413-SMAN-E-4352-V4.0, Layout 1

Total Page:16

File Type:pdf, Size:1020Kb

413-SMAN-E-4352-V4.0, Layout 1 Easy-Loading Thermal Printer GPT-4352(-60) GeBE Documen t No.: SMAN-E-41 3-V4.0 Printed: 09.07.20 07 Status: 18.01.2005 German: SMAN-D-4 12 Op e rati n g Ma n u a l A ctiv iti es at GeB E Printer: GeBE Elektr onik und Feinwerktechnik GmbH • E-Mail: [email protected] • www.oem-printer .com Key boards: GeBE Computer & Peripherie GmbH • E-Mail: [email protected] • www.tastatur en.com Inter net applications: www.GeBE.net The GeB E log o is a reg iste red trad em ark of GeB E Ele ktro nik und Feinwer kte chnik GmbH. All other bra nds nam ed in this bro chure ar e pro perties of the respec tive compan ies. Erro rs and change s res erv ed. The tec hnic al data given are non-co mm itta l informa tion and do not rep res ent any ass ura nc e of certain feature s. Our terms of pay me nt and del ivery app ly. Copyrig ht © 200 7 GeBE Ele ktro nik und Feinwer kte chnik Gm bH. All rights res erv ed. GeBE Elektr onik und Feinwerktechnik GmbH Beethovenstr. 15 • Germering • Germany • www.oem-printer .com Phone:++49 (0) 89/894141-0 • Fax:++49 (0) 89/8402168 • email: [email protected] GeBE E + F Gm bH • www .oe m- printe r .co m • GeBE Dok.N r .: SM AN-E- 413-V4 .0 Easy-L oad ing The rm al Printe r GPT-43 52( -60) 2 C onte nt 1 C onte nt 1 Con ten t 2 13 Option Mag netic Card Rea der 19 2 Saf ety Instruc tions 3 14 Charac ter Sets 20 14.1 GeBE Sta ndar d Charact er Set 20 3 Pac king List 4 14.2 Optiona l Cha rac ter Set s 20 4 Inst allation 5 15 4.1 Inst allation in a front panel 5 4.2 Par tial inst alla tion in plastic cas ing 5 16 Options Access orie s 22 4.3 Exa mple for inst alla tion and applica tion 5 16.1 Option s 22 16.2 Access ories 22 5 Con necting the Printer 6 16.2 .1 Mount ing fram es 22 5.1 Con necting the power sup ply (1) 6 16.2.2 Paper 22 5.2 Pow er Down (2) 6 16.2 .3 Power sup plies and char ging dev ices 22 5.3 Con necting the Char ger (3) 6 16.2 .4 Batteri es 22 16.2 .5 Cables 22 6 Prin ter Con figurati on 7 6.1 Con figu ration ove r Initi alisatio n-T extP r ese rve 7 17 Ser vice 22 6.2 Ent ries into the "TIN IT" 7 6.3 Sold er Brid ges 7 18 CE Certific atio n 23 7 Inte rfac es 8 19 Tech nica l Data 24 7.1 Ser ial Inte rfac e 8 7.1. 1 Ser ial inte rfac e RS232 (V.24) at connec tor J2 8 20 Mec hanical Dimens ions 24 7.1. 2 Tim ing der serielle n RS232 /TT L Sch nittstel le 8 7.2 Par alle l Interfac e 9 7.2. 1 Centr onic s Ada pter 9 7.2. 2 PIN-sei zure at the SUB-D 25 of the adapte r 9 7.2. 3 Tim ing of the Par allel Inte rfac e 9 7.3 Infrar ed Interfac es 10 7.4 US B 11 7.5 Blu eto oth® Wireles s Tech nolo gy 12 8 Ope rati on 13 8.1 Wh ich therma l paper is suit able ? 13 9 Key Functio ns 14 10 OPD-Menue® 15 11 Sta tus Mes sages 17 12 Bat ch File s 18 GeBE E + F GmbH • www .oe m- pri nter .co m • GeBE Do k.Nr .: SM AN-E- 413-V4 .0 Easy-L oad ing The rm al Printe r GPT-43 52(-60 ) Sa fety Inst ruct io ns 3 2 Safe ty In st ruct io ns Read ope rati ng manua l befor e ope rati on! During inst allation : Always disconn ect the power . Safe ope ration of this dev ice is only warrant eed , if the instruct ions in this operatin g man ual have been complie d with . Usage in accor dan ce with the ope rating man ual is requ ir ed for produ ct warrant y . If the user atte mpts to r epair the pr oduct, all factory war ranties will be null and void . Only use man ufactur er's par ts and acc essorie s! Mak e sure that the prin ter is saved against ove rvoltage after EN/IEC 609 50. • The device may only be opened or repair ed by autho- rized personal. Never open the device or carry out re- pairs yourself. Always contact an authorized technical servicer. You can find all necessary service information in the chapter "Service and Maintenance". • It is no longer possible to safely operate the device, if: • Before the device is tur ned on, make sure that the - the housing