Standard Operation Procedure. Elemental Analysis of Solution samples with Inductively Coupled Plasma Mass Spectrometry



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Standard Operation Procedure Elemental Analysis of Solution samples with Inductively Coupled Plasma Mass Spectrometry Soil & Plant Analysis Laboratory University of Wisconsin Madison http://uwlab.soils.wisc.edu October 2005, revised December 2005 1. Application This method covers the analysis of minor and trace elements in solution samples by ICP-MS (VG PlasmaQuad PQ2 Turbo Plus ICP-MS). 2. Summary of method 2.1 Principle: An aqueous sample is converted to aerosols via a nebulizer. The aerosols are transported to the inductively coupled plasma which is a high temperature zone (8,000 10,000ºC). The analytes are heated (excited) to the respective ions. In a quadrupole mass filter, these ions are separated based on their mass-tocharge ratios (For example, the massto-charge ratio is 7 for 7 Li +, 70 for 140 Ce ++, 140 for 140 Ce +, and 238 for 238 U +, respectively) and the ion intensities at different masses are measured (mass spectrometry). These ion intensities are proportional to the respective concentrations of analytes in the aqueous sample. The quantification is an external multi-point linear calibration by comparing the ion intensity of an unknown sample with that of a standard sample. Multielement calibration standard solutions are prepared from single- and multielement primary and/or in-house working standard solutions. Rhodium (Rh) is used as an internal reference standard. With respect to other kinds of analysis where chemical speciation is relevant (such as the concentration of ferrous iron or ferric iron), only total elemental concentration is analyzed by ICP-MS. 2.2 Brief procedure: Working standard solutions are freshly prepared from primary standard solutions and inhouse stock standard solutions. The sample introduction system (pump and nebulizer) is visually checked. The instrument is started and let stabilized. Unknown samples are measured along with standardization blanks, other kinds of blanks, working standard solutions, drift control samples, and quality control samples. After a batch of samples are measured, the data are downloaded to an Excel spreadsheet. The data are corrected in terms of standardization blanks, other relevant blanks, drift correction, and dilution 1

factor application. The results are normalized to the internal reference standard. The quantification is a multipoint external linear calibration. 3. Safety All relevant laboratory safety procedures are followed. 4. Interference This method covers the analysis of over 30 elements in different kinds of samples by ICP-MS. A general discussion of interferences is lengthy but not necessarily relevant to a specific element/isotope, which is especially true if the sample matrix is not specifically defined. Reading the published articles is recommended. There is an enormous amount of literature relevant to the analysis of metals and non-metals by ICP-MS. 5. Sample collection, preservation and handling Containers (bottles, vials, etc) typically are soaked in 10% nitric acid overnight and rinsed with de-ionized water for several times before use. Solution samples typically are acidified with nitric acid at a ratio of 1 5 ml of concentrated nitric acid to 1 liter of sample. Extra cautions need to be exercised in preventing contamination and preserving samples for some specific analyses. 6. Apparatus and device 6.1 ICP-MS: VG PlasmaQuad PQ2 Turbo Plus ICP-MS. 6.2 Fourteen-mL polystyrene test tubes (17 mm 100 mm. e.g. Falcon plastic tubes. Cat #14-959-8 by Fisher Scientific) for the ICP-MS autosampler are cleaned by soaking in 10% nitric acid overnight and rinsed with deionized water. The tubes are air-dried before use. 7. Reagents 7.1 Concentrated nitric acid (e.g. TraceMetal grade. Cat # A509-212 by Fisher Scientific). 7.2 Single-element and multi-element primary standard solutions (SPEC). 7.3 In-house ICP-OES working standard solutions (Details of the ICP-OES work standard solutions are presented in a separate document Elemental analysis of solution samples with ICP- OES ). 8. Measurement by ICP-MS 8.1 MS working standard 8.1.1 Set 14-ml Falcon tubes in the ICP-MS autosampler rack. 8.1.2 Add 10 ml of 2 % (v/v) nitric acid to each tube and label the tubes accordingly (i.e. MS 1, MS 2, MS 3, MS 4, MS 5 and MS 6). 8.1.3 The tube MS 1 serves as a calibration blank. 8.1.4 Prepare the MS working standard solutions in the rest 5 Falcon tubes from the in-house OES working standard solutions and from the SPEC primary standard solutions (CLMS-2, CLMS-3 and CLMS-4). Add the solutions following Table 1: Working standards for ICP-MS. Note: this method covers over 30 elements. Since the analysis by ICP- MS is flexible and can be easily expanded to other elements, and the standards of MS2 MS6 may not cover 2

