Acids and Bases Acids Release H+(Aq) When Dissolved in Water and Bases Release HO-(Aq)

Total Page:16

File Type:pdf, Size:1020Kb

Acids and Bases Acids Release H+(Aq) When Dissolved in Water and Bases Release HO-(Aq) Acids and Bases Acids release H+(aq) when dissolved in water and bases release HO-(aq). Strong acids and bases dissociate completely in water. Weak acids and bases are in equilibrium with H+(aq) and HO- (aq), respectively. Acids react with bases to form water in neutralization reactions. Outline • Strong Acids and Bases • Weak Acids • Homework Litmus paper for pH determination Strong Acids and Bases Strong Acids in Water Strong acids are those that completely dissociate in water. You've seen them all in a previous section: HCl, HBr, HI, H2SO4, HNO3, and HClO4. Chemistry 102 Prof. Shapley page 1 The concentration of solvated protons is equal to the moles of the acid added to each liter of water. When 0.05 mol of HNO3 is added to 50 mL water: [H+] = (0.05 mol)/(50 mL)(1 L/1000 mL) = 1.0 M pH = -log(1.0) = -log(100) = 0 When 0.05 mol of H2SO4 is added to 10 L water: [H+] = (0.05 mol)/(10 L) = 0.005 M = 5 x 10-3 = 100.70 x 10-3 pH = -log(10-2.3) = 2.3 Strong Bases in Water The strongest base that can exist in water is HO-. There are many hydroxide salts that provide HO- when dissolved in water. These include NaOH, KOH, Mg(OH)2, Ca(OH)2, and Al(OH)3. There are other bases that are even stronger than hydroxide but these react with water to make hydroxide. [Li+][NH2-] + H2O NH3 + Li+ + HO- [Na+][H-] + H2O H2(g) + Na+ + HO- Neutralization Reactions The reaction between a strong acid and an equal number of moles of a strong base produces water. This is a neutralization reaction because the resulting solution is neutral, neither acidic nor basic, with a pH of 7. When the molar quantity of acid does not equal the molar quantity of base, the pH of the solution depends on the quantity of acid or base that remains. 1. What is the pH of a solution resulting from the addition of 0.10 mol HCl and 0.07 mol NaOH to 1.0 L of water? Chemistry 102 Prof. Shapley page 2 2. What is the pH of a solution resulting from 50 mL of 0.02 M HCl and 50 mL of 0.10 M NaOH? Weak Acids Why are acids weak or strong? Every acid reacts with water. When it loses a proton, it transfers that proton to water. Water acts as a base + when it solvates the proton. The conjugate acid is protonated water and it is represented as (H3O) , + + + (H5O2) , (H2nOn) , or just as H (aq). The conjugate base is the acid minus its proton. A strong acid is completely dissociated in water while a weak acid is in equilibrium with its conjugate base in water. Let's look at the reaction of a strong acid, nitric acid or HNO3, and a weaker acid, nitrous acid or HNO2, in water. Chemistry 102 Prof. Shapley page 3 - Nitric acid is a stronger acid than nitrous acid because its conjugate base is more stable. The NO3 ion has - excess negative charge spread out over 3 oxygen atoms while the excess negative charge in NO2 is spread out over on 2 oxygen atoms. A conjugate base is more stable when the negative charge is on an electronegative element and when the charge is delocalized over multiple atoms. The more stable the conjugate base, the stronger the acid. A stable conjugate base is not very basic. A very strong acid has a very weak conjugate base and a very weak acid has a very strong conjugate base. Weak Acid Equilibrium Nitrous acid is in equilibrium with a proton and its conjugate base, NO2-. Because the concentration of water is constant, we can define a constant equal to the product of the concentration of water and the equilibrium constant. This constant, the Ka is 10-3.29 for HNO2. We can use the Ka to determine the pH of a solution of nitrous acid. For example, let's determine the pH of a solution made from 0.01 mole of HNO2 in 1.0 L of water. Some of the acid will dissociate into H+ and NO2- but we don't know w=how much. We'll call the molar concentration of solvated protons x so [H+] = x. This means that the concentration of NO2- must also be x because they form in equal amounts by the dissociation of the acid. The concentration Chemistry 102 Prof. Shapley page 4 It is always possible to solve for x by using the quadratic equation but most of the time we can solve it using an approximation. If we assume that the extent of dissociation is small, then the equilibrium concentration of acid doesn't change very much from its original concentration. We can then use the original acid concentration in the Ka expression. The approximation is a good one in this case because we get the same pH value using it as we did from the quadratic equation. Reaction between Weak Acids and Strong Bases Chemistry 102 Prof. Shapley page 5 Strong bases react completely with weak bases to form the conjugate base of the weak acid. Then there will be an equilibrium between the weak acid and its conjugate base in water. For example, let's look at the solution formed by mixing 0.010 mol HNO2 and 0.004 mol NaOH in 1.0 L water. Again, we can use an approximation to solve this. The approximation is valid because the extent of dissociation will be small when there is already some product present. Weak Acids and Strong Acids The acid dissociation constants of a selection of acids is in the tables. In the table are listed pKa values. pKa = -log(Ka) The very strong acids, those that are completely dissociated in water, are distinguished by examining their acid dissociation equilibrium in non-aqueous solvents and the pKa for water is estimated. The equilibrium constants for the weaker acids (pKa >0) are determined from pH measurements of solutions. Chemistry 102 Prof. Shapley page 6.
