1、Designation: D7501 09bStandard Test Method forDetermination of Fuel Filter Blocking Potential of Biodiesel(B100) Blend Stock by Cold Soak Filtration Test (CSFT)1This standard is issued under the fixed designation D7501; the number immediately following the designation indicates the year oforiginal a
2、doption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the determination by filtrationtime after col
3、d soak of the suitability for a biodiesel (B100)blend stock that meets all other requirements of SpecificationD6751 and has a cloud point below 68F (20C) to provideadequate low temperature operability performance to at leastthe cloud point of the finished blend.1.2 The formal precision of this test
4、method is included in13.1 on Precision.1.3 The values stated in inch-pound units are to be regardedas standard. The values given in parentheses are mathematicalconversions to SI units that are provided for information onlyand are not considered standard.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:2D4057 Practice for
6、 Manual Sampling of Petroleum andPetroleum ProductsD5452 Test Method for Particulate Contamination in Avia-tion Fuels by Laboratory FiltrationD6300 Practice for Determination of Precision and BiasData for Use in Test Methods for Petroleum Products andLubricantsD6751 Specification for Biodiesel Fuel
7、Blend Stock (B100)for Middle Distillate Fuels3. Terminology3.1 Definitions:3.1.1 biodiesel, nfuel comprised of mono-alkyl esters oflong chain fatty acids derived from vegetable oils or animalfats, designated as B100.3.1.2 bond, vto connect two parts of a system electricallyby means of a conductive w
8、ire to eliminate voltage differences.3.1.3 BXX blend, nfuel blend consisting of up to 20volume percent biodiesel designated as up to B20 conformingto the requirements of Specification D6751 with the remainderbeing a light middle or middle distillate grade diesel fuel andmeeting the requirements of t
9、his test method.3.1.3.1 DiscussionThe abbreviation BXX represents aspecific blend concentration in the range B2 to B20, where XXis the percent volume of biodiesel in the fuel blend.3.1.4 ground, vto connect electrically with earth.3.2 Definitions of Terms Specific to This Standard:3.2.1 air chamber,
10、 nunit to control temperature of samplefor cooling with maximum 0.5C variation from set point. Theunit shall use a microprocessor temperature controller withdigital set point and readout.Afood-grade refrigerator does notprovide adequate temperature stability for this test method.3.2.2 minor componen
11、t, nmaterial present in B100, typi-cally at concentrations well below 1% by mass.3.2.3 thermal history, nrange of temperatures that a batchor sample of B100 has experienced which can result inseparation or precipitation of minor components.3.2.3.1 DiscussionCooling some biodiesel fuels can resultin
12、precipitation or separation of minor components that havelimited solubility in B100. Heating these biodiesel fuels above40C is believed to redissolve most of these minor componentsand thus erase the thermal history of the sample.3.3 Abbreviations:3.3.1 CSFTCold Soak Filtration Test4. Summary of Test
13、 Method4.1 In this test method, 300 mL of biodiesel (B100) is storedat 40 6 1F (4.5 6 0.5C) for 16 h, allowed to warm to 77 62F (25 6 1C), and vacuum filtered through a single 0.7 mglass fiber filter at controlled vacuum levels of 2125 in. of Hg.1This test method is under the jurisdiction of ASTM Co
14、mmittee D02 onPetroleum Products and Lubricants and is the direct responsibility of SubcommitteeD02.14 on Stability and Cleanliness of Liquid Fuels.Current edition approved Oct. 1, 2009. Published November 2009. Originallyapproved in 2009. Last previous edition approved in 2009 as D750109a. DOI:10.1
15、520/D7501-09B.2For referenced 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
16、Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.4.2 The filtration time is reported in seconds.5. Significance and Use5.1 Some substances that are soluble or appear to be solublein biodiesel (B100) at room temperature will, upon cooling totemperatures above the cloud point or sta
17、nding at roomtemperature for extended periods, come out of solution. Thisphenomenon has been observed in both B100 and BXX blends.These substances can cause filter plugging. This methodprovides an accelerated means of assessing the presence ofthese substances in B100 and their propensity to plug fil
18、ters.5.1.1 B100 biodiesel fuels that give short filtration times areexpected to give satisfactory operation of BXX blends at leastdown to the cloud point of the biodiesel blends.5.2 The test method can be used in specifications as a meansof controlling levels of minor filter plugging components inbi
