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Metachem Ind
Metachem Ind
Metachem Ind
List of Products
Sr. MT/Month
Name of the Product
NO.
(A) Reactive Dyes
1 Reactive Blue 198. 50
2 Reactive Blue FNG. 50
3 Reactive Blue 19. 40
4 Reactive Blue 49. 50
5 Reactive Blue 220 50
6 Reactive Blue 221 50
7 Reactive Blue 222 50
Total (A) 340
(B) Dyes Intermediates
8 PNCBOSA 30
9 Chloranil Condense 30
10 Blue HEGN (198) Base 25
11 Aniline 2:4 DSA. 30
12 Aniline 2:5 DSA 30
13 Oxy-Sulphone 30
14 M. Acid 20
15 Blue - 49 BASE 20
16 Metanillic acid 20
17 4-Sulpho Anthralinic Acid 50
18 4-Sulpho Hydrazone 50
19 Sulpho O.A.V.S./ Sulpho V.S./ Sulpho J- Acid/ 30
Sulpho Gamma Acid
20 3;5 DABA 10
Total (B) 375
Total (A + B) 715
Manufacturing Process:
Blue 198(HEGN) base W/C condensate with Cynuration of aniline 2:4 DSA& then
clarify, standardize& spray dryer.
Chemical Reaction:
INPUT KG OUTPUT KG
Manufacturing Process:
Blue 198 base W/C condense with Cynuration of aniline 2:5 DSA & then cond. With
M.B.V.S ester then clarify & std. & spray dryer.
Mass Balance:
INPUT KG OUTPUT KG
2nd
Condensation
Manufacturing Process:
Mass Balance:
Mass Balance of Reactive Blue 19
INPUT KG OUTPUT KG
Oxilic Acid 90
Soda Bicarbonate 100 2nd Slurry
Water 650
Manufacturing Process:
Dump B-49 base press W/c in vessel with cold water 15 ͦC & take pH 7.0 to 7.2.
Check clear solution. Check real base by N. V. Then cool to 0 ͦC to 2 ͦC by external
chilling. Charge Cy. Chloride close main hole and stir for ½ hrs. Take pH 7.0 to 7.2
by soda solution and maintain for 4 hrs. Check N. V. of solution. It is 0.2%. If okay
then charge metanilic acid clear solution as fast as possible. Maintain pH 7.0 to 7.2
by soda solution. If pH stable start slowly heat up to 35 ͦC to 40 ͦC. check sample
and clarify.
Chemical Reaction:
Blue 49
O NH 2 O NH 2
N
SO 3 H Cl Cl 0 °C - 2 °C SO 3 H
+ N N
CH 3 CH 3
N
HN NH 2 Cl O HN NH Cl
O
CH 3 CH 3 CH 3 N N
CH 3
SO 3 H SO 3 H Cl
O NH 2
NH 2 NH 2
SO 3 H
+ +
CH 3 SO 3 H
N
O HN NH Cl SO 3 H
(50%) (50%)
CH 3 N N
CH 3
SO 3 H Cl
0 °C - 5 °C
O NH 2
SO 3 H
CH 3
N
O HN NH NH
CH 3 N N
CH 3
SO 3 H Cl SO 3 H
INPUT KG OUTPUT KG
Manufacturing Process:
Mass Balance:
INPUT KG OUTPUT KG
Manufacturing Process:
Chemical Reaction:
INPUT KG OUTPUT KG
Manufacturing Process:
MPDSA is cynurated with cynuric chloride at 5 ͦC& further condensed with M.B.V.S.
Ester. Then this product diazotized & coupled with H-acid to getcoupling mass-1.
S.T.acid is diazotized & further coupled with coupling mass-1 to get coupling mass-
2 which spraydried.
Chemical Reaction:
INPUT KG OUTPUT KG
MPDSA 135
Cyanuric Chloride 132
Soda ash 60 Cyanuration of
Celsolin Oil 3 MPDSA
Water 750
Ice 750
M.B.V.S. 200
M. B. V. S. Cle.
NaHCO3 60
Solution
Water 400
NaHCO3 70
Condensation 1
NaNO2 50
Diazotization of
HCl (30%) 300
Cond. Mass
Ice 750
H-Acid 210
Soda Ash 70 H-Acid Cle.
