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Cyanogen

Related Information: Chemical Sampling - Cyanogen
Method no.: PV2104

Control no.: T-PV2104-01-8907-CH

Matrix: Air

Target concentration: 10 ppm (20 mg/m3) OSHA TWA PEL

Procedure: Samples are collected by drawing a known volume of air through sampling tubes containing XAD-2 adsorbent which have been coated with 2-(hydroxmethyl) piperidine.  Samples are desorbed with toluene and analyzed by gas chromatography with a nitrogen-phosphorous detector (GC-NPD). 

Air volume and sampling rate studied: 0.2 L/min for 3 liters; upper limit: 0.2 L/min for 12 liters
 
Status of method: Stopgap method. This method has been only partially evaluated and is presented for information and trial use.

Date: July, 1989 Chemist: Mary E. Eide



Solvents Branch
OSHA Analytical Laboratory
Salt Lake City, UT




1. General Discussion
1.1 Background
1.1.1 History of procedure
 
The OSHA PEL for cyanogen is 10 ppm (20 mg/m3). 
Direct collection on various media was not attempted as cyanogen reacts with water to form hydrogen cyanide and cyanate, and would react with any water collected from the humidity in the air. The collection of the cyanogen with a XAD-2 tube coated with 2-(hydroxymethyl)piperidine (2-HMP XAD-2) was attempted and found to be successful. The cyanogen was stabilized by forming a derivative, and showed good desorption efficiencies, retention efficiencies, and storage.
 
1.1.2 Potential workplace exposure (Ref 5.1)
 
Workers are exposed to cyanogen in chemical manufacturing. Cyanogen is used as a fumigant, in welding and cutting heat-resistant metals, and as a rocket and missile propellant.
 
1.1.3 Toxic Effects (This section is for information purposes and should not be taken as the basis for OSHA policy.) (Ref 5.1)
 
Chronic exposure to cyanogen causes irritation to the respiratory tract and to exposed skin surfaces. Cyanogen forms hydrocyanic acid and cyanate in vivo. Exposure causes hoarseness, conjunctivitis, and edema of the eyelid; further exposure causes hemorragic exudate of the bronchi and trachea, followed by pulmonary edema, and death. In laboratory tests, exposure to 100 ppm. for 2-3 hours was fatal to cats, and at 400 ppm for 2 hours was fatal to rabbits. 

1.1.4 Physical properties (Ref 5.1 and 5.2):
Structure: structure
Synonyms: carbon nitride: dicyanogen; dicyan; ethedinitride; nitriloacetonitrile; oxalic acid dinitrile; oxalyl cyanide; oxalonitrile
Molecular weight: 52.04
Freezing point: -27.9C
Boiling point: -20.7C
Odor none up to 250 ppm, after that almond-like
Molecular formula: C2N2
CAS: 460-19-5
IMIS: 0800
RTECS: 27697 (GT1925000)
DOT: UN 1026
1.2 Limit defining parameters
1.2.1 The detection limit of the analytical procedure is 0.1 g. This is the smallest amount of cyanogen that could be detected under normal operating conditions.
 
1.2.2 The overall detection limit is 0.1 g. This corresponds to 0.016 ppm based on the 1 mL desorption volume, and 3 liters (all ppm amounts in this study are based on a 3-L air volume).
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 of 0.1 L/min sampling rate with the sampling tube in line.

2.1.2 Samples are collected using sampling tubes containing with XAD-2 coated with 2-(hydroxymethyl)piperidine. The tubes are 8 cm long and i.d. is 4 mm. and o.d. is 6 mm. The tube is packed with a 150 mg front section and a 75 mg backup section of the XAD-2 coated with 2-(hydroxymethyl) piperidine. There is a silanized glass wool plug before and after each section.
 2.2 Sampling technique
2.2.1 The ends of the sampling tubes are opened immediately before sampling.

