1、Designation: D 5004 89 (Reapproved 2004)e1An American National StandardStandard Test Method forReal Density of Calcined Petroleum Coke by XyleneDisplacement1This standard is issued under the fixed designation D 5004; the number immediately following the designation indicates the year oforiginal adop
2、tion 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.e1NOTEWarning notes were moved into text editorially in November 2004.1. Scope1.1 T
3、his test method is intended for the determination of thereal density (RD) of calcined petroleum coke. Real density, bydefinition, is obtained when the particle size of the testspecimen is smaller than 75 m (No. 200 sieve).1.2 The values stated in SI units are to be regarded asstandard.1.3 This stand
4、ard does not purport to address 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. For specificwarning statemen
5、ts, see Sections 10 and 11.1.2. Referenced Documents2.1 ASTM Standards:2D 346 Practice for Collection and Preparation of CokeSamples for Laboratory AnalysisD 1193 Specification for Reagent WaterD 2013 Method for Preparing Coal Samples for AnalysisD 2234 Test Methods for Collection of a Gross Sample
6、ofCoalD 4057 Practice for Manual Sampling of Petroleum andPetroleum ProductsD 4292 Test Method for Vibrated Bulk Density of CalcinedPetroleum CokeD 4930 Test Method for Dust Control Material on CalcinedPetroleum CokeE11 Specification for Wire Cloth and Sieves for TestingPurposes3. Terminology3.1 Def
7、initions:3.1.1 calcined cokegreen petroleum coke that has beenthermally treated to drive off the volatile matter and to developcrystalline structure.3.1.2 petroleum cokea solid, carbonaceous residue pro-duced by thermal decomposition of heavy petroleum fractionsor cracked stocks, or both.3.2 Definit
8、ions of Terms Specific to This Standard:3.2.1 bulk densitythe mass of the particles divided by thevolume they occupy that includes the space between theparticles. Refer to Test Method D 4292 for bulk densityprocedures.3.2.2 dedusting materialsee Test Method D 4930.3.2.3 real density(also referred to
9、 as true specific gravity),the mass divided by the volume occupied by the materialexcluding pores and voids. It is required, therefore, that voidsin the coke be eliminated and that pores in the material be filledby the fluid being displaced. This requirement is met for thepurposes of this test metho
10、d by reducing the coke particles toa size smaller than 75 m.3.2.3.1 DiscussionThe density of particles larger than 75m up to the largest that can be put into the helium pycnometercan also be determined, but must be designated as particledensity (PD). The precision data obtained for RD may not beappl
11、icable to PD.4. Summary of Test Method4.1 The mass of the sample is determined directly and thevolume derived by determining the mass of liquid displacedwhen the sample is introduced into a pycnometer.RD 5 M 3 D/L (1)where:1This test method is under the jurisdiction of ASTM Committee D02 onPetroleum
12、 Products and Lubricants and is the direct responsibility of SubcommitteeD02.05 on Properties of Fuels, Petroleum Coke and Carbon Material.Current edition approved Nov. 16, 2004. Published November 2004. Originallyapproved in 1989. Last previous edition approved in 1999 as D 5004 89 (1999).2For refe
13、renced ASTM standards, visit the ASTM website, 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, Wes
14、t Conshohocken, PA 19428-2959, United States.M = mass of sample,D = density of displaced liquid, andL = mass of displaced liquid.5. Significance and Use5.1 The density of petroleum coke directly influences thephysical and chemical properties of the manufactured carbonand graphite artifacts for which
15、 it is used. Density, therefore, isa major quality specification of calcined petroleum coke and isused as a control in coke calcination.6. Interferences6.1 Oil or other material sprayed on calcined petroleumcoke to control dust will interfere with the determination of realdensity so the oil must be
16、removed before reducing the sampleto 75 m.6.1.1 When a petroleum oil was used, it can be removed byflushing with a solvent such as methylene chloride, dichloro-ethane, or toluene. The solvent must be completely removedbefore proceeding with the RD determination. Heating to 10Cabove the boiling point
17、 of the solvent used or application ofvacuum is satisfactory for the removal of the dedusting oil.NOTE 1Consult the Material Safety Data Sheet (MSDS) for theselected solvent.6.1.2 An alternative method of oil removal is by heating thecalcined coke sample in an oven at 700C for 1 h.7. Apparatus7.1 Py
18、cnometer, or specific gravity bottle, 50 mL, with aground glass stopper with a capillary hole.3Bottles with a largeneck (12 to 13 mm outside diameter) are preferred.7.2 Water Bath, controlled to a temperature of 25 6 0.1C.NOTE 2This test method is written to be performed at 25 6 0.1C;however, some l