Ice 210 Solution
Water 380
S. T. A. 200
HCl (30%) 60
S.T.A.
NaNO2 50
Diazotization
Ice 380
Water 380
8. PNCBOSA
Manufacturing Process:
PNCB is sulphonated in presence of Oleum (65%) at 120 ͦc to 125 ͦC. Maintain for 8
hrs. then dump s/mass in water & salting & filter &C.F.
Mass Balance:
INPUT KG OUTPUT KG
Manufacturing process:
PNCBOSA is condensed with E.D.A. at 116ͦC& the mass is then isolate with HCl.
Product obtain is then reduction with C.I.P. when reaction is over filter red. Mass &
collect liq. This liq. Clarify & further condense with chloranil at 60ͦC. When reaction
over filter the mass & dry & Pulv. final product obtained.
Chemical Reaction:
Mass Balance:
INPUT KG OUTPUT KG
E.D.A. 5000
PNCBOSA 1000 E.D.A. E.D.A. Recovered 4400
SBC 250 Condensation
Water 1800
Manufacturing process:
Chlo. Cond is cyclisation in presence of Oleum (23%), Sulphuric acid (98%) &
sodium per sulphate at 18ͦC, when reaction over dump this mass in cold water
(20'c)as fast aspossible. Then temp. goes up to 50ͦC. When dumping over stir for
15minutes & start filter. Then wash with tap water up to congo paper faint. Then
dump press cake invessel & take pH 5.0 to5.5by soda ash & then spray dry and
final product obtain.
Chemical Reaction:
(I) Cyclisation:-
SO3Na O
NH2CH2CH2NH O NH
+
NH O NHCH2CH2NH2
O SO3Na
( Chlo. Cond )
NH2 CL O SO3H
NH O NHCH2CH2NH2
NH2CH2CH2NH O NH
SO3H O CL NH2
INPUT KG OUTPUT KG
Manufacturing process:
Sulphalinic Acid is sulphonated with Oleum (23%) at different temp. & then this
mass is dump in water. Aniline 2:4 DSA is isolated & cool. Filter slurry in Nutch &
wash & C.F.
Chemical Reaction:
NH 2 NH 2
SO 3 H
+ H 2S 2O 7
+ H2O
+ SO 3
Oleum Water Sulphur Trioxide
SO 3 H SO 3 H
Mass Balance:
Input KG Output KG
Manufacturing process:
Chemical Reaction:
NH 2 NH 2
SO 3 H
+ H 2 SO 4
+ H 2O + SO 3
HO 3 S + H 2S 2O 7 HO 3 S Water Sulphur Trioxide
SO 3 H
Metanilic Acid
Aniline 2, 4, 5-Trisulphonic Acid
NH 2 NH 2
SO 3 H SO 3 H
+ H 2O
+ H 2 SO 4
HO 3 S HO 3 S Sulphuric Acid
SO 3 H
Aniline 2, 5-Disulphonic Acid
Aniline 2, 4, 5-Trisulphonic Acid
Mass Balance:
Input KG Output KG
Hyflow 10
Activated Carbon 45 Spent Acid 5185
Hydrolysis
Steam 850
Water 3100
Manufacturing process:
Bromamine acid is condense with meta base cond. & cuprous chloride & S.B.C. at
72 ͦC for 10 hrs. When reaction over transfer cond. / mass in MS + RL+BL vessel.
Then charge HCl to get pH 1.5 to 1.0. Then heat 90 C for boil up. Then cool to 70
C and filter slurry in F. P. when filter over. Give wash of 5% salt solution gradually.
Then give air and dump F. P. Take water and charge press cake & spray dryer.
Final Powder obtain.
