Jersey Department of Health, Ammonium Hydroxide Has Sheet (MSDS) and the Label to Determine Product Not Been Tested for Its Ability to Affect Reproduction
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Chemical Storage Cabinets
Storage cabinets Incompatible chemicals must be kept separately to reduce the risk of mixing in case of accidental breakage or response to an emergency within the laboratory. (A starting point is to check the Safety Data Sheet for hazard and storage requirements.) Containers must be kept tightly closed and stored in cabinets which are suitable for the chemical. It is important to check materials which have a shelf life and safely dispose of before the date expires, and generally check the label to ensure it is still suitable and provides the necessary safety information. The condition of the cabinets needs to be checked to ensure that they are providing adequate containment of the materials being stored. Ensure spill trays are used which are capable of holding 110% volume of the largest container being stored in the tray. There may be occasions where the quantities being stored are very small and secondary containment of the chemicals within a cabinet provided would be deemed as providing adequate separation. The table below provides guidance on the type of materials being stored and the type of cabinet which is suitable for that material. This is not a definitive list and does not include ‘Highly Toxic’ materials. Separate guidance is in development. Hazard Group Type of cabinet Safety Sign and suggested Other information Max allowed (where wording applicable) Flammable Liquids Metal flammable storage Flammable liquids must 50 litres of highly flammable cabinet to BS EN 14470- never be stored in a liquid stored in any one E.g. alcohols, toluene, 1:2004, offering minimum refrigerator or freezer laboratory. -
Treating Irrigation Systems with Chlorine 1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. CIR1039 Treating Irrigation Systems with Chlorine 1 Kati W. Migliaccio, Brian Boman and Gary A. Clark2 Introduction Irrigation systems can become partially or completely clogged from biological growths of bacteria or algae which are often present in surface water and ground water. Bacteria and algae use chemical elements such as nitrogen, phosphorus, sulfur, or iron as nutrient sources to grow and develop (Figures 1 and 2) (Pitts et al., 2003). Thus, irrigation systems that also receive nutrients (such as natural background concentrations in the water or from fertigation) may experience greater rates of clogging. While all irrigation systems should have some Figure 1. Irrigation emitter clogged with algal growth. type of filtration system, this alone cannot effectively Credits: Brian Boman UF/IFAS remove microorganisms. Microorganism growth can result in clogged pipes, fittings, and emission devices of the chlorine chemical must be used to provide an (sprinklers, drippers, spray jets, etc.), decreasing effective water treatment program without damaging water application amounts and reducing application the irrigation system or the agricultural crop. uniformity and efficiency. The results of these are This publication provides a guide for using generally reduced agriculture productivity. A chlorine to treat inhibiting microorganism buildup in chemical method for removing microbial growth is irrigation systems. chlorination. Proper injection methods and amounts 1. This document is CIR1039, one of a series of the Agricultural and Biological Engineering Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Original publication date July 1992. -
(Oxy)Hydroxide Electrocatalysts for Water Oxidation Bryan R
www.acsami.org Research Article Effect of Selenium Content on Nickel Sulfoselenide-Derived Nickel (Oxy)hydroxide Electrocatalysts for Water Oxidation Bryan R. Wygant, Anna H. Poterek, James N. Burrow, and C. Buddie Mullins* Cite This: ACS Appl. Mater. Interfaces 2020, 12, 20366−20375 Read Online ACCESS Metrics & More Article Recommendations *sı Supporting Information ABSTRACT: An efficient and inexpensive electrocatalyst for the oxygen evolution reaction (OER) must be found in order to improve the viability of hydrogen fuel production via water electrolysis. Recent work has indicated that nickel chalcogenide materials show promise as electrocatalysts for this reaction and that their performance can be further enhanced with the generation of ternary, bimetallic chalcogenides (i.e., Ni1−aMaX2); however, relatively few studies have investigated ternary chalcogenides created through the addition of a second chalcogen (i.e., NiX2−aYa). To address this, we fi studied a series of Se-modi ed Ni3S2 composites for use as OER electrocatalysts in alkaline solution. We found that the addition of Se results in the creation of Ni3S2/NiSe composites composed of cross-doped metal chalcogenides and show that the addition of 10% Se reduces the overpotential required to reach a current density of 10 mA/cm2 by 40 mV versus a pure nickel sulfide material. Chemical analysis of the composites’ surfaces shows a reduction in the amount of nickel oxide species with Se incorporation, which is supported by transmission electron microscopy; this reduction is correlated with a decrease in the OER overpotentials measured for these samples. Together, our results suggest that the incorporation of Se into Ni3S2 creates a more conductive material with a less-oxidized surface that is more electrocatalytically active and resistant to further oxidation. -
