Methodological Recommendations for the Applications of the Mineral Resources Category in Mongolia to the Related Minerals
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WO 2017/106925 Al 29 June 2017 (29.06.2017) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2017/106925 Al 29 June 2017 (29.06.2017) P O P C T (51) International Patent Classification: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, C22B 26/12 (2006.01) C22B 3/06 (2006.01) DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, (21) International Application Number: KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, PCT/AU20 16/05 1278 MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, (22) International Filing Date: NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, 22 December 2016 (22. 12.2016) RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, (25) Filing Language: English ZA, ZM, ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 20159053 17 22 December 201 5 (22. 12.2015) AU GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, 2016900774 2 March 2016 (02.03.2016) AU TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, (72) Inventor; and DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (71) Applicant : HUNWICK, Richard [AU/AU]; 59 Abing LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, don Road, Roseville, New South Wales 2069 (AU). -
Design, Synthesis and Evaluation of Diphenylamines As MEK5 Inhibitors Suravi Chakrabarty
Duquesne University Duquesne Scholarship Collection Electronic Theses and Dissertations Fall 2014 Design, Synthesis and Evaluation of Diphenylamines as MEK5 Inhibitors Suravi Chakrabarty Follow this and additional works at: https://dsc.duq.edu/etd Recommended Citation Chakrabarty, S. (2014). Design, Synthesis and Evaluation of Diphenylamines as MEK5 Inhibitors (Master's thesis, Duquesne University). Retrieved from https://dsc.duq.edu/etd/388 This Immediate Access is brought to you for free and open access by Duquesne Scholarship Collection. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of Duquesne Scholarship Collection. For more information, please contact [email protected]. DESIGN, SYNTHESIS AND EVALUATION OF DIPHENYLAMINES AS MEK5 INHIBITORS A Thesis Submitted to the Graduate School of Pharmaceutical Sciences Duquesne University In partial fulfillment of the requirements for the degree of Master of Science (Medicinal Chemistry) By Suravi Chakrabarty December 2014 Copyright by Suravi Chakrabarty 2014 DESIGN, SYNTHESIS AND EVALUATION OF DIPHENYLAMINES AS MEK5 INHIBITORS By Suravi Chakrabarty Approved August 7, 2014 ________________________________ ________________________________ Patrick Flaherty, Ph.D. Aleem Gangjee, Ph.D., Chair, Thesis Committee Professor of Medicinal Chemistry Associate Professor of Medicinal Mylan School of Pharmacy Chemistry Distinguished Professor Graduate School Pharmaceutical Sciences Graduate School Pharmaceutical Sciences Duquesne University Duquesne -
Reactions of Lithium Nitride with Some Unsaturated Organic Compounds. Perry S
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1963 Reactions of Lithium Nitride With Some Unsaturated Organic Compounds. Perry S. Mason Jr Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Mason, Perry S. Jr, "Reactions of Lithium Nitride With Some Unsaturated Organic Compounds." (1963). LSU Historical Dissertations and Theses. 898. https://digitalcommons.lsu.edu/gradschool_disstheses/898 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been 64—5058 microfilmed exactly as received MASON, Jr., Perry S., 1938- REACTIONS OF LITHIUM NITRIDE WITH SOME UNSATURATED ORGANIC COMPOUNDS. Louisiana State University, Ph.D., 1963 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. REACTIONS OF LITHIUM NITRIDE WITH SOME UNSATURATED ORGANIC COMPOUNDS A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requireiaents for the degree of Doctor of Philosophy in The Department of Chemistry by Perry S. Mason, Jr. B. S., Harding College, 1959 August, 1963 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. -
Table of Contents