Recommended publications
  • (12) United States Patent (10) Patent No.: US 8,569,369 B2 Kramer Et Al
    USOO856.9369B2 (12) United States Patent (10) Patent No.: US 8,569,369 B2 Kramer et al. (45) Date of Patent: *Oct. 29, 2013 (54) AMINO ACID COMPOUNDS OTHER PUBLICATIONS (75) Inventors: Ronald Kramer, Phoenix, AZ (US); Jablecka et al., MedSci Monit 10(I):CR29-32 (2004). Alexander Nikolaidis, New Kallikratia Maynard et al., J. Nutr. 131:287-290 (2001). (GR) Ruel et al., J. Thorac Cardiovasc. Surg 135:762-77, 2008. Rytlewski et al., European Journal of Obstetrics & Gynecology and (73) Assignee: Thermolife International, LLC, Reproductive Biology 138:23-28 (2008). Phoenix, AZ (US) Schwedheim et al., Br J Clin Pharmacol 65(1):51-59 (2007). Smith et al., J. Thorac Cardiovasc. Surg 132:58-65 (2006). (*) Notice: Subject to any disclaimer, the term of this Rytlewski et al., Eur J. Clin Invest 35 (1):32-37 (2005). patent is extended or adjusted under 35 Ming et al., Circulation 110:3708-3714 (2004). U.S.C. 154(b) by 0 days. Romero et al., Cardiovascular Drug Reviews 24(3-4):275-290 (2006). This patent is Subject to a terminal dis Oka et al., Vasc Med 10:265-274 (2005). claimer. Hayashi et al., PNAS 102(38): 13681-13686 (2005). Grasemann et al., Eur Respir J 25:62-68 (2005). (21) Appl. No.: 13/468,231 Boger, J. Nutr 137:1650S-1655S (2007). Beghetti et al., J. Thorac Cardiovasc. Surg 132(6): 1501-1502 (2006). (22) Filed: May 10, 2012 Larsen et al., B. Acta Physiol 191(1):59-66 (2007). Berge, Journal of Pharmaceutical Sciences, Jan. 1977, vol.
    [Show full text]
  • Periodic Trends in the Main Group Elements
    Chemistry of The Main Group Elements 1. Hydrogen Hydrogen is the most abundant element in the universe, but it accounts for less than 1% (by mass) in the Earth’s crust. It is the third most abundant element in the living system. There are three naturally occurring isotopes of hydrogen: hydrogen (1H) - the most abundant isotope, deuterium (2H), and tritium 3 ( H) which is radioactive. Most of hydrogen occurs as H2O, hydrocarbon, and biological compounds. Hydrogen is a colorless gas with m.p. = -259oC (14 K) and b.p. = -253oC (20 K). Hydrogen is placed in Group 1A (1), together with alkali metals, because of its single electron in the valence shell and its common oxidation state of +1. However, it is physically and chemically different from any of the alkali metals. Hydrogen reacts with reactive metals (such as those of Group 1A and 2A) to for metal hydrides, where hydrogen is the anion with a “-1” charge. Because of this hydrogen may also be placed in Group 7A (17) together with the halogens. Like other nonmetals, hydrogen has a relatively high ionization energy (I.E. = 1311 kJ/mol), and its electronegativity is 2.1 (twice as high as those of alkali metals). Reactions of Hydrogen with Reactive Metals to form Salt like Hydrides Hydrogen reacts with reactive metals to form ionic (salt like) hydrides: 2Li(s) + H2(g) 2LiH(s); Ca(s) + H2(g) CaH2(s); The hydrides are very reactive and act as a strong base. It reacts violently with water to produce hydrogen gas: NaH(s) + H2O(l) NaOH(aq) + H2(g); It is also a strong reducing agent and is used to reduce TiCl4 to titanium metal: TiCl4(l) + 4LiH(s) Ti(s) + 4LiCl(s) + 2H2(g) Reactions of Hydrogen with Nonmetals Hydrogen reacts with nonmetals to form covalent compounds such as HF, HCl, HBr, HI, H2O, H2S, NH3, CH4, and other organic and biological compounds.
