Market Reactions to Changes in Demand for Naoh
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Solvay Process Company and a Portion of the Village of Solvay Which Grew up Company to Use Their Process
:«:..' :•' Telephone 2-3111 Telephone 2-3111 SYRACUSE JOTJRNAIi Saturday, July 28, 193C Page 8 - SOLVAY PROCESS AMONG STATE'S MIGHTIEST PLANTS MUM) NIK BURNS BRIGHTLY AIRVIEW OF THE SOLVAY PROCESS PLANT WHICH GREW FROM WILLIAM COGSWELL'S IDEA N HISTORY OF VAST IRKS j (This is the fifth of a series of articles whhb willjg <«.»r weklv in the Saturday edition of The Syracuse • ^ourZ^topermitSyracusaJto become iamiliar with the journal, to P"™;*' industrial and commercial enter- inside story of the great industrial a™ * develoo- \ prises which have played important parts in the develop lent of the city.) _ By BICHAKD B. WELCH. Bountiful Nature which supplied Syracuse with huge qnan- Itie* of salt and limestone coupled with the lewdness 0£ a Central New Yorker who saw the l-kto»tta.-* •btainahle raw materials gave Syracuse the.S*j'««- r^™*™™ ATIP of the largest heavy industries in the state. C°T^»M£nk of the history of the Solvay Process r™J»,»T« * subsidiary of the Allied Chemical and Dye Corp- STCE* tSTo William Browne Cog^eUmw, brain tie idea' of utilizing the resources of this section first KenXhdcredit for the formation and progress' »* tfe ^|My industry must also go to Bow and1 Hazard first P^nt tfthe company, and his son, Frederick B. Hazard, who succeeded him. SH; names which burn brightly in the industrial history 01 SMrCCog^ell was born in Oswego, Sept 22,1834 of a lixie- ,ge which dated back to Sir John Cogswell in If5- He was educated in Hamilton Academy at Oneida and in private schools of Syracuse. -
Sodium Hydroxide
Sodium hydroxide From Wikipedia, the free encyclopedia • Learn more about citing Wikipedia • Jump to: navigation, search Sodium hydroxide IUPAC name Sodium hydroxide Other names Lye, Caustic Soda Identifiers CAS number 1310-73-2 Properties Molecular NaOH formula Molar mass 39.9971 g/mol Appearance White solid Density 2.1 g/cm³, solid Melting point 318°C (591 K) Boiling point 1390°C (1663 K) Solubility in 111 g/100 ml water (20°C) Basicity (pKb) -2.43 Hazards MSDS External MSDS NFPA 704 0 3 1 Flash point Non-flammable. Related Compounds Related bases Ammonia, lime. Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references Sodium hydroxide (NaOH), also known as lye, caustic soda and sodium hydrate, is a caustic metallic base. Caustic soda forms a strong alkaline solution when dissolved in a solvent such as water. It is used in many industries, mostly as a strong chemical base in the manufacture of pulp and paper, textiles, drinking water, soaps and detergents and as a drain cleaner. Worldwide production in 1998 was around 45 million tonnes. Sodium hydroxide is the most used base in chemical laboratories. Pure sodium hydroxide is a white solid; available in pellets, flakes, granules and as a 50% saturated solution. It is deliquescent and readily absorbs carbon dioxide from the air, so it should be stored in an airtight container. It is very soluble in water with liberation of heat. It also dissolves in ethanol and methanol, though it exhibits lower solubility in these solvents than potassium hydroxide. -
(12) United States Patent (10) Patent No.: US 8,936,770 B2 Burba, III (45) Date of Patent: Jan
US00893677OB2 (12) United States Patent (10) Patent No.: US 8,936,770 B2 Burba, III (45) Date of Patent: Jan. 20, 2015 (54) HYDROMETALLURGICAL PROCESS AND (58) Field of Classification Search METHOD FOR RECOVERING METALS None See application file for complete search history. (75) Inventor: John L. Burba, III, Parker, CO (US) (56) References Cited (73) Assignee: Molycorp Minerals, LLC, Greenwood Village, CO (US) U.S. PATENT DOCUMENTS 2.916.357 A 12/1959 Schaufelberger (*) Notice: Subject to any disclaimer, the term of this 3,309,140 A * 3/1967 Gardner et al. ................... 