ASTM D2384-1983(2009) Standard Test Methods for Traces of Volatile Chlorides in Butane-Butene Mixtures《丁烷-丁烯混合物中挥发性氯化物的痕量的标准试验方法》.pdf

《ASTM D2384-1983(2009) Standard Test Methods for Traces of Volatile Chlorides in Butane-Butene Mixtures《丁烷-丁烯混合物中挥发性氯化物的痕量的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D2384-1983(2009) Standard Test Methods for Traces of Volatile Chlorides in Butane-Butene Mixtures《丁烷-丁烯混合物中挥发性氯化物的痕量的标准试验方法》.pdf（8页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D2384 83 (Reapproved 2009)Standard Test Methods forTraces of Volatile Chlorides in Butane-Butene Mixtures1This standard is issued under the fixed designation D2384; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the y

2、ear 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 These test methods cover the determination of the totalvolatile organic chlorides in concentrations from 10 to

3、100ppm in butane-butene mixtures. The amperometric finish is notdirectly applicable in the presence of other substances thatcombine with silver ion or oxidize chloride ion in dilute acidsolution. Bromides, sulfides, ammonia, tobacco smoke, andmore than 25 g of hydrogen peroxide in the test solutioni

4、nterfere in the spectrophotometric procedure.1.2 Dissolved sodium chloride is not quantitatively deter-mined using these test methods.1.3 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.4 This standard does not purport to addr

5、ess 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. Specific warningstatements are given in Sections 5, 8, 1

6、1, 14, 19, andAnnexA1.2. Referenced Documents2.1 ASTM Standards:2D329 Specification for AcetoneD1266 Test Method for Sulfur in Petroleum Products(Lamp Method)3. Summary of Test Methods3.1 Combination Test MethodsEither the lamp or oxy-hydrogen test method may be used for combustion.NOTE 1Lamp combus

7、tion is readily applicable to multiple testing.Although an oxy-hydrogen burner does not lend itself to multiple testing,it affords much more rapid analysis for a single sample than does the lampcombustion.3.1.1 Lamp CombustionThe sample is burned in an atmo-sphere of carbon dioxide and oxygen or in

8、purified air; thehalogen-containing combustion products are absorbed in dilutesodium carbonate solution.3.1.2 Oxy-Hydrogen CombustionThe sample is burned inan oxy-hydrogen atomizer burner, and the combustion productsare absorbed in a dilute solution of sodium carbonate.3.2 FinishesEither the amperom

9、etric titration or spectro-photometric finish may be used for the chloride ion determi-nation.3.2.1 Amperometric TitrationThe chloride ion in aqueoussolution is titrated amperometrically with standard silver ni-trate solution, using a saturated calomel electrode as referenceelectrode. The diffusion

10、currents are plotted against the corre-sponding volumes of silver nitrate solution used; the end pointis taken as the intersection of the two straight-line portions ofthe curve.3.2.2 Spectrophotometric FinishChloride ion in the ab-sorber solution is determined by reaction with mercuric thio-cyanate

11、to release thiocyanate, which forms a reddish orangecomplex with Fe+. The intensity of the color is measured at460 nm with a spectrophotometer or filter photometer.4. Significance and Use4.1 These test methods are used to determine trace amountsof volatile chlorides in butane-butene mixtures. Such i

12、nforma-tion is valuable in cases where chloride is deleterious in the useof this product; also, chloride contributes to corrosion prob-lems in processing units in instances where further processingof this material is involved.5. Purity of Reagents5.1 Purity of ReagentsReagent grade chemicals shall b

13、eused 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 specifications are available.3Other grades may be1These test methods are under the jurisdiction of

14、ASTM Committee D02 onPetroleum Products and Lubricants and are the direct responsibility of Subcommit-tee D02.D0.04 on C4 Hydrocarbons.Current edition approved July 1, 2009. Published November 2009. Originallyapproved in 1965. Last previous edition approved in 2004 as D238483(2004).DOI: 10.1520/D238

15、4-83R09.2For 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.3Reagent Chemicals, American Chemical Society Specifi

16、cations, AmericanChemical Society, Washington, DC. For Suggestions on the testing of reagents notlisted by the American Chemical Society, see Annual Standards for LaboratoryChemicals, BDH Ltd., Poole, Dorset, U.K., and the United States Pharmacopeiaand National Formulary, U.S. Pharmacopeial Conventi

17、on, Inc. (USPC), Rockville,MD.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.used, provided it is first ascertained that the reagent is ofsufficiently high purity to permit its use without lessening theaccuracy of the determination.

18、5.2 References to water shall be understood to meanchloride-free distilled or deionized water.5.3 (WarningIn view of the common occurrence ofchloride in reagents and laboratory air, special care must betaken during preparation and storage of reagents to avoidcontamination. They should be isolated fr

19、om other reagentsand used solely for these methods.Ablank determination mustbe performed each time a reagent is changed to ensure that itis not contaminated with chloride.It is also imperative that all glassware used in this determi-nation be cleaned thoroughly and rinsed four times withchloride-fre

20、e distilled or deionized water. Utmost caution mustbe taken during the analysis to prevent contamination fromchlorides.)6. Sampling6.1 Steam and dry a 10 to 25-mL corrosion-resistant metalsample cylinder having a 450-psi (3100 kPa) working pressureand equipped with a needle valve outlet at each end.