TABLE OF CONTENTS ACKNOWLEDGEMENTS iii TABLE OF CONTENTS iv LIST OF TABLES vi LIST OF FIGURES viii ABSTRACT xii CHAPTER 1 INTRODUCTION 1 1.1 Overview 1 1.2 Research Objectives and Organization of the Dissertation 2 CHAPTER 2 ALKLI SILICA REACTION AND RECYCLED CONCRETE 4 AGGREGATE 2.1 Alkali Silica Reaction (ASR) 4 2.1.1 ASR essentials 4 2.1.2 ASR mechanisms 5 2.1.3 ASR test methods review 7 2.1.4 Potential mitigation methods 9 2.2 Recycled Concrete Aggregate (RCA) 11 2.2.1 Recycled aggregate preview 11 2.2.2 RCA with ASR distress 13 2.2.3 RCA alkali contribution and alkali leaching 17 CHAPTER 3 PORE SOLUTION 19 3.1 Pore solution extraction 19 3.1.1 Instrumental introduction and description 19 3.1.2 Sample preparation 24 3.1.3 Extraction method and load scheme 25 3.2 Pore Solution Chemical Analysis 27 3.2.1 Alkali evolution process in pore solution 27 3.2.2 Pore solution test schemes and methods 29 3.2.3 Test results and analysis 32 iv CHAPTER 4 RCA ASR MITIGATION USING MINERAL ADMIXTURES 35 4.1 Fly Ash Mitigation 35 4.1.1 Fly ash as a concrete admixture 35 4.1.2 Mortar bar expansion test 38 4.1.3 Expansion results and comparison 42 4.1.4 Pore solution analysis 45 4.1.5 Mitigation mechanism analysis 49 4.2 Ground Granulated Blast Furnace Slag (GGBFS) Mitigation 54 4.2.1 Slag production and use in concrete 54 4.2.2 Expansion test results and comparison 55 4.2.3 Pore solution analysis and TGA 57 4.3 Silica Fume Mitigation 59 4.3.1 Expansion results and comparison 60 4.3.2 Pore solution analysis and TGA 65 4.3.3 Particle size issue 66 4.4 -
Synthetically Important Alkalimetal Utility Amides: Lithium, Sodium, And
Angewandte. Reviews R. E. Mulvey and S. D. Robertson DOI: 10.1002/anie.201301837 Alkali-Metal Amides Synthetically Important Alkali-Metal Utility Amides: Lithium, Sodium, and Potassium Hexamethyldisilazides, Diisopropylamides, and Tetramethylpiperidides Robert E. Mulvey* and Stuart D. Robertson* Keywords: alkali metals · heterometallic compounds · molecular structure · secondary amide · solution state Angewandte Chemie 11470 www.angewandte.org 2013 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Angew. Chem. Int. Ed. 2013, 52, 11470 – 11487 Angewandte Alkali-Metal Amides for Synthesis Chemie Most synthetic chemists will have at some point utilized a sterically From the Contents À demanding secondary amide (R2N ). The three most important examples, lithium 1,1,1,3,3,3-hexamethyldisilazide (LiHMDS), 1. Introduction 11471 lithium diisopropylamide (LiDA), and lithium 2,2,6,6-tetramethylpi- 2. Preparation and Uses in peridide (LiTMP)—the “utility amides”—have long been indis- Synthesis 11473 pensible particularly for lithiation (Li-H exchange) reactions. Like organolithium compounds, they exhibit aggregation phenomena and 3. Structures of 1,1,1,3,3,3- strong Lewis acidity, and thus appear in distinct forms depending on Hexamethyldisilazides 11475 the solvents employed. The structural chemistry of these compounds as 4. Structures of Diisopropylamide 11477 well as their sodium and potassium congeners are described in the absence or in the presence of the most synthetically significant donor 5. Structures of 2,2,6,6- solvents tetrahydrofuran (THF) and N,N,N,N-tetramethylethylene- Tetramethylpiperidide 11477 diamine (TMEDA) or closely related solvents. Examples of hetero- 6. Heterometallic Derivatives 11479 alkali-metal amides, an increasingly important composition because of the recent escalation of interest in mixed-metal synergic effects, are also 7. -
(12) Patent Application Publication (10) Pub. No.: US 2005/0044778A1 Orr (43) Pub
US 20050044778A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2005/0044778A1 Orr (43) Pub. Date: Mar. 3, 2005 (54) FUEL COMPOSITIONS EMPLOYING Publication Classification CATALYST COMBUSTION STRUCTURE (51) Int. CI.' ........ C10L 1/28; C1OL 1/24; C1OL 1/18; (76) Inventor: William C. Orr, Denver, CO (US) C1OL 1/12; C1OL 1/26 Correspondence Address: (52) U.S. Cl. ................. 