has been damaged. system voltage of your installation matches the supply - moisture r eached the inside of the device voltage of the device. The device characteristics are - smoke is coming from the inside of the device printed on the name plate and in the technical data. - the power supply cord is damaged - The name plate is located on the underside of the -the device stopped working properly . device. Tur n off the device immediately, when a failure occurs, as - For the technical data of the device, r efer to the mentioned above, and contact GeBE customer service. chapter "Technical Data". See chapter "Service and Maintenance". • The peripheral devices that are connected to the inter- •W e explicitly state that all product liability and guaratee faces and the DC cir cuits of this device have to meet claims are null and void, if the device has not been used the requir ements for safety extra-low voltage (SELV) in in accor dance with the instructions in this operating ma- accordance with EN/IEC 60950. nual or on the device itself! • Switching off the device does not completely discon- nect it from the power supply. Your device is only dis- connected completely, when the power plug is unplug- ged. • Please make sure that the power supply cable is run • Risk of explosion in case of incorrect battery exchange. in a way that nobody trips over it, and it cannot be da- • Please read how to safely exchange batteries in the maged by other devices. chapter "Exchanging Batteries". L as er K la ss e I • During operation, surfaces in the surrounding area of the print head may heat up. Therefor e, dir ect contact • The printer versions with an infrared interface contain a with the print head must be avoided to prevent bur ning light emitting diode of laser category I. This infrared accidents. transmitter does not pose a threat for the human eye or Do not put heat sensitive objects close to this heat skin, even with long periods of exposure. source. • The device complies with laser category I in accor dan- • Avoid constant high humidity and condensation. Pro- ce with EN60825-1/A2:2001 tect the device from being splashed and from getting in • It is pr ohibited to operate the device, if the housing is contact with chemicals. damaged. Please contact GeBE Service. You can find • Only use spare parts and accessories supplied or the information under "Service and Maintenance". For authorized by GeBE. The use of unauthorized parts or the description of the infrared interface, please r efer to accessories may affect the function and safety of the page 10. device. All parts included are listed in the chapter "Pa- cking List", while the original accessories are listed in the chapter "Parts and Accessories ". GeBE E + F GmbH • www .oe m- printe r .co m • GeBE Dok.N r .: SMAN -E-413 -V4.0 Eas y-Load ing The rmal Pri nter GPT-43 52( -60 ) 4 Pac ki ng Li st 3 P ac king List All printer sets GPT-4352(-60) contain: - tanspar ent LEVER (exchangeable) - 5 paper r olls: GPR-T01-058-031-007-060A resp. GPR-T01-058-060-007-0 60A for GPT-4352-60 - operating manual: SMAN-E-413 In addition the differ ent sets contain: GPT-4352 GPT-4352-60 SET1 GPT-4352-LV-82-24 -LC-at SET1 GPT-4352-60-LV-82 -24-LC- at • GKA-406: RS232 interface cabel, 500 mm • GKA-406: RS232 interface cabel, 500 mm • GKA-410: Power cable, • GKA-410: Power cable, one side open, 250 mm one side open, 250 mm SET2 GPT-4352-LV-82-24-V.24-EVAL-at SET2 GPT-4352-60-LV-82-24-V.24-EVAL-at • GKA-406: RS-232 interface cable 500 mm • GKA-406: RS-232 interface cable 500 mm • GKA-416: Connecting cable for charger, • GKA-416: Connecting cable for charger, 190 mm 190 mm • GNA-4,8V-1,6Ah-NiMH : Battery, • GNA-4,8V-1,6Ah-NiMH : Battery, 4x Mignon (AA) 4x Mignon (AA) • GNG-6V-0,8A-U : Charge r • GNG-6V-0,8A-U : Charge r SET3 GPT-43 52- LV-82- 24- SPI(4,5 V)-EVAL -at SET3 GPT-43 52- 60-LV- 82- 24-SPI (4,5 V)-EVAL -at • GKA-407: Connecting cable 12pol.
