ASTM E388-2004(2009) 2500 Standard Test Method for Wavelength Accuracy and Spectral Bandwidth of Fluorescence Spectrometers 《荧光分光计的光波波长精密度和光谱带宽的测试方法》.pdf

《ASTM E388-2004(2009) 2500 Standard Test Method for Wavelength Accuracy and Spectral Bandwidth of Fluorescence Spectrometers 《荧光分光计的光波波长精密度和光谱带宽的测试方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM E388-2004(2009) 2500 Standard Test Method for Wavelength Accuracy and Spectral Bandwidth of Fluorescence Spectrometers 《荧光分光计的光波波长精密度和光谱带宽的测试方法》.pdf（3页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E388 04 (Reapproved 2009)Standard Test Method forWavelength Accuracy and Spectral Bandwidth ofFluorescence Spectrometers1,2This standard is issued under the fixed designation E388; 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.1. Scope1.1 This test method covers the testing of the spectralbandwidth and wavelength accuracy of fluores

3、cence spectrom-eters that use a monochromator for emission wavelengthselection and photomultiplier tube detection. This test methodcan be applied to instruments that use multi-element detectors,such as diode arrays, but results must be interpreted carefully.This test method uses atomic lines between

4、 250 nm and 1000nm.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 standar

5、d to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Summary of Test Method2.1 The difference between the apparent wavelength and theknown wavelength for a series of atomic emission lines is usedas a test for wavelength ac

6、curacy. The apparent width of someof these lines is used as a test for spectral bandwidth.3. Apparatus3.1 Fluorescence Spectrometer to be tested.3.2 Atomic Discharge Lamps, Low-pressure, sufficientlysmall to be placed in the sample cell holder of the instrument.4. Reagent4.1 Scattering SuspensionDis

7、solve1gofglycogen perlitre of water, or use a dilute microsphere suspension contain-ing 1 mL of a commercially available, concentrated micro-sphere suspension.5. Procedure5.1 The emission lines given for mercury (Hg), neon (Ne),argon (Ar), krypton (Kr), and xenon (Xe) in Table 1 aretypically observa

8、ble using standard commercial fluorometers,although some of them may be too weak to detect on someinstruments.5.1.1 Most fluorescence instruments will not be able toresolve very closely spaced lines such as those for Hg at 312.57nm, 313.15 nm, and 313.18 nm, due to the relatively lowresolution monoc

9、hromators used in fluorescence equipmentcompared to those used in absorbance spectrometers. Evenlower resolution fluorometers may not resolve lines separatedby less than several nanometres such as those for Hg at 404.66and 407.78, or at 576.96 and 579.07 nm.5.1.2 In instruments using blazed grating

10、monochromators,additional weaker lines are found due to second order diffrac-tion of atomic lines. For instance, lines appear for Hg at 507.30and 593.46 nm, arising from the 253.65 and 296.73 nm lines,respectively.5.2 Calibration and Adjustment of Emission Monochroma-tor:5.2.1 With an atomic arc sou

11、rce properly aligned (see 5.3)inthe sample cell compartment, adjust the position of thewavelength dial to give maximum signal for each of the atomiclines and record the wavelength reading. The difference be-tween the observed value and the corresponding value in Table1 represents the correction that

12、 must be subtracted algebra-ically from the wavelength reading of the instrument. Thecorrections may be recorded or the monochromator adjusted togive the proper values. Since there may be some backlash inthe wavelength drive of scanning instruments, always approachthe peak position from the same dir

13、ection, if applicable.1This test method is under the jurisdiction of ASTM Committee E13 onMolecular Spectroscopy and Separation Science and is the direct responsibility ofSubcommittee E13.01 on Ultra-Violet, Visible, and Luminescence Spectroscopy.Current edition approved Oct. 1, 2009. Published Octo

14、ber 2009. Originallyapproved in 1969. Last previous edition approved in 2004 as E388 04. DOI:10.1520/E0388-04R09.2For 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

15、 standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.5.2.2 When calibrating scanning-type instruments, approachthe peak position in the same direction that the motor scans, ifyour instru

16、ment does not correct for backlash. Check theposition against that recorded while scanning and, if necessary,correct as in 5.2.1.5.3 In cases where the monochromator is designed so that alateral displacement of the calibration source from a positiondirectly in front of the entrance slit appears as a

17、 wavelengthshift, proceed as follows:5.3.1 Instead of placing the atomic lamp in front of theentrance slit of the monochromator, fill a sample cell with adilute scattering suspension, as described in 4.1.5.3.2 Place the cell in the sample position in the instrument.5.3.3 Illuminate the cell transver

18、sely with the atomic lamp,either from the side or from above.5.3.4 Adjust the wavelength to give the maximum signal foreach of the atomic lines given in Table 1; record the wave-length reading and proceed as in 5.2.5.4 Adjustment of Excitation Monochromator:5.4.1 After the emission monochromator has

19、 been cali-brated, adjust the excitation monochromator to match, asfollows:5.4.2 Place a sample cell containing either the dilute scat-tering suspension described in 4.1 in the sample cell compart-ment.5.4.3 With a continuous source in the normal source posi-tion of the instrument, illuminate the su