21、6.2 Pressure the prepared cylinder with dry hydrogen to 20psig (137.5 kPa gage) to afford a gas cushion preventingrupture due to liquid expansion on increase of temperature.6.3 Obtain a liquid sample from the purged sample line,filling the upright cylinder through the bottom needle valve,keeping the

22、 top valve closed. Do not purge the sample cylinder.LAMP COMBUSTION TEST METHOD7. Apparatus7.1 ASTM Lamp AssemblyUse the apparatus specified inTest Method D1266, including the liquefied petroleum gasburner assembly.8. Reagents8.1 Use the necessary reagents and materials specified inTest Method D1266

23、, in addition to the absorber solution asdescribed in 8.3.8.2 Hydrogen (WarningExtremely flammable (liquefied)gas under pressure. See Annex A1.1.)8.3 Sodium Carbonate Absorbent (2 g/L) Dissolve 2.0 gof anhydrous sodium carbonate (Na2CO3) in water and diluteto a litre with water.9. Procedure9.1 Prepa

24、re the combustion apparatus as described in Sec-tion 7 of Test Method D1266, Preparation of Apparatus, using35 mL of Na2CO3solution to charge the absorber.9.2 Weigh the vessel containing the sample to the nearest0.1 g. Support the sample vessel in an upright position so thatthe sample is burned from

25、 the gaseous phase. Connect thesample vessel to the auxiliary corrosion-resistant regulatingvalve by means of corrosion-resistant metal tubing (Fig. 1)(Note 2). Connect the bottom valve of the sample vessel to theregulated hydrogen supply. By means of short lengths ofchloride-free rubber tubing, con

26、nect the auxiliary valve outletto the side inlet of the gas burner and the lower inlet of the gasburner (Test Method D1266, Annex A3, Apparatus Detail, Fig.5) to the burner manifold.NOTE 2For steady burning, it may be necessary to surround theauxiliary valve with a heat-exchanger system. A convenien

27、t means iswinding insulated heating wire, having a resistance of 40 to 60 V, aroundthe auxiliary valve and connecting it to a suitable rheostat.Another meansis to place the regulating valve in a suitable metal beaker and cover thevalve body with water maintained at 60 to 80C.9.3 Open the valve on th

28、e sample vessel; then open theauxiliary valve to allow a small stream of vapor to escape.Quickly light the burner. Adjust the flow of CO2-O2mixtureand the sample so that the flame is approximately 35 mm highand clear blue in color; this color is reached just beyond thepoint at which a yellow color s

29、hows at the tip of the flame.Insert the burner into the chimney and readjust the flame ifnecessary. When the sample has burned almost to completion,open the valve on the bottom of the sample vessel and flush theresidual sample from the cylinder chamber by passing hydro-gen through the bottom valve f

30、or several minutes.FIG. 1 Diagrammatic Sketch of Butane-Butene Heat Exchange SystemD2384 83 (2009)29.4 When all of the residual material has been flushed fromthe sample vessel, turn off the hydrogen and close the valves onthe sample vessel. Disconnect the hydrogen flushing line andthe line to the he

31、ated auxiliary valve and weigh the samplevessel to the nearest 0.1 g. Draw the combustion atmospherethrough one absorber of a set to serve as a blank on the purityof this atmosphere. Rinse the chimneys and spray traps withwater and add the rinsings to the absorbers.9.5 Proceed in accordance with eit

32、her Section 16 or 21.OXY-HYDROGEN COMBUSTION TEST METHODALTERNATIVE TEST METHOD10. Apparatus10.1 Oxy-Hydrogen Burner4A flow diagram of a typicalapparatus is shown in Fig. 2. The apparatus shall consist ofthree parts: atomizer-burner, combustion chamber, and receiverwith spray trap. A blowout safety

33、port in the combustionchamber is desirable. The remainder of the apparatus shallconsist of a steel support stand with the necessary needlevalves and flow meters for precise control of air, oxygen,hydrogen, and vacuum.10.2 Vacuum Pump, having a capacity of at least 1200 L/h,and protected from corrosi

34、ve fumes by suitable traps.11. Reagents and Materials11.1 Hydrogen (WarningExtremely flammable (lique-fied) gas under pressure. See Annex A1.1.)11.2 Oxygen (WarningOxygen vigorously acceleratescombustion. See Annex A1.2.)11.3 Sodium Carbonate, Absorbent (2g/L)See 8.3.12. Procedure12.1 Follow the man

35、ufacturers instructions for preparingand operating the apparatus. Place 50 mL of the Na2CO3absorbent in the absorber. Burn all of the sample from the gasphase of the cylinder (Fig. 1)(WarningExtremely flam-mable (liquefied) gas under pressure. See Annex A1.1.). Flushthe residual gases from the cylin

