ASTM F1396-1993(2012) Standard Test Method for Determination of Oxygen Contribution by Gas Distribution System Components《测定气体分配系统组件氧气分布的标准试验方法》.pdf

《ASTM F1396-1993(2012) Standard Test Method for Determination of Oxygen Contribution by Gas Distribution System Components《测定气体分配系统组件氧气分布的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM F1396-1993(2012) Standard Test Method for Determination of Oxygen Contribution by Gas Distribution System Components《测定气体分配系统组件氧气分布的标准试验方法》.pdf（8页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: F1396 93 (Reapproved 2012)Standard Test Method forDetermination of Oxygen Contribution by Gas DistributionSystem Components1This standard is issued under the fixed designation F1396; the number immediately following the designation indicates the year oforiginal adoption or, in the case

2、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.INTRODUCTIONSemiconductor clean rooms are serviced by high-purity gas distribution systems. This test met

3、hodpresents a procedure that may be applied for the evaluation of one or more components considered foruse in such systems.1. Scope1.1 This test method covers a procedure for testing compo-nents for oxygen contribution to ultra-high purity gas distribu-tion systems at ambient temperature. In additio

4、n, this testmethod allows testing of the component at elevated ambienttemperatures as high as 70C.1.2 This test method applies to in-line components contain-ing electronics grade materials such as those used in asemiconductor gas distribution system.1.3 Limitations:1.3.1 This test method is limited

5、by the sensitivity of currentinstrumentation, as well as the response time of the instrumen-tation. This test method is not intended to be used for testcomponents larger than 12.7-mm (12-in.) outside diameternominal size. This test method could be applied to largercomponents; however, the stated vol

6、umetric flow rate may notprovide adequate mixing to ensure a representative sample.Higher flow rates may improve the mixing but excessivelydilute the sample.1.3.2 This test method is written with the assumption thatthe operator understands the use of the apparatus at a levelequivalent to six months

7、of experience.1.4 The values stated in SI units are to be regarded as thestandard. The inch-pound units given in parentheses are forinformation only.1.5 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 s

8、tandard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use. Specific hazardstatements are given in Section 6.2. Terminology2.1 Definitions:2.1.1 baselinethe instrument response under steady stateconditions.2.1.2 glove bagan e

9、nclosure that contains a controlledatmosphere. A glove box could also be used for this testmethod.2.1.3 heat trace heating of a component, spool piece, ortest stand by a uniform and complete wrapping of the item withresistant heat tape.2.1.4 minimum detection limit (MDL) of the instrumentthelowest i

10、nstrument response detectable and readable by theinstrument, and at least two times the amplitude of the noise.2.1.5 response timethe time required for the system toreach steady state after a change in concentration.2.1.6 spool piecea null component, consisting of astraight piece of electropolished

11、tubing and appropriate fittings,used in place of the test component to establish the baseline.2.1.7 standard conditions101.3 kPa, 0.0C (14.73 psia,32F).2.1.8 test componentany device being tested, such as avalve, regulator, or filter.2.1.9 test standthe physical test system used to measureimpurity l

12、evels.2.1.10 zero gasa purified gas that has an impurity concen-tration below the MDL of the analytical instrument. This gas isto be used for both instrument calibration and componenttesting.2.2 Symbols:2.2.1 P1The inlet pressure measured upstream of thepurifier and filter in the test apparatus.1Thi

13、s test method is under the jurisdiction of ASTM Committee F01 onElectronicsand is the direct responsibility of Subcommittee F01.10 on Contamina-tion Control.Current edition approved July 1, 2012. Published August 2012. Originallyapproved in 1992. Last previous edition approved in 2005 as F1396 93(20

14、05).DOI: 10.1520/F1396-93R12.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States12.2.2 P2The outlet pressure measured downstream of theanalyzer in the test apparatus.2.2.3 ppbvParts per billion by volume assuming ideal gasbehavior, equiva

15、lent to nmole/mole (such as nL/L). The sameas molar parts per billion (ppb).2.2.4 ppbwParts per billion by weight (such as ng/g).2.2.5 ppmvParts per million by volume assuming idealgas behavior, equivalent to mole/mole (such as L/L). Thesame as molar parts per million (ppm).2.2.6 ppmwParts per milli

16、on by weight (such as g/g).2.2.7 Q1the bypass sample flow not going through theanalytical system.2.2.8 Q2the total sample flow through the analyticalsystem.2.2.9 Qsthe flow through the spool piece or component.2.2.10 Tathe temperature of the air discharged by theanalyzers cooling exhaust.2.2.11 Tsth

17、e temperature of the spool piece or component.2.2.11.1 DiscussionPrecautions must be taken to insurethat the temperature measured by the thermocouple is as closeas possible to that of the spool piece and test component.Appropriate insulation and conductive shield should be used toachieve as uniform