299/4 patent is extended or adjusted under 35 3,711,591 A 1/1973 Hurst et al. U.S.C. 154(b) by 320 days. 3,808,305 A 4/1974 Gregor 3,937,783 A 2f1976 Wamser et al. 4,107,264 A 8/1978 Nagasubramanian et al. (21) Appl. No.: 13/010,609 4.278,640 A 7/1981 Allen et al. 4.326,935 A 4/1982 Moeglich (22) Filed: Jan. 20, 2011 4486,283 A 12/1984 Tejeda 4,676.957 A * 6/1987 Martin et al. ................ 423,215 (65) Prior Publication Data 4,740,281 A 4, 1988 Chlanda et al. US 2011 FO182786 A1 Jul. 28, 2011 (Continued) FOREIGN PATENT DOCUMENTS Related U.S. Application Data CN 1888.099 1, 2007 (60) Provisional application No. 61/297.536, filed on Jan. CN 101008047 8, 2007 22, 2010, provisional application No. 61/427,745, filed on Dec. 28, 2010, provisional application No. (Continued) 61/432,075, filed on Jan. 12, 2011. -
Salt In, Salt Out
chapter 2 Salt In, Salt Out Following their organizational meeting in November 1917, Yongli’s promoters began work on two Herculean tasks: searching for a plant design while raising the needed capital. In the process, problems of technology transfer, shifting government policy, and limitations of China’s capital market plagued them. Yongli’s challenge of Brunner, Mond’s formidable hold on the “well regulated” market and technology was both risky and difficult, which in turn made the task of raising the necessary capital even more daunting as it battled the Rev- enue Inspectorate over the gabelle waiver. Problems of Technology Transfer As Chen Diaofu and his colleagues demonstrated in Fan Xudong’s backyard, the chemistry behind the Solvay process was a public good. However, the engineering to make it work on an industrial scale was not.1 Sodium chloride (salt), one of the three main raw materials for the process, must be purified as a solution cleared of dirt, magnesium, and other impurities. The other essential chemical, ammonia, could be generated through burning coke, or added in liquid form. Reaction is then carried out by passing the concentrated and purified brine through the first of two absorption towers. Ammonia bubbles up to saturate the brine (NaCl + NH3, Step I). Separately, carbon dioxide is produced by heating limestone in a kiln at 950–1100°C. The calcium carbonate (CaCO3) in the limestone, the third main ingredient, is partially converted to quicklime (calcium oxide, CaO) and carbon dioxide: CaCO 3 → CO 2 + CaO ( Step II) The carbon dioxide and ammoniacal brine are then fed into a second tower for carbonation. -
OCCASION This Publication Has Been Made Available to the Public on The
OCCASION This publication has been made available to the public on the occasion of the 50th anniversary of the United Nations Industrial Development Organisation. DISCLAIMER This document has been produced without formal United Nations editing. The designations employed and the presentation of the material in this document do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations Industrial Development Organization (UNIDO) concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries, or its economic system or degree of development. Designations such as “developed”, “industrialized” and “developing” are intended for statistical convenience and do not necessarily express a judgment about the stage reached by a particular country or area in the development process. Mention of firm names or commercial products does not constitute an endorsement by UNIDO. FAIR USE POLICY Any part of this publication may be quoted and referenced for educational and research purposes without additional permission from UNIDO. However, those who make use of quoting and referencing this publication are requested to follow the Fair Use Policy of giving due credit to UNIDO. CONTACT Please contact [email protected] for further information concerning UNIDO publications. For more information about UNIDO, please visit us at www.unido.org UNITED NATIONS INDUSTRIAL DEVELOPMENT ORGANIZATION Vienna International Centre, P.O. Box 300, 1400 Vienna, Austria Tel: (+43-1) 26026-0 · www.unido.org · [email protected] k r i RESTRICTED MARKET STUDY F J <"* FOR SEA CHEMICALS PROJECT I N ICELAND PREPARED FOR NATIONAL RESEARCH COUNCIL REYKJAVIK, ICELAND BY WILLIAM B. -
Small Scale Distributed Ammonia Production