    [Show full text]
  • Guidance for Identification and Naming of Substance Under REACH
    Guidance for identification and naming of substances under 3 REACH and CLP Version 2.1 - May 2017 GUIDANCE Guidance for identification and naming of substances under REACH and CLP May 2017 Version 2.1 2 Guidance for identification and naming of substances under REACH and CLP Version 2.1 - May 2017 LEGAL NOTICE This document aims to assist users in complying with their obligations under the REACH and CLP regulations. However, users are reminded that the text of the REACH and CLP Regulations is the only authentic legal reference and that the information in this document does not constitute legal advice. Usage of the information remains under the sole responsibility of the user. The European Chemicals Agency does not accept any liability with regard to the use that may be made of the information contained in this document. Guidance for identification and naming of substances under REACH and CLP Reference: ECHA-16-B-37.1-EN Cat. Number: ED-07-18-147-EN-N ISBN: 978-92-9495-711-5 DOI: 10.2823/538683 Publ.date: May 2017 Language: EN © European Chemicals Agency, 2017 If you have any comments in relation to this document please send them (indicating the document reference, issue date, chapter and/or page of the document to which your comment refers) using the Guidance feedback form. The feedback form can be accessed via the EVHA Guidance website or directly via the following link: https://comments.echa.europa.eu/comments_cms/FeedbackGuidance.aspx European Chemicals Agency Mailing address: P.O. Box 400, FI-00121 Helsinki, Finland Visiting address: Annankatu 18, Helsinki, Finland Guidance for identification and naming of substances under 3 REACH and CLP Version 2.1 - May 2017 PREFACE This document describes how to name and identify a substance under REACH and CLP.
    [Show full text]
  • 140. Sulphuric, Hydrochloric, Nitric and Phosphoric Acids
    nr 2009;43(7) The Nordic Expert Group for Criteria Documentation of Health Risks from Chemicals 140. Sulphuric, hydrochloric, nitric and phosphoric acids Marianne van der Hagen Jill Järnberg arbete och hälsa | vetenskaplig skriftserie isbn 978-91-85971-14-5 issn 0346-7821 Arbete och Hälsa Arbete och Hälsa (Work and Health) is a scientific report series published by Occupational and Enviromental Medicine at Sahlgrenska Academy, University of Gothenburg. The series publishes scientific original work, review articles, criteria documents and dissertations. All articles are peer-reviewed. Arbete och Hälsa has a broad target group and welcomes articles in different areas. Instructions and templates for manuscript editing are available at http://www.amm.se/aoh Summaries in Swedish and English as well as the complete original texts from 1997 are also available online. Arbete och Hälsa Editorial Board: Editor-in-chief: Kjell Torén Tor Aasen, Bergen Kristina Alexanderson, Stockholm Co-editors: Maria Albin, Ewa Wigaeus Berit Bakke, Oslo Tornqvist, Marianne Törner, Wijnand Lars Barregård, Göteborg Eduard, Lotta Dellve och Roger Persson Jens Peter Bonde, Köpenhamn Managing editor: Cina Holmer Jörgen Eklund, Linköping Mats Eklöf, Göteborg © University of Gothenburg & authors 2009 Mats Hagberg, Göteborg Kari Heldal, Oslo Arbete och Hälsa, University of Gothenburg Kristina Jakobsson, Lund SE 405 30 Gothenburg, Sweden Malin Josephson, Uppsala Bengt Järvholm, Umeå ISBN 978-91-85971-14-5 Anette Kærgaard, Herning ISSN 0346–7821 Ann Kryger, Köpenhamn http://www.amm.se/aoh
    [Show full text]
  • WL-13 Safety Data Sheet, Canada (SDS-WL-13-CA
    WL- 13 Safety Data Sheet according to the Hazardous Products Regulation (February 11, 2015) SECTION 1: Identification 1.1. Product identifier Product form : Mixture Product name : WL- 13 1.2. Recommended use and restrictions on use No additional information available 1.3. Supplier Swagelok Supplier: 29495 F.A. Lennon Drive Distributor, add your contact information 44139 Solon, OH - United States T 440-349-5600 - F 440-519-3304 www.swagelok.com 1.4. Emergency telephone number Emergency number : Infotrac: North America: 1-800-535-5053 International: 1-352-323-3500 SECTION 2: Hazard identification 2.1. Classification of the substance or mixture Classification (GHS-CA) Not classified 2.2. GHS Label