Ca MW: Table 1 CAS: Table 1 RTECS: Table 1: CALCIUM and Compounds, As Ca 7020

CALCIUM and compounds, as Ca 7020
Ca MW: Table 1 CAS: Table 1 RTECS: Table 1
METHOD: 7020, Issue 2 EVALUATION: FULL Issue 1: 15 February 1984

Issue 2: 15 August 1994
OSHA : Table 1 PROPERTIES: soft, reactive metal; valence 2;

NIOSH: Table 1 MP 848 °C; VP not significant
ACGIH: Table 1
SYNONYMS: Quicklime (CaO); limestone (CaCO 3 ); marble (CaCO 3 ); hydrated lime (Ca(OH) 2 )
SAMPLING MEASUREMENT
SAMPLER: FILTER TECHNIQUE: ATOMIC ABSORPTION, FLAME

(0.8-µm cellulose ester membrane)
ANALYTE: calcium
FLOW RATE: 1 to 3 L/min
ASHING: conc. HNO 3 , 6 mL; 140 °C
VOL-MIN: 20 L @ 5 mg/m 3 60% (w/v) HClO 4 , 2 mL; 400 °C
-MAX: 400 L
FINAL
SHIPMENT: routine SOLUTION: 5% HCl; 100 mL
1000 µg/mL Cs; 1000 µg/mL La
SAMPLE
STABILITY: stable FLAME: air-acetylene, reducing
BLANKS: 2 to 10 field blanks per set WAVELENGTH: 422.7 nm
BACKGROUND
CORRECTION: none used
ACCURACY CALIBRATION: Ca 2+ in 5% HCl
RANGE STUDIED: 2.6 to 10.2 mg/m 3 [1] RANGE: 0.08 to 1.7 mg per sample [2]
(85-L samples)
ESTIMATED LOD: 0.001 mg per sample [3]
BIAS: - 0.39%
OVERALL PRECISION (ŜrT): 0.063 [1] PRECISION (Sr): 0.02 [1,3]
ACCURACY: ± 11.5%
APPLICABILITY: The working range is 1 to 20 mg/m 3 for an 85-L air sample. This is an elemental analysis, not compound
specific. Verify that the compounds in the samples are soluble with the ashing procedure. Aliquots of the samples can be
analyzed separately for many additional metals.
INTERFERENCES: The use of 1000 µg/mL Cs controls ionization in the flame caused by metals such as Na, K, Li, and Mg. The
presence of Si, Al, or H 3 PO 4 require the use of 1% (w/w) La as a releasing agent.
OTHER METHODS: This method combines and replaces P&CAM 173 [4] and S205 [2]. Method 7300 (ICP-AES) is an alternate
analytical method.
NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94

CALCIUM and compounds, as Ca: METHOD 7020, Issue 2, dated 15 August 1994 - Page 2 of 4
REAGENTS: EQUIPMENT:
1. Nitric acid, conc. 1. Sampler: cellulose ester membrane filter,

2. Hydrochloric acid, conc. 0.8-µm pore size, 37-mm diameter; in cassette
3. Hydrochloric acid, 5% (v/v). Add 50 mL conc. filter holder.
HCl to 500 mL water; dilute to 1 L. 2. Personal sampling pump, 1 to 3 L/min, with
4. Calibration stock solution, 1000 µg Ca/mL. flexible connecting tubing.
Commercially available or add 50 mL 3. Atomic absorption spectrophotometer with an
deionized water and minimum volume of HCl air-acetylene burner head and calcium hollow
(20 mL) to dissolve 2.498 g CaCO 3. Dilute to cathode lamp.
1 L with deionized water. 4. Regulators, 2-stage, for air and acetylene.
5. Cs solution, 50 mg/mL. Dissolve 73.40 g 5. Beakers, Phillips, 125-mL, or Griffin, 50-mL,
CsNO 3 in water to make 1 L solution. with watchglass covers.*
6. La solution, 50 mg/mL. Dissolve 156 g 6. Volumetric flasks, 25- and 100-mL.*
La(NO 3)3·6H 2O in water to make 1 L solution. 7. Micropipets, 5 to 500 µL.*
7. Distilled or deionized water. 8. Hotplate, surface temperature 140 and
8. Air, filtered. 400 °C.
9. Acetylene.
10. Perchloric acid, 60% w/v.
* Clean with conc. HNO 3 and rinse
* See SPECIAL PRECAUTIONS. thoroughly with distilled or deionized water
before use.
SPECIAL PRECAUTIONS: Perform all perchloric acid digestions in a perchloric acid fume hood.
SAMPLING:
1. Calibrate each personal sampling pump with a representative sampler in line.

2. Sample at an accurately known flow rate between 1 and 3 L/min for a total sample size of 20 to
400 L. Do not exceed 2 mg total dust loading on the filter.
SAMPLE PREPARATION:
NOTE: The following sample preparation gave quantitative recovery (see EVALUATION OF
METHOD). Steps 4 through 9 of Method 7300 or other quantitative ashing techniques
may be substituted, especially if several metals are to be determined on a single filter.
3. Open the cassette filter holders and transfer the samples and blanks to separate clean beakers.
4. Add 5 mL conc. HNO 3 and cover with a watchglass. Start reagent blanks at this point.
5. Heat on hotplate (140 °C) until most of the acid has evaporated.
6. Add 2 mL conc. HNO 3 and 1 mL 60% HClO 4.
7. Heat on 400 °C hotplate until dense fumes of perchloric acid appear.
8. Remove watchglass and rinse into the beaker with distilled water.
9. Place the beakers on the 400 °C hotplate and allow to go to dryness.
10. Cool each beaker and dissolve the residues in 5 mL 5% HCl.
11. Transfer the solution quantitatively to a 100-mL volumetric flask containing 2 mL of 50 mg/mL
Cs solution and 2 mL of 50 mg/mL La solution.
NOTE: Dilute to a smaller volume (e.g., 10 mL) with proportionally less Cs and La if required for
sensitivity of analysis for other metals in the sample.
12. Dilute to volume with 5% HCl.