Recommended publications
  • Nerve Agent - Lntellipedia Page 1 Of9 Doc ID : 6637155 (U) Nerve Agent
    This document is made available through the declassification efforts and research of John Greenewald, Jr., creator of: The Black Vault The Black Vault is the largest online Freedom of Information Act (FOIA) document clearinghouse in the world. The research efforts here are responsible for the declassification of MILLIONS of pages released by the U.S. Government & Military. Discover the Truth at: http://www.theblackvault.com Nerve Agent - lntellipedia Page 1 of9 Doc ID : 6637155 (U) Nerve Agent UNCLASSIFIED From lntellipedia Nerve Agents (also known as nerve gases, though these chemicals are liquid at room temperature) are a class of phosphorus-containing organic chemicals (organophosphates) that disrupt the mechanism by which nerves transfer messages to organs. The disruption is caused by blocking acetylcholinesterase, an enzyme that normally relaxes the activity of acetylcholine, a neurotransmitter. ...--------- --- -·---- - --- -·-- --- --- Contents • 1 Overview • 2 Biological Effects • 2.1 Mechanism of Action • 2.2 Antidotes • 3 Classes • 3.1 G-Series • 3.2 V-Series • 3.3 Novichok Agents • 3.4 Insecticides • 4 History • 4.1 The Discovery ofNerve Agents • 4.2 The Nazi Mass Production ofTabun • 4.3 Nerve Agents in Nazi Germany • 4.4 The Secret Gets Out • 4.5 Since World War II • 4.6 Ocean Disposal of Chemical Weapons • 5 Popular Culture • 6 References and External Links --------------- ----·-- - Overview As chemical weapons, they are classified as weapons of mass destruction by the United Nations according to UN Resolution 687, and their production and stockpiling was outlawed by the Chemical Weapons Convention of 1993; the Chemical Weapons Convention officially took effect on April 291997. Poisoning by a nerve agent leads to contraction of pupils, profuse salivation, convulsions, involuntary urination and defecation, and eventual death by asphyxiation as control is lost over respiratory muscles.
    [Show full text]
  • Warning: the Following Lecture Contains Graphic Images
    What the новичок (Novichok)? Why Chemical Warfare Agents Are More Relevant Than Ever Matt Sztajnkrycer, MD PHD Professor of Emergency Medicine, Mayo Clinic Medical Toxicologist, Minnesota Poison Control System Medical Director, RFD Chemical Assessment Team @NoobieMatt #ITLS2018 Disclosures In accordance with the Accreditation Council for Continuing Medical Education (ACCME) Standards, the American Nurses Credentialing Center’s Commission (ANCC) and the Commission on Accreditation for Pre-Hospital Continuing Education (CAPCE), states presenters must disclose the existence of significant financial interests in or relationships with manufacturers or commercial products that may have a direct interest in the subject matter of the presentation, and relationships with the commercial supporter of this CME activity. The presenter does not consider that it will influence their presentation. Dr. Sztajnkrycer does not have a significant financial relationship to report. Dr. Sztajnkrycer is on the Editorial Board of International Trauma Life Support. Specific CW Agents Classes of Chemical Agents: The Big 5 The “A” List Pulmonary Agents Phosgene Oxime, Chlorine Vesicants Mustard, Phosgene Blood Agents CN Nerve Agents G, V, Novel, T Incapacitating Agents Thinking Outside the Box - An Abbreviated List Ammonia Fluorine Chlorine Acrylonitrile Hydrogen Sulfide Phosphine Methyl Isocyanate Dibotane Hydrogen Selenide Allyl Alcohol Sulfur Dioxide TDI Acrolein Nitric Acid Arsine Hydrazine Compound 1080/1081 Nitrogen Dioxide Tetramine (TETS) Ethylene Oxide Chlorine Leaks Phosphine Chlorine Common Toxic Industrial Chemical (“TIC”). Why use it in war/terror? Chlorine Density of 3.21 g/L. Heavier than air (1.28 g/L) sinks. Concentrates in low-lying areas. Like basements and underground bunkers. Reacts with water: Hypochlorous acid (HClO) Hydrochloric acid (HCl).
