Parker O-Ring Reference Guide
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United States Patent Office Patented Aug
3,202,556 United States Patent Office Patented Aug. 24, 1965 2 mannan. As a consequence, crosslinking agents are used METHOD FOR GELiNGWATER-BEARNG3,282,555 EX to hasten the formation of gels, or they may be employed PLGSIVE COMPOSTIONS CONTAINNG GAYLAC to form gels which have desired physical properties at rel TOMANNAN (GUAS atively low gum concentrations, or even have properties Joseph D. Chrisp, Caymorf, Dai, assig or to E. I. du not obtainable by the use of the gum alone. An effective Poit de Neno Ers and Company, Wilmington, De., a and Well known crosslinking agent for the hydrated galac corporation of Delaware tomannans, especially for guar gum, is the borate ion No iPrawing. Fied July 23, 1963, Ser. No. 296,932 which acts as a crosslinking agent with hydrated guar gum 14 (Claims. (C. 49-20) to form cohesive structural gels. The process of cross 10 linking guar-containing compositions by adding borate This invention relates to a process for gelling aqueous ions has been employed in the manufacture of ammonium solutions of water-dispersible, non-ionic hydroxyl poly nitrate-based blasting agent compositions, as disclosed and mers. More particularly, this invention relates to a proc claimed in U.S. Patent No. 3,072,509. Such blasting ess for making water-bearing gels containing galactoman agents have a desirable body which resists dispersion of nans and to certain products obtained thereby including 5 the compositions by water and facilitates their handling explosives. and loading. Also, such crosslinked blasting agents are Water-soluble gums have been articles of commerce economical and safe to use, and have better storage prop for hundreds of years. -
Gasket Chemical Services Guide
Gasket Chemical Services Guide Revision: GSG-100 6490 Rev.(AA) • The information contained herein is general in nature and recommendations are valid only for Victaulic compounds. • Gasket compatibility is dependent upon a number of factors. Suitability for a particular application must be determined by a competent individual familiar with system-specific conditions. • Victaulic offers no warranties, expressed or implied, of a product in any application. Contact your Victaulic sales representative to ensure the best gasket is selected for a particular service. Failure to follow these instructions could cause system failure, resulting in serious personal injury and property damage. Rating Code Key 1 Most Applications 2 Limited Applications 3 Restricted Applications (Nitrile) (EPDM) Grade E (Silicone) GRADE L GRADE T GRADE A GRADE V GRADE O GRADE M (Neoprene) GRADE M2 --- Insufficient Data (White Nitrile) GRADE CHP-2 (Epichlorohydrin) (Fluoroelastomer) (Fluoroelastomer) (Halogenated Butyl) (Hydrogenated Nitrile) Chemical GRADE ST / H Abietic Acid --- --- --- --- --- --- --- --- --- --- Acetaldehyde 2 3 3 3 3 --- --- 2 --- 3 Acetamide 1 1 1 1 2 --- --- 2 --- 3 Acetanilide 1 3 3 3 1 --- --- 2 --- 3 Acetic Acid, 30% 1 2 2 2 1 --- 2 1 2 3 Acetic Acid, 5% 1 2 2 2 1 --- 2 1 1 3 Acetic Acid, Glacial 1 3 3 3 3 --- 3 2 3 3 Acetic Acid, Hot, High Pressure 3 3 3 3 3 --- 3 3 3 3 Acetic Anhydride 2 3 3 3 2 --- 3 3 --- 3 Acetoacetic Acid 1 3 3 3 1 --- --- 2 --- 3 Acetone 1 3 3 3 3 --- 3 3 3 3 Acetone Cyanohydrin 1 3 3 3 1 --- --- 2 --- 3 Acetonitrile 1 3 3 3 1 --- --- --- --- 3 Acetophenetidine 3 2 2 2 3 --- --- --- --- 1 Acetophenone 1 3 3 3 3 --- 3 3 --- 3 Acetotoluidide 3 2 2 2 3 --- --- --- --- 1 Acetyl Acetone 1 3 3 3 3 --- 3 3 --- 3 The data and recommendations presented are based upon the best information available resulting from a combination of Victaulic's field experience, laboratory testing and recommendations supplied by prime producers of basic copolymer materials. -
NOI to Prepare an Environmental Impact Statement For