186 SESSION LAWS [Chap
186 SESSION LAWS [Chap. Sec. 2. This act shall take effect and be in force from and after its passage. Approved April 13, 1925. CHAPTER 187—S. F. No. 984. An act to safeguard the distribution and sale of certain danger- ous caustic or corrosive acids, alkalis, and other substances. Be it enacted by the Legislature of the State of Minnesota: Section 1. Definitions.—That in this act, unless the context or subject-matter otherwise requires, A. The term "dangerous caustic or corrosive substance" means each and all of the acids, alkalis, and substances named below: (a) Hydrochloric acid and any preparation containing free or chemi- cally unneutralized hydrochloric acid (HC1) in a concentration of ten per centum or more; (b) Sulphuric acid and any preparation containing free or chemically unneulralized sulphuric acid (H2SO4) in a concentration of ten per centum or more; (c) Nitric acid or any preparation containing free or chemically unneutralized nitric acid (HNO3) in a concentration of five per centum or more; (d) Carbolic acid (C6H5OH), otherwise known as phenol, and any preparation containing carbolic acid in a concentration of five per centum or more; (e) Oxalic acid and any preparation containing free or chemically unneutralized oxalic acid (H2C2O4) in a con- centration of ten per centum or more; (f) Any salt of oxalic acid and any preparation containing any such salt in a concentration of ten per centum or more; (g) Acetic acid or any preparation con- taining free or chemically unneutralized acetic acid (HC2H3O2) in a concentration of -
The Influence of Sodium Hydroxide Concentration on the Phase, Morphology and Agglomeration of Cobalt Oxide Nanoparticles and Application As Fenton Catalyst
Digest Journal of Nanomaterials and Biostructures Vol.14, No.4, October-December 2019, p. 1131-1137 THE INFLUENCE OF SODIUM HYDROXIDE CONCENTRATION ON THE PHASE, MORPHOLOGY AND AGGLOMERATION OF COBALT OXIDE NANOPARTICLES AND APPLICATION AS FENTON CATALYST E. L. VILJOENa,*, P. M. THABEDEa, M. J. MOLOTOa, K. P. MUBIAYIb, B. W. DIKIZAa aDepartment of Chemistry, Vaal University of Technology Private, Bag X021, Vanderbijlpark 1900, South Africa bSchool of Chemistry, University of the Witwatersrand, 1 Jan Smuts Avenue, Braamfontein Johannesburg 2000, South Africa The concentration of NaOH was varied from 0.2 M to 0.7 M during the preparation of the cobalt oxide/cobalt oxide hydroxide nanoparticles by precipitation and air oxidation. Cubic shaped and less well defined Co3O4 nanoparticles formed at 0.2 M NaOH. An increase in the NaOH concentration increased the number of well-defined cubic shaped nanoparticles. Agglomerated CoO(OH) particles with different shapes formed at the highest NaOH concentration. The cubic shaped Co3O4 nanoparticles were subsequently used as catalyst for the Fenton degradation of methylene blue and it was found that the least agglomerated nanoparticles were the most catalytically active. (Received June 25, 2019; Accepted December 6, 2019) Keywords: Cobalt oxide, Nanoparticles, Precipitation, pH, Fenton reaction 1. Introduction Controlling the size and the shape of nanoparticles using simple, inexpensive precipitation methods without sophisticated capping molecules, remains a challenge. Literature has indicated that the concentration of the base (pH) is an important parameter to control the size, shape and phase of metal oxide nanoparticles. Obodo et al.[1] used chemical bath deposition at atmospheric pressure and 70 °C to precipitate Co3O4 crystallites on a glass substrate and they showed that the crystallite sizes were larger at a higher pH of 12 in comparison to when a pH of 10 was used. -
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. -
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. -
Sample Chapter Template for AFFA
The Training Material on “Dangerous Goods Handling (All modes)” has been produced under Project Sustainable Human Resource Development in Logistic Services for ASEAN Member States with the support from Japan-ASEAN Integration Fund (JAIF). Copyright Association of Southeast Asian Nations (ASEAN) 2014. All rights reserved. Dangerous Goods Handling Chapter 2: International Classification of Dangerous Goods Objectives This chapter will explain UN Transport regulations, its history and basis as model regulations for international classification system for other modes of transport. The linkage into the ASEAN Protocol 9 framework on the international carriage of dangerous goods in ASEAN will also be explained. 9 classes of dangerous goods classification shall be key content in this chapter. Other relevant basic terms such as Class, Division, Packaging Group (PG), UN Number (UNNO) and Proper Shipping Names (PSN) will also be covered. As supplement knowledge in classification of substances or mixtures that have more than one hazard, the explanation on precedence of hazard characteristics will be given. Basic hazard communication such as Labelling requirements, Dangerous Goods Declaration (DGD) or Multi-modal Dangerous Goods Form shall be explained. 1. Introduction 1.1 United Nations Recommendations on the Transport of Dangerous Goods (UNTDG/UNRTDG) These Recommendations have been developed by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods in the light of technical progress, the advent of new substances and materials, the exigencies of modern transport systems and, above all, the requirement to ensure the safety of people, property and the environment. They are addressed to governments and international organizations concerned with the regulation of the transport of dangerous goods. -
