) + 4LiH(s) Ti(s) + 4LiCl(s) + 2H2(g) Reactions of Hydrogen with Nonmetals Hydrogen reacts with nonmetals to form covalent compounds such as HF, HCl, HBr, HI, H2O, H2S, NH3, CH4, and other organic and biological compounds.