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本文(ASTM D847-2015 Standard Test Method for Acidity of Benzene Toluene Xylenes Solvent Naphthas and Similar Industrial Aromatic Hydrocarbons《苯 甲苯 二甲苯 溶剂石脑油和类似工业芳烃酸度的标准试验方法》.pdf)为本站会员(livefirmly316)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM D847-2015 Standard Test Method for Acidity of Benzene Toluene Xylenes Solvent Naphthas and Similar Industrial Aromatic Hydrocarbons《苯 甲苯 二甲苯 溶剂石脑油和类似工业芳烃酸度的标准试验方法》.pdf

1、Designation: D847 15Standard Test Method forAcidity of Benzene, Toluene, Xylenes, Solvent Naphthas,and Similar Industrial Aromatic Hydrocarbons1This standard is issued under the fixed designation D847; the number immediately following the designation indicates the year oforiginal adoption or, in the

2、 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.This standard has been approved for use by agencies of the U.S. Department of Defense.1. Scope*1.1

3、This test method is intended for the detection of acidityof benzene, toluene, xylenes, solvent naphthas, and similarindustrial aromatic hydrocarbons.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

4、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 specific hazardstatements see Section

5、 9.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent WaterD3437 Practice for Sampling and Handling Liquid CyclicProducts2.2 Other Documents:OSHA Regulations, 29CFR paragraphs 1910.1000 and1910.120033. Terminology3.1 Definitions:3.1.1 acidity, nfor purposes of this standard,

6、acidity isdefined as producing a persistent pink phenolphthalein endpoint with the addition of two (2) drops or more (0.1 mL) of 0.1N sodium hydroxide solution.3.1.2 acid reaction, na characteristic of materials produc-ing the acid-color of the indicator used under the conditionsprescribed in this t

7、est method.3.1.3 alkaline or basic reaction, na characteristic of thematerials producing the alkali-color of the indicator used underthe conditions prescribed in this test method.4. Summary of Test Method4.1 The acidity of aromatic hydrocarbons is detected usinga sodium hydroxide titration and a col

8、or change using aphenolphthalein indicator.5. Significance and Use5.1 This test method is suitable for setting specifications, foruse as an internal quality control tool, and for use in develop-ment or research work on industrial aromatic hydrocarbons andrelated materials. This test method gives an

9、indication ofresidual acidity and is a measure of the quality of the finishedproduct. It is an indication of the tendency of the product tocorrode equipment.6. Interferences6.1 Tests for acidity are not applicable in the presence ofcontaminating acidic or alkaline gases, soaps, salts, or othercompou

10、nds derived from the atmosphere or apparatus. Thecontainer holding the specimen, and the apparatus, water,indicator, and other materials used in the test shall be chosen sothat they themselves shall not appreciably affect the results.Since new corks used in specimen bottles often are bleachedwith ox

11、alic acid, it is advisable to rinse them thoroughly andcheck them for neutrality with the indicator used in the test.Glassware shall be of acid-resistant and alkali-resistant glass4and shall be rinsed with neutral distilled water before use. Theroom in which the test is performed shall be chosen so

12、as toprevent undue contamination by carbon dioxide, ammonia, orother interfering substances that may be present in the atmo-sphere.1This test method is under the jurisdiction of ASTM Committee D16 onAromatic Hydrocarbons and Related Chemicals and is the direct responsibility ofSubcommittee D16.01 on

13、 Benzene, Toluene, Xylenes, Cyclohexane and TheirDerivatives.Current edition approved Aug. 1, 2015. Published September 2015. Originallyapproved in 1945. Last previous edition approved in 2004 as D847 08. DOI:10.1520/D0847-15.2For referenced ASTM standards, visit the ASTM website, www.astm.org, orco

14、ntact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.3Available from U.S. Government Printing Office Superintendent of Documents,732 N. Capitol St., NW, Mail Stop: SDE, Washington, DC 2040

15、1, http:/www.access.gpo.gov.4Borosilicate glass or the equivalent has been found satisfactory for this purpose.*A Summary of Changes section appears at the end of this standardCopyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States16.2 The di

16、stilled water used in the test shall not alter thecomposition of the specimen nor otherwise interfere with thepurpose of the work. Although inert impurities often may beneglected, care must be exercised to correct for impurities or toeliminate them entirely if they are likely to interfere. When thed