44/320; 44/435; 44/378; 44/388; HOGAN & HARTSON LLP 44/385; 44/444; 44/443 ONE TABOR CENTER, SUITE 1500 1200 SEVENTEENTH ST DENVER, CO 80202 (US) (57) ABSTRACT (21) Appl. No.: 10/722,127 Metallic vapor phase fuel compositions relating to a broad (22) Filed: Nov. 24, 2003 Spectrum of pollution reducing, improved combustion per Related U.S. Application Data formance, and enhanced Stability fuel compositions for use in jet, aviation, turbine, diesel, gasoline, and other combus (63) Continuation-in-part of application No. 08/986,891, tion applications include co-combustion agents preferably filed on Dec. 8, 1997, now Pat. No. 6,652,608. including trimethoxymethylsilane. Patent Application Publication Mar. 3, 2005 US 2005/0044778A1 FIGURE 1 CALCULATING BUNSEN BURNER LAMINAR FLAME VELOCITY (LFV) OR BURNING VELOCITY (BV) CONVENTIONAL FLAME LUMINOUS FLAME Method For Calculating Bunsen Burner Laminar Flame Velocity (LHV) or Burning Velocity Requires Inside Laminar Cone Angle (0) and The Gas Velocity (Vg). LFV = A, SIN 2 x VG US 2005/0044778A1 Mar. 3, 2005 FUEL COMPOSITIONS EMPLOYING CATALYST Chart of Elements (CAS version), and mixture, wherein said COMBUSTION STRUCTURE element or derivative compound, is combustible, and option 0001) The present invention is a CIP of my U.S. -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
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— Studies on Lithium Acetylide Kenneth N. Campbell and Barbara K. Campbell, The University of Notre Dame In contrast to the large amount of work done on the acetylene derivatives of sodium, potassium and calcium, little attention has been paid to the analogous compounds of lithium. In 1898 Moissani prepared lithium acetylide on a small scale, by the action of acetylene on a liquid ammonia solution of lithium. He reported that lithium acetylide was less soluble in liquid ammonia than sodium acetylide, and that when isolated from the solvent, it was less stable, undergoing decomposition with evolu- tion of acetylene. On the basis of the weight of lithium acetylide obtained from a given weight of lithium, and from the amount of acetylene liberated on hydrolysis, he assigned to lithium acetylide the formula C2Li2.C2H2.2NH3. Since that time no references to lithium acetylide or lithium alkylacetylides have appeared in the literature. It was the pur- pose of the present work, therefore, to prepare and analyze lithium acetylide and a lithium alkylacetylide, and to compare their reactions with those of the better known sodium derivatives. Experimental Procedure Preparation of Lithium and Sodium Acetylides.—Acetylene gas, washed by bubbling through concentrated sulfuric acid, was passed into two liters of liquid ammonia, while 7 g. (1 mole) of metallic lithium, cut in small pieces, was added gradually, with stirring, at a rate such that the solution did not develop a permanent deep blue color. When the solution became colorless after the addition of the last piece of lithium, the flow of acetylene was stopped. -
Safety Data Sheet
SAFETY DATA SHEET Preparation Date: 7/21/2017 Revision Date: 7/21/2017 Revision Number: G1 1. IDENTIFICATION Product identifier Product code: S1725 Product Name: SULFUR, LUMP Other means of identification Synonyms: No information available CAS #: 7704-34-9 RTECS # WS4250000 CI#: Not available Recommended use of the chemical and restrictions on use Recommended use: In manufacturing sulfuric acid, carbon disulfide, sulfites, insecticides, plastics, enamels, metal-glass, cements; in vulcanizing rubber; in syntheses of dyes; in making gunpowder, matches; for bleaching wood pulp, straw, wool, silk, felt, linen; in making phosphatic fertilizers; bleaching of dried fruits; fungicide and acaricide; rodent repellent; soil conditioner; nucleating reagent for photographic film; used in cosmetics, such as acne ointments and lotions, and in antidandruff shampoos. 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) Flammable solids Category 2 Label elements Warning Flammable solids Product code: S1725 Product name: SULFUR, LUMP 1 / 14 Hazards not otherwise classified (HNOC) Not Applicable Other hazards Not available Precautionary Statements - Prevention Keep away from heat/sparks/open flames/hot surfaces. — No smoking Ground/bond container and receiving equipment Use explosion-proof electrical/ventilating/lighting/.../equipment Wear protective gloves Wear eye/face protection Prevent dust accumulations to minimize explosion hazard In case of fire: Use CO2, dry chemical, or foam to extinguish. -
