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ACETAMIDE |
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| Method No.: | PV2084 |
| Control No.: | T-PV2084-01-8706-CH |
| Matrix: | Air |
| Target concentration: | There is no TLV or OSHA PEL for acetamide. A target level of 10 ppm was used. |
| Procedure: | Samples are collected by drawing a known volume of air through a silica gel tube. Samples are desorbed with 1 mL methanol and analyzed by gas chromatography-with a nitrogen-phosphorous detector (GC-NPD). |
| Air volume and sampling rate: | 10 Liters at 0.1 Lpm |
| Status of method: | Stopgap method. This method has been only partially evaluated and is presented for information and trial use. |
| Date: | June, 1987 |
| Chemist: | Mary E. Eide |
Solvents Branch
OSHA Salt Lake Technical Center
Salt
Lake City, UT 84115-1802
- General Discussion
1.1 Background
1.1.1 History of procedure
The OSHA Laboratory recently received samples collected on silica gel tubes requesting analysis for acetamide. There is a NIOSH method S254 for the collection and analysis of dimethyl acetamide. This method recommends collection on silica gel tubes and analyzes them by gas chromatography with a flame ionization detector. A nitrogen-phosphorous detector was used since acetamide does not respond as well on a flame ionization detector. The silica gel tubes were found to have adequate desorption, retention, and storage stability.
1.1.2 Potential workplace exposure (Ref. 5.1)
Acetamide is used as a solubilizer, plasticizer, stabilizer, to denature alcohol, and in organic syntheses.
1.1.3 Toxic Effects (This section is for information purposes and should not be taken as the basis for OSHA policy.) (Ref. 5.2)
Acetamide is classified as a mild irritant with a low toxicity, but has been classified as a carcinogen by IARC as it tested positive as an animal carcinogen.
1.1.4 Physical properties (Ref. 5.1):
Physical Properties Compound:
CH3 CONH2 Molecular weight: 59.07 Melting point: 810°C Boiling point: 222°C Odor: mousy odor Color: white crystals Molecular formula: C2H5NO CAS: 60-35-5 IMIS: A625 1.2 Limit defining parameters
1.2.1 The detection limit of the analytical procedure is 10 ng. This is the smallest amount that could be detected under normal operating conditions. The injection volume is 1 µL (Figure 1).
1.2.2 The detection limit of the overall procedure is 10 ng/sample (0.4 ppm based on a 10 liter sample). This is the amount of analyte placed on a silica gel tube which corresponds to the detection limit of the analytical procedure.
1.3 Advantages
1.3.1 The sampling procedure is convenient.
1.3.2 The analytical method is reproducible and sensitive.
1.3.3 Reanalysis of samples is possible.
1.3.4 It may be possible to analyze other compounds at the same time.
1.3.5 Interferences may be avoided by proper selection of column and GC parameters.
1.4 Disadvantages
none known
2. Sampling procedure
2.1 Apparatus
2.1.1 A calibrated personal sampling pump, the flow of which can be determined within ± 5% at the recommended flow.
2.1.2 Silica gel tubes (20/40 mesh) containing a 150 mg adsorbing section with a 75 mg backup section separated by a 2 mm portion of urethane' foam, with a silanized glass wool plug before the adsorbing section and a 3 mm plug of urethane foam at the back of the backup section. The ends are flame sealed and the glass tube containing the adsorbent is 7 cm long, with a 6 mm O.D. and 4 mm I.D., SKC tubes or equivalent.
2.2 Sampling technique
2.2.1 The ends of the silica gel tube are opened immediately before sampling.
2.2.2 Connect the silica gel tube to the sampling pump with flexible tubing.
2.2.3 Tubes should be placed in a vertical position to minimize channeling, with the smaller section towards the pump.
2.2.4 Air being sampled should not pass through any hose or tubing before entering the silica gel tube.
2.2.5 Seal the silica gel tube with plastic caps immediately after sampling. Seal each sample lengthwise with OSHA Form-21.
2.2.6 With each batch of samples, submit at least one blank tube from the same lot used for samples. This tube should be subjected to exactly the same handling as the samples (break ends, seal, & transport) except that no air is drawn through it.
2.2.7 Transport the samples (and corresponding paperwork) to the lab for analysis.
2.2.8 Bulks submitted for analysis must be shipped in a separate container from the air samples.
2.3 Desorption efficiency
2.3.1 A loading of 241.8 µg on the tubes corresponds to 10.6 ppm based on a 10 liter air volume and the overall desorption efficiency of 94.4% (Table 1).
2.3.2 A solution of acetamide in methanol was prepared. Aliquots of this solution were liquid spiked onto eighteen tubes, six at each of the following loadings; 483.6, 241.8, and 96.72 µg. These levels correspond to 20, 10 and 4 ppm based on a 10 liter air volume. The tubes were allowed to equilibrate in the refrigerator overnight. They were opened, each section placed into a separate 2 mL vial, desorbed with 1 mL methanol, and allowed to desorb for 30 minutes with occasional shaking. They were analyzed by GC-NPD. The overall average desorption was 94.4% (Table 1).
Table 1
Desorption Efficiency
Tube# % Desorption % Desorption % Desorption 483.6 µg 241.8 µg 96.72 µg
1 90.3 92.5 95.7 2 91.6 94.8 92.4 3 92.7 97.1 94.1 4 95.3 96.5 94.1 5 95.3 95.3 94.1 6 96.1 96.0 94.1 average 93.6 95.4 94.1 overall average 94.4%
standard deviation ±1.83
2.4 Retention efficiency
A solution of acetamide in methanol was prepared, and aliquots were liquid spiked onto seven silica gel tubes, for a loading of 483.6 µg acetamide. These tubes had 10 liters of humid air (83% RH) drawn through them. They were desorbed and analyzed by GC-NPD. There was no acetamide detected in the backup portions of the tubes. The average amount recovered was 83.5% (Table 2).