18、a temperature as possible. The thermo-couple must be in contact with the outside wall of thecomponent or spool piece.2.2.12 V-1, V-2inlet and outlet valves of bypass loop,respectively.2.2.13 V-3, V-4inlet and outlet valves of test loop, respec-tively.3. Significance and Use3.1 This test method defin

19、es a procedure for testing compo-nents being considered for installation into a high-purity gasdistribution system. Application of this test method is expectedto yield comparable data among components tested for pur-poses of qualification for this installation.4. Apparatus4.1 Materials:4.1.1 Nitroge

20、n or Argon, clean and dry, as specified in 7.5.4.1.2 Spool Piece, that can be installed in place of the testcomponent is required. This piece is to be a straight section of316L electropolished stainless steel tubing with no restrictions.The length of the spool piece shall be 200 mm. The spool pieceh

21、as the same end connections as the test component.4.1.2.1 Components With Stub EndsUse compression fit-tings with nylon or teflon ferrules to connect the spool pieceand test component to the test loop. Keep the purged glove bagaround each component for the duration of the test. In the caseof long pi

22、eces of electropolished tubing, use two glove bags,one at each end.4.1.3 Tubing, used downstream of the test component shallbe 316L electropolished stainless steel seamless tubing. Thediameter of the sample line to the analyzer shall not be largerthan 6.4 mm (14 in.). The length of the sample line f

23、rom the tee(installed upstream of the pressure gage P2) to the analyzershall not be more than 600 mm, so as to minimize the effect(adsorption/desorption) of the sample line on the result. Thesample line shall have no more than two mechanical joints.4.1.4 Valves, diaphragm or bellows type, capable of

24、 unim-paired operation at 94C (200F). The use of all-welded,all-metal valves is preferred.4.2 Instrumentation:4.2.1 Oxygen AnalyzerThe oxygen analyzer is to beplaced downstream of the test component. Accurate baselinereadings must be obtained prior to and subsequent to each ofthe tests. Excessive de

25、viations in baseline levels (610 ppbv)before or after the tests require that all results be rejected. Theanalyzer must be capable of accurately recording changes inoxygen concentrations on a real time basis.4.2.2 Oxygen Analyzer CalibrationZero gas shall be at anoxygen level below the MDL of the ins

26、trument, supplied bypurified gas, with the purifier in close proximity to the analyzer.The instruments internal standard, if available, is to be usedfor the span calibration. Alternatively, span gas from a cylindermay be used.4.3 Pressure and Flow ControlUpstream pressure is to becontrolled with a r

27、egular upstream of the test component. Flowis to be controlled at a point downstream of the sampling portand monitored at that point. A mass flow controller is preferredfor maintaining the flow as described in 7.4. Sampling is to beperformed via a tee in the line, with a section of straight tubingbe

28、fore the mass flow controller. All lines must conform to4.1.3. Inlet pressure is monitored by P1. Test flow is the sum ofQ1and Q2. Q1is directly controlled, and Q2is the measuredflow through the analyzer. Refer to Fig. 1.4.4 Bypass LoopThe design of the bypass loop is notrestricted to any one design

29、. It could be, for example, a 3.2-mm(18-in) 316L stainless steel coil or a flexible tube section. Thisallows the flexibility necessary to install test components ofdifferent lengths.5. Hazards5.1 It is required that the user have a working knowledge ofthe respective instrumentation and that the user

30、 practice properhandling of test components for trace oxygen analysis. Goodlaboratory practices must also be understood.5.2 It is required that the user be familiar with propercomponent installation, and that the test components be in-stalled on the test stand in accordance with manufacturersinstruc

31、tions.FIG. 1 Test SchematicF1396 93 (2012)25.3 Do not exceed ratings (such as pressure, temperature,and flow) of component.5.4 Gloves are to be worn for all steps.5.5 Limit exposure of the instrument and test component toatmospheric contamination before and during the test.6. Calibration6.1 Calibrat

32、e instruments using standard laboratory prac-tices and manufacturers recommendations.7. Conditioning7.1 Ensure that adequate mixing of the test gas is attained.7.2 PressureTest component at 200 kPa gage (30 psig)measured at P2.7.3 Temperature Tsis to be in the ambient temperaturerange of 18 to 26C (

33、64 to 78F) and in the higher meantemperature range of 69 to 71C (156 to 160F). Tamust notdeviate more than 6 2C (4F) from the time of calibration tothe termination of the test. Tamust either be within the rangeof 18 to 26C (64 to 78F) or be consistent with the analyticalsystems manufacturers specifi

34、cations, whichever is morestringent.7.4 The flow rate Qsfor components is 1 standard L/minwith 6 2 % tolerance.7.5 The test gas shall be purified nitrogen or argon with amaximum oxygen concentration not exceeding an oxygenconcentration of 10 ppb. Gas quality must be maintained atflow specified in 7.

