MIL-STD-1442 Rev. A
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Standardal /Z<-Z
Hamilton Ui StandardAl HANL1r0N STNTVI) Bi;.TVGircr1h VP0FT SVHCA, 5712 1 0 L 'K-KY-o LaIUI P~FrcX.-19F TEST2 ?i0&at CONrxyhCT NO. TIAS 9-8159 NASA Aid!,zj.. SACECAFT CF.CErR ,_eb-r 1970 Prepared Byi/kA / 70 L.A. Wilis, axrer.mwtal Enineer Pae Aproved ByA1"" /Z<-Z -;' W. A. Blezhcr0 Chiet Pa tc Advanced -nginee.rin ONUMBE) AHRU) U NASA CR OR ?MX OR AD NUMBER) (CATEGORY) Hamilton L Standard cnisni _ This report contairs test results defining the operating chsractcristics of lithin peroxide to the extcnt required to quantify system level ponalties. The effects of chemical caulysts, bed cooling, che.,ical Panufacturing tech uiques, opera ing conditions, and cheaica) handling jroc Curea are evaluated. ii! StandardHamilton i5U TAlBLE OF CO_&E!PS Section me No. 1.0 SUMM4ARY 1 2 .0 INTRODUCTION 3 3.0 PROGRAM DEFINITION 3.1 Program Objectives 4 3.2 Test Objectives 4 3.3 Program Description 5 3.4 Test Conitions T 3.5 Test Facility 7 3.6 - Test Hardware 12 3.7 Planned Test Sequence 18 3.8 Test.Results 21 ho TEST DATA PRESENTATION 22 4.1 Performance Data 22 4.2 Chemical Analysis Data 1o6 5.0 PERFOrd4ICE ANALYSIS 109 5.1 Catalyst Evaluation 109 5.2 Bed Cooling Evaluation 134 5.3 Procedural Test Evaluation 0h5 5.4 Off Design Test Evaluation 153 5.5 End Item Canister Evaluation 157 5.6 Li 2O2 System Penalty Evaluation 163 6.0 RECOM ENDED FUTURE EFFORT 165 7.0 APPENDIX 167 7.1 Specification for Lithium Peroxide 167 Manufacturing 7.2 Specification for Lithium Peroxide Storage a68 7.3 Specification for Lithium Peroxide 170 Cartridge Loading iv Standard 5712 LIST OP TABLFS Table No. -
Transport of Dangerous Goods
ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions. -
162 Part 175—Indirect Food Addi
§ 174.6 21 CFR Ch. I (4–1–19 Edition) (c) The existence in this subchapter B Subpart B—Substances for Use Only as of a regulation prescribing safe condi- Components of Adhesives tions for the use of a substance as an Sec. article or component of articles that 175.105 Adhesives. contact food shall not be construed as 175.125 Pressure-sensitive adhesives. implying that such substance may be safely used as a direct additive in food. Subpart C—Substances for Use as (d) Substances that under conditions Components of Coatings of good manufacturing practice may be 175.210 Acrylate ester copolymer coating. safely used as components of articles 175.230 Hot-melt strippable food coatings. that contact food include the fol- 175.250 Paraffin (synthetic). lowing, subject to any prescribed limi- 175.260 Partial phosphoric acid esters of pol- yester resins. tations: 175.270 Poly(vinyl fluoride) resins. (1) Substances generally recognized 175.300 Resinous and polymeric coatings. as safe in or on food. 175.320 Resinous and polymeric coatings for (2) Substances generally recognized polyolefin films. as safe for their intended use in food 175.350 Vinyl acetate/crotonic acid copoly- mer. packaging. 175.360 Vinylidene chloride copolymer coat- (3) Substances used in accordance ings for nylon film. with a prior sanction or approval. 175.365 Vinylidene chloride copolymer coat- (4) Substances permitted for use by ings for polycarbonate film. 175.380 Xylene-formaldehyde resins con- regulations in this part and parts 175, densed with 4,4′-isopropylidenediphenol- 176, 177, 178 and § 179.45 of this chapter. -
United States Patent Office Patented May 26, 964 1