the concentration ranges of several elements in samples, the working standards may be made in different ways. 8.1.5 MS6 contains 20 ppb of Rh (SPEC CLMS-3 contains 10 ppm of Rh already). Spike 0.02 ml of 2 ppm Rh to MS1 MS5 as the IRS. The nominal concentration is 4 ppb. 8.2 Preparing sample solutions for ICP- MS 8.2.1 For routine samples, add solution samples (10 ml) to 14-mL Falcon tubes. 8.2.2 Spike 0.02 ml of 2 ppm Rh as the IRS. The nominal concentration is 4 ppb. 8.2.3 Prepare none-routine samples in some other methods, depending on the requested analyses, sample matrix, analyte concentrations, etc. For example, low-volume or overconcentrated samples are diluted before analysis. Turbid samples are left to stand overnight so that particles settle down to the bottom, or the samples are centrifugated so that particles are separated from the samples. 8.2.4 After a given amount of sample (weight or volume) is spiked with a given amount of rhodium (Rh), the concentration ratio of (analyte/rh) is later used for quantification. Any further dilution does not change the concentration ratio (see Appendix 1 of Elemental analysis of solution sample with ICP-OES ). 8.3 ICP-MS measurement 8.3.1 Clean the cones. 8.3.2 Set up the sample introduction system. Visually check the nebulization performance. Start the instrument. Let it stabilize. The relevant instrument conditions are listed in Table 2: ICP- MS Instrument Conditions. 8.3.3 In the instrument s software, edit the acquisition procedure. General sequence: calibration blanks (i.e. 2% nitric acid with 4 ppb of Rh), calibration standard solutions (i.e. MS2 MS6), QC or quality control sample(s), wash sample, 10-20 samples, QC(s), 10-20 samples, QC(s), and so on. 8.3.4 In the Menu, select spal acq containing 30+ isotopes. Edit the menu depending on specific samples or analytical requests. The analysis by ICP-MS is flexible and is easily expanded to other elements. In combination of 8.1 (MS working standard), both of the working standard and the acquisition menu can be changed accordingly for additional elements. 8.3.5 Tune the instrument. Check and confirm the instrument s general performance such as blank level, sensitivity, and stability. 8.3.6 Condition the cones by analyzing 10 15 sample solutions. Note: With materials being deposited to the cones during samples being analyzed, the cone s condition changes with time. The change is most significant after the cones are just cleaned. In this sense, the cones need to be conditioned or aged after being cleaned. If the cones have been slightly used and step 8.3.1 is skipped, the condition process may be skipped. 3