Small Scale Distributed Ammonia Production Less than 100 tons per day Contact: Doug Carpenter at Sustainable Fuels, Inc. [email protected] Presented By: Bill Ayres at R3Sciences, LP www.r3sciences.com Overview • Nitrogen Generation • Hydrogen Generation • Hydrogen Purification • Reaction Gas Blending • Reaction Gas Storage • Reaction Overview • Reactor • Ammonia Separation • Residual Gas Stream • FAQ Nitrogen Generation • Nitrogen from Air (79% Nitrogen) − Pressure Swing Adsorption (PSA) • Gas compression, adsorption on carbon media, depressurization, nitrogen desorption • Repeat until desired purity (>99.99%) − Cryogenic Liquefaction • High Cost • High Volume • Very High Purity ( >99.999%) − LN2 Delivery Hydrogen Generation • Traditional Catalytic Steam Reforming of Methane and Water-Gas Shift Reaction CH4 + 2H2O CO2 + 4H2 • Capture CO2 for Urea Production • Chloralkali Process 2NaCl + 2H2O Cl2 + H2 + 2NaOH • Electrolysis of Water 2H2O 2H2 + O2 • Pyrolysis (Gasification) of Biomass C6H12O6 + O2 + H2O CO + CO2 + H2 Hydrogen Purification • High Purity Hydrogen Required to Prevent Catalyst Degradation − Low H2O − Low Sulfur − Low CO2 and CO • Traditional Chemical Methods − Diethylene glycol water removal − Methyldiethanolamine for CO2 − ZnO, FeO remove H2S chemically − N-Formylmorpholine also for H2S • Palladium Membrane Separation • Pressure Swing Adsorption Reaction Gas Blending •Low pressure hydrogen and nitrogen are blended using mass flow controllers then compressed to 3000 psi Reaction Gas Storage • Renewable Sources (Solar, -
Economy of Salt in Chloralkali Manufacture
National Salt Conference 2008, Gandhidham Economy of Salt in Chloralkali Manufacture Vladimir M. Sedivy MSc (Hons) Chem Eng, IMD President, Salt Partners Ltd., Zurich, Switzerland Email: [email protected] Impurities in salt are costly. Impurities dissolve in electrolytic brine and need to be removed, employing expensive processes and chemicals. The cost of brine purification is high. Therefore, pure salt is more valuable. Chloralkali producers are willing to pay higher price for purer salt. This paper deals with the technical aspects of the use of salt in the chloralkali industry, explains under what conditions the consumption of brine purification chemicals can safely be reduced and offers the economic rules that can be used for estimating the additional value of pure salt. The main principles of high quality solar salt production and the related economy are explained. Advanced technologies, such as SOLARSAL saltworks design and operation, BIOSAL biological solar saltworks management and HYDROSAL salt purification process with hydroextraction of impurities facilitate profitable production of high quality solar salt for chloralkali industry, for human consumption and for exports. Salt is a most important raw material for chemical industry The annual world production of salt exceeds 200 million tons. Approximately one third of the total is produced by solar evaporation of sea water or inland brines. Another one third is obtained by mining of rock salt deposits, both underground and on the surface. The balance is obtained as brines, mainly by solution mining. Brines can be used directly, for example in diaphragm electrolysis, or thermally evaporated to produce vacuum salt. Salt type World production Solar salt 90,000,000 t/y Rock salt 60,000,000 t/y Brines and vacuum salt 80,000,000 t/y The chemical industry is the largest salt consumer of salt using about 60% of the total production. -
Fugitive Emissions)
AEAT/R/ENV/1000 Issue 1 Appendix 3 Energy (Fugitive Emissions) CONTENTS 1 INTRODUCTION 2 2 COAL MINING 2 3 SOLID FUEL TRANSFORMATION 3 3.1 Coke Production 3 3.2 Solid Smokeless Fuel Production 4 4 OIL AND NATURAL GAS 5 4.1 Offshore Flaring 6 4.2 Offshore Gas Use 7 4.3 Well Testing 8 4.4 Other Emissions from Platforms and Terminals 9 4.5 Loading Emissions 9 4.6 Leakage from the Gas Transmission System. 