ASTM D6656-2001(2010)e1 7500 Standard Test Method for Determination of Chromic Oxide in Wet Blue (Perchloric Acid Oxidation)《测定蓝湿皮中氧化铬含量的标准试验方法(高氯酸氧化)》.pdf

《ASTM D6656-2001(2010)e1 7500 Standard Test Method for Determination of Chromic Oxide in Wet Blue (Perchloric Acid Oxidation)《测定蓝湿皮中氧化铬含量的标准试验方法(高氯酸氧化)》.pdf》由会员分享，可在线阅读，更多相关《ASTM D6656-2001(2010)e1 7500 Standard Test Method for Determination of Chromic Oxide in Wet Blue (Perchloric Acid Oxidation)《测定蓝湿皮中氧化铬含量的标准试验方法(高氯酸氧化)》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D6656 01 (Reapproved 2010)1Standard Test Method forDetermination of Chromic Oxide in Wet Blue (PerchloricAcid Oxidation)1This standard is issued under the fixed designation D6656; the number immediately following the designation indicates the year oforiginal adoption or, in the case of

2、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.1NOTEThe SI statement was added and the Subcommittee name corrected in footnote 1 in November 2010.1. Scope1

3、.1 This test method covers the determination of chromicoxide in wet blue that has been partly or completely tannedwith chromium compounds. In general, the samples willcontain chromium content between 1 % and 5 % when calcu-lated as chromic oxide expressed upon a dry basis otherwisereferred to as moi

4、sture-free basis (mfb).1.2 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.3 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 sta

5、ndard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use. See Section 9 forspecific safety hazards.2. Referenced Documents2.1 ASTM Standards:2D6658 Test Method for Volatile Matter (Moisture) of WetBlue by Oven DryingD6659 Pra

6、ctice for Sampling and Preparation of Wet Bluefor Physical and Chemical TestsE180 Practice for Determining the Precision of ASTMMethods for Analysis and Testing of Industrial and Spe-cialty Chemicals33. Terminology3.1 DefinitionsThe terms and definitions employed withinthis method are commonly used

7、in normal laboratory practiceand require no special comment.4. Summary of Test Method4.1 The perchloric acid method may be applied to wet blue.Accurately weighed wet blue samples are digested in a blend ofconcentrated nitric acid and a prepared “oxidation mixture”consisting of sulfuric and perchlori

8、c acids. Once completed,oxidation of all tri-valent to haxavalent chrome is executed bycontrolled heating. Upon dilution, the chromium is indirectly(back) titrated volumetrically with standardized thiosulfateusing released iodine as the titrate. The perchloric acid methodrequires less manipulation t

9、han procedures based upon fusionof the ash. However, care must be taken because of potentialhazards in the use of this reagent.5. Significance and Use5.1 The procedure described is specific for chromium in wetblue. Vanadium is the only common interfering element and israrely present in quantity. The

10、 precision and accuracy of themethods are usually, at least, as good as the sampling of wetblue itself.5.2 The chromium content of wet blue is related to thedegree of tannage obtained, and hence may be a matter forspecification in the purchase of wet blue. The proceduredescribed provides adequate ac

11、curacy for this purpose.6. Apparatus6.1 Analytical Balanceaccurate and calibrated to 0.001 g.6.2 Erlenmeyer Flasks250 mL capacity or equivalent.6.3 Burette50 mL capacity of suitable calibration grade,minimum calibration of 0.1 mL.6.4 Glass Anti-Bumping Beadsor equivalent.6.5 Measuring Cylindersof 50

12、 mL capacity or equivalent.6.6 Small Glass Filter Funnel.6.7 Dessicatorof suitable size and design and chargedwith fresh dessicant.6.8 Weighing Vesselsof suitable size and design.6.9 Drying Ovenwith accurate variable temperature con-trols.1This test method is under the jurisdiction of ASTM Committee

13、 D31 on Leatherand is the direct responsibility of Subcommittee D31.02 on Wet Blue.Current edition approved Oct. 1, 2010. Published November 2010. Originallyapproved in 1996. Last previous edition approved in 2006 as D6656 - 02 (2006).DOI: 10.1520/D6656-01R10E01.2For referenced ASTM standards, visit

14、 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.3Withdrawn. The last approved version of this historical standard is referencedon www.astm.org.1Co

15、pyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.7. Reagents and Materials7.1 Purity of ReagentsAnalytical Reagent (AR) gradeshall be used in all tests. Unless otherwise indicated, it isintended that all reagents shall conform to specifi

16、cations of theCommittee on Analytical Reagents of the American ChemicalSociety, where such specifications are available.4Other gradesmay be used, provided it is first ascertained that the reagent isof sufficiently high purity to permit its use without lesseningthe accuracy of the determination.7.2 P

