Diethylenetriamine (2540)

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NIOSH Manual of Analytical Methods (1994)
National Institute for Occupational Safety and Health
Diethylenetriamine (2540)
2003140NIOSH Manual of Analytical Methods — Diethylenetriamine (2540)1994National Institute for Occupational Safety and Health
TRIETHYLENETETRAMINE
See ETHYLENEDIAMINE, Method 2540, for Procedure
(NH₂CH₂CH₂NHCH2)₂
MW: 146.2
CAS: 112-24-3
RTECS: YE6650000

METHOD: 2540, Issue 2
EVALUATION: UNRATED
Issue 1: 15 May 1989
Issue 2: 15 August 1994

OSHA:  
no PEL
NIOSH:  
no REL
ACGIH:  
no TLV (1 ppm = 5.98 mg/m 3
PROPERTIES:  
liquid; d 0.98 g/mL @ 20 °C; BP 277.4 °C; VP unknown; flash point 118 °C

SYNONYMS:  
diethylenetriamine; DETA; aminoethylethandiamine; 3-azapentane-1,5-diamine; bis(2-aminoethyl)amine

SAMPLER:  
SOLID SORBENT TUBE (1-naphthylisothiocyanate- coated XAD-2, 80 mg/40 mg)
FLOW RATE:  
0.01 to 0.1 L/min [1]
VOL-MIN:  
1 L @ 10 ppm
-MAX:  
20 L
SHIPMENT:  
routine
SAMPLE STABILITY:  
>30 days @ 20 °C [2]
BLANKS:  
2 to 10 field blanks per set

ACCURACY


RANGE STUDIED:  
0.016 to 8 mg/m 3; (10-L samples)
OVERALL PRECISION(Sˆ rT):  
0.06 [1]
BIAS:  
-1.9%
ACCURACY:  
±13.7%

Measurement


TECHNIQUE:  
HPLC, UV DETECTION
ANALYTE:  
naphthylisothiourea derivative of analytes
DESORPTION:  
2 mL dimethylformamide (DMF), ultrasonic 30 min
INJECTION VOLUME:  
10 μL
COLUMN:  
10-μm radial cyano, 10 cm x 8-mm ID in Waters RCM-100 radial compression mode
MOBILE PHASE:  
50/50 isoctane/isopropanol at 3 mL/min
CALIBRATION:  
standard solutions of derivatives in
RANGE:  
1 to 119 μg per sample
ESTIMATED LOD:  
0.3 μg per sample
PRECISION (Sr):  
0.018

APPLICABILITY:  
The working range for TETA is 0.08 to 160 mg/m 3 for a 10-L air sample. This method is the result of evaluation [2] of OSHA Method #60 for DETA, EDA, TETA [1]. The theoretical capacity of each front section is 1.6 mg of TETA.

INTERFERENCES:  
Other primary or secondary amines may react with the sampler coating reagent, and thereby reduce the sampler capacity.

OTHER METHODS:  
This replaces NIOSH Method P&CAM 276 [3]. The method of Anderson, et al., for EDA [4] is an alternate method using thiourea derivatization and HPLC analysis.