19、aboratories may not have the provisions to perform thetest at this temperature. It is permissible to perform the test procedure atany temperature between 20 and 40C providing that the water bath iscontrolled at 60.1C of the chosen temperature and the pycnometers arecalibrated at the same temperature
20、 that is used to determine the realdensity of the petroleum coke sample. This is possible due to the fact thatthe real density of calcined petroleum coke is not affected by temperaturechanges over a limited temperature range.7.3 Analytical Balance, accurate to 60.1 mg.7.4 Vacuum Desiccator, with gua
21、rd, connected to a vacuumsource capable of lowering pressure to 75 mm of Hg (10 kPa).7.5 Desiccator, with drying agent. Anhydrous calcium sul-phate is satisfactory.7.6 Drying Oven, preferably a vacuum oven, for tempera-ture to 120C.7.7 Lead Weights, for the pycnometers, to prevent tippingover in the
22、 water bath. These can be made by coiling solid wiresolder.7.8 Wire Sieve, 75 m (No. 200 mesh), meeting Specifica-tion E11.8. Reagents8.1 Purity of WaterReferences to distilled water shall beunderstood to mean reagent water as defined by Type III ofSpecification D 1193.8.2 Analytical reagent grade s
23、olvents are not required butcan be used. The technical grade of each of the following issatisfactory:8.2.1 Acetone, Xylene, and Ethyl Alcohol. (See 6.1.2.)9. Sample Preparation9.1 For recommended practice for obtaining, handling, andpreparing coke samples, refer to Practice D 346, MethodD 2013, Test
24、 Methods D 2234, and Practice D 4057. SeeSection 6.9.2 Crush 50 g of coke so that the entire sample will passthrough a 75 m (No. 200) sieve. Dry the crushed sample in adrying oven at 1156 5C to constant mass (approximately 8 h).Cool in a desiccator.NOTE 3Constant mass is considered to be achieved wh
25、en change inmass is less than 60.05 g after a 30 min test drying period.10. Pycnometer Calibration (Determination ofPycnometer Volume)10.1 Clean the pycnometer and its stopper with detergent,rinse thoroughly with water then with acetone. Place in adesiccator to dry, then weigh the empty pycnometer t
26、ogetherwith its stopper to 0.1 mg (mass Wo). The temperature of thepycnometer is to be close to room temperature when its weightis determined. (WarningCommercial pycnometers (specificgravity bottles) can either have not been calibrated at 25C orelse not calibrated to the accuracy required for this t
27、est method,so it is necessary that the pycnometer volume be determined.)NOTE 4Do not handle the pycnometer with bare fingers. Finger cotsor surgical gloves can be worn, or tongs can be used, when handling thepycnometer to prevent moisture from fingers influencing the weight.10.2 Fill the pycnometer
28、with freshly boiled (to remove air)and cooled distilled water, and replace the stopper. Immerse thepycnometer up to the neck in the 25 6 0.1C water bath for1 h. Use the lead weights to prevent tipping. Replace water thatleaves the capillary during this period. A syringe is convenientfor this purpose
29、.10.3 At the end of the temperature stabilization period,check the capillary to be certain it is completely filled. Removeexcess water on the stopper by dabbing with filter paper. Ifwater is inadvertently removed from the capillary it must bereplaced. Remove the pycnometer from the 25C bath, rinseim
30、mediately with acetone, dry, and weigh to 0.1 mg (mass W3).NOTE 5Avoid any heating after the pycnometer is removed from the25C bath. Heating will expand the water and cause loss from thecapillary. Water is not to be added to the capillary after the pycnometer isremoved from the 25C bath. The purpose
31、 for the immediate acetone rinseis to contract the contents so it will recede in the capillary. Ethyl alcoholcan be used in place of acetone. If laboratory temperature is 25C orabove, a water bath maintained at about 20C should be provided to coolthe pycnometer for about 1 min then dry and weigh. Do
32、 not chill thepycnometers so cold that moisture from the atmosphere will condense onthem and make accurate weighing impossible.3A Gay-Lussac pycnometer has been found suitable for this purpose.D 5004 89 (2004)e1210.4 Calculate the volume, v, of the pycnometer in cubiccentimetres using Eq 2. Round of
33、f to 0.001 cm3.v 5W32 Worw(2)where:Wo= mass of the empty pycnometer, g,W3= mass of the water filled pycnometer, g, andrw= density of water at 25C = 0.9970 g/cm3.10.5 Repeat 10.1-10.4 seven times over a two to three dayperiod. Individual values should not deviate from the mean bymore than 60.0015 cm3
34、. Use the mean value in all calculationsusing Eq 3. Re-determine the pycnometer volume every threemonths. The mass, Wo, should remain constant to within60.001 g. (WarningIf this test method is performed at atemperature other than 256 0.1C as stated in Note 2, then rwis the density of water at the te