elements, including precautionary statements GHS-CA labeling No labeling applicable 2.3. Other hazards No additional information available 2.4. Unknown acute toxicity (GHS-CA) No data available SECTION 3: Composition/Information on ingredients 3.1. Substances Not applicable 3.2. Mixtures Name Chemical name / Synonyms Product identifier % Classification (GHS-CA) Molybdenum(IV) sulfide Molybdenum disulfide / Molybdenum (CAS-No.) 1317-33-5 <= 10 Comb. Dust disulphide / Molybdenum sulfide / Molybdenum sulfide (MoS2) / Manganese tetroxide Sodium nitrite Diazotizing salts / Nitrous acid, (CAS-No.) 7632-00-0 <= 1.8 Acute Tox. 3 (Oral), H301 sodium salt / Nitrous acid, sodium Aquatic Acute 1, H400 salt (1:1) / SODIUM NITRITE Full text of hazard classes and H-statements: see section 16 SECTION 4: First-aid measures 4.1. Description of first aid measures First-aid measures after inhalation : Allow victim to breathe fresh air. Allow the victim to rest. First-aid measures after skin contact : Remove affected clothing and wash all exposed skin area with mild soap and water, followed by warm water rinse.
    [Show full text]
  • Acids and Bases
    Name Date Class CHAPTER 14 REVIEW Acids and Bases SECTION 1 SHORT ANSWER Answer the following questions in the space provided. 1. Name the following compounds as acids: sulfuric acid a. H2SO4 sulfurous acid b. H2SO3 hydrosulfuric acid c. H2S perchloric acid d. HClO4 hydrocyanic acid e. hydrogen cyanide 2. H2S Which (if any) of the acids mentioned in item 1 are binary acids? 3. Write formulas for the following acids: HNO2 a. nitrous acid HBr b. hydrobromic acid H3PO4 c. phosphoric acid CH3COOH d. acetic acid HClO e. hypochlorous acid 4. Calcium selenate has the formula CaSeO4. H2SeO4 a. What is the formula for selenic acid? H2SeO3 b. What is the formula for selenous acid? 5. Use an activity series to identify two metals that will not generate hydrogen gas when treated with an acid. Choose from Cu, Ag, Au, Pt, Pd, or Hg. 6. Write balanced chemical equations for the following reactions of acids and bases: a. aluminum metal with dilute nitric acid ϩ → ϩ 2Al(s) 6HNO3(aq) 2Al(NO3)3(aq) 3H2(g) b. calcium hydroxide solution with acetic acid ϩ → ϩ Ca(OH)2(aq) 2CH3COOH(aq) Ca(CH3COO)2(aq) 2H2O(l ) MODERN CHEMISTRY ACIDS AND BASES 117 Copyright © by Holt, Rinehart and Winston. All rights reserved. Name Date Class SECTION 1 continued 7. Write net ionic equations that represent the following reactions: a. the ionization of HClO3 in water ϩ → ϩ ϩ Ϫ HClO3(aq) H2O(l ) H3O (aq) ClO3 (aq) b. NH3 functioning as an Arrhenius base ϩ → ϩ ϩ Ϫ NH3(aq) H2O(l ) ← NH4 (aq) OH (aq) 8.
    [Show full text]
  • Mechanisms of Nitric Oxide Reactions Mediated by Biologically Relevant Metal Centers
    Struct Bond (2014) 154: 99–136 DOI: 10.1007/430_2013_117 # Springer-Verlag Berlin Heidelberg 2013 Published online: 5 October 2013 Mechanisms of Nitric Oxide Reactions Mediated by Biologically Relevant Metal Centers Peter C. Ford, Jose Clayston Melo Pereira, and Katrina M. Miranda Abstract Here, we present an overview of mechanisms relevant to the formation and several key reactions of nitric oxide (nitrogen monoxide) complexes with biologically relevant metal centers. The focus will be largely on iron and copper complexes. We will discuss the applications of both thermal and photochemical methodologies for investigating such reactions quantitatively. Keywords Copper Á Heme models Á Hemes Á Iron Á Metalloproteins Á Nitric oxide Contents 1 Introduction .................................................................................. 101 2 Metal-Nitrosyl Bonding ..................................................................... 101 3 How Does the Coordinated Nitrosyl Affect the Metal Center? .. .. .. .. .. .. .. .. .. .. .. 104 4 The Formation and Decay of Metal Nitrosyls ............................................. 107 4.1 Some General Considerations ........................................................ 107 4.2 Rates of NO Reactions with Hemes and Heme Models ............................. 110 4.3 Mechanistic Studies of NO “On” and “Off” Reactions with Hemes and Heme Models ................................................................................. 115 4.4 Non-Heme Iron Complexes ..........................................................