8.3.7 Check the instrument blank levels again, especially the blank levels of Cr, Cu, Zn, Mo and Pb. 8.3.8 Set the sample rack(s) into place. Start the whole acquisition sequence. 9. Data processing after ICP-MS analysis 9.1 Download all of the acquisition data into an in-house Microsoft Excel spreadsheet SPAL program. Check the intensities of: internal reference standard (IRS, Rh: drifting down with increasing time and drifting up/down accordingly with sample matrix), calibration blanks and other kinds of blanks (no significant contaminations), quality control samples (drifting in an expected manner), and other samples (the change of acquisition mode from pulse counting to analog counting, extraordinarily high/low intensities). 9.2 Back in the procedure of the ICP-MS software, select/set/change the IRS concentration for the procedure. Edit IRS concentrations for individual samples if there are differences (e.g. MS6 contains 20 ppb while most samples contain 4 ppb of Rh). 9.3 Use the calibration blank (MS1) as the blank for other working standard solutions (MS2 MS6), calculate the slopes. Inspect the calibration lines. 9.4 Calculate the concentrations of other samples (conc. = intensity/slope). No blank correction yet for other samples at this step. 9.5 Download all of the concentration data into the in-house Microsoft Excel spreadsheet SPAL program. 9.6 Use the result of the quality control (QC) sample to correct for drift (with time). It is assumed that the drift is linear between two bracketing QC samples. 9.7 Use the calibration blank (MS-1) as the blank for the samples, carry out blank subtraction. 9.8 If relevant, use the digestion blank to correct the digest blank for digested samples, or use the appropriate blank for some other kind of blank correction. 9.9 Check the results against their respective detection limits. 9.10 Apply dilution factors if appropriate. 9.11 Generate out-going reports. 10. Quality assurance (QA) and quality control (QC) An ICP-MS instrument is used for broad applications in unlimited situations. A general discussion about QA/QC practice is not specific to a particular application, yet detailed discussions about various applications become too lengthy and are beyond the scope of this procedure. It should be reminded that the QA/QC for any specific isotope/element has to be evaluated under certain specifications/conditions. The time in setting the QA/QC criteria is well spent only when the sample matrix is defined, the instrument and its condition are defined, and the target isotope/element is defined. Presented here are some basic operations. 10.1 The calibration standards are made from primary standards and in-house ICP-OES working standards. The inhouse ICP-OES working standards are made from primary standards of several independent sources and confirmed by using some other independent primary solutions (The details of the in-house ICP-OES working standards are presented in Appendix 3 Strategies and 4

implementation of quality assurance (QA) and quality control (QC) in the elemental analysis of solution samples with ICP-MS). In this way, the quality of the calibration standard is assured. 10.2 Samples are diluted to different ratios and measured. The results are used to evaluate matrix effects and dynamic ranges (calibration ranges). 10.3 Samples are analyzed by the calibration of internal standard addition. 10.4 Samples are analyzed by using ICP- OES. 10.5 Some basic performance or data are listed in Table 3: The analysis by ICP- MS. An in-house quality control water (msqc) is diluted by five times and is analyzed each time for a batch of unknown samples. The results of the msqc water are confirmed against the expected values. 10.6 The in-house quality control water (msqc) was made in 1998. The expected values are compiled from the side-by-side analysis of this msqc water with NIST 1643d water, the historical results of this msqc water by the ICP-MS analysis, and the historical results of this msqc water by the ICP-OES analysis. The results are presented in Table 4: In-house msqc value. excellent agreement for most isotopes/elements. 10.6.3 The concentrations of those elements in red color in Table 4 apparently increased with time. As discussed in Appendix 3 of Solution samples by ICP-OES, this is due to the release of these elements from the container glass bottle (Platinum is the exception). 10.6.4 The ICP-MS results of magnesium and vanadium might be interfered and less reliable than the results by ICP-OES. The analysis of selenium by ICP-MS might be better than that by ICP-OES. End 10.6.1 The historical results of this msqc water by ICP-OES and some limited discussion are given in Appendix 3 Strategies and implementation of quality assurance (QA) and quality control (QC) in the elemental analysis of solution samples with ICP-OES. 10.6.2 As presented in Table 4, the values obtained in 1998 by ICP-MS and the values obtained in 2005 are in an 5