3,134,646 United States Patent Office Patented May 26, 964 1. 2 3,134,646 anhydrous lithium peroxide. The rapid drying step PREPARATION 6Fiff UM PEROXIDE. serves not only to effect the removal of water added Ricardo O. Bach, Gastonia, N.C., assignor to Lithium through the water solutions of the reactants and, addi Corporation of America, inc., New York, N.Y., a cor tionally, formed in the course of the reaction, but serves, poration of Minnesota also, and quite surprisingly, to bring about the important No Drawing, Filed Jan. 5, 1962, Set. No. 166,395 function of effecting rapid transfer of the active oxygen 10 Claims. (CI. 23-184) of the hydrogen peroxide to the lithium hydroxide to consummate formation of the desired lithium peroxide. This invention relates to an improved method of pro The lithium hydroxide (which term also includes ducing substantially anhydrous lithium peroxide, and to O lithium hydroxide hydrates such as lithium hydroxide the product produced thereby. monohydrate) is most advantageously used in the form Methods for the production of substantially anhydrous of a strong to substantially saturated aqueous solution, lithium peroxide have long been known in the art. More for instance, from about 8 or 10 to 12% concentration. recently, improvements in such methods have been pro In those instances where the resulting lithium hydroxide posed as disclosed, for instance, in U.S. Patents Nos. 5 solutions contain insoluble impurities as, for instance, 2,448,485 and 2,962,358. However, each of the methods lithium carbonate, it is desirable to filter the solutions disclosed in these patents has certain significant disad to remove said impurities so as to bring about greater vantages, particularly from an economic standpoint, purity of the final substantially anhydrous lithium which make their utilization in commercial operations peroxide. -
Chemical Chemical Hazard and Compatibility Information
Chemical Chemical Hazard and Compatibility Information Acetic Acid HAZARDS & STORAGE: Corrosive and combustible liquid. Serious health hazard. Reacts with oxidizing and alkali materials. Keep above freezing point (62 degrees F) to avoid rupture of carboys and glass containers.. INCOMPATIBILITIES: 2-amino-ethanol, Acetaldehyde, Acetic anhydride, Acids, Alcohol, Amines, 2-Amino-ethanol, Ammonia, Ammonium nitrate, 5-Azidotetrazole, Bases, Bromine pentafluoride, Caustics (strong), Chlorosulfonic acid, Chromic Acid, Chromium trioxide, Chlorine trifluoride, Ethylene imine, Ethylene glycol, Ethylene diamine, Hydrogen cyanide, Hydrogen peroxide, Hydrogen sulfide, Hydroxyl compounds, Ketones, Nitric Acid, Oleum, Oxidizers (strong), P(OCN)3, Perchloric acid, Permanganates, Peroxides, Phenols, Phosphorus isocyanate, Phosphorus trichloride, Potassium hydroxide, Potassium permanganate, Potassium-tert-butoxide, Sodium hydroxide, Sodium peroxide, Sulfuric acid, n-Xylene. Acetone HAZARDS & STORAGE: Store in a cool, dry, well ventilated place. INCOMPATIBILITIES: Acids, Bromine trifluoride, Bromine, Bromoform, Carbon, Chloroform, Chromium oxide, Chromium trioxide, Chromyl chloride, Dioxygen difluoride, Fluorine oxide, Hydrogen peroxide, 2-Methyl-1,2-butadiene, NaOBr, Nitric acid, Nitrosyl chloride, Nitrosyl perchlorate, Nitryl perchlorate, NOCl, Oxidizing materials, Permonosulfuric acid, Peroxomonosulfuric acid, Potassium-tert-butoxide, Sulfur dichloride, Sulfuric acid, thio-Diglycol, Thiotrithiazyl perchlorate, Trichloromelamine, 2,4,6-Trichloro-1,3,5-triazine -
The Structure of Alkali Silicate Glasses and Melts: a Multi-Spectroscopic Approach
The structure of alkali silicate glasses and melts: A multi-spectroscopic approach by Cedrick A. O'Shaughnessy A thesis submitted in conformity with the requirements for the degree of Doctor of Philosophy in Geology Graduate Department of Earth Sciences University of Toronto c Copyright 2019 by Cedrick A. O'Shaughnessy Abstract The structure of alkali silicate glasses and melts: A multi-spectroscopic approach Cedrick A. O'Shaughnessy Doctor of Philosophy in Geology Graduate Department of Earth Sciences University of Toronto 2019 The structure of alkali silicate glasses and melts is investigated using a multi-spectroscopic approach. Raman