19、odiesel and biodiesel blends.6. Apparatus6.1 Filtration SystemArrange the following componentsas shown in Fig. 1.6.1.1 Funnel and Funnel Base, with a stainless steel filtersupport for a 47-mm diameter glass fiber filter, and locking ringor spring action clip, capable of receiving 300 mL.NOTE 1Sinter
20、ed glass supports were found to give much higherfiltration times during initial studies and are not recommended to be used.6.1.2 Ground/Bond Wire, 0.912-2.59-mm (No. 10 throughNo. 19) bare stranded flexible, stainless steel or copperinstalled in the flasks and grounded as shown in Fig. 1.6.1.3 Elect
21、rical Bonding Apparatus, as described in TestMethod D5452 or by using other suitable means of electricalgrounding that ensure safe operation of the filtration apparatusand flask.6.1.4 Receiving Flask, 1-L borosilicate glass vacuum filterflask, into which the filtration apparatus fits, and equipped w
22、itha sidearm to connect to the safety flask.6.1.5 Safety Flask, 1-L borosilicate glass vacuum filter flaskequipped with a sidearm to connect the vacuum system. A fueland solvent resistant rubber hose, through which the groundingwire is connected to the sidearm of the receiving flask to thetube, pass
23、es through the rubber stopper in the top of the safetyflask.6.1.6 Vacuum System, capable of producing a vacuum of 70to 100 kPa below atmospheric pressure when measured at thesafety flask. A mechanical vacuum pump may be used if it hasthis capability.NOTE 2Water aspirated vacuum will not provide rela
24、tive vacuumwithin the prescribed range.6.1.7 Chilling Apparatus, either 6.1.7.1 or 6.1.7.2 may beused.6.1.7.1 Circulating Water Bath, capable of sustaining atemperature of 40 6 1F (4.5 6 0.5C).6.1.7.2 Air Chamber, capable of sustaining a temperature of40 6 1F (4.5 6 0.5C). The unit shall use micropr
25、ocessortemperature control and have a digital temperature control/display.6.1.8 Circulating Water Bath, capable of sustaining a tem-perature of 77 6 1F (25 6 0.5C).FIG. 1 Schematic of Filtration SystemD7501 09b26.1.9 Whatman Glass Fiber Filters (GF/F),3plain, 47-mmdiameter, nominal pore size 0.7-m.
26、Acid treated low metalTCLP filters are not suitable for this purpose.6.2 Other Apparatus:6.2.1 Forceps, approximately 12-cm long, flat-bladed, withnon-serrated, non-pointed tips.6.2.2 Graduated Cylinders, to contain at least 0.5 L of fluidand marked at 10-mL intervals. Samples that filter slowly may
27、require 100-mL graduated cylinders.6.2.3 Petri Dishes, approximately 12.5 cm in diameter, withremovable glass supports for glass fiber filters.6.2.3.1 Small Watch Glasses, approximately 5 to 7 cm indiameter, have been found suitable to support the glass fiberfilters.NOTE 3B100 will dissolve some pla
28、stics. This can cause the filters toadhere to the plastic.6.2.4 Protective Cover, polyethylene film or clean alumi-num foil.6.2.5 Timer, capable of displaying elapsed times of at least900 s to the nearest 0.1 s.6.2.6 Thermometer or RTD Sensor, for measuring sampletemperature, should be capable of me
29、asurement 61F(60.5C).7. Reagents and Materials7.1 Purity of ReagentsReagent grade chemicals shall beused in all tests. Unless otherwise indicated, it is intended thatall reagents shall conform to the specifications of the Commit-tee on Analytical Reagents of the American Chemical Society,where such
30、specifications are available. Other grades may beused, provided it is first ascertained that the reagent is ofsufficient purity to permit its use without lessening the accu-racy of the determination.7.2 Flushing FluidsFlushing fluids are not required forthe test as the filter is not weighed. However
31、, heptane orisooctane may be used to wash the apparatus after filtration toremove any residue.7.2.1 Heptane,(WarningFlammable.)7.2.2 2,2,4-trimethylpentane (isooctane),(WarningFlammable.)7.3 Liquid or Powder Detergent, water-soluble, for cleaningglassware.8. Sampling8.1 A separate representative sam
32、ple shall be collected forthis test method. Samples may preferentially be obtaineddynamically from a sampling loop in a distribution line or fromthe flushing line of a field sampling kit. Ensure that the line tobe sampled is flushed with fuel before collecting the sample.Alternatively, circulate or
33、agitate the contents of the tank inorder to collect a representative sample that includes anyprecipitates that might have settled in the tank. One option is tosample the tank immediately after filling, before the contentshave time to settle.8.1.1 Where it is necessary to obtain samples from staticst
34、orage using a sampling container or intermediate containers,follow the procedures given in Practice D4057 or equivalent,taking precautions for cleanliness of all equipment used. Thisis interpreted to mean a representative sample in accordancewith Practice D4057, and refers to an “all-levels” sample.
