Microstructural and Compressive Strength Analysis for Cement Mortar with Industrial Waste Materials
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SDS Contains All of the Information Required by the HPR
SAFETY DATA SHEET Preparation Date: 7/7/2015 Revision Date: 7/6/2018 Revision Number: G2 1. IDENTIFICATION Product identifier Product code: C1115 Product Name: CALCIUM HYDROXIDE, POWDER, REAGENT, ACS Other means of identification Synonyms: Calcium hydrate Carboxide Calcium dihydroxidede calcium (French) CAS #: 1305-62-0 RTECS # EW2800000 CI#: Not available Recommended use of the chemical and restrictions on use Recommended use: Fireproofing coatings. water treatment. Buffering agent. In paper manufacture process. Chemical intermediate. In dental cement. In lubricants. In mortar, plaster, cement and other building and paving materials. In fungicides. In pesticides. In SBR rubber vulcanization. Uses advised against No information available Supplier: Spectrum Chemical Mfg. Corp 14422 South San Pedro St. Gardena, CA 90248 (310) 516-8000 Order Online At: https://www.spectrumchemical.com Emergency telephone number Chemtrec 1-800-424-9300 Contact Person: Martin LaBenz (West Coast) Contact Person: Ibad Tirmiz (East Coast) 2. HAZARDS IDENTIFICATION Classification This chemical is considered hazardous according to the 2012 OSHA Hazard Communication Standard (29 CFR 1910.1200) Considered a dangerous substance or mixture according to the Globally Harmonized System (GHS) Skin corrosion/irritation Category 2 Serious eye damage/eye irritation Category 1 Specific target organ toxicity (single exposure) Category 3 Label elements Danger Product code: C1115 Product name: CALCIUM 1 / 13 HYDROXIDE, POWDER, REAGENT, ACS Hazard statements Causes skin irritation Causes serious eye damage May cause respiratory irritation Hazards not otherwise classified (HNOC) Not Applicable Other hazards Not available Precautionary Statements - Prevention Wash face, hands and any exposed skin thoroughly after handling Avoid breathing dust/fume/gas/mist/vapors/spray Use only outdoors or in a well-ventilated area Wear protective gloves Wear eye/face protection Precautionary Statements - Response IF IN EYES: Rinse cautiously with water for several minutes. -
Alkali-Silica Reactivity: an Overview of Research
SHRP-C-342 Alkali-Silica Reactivity: An Overview of Research Richard Helmuth Construction Technology Laboratories, Inc. With contributions by: David Stark Construction Technology Laboratories, Inc. Sidney Diamond Purdue University Micheline Moranville-Regourd Ecole Normale Superieure de Cachan Strategic Highway Research Program National Research Council Washington, DC 1993 Publication No. SHRP-C-342 ISBN 0-30cL05602-0 Contract C-202 Product No. 2010 Program Manager: Don M. Harriott Project Maxtager: Inam Jawed Program AIea Secretary: Carina Hreib Copyeditor: Katharyn L. Bine Brosseau May 1993 key words: additives aggregate alkali-silica reaction cracking expansion portland cement concrete standards Strategic Highway Research Program 2101 Consti!ution Avenue N.W. Washington, DC 20418 (202) 334-3774 The publicat:Lon of this report does not necessarily indicate approval or endorsement by the National Academy of Sciences, the United States Government, or the American Association of State Highway and Transportation Officials or its member states of the findings, opinions, conclusions, or recommendations either inferred or specifically expressed herein. ©1993 National Academy of Sciences 1.5M/NAP/593 Acknowledgments The research described herein was supported by the Strategic Highway Research Program (SHRP). SHRP is a unit of the National Research Council that was authorized by section 128 of the Surface Transportation and Uniform Relocation Assistance Act of 1987. This document has been written as a product of Strategic Highway Research Program (SHRP) Contract SHRP-87-C-202, "Eliminating or Minimizing Alkali-Silica Reactivity." The prime contractor for this project is Construction Technology Laboratories, with Purdue University, and Ecole Normale Superieure de Cachan, as subcontractors. Fundamental studies were initiated in Task A. -
Silica Fume As a Scm for Pervious Concrete