spectroscopy is used to characterize the local to intermediate range order within the glasses. We show that the distribution of rings varies as a function of composition, with 3-membered rings gaining importance with increasing alkali content. We apply a newly developed model for the fitting of the high n frequency envelope related to SiO4 symmetric stretch vibrations of Q species. These fits are interpreted using the idea of modifier bound bridging oxygen. The proportions of the different Qn species vary with alkali concentration with Q4 species breaking down to form lower order Qn species with increasing alkali 2 content. The Q peak appears at increasingly higher concentrations of M2O with increasing cation size. This leads us to believe that cations with a higher charge density cluster more readily than cations with a lower charge density. At the ∼20 mol. % composition we see a change in the silicate network, as shown by the absence of a Q4 peak and the proportion of 3-membered rings. -
Design Guidelines for Carbon Dioxide Scrubbers I
"NCSCTECH MAN 4110-1-83 I (REVISION A) S00 TECHNICAL MANUAL tow DESIGN GUIDELINES FOR CARBON DIOXIDE SCRUBBERS I MAY 1983 REVISED JULY 1985 Prepared by M. L. NUCKOLS, A. PURER, G. A. DEASON I OF * Approved for public release; , J 1"73 distribution unlimited NAVAL COASTAL SYSTEMS CENTER PANAMA CITY, FLORIDA 32407 85. .U 15 (O SECURITY CLASSIFICATION OF TNIS PAGE (When Data Entered) R O DOCULMENTATIONkB PAGE READ INSTRUCTIONS REPORT DOCUMENTATION~ PAGE BEFORE COMPLETING FORM 1. REPORT NUMBER 2a. GOVT AQCMCSION N (.SAECIP F.NTTSChALOG NUMBER "NCSC TECHMAN 4110-1-83 (Rev A) A, -NI ' 4. TITLE (and Subtitle) S. TYPE OF REPORT & PERIOD COVERED "Design Guidelines for Carbon Dioxide Scrubbers '" 6. PERFORMING ORG. REPORT N UMBER A' 7. AUTHOR(&) 8. CONTRACT OR GRANT NUMBER(S) M. L. Nuckols, A. Purer, and G. A. Deason 9. PERFORMING ORGANIZATION NAME AND ADDRESS 10. PROGRAM ELEMENT, PROJECT. TASK AREA 6t WORK UNIT NUMBERS Naval Coastal PanaaLSystems 3407Project CenterCty, S0394, Task Area Panama City, FL 32407210,WrUnt2 22102, Work Unit 02 II. CONTROLLING OFFICE NAME AND ADDRE1S t2. REPORT 3ATE May 1983 Rev. July 1985 13, NUMBER OF PAGES 69 14- MONI TORING AGENCY NAME & ADDRESS(if different from Controtling Office) 15. SECURITY CLASS. (of this report) UNCLASSIFIED ISa. OECL ASSI FICATION/DOWNGRADING _ __N•AEOULE 16. DISTRIBUTION STATEMENT (of thia Repott) Approved for public release; distribution unlimited. 17. DISTRIBUTION STATEMENT (of the abstract entered In Block 20, If different from Report) IS. SUPPLEMENTARY NOTES II. KEY WORDS (Continue on reverse side If noceassry and Identify by block number) Carbon Dioxide; Scrubbers; Absorption; Design; Life Support; Pressure; "Swimmer Diver; Environmental Effects; Diving., 20. -
Hazardous Material Inventory Statement
City of Brooklyn Park FIRE DEPARTMENT 5200 - 85th Avenue North Brooklyn Park MN 55443 Phone: (763)493-8020 Fax: (763) 493-8391 Hazardous Materials Inventory Statement Users Guide A separate inventory statement shall be provided for each building. An amended inventory statement shall be provided within 30 days of the storage of any hazardous materials or plastics that changes or adds a hazard class or which is sufficient in quantity to cause an increase in the quantity which exceeds 5 percent for any hazard class. The hazardous materials inventory statement shall list by hazard class categories. Each grouping shall provide the following information for each hazardous material listed for that group including a total quantity for each group of hazard class. 1. Hazard class. (See attached Hazardous Materials Categories Listing) 2. Common or trade name. 3. Chemical Abstract Service Number (CAS number) found in 29 Code of Federal Regulations (C.F.R.). 