Exposure to Potassium Hydroxide Can Cause Headache, Eye Contact Dizziness, Nausea and Vomiting
Right to Know Hazardous Substance Fact Sheet Common Name: POTASSIUM HYDROXIDE Synonyms: Caustic Potash; Lye; Potassium Hydrate CAS Number: 1310-58-3 Chemical Name: Potassium Hydroxide (KOH) RTK Substance Number: 1571 Date: May 2001 Revision: January 2010 DOT Number: UN 1813 Description and Use EMERGENCY RESPONDERS >>>> SEE LAST PAGE Potassium Hydroxide is an odorless, white or slightly yellow, Hazard Summary flakey or lumpy solid which is often in a water solution. It is Hazard Rating NJDOH NFPA used in making soap, as an electrolyte in alkaline batteries and HEALTH - 3 in electroplating, lithography, and paint and varnish removers. FLAMMABILITY - 0 Liquid drain cleaners contain 25 to 36% of Potassium REACTIVITY - 1 Hydroxide. CORROSIVE POISONOUS GASES ARE PRODUCED IN FIRE DOES NOT BURN Reasons for Citation Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; f Potassium Hydroxide is on the Right to Know Hazardous 4=severe Substance List because it is cited by ACGIH, DOT, NIOSH, NFPA and EPA. f Potassium Hydroxide can affect you when inhaled and by f This chemical is on the Special Health Hazard Substance passing through the skin. List. f Potassium Hydroxide is a HIGHLY CORROSIVE CHEMICAL and contact can severely irritate and burn the skin and eyes leading to eye damage. f Contact can irritate the nose and throat. f Inhaling Potassium Hydroxide can irritate the lungs. SEE GLOSSARY ON PAGE 5. Higher exposures may cause a build-up of fluid in the lungs (pulmonary edema), a medical emergency. FIRST AID f Exposure to Potassium Hydroxide can cause headache, Eye Contact dizziness, nausea and vomiting. -
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. -
Dangerous Goods Classifications
Dangerous Goods Classifications Dangerous Goods Classifications Click on a class to read more details: 1. Explosives 2. Gases 3. Flammable Liquids 4. Flammable Solids 5. Oxidizing Substances 6. Toxic & Infectious Substances 7. Radioactive Material 8. Corrosives 9. Miscellaneous Dangerous Goods CLASS 1: EXPLOSIVES Explosives are materials or items which have the ability to rapidly conflagrate or detonate as a consequence of chemical reaction. Subclass Subclass 1.1: Explosives with a mass explosion hazard Consists of explosives that have a mass explosion hazard. A mass explosion is one which affects almost the entire load instantaneously. Subclass 1.2: Explosives with a severe projection hazard Consists of explosives that have a projection hazard but not a mass explosion hazard. Subclass 1.3: Explosives with a fire Consists of explosives that have a fire hazard and either a minor blast hazard or a minor projection hazard or both but not a mass explosion hazard. Subclass 1.4: Minor fire or projection hazard Consists of explosives that present a minor explosion hazard. The explosive effects are largely confined to the package and no projection of fragments of appreciable size or range is to be expected. An external fire must not cause virtually instantaneous explosion of almost the entire contents of the package. Subclass 1.5: An insensitive substance with a mass explosion hazard Consists of very insensitive explosives with a mass explosion hazard (explosion similar to 1.1). This division is comprised of substances which have a mass explosion hazard but are so insensitive that there is very little probability of initiation or of transition from burning to detonation under normal conditions of transport. -
N-BUTYL ALCOHOL
Right to Know Hazardous Substance Fact Sheet Common Name: n-BUTYL ALCOHOL Synonyms: Propyl Carbinol; n-Butanol CAS Number: 71-36-3 Chemical Name: 1-Butanol RTK Substance Number: 1330 Date: November 1998 Revision: January 2008 DOT Number: UN 1120 Description and Use EMERGENCY RESPONDERS >>>> SEE BACK PAGE n-Butyl Alcohol is a colorless liquid with a strong, sweet Hazard Summary alcohol odor. It is used as a solvent for fats, waxes, shellacs, Hazard Rating NJDOH NFPA resins, gums, and varnish, in making hydraulic fluids, and in HEALTH - 2 medications for animals. FLAMMABILITY - 3 REACTIVITY - 0 f ODOR THRESHOLD = 1 to 15 ppm FLAMMABLE f Odor thresholds vary greatly. Do not rely on odor alone to POISONOUS GASES ARE PRODUCED IN FIRE determine potentially hazardous exposures. CONTAINERS MAY EXPLODE IN FIRE Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; Reasons for Citation 4=severe f n-Butyl Alcohol is on the Right to Know Hazardous f n-Butyl Alcohol can affect you when inhaled and by Substance List because it is cited by OSHA, ACGIH, DOT, passing through the skin. NIOSH, DEP, IRIS, NFPA and EPA. f Contact can irritate and burn the skin. f This chemical is on the Special Health Hazard Substance f n-Butyl Alcohol can irritate and burn the eyes with possible List. eye damage. f Inhaling n-Butyl Alcohol can irritate the nose, throat and lungs. f Exposure to n-Butyl Alcohol can cause headache, dizziness, nausea and vomiting. SEE GLOSSARY ON PAGE 5. f n-Butyl Alcohol can damage the liver, kidneys, hearing, and sense of balance.