THE EFFECTS OF UTILIZING SILICA FUME IN PORTLAND CEMENT PERVIOUS CONCRETE A THESIS IN Civil Engineering Presented to the Faculty of the University of Missouri-Kansas City in partial fulfillment of the requirements for the degree MASTER OF SCIENCE By DANIEL ALLEN MANN B.S. University of Missouri-Kansas City, 2012 Kansas City, Missouri 2014 © 2014 DANIEL ALLEN MANN ALL RIGHTS RESERVED THE EFFECTS OF UTILIZING SILICA FUME IN PORTLAND CEMENT PERVIOUS CONCRETE Daniel Allen Mann, Candidate for the Master of Science Degree University of Missouri-Kansas City, 2014 ABSTRACT Silica fume has long been used as a supplementary cementing material to provide a high density, high strength, and durable building material. Silica fume has a particle size a fraction of any conventional cement, which allows it to increase concrete strength by decreasing the porosity especially near the aggregates surface. Because Portland Cement Pervious Concrete (PCPC) has a smaller bond area between aggregate and paste, silica fume has significant impacts on the properties of the PCPC. The research in this paper studies the workability of a cement paste containing silica fume in addition to analyzing the results of testing on Portland Cement Pervious Concrete mixtures that also contained silica fume. Testing conducted included a study of the effects of silica fume on cement’s rheological properties at various dosage rates ranging from zero to ten percent by mass. It was determined that silica fume has negligible effects on the viscosity of cement paste until a dosage rate of five percent, at which point the viscosity increases rapidly. In addition to the rheological testing of the cement paste, trials were also conducted on the pervious concrete samples. -
ACUMER™ 9000 Mineral Slurry Dispersant
Technical Data ACUMER™ 9000 Mineral Slurry Dispersant Description ACUMER™ 9000 is a sodium salt of an acrylic acid-based polymer. It is a highly effective dispersant for aqueous calcium hydroxide and magnesium hydroxide slurries. Features and • Controlling phase separation Benefits • Reducing caking and clogging of equipment • Aiding the remixing of slurries after settling Typical Properties Property Typical Value Appearance Clear, light amber solution Total solids, % 44 pH 7.5 Density (lb/gal, @ 25°C) 10.8 Brookfield viscosity, (mPa.s/cps @ 25°C) 500 These properties do not constitute specifications. Performance Many problems can be encountered in producing calcium hydroxide or magnesium hydroxide slurries, including: • Wettability • Phase separation • Caking • Pumping • Pipe clogging • Remixing after setting • Slurry viscosity Calcium Hydroxide Figure 1 shows the efficiency of ACUMER 9000 as a dispersant for 30% calcium hydroxide slurry. Figure 1. ACUMER 9000 Dosage vs. Viscosity (30% Lime Slurry) Page 1 of 4 ®™Trademark of The Dow Chemical Company (“Dow”) or an affiliated company of Dow Form No. 812-00352-0216BBI ACUMER™ 9000 / Dow Oil, Gas & Mining The following table shows the positive effect of ACUMER™ 9000 dosage on lime slurry stability. Lower dosage (0.2%) gives higher slurry viscosity and lower syneresis (liquid phase separation). The desired slurry properties can be controlled by optimizing the dispersant dosage. Effect of ACUMER 9000 Dispersant on 30% Lime Slurry1 Stability After 8 Days at Room Temperature Initial Make-Down Dosage, % (solids basis) Syneresis Gel3 Flowed4 Viscosity2 0.2 2080 1.7 98.3 93.3 0.4 810 12.0 88.0 97.1 0.6 382 16.5 83.5 96.3 130% lime slurry was prepared by mixing 210 grams of slaked lime with 490 grams of deionized water (including additives) for five minutes in a Waring blender at high speed. -
Thermodynamics of Cement Hydration
UNIVERSITY OF ABERDEEN DEPARTMENT OF CHEMISTRY Thermodynamics of Cement Hydration by Thomas Matschei Dipl.-Ing., Bauhaus University Weimar A Thesis presented for the degree of Doctor of Philosophy at the University of Aberdeen Aberdeen, 06 December 2007 Declaration This Thesis is submitted to the University of Aberdeen for the degree of Doctor of Philosophy. It is a record of the research carried out by the author, under the supervision of Professor F.P. Glasser. It has not been submitted for any previous degree or award, and is believed to be wholly original, except where due acknowledgement is made. Thomas Matschei Aberdeen, December 2007 Abstract 3 Abstract The application of thermodynamic methods to cement science is not new. About 80 years ago, Bogue wrote a series of equations describing the relationship between clinker raw meal chemical composition and the mineralogy of the finished clinker. These enabled the amounts of minerals to be calculated from a bulk chemical composition. Fundamental to the equations was a precise description of the high temperature equilibrium achieved during clinkering. Bogue admitted four oxide components into the calculation; lime, alumina, silica and ferric oxide and assumed that equilibrium was attained (or very nearly attained) during clinkering. This approach, which is, with modifications, still a widely used tool to quantify cement clinkering, was one of the main motivations of this work. Thus the overall aim of this Thesis is to provide a generic toolkit, which enables the quantification of cement hydration. The use of thermodynamic methods in cement hydration was often doubted, as the water-cement system was considered to be too complex. -