20、spension.5.4.4 Set the wavelength positions of both excitation andemission monochromators at a previously determined settingused for calibration of the emission monochromator.5.4.5 Adjust the wavelength position of the excitationmonochromator to give a maximum signal, and record thewavelength readin

21、g. The difference between the observedvalue on the dial and the corresponding value in 5.1 representsthe correction that must be subtracted algebraically from thereading of the instrumentation. The corrections may be eitherrecorded, or the monochromator may be adjusted to give theproper value. It is

22、 possible to perform the latter using thecontrol software for some spectomaters. As stipulated in 5.2.1,always approach the desired wavelength position in the samedirection that the scan motor scans, if applicable.5.4.6 The match of the excitation monochromator with theemission monochromator may be

23、checked at wavelengthsabove or below that used in 5.4.5.NOTE 1Some fluorescence spectrometers are designed to allow theuser to place an atomic lamp before the excitation monochromator. Thelamp is installed into the instrument either by the manufacturer or by theuser as specified by the manufacturer.

24、 In this case, wavelength accuracycan be calibrated for the excitation monochromator using a procedure thatparallels that given in 5.2 for the emission monochromator. A scatteringsolution or other scattering media can then be placed at the sampleposition to scatter atomic lamp light into the emissio

25、n monochromator tocalibrate emission wavelength accuracy using a procedure that parallelsthat given in 5.4 for the excitation monochromator.5.5 Slit Width Effects:5.5.1 Use the narrowest practical slit widths in calibratingthe wavelength scale. In cases when monochromator slits arenot filled, or whe

26、n intensity of fluorescence varies rapidly withwavelength, there may be an apparent wavelength error withwide slits. Under the most unfavorable conditions this errormay approach one spectral bandwidth, so that narrow slitsshould be used for accurate wavelength measurements. As themagnitude of the er

27、ror may depend on characteristics of boththe instrument and the sample, a generally applicable correc-tion for slit widths is not practical.5.5.2 For greatest accuracy at important wavelengths ofspecific compounds, measure the peak wavelength as a func-tion of slit width and plot a correction curve.

28、TABLE 1 Atomic Emission LinesAfor Wavelength AccuracyHg Ne Ar Kr Xe253.65 336.99 633.44 830.03 696.54 427.40 645.63 450.10296.73 341.79 638.30 836.57 706.72 428.30 722.41 458.28302.15 345.42 640.11 837.76 727.29 431.96 758.74 462.43312.57 346.66 640.22 841.72 738.40 436.26 760.15 467.12313.15 347.26

29、 650.65 841.84 750.39 437.61 768.53 469.70313.18 350.12 653.29 846.34 751.47 440.00 769.45 473.42334.15 352.05 659.90 857.14 763.51 442.52 785.48 480.70365.02 359.35 667.83 859.13 772.38 445.39 805.95 482.97404.66 533.08 671.70 863.46 794.82 446.37 810.44 484.33407.78 534.11 692.95 864.70 800.62 450

30、.24 811.29 491.65435.84 540.06 703.24 865.44 801.48 557.03 819.00 492.32546.07 576.44 717.39 865.55 810.37 564.96 826.32 711.96576.96 582.01 724.52 867.95 811.53 567.25 828.10 764.20579.07 585.25 743.89 868.19 826.45 583.29 829.81 823.16588.19 783.91 870.41 840.82 587.09 850.89 828.01594.48 792.71 8

31、77.17 842.46 599.39 877.67 834.68597.55 793.70 878.06 912.30 601.21 975.18 840.92603.00 794.32 885.39 922.45 605.61 881.94607.43 808.25 920.18 965.78 895.22609.62 811.85 930.09 979.97614.31 812.89 932.65 992.32616.36 813.64 942.54621.73 825.94 948.67626.65 826.61 953.42630.48 826.71AWavelength value

32、s have been obtained from Harrison, G.R., MIT Wavelength Tables, Wavelengths by Element, Vol 2, MIT Press, Cambridge, MA, 1982; and Zaidel,A.N., Prokofev, V.K., Raiskii, S.M., Slavnyi, V.A., and Shreider, E.Ya., Tables of Spectral Lines, Plenum Press, New York, NY, 1970.E388 04 (2009)25.6 Spectral B

33、andwidth of Monochromator:5.6.1 Use the well-separated atomic lines such as those forHg at 253.65, 435.84, and 546.07 nm. Do not use second orderlines.5.6.2 Take sets of readings at wavelengths on both sides ofthe reading of maximum intensity.5.6.3 Record the wavelength positions on both sides of th

34、epeak maximum that correspond 50 % and 5 % of the maxi-mum. The wavelength interval between the 50 % points is thespectral bandwidth of the monochromator. This test is used asan indication of the approximate resolving power that may beexpected from the instrument. The wavelength interval be-tween th

35、e 5 % points is an indication of the degree of isolationthat may be achieved between adjacent wavelengths.6. Precision and Bias6.1 The precision of this test method is undetermined, but ismost likely limited by the wavelength repeatability of thefluorescence spectrometer.6.2 Bias does not have meani

36、ng for this test method.7. Keywords7.1 fluorescence spectrometers; fluorometer; molecular lu-minescence; molecular spectroscopy; spectrofluorometerASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users o

37、f 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 must be reviewed every fiv

38、e 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 theresponsible technical c

39、ommittee, 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 C700, 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).E388 04 (2009)3