    [Show full text]
  • Organic & Biomolecular Chemistry
    Organic & Biomolecular Chemistry Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/obc Page 1 of 7 Organic & Biomolecular Chemistry Journal Name RSCPublishing ARTICLE Selective chromo-fluorogenic detection of DFP (a Sarin and Soman mimic) and DCNP (a Tabun mimic) Cite this: DOI: 10.1039/x0xx00000x with a unique probe based on a boron dipyrromethene (BODIPY) dye Manuscript Received 00th January 2012, Accepted 00th January 2012 Andrea Barba-Bon,a,b Ana M. Costero,a,b* Salvador Gil,a,b Ramón Martínez- a,c,d a,c,d DOI: 10.1039/x0xx00000x Máñez, * and Félix Sancenón www.rsc.org/ A novel colorimetric probe (P4) for the selective differential detection of DFP (a Sarin and Soman mimic) and DCNP (a Tabun mimic) was prepared.
    [Show full text]
  • Chapter 6 PRETREATMENT for NERVE AGENT EXPOSURE
    Pretreatment for Nerve Agent Exposure Chapter 6 PRETREATMENT FOR NERVE AGENT EXPOSURE MICHAEL A. DUNN, M.D., FACP*; BRENNIE E. HACKLEY, JR., PH.D.†; AND FREDERICK R. SIDELL, M.D.‡ INTRODUCTION AGING OF NERVE AGENT–BOUND ACETYLCHOLINESTERASE PYRIDOSTIGMINE, A PERIPHERALLY ACTING CARBAMATE COMPOUND Efficacy Safety Wartime Use Improved Delivery CENTRALLY ACTING NERVE AGENT PRETREATMENTS NEW DIRECTIONS: BIOTECHNOLOGICAL PRETREATMENTS SUMMARY *Colonel, Medical Corps, U.S. Army; Director, Clinical Consultation, Office of the Assistant Secretary of Defense (Health Affairs), Washing- ton, D.C. 20301-1200; formerly, Commander, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Mary- land 21010-5425 †Scientific Advisor, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland 21010-5425 ‡Formerly, Chief, Chemical Casualty Care Office, and Director, Medical Management of Chemical Casualties Course, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland 21010-5425; currently, Chemical Casualty Consultant, 14 Brooks Road, Bel Air, Maryland 21014 181 Medical Aspects of Chemical and Biological Warfare INTRODUCTION Nerve agents are rapidly acting chemical com- cal as well and may impair physical and mental pounds that can cause respiratory arrest within performance. A pretreatment must be administered minutes of absorption. Their speed of action im- to an entire force under a nerve agent threat. Any poses a need for rapid and appropriate reaction by resulting performance decrement, even a compara- exposed soldiers, their buddies, or medics, who tively minor one, would make pretreatment use must administer antidotes quickly enough to save unacceptable in battlefield situations requiring lives. A medical defense against nerve agents that maximum alertness and performance for survival.