Brownmillerite Ca2(Al, Fe )2O5 C 2001-2005 Mineral Data Publishing, Version 1
3+ Brownmillerite Ca2(Al, Fe )2O5 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: mm2. As square platelets, to about 60 µm; massive. Physical Properties: Hardness = n.d. D(meas.) = 3.76 D(calc.) = 3.68–3.73 Optical Properties: Semitransparent. Color: Reddish brown. Optical Class: Biaxial (–). Pleochroism: Distinct; X = Y = yellow-brown; Z = dark brown. Orientation: Y and Z lie in the plane of the platelets; extinction in that plane is diagonal. α = < 2.02 β = > 2.02 γ = > 2.02 2V(meas.) = n.d. Cell Data: Space Group: Ibm2. a = 5.584(5) b = 14.60(1) c = 5.374(5) Z = 2 X-ray Powder Pattern: Near Mayen, Germany. 2.65 (vs), 7.19 (s), 2.78 (s), 1.93 (s), 2.05 (ms), 3.65 (m), 1.82 (m) Chemistry: (1) (2) (3) TiO2 1.5 1.9 Al2O3 17.2 22.3 13.1 Fe2O3 30.5 27.6 41.9 Cr2O3 0.1 n.d. MgO n.d. n.d. CaO 46.2 44.8 43.7 insol. 4.0 LOI 0.5 Total 94.4 100.3 100.6 (1) Near Mayen, Germany; by semiquantitative spectroscopy. (2) Hatrurim Formation, Israel; corresponds to Ca1.99(Al1.09Fe0.86Ti0.05)Σ=2.00O5. (3) Do.; corresponds to Ca1.95(Fe1.31Al0.64 Ti0.06)Σ=2.01O5. Occurrence: In thermally metamorphosed limestone blocks included in volcanic rocks (near Mayen, Germany); in high-temperature, thermally metamorphosed, impure limestones (Hatrurim Formation, Israel). Association: Calcite, ettringite, wollastonite, larnite, mayenite, gehlenite, diopside, pyrrhotite, grossular, spinel, afwillite, jennite, portlandite, jasmundite (near Mayen, Germany); melilite, mayenite, wollastonite, kalsilite, corundum (Kl¨och, Austria); spurrite, larnite, mayenite (Hatrurim Formation, Israel). -
The Effect of Various Hydroxide and Salt Additives on the Reduction of Fluoride Ion Mobility in Industrial Waste
sustainability Article The Effect of Various Hydroxide and Salt Additives on the Reduction of Fluoride Ion Mobility in Industrial Waste Tadas Dambrauskas 1,* , Kestutis Baltakys 1, Agne Grineviciene 1 and Valdas Rudelis 2 1 Department of Silicate Technology, Kaunas University of Technology, LT-50270 Kaunas, Lithuania; [email protected] (K.B.); [email protected] (A.G.) 2 JSC “Lifosa”, LT-57502 Kedainiai, Lithuania; [email protected] * Correspondence: [email protected] Abstract: In this work, the influence of various hydroxide and salt additives on the removal of F− ions from silica gel waste, which is obtained during the production of AlF3, was examined. The leaching of the mentioned ions from silica gel waste to the liquid medium was achieved by the application of different techniques: (1) leaching under static conditions; (2) leaching under dynamic conditions by the use of continuous liquid medium flow; and (3) leaching in cycles under dynamic conditions. It was determined that the efficiency of the fluoride removal from this waste depends on the w/s ratio, the leaching conditions, and the additives used. It was proven that it is possible to reduce the concentration of fluorine ions from 10% to <5% by changing the treatment conditions and by adding alkaline compounds. The silica gel obtained after the leaching is a promising silicon dioxide source. Keywords: fluorine ions; silica gel waste; leaching; hydroxide additives Citation: Dambrauskas, T.; Baltakys, K.; Grineviciene, A.; Rudelis, V. The 1. Introduction Effect of Various Hydroxide and Salt Waste management and the reduction of pollution are the priority areas of environ- Additives on the Reduction of mental protection in the World [1–4]. -
How to Make Concrete More Sustainable Harald Justnes1
