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Caves and Caverns: Their Interest for Chemists and Geologists
4 ENVIRONMENT his Nob"; and many a person today shudders slightly when referring to "The Talkies". I wonder what the final word will be that slips into an Oxford Dictionary of the future to express the combination of Television and Talkie. CAVES AND CAVERNS: THEIR INTEREST FOR CHEMISTS AND GEOLOGISTS. By w. L. HAVARD, Assistant Master, Sydney Technical High School. Caves, whether they be holes in the ground, gapes in the mountain side, or wounds in the rocky face of a sea cliff, have always played a romantic part in the history and literature of the world ; mystery dwells about their thresholds, while their pitchy halls and hidden ways are the home of fairies, gnomes and sibyls, of dwarfs that toil at Vulcan's bidding. From caves, too, spake the oracles, voices of destiny heard beside the cradle and the death bed of pagan nations. Primitive man made caverns his home, peoples of early civilization made then their burying-plaees. In many parts of the world caves are natural museums which gathered through the ages relics not only of man and his tools and weapons, but of many varied kinds of animals and birds. Who would imagine the hyena, tiger, bear, rhinoceros, elephant or hippopotamus roaming in England? Yet English caves hold the bones of these animals besides those of a more familiar kind. Caves have been used successfully as hiding-places, retreats and strongholds for bandits, smugglers, pilgrims, prophets, kings. During the ·Great War certain English caves · were used ·for the storage of ammunition. During the war between Great Britain and the United States in 1812 the Mammoth Cave of Kentucky played its part in the crude manufacture of one of the essential ingredients of gun powder. -
Alkalinity Management in Soilless Substrates and Landscape Architecture Roberto G
Purdue extension HO-242-W Commercial Greenhouse and Nursery Production Purdue Department of Horticulture Alkalinity Management in Soilless Substrates and Landscape Architecture Roberto G. Lopez and Michael V. Mickelbart, Purdue Horticulture and Landscape Architecture www.hort.purdue.edu Ohio State University Horticulture Claudio Pasian, Ohio State University Horticulture and Crop Science and Crop Science www.hcs.osu.edu Purdue Floriculture Greenhouse and nursery growers often assume yellow and pale leaves are signs of nutritional flowers.hort.purdue.edu deficiencies. Sometimes, however, the problem may be due to a lack of specific nutrients in the substrate — in other cases, the nutrients may be present but high substrate pH makes them unavailable to the plant. Growers commonly add sulfuric or other acids to irrigation water to help lower substrate pH or apply iron chelates to quickly “green up” their crops before shipping. Unfortunately, growers often do not have a clear understanding of the underlying causes behind increased substrate pH — water alkalinity, rather than water pH, is typically the source of the problem. The purpose of this publication is to help growers differentiate between high pH and high alkalinity and how to manage alkalinity in soilless substrates. What Is pH? The pH scale measures the concentration of hydrogen ions (H+) in a solution. Examples of solutions are tap water and the water in the substrate inside a pot. The pH scale ranges from 0 to 14. A value of 7.0, which is pure water, is neutral. Values less than 7.0 are called acidic, and values greater than 7 are called basic or alkaline. -
Summary Statistics for Selected Common Ions, Including Dissolved