35、mperature chosen for themeasurement. The density of water at temperatures other than25C is available in numerous standard reference journals.)11. Determination of the Density of Xylene11.1 Follow the procedure in 10.1-10.3, but use xyleneinstead of water. Calculate the density, rx, of xylene at 25C
36、ing/cm3using Eq 3. Round off to 0.0001 g/cm3.(WarningAvoid any heating after the pycnometer is removed from the25C bath. Heating will expand the xylene and cause loss fromthe capillary. Xylene is not to be added to the capillary after thepycnometer is removed from the 25C bath.rx5W22 Wov(3)where:Wo=
37、 mass of the empty pycnometer, g,W2= mass of the xylene-filled pycnometer, g, andv = pycnometer volume, cm3.)12. Procedure12.1 Clean the pycnometer and its stopper with detergentand rinse thoroughly with water then with acetone and dry ina desiccator.12.2 Weigh the pycnometer with its stopper to 0.1
38、 mg (massWo). The temperature of the pycnometer is to be close toambient room temperature. (See Note 4.)12.3 Introduce approximately 10 g of the dried and cooledanalysis sample into the clean, dry, pycnometer. Less samplecan be used but should not be less than 5 g.12.4 Replace the stopper, remove an
39、y coke adhering to theouter pycnometer surface, and re-weigh. The difference be-tween this mass and Wois the sample mass (mass Ws).12.5 Fill the pycnometer with enough xylene to wet andcover the sample and swirl gently to aid wetting and to displaceair. Add additional xylene until the pycnometer is
40、abouttwo-thirds full and place it, without stopper, in the vacuumdesiccator at as low an absolute pressure (or high a vacuum) aspossible to remove air from the coke but to avoid excessiveevaporation of the xylene. If a means is available, vibrate thepycnometer gently and intermittently while in the
41、desiccator toassist in the elimination of air. Leave under vacuum until allbubbling stops. It is recommended that time under vacuum beat least 30 min.12.6 Remove the pycnometer from the desiccator, fill it withxylene, and place it in the 25 6 0.1C bath with stopper inplace. Immerse the pycnometer up
42、 to the neck in the water bathfor 1 h. Use the lead weights to prevent tipping. Replace xylenethat leaves the capillary during this period. A syringe isconvenient for this purpose.12.7 At the end of the temperature stabilization period,check the capillary to be certain it is completely filled. Remov
43、eexcess xylene on the stopper by dabbing with filter paper. Ifxylene is inadvertently removed from the capillary, it must bereplaced. Remove the pycnometer from the 25C bath, rinseimmediately with acetone, dry, and weigh to 0.1 mg (mass W1).12.8 Upon completion of the test procedure, clean and dryth
44、e pycnometers. To facilitate cleaning of the pycnometers,remove a portion of the xylene and replace with acetone. Thenshake this xylene/acetone mixture and facilitate removal of thepetroleum coke from the pycnometers. Clean the pycnometersas specified in 10.1 before reuse.13. Calculation13.1 Determi
45、ne the density of the sample in g/cm3from Eq4 as follows:density 5 WsSrxWs2 W12 W2!D(4)where:Ws= mass of sample, g,rx= density of xylene at 25C, g/cm3,W1= mass of the pycnometer filled withsample and xylene, g,W2= mass of the pycnometer filled withxylene alone, g,Ws(W1W2) = mass of xylene displaced
46、by coke,g, andrxWs2 W12 W2!= volume of xylene displaced bycoke, cm3.14. Report14.1 Report to the third decimal place the average ofduplicate determinations that agree within 0.007 g/cm3. Whenthis agreement is not met, the values are considered suspectand another duplicate set shall be run. Report th
47、e average of allresults agreeing within 0.007 g/cm3. If the second set also failsto agree within 0.007 g/cm3, report the average of all fourvalues. The operator shall also report if the second set ofduplicate determinations fail to agree within 0.007 g/cm3.15. Precision and Bias415.1 The precision o
48、f this test method as determined by thestatistical examination of interlaboratory test results is asfollows:15.1.1 RepeatabilityThe difference between successiveresults by the same operator using the same apparatus underconstant operating conditions on identical test materials, will inthe long run,
49、in normal and correct operation of the test4Supporting data have been filed at ASTM International Headquarters and maybe obtained by requesting Research Report RR: D02-1007.D 5004 89 (2004)e13method, exceed the following values only in one case intwenty: repeatability = 0.0067.15.1.2 ReproducibilityThe difference between two singleand independent results obtained by different operators work-ing in different laboratories on identical test materials, will inthe long run, in normal and correct operation of the testmethod, exceed the