Journal of Advanced Concrete Technology Vol. 13, 147-154, March 2015 / Copyright © 2015 Japan Concrete Institute 147 Scientific paper How to Make Concrete More Sustainable Harald Justnes1 A selected paper of ICCS13, Tokyo 2013. Received 12 November 2013, accepted 16 February 2015 doi:10.3151/jact.13.147 Abstract Production of cement is ranking 3rd in causes of man-made carbon dioxide emissions world-wide. Thus, in order to make concrete more sustainable one may work along one or more of the following routes; 1) Replacing cement in con- crete with larger amounts of supplementary cementing materials (SCMs) than usual, 2) Replacing cement in concrete with combinations of SCMs leading to synergic reactions enhancing strength, 3) Producing leaner concrete with less cement per cubic meter utilizing plasticizers and 4) Making concrete with local aggregate susceptible to alkali silica reaction (ASR) by using cement replacements, thus avoiding long transport of non-reactive aggregate. 1 Introduction SCMs, also uncommon ones like calcined marl 2. Replacing cement in concrete with combinations of The cement industry world-wide is calculated to bring SCMs leading to synergic reactions enhancing about 5-8% of the total global anthropogenic carbon strength dioxide (CO2) emissions. The general estimate is about 3. Producing leaner concrete with less cement per cubic 1 tonne of CO2 emission per tonne clinker produced, if meter utilizing plasticizers. fossil fuel is used and no measures are taken to reduce it. 4. Making concrete with local aggregate susceptible to The 3rd rank is not because cement is such a bad mate- alkali silica reaction (ASR) by using cement re- rial with respect to CO2 emissions, but owing to the fact placements, thus avoiding long transport of non- that it is so widely used to construct the infrastructure reactive aggregate and buildings of modern society as we know it. -
Experimental Investigation of Self Healing Behavior of Concrete Using Silica Fume and GGBFS As Mineral Admixtures
ISSN (Print) : 0974-6846 Indian Journal of Science and Technology, Vol 8(36), DOI: 10.17485/ijst/2015/v8i36/87644, December 2015 ISSN (Online) : 0974-5645 Experimental Investigation of Self Healing Behavior of Concrete using Silica Fume and GGBFS as Mineral Admixtures RA. B. Depaa* and T. Felix Kala Dr. MGR Educational and Research Institute University, Chennai - 600095, Tamil Nadu, India; [email protected], [email protected] Abstract The process of self-healing of concrete has been gaining momentum nowadays due to increased deterioration of concrete structures subjected to adverse environmental conditions. Admixtures like silica fume and ground granulated blast furnace slag is one of the self healing agents being experimented recently. The method of usage of Silica fume and ggbfs, the waste derivatives from coal and steel industries, strength and durability testing of these mixes for achieving the self healing prop- erty has been presented. The effects of self-healing on normal concrete by adding small amounts of GGBFS and silica fume to concrete is studied. For this purpose, silica fume is added to concrete at percent of 0%, 2.5%, 5%, 7.5%, 10%, 12.5% and cement has been replaced with GGBFS by 35% and 55% respectively. The adopted water binder ratio for silica fume specimensand GGBFS to mixes generate is 0.45. microcracks M30 mix designfor studying is being the done durability as per properties the Indian of Standard the specimens. Code IS: The 10262-1982. strength properties The specimens of con- are first tested for compressive strength at 28 days, then 70% and 90% of the compressive load is applied to another set of crete specimens made using silica fume and GGBFS are tested for compressive strength and the durability properties are studied using sorptivity index test. -
Silica Fume and Metakaolin As Supplementary Cementing Materials- a Review
ISSN(Online): 2319-8753 ISSN (Print): 2347-6710 International Journal of Innovative Research in Science, Engineering and Technology (A High Impact Factor, Monthly, Peer Reviewed Journal) Visit: www.ijirset.com Vol. 6, Issue 10, October 2017 Silica Fume and Metakaolin as Supplementary Cementing Materials- A Review Syed Abuthahir 1, Nirmalkumar2 P.G. Student, Department of Civil Engineering, Kongu Engineering College, Perundurai, Erode, India1 Professor, Department of Civil Engineering, Kongu Engineering College, Perundurai, Erode, India2 ABSTRACT:The replacement of cement by various mineral admixtures as supplementary cementing materials for concrete has gained a global attention in recent years. This replacement becomes efficient not only by increasing the strength and durability of the concrete but also reduces the usage of the ordinary cement thereby curtailing the