Common Ions Precambrian Aquifers Summary statistics for selected common ions, Generally, water from the Precambrian aquifers including dissolved solids, calcium, magnesium, is fresh (less than 1,000 mg/L dissolved solids concen- sodium, percent sodium, sodium-adsorption ratio tration). Calcium and bicarbonate generally are dominant among the common ions. Water from the (SAR), potassium, bicarbonate, carbonate, sulfate, Precambrian aquifers has the highest median chloride chloride, fluoride, bromide, iodide, and silica, are concentration, lowest mean and median concentrations presented in table 4. The significance of the various of calcium, magnesium, and bicarbonate, and the common ions is described in table 1. Boxplots are pre- lowest median sulfate (equal to the Deadwood aquifer) sented in figure 16 for each of the common ions, except of the major aquifers. for carbonate. The water type for the various aquifers The water type of the Precambrian aquifers also is discussed in this section. Trilinear diagrams generally is a calcium bicarbonate or a calcium magne- (fig. 17) are presented for each of the aquifers. sium bicarbonate type but also can be a mixed type Changes in water type as ground water flows down- (fig. 17). The original rock mineralogy, degree of gradient are discussed for the Madison, Minnelusa, and metamorphism, and degree of weathering all can Inyan Kara aquifers. contribute to the variations in water type. Two of 56 samples from Precambrian aquifers Specific conductance can be used to estimate the exceed the SMCL of 500 mg/L for dissolved solids. concentration of dissolved solids using the equations Two of 112 samples exceed the SMCL of 250 mg/L for presented in table 5. -
( 12 ) United States Patent
US010682325B2 (12 ) United States Patent ( 10 ) Patent No.: US 10,682,325 B2 Comb et al. (45 ) Date of Patent : * Jun . 16 , 2020 (54 ) COMPOSITIONS AND METHODS FOR THE 3,988,466 A 10/1976 Takagi et al. TREATMENT OF LIVER DISEASES AND 4,496,703 A 1/1985 Steinmetzer 4,871,550 A 10/1989 Millman DISORDERS ASSOCIATED WITH ONE OR 4,898,879 A 2/1990 Madsen et al . BOTH OF HYPERAMMONEMIA OR 4,908,214 A 3/1990 Bobee et al. MUSCLE WASTING 5,028,622 A 7/1991 Plaitakis 5,034,377 A 7/1991 Adibi et al. 5,106,836 A 4/1992 Clemens et al . ( 71) Applicant: AXCELLA HEALTH INC . , 5,229,136 A 7/1993 Mark et al. Cambridge , MA (US ) 5,276,018 A 1/1994 Wilmore 5,348,979 A 9/1994 Nissen et al . (72 ) Inventors : William Comb , Melrose , MA (US ); 5,356,873 A 10/1994 Mark et al . Sean Carroll, Cambridge, MA (US ) ; 5,405,835 A 4/1995 Mendy Raffi Afeyan , Boston , MA (US ) ; 5,438,042 A 8/1995 Schmidl et al. 5,504,072 A 4/1996 Schmidl et al. Michael Hamill, Wellesley , MA (US ) 5,520,948 A 5/1996 Kvamme 5,571,783 A 11/1996 Montagne et al. (73 ) Assignee : AXCELLA HEALTH INC . , 5,576,351 A 11/1996 Yoshimura et al . Cambridge, MA (US ) 5,712,309 A 1/1998 Finnin et al . 5,719,133 A 2/1998 Schmidl et al. Subject to any disclaimer, the term of this 5,719,134 A 2/1998 Schmidl et al. -
Synthesis Methods and Favorable Conditions for Spherical Vaterite Precipitation: a Review
crystals Review Synthesis Methods and Favorable Conditions for Spherical Vaterite Precipitation: A Review Donata Konopacka-Łyskawa Department of Process Engineering and Chemical Technology, Faculty of Chemistry, Gda´nskUniversity of Technology, Narutowicza 11/12, 80-233 Gda´nsk,Poland; [email protected]; Tel.: +48-58-347-2910 Received: 15 March 2019; Accepted: 18 April 2019; Published: 25 April 2019 Abstract: Vaterite is the least thermodynamically stable anhydrous calcium carbonate polymorph. Its existence is very rare in nature, e.g., in some rock formations or as a component of biominerals produced by some fishes, crustaceans, or birds. Synthetic vaterite particles are proposed as carriers of active substances in medicines, additives in cosmetic preparations as well as adsorbents. Also, their utilization as a pump for microfluidic flow is also tested. In particular, vaterite particles produced as polycrystalline spheres have large potential for application. Various methods are proposed to precipitate vaterite particles, including the conventional solution-solution synthesis, gas-liquid method as well as special routes. Precipitation conditions should be carefully selected to obtain a high concentration of vaterite in all these methods. In this review, classical and new methods used for vaterite precipitation are presented. Furthermore, the key parameters affecting the formation of spherical vaterite are discussed. Keywords: vaterite; calcium carbonate; polymorph; precipitation; synthesis; carbonation 1. Introduction Vaterite is the least thermodynamically stable anhydrous calcium carbonate polymorph and it easily transforms into more stable calcite or aragonite in the presence of water. This form of calcium carbonate mineral was named to honor the German chemist and mineralogist, Heinrich Vater, in 1903. -