4. Whether the material is pure or a mixture, and whether the material is a solid, liquid or gas 5. Maximum aggregate quantity stored at any one time. 6. Maximum aggregate quantity In-Use (Open to atmosphere) at any one time. 7. Maximum aggregate quantity In-Use (Closed to atmosphere) at any one time. 8. Storage conditions related to the storage type, high-pile, encapsulated, non-encapsulated. Attached is a listing of categories that all materials need to be organized to. Definitions of these categories are also attached for your use. At the end of this packet are blank forms for completing this project. For questions regarding Hazardous Materials Inventory Statement contact the Fire Department at 763-493-8020. -
Zllniit?Dstates Patent' ”
, 2,962,358 zllniit?dstates Patent‘ ” ICC. Patented Nov. 29,1969 7 l . , r 2 . percent recovery of the theoretical amount of lithium peroxide available-can be obtained. 2,96%“ The drying may bedone underatmosphen'c pressure at 1 METHOD on MAKING LITHIUM PERoxmE suitable temperatures to keep decomposition of the lithium IN METHANOL peroxide at a ' ‘Ethyl alcohol can be used, as well as methanol, and Henry H. Strater, May?eld Heights, Ohio, assignor to commercial strength alcohols are satisfactory. The re 8: Chemicals, Willoughby, Ohio, a corporation action of the invention will occur at room tempera 0 o ture. No Drawing. Filed June 2, 1958, Ser. No. 738,959 10 Should it be desired to recover the lithium present in the end ?ltrate material, the ?ltrate can be heated to 4 Claims. (Cl. 23-184) distill the alcohol therein which can be recovered for further use. The water present also is evaporated o? and the residue material will have been partially con The present invention relates to a method of preparing 15 verted from lithium peroxide over to lithium hydroxide. lithium' peroxide, and particularly relates to the prepara Such end product can be puri?ed in any conventional tion of such material in an alcohol reacting medium. manner and be again used in the practice of the process, Heretofore there have been some methods proposed or it can be used for other purposes, as desired. for the production of lithium peroxide, vbut none of such The reaction conditions are readily controllable by methods have been completely satisfactory for low cost 20 the process described, as the hydrogen peroxide is slowly eifective production of lithium peroxide, so far as I am added to the reacting materials and no excessive tem aware. -
Safety Data Sheet
Safety Data Sheet Issue Date: 19-Sep-2013 Revision Date: 10-Dec-2016 Version 2 1. PRODUCT AND COMPANY IDENTIFICATION Product Identifier Product Name United 482 O2 PLUS Other means of identification SDS # UNITED-482 UN/ID No UN1457 Recommended use of the chemical and restrictions on use Recommended Use Water Soluble Packets Uses Advised Against For industrial and institutional use only. Details of the supplier of the safety data sheet Supplier Address United Laboratories, Inc. 320 37th Avenue St. Charles, IL 60174 www.unitedlabsinc.com www.unitedlabsinc.ca Emergency Telephone Number Company Phone Number 800-323-2594 (to reorder) Emergency Telephone (24 hr) INFOTRAC 1-800-535-5053 (North America) 1-352-323-3500 (International) 2. HAZARDS IDENTIFICATION Classification OSHA Regulatory Status-This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Serious eye damage/eye irritation Category 1 Oxidizing Solids Category 2 Signal Word Danger Hazard Statements Causes serious eye damage. May intensify fire; oxidizer. Precautionary Statements – Prevention Wear eye protection/face protection. Take any precaution to avoid mixing with combustibles. Keep away from heat/sparks/ open flames/hot surfaces. No smoking. Keep/store away from clothing/combustible materials. _____________________________________________________________________________________________ Page 1 / 7 Revision Date: 10-Dec-2016 UNITED-482 - United 482 O2 PLUS _____________________________________________________________________________________________ Precautionary Statements - Response In case of fire: use water to extinguish. If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a poison center or physician. Precautionary Statements - Storage Store in accordance with local, national and regional rules, laws and regulations. -
