Separation of isomers in p-chlorophenol
First, the experimental conditions
1
,
instrument:
GC508
Detector:
FID
2
,
workstation:
N2000
3
,
Column:
CS
-
05 30m
×
0.32mm
×
0.4
μ
m
Changzhou
4
,
temperature
:
COL 120
°C
INJ 250°C
DET 220°C
5
,
Carrier gas:
N2
Pre-column pressure:
0.03Mpa
Split ratio:
100
:
1
6
,
hydrogen:
0.08 Mpa
7
,
air:
0.05 Mpa
8
,
Injection volume:
0.1
μ
L
Second, the chromatogram
5.62
─
phenol
9.62
─
O-chlorophenol
10.52
─
P-chlorophenol
10.88
─
M-chlorophenol
Third, the results and discussion
1
,
The experimental conditions can better separate the isomers in p-chlorophenol, and the outflow order is adjacent, opposite, and intervening.
2
,
Before the analysis, you need to adjust the split ratio to
100
:
1
, the injection volume is as small as possible, otherwise the alignment and meta position will not be complete
separate.
3
,
The method is equally applicable to the quality detection of o-chlorophenol and m-chlorophenol.
4
, quantitative method: peak area normalization method.
Need analysis method, please call
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