Solicit Proposals for a Firm to Provide a Chemical Tracking Software System at the Collge of New Jersey
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Portable Oxygen Dispensing Device
CIKITUSI JOURNAL FOR MULTIDISCIPLINARY RESEARCH ISSN NO: 0975-6876 Portable Oxygen Dispensing Device Mr. Pritaj Yadav, Dept. of Computer Science and Engineering Rabindranath Tagore University, Bhopal Abstract A portable oxygen dispensing device, comprises a body which comprises of six chambers to generate oxygen, and a wearable mask attached to the body , a first chamber consists of a micro-capsule comprising a sodium superoxide, a second chamber is connected to the first chamber for storing solid carbon di-oxide, a third chamber is connected with the first chamber and second chamber, and contains a solution of solution of hydrogen peroxide and non-ionic surfactant such as ethoxylated aliphatic alcohol and a and a fourth chamber is connected with the first chamber and the third chamber, consists of a hydrogen peroxide and ethoxylated aliphatic alcohol to feed the first chamber, a fifth chamber consists of a zeolite for absorbing noxious gases and a sixth chamber consists of an anti-oxidant to prevent the body from harmful reactions [1], [2]. Key words: micro-capsule, chamber, non-ionic surfactant, hydrogen peroxide. Introduction In the present scenario, environment is threatened by air pollution due to addition of harmful substances, poisonous gases and smoke that are released in the surrounding air from industries which are working on chemicals such as nitrogen dioxide, sulphur dioxide etc. To live a healthy life, fresh air is very important that is free from various poisonous gasses and other pollutants. Many devices like respirators and rebreathers are used to provide oxygen by absorbing carbon di-oxide and protect the user from respiratory problems but these devices are limited by the rate at which they provide oxygen and the conditions under which they are used. -
Regulated Substance List
INSTRUCTIONS FOR THE UNIFIED PROGRAM (UP) FORM REGULATED SUBSTANCE LIST CHEMICAL NAME CAS # TQ Listing CHEMICAL NAME CAS # TQ Listing (Lbs) Basis (Lbs) Basis Acetaldehyde 75-07-0 10,000 g Cantharidin 56-25-7 100/10,0001 * Acetone Cyanohydrin 75-86-5 1,000 Carbachol Chloride 51-83-2 500/10,0001 Acetone Thiosemicarbazide 1752-30-3 1,000/10,0001 Acetylene (Ethyne) 74-86-2 10,000 f Carbamic Acid, Methyl-,o- Acrolein (2-Propenal) 107-02-8 500 b (((2,4-Dimethyl-1,3-Dithiolan- Acrylamide 79-06-1 1,000/10,0001 2-YL) Methylene)Amino)- 26419-73-8 100/10,0001 Acrylonitrile (2- Propenenitrile) 107-13-1 10,000 b Carbofuran 1563-66-2 10/10,0001 Acrylyl Chloride Carbon Disulfide 75-15-0 10,000 b (2-Propenoyl Chloride) 814-68-6 100 b Carbon Oxysulfide Aldicarb 116-06-3 100/10,0001 (Carbon Oxide Sulfide (COS)) 463-58-1 10,000 f Aldrin 309-00-2 500/10,0001 Chlorine 7782-50-5 100 a,b Allyl Alcohol (2-Propen-1-ol) 107-18-6 1,000 b Chlorine Dioxide Allylamine (2-Propen-1-Amine) 107-11-9 500 b (Chlorine Oxide (ClO2)) 10049-04-4 1,000 c Aluminum Phosphide 20859-73-8 500 Chlorine Monoxide (Chlorine Oxide) 7791-21-1 10,000 f Aminopterin 54-62-6 500/10,0001 Chlormequat Chloride 999-81-5 100/10,0001 Amiton Oxalate 3734-97-2 100/10,0001 Chloroacetic Acid 79-11-8 100/10,0001 Ammonia, Anhydrous 2 7664-41-7 500 a,b Chloroform 67-66-3 10,000 b Ammonia, Aqueous Chloromethyl Ether (conc 20% or greater) 7664-41-7 20,000 a,b (Methane,Oxybis(chloro-) 542-88-1 100 b * Aniline 62-53-3 1,000 Chloromethyl Methyl Ether Antimycin A 1397-94-0 1,000/10,0001 (Chloromethoxymethane) -
United States Patent Office Patented Sept
3,149,913 United States Patent Office Patented Sept. 22, 1964 2 may vary over a wide range and may be as little as 1% 3,49,913 and as much as 50% and even higher. Particularly ad PROCESS FOR PRODUCING NETROSYL vantageous is the use of nitric acid in amounts such that SULFURECACE) d the resulting nitrosylsulfuric acid concentration approxi ALouis L. Ferstandig, El Cerrito, and Paul C. Condit, San 5 mates saturation values in order to afford maximum pro Asseino,poration, Calif.,San Francisco,assignors toCalif., California a corporation Research Cor of duction per unit reactor volume and yet avoid deposition Beavy are of solids. The solubility of nitrosylsulfuric acid in ap No Drawing. Fied June 14, 1961, Ser. No. 116,957 proximately 100% sulfuric acid ranges from about 48 3 (Caims. (CE. 23-39) grams per 100 grams of solution at 0° C. up to about 68 grams at 50 C. with, of course, a lesser solubility below This invention relates to a proces for the production of O 0 C. and a greater above 50° C. Although the presence nitrosylsulfuric acid. of the precipitated nitrosylsulfuric acid is usually a source Nitrosyisulfuric acid is particularly desirable for use of mechanical inconvenience, advantage may be taken of in the production of caprolactam from hexahydrobenzoic it by removal of the solid nitrosylsulfuric acid by filtra acid. Nitrosylsulfuric acid has long been known as an 5 tion and subsequent recycle of the mother liquor to the intermediate in connection with the lead-chamber sulfuric reaction Zone. acid process in which it is converted to Sulfuric acid with in general, the effective temperature range of the process concurrent liberation of nitric oxide in a reaction with is defined by the requirement that the reaction medium be sulfur dioxide. -