Chemical Reaction:
(I) Bromamine Condensation:-
O NH2
NH2
SO 3H + NaHCo3
+ CuCl2
SO 2CH2CH2OH
O Br
( Bromamine Acid ) ( M. Base Condense )
O NH2
SO 3H
O NH
SO 2CH2CH2OH
( Oxy. Sulphone )
Input KG Output KG
Water 2000
Slurry
Manufacturing process:
Macitinline acid is nitrated by nitric acid & H2SO4. Then isolate N. Mass in chilled
water. Filter &C.F. Nitro w/cake. Then this nitro w/cake reduction in presence of
C.I.powder & acetic acid at 80ͦC. Then filter reduction Mass & collect amino
solution. Check N.V.& set N.V. 7.0 to7.5%. Isolate by HCl (30%) at 3.0 to3.5pH.
Check f/l. Then heat 75ͦC& check f/l 0.2% to0.3%.
Chemical Reaction:
(I) Sulphonation:-
CH3
CH3
H2S2O7 SO3H
+ + H2SO4
H3C CH3 H2SO4
H3C CH3
( Mesitylene Acid )
(II) Nitration:-
CH3
CH3
O 2N SO 3H
SO 3H 2(HNO3) + 2(H2O) + H2SO4
+ H2SO4 H3C CH3
H3C CH3
NO 2
(III) Reduction:-
CH3 CH3
SO 3H H2 N SO 3H
O 2N
Fe/HCl/H2O
+ Na2CO3 CH3
H3C CH3 H3 C
NO2 NH2
Input KG Output KG
Water 1500
Isolation
Ice 2200
NaOH 150
Nitro slurry
Water 1500
Isolation
Manufacturing process:
Bromammine acid is condense with M. Acid at 8.5 to 9.0pH in presence of copper
oxide & nitrogen gas purging. At 72ͦC slowly by slowly external heating. The
reaction take 12 to 15hrs.check unreacted bromamine content. If nil then charge
common salt & Dicamol & stop stirrer. Filter mass & wash press cake by hot water.
Collect filtrate in another vessel. Charge HCl (30%) to get pH 4.0 to 4.2 to isolate
M-acid. Start filter in F.P. &collect filtrate in another vessel. (Press cake is recover
m-acid use for next batch). Check volume & take pH 1.0 by HCl(30%) charging.
Check spot & startfilter. Give wash of 30% HClsolution gradually.Give slow air &
dump F.P. Cake in vessel with water. Take pH 4.5 by soda ash & spray dryer.
Chemical Reaction:
(I) Bromamine Condensation:-
NH2 SO3H
O
SO3H H3C CH3
+ + CuO + N2 gas + Na2Co3
H2N NH2
O Br CH3
O NH2
SO3Na
CH3
O NH NH2
H3C CH3
SO3Na
( Blue 49 Base )
INPUT KG OUTPUT KG
Water 1800
Slurry
Soda Ash 180
Manufacturing process:
Nitro Benzene reacted with Oleum (65%) at 105 ͦCfor 4 hrs. Maintain Check TLC &
acidity. Then dump S/mass water + lime powder + Soda ash solution slowly at 60
C to 80 C. Take pH 7.0 by lime powder & stir for 1 hrs. Filter slurry in nutch &
wash with hot water. Collect nitro solution. Check N V and real. Then reduction of
nitro solution in presence of iron powder & HCl. Heat mass up to 95 C and check
clear spot and A. R. + B. R. by N. V. ok. Then charge soda ash to get pH 8.5 to
9.0 to –Ve test. Filter mass in F. P. and wash with hot water and receive amino
solution & check N. V. & real charge sulphuric acid slowly to get pH 1.5 Material
isolate. Check F/L & filter slurry in nutch. Then C. F. & Dry in SFD
Chemical Reaction:
(I) Sulphonation:-
NO2
NO2 NO2
H2S2O7 + Na2CO3
+ H2SO4
SO3H
SO3Na
(II) Reduction:-
NO2 NH2
INPUT KG OUTPUT KG
Soda Ash 50
Lime Stone Powder 1100 Drawning CO2 Gas Evap. 150
Water 500
Manufacturing process:
O.N.T. is sulphonated with sulphuric acid (98%) and leum (65%) at 65 C maintain
for 12 hrs. Then S/mass is dilute in water and hydrolyze by NaOH and water. Then
clarify it, isolate material by 70% sulfuric acid then filter & C.F.