35、4. The test gas must be passed through afilter having a pore size rating of 0.02 m or finer. the filtermust be compatible with the 94C (200F) bake-out.8. Preparation of Apparatus8.1 A schematic drawing of a recommended test apparatuslocated inside a clean laboratory is shown in Fig. 1. Deviationsfro

36、m this design are acceptable as long as baseline levelsconsistent with 4.2.1 can be maintained. Nitrogen or argon gasis purified to remove water and hydrocarbons. The base gas isthen filtered by an electronics grade, high purity, point of usefilter (pore size rating # 0.02 m) before it is delivered

37、to thetest component.8.2 A bypass loop may be used to divert gas flow throughthe test stand and the analyzer whenever the spool piece or atest component is installed or removed from the test stand. Thisprevents the ambient air from contaminating the test apparatusand the oxygen analyzer; thus, the a

38、nalyzer baseline remainsthe same. A glove bag is used to enclose test component linesof the test apparatus during the installation and removal of thespool piece and the test piece.8.3 A trace oxygen analyzer capable of detecting oxygenconcentration levels down to 2 ppb is connected to the teststand

39、to sample the gas flowing through the test piece. Thepurified and filtered base gas from the test stand containing 10 ppb oxygen is used as the zero oxygen gas source for theanalyzer. Since the analyzer is sensitive to the sample flow rate,the metering valves within the analyzer should be adjusted t

40、oyield the flow rates required by the specification for an inletpressure of 30 psig. The gas flow rate Qsis set to 1 L/min.8.4 Inlet gas pressure is controlled by a pressure regulatorand measured immediately upstream of the purifier by anelectronic grade pressure gage. Flow measurement is carriedout

41、 by a mass flow controller (MFC) located downstream of theanalyzer. The outlet pressure of the gas is measured immedi-ately downstream of the analyzer by another electronic gradepressure gage. The MFC along with its digital readout shouldbe calibrated before use to control and display the gas flow r

42、ateQ1.8.5 The temperature of the spool piece, test specimen,analyzer cell compartment, and the oxygen concentrationmeasured by the analyzer can either be recorded continuouslyby a 25 channel data logger or collected and stored in acomputer using a data acquisition program.9. Procedure (see Fig. 2)9.

43、1 Bake-OutWith the spool piece installed and valvesV-1, V-2, V-3, and V-4 open, bake out the system (downstreamof purifier to upstream of analyzer, exclusive of the exhaustleg) at 94C (200F) until outlet oxygen concentration is stablebelow 20 ppbv. Flow of the gas is specified in 7.4. Cool tolower T

44、s. Close valves V-1 and V-2.9.2 BaselineFlow gas through the test stand with the spoolpiece installed on the test stand. Use the flow rate as defined in7.4. Flow for 30 min after the oxygen concentration hasattained a level of 20 ppbv. Utilizing heat tape, heat the spoolpiece and upstream tubing to

45、within 80 mm of the upstreamvalve. Monitor the oxygen of the outlet and the Ts, as specifiedin 7.3. The time required to reach the higher Tsmust be lessthan or equal to 10 min. Continue testing for 30 min after astable baseline is reestablished (20 ppbv) as specified in 9.1.Cool until the lower Tsis

46、 reached.9.3 Place the spool piece, test component (in originalbagging), and fittings into a glove bag or nitrogen tent withoutdisconnecting. Purge the glove bag with approximately fiveglove bag volumes of inert gas. Disconnect the spool piecewhile maintaining the flow through the system. Maintain t

47、hespool piece in the proximity of the positive flow. Reinstall thespool piece on the test stand. The entire disconnection andreinstallation must be performed within 2 min. Maintain flowthrough the analyzer during disconnection and installation viathe bypass loop, using valves V-1, V-2, V-3, and V-4

48、(if V-1 andV-2 are open, then V-3 and V-4 will be closed). DuringFIG. 2 Test Procedure SequenceF1396 93 (2012)3disconnection, open valves V-1 and V-2 first, then close V-3and V-4. After connection, reverse the order. Keep the purgedglove bag around each component for the duration of the test.In the

49、case of long pieces of electropolished tubing, use twoglove bags, one at each end.9.4 Initiate flow through the spool piece in accordance with8.4. Monitor Tsand Tain accordance with 8.3. Monitor oxygenuntil a stable baseline, in accordance with 9.2, is reestablished(20 ppbv). Utilizing heat tape, heat the spool piece andupstream tubing to within 80 mm of the upstream valve. Turnon the current and monitor the oxygen of the outlet and the Ts,in accordance with 8.3. The time required to reach the higherTsmust be less than o