    [Show full text]
  • Efficacy of the Repon1 Mutant IIG1 to Prevent Cyclosarin Toxicity in Vivo and to Detoxify Structurally Different Nerve Agents in Vitro
    Arch Toxicol (2014) 88:1257–1266 DOI 10.1007/s00204-014-1204-z MOLECULAR TOXICOLOGY Efficacy of the rePON1 mutant IIG1 to prevent cyclosarin toxicity in vivo and to detoxify structurally different nerve agents in vitro Franz Worek · Thomas Seeger · Moshe Goldsmith · Yacov Ashani · Haim Leader · Joel S. Sussman · Dan Tawfik · Horst Thiermann · Timo Wille Received: 30 September 2013 / Accepted: 16 January 2014 / Published online: 30 January 2014 © Springer-Verlag Berlin Heidelberg 2014 Abstract The potent human toxicity of organophos- alkylmethylfluorophosphonates but had low efficiency with phorus (OP) nerve agents calls for the development of the phosphoramidate tabun and was virtually ineffective effective antidotes. Standard treatment for nerve agent with the nerve agent VX. This quantitative analysis vali- poisoning with atropine and an oxime has a limited effi- dated the model for predicting in vivo protection by cata- cacy. An alternative approach is the development of cata- lytic bioscavengers based on their catalytic efficiency, the lytic bioscavengers using OP-hydrolyzing enzymes such level of circulating enzyme, and the dose of the intoxicat- as paraoxonases (PON1). Recently, a chimeric PON1 ing nerve agent. The in vitro and in vivo results indicate mutant, IIG1, was engineered toward the hydrolysis of the that IIG1 may be considered as a promising candidate toxic isomers of soman and cyclosarin with high in vitro bioscavenger to protect against the toxic effects of a range catalytic efficiency. In order to investigate the suitabil- of highly toxic nerve agents. ity of IIG1 as a catalytic bioscavenger, an in vivo guinea pig model was established to determine the protective Keywords Nerve agents · Paraoxonase · Mutant · effect of IIG1 against the highly toxic nerve agent cyclo- Detoxification · Protection · Bioscavenger sarin.
    [Show full text]
  • Soman (GD) Team (NRT) Quick Reference Guides (Qrgs) for Chemical Warfare Agents
    NRT Quick Reference Guide: For references, please see Key References Cited/Used in National Response Soman (GD) Team (NRT) Quick Reference Guides (QRGs) for Chemical Warfare Agents. [January 2015 Update] QRGs are intended for Federal OSC/RPMs. Agent Classification: Schedule 1 Chemical Warfare Nerve Agent; CAS: 96-64-0; Formula: C7H16FO2P; Molecular Weight: 182.18 g/mol. Description: Colorless liquid that with aging may discolor to dark brown; generally odorless, but sometimes has odor of camphor or rotting fruit. GD is a lethal cholinesterase inhibitor with a mechanism of toxicity similar to organophosphate insecticides, though it is much more potent. GD is less volatile than Sarin (GB); it is much more volatile than persistent agents VX or Sulfur Mustard (HD). Environmental breakdown products of GD, including methylphosphonic acid (MPA), are relatively non-toxic. Other breakdown products include fluoride ion, which may exist as hydrofluoric acid (HF) depending on the pH. GD can react violently with bases, weak acids and strong oxidizers, and may decompose when in contact with metals, evolving flammable hydrogen gas. GD is combustible but not easily ignited when heated; GD vapors can form explosive mixtures with air. Persistence: GD is considered a “low persistent” chemical warfare agent. Vapor: minutes to hours; liquid: hours to days. Persistence will depend upon the amount and purity of the agent, method of release, environmental conditions, and types of surfaces and materials impacted. Porous, permeable, organic or polymeric materials such as carpets and vinyl tiles can accumulate agent by sorbing GD vapors and liquids, acting as “sinks,” thereby prolonging persistence. Physical properties are listed at/near STP unless otherwise indicated.
