1、Designation: D 3495 00 (Reapproved 2006)Standard Test Method forHexane Extraction of Leather1This standard is issued under the fixed designation D 3495; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision. A n
2、umber in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1. Scope1.1 This test method covers the quantitative extraction of
3、 alltypes of leather with hexane. This test method does not applyto wet blue.1.2 This standard 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 determ
4、ine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D 2813 Practice for Sampling Leather for Physical andChemical TestsD 3790 Test Method for Volatile Matter (Moisture) ofLeather by Oven Drying3. Significance and Use3.1 This test method measures t
5、he amount of hexane-soluble lubricant present in all types of leather. Adequatelubrication prevents abrasion of leather fibers during flexing.This lubrication is generally obtained from the fat liquor addedat the tannery. Some lubrication is also obtained from naturalgrease produced during the life
6、of the animal.4. Apparatus4.1 Analytical Balance.4.2 Soxhlet Apparatus, consisting of a boiling flask, extrac-tion tube, and condenser.4.3 Forced Circulating Air Oven, capable of maintaining thespecified temperature.4.4 Electric Hot Plate.4.5 Extraction Thimbles, fat-free, cellulose, Alundum, orfrit
7、ted.4.6 Absorbent Cotton, fat-free.4.7 Steam Bath.5. Reagent5.1 Hexane, ACS Reagent Grade conforming to the follow-ing requirements:5.1.1 Color (APHA)10 max.5.1.2 Density (g/mL) at 25C0.687 max.5.1.3 Boiling Range1 to 95 mL, not more than 4.0C.5.1.4 Residue After Evaporation0.001 % max.5.1.5 Acidity
8、 (as CH3COOH)To pass test (limit 0.002 %).5.1.6 Sulfur Compounds (as S)0.005 % max.5.1.7 ThiopheneTo pass test.NOTE 1This reagent grade hexane is generally a mixture of severalisomers of hexane (C6H14), predominantly n-hexane and methylcyclopen-tane (C6H12).6. Test Specimens6.1 The leather shall be
9、sampled in accordance with MethodD 2813. Leather test specimens shall be obtained from thecomposite sample prepared by random sampling, cutting, andmixing equal portions of leather representing the lot that isbeing analyzed. The well-mixed leather pieces shall be groundin a mill (Wiley or equal) hav
10、ing a No. 5 (4-mm) sieve. Theground leather that passes through this 4-mm sieve shall bemixed well and used as the composite sample.7. Procedure7.1 Determine the moisture content of the composite samplefrom which the ground leather for hexane extraction is taken inaccordance with Test Method D 3790.
11、 Determine the weight ofthe ground leather taken from the composite sample formoisture content at the same time and under the same ambientconditions as the weight of the ground leather taken for hexaneextraction.7.2 Weigh5gofground leather taken from the composite tothe nearest 0.001 g and record th
12、is value as W1. Loosely packthis material in an appropriately sized extraction thimble andcover with a pad of fat-free cotton. Place the loaded thimble in1This test method is under the jurisdiction of ASTM Committee D31 on Leatherand is the direct responsibility of Subcommittee D31.06 on Chemical An
13、alysis.Current edition approved April 1, 2006. Published April 2006. Originallyapproved in 1976. Last previous edition approved in 2000 as D 3495 00.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStanda
14、rds 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 States.the Soxhlet extraction tube. Dry an extraction flask in an ovenfor1hat1006 2C, cool in a desiccat
15、or, and weigh to thenearest 0.001 g. Record this value as W2. Fill the flaskapproximately two-thirds full with hexane, assemble the appa-ratus, circulate the water through the condenser, and heat theflask until the extraction of the leather has continued for aminimum of 50 cycles. If the Soxhlet dri
16、ps continuouslyinstead of cycling, extract the leather for a minimum of 5 husing maximum heat. At the end of the extraction period,remove the flask containing the extraction solvent and drive offthe hexane. When 10 to 20 mL of hexane remain, heat gentlyon a steam bath until the odor of the solvent c
17、an no longer bedetected. Facilitate the removal of the hexane by utilizing avacuum or a gentle stream of filtered (oil- and water-free) air.After the hexane has been removed, dry the flask containingthe extracted matter in a forced circulating air oven at 100 62C, for 2 h, cool to room temperature i
18、n a desiccator andweigh. Continue drying for successive 2-h periods until con-stant weight is obtained. When successive weighings vary byless than 6 0.005 g, consider the weight constant. Record thisweight to the nearest 0.001 g as W3. No more than threesuccessive 2-h drying periods shall be allowed
19、. If constantweight has not been obtained after the third drying, the resultsof the second drying period shall be repeated.8. Calculation8.1 Calculate the percentage of hexane-soluble matter, on amoisture-free basis, as follows:Hexane2soluble matter, % 5W32 W2W13100 2 % moisture!1003 100(1)where:W1=
20、 original weight of extracted leather,W2= weight of extraction flask, andW3= weight of extraction flask and hexane-soluble matter.9. Report9.1 Report the hexane-soluble matter in the leather as theaverage value obtained from the test results to nearest 0.01 %.9.2 State that the results are calculate
21、d on a moisture-freebasis.10. Precision and Bias10.1 Interlaboratory Test Data3An interlaboratory testwas run in 1972 in which each of 7 laboratories tested duplicatespecimens from each of 15 different types of leather. Alllaboratories tested the following leathers: chamois, yellowlace, crust sheeps
22、kin, crust goatskin, vegetable-strap leather,chrome-retan side leather, vegetable-skirting leather,vegetable-retan side leather, latigo-lace leather, white-laceleather, suede sheepskin, horsehide (finished), white-sideleather, chrome-split leather, and silicone-treated militaryleather. The component
23、s of variance for hexane-soluble matterexpressed as standard deviations were calculated to be:Within2laboratory single operator!component0.14 percentage points (2)Between2laboratory component0.41 percentage points (3)10.2 PrecisionFor the components of variance reported in9.1, two averages of two ob
24、servations each of hexane solublematter should be considered significantly different at the 95 %probability level if the difference equals or exceeds thefollowing critical differences:Within2laboratory single operator! precision 0.59 percentage points(4)Between2laboratory precision 1.41 percentage p
25、oints see Note3!(5)NOTE 2The critical differences were calculated using t = 1.960,which is based on infinite degrees of freedom.NOTE 3The calculated values of the critical differences should beconsidered to be a general statement particularly with respect to between-laboratory precision. Before a me
26、aningful statement can be made abouttwo specific laboratories, the amount of statistical bias, if any, betweenthem must be established, with each comparison being based on recentdata obtained on randomized specimens from one sample of the materialto be tested. The interlaboratory test showed that fo
27、r certain leatherscontaining more than 18 % hexane-soluble matter the between-laboratorycritical difference could be as high as 3 percentage points.10.3 BiasNo justifiable statement on bias can be made,since the true value of hexane-soluble matter cannot beestablished by an accepted reference method
28、.11. Keywords11.1 extractables; extraction; fat liquor; hexanesolublelubricant; lubricationASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination
29、 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 technical committee and must be reviewed every five years andif not revised, either reapproved or withdraw
30、n. Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your co
31、mments 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 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single o
32、r 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).3Supporting data have been filed atASTM Headquarters and may be obtained byrequesting Research Report RR: D-31-1003.D 3495 00 (2006)2
