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Project Review (35,36,37,41)
Project Review (35,36,37,41)
Technology
(2019-2020)
Subject : Project I
(2170001)
SUBMITTED BY:
SUBMITTED TO:
Sr. Name Enrollment No.
1 Patel Armin 160420105019 Prof. Anand Upadhyay
4 Process overview
5 Planning
2
Introduction
3
Why Dwsim?
4
Cyclohexanol and Cyclohexanone
5
Process Over View
6
• Figure provides an overview of these process routes.
7
Oxidation of cyclohexane
• Cyclohexanol is widely produced by the liquid-phase air oxidation
of cyclohexane to cyclohexanol and cyclohexanone. The reaction
can be carried out with or without catalyst.The intermediate
cyclohexyl hydroperoxide and the products, cyclohexanol and
cyclohexanone, are more readily oxidized than cyclohexane.
Therefore, to maximize the yield, the conversion of cyclohexane in
the air oxidizers must be kept low (under 6%). Depending on the
conversion, the total yield of alcohol, ketone, and hydroperoxide
varies from 70 to 90%.
8
Hydrogenation of phenol
• Cyclohexanol can be produced by vapor or liquid-phase
hydrogenation of phenol using metal catalysts. The commonly
employed catalyst is nickel or a nickel alloy with copper, cobalt, or
manganese. The reaction gives very high yield 95%-99% at nearly
100% conversion. Very high selectivity for cyclohexanol can be
achieved for instance, a Raney nickel catalyst can give a 99.9%
selectivity for cyclohexanol.
9
Hydration of cyclohexene
• Reaction is carried out using a nickel catalyst. The conversion per
pass is about 50%, at which point the product consists of about 35%
cyclohexene, 15% cyclohexane, and 50% unconverted benzene. The
selectivity of this reaction is very sensitive to impurities such as
sulfur and iron. Therefore, the benzene must be purified and the
hydrogenation vessel is lined with an inert material.
10
Planning
11