Va 0047.Doc 8/10/01 3
BEFORE THE STATE OF FLORIDA DEPARTMENT OF ENVIRONMENTAL PROTECTION In re: Environmental Engineering Consultants, Inc. Petition for Variance _________________________________/ OGC File No. 01-0790 FINAL ORDER GRANTING PETITION FOR VARIANCE FROM RULE 62-522.300(3), F.A.C. On May 9, 2001, Environmental Engineering Consultants (EEC), Inc., filed a petition for variance from requirements in rule 62- 522.300(3) of the Florida Administrative Code. The petition was for a variance from rule 62-522.300(3), which prohibits a zone of discharge for discharges through wells, in order to use an in-situ remediation process. This process involves the use of wells or borings which is considered installation of one or more temporary Class V underground injection control wells at the site of contamination. A notice of receipt of the petition was published in the Florida Administrative Weekly on June 1, 2001. 1. Petitioner is located at 5119 North Florida Avenue, Tampa, Florida 33603. 2. EEC, Inc., wants to perform enhanced in-situ aerobic biodegradation using a powder containing 75% food grade calcium peroxide and 25% calcium hydroxide (manufactured by FMC Corporation) mixed with chlorine free potable water to clean up sites contaminated with gasoline, diesel fuel, and other chemicals containing primarily aromatic hydrocarbons. Va_0047.doc 8/10/01 3. Under rule 62-520.420 of the Florida Administrative Code, the standards for Class G-II ground waters include the primary and secondary drinking water standards of rules 62-550.310 and 62- 550.320 of the Florida Administrative Code, and the minimum criteria of rule 62-520.410 of the Florida Administrative Code. -
Effects of Solid Oxygen Fertilizers and Biochars on Nitrous Oxide
www.nature.com/scientificreports OPEN Efects of solid oxygen fertilizers and biochars on nitrous oxide production from agricultural soils in Florida Tanumoy Bera1,2, Kanika S. Inglett2 & Guodong D. Liu1* Elevated levels of nitrous oxide (N2O) emissions are a matter of concern in agricultural soils especially when fooding (hypoxic conditions) results from over irrigation or frequent rains. This study is the frst to report the use of two solid oxygen fertilizers (SOFs, calcium peroxide and magnesium peroxide) to reduce N2O production in mineral and organic soils amended with N fertilizer in a short-term laboratory incubation besides two biochars. In general, organic soil had greater N2O production than mineral soil. Soils amended with nitrogen fertilizer exhibited increased N2O production, by 74 times in mineral soil and 2 times in organic soil. Both solid oxygen fertilizers in mineral soil (98–99%) and calcium peroxide in organic soil (25%) successfully reduced N2O production than corresponding N fertilized treatments. Additionally, a greater level of available nitrate–N (52–57 and 225 mg kg−1 in mineral and organic soil, respectively) was recorded with the solid oxygen fertilizers. Corn residue biochar with N fertilizer increased N2O production in mineral soil but decreased in organic soil, while pine bark biochar with N did not afect the N2O production in either soil. Depending on soil, appropriate SOFs applied were able to reduce N2O production and maintain greater nitrate–N levels in fooded soil. Thus, solid oxygen fertilizers can potentially be used as an efective way to reduce N2O emission from hypoxic soil in agricultural production systems.