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CATALYTIC REDUCTION OF AROMATIC MONO NITRO



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169339.pptx, 169339.pptx, 7
CATALYTIC REDUCTION OF AROMATIC MONO NITRO 
COMPOUNDS OF DIFFERENT STRUCTURE IN LIQUID PHASE 
 
Kairdenov
 Sh.A., 
Zharkyn
 M.K. 
Karimbaev
 S.E. 
Supervisor Prof. L.R. Sassykova 
Al-Farabi Kazakh National University 
larissa.rav@mail.ru 
Aromatic mono-, di- and polyamines are widely applied in the production of 
synthetic dyes, photochemicals, fuel stabilizers and additives lubricating oils, 
chemical plant protection products, synthetic fibers, sorbents, medicines. The total 
production of amines in the world is more than 3-4 million tons/year. Obviously that 
the problem of improving the technology of obtaining these compounds can be 
considered actual. The most important way of amines producing is catalytic reduction 
of nitro compounds by hydrogen on catalysts. 
In this work catalytic reduction of mono nitro compounds, nitrobenzene (NB), 
ortho, para-, ortho-nitrophenols (o-NP, p-NP, o-NP), ortho, meta-, para-nitroanilines 
(o-NA, m-NA, p-NA) and p-nitrodiethyl aniline (p-NDA) has been investigated. The 
enlarged laboratory tests on the synthesis of p-phenylenediamine, o-aminophenol, 
and p-aminophenol under optimal process conditions on the most effective and 
selective catalysts have been performed. For the charge, 50 g of the substance and 
200 ml of solvent were taken. The distilled water, C
1
-C
5
alcohols of the grade “CP” 
were used as solvents. The reaction was carried out at the installation on the basis of 
“catalytic duck” and a high-pressure kinetic unit (HPKU), consisting of an advanced 
Vishnevsky autoclave with intensive mixing and a measuring part. The process was 
performed with electrolytic hydrogen from a balloon (99.8%); for gas-liquid 
chromatography (GLC) helium (99.992%) was used. For the research the catalysts 
based on Pt and Pd and deposited on γ-Al
2
O
3
and coal (C), prepared by applying 
appropriate compounds to the carrier by impregnation have been applied.
It was found that the studied nitro compounds on decreasing the initial rate of 
hydrogenation form a series: NB> p-NA > m-NA> p-NDA (p-NP) >> o-NP. The 
high catalytic activity of Pd-based catalysts compared to the Ni catalyst allowed the 
reaction to be carried out under milder conditions. The results of enlarged tests show 
that using relatively small amounts of catalysts (0.48-0.6 g of catalyst by 
hydrogenating 50 g of an aromatic nitro compound) it is possible to obtain high 
amine yields of 90-98.7%.


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