    [Show full text]
  • Nerve Agents (Ga, Gb, Gd, Vx) Tabun (Ga) Cas # 77-81-6 Sarin (Gb) Cas # 107-44-8 Soman (Gd) Cas # 96-64-0 Vx Cas # 50782-69-9
    NERVE AGENTS (GA, GB, GD, VX) TABUN (GA) CAS # 77-81-6 SARIN (GB) CAS # 107-44-8 SOMAN (GD) CAS # 96-64-0 VX CAS # 50782-69-9 Division of Toxicology ToxFAQsTM April 2002 This fact sheet answers the most frequently asked health questions (FAQs) about nerve agents. For more information, call the ATSDR Information Center at 1-888-422-8737. This fact sheet is one in a series of summaries about hazardous substances and their health effects. It is important you understand this information because this substance may harm you. The effects of exposure to any hazardous substance depend on the dose, the duration, how you are exposed, personal traits and habits, and whether other chemicals are present. HIGHLIGHTS: Exposure to nerve agents can occur due to accidental release from a military storage facility. Nerve agents are highly toxic regardless of the route of exposure. Exposure to nerve agents can cause tightness of the chest, excessive salivation, abdominal cramps, diarrhea, blurred vision, tremors, and death. Nerve agents (GA, GB, GD, VX) have been identified at 5 of the 1,585 National Priorities List sites identified by the Environmental Protection Agency (EPA). What are nerve agents GA, GB, GD, and VX? ‘ GA, GB, GD, and VX will be broken down in water quickly, but small amounts may evaporate. Nerve agents GA(tabun), GB (sarin), GD(soman), and VX are ‘ GA, GB, GD, and VX will be broken down in moist soil manufactured compounds. The G-type agents are clear, quickly. Small amounts may evaporate into air or travel colorless, tasteless liquids miscible in water and most below the soil surface and contaminate groundwater.
    [Show full text]
  • Wilmsmeyer a D 2012.Pdf
    Ultrahigh Vacuum Studies of the Fundamental Interactions of Chemical Warfare Agents and Their Simulants with Amorphous Silica Amanda Rose Wilmsmeyer Dissertation submitted to the faculty of the Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy In Chemistry John R. Morris, Chair Louis A. Madsen James M. Tanko Brian M. Tissue Edward F. Valeev August 3, 2012 Blacksburg, VA Keywords: surface chemistry, chemical warfare agent simulants, hydrogen bonding, ultrahigh vacuum, temperature programmed desorption, infrared spectroscopy Ultrahigh Vacuum Studies of the Fundamental Interactions of Chemical Warfare Agents and Their Simulants with Amorphous Silica Amanda Rose Wilmsmeyer Abstract Developing a fundamental understanding of the interactions of chemical warfare agents (CWAs) with surfaces is essential for the rational design of new sorbents, sensors, and decontamination strategies. The interactions of chemical warfare agent simulants, molecules which retain many of the same chemical or physical properties of the agent without the toxic effects, with amorphous silica were conducted to investigate how small changes in chemical structure affect the overall chemistry. Experiments investigating the surface chemistry of two classes of CWAs, nerve and blister agents, were performed in ultrahigh vacuum to provide a well-characterized system in the absence of background gases. Transmission infrared spectroscopy and temperature-programmed desorption techniques were used to learn about the adsorption mechanism and to measure the activation energy for desorption for each of the simulant studied. In the organophosphate series, the simulants diisopropyl methylphosphonate (DIMP), dimethyl methylphosphonate (DMMP), trimethyl phosphate (TMP), dimethyl chlorophosphate (DMCP), and methyl dichlorophosphate (MDCP) were all observed to interact with the silica surface through the formation of a hydrogen bond between the phosphoryl oxygen of the simulant and an isolated hydroxyl group on the surface.
    [Show full text]
  • Nerve Agent Tables
    Report any release of WMD to the National Response Center 1-800-424-8802 NRT Quick Reference Guide: For References, Please See: Key References Cited/Used* in National Response Team Soman (GD) (NRT) Quick Reference Guides (QRGs) for Chemical Warfare Agents. Agent Classification: Chemical Warfare Nerve Agent CAS: 96-64-0 Description: Colorless liquid; generally odorless, possibly fruity. GD was manufactured as a warfare agent and is a lethal cholinesterase inhibitor. It has the same mechanism of toxicity as organophosphate insecticides but is much more potent. GD is considered to have low persistence; though it is less volatile than sarin (GB), it is much more vola- tile than persistent agents VX or sulfur mustard (HD). While considered relatively non-persistent, liquid GD could be present for hours to days if in large amounts, or in cold or enclosed environments. Breakdown/hydrolysis in water (especially treated water) is expected. Environmental breakdown products of GD are relatively nontoxic. Signs/symp- toms of exposure to GD will occur within minutes or hours, depending on the dose. Even relatively low dose exposure to GD can be fatal; administration of antidotes within 2 minutes of exposure may be effective. (See First Aid/Decon below) Persistence: vapor: minutes-hours; liquid: hours to days depending on amount, temperature, rain or other weather conditions, and type of surface. Molecular Weight: 182.18 g/mol Vapor Density: 6.33 (air = 1) Aqueous Solubility: 21 g/L 68°F Volatility: 3900 mg/m3 77°F Boiling Point: 388°F Soluble: organic solvents Agent Characteristics Freezing point: -44°F Flashpoint: 250°F Specific Gravity: 1.02 g/ml 68°F Vapor Pressure: 0.4 mm Hg @ 77°F Conversion Factors: 1ppm= 7.5 mg/m3; °C = 0.56 × (°F – 32) Air Release: Because it is somewhat volatile, GD is not generally considered a “persistent” agent.
