ASTM E1690-2001 Standard Test Method for Determination of Ethanol Extractives in Biomass《测定生物物质中乙醇萃取物的标准试验方法》.pdf

1、Designation: E 1690 01Standard Test Method forDetermination of Ethanol Extractives in Biomass1This standard is issued under the fixed designation E 1690; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A

2、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 the determination of ethanolsoluble extractives, expressed as a percentage of the oven-driedbiomass, of hard a

3、nd soft woods, herbaceous materials (such asswitchgrass and sericea), agricultural residues (such as cornstover, wheat straw, and bagasse), and wastepaper (such asoffice waste, boxboard, and newsprint). All results are reportedrelative to the oven-dried weight of the sample.NOTE 1This method may not

4、 be suitable for hard and soft woodsamples that include bark or those with more than 10% extractablematerials.1.2 The values stated in SI units are to be regarded as thestandard.1.3 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is therespons

5、ibility 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 1107 Test Method for Alcohol-Benzene Solubility ofWoodE 1756 Test Method for Determination o

6、f Total Solids inBiomassE 1757 Practice for Preparation of Biomass for Composi-tional Analysis3. Terminology3.1 Definitions:3.1.1 ethanol extractivesthe residue remaining afterevaporation of the ethanol solvent. These are materials that areremoved from the biomass by extraction with 190 proofethanol

7、.3.1.2 oven-dried weightthe moisture-free correctedweight of the prepared biomass sample. The correction factoris determined in accordance with Test Method E 1756.3.1.3 prepared biomassthe biomass that has been pre-pared in accordance with Practice E 1757.4. Significance and Use4.1 Ethanol extractiv

8、es are any materials found in biomassthat are soluble in ethanol. They are not considered to be partof the structural components of biomass and should be re-moved prior to any chemical analysis of the sample. Theprolonged extraction removes nonstructural materials that caninclude waxes, fats, resins

9、, tannins, gums, sugars, starches, andpigments. Removing hydrophobic materials from the biomassmakes it easier to wet the material for the analysis of structuralcomponents in the biomass.4.2 This test method yields results comparable to TestMethod D 1107.5. Apparatus5.1 Soxhlet Extraction Apparatus,

10、 glass, of a size (100 mL)suitable for containing the sample and a 250-mL collectionflask.5.2 Alundum Extraction Thimbles, medium porosity (10 to15-m pore), sized to fit the Soxhlet extractor.5.3 Analytical Balance, sensitive to 0.1 mg.5.4 Rotary Evaporator with Vacuum and Water Bath, con-figured wi

11、th a “bump” or safety trap, condenser, and receivingvessel. A water aspirator will generally provide sufficientvacuum (150 torr).5.5 Vacuum Oven, controllable to 40 6 1C and withvacuum between 75 and 100 torr.6. Reagents and Materials6.1 Ethyl Alcohol, 190 proof, USP grade.1This test method is under

12、 the jurisdiction of ASTM Committee E48 onBiotechnology and is the direct responsibility of Subcommittee E48.05 on BiomassConversion.Current edition approved November 10, 2001. Published February 2002.Originally published as E 1690-95. Last previous edition E 1690-95.2For referenced ASTM standards,

13、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, West Conshohocken, PA 1942

14、8-2959, United States.7. Sampling7.1 The sample is milled material prepared in accordancewith Practice E 1757.8. Procedure8.1 Dry the Soxhlet extraction thimble in a drying oven at105C overnight. Remove it and allow it to cool to roomtemperature in a desiccator.8.2 Weigh the Soxhlet extraction thimb

15、le to the nearest 0.1mg, and record the weight as Wt. Add a suitable quantity ofsample to the extraction thimble. Do not over fill the thimble;the largest sample should still leave approximately 1 cm of freespace in the top of the thimble. Weigh to the nearest 0.1 mg,and record this weight as Wst.NO

16、TE 2The precision for quantitation of the extractives weight isbased on a nominal 7-g prepared sample weight. Smaller samples willintroduce a larger relative error.NOTE 3The samples for total solids determination should be weighedout at the same time as those for extractives determination. If this i