2.2.2 Connect the sampling tubes 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 sampling tube.

2.2.5 Seal the sampling tubes with plastic caps immediately after sampling. Seal each sample lengthwise with OSHA Form-21 sealing tape. 

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 samples.
2.3 Desorption efficiency

Six tubes were spiked with cyanogen gas at each loading of 3.64 g (0.57 ppm), 16.5 g (2.58 ppm), 32.9 g (5.15 ppm), and 64.0 g (10.0 ppm). They were compared to standards prepared by spiking cyanogen into a solution of 15 mg/mL 2-(hydroxymethyl) piperidine in toluene. Samples and standards were allowed to react overnight. The samples were opened, each section placed into a separate 2 mL vial, desorbed with 1 mL of the desorbing solution, desorbed for 30 minutes with occasional shaking, and were analyzed by GC-NPD. The overall average was 99.0% recovered (Table 2.3).

Table 2.3
Desorption Efficiency

% Recovered
Tube # 0.05 PEL 0.25 PEL 0.5 PEL 1 PEL
3.64 g 16.5 g 32.9 g 64.0 g

1
99.3
97.9
94.4
96.2
2
98.6
99.1
101
97.9
3
103
100
102
98.2
4
97.4
95.8
100
101
5
98.8
101
100
98.2
6
100
99.9
99.9
95.5
average
99.5
99
99.6
97.8
overall average
99.0
standard deviation 
2.09



2.4 Retention efficiency

Six tubes were spiked with 35 L cyanogen gas, or 64.3 g (10.1 ppm) cyanogen, allowed to equilibrate overnight, and had 12 liters humid air (93% RH) pulled through them. They were opened, desorbed, and analyzed by GC-NPD. There was no cyanogen found on the backup portions of the tubes (Table 2.4). The retention efficiency averaged 99.8%.

Table 2.4
Retention Efficiency

Tube # % Recovered % Recovered Total
'A' 'B'

1 96.6 0.0 96.6
2 102 0.0 102
3 97.5 0.0 97.5
4 99.6 0.0 99.6
5 101 0.0 101
6 102 0.0 102
average
99.8



2.5 Storage
 
Sampling tubes were spiked with 63.6 g (9.96 ppm) cyanogen and stored at room temperature until opened and analyzed. The recoveries averaged 98.6 % for the 13 days stored (Table 2.5). 

Table 2.5
Storage Study

Day % Recovered

6 97.9
6 94.3
6 96.4
6 98.2
6 99.2
13 102
13 101
13 99.8
13 97.6
13 100
average 98.6



2.6 Precision

The precision was calculated using the area counts from six injections of each standard at concentrations of 3.64 g/mL, 16.5 g/mL, 32.9 g/mL, and 64.0 g/mL. The pooled coefficient of variance (Pooled CV) was 0.0257 (Table 2.6). 

Table 2.6
Precision Study

Injection 3.64 16.5 32.9 64.0
Number g/mL g/mL g/mL g/mL

1 129360 617890 1260600 2004500
2 130840 578030 1298100 2048300
3 127230 582110 1307300 1927600
4 124970 615870 1294900 1959700
5 132100 574430 1300200 1914100
6 127550 617730 1300700 1915500
Average 128675 597577 1293533 1961617
Standard Deviation 2606 21496 16689 54586
CV 0.0203 0.0360 0.0130 0.0278
Pooled CV 0.0257

where:

CV (Coefficient of Variable) =  standard devation

average
Pooled CV =


A1(CV1)2 + A2(CV2)2 + A3(CV3)2 + A4(CV4)2

A1 + A2 + A3 + A4


A(1),A(2),A(3),A(4) = # of injections at each level
CV1,CV2,CV3,CV4 = coefficients at each level

2.7 Air volume and sampling rate studied
2.7.1 The air volume studied is 3 liters. Retention efficiencies were studied at 12 liters with no loss of sample, so larger air volumes can be taken.

2.7.2 The sampling rate studied is 0.2 liters per minute.
2.8 Interferences

Suspected interferences should be listed on sample data sheets.