    [Show full text]
  • List of Certified Energy Auditors
    LIST OF CERTIFIED ENERGY AUDITORS S No Regn No Name of the Candidate IST EXAM - MAY 2004 1 EA-0001 Atul Pratap Singh 2 EA-0007 Padmanabha Ramanuja Chari 3 EA-0009 Jitendra Jain 4 EA-0011 G Rudra Narsimha Rao 5 EA-0012 Pradeep Shrikrishna Lothe 6 EA-0015 Ram Kumar Yadav 7 EA-0016 Prabir Chattoraj 8 EA-0019 Aswini Kumar Sahu 9 EA-0021 Hitendera Mehtani 10 EA-0028 Premkumar 11 EA-0029 Subesh Kumar 12 EA-0030 L Rafique Ali 13 EA-0032 Pramod Kumar Dangaich 14 EA-0035 I Thanumoorthi 15 EA-0036 Devesh Kumar Singhal 16 EA-0038 T Senthil Kumar 17 EA-0043 Anand Narayan Kale 18 EA-0044 G V Jagadeesh Kumar 19 EA-0045 P Chandramouli 20 EA-0046 Deepak Kaushik 21 EA-0055 Rajeev Kumar Pahwa 22 EA-0061 Vishnu J Mulchandani 23 EA-0064 Babu M 24 EA-0075 Dilip Sarda 25 EA-0077 J Swaminathan 26 EA-0081 Mahendra Manohar Dandekar 27 EA-0083 Avinash Kumar 28 EA-0086 M Bhaskar 29 EA-0092 Dhirendra Bansal 30 EA-0104 Pande Madhav 31 EA-0108 Rakesh Sahay 32 EA-0114 Dipak Kumar Bhattacharya 33 EA-0115 Manu Chawla 34 EA-0119 Shishir Saxena 35 EA-0122 Amar Gupta 36 EA-0128 Mukul Ghanekar 37 EA-0132 Binobananda Jha 38 EA-0133 Ramesh Babu Guptha Paluri 39 EA-0136 Sukuru Ramarao 40 EA-0142 Sanjay Bhanudasrao Joshi 41 EA-0148 Mahesh Kumar Madan 42 EA-0149 Swapan Kumar Dutta 43 EA-0155 Desai Gaurang 44 EA-0157 Raj Kumar Porwal 45 EA-0159 Devanand Patil 46 EA-0160 Achyuta Nanda Mohanty 47 EA-0178 Mahesh Chandani 48 EA-0179 R K Aggarwal 49 EA-0183 G Pasupathy 50 EA-0184 Sandeep Kumar Jain 51 EA-0185 B D Gupta 52 EA-0187 Mohammad Abul Kalam 53 EA-0191 Arun Kanti Bala 54 EA-0192 G Sankar 55 EA-0200 R Balasubramanian 56 EA-0203 V Kumaran 57 EA-0205 Sarvesh Kumar 58 EA-0207 C Sethuraman 59 EA-0216 Pramath Sanghavi 60 EA-0220 Pawan B Agarwal 61 EA-0223 Subrat Kishore Nayak 62 EA-0232 Upendra Pratap Singh 63 EA-0233 Shailendra Pandey 64 EA-0236 Tukaram K.
