Caustic Soda Handbook March 2018
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Potash Case Study
Mining, Minerals and Sustainable Development February 2002 No. 65 Potash Case Study Information supplied by the International Fertilizer Industry Association This report was commissioned by the MMSD project of IIED. It remains the sole Copyright © 2002 IIED and WBCSD. All rights reserved responsibility of the author(s) and does not necessarily reflect the views of the Mining, Minerals and MMSD project, Assurance Group or Sponsors Group, or those of IIED or WBCSD. Sustainable Development is a project of the International Institute for Environment and Development (IIED). The project was made possible by the support of the World Business Council for Sustainable Development (WBCSD). IIED is a company limited by guarantee and incorporated in England. Reg No. 2188452. VAT Reg. No. GB 440 4948 50. Registered Charity No. 800066 1 Introduction 2 2 Global Resources and Potash Production 3 3 The use of potassium in fertilizer 4 3.1 Potassium Fertilizer Consumption 4 3.2 Potassium fertilization issues 6 Appendix A 8 1 Introduction Potash and Potassium Potassium (K) is essential for plant and animal life wherein it has many vital nutritional roles. In plants, potassium and nitrogen are the two elements required in greatest amounts, while in animals and humans potassium is the third most abundant element, after calcium and phosphorus. Without sufficient plant and animal intake of potassium, life as we know it would cease. Human and other animals atop the food chain depend upon plants for much of their nutritional needs. Many soils lack sufficient quantities of available potassium for satisfactory yield and quality of crops. For this reason available soil potassium levels are commonly supplemented by potash fertilization to improve the potassium nutrition of plants, particularly for sustaining production of high yielding crop species and varieties in modern agricultural systems. -
Liquid Lye MSDS
MATERIAL SAFETY DATA SHEET LIQUID LYE Revision Number 4, Revision Date 10.01.29 1. IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND THE COMPANY/UNDERTAKING Product Code CON151BT Product Name LIQUID LYE Synonyms Liquid Sodium Hydroxide (50%) Manufacturer and Supplier CHEM CLEAN LTD #1 Trincity Drive Trincity Industrial Estate Trincity Trinidad and Tobago EMERGENCY TELEPHONE NUMBER (868) 662-2615 2. COMPOSITION/INFORMATION ON INGREDIENTS CAS CHEMICAL NAME % WEIGHT 1310-73-2 Sodium Hydroxide 49 min 3. HAZARDS IDENTIFICATION Emergency Overview: ♦ Corrosive ♦ Based upon available toxicity information for this and closely related materials, it is anticipated that this material will be harmful if ingested and can cause serious tissue damage Eye Contact ♦ Causes severe burns Skin Contact ♦ Causes severe irritation and chemical burns Inhalation ♦ None, if used in adequately ventilated area Ingestion ♦ Harmful if swallowed ♦ Causes serious damage to tissues General Advice ♦ See First Aid Section Properties affecting Health Principle Routes of ♦ Eye Exposure ♦ Skin 4. FIRST AID MEASURES General Advice ♦ Show this Safety Data Sheet to the Doctor in attendance Page 1 of 6 LIQUID LYE Skin Contact ♦ Immediately apply vinegar if readily available ♦ Immediately flush skin with plenty of cool running water for at least 15 minutes ♦ Immediately remove contaminated clothing ♦ Immediate Medical Attention is required if irritation persists or burns develop Eye Contact ♦ In case of eye contact, remove contact lens and rinse immediately with plenty of water, -
MORDANTING NATURAL DYES IRON SULPHATE (Ferrous Sulphate) Is Usually Used to Change the Colour of a Dye