    [Show full text]
  • Arsine Back up Data Report
    NIOSH Manual of Analytical Methods (NMAM) 5th Edition BACKUP DATA REPORT NIOSH Method No. 6001 Title: Arsine Analyte: Arsine Author/developer: Developed under contract Date: 1976 Note: Method 6001 is a combination of two older, previously published methods: S229 and P&CAM 265. Therefore, the backup data report is a combination of the two methods’ reports. The backup data report for method S229 is a regular written report. The backup data report for P&CAM 265, however, is in the form of a published journal article. The written report for S229 follows, the journal article for P&CAM can be seen here as a pdf. Disclaimer: Mention of any company or product does not constitute endorsement by the National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention. In addition, citations to websites external to NIOSH do not constitute NIOSH endorsement of the sponsoring organizations or their programs or products. Furthermore, NIOSH is not responsible for the content of these websites. All web addresses referenced in this document were accessible as of the publication date. NIOSH Manual of Analytical Methods (NMAM), Fifth Edition Backup Data Report Method S229 Substance: Arsine OSHA Standard: 0.2 mg/m3 Chemical Used: Arsine in Nitrogen (14 ppm), Linde Specialty Gases Procedure The general procedure used is described in NIOSH Method 6001. The collection method has been adapted from P&CAM 127. The charcoal used was Lot 105 activated coconut charcoal supplied by SKC, Inc., Pittsburgh, PA. Desorption efficiency tests have not been carried out because the low concentration of the arsine source would require that large volumes of gas (200-800 ml) had to be injected directly into the charcoal tube.
    [Show full text]
  • Amino-Nitrogen Contents of Wool and Collagen
    U. S. DEPARTMENT OF COMMERCE NATIONAL BUREAU OF STANDARDS RESEARCH PAPER RP787 Part of Journal of Research of the National Bureau of Standards, Volume 14, May 1935 AMINO-NITROGEN CONTENTS OF WOOL AND COLLAGEN By Joseph R. Kanagy 1 and Milton Harris 2 ABSTRACT When wool, collagen, and arginine were treated with nitrous acid, increasing amounts of nitrogen were evolved with time. The continued evolution of nitro­ gen was due to the action of nitrous acid on the guanidine nuclei of these materials. A new method for the determination of the arginine content of a protein is given. The method is based on the relative rates of evolution of nitrogen from the guanidine nuclei in a protein and in arginine. Evidence is presented t o show that the action of nitrous acid on the guanidine nucleus is different from its action on a free amino group. The free amino-nitro­ gen contents of wool and collagen were calculated by subtracting from the total nitrogen evolved that portion of nitrogen which came from the guanidine nuclei. The values obtained for the percentages of the total nitrogen as amino nitrogen are 2.53 for wool and 2.77 for collagen. CONTENTS Page I. Introduction ___ _____________ __________________________________ _ 563 II. Materials and methods _____________________________________ ____ _ 564 III. 566 IV. 569 Conclu~on _____________________________ __ _____________________ _ V. ~frc~~~~~~~~~~======================= ===== ========= =========== 573 VI. References __ _____ ___________ _____ ___________________ _______ ___ _ 573 I. INTRODUCTION The free amino groups in wool and collagen have been related to the combination of these materials with acids, dyes, and tannins by various investigators.