17、urity of WaterUnless otherwise indicated, referenceto water shall be understood to mean distilled water or water ofequal purity.7.3 Commercial ReagentsThe use of commercially avail-able pre-standardized analytical reagents and solutions isappropriate, providing those reagents and solutions have been

18、prepared according to and conform to the previously men-tioned specifications (see 7.1).7.4 Nitric Acid(HNO3), 70 % w/w.7.5 Perchloric Acid(HClO4), 60-62 % w/w. 70 % or 72 %w/w perchloric acid may be substituted; however, storage issomewhat more hazardous.7.6 Sulfuric Acid(H2SO4), 96-98 % w/w.7.7 Po

19、tassium Iodide(KI), 99-100 % purity.7.8 Potassium Iodide Solution(KI), 10 % w/w. Dissolve10g(6 0.1 g) of potassium iodide into 100 ml of water.7.9 Starch Indicator Solution2 % or equivalent. Preparedaccording to accepted procedures available in analytical hand-books.7.10 Oxidizing MixtureMix 1666 mL

20、 of concentratedsulfuric acid into an appropriate glass container that contains2500 mL of perchloric acid using extreme caution whileadding. Cool the mixture to room temperature before use.7.11 Phosphoric Acid(H3PO4), 40 % w/w. Dilute 45 mLof 85 % phosphoric acid with water to 100 ml.7.12 Hydrochlor

21、ic Acid(HCl, 1:1 dilution of 37 %, w/w).Used in standardization of thiosulfate solution.7.13 Potassium Dichromate(K2Cr2O7). Used in standard-ization of thiosulfate solution.7.14 Sodium Carbonate(Na2CO3). Used in preparation ofthiosulfate solution.7.15 Sodium Thiosulfate(Na2S2O35H2O). Used to pre-par

22、e thiosulfate solution.7.16 Sodium Thiosulfate Standard Solution(Na2S2O3),0.1N (6 0.0002). Dissolve 24.85 g of sodium thiosulfate(Na2S2O35H2O) in previously boiled water, add 1.00 g ofsodium carbonate (Na2CO3) and dilute to 1000 mL.8. Standardization8.1 Dry potassium dichromate (K2Cr2O3) in an oven

23、at 130C for 2 h and cool in a dessicator. Once cool, weigh about 0.2g(6 0.0001 g) of this dry potassium dichromate into a clean250 ml, glass-stoppered Erlenmeyer flask. Dissolve in 50 mLwater; add 4 ml of hydrochloric acid (HCl, 1:1) and 20 ml ofKI solution. Stopper the flask and allow to stand for

24、5 min. inthe dark. Titrate with the thiosulfate solution that is to bestandardized. When the solution color has faded to brownish-green, add 2 ml of 2 % starch solution and continue titratinguntil the deep blue color changes to a clear green. Record thevolume of titrant used. Calculate the Normality

25、 of the thiosul-fate solution as follows:Normality 5 A 4 0.04903 3 B!where:A = grams of K2Cr2O7used, andB = ml required for titration.8.2 Shelf LifeThe thiosulfate solution is relatively stable.However, it should be re-standardized at least once everymonth. Alternatively, a commercially available pr

26、e-standardized analytical solution may be substituted.9. Hazards9.1 Chemicals used can be harmful or explosive, or both.9.2 The improper use of perchloric acid can lead to violentand serious explosions. In general, these can be traced tosituations where concentrated perchloric acid has come incontac

27、t with organic or easily oxidized materials.9.3 The exact procedures given must be followed and thedigestion, once started, should be kept from possible contactwith other organic matter. The digestion should never beallowed to boil dry. The perchloric acid should never be usedwithout the accompanyin

28、g use of nitric and sulfuric acids.9.4 Any spills involving perchloric acid should be flushedwith water and a liquid acid neutralizer.9.5 The use of a perchloric acid hood, reserved for perchlo-ric acid digestion, equipped with wash-down facilities andconstructed entirely of non-porous inorganic mat

29、erial is re-quired.9.6 Perchloric acid bottles should be stored on a ceramic ornon-porous tray or shelf and never on a wooden or perviousshelf.9.7 Perchloric acid must not be permitted to go dry in thepresence of organics, metals or metal salts.9.8 It is advisable to keep only a one pound (0.45 kg)

30、bottleof acid in a working area.10. Test Specimens10.1 The test specimen shall be 3-5 g of wet blue from acomposite sample prepared according to Practice D6659 andweighed to an accuracy of 0.001 g.11. Procedure11.1 Accurately weigh between 3 and5g(6 0.001 g) of theprepared wet blue sample into a 250

