1974
DOI: 10.1016/s0021-9673(01)85410-8
|View full text |Cite
|
Sign up to set email alerts
|

Thin-layer and high-speed liquid chromatography of the derivatives of 1,4-phenylenediamine

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1977
1977
1984
1984

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 17 publications
(1 citation statement)
references
References 18 publications
0
1
0
Order By: Relevance
“…Analysis. Colorimetry tests were ruled out (interference, extract discoloration) and gas chromatography (GC) chosen rather than thin-layer chromatography (TLC) (see Ivan & Ciutacu 1974, Uchytil 1974 Warner 1969 for the following reasons: a) GC makes for easier separation of the eluted compounds, especially when oils and phthalates are involved; b) because of its relatively high detection limit (using a catharometer), it is possible to make a thin-layer chro· matography of selected parts of the chromatogram (after trapping); c) it is easier to combine selective infrared spectrophotometry; the trapped quantity is also sufficient to obtain an ultra-violet spectrum. The procedure is as follows: the nitromethanic extract, after being dried at 50-60°C, is dissolved in acetone and injected into a 2 m X 0.6 cm chromatograph column filled with Chromosorb® with 7.5 % Apiezon L, set at 150 rising to 300°C (temperature increase 6°C/min), and then maintained at 300°C.…”
Section: Analytical-chemical Investigation Of the Antiozonants Of Thementioning
confidence: 99%
“…Analysis. Colorimetry tests were ruled out (interference, extract discoloration) and gas chromatography (GC) chosen rather than thin-layer chromatography (TLC) (see Ivan & Ciutacu 1974, Uchytil 1974 Warner 1969 for the following reasons: a) GC makes for easier separation of the eluted compounds, especially when oils and phthalates are involved; b) because of its relatively high detection limit (using a catharometer), it is possible to make a thin-layer chro· matography of selected parts of the chromatogram (after trapping); c) it is easier to combine selective infrared spectrophotometry; the trapped quantity is also sufficient to obtain an ultra-violet spectrum. The procedure is as follows: the nitromethanic extract, after being dried at 50-60°C, is dissolved in acetone and injected into a 2 m X 0.6 cm chromatograph column filled with Chromosorb® with 7.5 % Apiezon L, set at 150 rising to 300°C (temperature increase 6°C/min), and then maintained at 300°C.…”
Section: Analytical-chemical Investigation Of the Antiozonants Of Thementioning
confidence: 99%