1、Designation: D 6423 99 (Reapproved 2004)An American National StandardStandard Test Method forDetermination of pHe of Ethanol, Denatured Fuel Ethanol,and Fuel Ethanol (Ed75-Ed85)1This standard is issued under the fixed designation D 6423; the number immediately following the designation indicates the
2、 year oforiginal adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers a procedure to determine a
3、measure of the acid strength of high ethanol content fuels.These include ethanol, denatured fuel ethanol, and fuel ethanol(Ed75-Ed85). The test method is applicable to fuels containingnominally 70 volume % ethanol, or higher, as described inSpecifications D 4806 and D 5798.1.2 Acid strength as measu
4、red in this test method is definedas pHe. A pHe value for alcohol solutions is not directlycomparable to pH values of water solutions.1.3 The value of pHe will depend somewhat on the fuelblend, the stirring rate, and the time the electrode is in the fuel.1.4 This standard does not purport to address
5、 all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 4806 Specificat
6、ion for Denatured Fuel Ethanol for Blend-ing with Gasolines for Use as Automotive Spark-IgnitionEngine FuelD 5798 Specification for Fuel Ethanol (Ed75-Ed85) forAutomotive Spark-Ignition Engines3. Terminology3.1 Definitions:3.1.1 ethanol, nethyl alcohol, the chemical compound,C2H5OH.3.1.2 denaturants
7、, nnatural gasoline, gasoline compo-nents, unleaded gasoline, or toxic or noxious materials added tofuel ethanol to make it unsuitable for beverage use but notunsuitable for automotive fuel use.3.1.3 denatured fuel ethanol, nfuel ethanol made unfit forbeverage use by the addition of denaturants.3.1.
8、4 fuel ethanol (Ed75-Ed85), na blend of ethanol andhydrocarbons of which the ethanol portion is nominally 75 to85 volume % denatured ethanol.3.2 Definitions of Terms Specific to This Standard:3.2.1 pHe, na measure of the acid strength of alcoholfuels defined by this apparatus and procedure.4. Summar
9、y of Test Method4.1 The sample is analyzed at room temperature using aspecified electrode system and a pH meter with a sufficientlyhigh impedance and recommended for use with ion-specificelectrodes.4.2 Readings are taken at exactly 30 s because the meterreading will drift throughout the analysis due
10、 to solvent effectson the electrode.4.3 The electrode is soaked in water-based pH 7 bufferbetween readings to prepare it for the next sample. Thisrehydrates the glass electrode, a necessary step to preserve theelectrodes response characteristics.5. Significance and Use5.1 The acid strength, as measu
11、red by pHe, is a goodpredictor of the corrosion potential of ethanol fuels. It ispreferable to total acidity because total acidity does notmeasure acid strength; overestimates the contribution of weakacids, such as carbonic acid; and may underestimate thecorrosion potential of low concentrations of
12、strong acids, suchas sulfuric acid.6. Apparatus6.1 pH meterAll types of commercially available pHmeters with a sufficiently high impedance and recommendedfor use with ion-specific electrodes are acceptable for this test1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum Pro
13、ducts and Lubricants and is the direct responsibility of SubcommitteeD02.A0 on Gasoline and Oxygenated Fuels.Current edition approved July 1, 2004. Published July 2004. Originally approvedin 1999. Last previous edition approved in 1999 as D 6423 - 99.2For referenced ASTM standards, visit the ASTM we
14、bsite, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United St
15、ates.method. Temperature compensation and readability to 0.01 pHunit are recommended.6.2 ElectrodeORION Ross Sure-Flow combination elec-trode3with a glass body shall be used. Because the measure-ment is (of necessity) not made at equilibrium, it is essentialthat this exact electrode be used to ensur
16、e the reproducibility ofresults. Other electrodes (even those of similar design) willlikely give different results under some or all conditions due tothe use of a different size or type of glass membrane for the pHelectrode, a different type of salt bridge junction, or other smalldifferences, which
17、may affect their nonequilibrium response.6.3 Temperature CompensatorThe thermocompensator isa temperature-sensitive resistance element immersed in thesample with the electrodes. The thermocompensator automati-cally corrects for the change in slope of the glass electroderesponse (with change in tempe
18、rature) but does not correct foractual changes in sample pH with temperature. Becausetemperature compensation corrects only for changes in pHelectrode response with temperature, the fuel sample must be at22 6 2C.6.4 Beakers, borosilicate glass, 100 mL.6.5 Magnetic StirrerAny laboratory magnetic stir
19、rer canbe used, along with a TFE-fluorocarbon-coated stirring barapproximately 19 to 25-mm long.6.6 Timer, capable of measuring seconds.7. Reagents and Materials7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents confor
20、m to the specifications of the Committee onAnalytical Reagents of the American Chemical Society wheresuch specifications are available.4Other grades may be used,provided it is first ascertained that the reagent is of sufficientlyhigh purity to permit its use without lessening the accuracy ofthe dete
21、rmination.7.2 Buffer SolutionsCommercially available, preparedbuffer solutions (pH=4.00 and pH=7.00) are acceptable for thestandardization.7.3 1 M Hydrochloric Acid (HCl)Mix one volume ofconcentrated (12 M) HCl with eleven volumes of distilledwater.7.4 3 M Potassium Chloride (KCl)The electrode isshi
22、pped with this filling solution already prepared.7.5 1 M Sodium Hydroxide (NaOH)Dissolve4gofNaOHpellets in 100 mL of distilled water.7.6 1 M Sulfuric Acid (H2SO4)Mix one volume of con-centrated (18 M) H2SO4with 17 volumes of distilled water.8. Sample Containers8.1 Care must be used in sample contain
23、er selection to avoidreactions that change the pHe of the sample. Do not use steel,plated steel, or epoxy-coated steel containers or PVC-coatedglass bottles for samples. Avoid closures with a paper seal.Fluorinated high-density polyethylene and spun aluminumsample containers with polyethylene closur
24、es are acceptable.Glass bottles without a PVC coating and utilizing TFE-fluorocarbon or polyethylene cap seals are also acceptable.8.2 Rinse the container with a portion of the fuel to besampled before taking the sample.9. Standardization of Assembly9.1 Turn on the pH meter and allow it to warm upth
25、oroughly in accordance with the manufacturers instructions.Note the temperature of the sample to be tested. If temperaturecompensation is to be manual, adjust the temperature dial ofthe meter to correspond to the temperature of the sample to betested and allow time for all buffers, solutions, and th
26、eelectrode to equilibrate thermally.9.2 Clean/rehydrate the electrode after every ten samplesand new electrodes before first use in alcohol solutions byalternately soaking several times in 1 M NaOH solution and 1MH2SO4(or 1 M HCl) for about 30 s each. Remove theelectrode and rinse it well with disti
27、lled water into a wastecontainer.9.3 Calibrate the pH meter to pH=7.00 with a water-basedpH=7.00 buffer solution. Remove the electrode and rinse itwith distilled water into a waste container.9.4 Calibrate the pH meter to pH=4.00 with a water-basedpH=4.00 buffer solution, using the slope adjustment.