31、 mL Erlenmeyer flask.Record the weight to the nearest 0.001 g.11.2 Using extreme care, add 20 mL of nitric acid (HNO3)to the flask.11.3 Next, carefully and slowly add 25 mL of the OxidizingMixture to the flask.11.4 Add a few glass anti-bumping beads (these will allowthe solution to boil evenly), the

32、n place the filter funnel into theneck of the flask.4Reagent Chemicals, American Chemical Society Specifications , AmericanChemical Society, Washington, DC. For suggestions on the testing of reagents notlisted by the American Chemical Society, see Analar Standards for LaboratoryChemicals, BDH Ltd. P

33、oole, Dorset, UK and the United States Pharmacopoeia andNational Formulary, U.S. Pharmacopoeial Convention, Inc. (USPC), Rockville,MD.D6656 01 (2010)1211.5 Under the perchloric hood, heat the solution gentlyunder reflux conditions (using the funnel as a condenser in theneck of the flask) until all o

34、rganic matter is destroyed and thesolution color changes to a clear red-orange, indicating oxida-tion of the chromium. Do not allow the sample to boil todryness.11.6 Heat the solution for an additional 2 min to ensurecomplete oxidation; then rapidly cool the solution, rinse andremove the funnel, the

35、n dilute to 125 mL with water. Rapidcooling can be achieved with the use of a cold water bath.11.7 Re-heat the solution to boiling and continue for 7 to 10min in order to expel and any chlorine or oxides of nitrogen.11.8 Remove the flask from the heat and allow the solutionto cool to room temperatur

36、e.11.9 Once cool, add 30 mL of phosphoric acid and 25 mL ofthe 10 % potassium iodide solution, then stopper the flask.11.10 Place the flask in the dark and allow to stand for 5 minto allow complete release of iodine (dark brown color).11.11 Titrate volumetrically with 0.1 N, standardized so-dium thi

37、osulfate.11.12 When the solution color has faded to a pale yellow-brown, add approximately 2 ml of the starch indicator solution.Continue the titration until the deep blue color changes to aclear blue-green.11.13 Record the titration volume.11.14 If the titration volume is less than 5 mL or more tha

38、n50 ml, repeat the entire procedure, after adjusting the sampleweight so that the titration volume is toward the middle of theburette.11.15 Calculate the results in accordance with Section 12.12. Calculation12.1 Calculate the chromium content as the percentage ofchromic oxide (Cr2O3) in the leather

39、as follows:Chromic Oxide Cr2O3!,% 5 T 3 N 3 E 3 100 4 W!where:T = titration volume of sodium thiosulfate solution usedin milliliters (ml),N = Normality of the sodium thiosulfate solution,E = 0.025332 = chromic oxide (Cr2O3) equivalenceweight per milliliter (g/mL),W = weight of original wet blue spec

40、imen (as received) ingrams (g), and100 = conversion to percent.12.2 The above calculation provides the Cr2O3content ofthe wet blue on an “as received” basis. Since the chromiumcontent of wet blue is expressed upon a dry (moisture-free)basis, a moisture determination must be run in accordance withTes

41、t Method D6658.IfD is found to be the moisture content inthe wet blue sample, then calculate the Cr2O3upon a dry basis(mfb) as follows:Chromic Oxide Cr2O3!,%5 T 3 N 3 E 3 100 4 W! 3 1 4 1 D4 100!#!where:T, N, E and W = the same significance as in the previouscalculation.13. Report13.1 Report the per

42、centage of Cr2O3to the nearest 0.01 %for each and all values.13.2 Duplicate runs that agree within 0.09 % absolute areacceptable for averaging (95 % confidence level).14. Precision and Bias14.1 ReproducibilityThe average difference between tworesults (each the average of duplicate determinations) ob

43、tainedby analysis in different laboratories will approximate 0.06 %on an absolute basis. Two such values should be consideredsuspect (95 % confidence level) if they differ by more than0.2 % absolute.14.2 BiasThe test method yields results that average1.75 % lower in relation to the standard sample o

44、f NBSK2Cr2O7. The 99 % confidence limits on this value are 1.50 to2.00 %, as determined by triplicate analyses in five laborato-ries.NOTE 1The estimates of checks for duplicates and reproducibility in14.1 and 14.2 are based on an interlaboratory study of four leather samplesrun in triplicate in each

45、 of laboratories. The precision statements weredeveloped5using Practice E180.15. Keywords15.1 blue stock; chrome content; chromic oxide; perchloricacid oxidation; wet blueASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedi

46、n 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 technical committee and mu

47、st 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 International Headquarters. Your comments will receive careful consideration at a meeting of th

48、eresponsible 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 Barr Harbor Drive, PO Box C70

49、0, 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). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).5The actual data upon which the results are based are reported in Journal,American Leather Chemists Assn. JALCA, Vol. 54, 1959, p. 2.D6656