Chemical Reaction:
CH 3
CH3 COOH
NO 2
NO 2 NH2
Sulphonation Hydrolysis
+ H2SO 4 + H2SO 4.SO 3
-2SO 3
Sulphuric Acid Oleum
Ortho Nitro Toluene -2H2O
SO 3H SO 3H
Input KG Output KG
O.N.T. 1800
Oleum (65%) 1980 Sulphonation
Sulfuric Acid 1000
Water 3500
Hydrolysis
NaOH 2150
Manufacturing process:
4 Sulpho Anthranilic Acid is diazotize by sodium nitrite and HCl. Then it is coupled
by S. B. S. in presence of C. S. Lye (48%). Then mass is reacting with
benzaldehyde & HCl to get product.
Chemical Reaction:
(I) Diazotisation:-
COOH COOH
NH2 N=NCL
+ NaNo2 + 2(HCl)
SO3H SO3H
(II) Reduction:-
COOH
COOH
NHNH2
N=N-CL + SBS + NaOH
SO 3H
SO 3H
(III) Condensation:-
COOH
COOH CHO
N=N-CH
NHNH2
+
SO3H
SO 3H
(Benzaldehyde)
( 4- Sulpho Hydrozone )
Input KG Output KG
Manufacturing process:
OAVS is sulphonated with Sulphuric acid (98%), oleum (65%) at 140 ͦC then dump
s. mass in cold water below 10 ͦC to 15 ͦC. Then salting by KCl & check F/L& filter &
C.F.
Chemical Reaction:
Sulpho OAVS
(I) Sulphonation:-
NH2 NH2
OCH3
OCH3 H2S2O7
+ H2SO4 HO3S
SO2CH2CH2OSO 3H
SO 2CH2CH2OSO 3H
Sulpho VS
(I) Sulphonation:-
NH2 NH2
H2S2O7 SO3H
+ H2SO4
SO2CH2CH2OSO 3H SO2CH2CH2OSO 3H
( Sulpho V.S )
Sulpho J Acid
(I) Sulphonation:-
OH
OH
H2S2O7
+ H2SO4
H 2N H 2N SO 3H
SO 3H
SO3H
( J. Acid )
( Sulpho J- Acid )
(I) Sulphonation:-
OH OH
NH2 H2S2O7 NH2
+ H2SO4
NO3S HO 3S SO 3H
( Gamma Acid )
( Sulpho Gamma Acid )
Mass Balance:
Mass Balance of Sulfo OAVS
INPUT KG OUTPUT KG
KCl 650
Water 1500 Dumping
Ice 2500
Manufacturing process:
Benzoic acid is nitrated in presence of Nitric acid & Sulphuric acid. When reaction
over transfer n/mass in water & isolated. Filter & C.F. Then reduction of nitro
compound in presence of iron powder &HCl (30%). Then maintain temp up to
reduction over. When reduction overcharge soda ash to -ve iron test. Then filter
mass in F.P. & wash with water. Collect amino in isolation vessel. Isolate by HCl
(30%) &filter & get final product.
Chemical Reaction:
(I) Nitration:-
COOH COOH
HNO3
+
H2SO4
O 2N NO2
(II) Reduction:-
COOH
COOH
Fe/HCl/H2O
+ H2 N
Na2CO3 NH2
O 2N NO2
( 3:5 DABA )
INPUT KG OUTPUT KG
Water 2500
Drawning
Filtration &
Centrifuge
Soak pit
4.0
7.0
Boiler Cooling
SBS (30-35%)
10.0 40
25
4.0 Steam
Ice 30
Water
retained with
RM 71
Spray drying 10
Drying
for product Bleed
Loss 39 3.0
recovery off
77
ETP
77+ 3.0 + 25.0 +25.0 + 1.0+ 10 =141
Permeates
RO water 85.0*
141
Evaporation Salt
Spray Dryer
loss 54.25 1.75
56.0