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. -
New Synthesis Routes for Production of Ε-Caprolactam by Beckmann
New synthesis routes for production of ε-caprolactam by Beckmann rearrangement of cyclohexanone oxime and ammoximation of cyclohexanone over different metal incorporated molecular sieves and oxide catalysts Von der Fakultät für Mathematik, Informatik und Naturwissenschaften der RWTH Aachen University zur Erlangung des akademischen Grades eines Doktors der Naturwissenschaften genehmigte Dissertation vorgelegt von Anilkumar Mettu aus Guntur/Indien Berichter: Universitätprofessor Dr. Wolfgang F. Hölderich Universitätprofessor Dr. Carsten Bolm Tag der mündlichen Prüfung: 29.01.2009 Diese Dissertation ist auf den Internetseiten der Hochschulbibliothek online verfügbar. Dedicated to my Parents This work reported here has been carried out at the Institute for Chemical Technolgy and Heterogeneous Catalysis der Fakultät für Mathematik, Informatik und Naturwissenschaften in the University of Technology, RWTH Aachen under supervision of Prof. Dr. Wolfgang F. Hölderich between June 2005 and August 2008. ACKNOWLEDGEMENTS I would like to express my deepest sence of gratitude to my supervisor Prof. Dr. rer. nat. W. F. Hölderich for giving me the opportunity to do my doctoral study in his group. His guidance and teaching classes have allowed me to grow and learn my subject during my Ph.d. He has provided many opportunities for me to increase my abilities as a researcher and responsibilities as a team member. I am grateful for the financial support of this work from Sumitomo Chemicals Co., Ltd, Niihama, Japan (Part One) and Uhde Inventa-Fischer GmBH, Berlin (Part Two). Our collaborators at Sumitomo Chemicals Co., Ltd (Dr. C. Stoecker) and Uhde Inventa- Fischer GmBH (Dr. R. Schaller and Dr. A. Pawelski) provided thoughtful guidance and suggestions for each project. -
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. -
COMBINED LIST of Particularly Hazardous Substances
COMBINED LIST of Particularly Hazardous Substances revised 2/4/2021 IARC list 1 are Carcinogenic to humans list compiled by Hector Acuna, UCSB IARC list Group 2A Probably carcinogenic to humans IARC list Group 2B Possibly carcinogenic to humans If any of the chemicals listed below are used in your research then complete a Standard Operating Procedure (SOP) for the product as described in the Chemical Hygiene Plan. Prop 65 known to cause cancer or reproductive toxicity Material(s) not on the list does not preclude one from completing an SOP. Other extremely toxic chemicals KNOWN Carcinogens from National Toxicology Program (NTP) or other high hazards will require the development of an SOP. Red= added in 2020 or status change Reasonably Anticipated NTP EPA Haz list COMBINED LIST of Particularly Hazardous Substances CAS Source from where the material is listed. 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide Acutely Toxic Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- Acutely Toxic 1-(2-Chloroethyl)-3-(4-methylcyclohexyl)-1-nitrosourea (Methyl-CCNU) Prop 65 KNOWN Carcinogens NTP 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) IARC list Group 2A Reasonably Anticipated NTP 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) (Lomustine) Prop 65 1-(o-Chlorophenyl)thiourea Acutely Toxic 1,1,1,2-Tetrachloroethane IARC list Group 2B 1,1,2,2-Tetrachloroethane Prop 65 IARC list Group 2B 1,1-Dichloro-2,2-bis(p -chloropheny)ethylene (DDE) Prop 65 1,1-Dichloroethane -
CA004600 SDS.Pdf