36、der chamber by passinghydrogen through the bottom valve for several minutes, burn-ing the flushed gases.)12.2 When combustion is completed, rinse all water-cooledportions of the apparatus and the spray trap with a spray ofwater. Collect all rinsings in the absorbent.12.3 Proceed in accordance with e

37、ither Section 16 or 21.12.4 Prepare a blank by placing 50 mL of the Na2CO3absorbent in the absorber. Operate the apparatus for the sameperiod of time, under the same conditions that were used forthe combustion of the sample, but without a sample and thesample inlet closed to the atmosphere. Burn app

38、roximately thesame volume of hydrogen as was used to flush the samecylinder. When combustion of the hydrogen is complete, rinseall water-cooled portions of the apparatus and the spray trapwith a spray of water. Collect all rinsings in the absorbent.Proceed as in 12.3.AMPEROMETRIC TITRATION FINISH13.

39、 Apparatus13.1 Potentiometer-Galvanometer Assembly, capable of ap-plying a cell potential up to 3 V with an accuracy of 1 % of fullscale, and capable of indicating the cell current by means of agalvanometer having a sensitivity of 0.005 to 0.008 A/mmscale division. A multiposition galvanometer shunt

40、 for adjust-ment of current measurement sensitivity should also be pro-vided; shunt ratios to give sensitivities of approximately 0.05to 0.08, and 0.10 to 0.16 A/mm should be included.13.2 Titration AssemblyAn apparatus similar to thatshown in Fig. 3, consisting of a rotating (600 rpm) platinumelect

41、rode, a saturated calomel reference electrode with saltbridge, a means of blanketing the solution with nitrogen, and aholder for a 10-mL buret.13.3 Calomel Electrode, constructed as shown in Fig. 3.13.4 Platinum Electrode, rotating-hook type. A suitableelectrode may be constructed as follows: Seal a

42、 platinum wire0.03 to 0.05 in. (0.76 to 1.3 mm) in diameter and 0.75 to 1.0 in.(19.1 to 25.4 mm) long into the end of a 6-mm outside diametersoft glass tube that has been shaped into a stirrer blade. Bendthe extending platinum wire upwards at its midpoint to form anangle of 90. Place a few drops of

43、mercury in the glass tube andmake electrical contact between the mercury and the connec-tion on the amperometric titrator with a piece of copper wire(insulate the exposed wire to prevent shorting).4The Wickbold Burner Apparatus obtainable from the Atlas Instrument Co.,8902 E. 11th St., Tulsa, OK, or

44、 the Richfield Burner Apparatus obtainable from theGreiner Glass Blowing Laboratories, 3604 E. Medford St., LosAngeles, CA90034,has been found suitable for this purpose. If you are aware of alternative suppliers,please provide this information to ASTM International Headquarters. Your com-ments will

45、receive careful consideration at a meeting of the responsible technicalcommittee,1which you may attend.1Atomizer-burner 4Three-way stopcock2Sample tube 5Absorber3Combustion chamber 6Spray trapFIG. 2 Flow Diagram of a Typical Oxy-Hydrogen CombustionApparatusD2384 83 (2009)313.5 BuretA 10-mL semi-micr

46、o buret, with the tip con-structed so as to be able to dip below the surface of the solutionbeing titrated.14. Reagents14.1 Acetone (99.5 %) (WarningExtremely flammable.Vapor may cause fire. See Annex A1.3.)Refined acetoneconforming to Specifications D329.14.2 Agar SolutionDissolve2gofagar-agar powd

47、er in100 mL of hot water (80 to 100C) containing 20 g ofpotassium nitrate (KNO3).14.3 Bromthymol Blue Indicator Solution Dissolve 0.10 gof the solid indicator in 100 mL of hot water, cool, and add 1mL of chloroform as a preservative. Discard the solution whenit is 1 week old.NOTE 3Remove possible ob

48、jectionable amounts of chloride by pass-ing the solution through an ion-exchange resin in the hydroxyl form.Neutralize the resulting alkaline solution to the bromthymol blue end pointby titration with HNO3(3 + 97).14.4 Chloride, Standard Solution (10 g Cl/mL)Dilute asuitable volume of 1 + 10 assayed

49、 hydrochloric acid to obtaina solution containing 10 g Cl/mL.14.5 Gelatin Solution (10 g/L)Dissolve1gofgelatin in100 mL of hot water and add 1 mL of chloroform as apreservative. Discard the solution when it is 1 week old.14.6 Hydrogen Peroxide SolutionPrepare by diluting 1volume of concentrated hydrogen peroxide solution (H2O2,30 %) with 4 volumes of water. Store in a dark-coloredglass-stoppered bottle.14.7 Mercury-Calomel MixturePrepare a mixture of mer-cury and calomel (mercurous chloride, Hg2Cl2) by vigorouslyshaking 10 g of calom