17、sperformed at a later time, it can introduce an error in the calculationbecause ground biomass can gain or lose moisture rapidly when exposedto the atmosphere.8.3 Place several boiling chips into a 250-mL flask. Weighthe flask, with chips, to the nearest 0.1 mg, and record thisweight as the tare wei

18、ght of the flask, Wf.8.4 Assemble the Soxhlet apparatus using at least 160 mLof190 proof ethanol. Insert the thimble, and heat at reflux for 24h. Check the reflux rate periodically, and adjust the heating rateto provide four to five solvent exchanges per hour in theSoxhlet thimble. Approximately 100

19、 to 120 solvent exchangesare required during the 24-h period.8.5 Remove the thimble when the extraction time is com-plete, and transfer the sample carefully to a Buchner funnel.Remove any residual solvent by vacuum filtration, and washthe sample thoroughly with 190 proof ethanol, collecting all ofth

20、e filtrate. Allow the biomass to air dry in the Buchner funnelwhile it is still attached to the vacuum system.NOTE 4If the extractives-free sample is to be analyzed further, storethe air-dried extractives-free sample in a freezer at 10C until needed.8.6 Combine the filtrate from the previous step an

21、d anysolvent from the upper section of the Soxhlet apparatus withthe solvent in the 250-mL flask. Place the flask on the rotaryevaporator, and remove the solvent under vacuum. Use a waterbath temperature of 45 6 5C to heat the flask duringevaporation.8.7 Place the flask in a vacuum oven (75 to 100 t

22、orr) at 406 1C for 24 6 1 h after all of the visible solvent is removedby the rotary evaporator. Remove the flask at this time, andallow it to cool to room temperature in a desiccator. Weigh theflask to the nearest 0.1 mg. Record this weight as Wef.9. Calculation9.1 Calculate the weight of oven-drie

23、d biomass used for theextraction:Ws5 Wst2 Wt! 3 T/100 %! (1)where:Ws= weight of moisture-free solids in the preparedsample, g,Wst= weight of sample and thimble (8.2), g,Wt= tare weight of thimble (8.2), g, andT = percentage of total solids in the sample, as deter-mined in accordance with Test Method

24、 E 1756.9.2 Calculate the percent of extractives on a 105C oven-dried weight basis:% extractives 5 Wef2 Wf!/Ws# 3 100 % (2)where:% extractives = percentage of extractives based on theoven-dried weight,Wef= weight of extractives, flask, and boilingstones (8.7), g,Wf= tare weight of flask with boiling

25、 stones(8.3), g, andWs= weight of moisture-free solids in the pre-pared sample (9.1), g.10. Report10.1 Report the percent extractives based on the oven-driedweight of the sample.11. Precision and Bias11.1 Precision:11.1.1 Data obtained by replicate testing of a hybrid poplarsample in one laboratory

26、yielded a standard deviation inextractive content of 0.15 % and a CV % of 7.6 %. Replicatetesting of a National Institute of Standards and Technology(NIST) No. 8494 wheat straw yielded a standard deviation of0.20 % and a CV % of 1.6 %, and NIST No. 8493 Pinus radiata(Monterey Pine) yielded a standar

27、d deviation of 0.20 % and aCV % of 8.0 %.11.1.2 No data are available at this time on replicate testingin independent laboratories.11.2 BiasProlonged heating of the extractive residue maybias the reported results low because of the evaporation ofsemivolatile constituents. Insufficient heating or usi

28、ng inad-equate vacuum can bias the results high because of incompleteremoval of the ethanol solvent.12. Keywords12.1 agricultural residue; biomass; extractives; herbaceous;waste paper; woodE1690012ASTM International takes no position respecting the validity of any patent rights asserted in connectio

29、n 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 standard is subject to revision at any time by the responsible

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31、eration 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 below.This standard is copyrighted by ASTM International, 100 Bar

32、r 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).E1690013