2.9 Safety precautions 
2.9.1 Sampling equipment should be placed on an employee in a manner that does not interfere with work performance or safety.

2.9.2 Safety glasses should be worn at all times.

2.9.3 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-phosphorous detector. 

3.1.2 GC column capable of separating the analyte and an internal standard from any interferences. The column used in this study was a 30-meter 0.5-m df SP2250 capillary column, 0.32 mm i.d.

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.

3.1.5 A 10-L syringe or other convenient size for sample injection.
 
3.1.6 Pipets for dispensing the desorbing solution.
 
3.1.7 Gas tight syringe 25 L or other convenient size for preparing standards.
 3.2 Reagents
3.2.1 Purified GC grade hydrogen, nitrogen, and air. 

3.2.2 Cyanogen 98% purity.

3.2.3 Toluene, Reagent grade.

3.2.4 2-(Hydroxymethyl) piperidine, Reagent grade. 

3.2.5 Dimethyl formamide, Reagent grade.

3.2.6 Desorbing solution is 0.2 L/mL dimethyl formamide in toluene. 
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 of the desorbing solution of 0.2 L/mL dimethyl formamide in toluene.

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 spiking a known quantity of cyanogen onto a 150 mg portion of the 2-HMP XAD-2.

3.4.2 Cyanogen gas was spiked onto the resin using a gas-tight syringe. A spike of 35 L corresponds to 64.0 g cyanogen at 657 mmHg, 22C, and a 98% purity gas. This is equal to 10.0 ppm based on a 3-L air volume, or 2.5 ppm based on a 12-liter air volume.

3.4.3 A series of standards are prepared covering the range from detection limit to the highest sample. The standards should bracket the samples. At least five differing concentrations should be made so that there are enough data points to plot a curve.
3.5 Analysis
3.5.1 Gas chromatograph conditions.

Flow rates (mL/min) Temperature (C)
Nitrogen (make-up): 30  Injector: 180
Hydrogen (carrier): 1  Detector: 250
Hydrogen (detector): 2  Column: 140
Air: 30
Injection size: 1L
Elution time: 34.4 min
Chromatogram: For problems with accessibility in using figures please contact the SLTC at (801) 233-4900.
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 retention time of the analyte or the internal standard 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 It was found that cyanogen chloride formed the same derivative.

3.6.3 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 A curve with area counts versus concentration is calculated from the calibration standards.

3.7.2 The area counts for the samples are plotted with the calibration curve to obtain the concentration of cyanogen in solution. 

3.7.3 To calculate the concentration of analyte in the air sample the following formulas are used:

  (µg/mL) (desorption volume)  
(desorption efficiency)
  =   mass of analyte in sample


  (mass of analyte in sample)  
molecular weight
  =   number of moles of analyte


(number of moles of analyte) (molar volume at 25C & 760mm Hg) =   (volume the analyte will occupy at 25C & 760mm Hg)


  (volume analyte occupies) (106) *  
(air volume)
  =  ppm


* All units must cancel.

3.7.4 The above equations can be consolidated to form the following formula. To calculate the ppm of analyte in the sample based on a 10 liter air sample:

ppm =  (μg/mL)(DV)(24.46)(106)(g)(mg)

(10 L)(DE)(MW)(1000 mg)(1000 mg)


g/mL = Concentration of analyte in sample or standard
24.46 = Molar volume (liters/mole) at 25C and 760 mmHg.
MW = Molecular weight (g/mole)
DV = Desorption volume
10 L = 10 liter air sample
DE = Desorption efficiency


3.7.5 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 studies should be performed. 

5. References
5.1 "Documentation of the Threshold Limit Values and Biological Exposure Indices", Fifth Edition, American Conference of Governmental Industrial Hygienists Inc., Cincinnati, OH, 1986, p. 154.

5.2 Windholz, M., "The Merck Index", Tenth Edition, Merck & Co., Rahway N.J., 1983, p. 385.