17、istilled water does not show an acid or alkaline reaction, itmay be used without further adjustment to neutrality. However,if the water shows an acid or alkaline reaction, it shall bebrought to a persistent pink end point before use by titrationwith standard 0.01 N NaOH solution (see 8.4) or standar

18、d 0.01N H2SO4, respectively (see 8.5).7. Apparatus7.1 Graduate, 100-mL.47.2 Bottle, 500-mL glass-stoppered.48. Reagents8.1 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 Commi

19、t-tee on Analytical Reagents of the American Chemical Society,where such specifications are available.5Other grades may beused, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.8.2 Phenolphthalein Ind

20、icator SolutionDissolve 0.5 g ofphenolphthalein in 100 mL of ethyl alcohol (95 %). Add 0.01N NaOH solution cautiously until a faint pink color appears;then just remove the color with a drop or two of 0.01 N acid.8.3 Sodium Hydroxide, Standard Solution (0.1 N).8.4 Sodium Hydroxide, Standard Solution

21、(0.01 N).8.5 Sulfuric Acid, Standard (0.01 N).8.6 Purity of Water: Distilled Water, NeutralBoil vigor-ously for 30 min, 1 to 2 L of distilled water conforming to TypeIII of Specification D1193. Insert a stopper carrying a guardtube of soda lime. Rinse a 200-mL flask with this distilledwater, add a 1

22、00-mLportion, and titrate in a closed system with0.01 N NaOH solution: or heat to boiling and titrateimmediately, taking care that the temperature does not fallbelow 80C during the titration. If more than 1 drop (0.05 mL)of 0.01 N NaOH solution is required to obtain an end pointwith phenolphthalein,

23、 adjust the pH of the water to be used byadding the calculated amount of NaOH solution. Repeat theblank titration, and readjust if necessary until the blank titrationon 100 mL of the distilled water is 1 drop (0.05 mL) or less ofthe 0.01 N NaOH solution. The distilled water now will beneutral or ver

24、y slightly acid to the phenolphthalein indicator.9. Hazards9.1 Consult current OSHA regulations, suppliers SafetyData Sheets, and local regulations for all materials used in thistest method.10. Sampling10.1 Sample the material in accordance with PracticeD3437.11. Procedure11.1 Add 100 6 5 mLof the s

25、ample in a 500-mLbottle.Add100 mL of neutral distilled water (see 8.6) and 2 drops ofphenolphthalein indicator solution. Stopper and shake thor-oughly. Without separating the layers, titrate the acidity, if any,with standard 0.1 N NaOH to the first persistent shade of pink,shake thoroughly after eac

26、h addition. Record Pass if 2 drops orless of 0.1 N NaOH solution produces a persistent pink endpoint. If more than 2 drops are required to produce a persistentpink end point, record Fail.12. Interpretation of Results12.1 Unless otherwise indicated in the applicablespecifications, the test results sh

27、all be interpreted as follows:12.1.1 A specimen shall be said to pass and to contain nofree acid, that is, show no evidence of acidity, if 2 drops or lessof 0.1 N NaOH solution produces a persistent pink end point inthe test bottle.13. Precision and Bias13.1 In the case of pass/fail data, no general

28、ly acceptedmethod for determining precision is currently available.14. Quality Guidelines14.1 In the case of pass/fail data, no generally acceptablemethod for determining that this test is under statistical controlis currently available.15. Keywords15.1 acidity; aromatic hydrocarbons5Reagent Chemica

29、ls, 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., Poole, Dorset, U.K., and the United States Pharmacopeiaand National F

30、ormulary, U.S. Pharmacopeial Convention, Inc. (USPC), Rockville,MD.D847 152SUMMARY OF CHANGESCommittee D16 has identified the location of selected changes to this standard since the last issue (D847 08)that may impact the use of this standard. (Approved August 1, 2015.)(1) Made revisions to Sections

31、 1, 2, 4, 6, 7, 8 11, and 12.(2) Revised definition for acidity.(3) Added Section 14, Quality Guidelines.ASTM 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

32、 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 must be reviewed every five years andif not revised, either reapprov

33、ed 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 theresponsible technical committee, which you may attend. If you fee

34、l 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 C700, West Conshohocken, PA 19428-2959,United States. Individual repr

35、ints (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 Copyright Clearance Center, 222Rosewood Drive, Danvers, MA 01923, Tel: (978) 646-2600; http:/ 153

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