Table 2
Retention Efficiency
Tube # % Recovered 'A' % Recovered 'B' % Total
1 82.5 0.0 82.5 2 84.3 0.0 84.3 3 85.2 0.0 85.2 4 83.4 0.0 83.2 5 83.9 0.0 83.9 6 83.0 0.0 83.0 7 82.1 0.0 82.1 Average 83.5 Average (desorption corrected) 88.4
2.5 Storage
A solution of acetamide in methanol was prepared, and aliquots were spiked onto three tubes for a loading of 483.6 µg acetamide. These were stored at room temperature (24°C) for seven days. The amount recovered averaged 94.1% (Table 3).
Table 3
Storage Stability
Tube # % Recovered
1 91.8 2 94.7 3 96.2 Average
94.1
Average (desorption corrected)
99.8
2.6 Air volume and sampling rate studied
2.6.1 The air volume studied was 10 liters.
2.6.2 The sampling rate studied was 0.1 liter per minute.
2.7 Interferences
Suspected interferences should be listed on sample data sheets.
2.8 Safety precautions
2.8.1 Sampling equipment should be placed on an employee in a manner that does not interfere with work performance or safety.
2.8.2 Safety glasses should be worn at all times.
2.8.3 Follow all safety practices that apply to the workplace being sampled.
3. Analytical method
3.1 Apparatus
3.1.1 Gas chromatograph equipped with a nitrogen-phosphorus detector in the nitrogen mode.
3.1.2 GC column capable of separating the analyte from any interferences. A 6 ft 10% UCON 50-HB-5100 on 80/100 Chrom WAW with 2% KOH was used for this stop-gap method.
3.1.3 An electronic integrator or some other suitable method of measuring peak areas.
3.1.4 Two milliliter vials with Teflon-lined caps for sample desorption.
3.1.5 A 10 µL syringe or other convenient size for sample injection.
3.1.6 Pipets for dispensing the methanol.
3.1.7 Volumetric flasks - 10 mL and other convenient sizes for preparing standards.
3.1.8 A balance capable of weighing milligram quantities.
3.2 Reagents
3.2.1 Purified GC grade nitrogen, hydrogen, and air.
3.2.2 Reagent grade methanol.
3.2.3 Reagent grade acetamide.
3.3. Sample preparation
3.3.1 Sample tubes are opened and the front and back
section of each tube are placed in separate 2 mL vials.
3.3.2 Each section is desorbed with 1 mL methanol.
3.3.3 The vials are sealed immediately and allowed to desorb for 30 minutes with occasional shaking.
3.4 Standard preparation
3.4.1 Standards are prepared by diluting a known quantity of acetamide with methanol.
3.4.2 At least two separate stock standards should be made. Dilutions of these stocks are made at five different levels covering the range of the samples. The standards used ranged from 9.67 to 483.6 µg/mL.
3.5 Analysis
3.5.1 Gas chromatograph conditions.
Gas chromatograph conditions Flow rates (mL/min) Temperature (°C) Nitrogen (carrier): 24 Injector: 200 Hydrogen (detector): 3 Detector: 220 Air (detector): 50 Column: 150 Injection size: 1 µL Elution time: 2.23 min Chromatogram: (See Figure 2) Attenuation: 6 3.5.2 Peak areas are measured by an integrator or other suitable means.
3.6 Interferences (analytical)
3.6.1 Any compound having the general reten.tion time of the analyte used is an interference. Possible interferences should be listed on the sample data sheet. GC parameters should be adjusted if necessary so these interferences will.pose no problems.
3.6.2 Retention time data on a single column is.not considered proof of chemical identity. Samples over the target concentration should be confirmed by GC/Mass Spec or other suitable means.
3.7 Calculations
3.7.1 To calculate the concentration of analyte in the air sample the following formulas are used:
(µg/mL) (desorption volume)
=
mass of analyte in sample (desorption efficiency)
(mass of analyte in sample)
=
number of moles of analyte molecular weight
(number of moles) (molar volume)
of analyte at 25°C and 760 mmHg=
volume the analyte will occupy at 25°C & 760 mmHg (volume analyte occupies) (106) *
=
ppm
(air volume)
* All units must cancel.
3.7.2 The above formulas can be combined to the formula given below. To calculate the ppm of analyte in the sample based on a 10 liter air sample, and a 1 mL desorbing solution:
(µg/mL)(1 mL)(24.45)(106) × (g) × (mg)
=
ppm (10 L) (DE) (MW)
(1000 mg)
(1000 µg)
µg/mL =
concentration of analyte in sample or standard 24.45 =
Molar volume (liters/mole) at 25°C and 760 mmHg. MW =
Molecular weight (g/mole) 1 mL =
Desorption volume 10 L =
10 liter air sample DE =
Desorption efficiency
3.7.3 This calculation is done for each section of the sampling tube and the results added together.
3.8 Safety precautions
3.8.1 All handling of solvents should be done in a hood.
3.8.2 Avoid skin contact with all solvents. 3.8.3. Wear safety glasses at all times.
4. Recommendations for further study
Collection efficiencies need to be performed to investigate the apparent loss indicated by the retention study. Longer storage tests should also be performed.
Figure 1. Detection limit standard of 10 µg/mL acetamide in methanol
Figure 2. Standard of acetamide in methanol at a concentration of 483.6 µg/mL.
5. References
5.1 Windholz, M., "The Merck Index". Tenth Edition, Merck & Co., Rahway N.J., 1983, p. 6.
5.2 Sax, N. "Dangerous Properties of Industrial Materials", Fifth Edition, Van Nostrand Reinhold Co., New York, 1979, p. 322.