MORDANTING NATURAL DYES IRON SULPHATE (Ferrous Sulphate) is usually used to change the colour of a dye. It also makes natural dyes Most natural dyes have great affinity for fibre but more light and wash fast. More often used with cellulose poor light and wash fastness. If the fibre is pre than protein as it can make protein fibres brittle and harsh. mordanted you create a bond between the dye Iron changes shades to deeper, darker shades and is better and the fibre which will improve this dramatically. used in a premordant bath than directly into the dyebath. The most common and least environmentally toxic Use at a maximum of 2 to 4 % WOF . are Alum, Iron and Tannin. Copper is a useful mordant but is toxic to marine COPPER (Copper Sulphate)tends dull colours and turn life and humans. It needs to be handled and them blue green ie. yellows become greens, pinks become disposed of carefully. Historically Tin and Chrome purple. You can use Copper as a premordant or as an after have been used but are hazardous to the treatment to adjust colours. Colours dyed with Copper are environment & your health and need to be usually more lightfast than those dyed with Alum. Copper disposed of with great care. For that reason we has a less harsh effect on Protein fibres than Iron. Dispose recommend only using Alum, Iron, Copper and of Copper solution responsibly by exhausting your Tannin. Copper is probably the least safe but will dyebaths, diluting the residue with clean water and don’t give you much brighter shades and is safe to use put it down the storm water. -
SODIUM HYDROXIDE @Lye, Limewater, Lyewater@
Oregon Department of Human Services Office of Environmental Public Health (503) 731-4030 Emergency 800 NE Oregon Street #604 (971) 673-0405 Portland, OR 97232-2162 (971) 673-0457 FAX (971) 673-0372 TTY-Nonvoice TECHNICAL BULLETIN HEALTH EFFECTS INFORMATION Prepared by: ENVIRONMENTAL TOXICOLOGY SECTION OCTOBER, 1998 SODIUM HYDROXIDE @Lye, limewater, lyewater@ For More Information Contact: Environmental Toxicology Section (971) 673-0440 Drinking Water Section (971) 673-0405 Technical Bulletin - Health Effects Information Sodium Hydroxide Page 2 SYNONYMS: Caustic soda, sodium hydrate, soda lye, lye, natrium hydroxide CHEMICAL AND PHYSICAL PROPERTIES: - Molecular Formula: NaOH - White solid, crystals or powder, will draw moisture from the air and become damp on exposure - Odorless, flat, sweetish flavor - Pure solid material or concentrated solutions are extremely caustic, immediately injurious to skin, eyes and respiratory system WHERE DOES IT COME FROM? Sodium hydroxide is extracted from seawater or other brines by industrial processes. WHAT ARE THE PRINCIPLE USES OF SODIUM HYDROXIDE? Sodium hydroxide is an ingredient of many household products used for cleaning and disinfecting, in many cosmetic products such as mouth washes, tooth paste and lotions, and in food and beverage production for adjustment of pH and as a stabilizer. In its concentrated form (lye) it is used as a household drain cleaner because of its ability to dissolve organic solids. It is also used in many industries including glassmaking, paper manufacturing and mining. It is used widely in medications, for regulation of acidity. Sodium hydroxide may be used to counteract acidity in swimming pool water, or in drinking water. IS SODIUM HYDROXIDE NATURALLY PRESENT IN DRINKING WATER? Yes, because sodium and hydroxide ions are common natural mineral substances, they are present in many natural soils, in groundwater, in plants and in animal tissues. -
The Art of Mordanting and Staining and the Complete Treatment of Wood
The Artof/Aordanting and Staining ' N:i^\><v 5W^ \\ \ ^^^ Class. X ) 3^^ Book -A fe Copyright }1® - COPYRIGHT DEPOSIT. C^z-A-^^UX-ftUv^w*^ %««<«^vvwn''v<^t'^"t^'>vva-'VU'nH^ , THE ART OF M ORD A NTI NG AND STAINING AND THE COMPLETE TREATMENT OF WOOD SURFACES A HANDBOOK AND AID FOR ARCHITECTS, CABINET MAKERS, DECORATORS, PAINTERS, PIANO FACTORIES AND TRADE SCHOOLS BY WILLIAM ZIMMERMANN INSTRUCTOR OF CHKMISTRY IN POLYTECHNIC INSTITUTE, BARMEN, GERMANY BOSTON, MASS.: THE ARTI-STAIN CO. 1911 \J> First English Edition Copyright 191 i BY W. F. PURSCHER All Rights Reserved ^ r/> ARTI-STAIN CO. Sole Agents for U. S. A. and the Dominion of Canada / !)CI.A28t)433 PREFACE Since the appearance of the Fifth Edition of this work in 1908, it has again been considerably enlarged and revised and the results incorporated in the present Sixth Edition. In the portion relating to staining, the chapter on Brown Stains, which occupy an important position in connection with modern furniture and fittings, has been completely revised and enlarged by the introduction of the new and practically-tested Special-Oak Stains, An- thracene Stains and Genuine-Mahogany Stains, which have been very favorably received. Because of their lesser importance, the number of staining formulas for bright colors has been diminished, but these have been replaced by staining formulas for new products of greater fastness to light. All suggestions and experiments since the last edition have been incorporated here. The Sample Card of colors (in the Supplement) has been made to correspond with the new formulas in the book. -