Federal Register / Vol. 64, No. 34 / Monday, February 22, 1999 / Notices 8553 reauthorization of OERI and will hear DEPARTMENT OF ENERGY Orders are summarized in the attached committee and officers' reports. A final appendix. [FE Docket Nos. 99±01±NG, 99±03±NG, 99± agenda will be available from the Board 02±NG, 99±04±NG, 92±24±NG, 99±05±NG, These Orders may be found on the FE office on March 10, 1999, and will be and 99±06±NG] web site at http://www.fe.doe.gov., or posted on the Board's web site, http:// on the electronic bulletin board at (202) www.ed.gov/offices/OERI/NERPPB/. Office of Fossil Energy; Orders 586±7853. Granting and Transferring Records are kept of all Board They are also available for inspection Authorizations To Import and/or Export proceedings and are available for public and copying in the Office of Natural Gas Natural Gas inspection at the office of the National & Petroleum Import & Export Activities, Educational Research Policy and OGE Energy Resources, Inc., National Fuel Docket Room 3E±033, Forrestal Priorities Board, Suite 100, 80 F St., Gas Distribution Corporation, Renaissance Building, 1000 Independence Avenue, NW, Washington, D.C. 20208±7564. Energy (U.S.) Inc., Selkirk Cogen Partners, SW, Washington, DC 20585, (202) 586± L.P., Coral Energy Resources, L.P. (Successor 9478. The Docket Room is open between Dated: February 16, 1999. to Salmon Resources Ltd.), Transco Energy the hours of 8:00 a.m. and 4:30 p.m., Eve M. Bither, Marketing Company, and Petro-Canada Hydrocarbons Inc. -
United States Patent Office 368)
Patented May 8, 1945 2,375,638 UNITED STATES PATENT OFFICE 368). OSPORCAC) AND METHOD OF PSEPARNG SE SAE Leonard H. Egguani, Winona, illinn. No Drawing. App3.cation May 17, 1942, Seria Ne, 393,938 6 Claims. (C. 23-166) This invention relates to the provision and pro phosphorus pentoxide P2O5, to about four molec diction of phosphorus pentoxide derivatives and ular equivalents of the boric acid B(OH) are has as a general object the provision and prepa employed in the reaction which is represented by ration of a novel boro-phosphoric acid and a the following equation: . method of preparing various salts thereof. A more specific object of the invention is the provision of a novel powdery non-hygroscopic While do not wish the invention imited to acid comprising acid oxide groups of boron and any theory of the reactions which may be in phosphorus together with certain molecular pro voived, in view of the generai belief stated above, portions of water. C it Enight toe we to point out by way of possible Another object of the invention is the pro explanation that i believe the two molecular vision of a novel boro-phosphoric acid which has equivalents of the phosphorus pentoxide, 2Paos, a relatively great capacity for neutralizing bases abstract from the four noiecular equivalents of and which can be readily stored and handled as the horic acid, 43(OH)3, three Eholecular equiva other non-corrosive powders without requiring lents of Water. Tiki as the boron oxide groups experasive subber-coated or rubber-lined equip ray be C33 'feite it one notects r equivalent ment and containers. -
Expanding the Modular Ester Fermentative Pathways for Combinatorial Biosynthesis of Esters from Volatile Organic Acids
ARTICLE Expanding the Modular Ester Fermentative Pathways for Combinatorial Biosynthesis of Esters From Volatile Organic Acids Donovan S. Layton,1,2 Cong T. Trinh1,2,3 1 Department of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, Tennessee 2 BioEnergy Science Center (BESC), Oak Ridge National Laboratory, Oak Ridge, Tennessee 3 Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, Tennessee; telephone: þ865-974-8121; fax: 865-974-7076; e-mail: [email protected] Biotechnol. Bioeng. 2016;113: 1764–1776. ABSTRACT: Volatile organic acids are byproducts of fermentative ß 2016 Wiley Periodicals, Inc. metabolism, for example, anaerobic digestion of lignocellulosic KEYWORDS: modular chassis cell; carboxylate; ester; acyl acetate; biomass or organic wastes, and are often times undesired inhibiting acyl acylate; ester fermentative pathway cell growth and reducing directed formation of the desired products. Here, we devised a general framework for upgrading these volatile organic acids to high-value esters that can be used as flavors, fragrances, solvents, and biofuels. This framework employs the acid-to-ester modules, consisting of an AAT (alcohol Introduction acyltransferase) plus ACT (acyl CoA transferase) submodule and an alcohol submodule, for co-fermentation of sugars and organic Harnessing renewable or waste feedstocks (e.g., switchgrass, corn acids to acyl CoAs and alcohols to form a combinatorial library of stover, agricultural residue, or municipal solid waste) -