Table 1: Working standards for ICP-MS The ICP-MS working standards (MSn, n = 2-6) are made from the in-house ICP-OES working standards (OESn, n = 1-5) and SPEC primary standards (CLMSn, n = 2-4). MS1 = OES1 = 2 % nitric acid. OES5 actually is reserved for future use. Elements of black color in CLMS 2&4 are from CLMS2. Elements of red color in CLMS 2&4 are from CLMS4. selected MS2 MS3 MS4 MS5 MS6 In-house OES working standards SPEC CLMS ml from these standards, to ppb unit OES2 OES3 OES4 OES5 2&4 3 OES2 OES3 OES4 2&4 3 ppm ppm ppm ppm ppm ppm 0.02 0.02 0.02 0.02 0.02 Li 2 10 10 yes 4 20 20 Be 1 1 10 yes 2 2 20 B 2 10 10 yes 4 20 20 Na 20 100 10 40 200 20 Mg 2 20 100 300 10 4 40 200 20 Al 2 10 100 10 4 20 200 20 Si 5 10 10 10 20 P 5 20 100 400 10 10 40 200 20 S 2 20 100 400 10 4 40 200 20 K 5 20 100 500 10 10 40 200 20 Ca 2 20 100 400 10 4 40 200 20 Ti 2 5 10 yes 4 10 20 V 1 5 10 yes 2 10 20 Cr 0.5 2 10 yes 1 4 20 Mn 1 1 4 40 10 2 2 8 20 Fe 2 10 100 10 4 20 200 20 Co 1 5 10 yes 2 10 20 Ni 2 5 10 yes 4 10 20 Cu 2 2 20 10 yes 4 4 40 20 Zn 1 1 20 10 yes 2 2 40 20 Ga 10 yes 20 Ge 10 yes 20 As 2 5 10 yes 4 10 20 Se 2 5 10 yes 4 10 20 Rb 10 yes 20 Sr 2 10 yes 4 20 Y 5 10 10 20 Zr 10 20 Nb 10 20 Mo 1 10 10 yes 2 20 20 Ru 10 yes 20 Rh 10 IRS 20

Table 1: Working standards for ICP-MS (cont'd) selected MS2 MS3 MS4 MS5 MS6 In-house OES working standards SPEC CLMS ml from these standards, to ppb unit OES2 OES3 OES4 OES5 2&4 3 OES2 OES3 OES4 2&4 3 ppm ppm ppm ppm ppm ppm 0.02 0.02 0.02 0.02 0.02 Pd 10 yes 20 Ag 1 2 10 yes 2 4 20 Cd 1 1 10 yes 2 2 20 In 10 yes 20 Sn 10 yes 20 Sb 2 5 10 yes 4 10 20 Te 10 20 Cs 10 yes 20 Ba 1 10 10 yes 2 20 20 Hf 10 20 Ta 10 20 W 10 20 Re 10 20 Ir 10 20 Pt 10 yes 20 Au 10 yes 20 Tl 2 5 10 yes 4 10 20 Pb 2 5 10 yes 4 10 20 Bi 1 2 10 yes 2 4 20 U 10 yes 20

Table 2: ICP-MS Instrument Conditions ICP-MS VG PlasmaQuad PQ2 Turbo Plus ICP-MS Plasma forward power Plasma reflected power 1350 W < 5 W Coolant gas flow rate Auxiliary gas flow rate Nebulizer gas flow rate 14 liter/min 0.6 liter/min 0.83 liter/min Nebulizer Spray chamber Spray chamber temperature Sampling depth Sample cone Skimmer cone Ion lenses setting Conikal (nominal flow rate: 1 ml/min) Double-pass Scott-type Water-cooled at 5C 10 mm 1.0 mm nickel 0.7 mm nickel Optimized on 115In Sample uptake rate Sample uptake time Acquisition time Wash time 0.85 ml/min 50 s 60 s twice 15 s Acquisition menu spal acq Detector mode Dual Acquisition format Scan Dwell PC 320 us Dwell analog 640 us Channels/amu 24 Start mass End mass 5.6 amu 238.4 amu Mass skip range 10.4-48.6 (Mass skip range may be 53.4-57.6 set to different values 78.4-80.6 depending on specific 88.4-96.6 samples) 123.4-132.6 136.4-194.6 210.4-236.6