    [Show full text]
  • AMMONIA and NITRIC ACID CONCENTRATIONS · in EQUILIBRIUM with ATMOSPHERIC AEROSOLS: EXPERIMENT VS • THEORY Lynn M
    AMMONIA AND NITRIC ACID CONCENTRATIONS · IN EQUILIBRIUM WITH ATMOSPHERIC AEROSOLS: EXPERIMENT VS • THEORY Lynn M. Rildemann,+ Armistead G. Russell,* Glen R. Cass+ California Institute of Technology Pasadena, California 91125 ABSTRACT The equilibrium between gaseous ammonia, nitric acid, and aerosol nitrate is discussed on the basis of a recent field experiment in Southern California. Comparison is drawn between theoretical equilibrium calculations and simultaneous measurements of nitric acid, ammonia, ammonium ion, nitrate ion, sulfate ion, other ionic species, temperature and dewpoint. Particulate .and gaseous pollutant concentrations at some inland sampling sites are readily explained if the aerosol is assumed to exist as an external mixture with all particulate nitrate and ammonium available to form pure NR • At other monitoring sites, especially near the 4No3 coast, aerosol nitrate is found in the presence of NR and RN0 concentrations that 3 3 thermodynamic calculations show are too low to produce pure NR No • This can be 4 3 explained when the amount of aerosol nitrate that can be derived from reaction of nitric acid with sea salt and soil dust is taken into account. A calculation approach that accounts for the presence of mixed sulfate and nitrate salts improves the agreement between predicted and observed pollutant concentrations in the majority of cases studied. Uncertainties in these calculations arise from a number of sources including the thermodynamic quantities, and the effect of these uncertainties on the comparison between
    [Show full text]
  • Nitration of Toluene (Electrophilic Aromatic Substitution)
    Nitration of Toluene (Electrophilic Aromatic Substitution) Electrophilic aromatic substitution represents an important class of reactions in organic synthesis. In "aromatic nitration," aromatic organic compounds are nitrated via an electrophilic aromatic substitution mechanism involving the attack of the electron-rich benzene ring on the nitronium ion. The formation of a nitronium ion (the electrophile) from nitric acid and sulfuric acid is shown below. The sulfuric acid is regenerated and hence acts as a catalyst. It also absorbs water to drive the reaction forward. Figure 1: The mechanism for the formation of a nitronium ion. The methyl group of toluene makes it around 25 times more reactive than benzene in electrophilic aromatic substitution reactions. Toluene undergoes nitration to give ortho and para nitrotoluene isomers, but if heated it can give dinitrotoluene and ultimately the explosive trinitrotoluene (TNT). Figure 2: Reaction of nitric acid and sulfuric acid with toluene. Procedure: 1. Place a 5 mL conical vial, equipped with a spin vane, in a crystallizing dish filled with ice-water placed on a stirrer. 2. Pour 1.0 mL of concentrated nitric acid into the vial. While stirring, slowly add 1.0 mL of concentrated sulfuric acid. 3. After the addition of sulfuric acid is complete, add 1.0 mL of toluene dropwise and slowly over a period of 5 minutes (slow down if you see boiling. Reaction produces a lot of heat). 4. While Stirring, allow the contents of the flask to reach the room temperature. Stir at room temperature for another 5 minutes. 5. Add 10 mL of water into a small separatory funnel.
    [Show full text]
  • Supporting Information
    Electronic Supplementary Material (ESI) for Green Chemistry This journal is © The Royal Society of Chemistry 2014 Supporting information A Carbon-Based Photocatalyst Efficiently Converted CO2 to CH4 and C2H2 In Visible Light Tongshun Wu,a Luyi Zou,b Dongxue Han,*a Fenghua Li,a Qixian Zhang a and Li Niua a State Key Laboratory of Electroanalytical Chemistry, c/o Engineering Laboratory for Modern Analytical Techniques, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences Changchun 130022, P.R. China bState Key Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun 130023, P. R. China E-mail: [email protected] 1. Preparation of photocatalyst 1.1 Preparation of previously exfoliated graphite (PEG) In order to fully exfoliate graphite into graphene, a solid-exfoliation process was employed to prepare PEG. Natural flaked graphite was mixed and saturated with acids consisting of concentrated sulfuric acid and concentrated nitric acid in a volume ratio of 4:1. The reaction system was stirred with excess FeCl3 or NH4NO3 (>0.25 g/ml in the mixture) for 24 h to form the intercalated graphite compound. The concentration of nitric acid should be maintained at 10 mol/L (as higher concentrations will reduce the 1 Electronic Supplementary Material (ESI) for Green Chemistry This journal is © The Royal Society of Chemistry 2014 conductance of the resulting graphene). The mixture was then carefully vacuum filtered and washed with deionized water for 5 times until the pH of the solution was 6. After being dried at 60 °C in a vacuum oven for 2 h, the graphite was loaded in a ceramic vessel, placed in a microwave oven, and irradiated at 500 W for 90 s.
    [Show full text]