Public Health Goal for ANTIMONY in Drinking Water
Public Health Goal for ANTIMONY in Drinking Water Prepared by Pesticide and Environmental Toxicology Section Office of Environmental Health Hazard Assessment California Environmental Protection Agency December 1997 LIST OF CONTRIBUTORS PHG PROJECT MANAGEMENT REPORT PREPARATION SUPPORT Project Officer Author Administrative Support Anna Fan, Ph.D. Lubow Jowa, Ph.D. Edna Hernandez Coordinator Chemical Prioritization Primary Reviewer Laurie Bliss Report Outline Robert Brodberg, Ph.D. Sharon Davis Joseph Brown, Ph.D. Kathy Elliott Coordinator Secondary Reviewer Vickie Grayson David Morry, Ph.D. Michael DiBartolomeis, Ph.D. Michelle Johnson Yi Wang, Ph.D. Juliet Rafol Final Reviewers Genevieve Shafer Document Development Anna Fan, Ph.D. Tonya Turner Michael DiBartolomeis, Ph.D. William Vance, Ph.D. Coordinator Library Support George Alexeeff, Ph.D. Editor Mary Ann Mahoney Hanafi Russell, M.S. Michael DiBartolomeis, Ph.D. Valerie Walter Yi Wang, Ph.D. Website Posting Public Workshop Robert Brodberg, Ph.D. Michael DiBartolomeis, Ph.D. Edna Hernandez Coordinator Laurie Monserrat, M.S. Judy Polakoff, M.S. Judy Polakoff, M.S. Organizer Hanafi Russell, M.S. Methodology/Approaches/ Review Comments Joseph Brown, Ph.D. Robert Howd, Ph.D. Coordinators Lubow Jowa, Ph.D. David Morry, Ph.D. Rajpal Tomar, Ph.D. Yi Wang, Ph.D. We thank the U.S. EPA’s Office of Water, Office of Pollution Prevention and Toxic Substances, and National Center for Environmental Assessment for their peer review of the PHG documents, and the comments received from all interested parties. ANTIMONY in Drinking Water ii December 1997 California Public Health Goal (PHG) PREFACE Drinking Water Public Health Goal of the Office of Environmental Health Hazard Assessment This Public Health Goal (PHG) technical support document provides information on health effects from contaminants in drinking water. -
Table of Contents
UNIVERSITY OF MISSOURI-KANSAS CITY CHEMICAL MANAGEMENT PLAN Revised May 2016 UMKC CHEMICAL MANAGEMENT PLAN This document constitutes the Chemical Management Plan (CMP) for the University of Missouri-Kansas City (UMKC). It was developed by the Environmental Health and Safety Department (EHS), to ensure the safe and proper use of hazardous and non- hazardous chemicals and to comply with applicable governmental regulations addressing the disposal of these chemicals. In addition, it was developed to foster waste minimization, and to provide the faculty and the staff with a management program to reduce the potential for accidents involving hazardous chemicals and/or wastes. Elements of the CMP include: a. a procedure for identifying potential or actual hazardous chemicals or wastes b. a procedure for periodic reexamination of those hazardous chemicals or wastes identified by the procedure in (a.) above as well as a systematic method for identification and evaluation of any new potential or actual hazardous chemicals or wastes c. procedures for labeling, and inventorying hazardous chemicals or wastes d. a procedure for identification and training of personnel directly responsible for ensuring that (a.), (b.), and (c.) are implemented e. a procedure for monitoring, recording, and reporting compliance with the CMP f. a procedure by which information generated by the CMP is provided to the persons performing waste analyses Each element is addressed as part of the complete CMP in the following paragraphs. 4 Table of Contents 1 Definitions 7 2 Identification -
Boron Compounds As Additives to Lubricants