Table 3: The analysis by ICP-MS Mass Slope LOD cblk msqc/5 cps/ppb ppb ppb ppb 1 Li 7 19775 0.02 1.15 6.2 2 Be 9 3893 0.06 0.01 4.1 3 B 10 506 0.20 0.83 35.3 4 Ti 49 346 0.20 0.30 5.4 5 V 51 5582 0.03 0.27 7.4 6 Cr 52 4949 0.10 0.44 8.5 7 Co 59 6492 0.01 0.01 3.4 8 Ni 60 1521 0.10 0.36 3.7 9 Cu 65 1699 0.10 0.04 18.8 10 Zn 66 553 0.30 1.63 10.1 11 Ga 71 4455 0.02 0.01 0.4 12 Ge 74 837 0.20 0.07 11.8 13 As 75 673 0.10 0.15 11.6 14 Se 82 61 2.00 1.42 14.6 15 Rb 85 4823 0.02 0.01 36.4 16 Sr 86 702 0.01 0.13 8.8 17 Mo 98 1506 0.05 0.02 4.8 18 Ru 101 1116 0.02 0.01 3.8 19 Pd 108 1793 0.06 0.02 6.1 20 Ag 109 3071 0.02 0.01 3.2 21 Cd 111 602 0.06 0.03 22.5 22 In 115 6789 0.01 0.002 0.04 23 Sn 118 1463 0.03 0.02 9.7 24 Sb 121 1536 0.02 0.01 7.8 25 Cs 133 5520 0.01 0.004 8.5 26 Ba 135 390 0.10 0.06 9.2 27 Pt 195 1553 0.05 0.01 3.7 28 Au 197 1952 0.03 0.01 0.4 29 Tl 205 4822 0.02 0.003 5.8 30 Pb 208 3313 0.03 0.04 13.1 31 Bi 209 3964 0.02 0.02 5.8 32 U 238 6461 0.02 0.003 7.2

Table 4: In-house msqc value Si, P, S and Cl: ppm. Others: ppb 1998 2005 ICP-MS 2005 ICP-OES 1998 2005 ICP-MS 2005 ICP-OES avg avg sd avg sd avg avg sd avg sd Li 7 31 31 2 30 1 Ag 109 15.8 16.3 0.4 Be 9 20 20 1 Cd 111 113 112 7 112 2 B 10 178 176 9 175 2 In 115 0.2 0.2 0.1 Na 23 135 306 5 Sn118 48 49 1 Mg 26 287 282 17 265 13 Sb 121 38 40 2 Al 27 32 63 9 82 9 Te 125 120 Si 28 1.4 2.9 0.0 I 127 8 P 31 2.9 3.1 0.1 Cs 133 42 43 1 S 34 4.6 4.6 0.1 Ba 138 46 46 2 46 1 Cl 35 25.0 La 139 54 K 39 135 10 Ce 140 54 Ca 44 418 831 26 Pr 141 31 Sc 45 57 Nd 146 55 Ti 49 27 29 2 26 1 Sm 147 55 V 51 43 43 2 37 2 Eu 153 0.02 Cr 52 43 43 3 42 1 Gd 157 52 Mn 55 46 49 2 51 0 Tb 159 19 Fe 56 166 221 4 228 3 Dy 163 32 Co 59 17 17 1 16 2 Ho 165 31 Ni 60 18 18 1 19 2 Er 167 31 Cu 65 93 95 5 95 3 Tm 169 31 Zn 66 49 51 3 52 3 Yb 172 31 Ga 69 2.1 1.9 0.2 Lu 175 31 Ge 74 57 61 5 Hf 178 32 As 75 55 59 5 61 13 Ta 181 28 Br 81 W 184 24 Se 82 74 72 3 56 10 Os 189 12 Rb 85 173 182 3 Ir 193 31 Sr 88 43 45 1 44 1 Pt 195 30 19 2 Y 89 28 26 1 29 3 Au 197 2.2 2.1 0.6 Zr 90 70 Tl 205 29 29 1 Nb 93 31 Pb 208 64 64 2 69 6 Mo 98 25 25 1 22 3 Bi 209 29 29 1 Ru 99 19 19 2 Th 232 36 Pd 105 30 31 1 U 238 36 36 1