Carbon Dioxide Capture from Atmospheric Air Using Sodium
Environ. Sci. Technol. 2008, 42, 2728–2735 Carbon Dioxide Capture from Nearly all current research on CCS focuses on capturing CO2 from large, stationary sources such as power plants. Atmospheric Air Using Sodium Such plans usually entail separating CO2 from flue gas, compressing it, and transporting it via pipeline to be Hydroxide Spray sequestered underground. In contrast, the system described in this paper captures CO2 directly from ambient air (“air § capture”). This strategy will be expensive compared to capture JOSHUAH K. STOLAROFF, from point sources, but may nevertheless act as an important DAVID W. KEITH,‡ AND complement, since CO emissions from any sector can be GREGORY V. LOWRY*,† 2 captured, including emissions from diffuse sources such as Chemical and Petroleum Engineering, University of Calgary, aircraft or automobiles, where on-board carbon capture is and Departments of Civil and Environmental Engineering very difficult and the cost of alternatives is high. Additionally, and Engineering and Public Policy, Carnegie Mellon in a future economy with low carbon emissions, air capture University, Pittsburgh, Pennsylvania 15213 might be deployed to generate negative net emissions (1). This ability to reduce atmospheric CO2 concentrations faster Received October 15, 2007. Revised manuscript received than natural cycles allow would be particularly desirable in February 05, 2008. Accepted February 06, 2008. scenarios where climate sensitivity is on the high end of what is expected, resulting in unacceptable shifts in land usability and stress to ecosystems. In contrast to conventional carbon capture systems for Previous research has shown that air capture is theoreti- cally feasible in terms of thermodynamic energy require- power plants and other large point sources, the system described ments, land use (2), and local atmospheric transport of CO2 in this paper captures CO2 directly from ambient air. -
United States Patent Office Patented Nov
3,352,642 United States Patent Office Patented Nov. 14, 1967 2 stabilized during storage for long periods of time with 3,352,642 out degradation of its oxidizing properties. STABLZATION OF OZONE Lawrence J. Heidt, Arlington, and Vincent R. Landi, In accordance with these and other objects, the present rookine, Mass., assignors to Massachusetts in invention involves the stabilization of ozone through the stitute of Technology, Cambridge, Mass., a corpo use of base, and in particular, sodium hydroxide and ration of Massachusetts other sources of hydroxyl-ion. This is a wholly new and No Drawing. Fied June 29, 1964, Ser. No. 378,990 Surprising approach to the problem of stabilizing ozone. 15 Clains. (Cl. 23-222) In fact, it has heretofore been generally believed that sodium hydroxide would have the opposite effect upon This invention relates to a method for the stabilization O oZone. For example, the Encyclopedia of Chemical Tech of ozone and in particular to a method whereby ozone nology, vol. 9, p. 735, reports that the ozone decomposi can be stored and transported with a much slower rate tion reaction is greatly accelerated by increasing the of decomposition than was heretofore thought possible. hydroxyl-ion concentration. Other references are made Ozone (O3) is an unstable blue gas which is formed in the same volume and article on ozone to the supposedly photochemically in nature in the earth's stratosphere but 5 detrimental effect of sodium hydroxide on the stability which exists only in great dilution with air or oxygen at of ozone. It is also reported in the article that the de ground levels. -
STATES PATENT OFFICE 2,497,519 ART of STABLZNG RAYON TYPE FABRIC Archibald S