ISSN: 1402-1544 ISBN 978-91-86233-XX-X Se i listan och fyll i siffror där kryssen är LICENTIATE T H E SIS Faiz Ullah to Shah Lubricants Additives Compounds Boron as Division of Chemical Engineering Division of Machine Elements Boron Compounds as Additives to Lubricants ISSN: 1402-1757 ISBN 978-91-7439-027-8 Synthesis, Characterization and Tribological Luleå University of Technology 2009 Optimization Synthesis, Characterization and Tribological Optimization Tribological Characterization and Synthesis, Faiz Ullah Shah Boron Compounds as Additives to Lubricants: Synthesis, Characterization and Tribological Optimization Faiz Ullah Shah Division of Chemical Engineering & Division of Machine Elements Luleå University of Technology SE- 971 87 Luleå SWEDEN November 2009 Printed by Universitetstryckeriet, Luleå 2009 ISSN: 1402-1757 ISBN 978-91-7439-027-8 Luleå www.ltu.se The most fundamental and lasting objective of synthesis is NOT production of new compounds but PRODUCTION OF NEW PROPERTIES George S. Hammond. Norris Award lecture, 1968 SUMMARY Developing new technological solutions, such as use of lightweight materials, less harmful fuels, controlled fuel combustion processes or more efficient exhaust gas after-treatment, are possible ways to reduce the environmental impact of machines. Both the reduction of wear and the friction control are key issues for decreasing of energy losses, improving efficiency and increasing of the life-span of an engine. Dialkyldithiophosphates (DTPs) of different metals have been extensively used as multifunctional additives in lubricants to control friction and reduce wear in mechanical systems. Among these DTP-compounds, zinc dialkyldithiophosphates (ZnDTPs) are the most common additives used for more than 60 years. These additives form protective films on steel surfaces and, thus, control friction and reduce wear. -
Treaty Series
Treaty Series Treaties and internationalagreements registered or filed and recorded with the Secretariat of the United Nations VOLUME 446 Recueil des Traites Traites et accords internationaux enregistres ou classes et inscrits au repertoire au Secrtariat de l'Organisationdes Nations Unies United Nations * Nations Unies New York, 1963 Treaties and international agreements registered or filed and recorded with the Secretariat of the United Nations VOLUME 446 1962 I. Nos. 6397-6409 TABLE OF CONTENTS Treaties and internationalagreements registered /rom 29 November 1962,to 4 December 1962 Page No. 6397. Denmark and People's Republic of China: Exchange of notes constituting an agreement relating to mutual exemption from taxation of residents of either State who are temporarily staying in the other State for educational purposes. Copenhagen, 7 and 23 Septem- ber 1961 .............. .............. ........ 3 No. 6398. United States of America and Denmark: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ............ 9 No. 6399. United States of America and Finland: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ......... ... 19 No. 6400. United States of America and Israel: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ......... ... 29 No. 6401. United States of America and New Zealand: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ......... ... 39 No. 6402. United States of America and Norway: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). -
ANTIMONY by James F
ANTIMONY By James F. Carlin, Jr. Domestic survey data and tables were prepared by Mahbood Mahdavi, statistical assistant, and the world production table was prepared by Regina R. Coleman, international data coordinator. More than one-half of the primary antimony used in the merging operations with Laurel, the unified operation would United States during 2004 went into flame-retardants; most of increase its competitive position. manufacturing for the joint the remainder was used by the ceramic, chemical, glass, and venture will be consolidated into the existing Great Lakes transportation industries. Secondary antimony, which was antimony production facility in Reynosa, mexico. the Laurel derived almost entirely from recycled lead-acid batteries, was production facility in La Porte, tX, which employed 4 people, used in the manufacture of new batteries. in 2004, the average ceased production by yearend 2004; production of raw materials price of antimony was 20% higher than that of 2003. for flame-retardants and catalyst grades of antimony oxide was There was no domestic antimony mine production during the transferred to the Great Lakes facility in mexico (Great Lakes year. most primary antimony metal and oxide were produced Chemical Corp., 2004). domestically from imported raw material. most domestic At yearend 2004, the United States had only one antimony smelting consisted of upgrading imported antimony trioxide to a smelter, the United States Antimony Corp. (USAC), based in higher purity. Primary antimony metal and oxide were produced Montana. USAC produced antimony metal for bearings, lead by two companies operating two plants––one in montana and alloys, and ordnance; antimony oxide as a raw material for one in texas. -