Safety Data Sheet SECTION 1: Identification 1.1. Product Identifier Trade Name or Designation: Ammonium Bifluoride, 15.5 g/L, Aqueous Product Number: A-0046 Other Identifying Product Numbers: A-0046-4L 1.2. Recommended Use and Restrictions on Use General Laboratory Reagent 1.3. Details of the Supplier of the Safety Data Sheet Company: Reagents Inc. Address: 4746 Sweden Road Charlotte, NC 28224 USA Telephone: 800-732-8484 1.4. Emergency Telephone Number (24 hr) CHEMTREC (USA) 800-424-9300 CHEMTREC (International) 1+ 703-527-3887 SECTION 2: Hazard(s) Identification 2.1. Classification of the Substance or Mixture (in accordance with OSHA HCS 29 CFR 1910.1200) For the full text of the Hazard and Precautionary Statements listed below, see Section 16. Hazard Hazard Class Category Statement Precautionary Statements Skin Corrosion / Irritation Category 1 H314 P260, P264, P280, P301+P330+P331, P303+P361+P353, P363, P304+P340, P310, P321, P305+P351+P338, P405, P501 Eye Damage / Irritation Category 1 H318 P280, P305+P351+P338, P310 Specific Target Organs/Systemic Toxicity Following Single Category 1 H370 P260, P264, P270, P307+P311, P321, P405, Exposure P501 Specific Target Organs/Systemic Toxicity Following Repeated Category 2 H373 P260, P314, P501 Exposure Corrosive to Metals Category 1 H290 P234, P390, P406 Product Number: A-0046 Page 1 of 10 Safety Data Sheet 2.2. GHS Label Elements Pictograms: Signal Word: Danger Hazard Statements: Hazard Number Hazard Statement H290 May be corrosive to metals. H314 Causes severe skin burns and eye damage. H318 Causes serious eye damage. H370 Causes damage to organs. H373 May cause damage to organs through prolonged or repeated exposure. -
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. -
Ammonium Bifluoride CAS No
Product Safety Summary Ammonium Bifluoride CAS No. 1341-49-7 This Product Safety Summary is intended to provide a general overview of the chemical substance. The information on the summary is basic information and is not intended to provide emergency response information, medical information or treatment information. The summary should not be used to provide in-depth safety and health information. In-depth safety and health information can be found in the Safety Data Sheet (SDS) for the chemical substance. Names • Ammonium bifluoride (ABF) • Ammonium difluoride • Ammonium acid fluoride • Ammonium hydrogen difluoride • Ammonium fluoride compound with hydrogen fluoride (1:1) Product Overview Solvay Fluorides, LLC does not sell ammonium bifluoride directly to consumers. Ammonium bifluoride is used in industrial applications and in other processes where workplace exposures can occur. Ammonium bifluoride (ABF) is used for cleaning and etching of metals before they are further processed. It is used as an oil well acidifier and in the etching of glass or cleaning of brick and ceramics. It may also be used for pH adjustment in industrial textile processing or laundries. ABF is available as a solid or liquid solution (in water). Ammonium bifluoride is a corrosive chemical and contact can severely irritate and burn the skin and eyes causing possible permanent eye damage. Breathing ammonium bifluoride can severely irritate and burn the nose, throat, and lungs, causing nosebleeds, cough, wheezing and shortness of breath. On contact with water or moist skin, ABF can release hydrofluoric acid, a very dangerous acid. Inhalation or ingestion of large amounts of ammonium bifluoride can cause nausea, vomiting and loss of appetite. -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Hydrogen Generation from Magnesium Hydride by Using Organic Acid Yen-Hsi Ho University of Wisconsin-Milwaukee
University of Wisconsin Milwaukee UWM Digital Commons Theses and Dissertations August 2013 Hydrogen Generation from Magnesium Hydride By Using Organic Acid Yen-Hsi Ho University of Wisconsin-Milwaukee Follow this and additional works at: https://dc.uwm.edu/etd Part of the Mechanical Engineering Commons, and the Oil, Gas, and Energy Commons Recommended Citation Ho, Yen-Hsi, "Hydrogen Generation from Magnesium Hydride By Using Organic Acid" (2013). Theses and Dissertations. 286. https://dc.uwm.edu/etd/286 This Thesis is brought to you for free and open access by UWM Digital Commons. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of UWM Digital Commons. For more information, please contact [email protected]. HYDROGEN GENERATION FROM MAGNESIUM HYDRIDE BY USING ORGANIC ACID by Yen-Hsi Ho A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Engineering at The University of Wisconsin-Milwaukee August 2013 ABSTRACT HYDROGEN GENERATION FROM MAGNESIUM HYDRIDE BY USING ORGANIC ACID by Yen-Hsi Ho The University of Wisconsin-Milwaukee, 2013 Under the Supervision of Professor Tien-Chien Jen In this paper, the hydrolysis of solid magnesium hydride has been studied with the high concentration of catalyst at the varying temperature. An organic acid (acetic acid, CH3COOH) has been chosen as the catalyst. The study has three objectives: first, using three different weights of MgH2 react with aqueous solution of acid for the hydrogen generation experiments. Secondly, utilizing acetic acid as the catalyst accelerates hydrogen generation. Third, emphasizing the combination of the three operating conditions (the weight of MgH2, the concentration of acetic acid, and the varying temperature) influence the amount of hydrogen generation.