environmental hazardous due to cement manufacturing industries. This paper reviews the work carried out on the use of silica fume (SF) and Metakaolin (MK) as supplementary cementing materials as a partial replacement for cement. The literature demonstrates that both SF and MK are effective and causes significant improvement in various properties of the concrete in both fresh and harden state. KEYWORDS: Metakaolin, Silica Fume, Compressive Strength, Durability Properties. I.INTRODUCTION Major of the construction company relies on the concrete. Cement is major constituent of concrete. The annual global production of ordinary portland cement is about 3 Gt. Cement becomes a dominant binder due to its versatility, durability, and its demand increases dramatically. Even though it is a vital material, it production directly affects the environment by releasing 0.87t of carbon dioxide for every tonne of cement produced. -
Evolution of Geochemical Conditions in SFL 3-5
SE0000146 R-99-15 Evolution of geochemical conditions in SFL 3-5 Fred Karlsson Svensk Kambranslehantering AB Maria Lindgren, Kristina Skagius, Marie Wiborgh Kemakta Konsult AB Ingemar Engkvist Barseback Kraft AB December 1999 Svensk Karnbranslehantering AB Swedish Nuclear Fuel and Waste Management Co Box 5864 SE-102 40 Stockholm Sweden Tel 08-459 84 00 +46 8 459 84 00 Fax 08-661 57 19 +46 8 661 57 19 J> ISSN 1402-3091 SKB Rapport R-99-15 Evolution of geochemical conditions in SFL 3-5 Fred Karlsson Svensk Karnbranslehantering AB Maria Lindgren, Kristina Skagius, Marie Wiborgh Kemakta Konsult AB Ingemar Engkvist Barseback Kraft AB December 1999 Keywords: geochemical conditions, deep repository, near-field chemistry, concrete, evolution, LILW. Abstract The evolution of geochemical conditions in the repository for long-lived low- and intermediate-level waste, SFL 3-5, and in the vicinity of the repository are important when predicting the retention of radionuclides and the long-term stability of engineered barriers. In this study the initial conditions at different repository sites at 300 - 400 m depth, the influence of repository construction and operation, the expected conditions after repository closure and saturation, and the evolution in a long-term perspective are discussed. Groundwaters that are found at these depths have near-neutral pH and are reducing in character, but the composition can vary from saline to non-saline water. The water chemistry in the near-field will mainly be influenced by the composition of the groundwater and by the large amounts of cementitious material that can be found in the repository. -
Crystal Structure of the High-Pressure Phase of Calcium Hydroxide, Portlandite: in Situ Powder and Single-Crystal X-Ray Diffraction Study
American Mineralogist, Volume 98, pages 1421–1428, 2013 Crystal structure of the high-pressure phase of calcium hydroxide, portlandite: In situ powder and single-crystal X-ray diffraction study RIKO IIZUKA,1,2,3,* TAKEHIKO YAGI,1,3 KAZUKI KOMATSU,2 HIROTADA GOTOU,1 TAKU TSUCHIYA,3 KEIJI KUSABA,4 AND HIROYUKI KAGI2 1Institute for Solid State Physics, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, 277-8581, Japan 2Geochemical Research Center, Graduate School of Science, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan 3Geodynamics Research Center, Ehime University, 2-5 Bunkyo-cho, Matsuyama 790-8577, Japan 4Department of Materials Science, Nagoya University, Nagoya, 464-8603, Japan ABSTRACT The crystal structure of a high-pressure phase of calcium hydroxide, Ca(OH)2 (portlandite), was clarified for the first time using the combination of in situ single-crystal and powder X-ray diffraction measurements at high pressure and room temperature. A diamond-anvil cell with a wide opening angle and cell-assembly was improved for single-crystal X-ray diffraction experiments, which allowed us to successfully observe Bragg reflections in a wide range of reciprocal space. The transition occurred at 6 GPa and the crystal structure of the high-pressure phase was determined to be monoclinic at 8.9 GPa and room temperature [I121; a = 5.8882(10), b = 6.8408(9), c = 8.9334(15) Å, β = 104.798(15)°]. The transition involved a decrease in molar volume by approximately 5.8%. A comparison of the structures of the low- and high-pressure phases indicates that the transition occurs by a shift of CaO6 octahedral layers in the a-b plane along the a-axis, accompanied by up-and-down displacements of Ca atoms from the a-b plane.