Patented Feb. 14, 1950 2497,519 UNITED STATES PATENT OFFICE 2,497,519 ART OF STABLZNG RAYON TYPE FABRIC Archibald S. Stevenson, Pawtucket, and Leo Beer, Providence, R. I., assignors to Alrose Chemical Company, Cranston, R. ., a corporation of Rhode Island No Drawing. Application December 4, 1946, Serial No. 13,918 15 Claims. (C. 8-125) 2 The textile fabric with the stabilization of the alternative, costly ventilating equipment is which the present invention is concerned, con 'equired, and tains Synthetic fibers of regenerated cellulose, h. Fabrics treated with resins frequently cause Such as viscose or cupra-ammonium rayon or of dermatitis when worn by persons whose skin is cellulose-acetate or other cellulose derivative, the Sensitive to such resins. fabric consisting of any of said fibers, alone or in It is among the objects of the present inven admixture with one or more of the other fibers, tion to produce textile fabrics of the rayon-type with or without components of wool, cotton or which are stabilized to a highly satisfactory de other fiber, natural or synthetic. Fabric of the gree against laundering shrinkage, without there character referred to is designated hereinafter () by incurring excessive loss of yardage and with both in the specification and the claims in the in out the need to this end for incorporating in or terest of brevity as "rayon-type fabric.' on the fibre any foreign substance, or altering As conducive to a clear understanding of the the molecular structure of the fiber or detracting from the weight or the tensile strength or the invention, it is noted that if such rayon-type abrasion resistance of the fibre or fabric or in fabric were subjected to the action of caustic 5 pairing the hand of feel thereof, or objectionably under conditions similar to those of mercerizing detracting from its luster. -
Chemical Compatibility Guide
APPENDIX E CHEMICAL COMPATIBILITY GUIDE DISCLAIMER: This chart is intended to provide general guidance on chemical compatibility and should not be used for product selection. The chart is based on industry data and may not be applicable to your specific applications. Temperature, fluid concentration and other process conditions may affect the material compatibility. If there is uncertainty about the suitability of the material with the process chemical, Macnaught recommends physical testing of the sample material with the chemical. If further assistance is required, Macnaught's Technical Support Team can provide advice to assist with selection. S Recommended S E E L L RI Data not available RI E E E — E E E S S ST ST 61 Not recommended 61 0 0 S S 6 6 S S E E M M N N L L O O N N I I T T N N A A Y Y O O T T R R N N M M B B S S E E O O S S R R M M UMINIU UMINIU F F 6 6 T T A A K K 1 1 AL PP AL PP C VI PT F C VI PT F 3 3 Acetaldehyde — Aluminum Chloride 20% — — Acetamide — Aluminum Fluoride — — — Acetate Solvent — — — Aluminum Hydroxide — — Acetic Acid — — — Aluminum Nitrate — — — Aluminum Potassium Acetic Acid 20% Sulfate 10% — — — — Acetic Acid 80% — — — Aluminum Sulfate — Acetic Acid, Glacial — — Alums — — — — — Acetic Anhydride — Amines — — — — Acetone — Ammonia 10% — — Acetyl Chloride (dry) — — Ammonia Nitrate — — — — — Acetylene Ammonia, anhydrous — — — Acrylonitrile — — — Ammonia, liquid — — — Adipic Acid — Ammonium Acetate — — — Alcohols: Amyl — — — — Ammonium Bifluoride — — — — Alcohols: Benzyl — — — — Ammonium Carbonate — — Alcohols: -
Experimental Study on Capture of Carbon Dioxide and Production of Sodium Bicarbonate from Sodium Hydroxide
Environ. Eng. Res. 2016 Research Article http://dx.doi.org/10.4491/eer.2016.042 pISSN 1226-1025 eISSN 2005-968X In Press, Uncorrected Proof Experimental study on capture of carbon dioxide and production of sodium bicarbonate from sodium hydroxide † Jae-Goo Shim , Dong Woog Lee, Ji Hyun Lee, No-Sang Kwak KEPCO Research Institute, 105 Munji-ro, Yuseong-gu, Daejeon, 54056, Korea Abstract Global warming due to greenhouse gases is an issue of great concern today. Fossil fuel power plants, especially coal-fired thermal power plants, are a major source of carbon dioxide emission. In this work, carbon capture and utilization using sodium hydroxide was studied experimentally. Application for flue gas of a coal-fired power plant is considered. Carbon dioxide, reacting with an aqueous solution of sodium hydroxide, could be converted to sodium bicarbonate (NaHCO3). A bench-scale unit of a reactor system was designed for this experiment. The