Safe Handling and Disposal of Chemicals Used in the Illicit Manufacture of Drugs
Vienna International Centre, PO Box 500, 1400 Vienna, Austria Tel.: (+43-1) 26060-0, Fax: (+43-1) 26060-5866, www.unodc.org Guidelines for the Safe handling and disposal of chemicals used in the illicit manufacture of drugs United Nations publication USD 26 Printed in Austria ISBN 978-92-1-148266-9 Sales No. E.11.XI.14 ST/NAR/36/Rev.1 V.11-83777—September*1183777* 2011—300 Guidelines for the Safe handling and disposal of chemicals used in the illlicit manufacture of drugs UNITED NATIONS New York, 2011 Symbols of United Nations documents are composed of letters combined with figures. Mention of such symbols indicates a reference to a United Nations document. ST/NAR/36/Rev.1 UNITED NATIONS PUBLICATION Sales No. E.11.XI.14 ISBN 978-92-1-148266-9 eISBN 978-92-1-055160-1 © United Nations, September 2011. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. Requests for permission to reproduce this work are welcomed and should be sent to the Secretary of the Publications Board, United Nations Headquarters, New York, N.Y. 10017, U.S.A. or also see the website of the Board: https://unp.un.org/Rights.aspx. Governments and their institutions may reproduce this work without prior authoriza- tion but are requested to mention the source and inform the United Nations of such reproduction. -
The Solubility of Magnesium Carbonate in Aqueous Solutions of Certain
c THE SOLUBILITY OF MAGNESIUM CARBONATE IN AQUEOUS SOLUTIONS OF CERTAIN ELECTROLYTES I BY F. K. CAMERON AND A. SEIDEIJ, P The work herein described was done in connection with and for the most part antedated that upon the solubility of cal- cium carbonate in solutions of other salts, which has already been described.z The solubility of magnesium carbonate is obviously depen- dent upon the partial pressure of the carbon dioxide in the at- mosphere or gas phase in contact with the solution. This has led to the development of this investigation in three parts : I, When the solutions were in contact with ordinary atnios- pheric air containing a small and practically constant percent- age of carbon dioxide. 2. When the atmosphere in contact with the solutions con- tained practically nothing but carbon dioxide and water. 3. When the solutions were in contact with an atmosphere practically free from carbon dioxide. Under these several conditions the ratio of normal carbon- ate to hydrogen carbonate or bicarbonate for any given concen- tration of solution might be expected to vary greatly. Moreover, it was found, in the case of solutions of mag- nesium carbonate, that temperature changes frequently prodiiced relatively large changes in the solubility, and it was therefore necessary to take precautions to prevent variations in this re- spect during the progress of the work. Unless otherwise stated the work described here was done at 23' C. As is well known, solution studies of magnesium carbonate, when other salts are present, have always given great difficulty Published by the permission of the Secretary of Agriculture. -
US3099524.Pdf
3,099,524 United States Patent 0 Patented July 30, 1963 1 2 aluminium and magnesium with a mixture of sodium 3,099,524 hydroxide and sodium canbonate in appropriate amounts. ANTAClD CGMPOSITIONS The aluminium and magnesium salts are preferably the Frederick Grossmith, Pinner, England, assignor to chlorides. Beecham Research Laboratories Limited, Breutford, A further method for preparing the compounds of the Middlesex, England present invention is to suspend a magnesium hydroxo Filed June 28, 1960, Ser. No. 39,245 Claims priority, application Great Britain July 2, 1959 aluminate of the type disclosed in by said co?pending 6 Claims. (Cl. 23—l4) application Serial No. 842,042, ?led September 24, 1959, in a liquor containing bicarbonate ions. A suitable