10 4.7 Petrol Distribution 11 4.8 Refineries and Petroleum Processes 11 4.9 Gasification Processes 12 5 REFERENCES 13 AEA Technology A3.1 AEAT/R/ENV/1000 Issue 1 1 Introduction This Appendix outlines the emissions of greenhouse gases arising from the production, extraction of coal, oil and natural gas; their storage, processing and distribution. These emissions are fugitive emissions and are reported in IPCC Table 1B. Emissions from fuel combustion during these processes are reported in IPCC Table 1A and are described in Appendix 2. In certain cases the methodology of some of these fuel combustion emissions are discussed in this Appendix, because they have links with the methodologies used for fugitive emissions. 2 Coal Mining The NAEI reports emissions of methane from coal mining in the categories deep mined coal; coal storage and transport; open cast coal. These map onto the IPCC categories 1B1ai Underground Mines-mining, 1B1ai Underground Mines-post-mining and 1B1aii Surface Mines respectively. Emissions are calculated from saleable coal production statistics reported in DTI, (2001). Data on the shallower licensed mines are not published and were supplied to us by Barty (1995) up to 1994. -
Production of Caustic Soda Using Solar Powered Diaphragm Cells
IOSR Journal of Applied Chemistry (IOSR-JAC) e-ISSN: 2278-5736.Volume 8, Issue 2 Ver. I. (Feb. 2015), PP 09-16 www.iosrjournals.org Production of Caustic Soda Using Solar Powered Diaphragm Cells Eng. Wegdan Ahmad Osman Ahmad1 Khartoum, Sudan2 Dr. Abdelsalam Abdelmaged3 Department of Chemical Engineerin, Faculty of Engineering, Al-Neelain University Khartoum, Sudan (E-mail: [email protected]) Department of Chemical, Faculty of Engineering, Al-Neelain University, Head of Department of Chemical Engineering Khartoum, Sudan (E-mail: [email protected]) Abstract: we showed in this paper the possibility of producing caustic soda directly from solar powered electrolytic diaphragm cells in comparison with present conventional modes of electrochemical production.,The results showed that this method has superior economic characteristics. The non-asbestos diaphragm cell showed similar trend with the conventional asbestos diaphragm cell performances indicating higher yield of caustic soda per d.c Watt. The asbestos and non-asbestos diaphragms served to hinder the formation of unwanted substances as well as permit reasonable production of the desired products. Quantitative analysis showed that the quantity and concentration of caustic soda produced varied with the current and voltage obtained from the solar panels which were dependent upon the intensity of the sun on any particular day and the length of time the panels were exposed to sunlight.[1] Keywords: caustic soda, asbestos, diaphragm cells, solar, non-asbestos, economic . I. Introduction Among the various strategies aimed to meet energy demand, efficient use of energy and its conservations emerges out to be the least cost option. Energy Conversation assumes special significance due to the limited availability of energy, and heavy dependence on imports for this purpose. -
Solvay Process & Local History Archive
Solvay Public Library Solvay Process & Local History Archive 615 Woods Road, Solvay, NY 13209 Phone (315) 468-2441, Fax (315) 468-0373 www.solvaylibrary.org LOCAL HISTORY SUBJECT HEADINGS (SV) October 3, 2017 Atlantic States Legal Foundation Biography – Abell, Flavel L. Antonini, Henry Atwood, Clinton H. Auchincloss, Sarah S. Bacon, Nathaniel Terry Bodot, Jean-Nicholas Bodot, John Campagnoni, William L. Casey, Daniel & Betty Clapp, John T. Clark, Hezikiah E. Coleman Family Cogswell. William B. Cominolli, Rita Cooper, Harriet Miller Croasdale, Robert Darrow, Beverly DeLallo, Leonard DeLawyer, Mark W. Demport, Charles See also LH 921 DEM D'eredita, Carmen Desantis, Mario D’Onofrio, Joan Duvall, Claude Fitzgerald, Mary E. Gere Family Gill, Irving J. Green, Andrew H. Grodevant family Hadley, E. Earl Handlon, Anne Emily Haas, Ruth Alice Hazard family – Caroline Hazard Deeds Dora Hazard Frederick R. Hazard Genealogy History John N. Hazard Maps of Uplands Development Photographs Solvay Public Library Solvay Process & Local History Archive 615 Woods Road, Solvay, NY 13209 Phone (315) 468-2441, Fax (315) 468-0373 www.solvaylibrary.org Rowland Gibson Hazard Upland Farm Upland Farms photographs Ippolito, Tom Kinsella, Edward Kinsella Family Lewis, Joe See also, Joseph L. Lewis Collection Major, Stanley E. Mandigo, Roy A. Marcellus, Clyde D. Mashall, Ty McCollum, Dr. Frank R. McConnell, James Mertens family Mioli, Milo Miscellaneous… Murphy, Clara Hill Murtagh, Anna L. Palerino, Vincent Parsons, Willis Pass, James A. Pennock, John D. Petrocci, Gariele Pettitt, David Pirro, Rocco inc. Carmen Rocco Porter, Dr. Wilfred W. Powell, Edward A. Quinlan, Patrick R. Randall, James A. Richards, Charles O. Riley, Helen Salvetti, Arthur Scott, Jeannette Seymour, Albert P. -
