OXIDATION TYPES OF OXIDATION OXIDIZING AGENTS OXIDATION OF ACETALDEHYDE
The removal of hydrogen or addition of oxygen in a OXIDATION compound is called
TYPES OF OXIDATION OXIDIZING AGENTS OXIDATION OF ACETALDEHYDE
OXIDATION Dehydrogenation Introduction of Oxygen OF and OXIDATION TYPES Dehydrogenation Oxidation Dehydrogenation along with molecular OXIDIZING AGENTS condensation OXIDATION Oxidation of Sulfur Compounds OF ACETALDEHYDE Oxidation of Olefins
Nitric Acid Fuming Sulfuric Acid Hypochlorous acid and Salts OXIDATION PeroxidesOF OXIDATION TYPES Lead Peroxide (PbO2) OXIDIZING AGENTS Hydrogen Peroxide (H2O2) OXIDATION OF ACETALDEHYDE Manganese Peroxide (MnO2) Sodium Peroxide (Na2O2) Permanganates Dichromates Chromic Acid Solution
w
r i n e
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A ce ta ld e h y d e fro m A c e ty le n e H y d r a tio n
w
e a t c h a n
c o
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w
s t e a m
h e a t e x c h a n
l e d
a t e r
g e r
g
S cru b b er
h
C
g
OXIDATION TYPES OF OXIDATION OXIDIZING AGENTS OXIDATION OF ACETALDEHYDE e x
W
A ceta ld eh y d e S till
n i t r o
a t e r A c etic A cid S till
b
a s t e
O
X
K
E
I D I Z T T L
I N E
e r
s t e
G
c a t a l y s t
e a k H C H O 3
A
c i d
R C
e f i n e d H O
3 HC
a i r a t ( l b i n2 / )
7
0
A
C C
R E
U T
D I C
E A
CA
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E F I N E D IC D E T I C A C
OXIDATION OF ACETALDEHYDE
e x
hh
e a t cc h a n
c o w
o
n i t r o
g e r
A c e t a l d e h y d e f r oo mm A c e t y l e n e H y d r a t i oo nn
This crude Acetaldehyde passes to heat w aa s s tt e e and then to Acetaldehyde Still, exchanger O X I D it comes to 99 – 99.8 % pure K E T
e e a a k k AA c c i i d d C HH O O H C 33 H
RR ee ff i i nn ee dd CC 3 3HCHC HH OO
g
e r
s t e T
I Z L
The steam is introduced in Still just because of heating purpose WW CC
e n
h e a t e x c h a n
l e d
a t e r
g
a t e r A c etic A cid S till
Hydrolysis of Acetylene: C2H2 (g) + H2O (l) → CH3CHO (l) ss tt ee aa mm
w
S cru b b er
A ceta ld eh y d e S till
Acetaldehyde is produced by hydration bb r r i ni n45 e e – 55 % of Acetylene in crude form having strength
a i r a t ( l b i n2 / )
I N E
G
c a t a l y s t
7
0
A
C C
R E
U T
D I C
E A
CA
R
E F I N E D IC D E T I C A C
OXIDATION OF ACETALDEHYDE
n
g
A ce ta ld e h y d e fro m A c e ty le n e H y d r a tio n
3
3
A
C
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T
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Nitrogen is vented through a series of condensers at the top
e r
A c etic A cid S till
r
SS cc rr uu bb bb ee rr
A ceta ld eh y d e S till
Kettle is made up of an aluminum-lined steel vessel, fitted with aluminum coils for heating and cooling purpose w a t e b r i n e Acetaldehyde of 99.0 - 99.8% strength pre-cooled nn i i t t r rto o o 0-5°C gg e e n n is introduced in the vessel Potassium acetate catalyst is added h e a t K 2 Cr 2 O 7 c c oo oo l e d e x c h a w w a a t te e r r CHs 3CHO t e a m→ CH3oxygen COOH absorption from the When h reaction starts, e a t incoming e x c h a n g e r air complete andthe heat removed by cooling w is a s almost t e OO XX I I DD II ZZ II N G water KK EE TT TT LL E to maintain the temp The temperature is controlled that cc aa t t a a l l y y s s t t after 1 hour, it should be 27°C after 2 hours, it should be 28–30°C after 4 hours, it should be 60°C aa i i rr a t 7 0 Reaction time is about 12–14 hours ( ( l l bb i n2 / ) i n W e a k A c i d R e f i n e d R U D E The of kettle keepsC 65.3psi C HC H O C HCpressure H O
s t e
CA
R
E F I N E D IC D E T I C A C
OXIDATION OF ACETALDEHYDE w
r i n e n i t r o
A ce ta ld e h y d e fro m A c e ty le n e H y d r a tio n W C
w
c o
o
w
s t e a m
l e d
a t e r
g e r
e x c h aa nn gg e e r r
S cru b b er
e a t c h a n
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Acetic acid is collected from plant having a strength 65% h e a tt
A ceta ld eh y d e S till
h e x
g
a t e rr A c e tic A c id S till
b
s t e
a s t e O
X K
E
I D I Z T T L
I N E
G
To increasing c a the t a l purity, y s t we use AceticAcid Still just like in Acetaldehyde Still and by this process we get Acetic acid of strength exceeding a i r a 96%. t 7 0 e a k H C H O 3
A
c i d
R C
e f i n e d H O 3 HC
( l b i n2 / )
C A C
R E
U DD EE R E FF II NN EE D D TT II CC AA CAC I CI D D E TT I I CC AA C C
MUHAMMAD SERVER REHMANI MUHAMMAD ASIF SALEEM