28、The slopemust be in the 95 to 100 % range, or the electrode will have tobe cleaned or replaced. Remove the electrode and rinse it withdistilled water into a waste container. Return the electrode tothe pH=7.00 buffer.10. Procedure10.1 Fill the electrode as needed with 3M KCl solution,which is supplie
29、d with the electrode.10.2 Standardize the assembly with two reference buffersolutions, as described in 9.3 and 9.4.10.3 Start with a new aliquot (fresh portion) of ethanolsample for each measurement. (Poor repeatability can be partlydue to a poorly buffered sample. High-purity solutions arepoorly bu
30、ffered because they do not contain compounds thattend to stabilize pH. Since some alcohols meet this criteria, itis important that a fresh sample be used for each measurementand that electrodes be in top condition.)10.4 Place about 50 mL of sample in a 100-mL beakercontaining a magnetic stirring bar
31、 and either a thermometer(for meters with manual temperature compensation) or an ATCprobe (for meters with automatic temperature compensation),and ensure the sample is at 22 6 2C.10.5 Remove the electrode from the pH=7.00 buffer, andrinse the electrode with distilled water into a waste container.10.
32、6 Blot the electrode to remove excess water.10.7 Insert the electrode into the room-temperature stirredethanol sample, start the timer, and measure the pHe at exactly3The specified electrode (ORION Cat. No. 8172BN) is available from manylaboratory supply companies or from the manufacturer: Orion Res
33、earch Incorpo-rated, Laboratory Products Group, The Schrafft Center, 529 Main Street, Boston,MA 02129.4Reagent Chemicals, American Chemical Society Specifications, AmericanChemical Society, Washington, D.C. For suggestions on the testing of reagents notlisted by the American Chemical Society, see An
34、alar Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.D 6423 99 (2004)230 6 1 s. Stirring must be rapid enough to cause a small tomoderate vortex about 6 to 8 mm deep.
35、Note that the readingwill still be slowly changing after 30 s due to dehydration ofthe glass pH electrode, which causes a shift in its output. If thereading is not rising at the 30-s point for low pHe fuels(pHe5), or gives poor repeatability in some solutions (thosewith low buffering capacity), the
36、electrode probably needs tobe cleaned or replaced.10.8 Remove the electrode from the sample and rinse it withdistilled water into a waste container. Return the electrode tothe pH=7.00 buffer to rehydrate the glass pH electrode.10.9 Soak the electrode in the buffer until the reading fallsbelow 7.05,
37、but soak for at least 20 s. Recalibrate to pH=7.00if the pH is still above 7.05 after 5 min.10.10 Clean/rehydrate the electrode as described in 9.2 afterten alcohol samples have been measured. The electrode maygive poor repeatability or high results (in alcohols) withoutperiodic pretreatment by soak
38、ing in acid and base before use,probably because the glass electrode is contaminated or notfully hydrated.10.11 Start with 10.3 for the next sample.11. Precision and Bias11.1 PrecisionThe precision of this test method as deter-mined by statistical examination of the interlaboratory testresults is as
39、 follows:11.1.1 RepeatabilityThe difference between successivetest results, obtained by the same operator using the sameapparatus under constant operating conditions on identical testmaterial, would in the long run, in the normal and correctoperation of this test method, exceed 0.29 pHe in only one
40、casein twenty.11.1.2 ReproducibilityThe difference between two singleand independent test results, obtained by different operatorsworking in different laboratories on identical test material,would in the long run, in the normal and correct operation ofthis test method, exceed 0.52 pHe in only one ca
41、se in twenty.11.2 BiasSince there is no material having an acceptedreference value for pHe, bias cannot be determined.12. Keywords12.1 acid strength; automotive spark ignition engine fuel;corrosion potential; denatured fuel ethanol; ethanol; fuel etha-nol; pHeASTM International takes no position res
42、pecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This
43、standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM Intern
44、ational Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown be
45、low.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org).D 6423 99 (2004)3