35、(WarningSamples obtained from static storage can giveresults which are not representative of the bulk contents of thetank because of particulate matter settling.)8.2 Precautionsto avoid sample contamination include:8.2.1 Selection of an appropriate sampling point.8.2.2 Use of clean sample containers
36、. Visually inspect thesample container before taking the samples to verify that thereare no visible particles present inside the container.8.2.3 Keeping a clean protective cover over the top of thesample container until the cap is replaced after filling.8.2.4 If the primary sample container cannot b
37、e selectedsuch that it is suitable for this test procedure, the sample shallpass through only a minimum number of intermediate contain-ers prior to placement in the final container.8.2.5 After filling the sample container with 300 mL ofsample, protect the fuel sample from prolonged exposure tolight
38、by wrapping the container in aluminum foil or storing itin the dark to reduce the possibility of particulate formation bylight-promoted reactions.8.3 If 300 mL of sample is not received in a 500-mL bottleor the sample has been received in a container not suitable forthis test, follow the sampling co
39、ndition procedure in 8.4.8.4 Sample Conditioningfor samples received that mighthave been cooled to temperatures below 68F (20C):8.4.1 Upon receipt of a biodiesel blend stock (B100)sample, the entire sample is to be heated to 104F (40C) forat least 3 h under an inert atmosphere to erase any thermalhi
40、story and to dissolve any solids that might have precipitatedduring transit. After heating for the required time, allow thesample to sit for 24 h at a temperature no lower than 68F(20C).8.4.2 This sample conditioning step may be omitted if thesample was collected from a heated tank at a productionfa
41、cility. In this case, proceed directly to 8.5.8.4.3 If there is any doubt about the thermal history of thesample, the sample conditioning step shall be performed.8.5 Analyze fuel samples as soon as possible after sampling.8.6 Shake the sample vigorously for 1 min. If the sample isnot already in a 50
42、0-mL bottle suitable for this test procedure,transfer 300 mL to a clean, fresh 500 6 15-mL bottle. If a300-mL sample was received is already in such a bottle,proceed with the test procedure in Section 11.9. Preparation of Apparatus and Sample Containers9.1 Clean all components of the filtration appa
43、ratus usingthe reagents described in 7.2 and 7.3.9.1.1 Filtration apparatus shall be clean and dry prior to use.9.1.2 Remove any labels, tags, and so forth.10. Preparation of Glass Fiber Filter10.1 Each filtration uses one filter as specified in 6.1.9. Theglass fiber filter used for each individual
44、test may be identifiedby marking the petri dish used to hold and transport the filter.10.2 Clean all glassware used in preparation of glass fiberfilter as described in 9.1.3Whatman filters were used in the ILS. See Section 13.D7501 09b310.3 Using forceps, place the filter on clean glass supportrods
45、or watch glasses in petri dish.10.4 Place the petri dish, with its lid slightly ajar, in a dryingoven at 194F (90 6 2C and leave it for 30 min.10.5 Remove the petri dish from the drying oven. Keep thepetri dish cover ajar, such that the filter is protected fromcontamination from the atmosphere.Allow
46、 30 min for the filterto come to equilibrium with room air temperature and humid-ity.10.6 Using clean forceps, place the filter centrally on thefilter support of the filtration apparatus (see Fig. 1). Install thefunnel and secure with locking ring or spring clip.10.7 Protect the funnel opening of th
47、e assembled filtrationapparatus with a clean protective cover until ready for use.11. Procedure11.1 Place 300 mL of sample in a 500 mL glass bottle andset in a liquid or air chamber at 40 6 1F (4.5 6 0.5C) for 166 0.25 h. A refrigerator is not suitable for this procedure.11.2 After the 16-h cold soa
48、k at 40 6 2F (4.5 6 1.1C) iscompleted, remove sample from bath and place in a circulatingwater bath with the temperature set to 77 6 1F (25 6 0.5C)according to 11.2.1 or 11.2.2. The sample shall be completelyliquid before filtration.11.2.1 If the sample is completely liquid after the 16-h coldsoak,
49、heat the sample at 77 6 1F (25 6 0.5C) for 2 6 0.25h. Otherwise follow 11.2.2.11.2.2 If the sample is solid or contains any solids or hazeafter the 16-h cold soak, heat the sample at 77 6 1F (25 60.5C) for 4 6 0.25 h.11.2.3 Verify that the sample is at 77 6 1F (25 6 0.5C) bydipping without stirring or agitating the sample with an RTDsensor or thermometer.11.3 Filter the samples as quickly as possible upon removalfrom the warming bath once the desired warming time haselapsed according to 11.2.1 or 11.2.2, whichever applies.