capture scale of the reactor system was 2 kg of carbon dioxide per day. The detailed operational condition could be determined. The purity of produced sodium bicarbonate was above 97% and the absorption rate of CO2 was above 95% through the experiment using this reactor system. The results obtained in this experiment contain useful information for the construction and operation of a commercial-scale plant. Through this experiment, the possibility of carbon capture for coal power plants using sodium hydroxide could be confirmed. This is an Open Access article distributed under the terms Received March 14, 2016 Accepted May 10, 2016 of the Creative Commons Attribution Non-Commercial Li- † cense (http://creativecommons.org/licenses/by-nc/3.0/) Corresponding Author which permits unrestricted non-commercial use, distribution, and repro- E-mail: [email protected] duction in any medium, provided the original work is properly cited. -
Potassium and Phosphorus Have No Effect on Severity of Charcoal Rot of Soybean
Can. J. Plant Pathol., 2016 http://dx.doi.org/10.1080/07060661.2016.1168869 Disease control/Moyens de lutte Potassium and phosphorus have no effect on severity of charcoal rot of soybean ALEMU MENGISTU1, XINHUA YIN2, NACER BELLALOUI3, ANGELA M. McCLURE2, DON D. TYLER4 AND KRISHNA N. REDDY5 1Crop Genetics Research Unit, United States Department of Agriculture, Agricultural Research Service (USDA-ARS), Jackson, TN, 38301, USA 2Department of Plant Sciences, University of Tennessee, Jackson, TN, 38301, USA 3Crop Genetics Research Unit, USDA-ARS, Stoneville, MS, 38776, USA 4Department of Biosystems Engineering and Soil Science, University of Tennessee, Jackson, TN, 38301, USA 5Crop Production Systems Research Unit, USDA-ARS, Stoneville, MS, 38776, USA (Accepted 17 March 2016) Abstract: Charcoal rot of soybean [Glycine max (L.) Merr.] caused by Macrophomina phaseolina is a disease of economic significance throughout the world. The effects of potassium (K) and phosphorus (P) fertilizer on disease development are unknown. Therefore, two separate trials were conducted in the field during 2008, 2009 and 2010 at Jackson and Milan, TN, USA to evaluate the effects of K and P on severity of −1 −1 charcoal rot. Rates of K (0, 45, 90, 134 and 179 kg K2Oha ) and P (0, 22, 45, 67 and 90 kg P2O5 ha ) were used, with a sixth rate ranging from 0–22 for P and 0–37 for K equal to the recommended K or P fertilizer application based on annual soil testing. The colony forming units of M. phaseolina in soil indicated no significant response for any P treatments in five of six location-by-year and for K applications in all six location-by-year environments. -
Fertilizer Guide
Jts - Using Wood Ashes in Fertilizer the Home Garden FG61 Guide Revised May 1982 Wood ashes can be useful as a fertilizer and magnesium oxides in fresh ash can react with liming material in home gardens, particularly on water to produce hydroxides or with carbon dioxide acid soils low in potassium. to produce carbonates. Calcium and magnesium oxides, hydroxides, and carbonates are found in Wood contains a small proportion of mineral, or commercial liming materials. inorganic matter. When wood is burned, mineral matter is left behind as a white-gray ash. Potassium (K) Hardwoods, or deciduous trees, when burned, produce a greater percent of ash than softwoods, Potassium is found in wood ash as potassium car- or conifers. Within a given tree, different bonate and potassium oxide. The potash content parts produce varying amounts of ash. Generally (K 0) of wood ash varies from 10 to 35%. These the percent of ash in the bark exceeds that of compounds, like lime, have a neutralizing effect the branches with the branches containing more on soil acidity. ash than the stem wood. The ash content not only Phosphorus (P) varies with tree species or the part of a tree, but also with the age of the tree, season of The content of phosphorus (as P^O ) in wood ash felling and method of burning. For woods in is usually less than 10%. temperate regions, the ash content usually ranges from 0.2% to 1.0%, occasionally approaching 3% to Fertilizer Value of Wood Ash 4%. The fertilizer value of wood ash depends on the Prior to World War II, wood ashes were used on a type of wood burned.