Chemical Matrix
Chemical Matrix - Ceramics Studio Recommended Personal Protective Key Hazardous Properties Storage Location Disposal Equipment Face Body Hands Protection Respiratory Respiratory Product Form / Phase Key Composition Combustible High Toxicity High Flash Point F Flash Point Plaster Room Plaster Sanitary Drain Sanitary Compressed Gas Compressed Strong Acid/Base Strong Non-Haz Disposal Non-Haz Non-Flam Cabinet Non-Flam Glaze Mixing Room Haz Waste Disposal Waste Haz Flammables Cabinet Flammable/Explosive Potentially SensitizingPotentially MSDS Strong Oxidizer / Reducer Oxidizer Strong Cartirdge Face Shield Nitrile Gloves Nitrile Use with Local Only Exhaust Ventilation with Use Non-Flam Cupboard / Shelving / Counter Cupboard Non-Flam Chemical Splash Apron Chemical Safety Glasses Safety Chemical Flame Resistant Lab Coat Lab Resistant Flame Half Face Respitator with P100 P100 with Respitator Face Half Chemical Protective Gloves per per Gloves Protective Chemical Acetone Liquid Acetone -4 X X X X X X X Albany Slip Powder Silty glacial clay used for pottery, contains up to 30% quartz free silica according to Columbus Clay web X X X X X X MSDS Alumina Hydrate Powder Alumina Hydrate X X X X X X Angelos Copperslip Liquid (thick) Copper oxide, frit 3110, CMC gum, bentonite X X Antimony oxide Powder Antimony oxide X X X X X X X X Baking Soda Powder Sodium bicarbonate X X X X X X X Bell Dark Ball Clay Powder Kaolinite, plus up to 30% quartz free silica X X X X X X Bernard Slip Clay Powder Clay, plus up to 30% silica, some considered respirable according -
Acutely / Extremely Hazardous Waste List
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extemely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extemely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extemely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extemely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extemely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extemely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extemely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extemely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extemely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extemely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extemely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extemely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extemely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
The Action of Nitrogen on Lithium Carbide. by S
‘478 GENERAL, PHYSICAL AND INORGANIC. chain action as suggested by Daneel,’ then anything which alters the degree of association of the water would influence the magnitude of this effect. In order, therefore, to estimate the degree of ionization of strong acids or alkalies in concentrated solutions, the best procedure would probably be to make use of the equation 7 = AjAb (34) in which A is the equivalent conductance of the solution for which r is desired, and above which the vapor pressure of the water is p. A’, is the equivalent conductance of fie electrolyte at infinit dilution in a solu- tion to which a suitable non-electrolyte has been added, so as to give it the same viscosity and the same vapor pressure, p, as the first solution. In the absence of any experimental data, however, equation (34) must be regarded merely as a suggestion. Summary. I. It is pointed out that in calculating the degree of ionization of an electrolyte by the conductivity method, the neglect of the viscosity effect may produce errors as high as 7 and 8 per cent., even at such low concentrations as 0.1 normal and for such simple electrolytes as uni- univalent salts. 2. The relation A = kj” (in which A is the equivalent conductance of an ion, f is the fluidity of the solution, m is a constant not far from unity and dependent chiefly upon the nature of the ion, and k is a propor- tionality constant) is proposed, provisionally as the most logical basis for formulating the viscosity correction in calculating the degree of ioniza- tion, y, in moderately concentrated solutions.