    [Show full text]
  • Soman-Induced Neuro-Inflammatory Reaction in Mouse Brain. Some Effects of a Combination of Atropine and Ketamine
    Soman-Induced Neuro-Inflammatory Reaction in Mouse Brain. Some Effects of a Combination of Atropine and Ketamine Dr. Franck Dhote, Dr. André Peinnequin, Dr. Pierre Carpentier, Dr. Valérie Baille, Ms. Claire Delacour, Ms. Annie Foquin, Pr. Guy Lallement, Dr. Frédéric Dorandeu Centre de Recherches du Service de Santé des Armées « Emile Pardé » -CRSSA- 24, avenue des maquis du Grésivaudan 38702 La Tronche Cedex France Email : [email protected] / [email protected] / [email protected] / [email protected] / [email protected] / [email protected] / [email protected] ABSTRACT Organophosphorus nerve agent (OP) poisoning induces death through different mechanisms including respiratory and cardiovascular major dysfunctions. Epileptic seizures, status epilepticus and seizure- related brain damage (SRBD) complicate the clinical picture. Recently different publications showed that neuro-inflammatory events take place during OP-induced seizures but their role in SRBD and post-status epilepticus epileptogenesis is not clear. Antagonists of the NMDA ionotropic glutamate receptors are currently the only drugs able to arrest seizures and provide neuroprotection when treatment is initiated up to one hour after poisoning. We recently reported that racemic ketamine, or the more active isomer S(+) ketamine, in combination with atropine sulphate (AS), could counteract lethality, seizures and SRBD in soman poisoned guinea-pigs. Moreover peripheral anti-inflammatory properties of ketamine have been described. To complement former studies restricted to shorter time courses, we undertook a quantitative RT-PCR analysis of the brain genic response to soman (IL-1β, TNFα, IL-6, ICAM-1 and SOCS3) up to 7 days after poisoning in a mouse model of severe convulsions and neuropathy (HI-6, 50 mg/kg i.p.
    [Show full text]
  • Composites Based on Conductive Polymer with Carbon Nanotubes in DMMP Gas Sensors – an Overview
    Nr 2 (83–154) LUTY 2021 Tom LXVI POLIMERY Composites based on conductive polymer with carbon nanotubes in DMMP gas sensors – an overview N.M. Nurazzi1) (ORCID ID: 0000-0001-7697-0511), M.M. Harussani1), N.D. Siti Zulaikha1) (0000-0001-6706-7216), A.H. Norhana1) (0000-0001-8077-824X), M. Imran Syakir2) (0000-0002-3805-9919), A. Norli1), *) (0000-0002-8519-3379) DOI: dx.doi.org/10.14314/polimery.2021.2.1 Abstract: A number of recent terrorist attacks make it clear that rapid response, high sensitivity and sta- bility are essential in the development of chemical sensors for the detection of chemical warfare agents. Nerve agent sarin [2-(fluoro-methyl-phosphoryl) oxypropane] is an organophosphate (OP) compound that is recognized as one of the most toxic chemical warfare agents. Considering sarin’s high toxicity, being odorless and colorless, dimethyl methylphosphonate (DMMP) is widely used as its simulant in the laboratory because of its similar chemical structure and much lower toxicity. Thus, this review serves to introduce the development of a variety of fabricated chemical sensors as potential sensing materials for the detection of DMMP in recent years. Furthermore, the research and application of carbon nanotubes in DMMP polymer sensors, their sensitivity and limitation are highlighted. For sorption-based sensors, active materials play crucial roles in improving the integral performances of sensors. The novel active materials providing hydrogen-bonds between the polymers and carbon nanotubes are the main focus in this review. Keywords: carbon nanotubes, DMMP, chemical sensor, conductive polymer. Kompozyty na osnowie polimeru przewodzącego z udziałem nanorurek węglowych w czujnikach gazu DMMP – przegląd literatury Streszczenie: Przeprowadzone w ostatnich latach liczne ataki terrorystyczne jasno wskazują, że w wy- padku czujników do wykrywania chemicznych środków bojowych są niezbędne: ich wysoka czułość, szybka reakcja i stabilność.
    [Show full text]