Topic: Catalytic Wet Air Oxidation: Dept. of Chemical Engineering IIT Delhi
Topic: Catalytic Wet Air Oxidation: Dept. of Chemical Engineering IIT Delhi
Topic: Catalytic Wet Air Oxidation: Dept. of Chemical Engineering IIT Delhi
To perform catalytic wet air oxidation of a multicomponent reactant. To go through literature and find suitable catalyst and conditions for the reaction. To find temperature and other conditions optimum for the reaction To understand the Deactivation rate and methods to regenerate the catalyst
Involves the liquid phase oxidation of organic or oxidizable inorganic components . Complex organic compounds are mostly oxidized into carbon dioxide and water along with simpler forms .
Useful when concentration of organic pollutant are too low or when organic pollutant are toxic
2 11 1 4 10 5
Based on oxidation of carbon of organic matter to carbon dioxide Carbon dioxide is swept into a non dispersive infrared analyzer Steam is condensed and removed Includes both organic and inorganic carbon in the sample Sample Injected : 100 microlitres Temperature : 8000C T.O.C. for the sample : 133.2 mg/ltr
Sample : Organic Raffinate Temperature : 100C Air flow rate : 2 ltr/min Initial T.O.C : 133.2 mg/ltr
Time (hr)
1 2 3 4 5
T.O.C (mg/ltr)
118.67 108.43 96.27 87.48 78.09
Experiment 1: Temperature 10 0C
140
120
T.O.C (mg/ltr)
100
80
60
40
20
0 0 1 2 3 4 5 6
Time (hr)
Sample : Organic Raffinate Temperature : 300C Air flow rate : 2 ltr/min Initial T.O.C : 133.2 mg/ltr
Time (hr)
1 2 3 4 5
T.O.C (mg/ltr)
109.67 102.45 91.42 81.28 69.32
Experiment 2: Temperature 30 0C
140
120
100
T.O.C (mg/ltr)
80
60
40
20
0 0 1 2 3 4 5 6
Time (hr)
Sample : Organic Raffinate Temperature : 700C Air flow rate : 2 ltr/min Initial T.O.C : 133.2 mg/ltr
Time (hr)
1 2 3 4 5
T.O.C (mg/ltr)
105.9 93.11 82.55 74.25 52.63
Experiment 3 : Temperature 70 0C
140
120
100
T.O.C (mg/ltr)
80
60
40
20
0 0 1 2 3 4 5 6
time (hr)
100
T.O.C (mg/ltr)
80
60
40
20
0 0 1 2 3 4 5
Time (hr)
Sample : Organic Raffinate Temperature : 300C Catalyst : Alumina ( 2 g/ltr) Air flow rate : 2 ltr/min Initial T.O.C : 133.2 mg/ltr
Time (hr)
1 2 3 4 5
T.O.C (mg/ltr)
107.63 101.08 87.49 77.28 66.32
120
100
T.O.C (mg/L)
80
60
Using Alumina
40
20
0 0 1 2 3 4 5
time (hr)
Calculations
Total Alumina taken - 10 gram
Sample : Organic Raffinate Temperature : 300C Catalyst : Pt/Alumina ( 2 g/ltr) Air flow rate : 2 ltr/min Initial T.O.C : 133.2 mg/ltr
Time (hr)
1 2 3 4 5
T.O.C (mg/ltr)
102.32 90.58 79.44 68.79 59.26
Experiment 5
Experiment : Using Pt/alumina
140
120 100 80 60 40 20 0 0 1 2 3 4 5 With Pt/alumina
T.O.C (mg/ltr)
Time (hr)
Comparison at 30C
Comparison :
140
120
80
T.O.C with Alumina T.O.C. without catalyst T.O.C with pt/Alumina catalyst
60
40
20
0 0 1 2 3 4 5
1.
2.
Catalytic Wet Air Oxidation Catalytic wet air oxidation at different temperature using Pt/Alumina catalyst Wet air oxidation of the sample using catalyst like ceria with platinum
1.
Characterization
Physical properties like EDX, Metal dispersion, surface area, pore area
1.
2.
Deactivation Deactivation of supported metals by carbon or coke may occur chemically owing to chemisorptions or carbide formation or physically and mechanically Blocking of surface sites, metal crystallite encapsulation, plugging of pores, and destruction of catalyst pellets by carbon laments Regeneration Carbon and coke formation is relatively easily reversed through gasication with hydrogen, water, or oxygen
1.
Compared to conventional wet oxidation, catalytic wet oxidation offers lower energy requirements and much higher oxidation efficiencies Literature only shows catalytic wet air oxidation of single component reactant Result would be compared on the basis of T.O.C. rather than conversion; leading to better results
LITERATURE REVIEW
Presently reading the following manuscripts:
Mishra et al. (1995) Wet Air Oxidation.
Luck(1996) A review of industrial catalytic wet air oxidation process J. Levec and A. Pintar. Catal. Today 24 (1995) M. J. Dietrich et al. (1996) Wet Air Oxidation of Hazardous Oraanics in Wastewater. F. Luck (1994) Wet air oxidation: past, present and future.