This invention relates to improvements in antacid 10 liquor is a dilute solution of magnesium bicarbonate. compositions and is particularly concerned with new A still further method for preparing the magnesium chemical compounds which have been found to have bicarbonate hydroxoaluminates, which method minimises desirable antacid properties being eminently suitable for the formation of a basic magnesium carbonate impurity, medicinal use for the treatment of gastric hyperacidity. is to react a solution containing aluminium and mag In my co-pending application Serial No. 842,042, ?led 15 nesium salts in appropriate amounts with sodium hy September 24, 1959, now abandoned, I have disclosed droxide at a suitable rate of delivery. An addition of certain novel compounds which are formed by reacting ‘sodium bicarbonate is made at an appropriate stage and aluminium and magnesium salts with caustic allcalis, in a ?nal addition of mixed sodium hydroxide and sodium which the magnesium content, expressed as Mg(OI-I)2, bicarbonate is made to precipitate all the magnesium lies between the approximate limits 2.5% to 75% by 20 without allowing the pH to rise too high. -
Hydrogeological Evaluation Report (PDF)
Enbridge Line 6B MP 608 Releases Marshall, MI Evaluation of Potential Impact of Released Oil on Groundwater used for Drinking Water (Hydrogeological Evaluation Report) Prepared: October 30, 2010 Enbridge Line 6B MP 608 Release Marshall, MI Evaluation of Potential Impact of Released Oil on Groundwater used for Drinking Water (Hydrogeological Evaluation Report) Prepared October 30, 2010 Table of Contents 1.0 Introduction ........................................................................................................................................... 1 1.1 Background ............................................................................................................................. 1 1.2 Purpose and Overview ............................................................................................................ 2 1.3 Site Setting .............................................................................................................................. 2 1.4 Goals ....................................................................................................................................... 3 2.0 Historical Information on the Kalamazoo River ................................................................................. 5 2.1 Kalamazoo River .................................................................................................................... 5 2.2 Regional Geological Setting ................................................................................................... 6 2.3 Regional Hydrogeology -
Mineral Carbonation and Industrial Uses of Carbon Dioxide 319 7
Chapter 7: Mineral carbonation and industrial uses of carbon dioxide 319 7 Mineral carbonation and industrial uses of carbon dioxide Coordinating Lead Author Marco Mazzotti (Italy and Switzerland) Lead Authors Juan Carlos Abanades (Spain), Rodney Allam (United Kingdom), Klaus S. Lackner (United States), Francis Meunier (France), Edward Rubin (United States), Juan Carlos Sanchez (Venezuela), Katsunori Yogo (Japan), Ron Zevenhoven (Netherlands and Finland) Review Editors Baldur Eliasson (Switzerland), R.T.M. Sutamihardja (Indonesia) 320 IPCC Special Report on Carbon dioxide Capture and Storage Contents EXECUTIVE SUMMARY 321 7.3 Industrial uses of carbon dioxide and its emission reduction potential 330 7.1 Introduction 322 7.3.1 Introduction 330 7.3.2 Present industrial uses of carbon dioxide 332 7.2 Mineral carbonation 322 7.3.3 New processes for CO2 abatement 332 7.2.1 Definitions, system boundaries and motivation 322 7.3.4 Assessment of the mitigation potential of CO2 7.2.2 Chemistry of mineral carbonation 323 utilization 333 7.2.3 Sources of metal oxides 324 7.3.5 Future scope 334 7.2.4 Processing 324 7.2.5 Product handling and disposal 328 References 335 7.2.6 Environmental impact 328 7.2.7 Life Cycle Assessment and costs 329 7.2.8 Future scope 330 Chapter 7: Mineral carbonation and industrial uses of carbon dioxide 321 EXECUTIVE SUMMARY This Chapter describes two rather different options for carbon and recycled using external energy sources. The resulting dioxide (CO2) storage: (i) the fixation of CO2 in the form of carbonated solids must be stored at an environmentally suitable inorganic carbonates, also known as ‘mineral carbonation’ or location. -