CALIBRATION AND QUALITY CONTROL:
13. Add known amounts, covering the range 0 to 500 µg Ca per sample, of calibration stock
solution to 100-mL volumetric flasks containing 2 mL each of the 50 mg/mL Cs and La solutions
and dilute to volume with 5% HCl.
14. Analyze the working standards along with the samples and blanks (steps 19 and 20).
15. Prepare a calibration graph of absorbance vs. solution concentration (µg/mL).
16. Aspirate a standard for every 10 samples to check instrument drift.
17. Check recoveries with at least one spiked media blank per 10 samples.
18. Use method of additions occasionally to check for interferences.
MEASUREMENT:
19. Set spectrophotometer according to manufacturer's recommendations and to conditions on

page 7020-1.
20. Aspirate standards and samples. Record absorbance readings.
NOTE: If the absorbance values for the samples are above the linear range of the standards,
dilute the solutions with 5% HCl and an appropriate amount of the 50 mg/mL Cs and La
solutions, reanalyze, and apply the appropriate dilution factor in the calculations.
CALCULATIONS:
21. Using the measured absorbances, calculate the corresponding concentrations (µg/mL) of
calcium in the sample, C s, and average media blank, C b, from the calibration graph.
22. Using the solution volumes (mL) of the sample, V s, and media blanks, V b, calculate the
concentration, C (mg/m 3), of calcium in the volume of air sampled, V (L):
EVALUATION OF METHOD:
Method S205 [2] was issued on September 26, 1975, and validated over the range 2.6 to 10.2 mg/m 3
using an 85-L air sample by lab testing with spiked filters and generated atmospheres of CaO, verified
by EDTA titration [1]. Collection efficiency of 1.00 was determined for the sampling device. Precision
and accuracy data are given on page 7020-1. An additional check showed an estimated LOD of 1 µg
Ca per sample [3].
REFERENCES:
[1] Documentation of the NIOSH Validation Tests, S205, U.S. Department of Health, Education, and
Welfare, Publ. (NIOSH) 77-185 (1977).
[2] V. 3, S205, U.S. Department of Health, Education, and Welfare, Publ. (NIOSH) 77-157-C (1979).
[3] User check, UBTL, NIOSH Seq. #3990-Q (unpublished, November 29, 1983).
[4] Ibid, NIOSH Manual of Analytical Methods, 2nd ed., Vol. 5, P&CAM 173, U.S. Department of Health,
Education, and Welfare, Publ. (NIOSH) 79-141 (1979).
METHOD REVISED BY:
Mark Millson, NIOSH/DPSE and R. DeLon Hull, Ph.D., NIOSH/DBBS; S205 originally validated under
NIOSH Contract CDC-99-74-45.

TABLE 1: General Information
FORMULA M.W. CAS # RTECS # EXPOSURE LIMITS (mg/m 3)

OSHA NIOSH ACGIH
Ca 40.08 7440-70-2 EV8040000 -- -- --
CaO 56.08 1305-78-8 EW3100000 5 2 2
Ca(OH) 2 74.10 1305-62-0 EW2800000 None 5 5
Ca(CO 3)2 100.09 471-34-1 EV9580000 15 (total); 10 (total); 10

total dust 5 (resp.) 5 (resp.)

Ca MW: Table 1 CAS: Table 1 RTECS: Table 1: CALCIUM and Compounds, As Ca 7020

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CALCIUM and compounds, as Ca 7020

Ca MW: Table 1 CAS: Table 1 RTECS: Table 1

METHOD: 7020, Issue 2 EVALUATION: FULL Issue 1: 15 February 1984

OSHA : Table 1 PROPERTIES: soft, reactive metal; valence 2;

SAMPLER: FILTER TECHNIQUE: ATOMIC ABSORPTION, FLAME

BLANKS: 2 to 10 field blanks per set WAVELENGTH: 422.7 nm

ACCURACY CALIBRATION: Ca 2+ in 5% HCl

NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94

1. Nitric acid, conc. 1. Sampler: cellulose ester membrane filter,

1. Calibrate each personal sampling pump with a representative sampler in line.

NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94

CALIBRATION AND QUALITY CONTROL:

19. Set spectrophotometer according to manufacturer's recommendations and to conditions on

METHOD REVISED BY:

NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94

TABLE 1: General Information

FORMULA M.W. CAS # RTECS # EXPOSURE LIMITS (mg/m 3)

Ca 40.08 7440-70-2 EV8040000 -- -- --

CaO 56.08 1305-78-8 EW3100000 5 2 2

Ca(OH) 2 74.10 1305-62-0 EW2800000 None 5 5

Ca(CO 3)2 100.09 471-34-1 EV9580000 15 (total); 10 (total); 10

NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94

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