Soda Ash Sodium Carbonate
Alkali-Chlorine & Allied Chemicals Course : ACCE-2221 2nd Year : Even Semester Group-A : Chapter-2 30 January 2016 Course Outline 1. Alkali, Chlorine and Allied Chemicals 2. Sodium Chloride as raw material 3. Manufacture of soda ash, Caustic soda, Chlorine. 4. Manufacture of hypochlorite's and bleaching powder. 30 January 2016 Alkali In chemistry, an alkali is a basic, ionic salt of an alkali metal or alkaline earth metal chemical element. Some authorsalso define an alkali as a base that dissolves in water. A solution of a soluble base has a pH greater than 7.0. 30 January 2016 Allied Chemicals Caustic potash Caustic soda Chlorine compressed or liquefied Potassium carbonate Potassium hydroxide Sal soda (washing soda) Sodium bicarbonate Sodium carbonate (soda ash) 30 January 2016 Alkali Metal 30 January 2016 Alkali 30 January 2016 Alkali 30 January 2016 Common properties of Alkali Moderately concentrated solutions (over 10−3 M) have a pH of 7.1 or greater. This means that they will turn phenolphthalein from colorless to pink. Concentrated solutions are caustic (causing chemical burns). Alkaline solutions are slippery or soapy to the touch, due to the saponification of the fatty substances on the surface of the skin. Alkalis are normally water soluble, although some like barium carbonate are only soluble when reacting with an acidic aqueous solution. 30 January 2016 What is soda ash? Sodium carbonate (also known as washing soda, soda ash and soda crystals), Na2CO3, is a sodium salt of carbonic acid (soluble in water). It most commonly occurs as a crystalline hepta-hydrate, which readily effloresces to form a white powder, the monohydrate. -
Dynamic Model of Chloralkali Membrane Process
Available online at www.sciencedirect.com ScienceDirect Procedia Engineering 170 ( 2017 ) 473 – 481 Engineering Physics International Conference, EPIC 2016 Dynamic Model of Chloralkali Membrane Process T Budiartoa, E Eschea, J U Repkea, E Leksonob a Process Dynamics and Operations Group, DBTA , Technische Universität Berlin, Str. des 17. Juni 135, D-10623 Berlin, Germany* bEngineering Physics Group, Institut Teknologi Bandung, Str. Ganesha 10, 40132 Bandung, Indonesia† Abstract Chloralkali is one of the most important and energy intensive processes in the chemical industry. The process produces chlorine through electrochemical conversion. The process’s energy consumption is a major production cost for the chloralkali industry. Since the demand for energy efficiency and environmentally friendly processes in industry increases, ion exchange membranes are used intensively in the process. One of the prospective energy sources for this process is renewable energy, which shows strong fluctuations and highly unpredictable behavior. Dynamic behavior of the process becomes important to measure and predict the feasibility of the process. Therefore, modelling of the process dynamics is required. Rigorous model of material balance and voltage balance of the process are developed and investigated in this paper. The material transport phenomena inside the electrolyser are modelled considering a number of driving forces. The developed model also predicts the voltage and current density of the cell. The process simulation result is compared to experimental data. © 2017 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (©http://creativecommons.org/licenses/by-nc-nd/4.0/ 2016 The Authors. Published by Elsevier Ltd. ). Peer-review under responsibility of the organizing committee of the Engineering Physics International Conference 2016 Keywords: chloralkali; dynamic model; electrochemical process; demand response potential 1.