Avian Eggshell Biomineralization: an Update on Its Structure, Mineralogy and Protein Tool Kit J
Gautron et al. BMC Molecular and Cell Biology (2021) 22:11 BMC Molecular and https://doi.org/10.1186/s12860-021-00350-0 Cell Biology REVIEW Open Access Avian eggshell biomineralization: an update on its structure, mineralogy and protein tool kit J. Gautron1* , L. Stapane1, N. Le Roy1, Y. Nys1, A. B. Rodriguez-Navarro2 and M. T. Hincke3 Abstract The avian eggshell is a natural protective envelope that relies on the phenomenon of biomineralization for its formation. The shell is made of calcium carbonate in the form of calcite, which contains hundreds of proteins that interact with the mineral phase controlling its formation and structural organization, and thus determine the mechanical properties of the mature biomaterial. We describe its mineralogy, structure and the regulatory interactions that integrate the mineral and organic constituents. We underline recent evidence for vesicular transfer of amorphous calcium carbonate (ACC), as a new pathway to ensure the active and continuous supply of the ions necessary for shell mineralization. Currently more than 900 proteins and thousands of upregulated transcripts have been identified during chicken eggshell formation. Bioinformatic predictions address their functionality during the biomineralization process. In addition, we describe matrix protein quantification to understand their role during the key spatially- and temporally- regulated events of shell mineralization. Finally, we propose an updated scheme with a global scenario encompassing the mechanisms of avian eggshell mineralization. With this large dataset at hand, it should now be possible to determine specific motifs, domains or proteins and peptide sequences that perform a critical function during avian eggshell biomineralization. The integration of this insight with genomic data (non- synonymous single nucleotide polymorphisms) and precise phenotyping (shell biomechanical parameters) on pure selected lines will lead to consistently better-quality eggshell characteristics for improved food safety. -
Effect of Some Deacidification Agents on Copper-Catalyzed Degrardation
Preservation Research and Testing Series No. 9501 Effect of Some Deacidification Agents on Copper-Catalyzed Degradation of Paper C. J. Shahani and F. H. Hengemihle Preservation Research and Testing office Preservation Directorate Library of Congress Washington, DC November 1995 Effect of Some Deacidifying Agents on Copper-Catalyzed Degradation of Paper Preservation Research and Testing Series No. 9501 November 1995 Page 1 of 12 Library of Congress ♦ Preservation Directorate www.loc.gov/preservation/ Effect of Some Deacidification Agents on Copper-Catalyzed Degradation of Paper Conservation of Historic and Artistic Works on Paper Organized by the Canadian Conservation Institute Ottawa, Canada, October 3-7, 1988 Introduction Paper conservators are all too familiar with artifacts in which iron gall ink or copper in verdigris pigment has caused severe deterioration of the paper base. But even trace concentrations of these metals, which are generally present in paper, contribute significantly to its aging by catalyzing oxidation reactions.1,2,3 Copper and iron contaminants can also cause foxing in paper.4,5 Williams and his co-workers observed that paper samples containing copper acetate, which degraded rapidly when aged at 90˚C and 50˚C relative humidity (RH), were stabilized appreciably after deacidification treatment with magnesium bicarbonate.3 However, deacidification by a Barrow two-step treatment with calcium hydroxide and calcium bicarbonate solutions did not stabilize against the degradative effect of copper acetate to a comparable