Biocatalytic Synthesis of Flavor Ester “Pentyl Valerate” Using Candida Rugosa Lipase Immobilized in Microemulsion Based Organogels: Effect of Parameters and Reusability
Hindawi Publishing Corporation BioMed Research International Volume 2014, Article ID 353845, 14 pages http://dx.doi.org/10.1155/2014/353845 Research Article Biocatalytic Synthesis of Flavor Ester ‘‘Pentyl Valerate’’ Using Candida rugosa Lipase Immobilized in Microemulsion Based Organogels: Effect of Parameters and Reusability Tripti Raghavendra,1 Nilam Panchal,1 Jyoti Divecha,2 Amita Shah,1 and Datta Madamwar1 1 BRD School of Biosciences, Sardar Patel Maidan, Sardar Patel University, Satellite Campus, Vadtal Road, P.O. Box 39, Vallabh Vidyanagar, Gujarat 388120, India 2 Department of Statistics, Sardar Patel University, Vallabh Vidyanagar, Gujarat 388120, India Correspondence should be addressed to Datta Madamwar; datta [email protected] Received 28 February 2014; Revised 5 May 2014; Accepted 19 May 2014; Published 1 July 2014 Academic Editor: Yunjun Yan Copyright © 2014 Tripti Raghavendra et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Pentyl valerate was synthesized biocatalytically using Candida rugosa lipase (CRL) immobilized in microemulsion based organogels ∘ (MBGs). The optimum conditions were found to be pH 7.0, temperature of 37 C, ratio of concentration of water to surfactant (Wo) of 60, and the surfactant sodium bis-2-(ethylhexyl)sulfosuccinate (AOT) for MBG preparation. Although kinetic studies revealed that the enzyme in free form had high affinity towards substrates ( = 23.2 mM for pentanol and 76.92 mM for valeric acid) whereas, after immobilization, the values increased considerably (74.07 mM for pentanol and 83.3 mM for valeric acid) resulting in a slower reaction rate, the maximum conversion was much higher in case of immobilized enzyme (∼99%) as compared to free enzyme (∼19%). -
Articles Is an Important Step for the For- Mation and Transformation of Atmospheric Particles
Atmos. Chem. Phys., 15, 5585–5598, 2015 www.atmos-chem-phys.net/15/5585/2015/ doi:10.5194/acp-15-5585-2015 © Author(s) 2015. CC Attribution 3.0 License. Compilation and evaluation of gas phase diffusion coefficients of reactive trace gases in the atmosphere: Volume 2. Diffusivities of organic compounds, pressure-normalised mean free paths, and average Knudsen numbers for gas uptake calculations M. J. Tang1, M. Shiraiwa2, U. Pöschl2, R. A. Cox1, and M. Kalberer1 1Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK 2Multiphase Chemistry Department, Max Planck Institute for Chemistry, 55128, Mainz, Germany Correspondence to: M. J. Tang ([email protected]) and M. Kalberer ([email protected]) Received: 26 January 2015 – Published in Atmos. Chem. Phys. Discuss.: 25 February 2015 Revised: 24 April 2015 – Accepted: 3 May 2015 – Published: 21 May 2015 Abstract. Diffusion of organic vapours to the surface of 1 Introduction aerosol or cloud particles is an important step for the for- mation and transformation of atmospheric particles. So far, Organic aerosols are ubiquitous in the atmosphere and can however, a database of gas phase diffusion coefficients for or- account for a dominant fraction of submicron aerosol par- ganic compounds of atmospheric interest has not been avail- ticles (Jimenez et al., 2009). Organic aerosols affect climate able. In this work we have compiled and evaluated gas phase by scattering and adsorbing solar and terrestrial radiation and diffusivities (pressure-independent diffusion coefficients) of serving as cloud condensation nuclei and ice nuclei (Kanaki- organic compounds reported by previous experimental stud- dou et al., 2005; Hallquist et al., 2009).