Title of Invention

A PROCESS FOR THE MANUFACTURE OF ACTIVE CARBON FROM COKE BREEZE

Abstract This invention describes a process for the manufacture of active carbon from coke breeze in a fluid bed reactor, pre-heated at 600 degree Celsius, allowing the temperature of the reactor, containing crushed and screened coke breeze, to rise steadily to 900 degree Celsius, injecting superheated steam from below the reactor, allowing the carbon materials to remain in a fluidized state for a time period in the range of 1 to 2 hours. After the activation period is over, the reactor is allowed to cool down to 350 degree Celsius. The product is discharged after adjusting the pH between 6.5-7.0 by known methods. The active carbon so obtained is useful for removing toxicants from effluent water from coke plants 13
Full Text The present invention relates to a process for the manufacture of active carbon from coke breeze.
This invention particularly relates to preparation of highly porous, relatively dense active carbon from comparatively cheap raw material like coke breeze, abundantly available from coke oven plants, for removal of toxicants from effluent water of coke plants.
This invention finds its usage in removing toxicants from effluent water from coke oven plants. In this invention, active carbon obtained from relatively cheap raw materials like coke breeze, which is abundantly available from coke oven plants, is used and at the same time environmental pollution hazard is controlled unlike other conventional raw materials and impregnation methods.
High quality activated carbon is required for decolourising purposes in sugar industry, oil industry, alcoholic beverages, pharmaceutical indusl Itry and for gas & vapour adsorbing purposes in gas mask industry and environmental pollution control measures and in recent times for industrial waste water treatment purposes as well as in the processing of drinking water. Indian cokeries produce significant amount of coke breeze. The use of coke breeze is very limited. It is used in sintering as well as for the production of briquettes. Coke producing industry is facing acute problems for marketing the coke breeze. The market demand for coke breeze in India is 1,35,000 metric tons against present installed capacity of 75000 metric tons.
In recent times, active carbon is being used for removal of toxic organic substances from mine water, waste water etc. While conventional waste water treatment methods, such as ion exchanges, reverse osmosis, chemical oxidation, precipitation and gas tripping are effective in removing toxicants, application of granular activated carbon has good scope, particularly in areas like regeneration, more efficient and low cost technology, adsorbate recovery and reuse and prediction of application in waste water treatment. In view of acute shortage of drinking water supply in rural and urban areas and constant pollution of surface water by discharge of toxic industrial effluents, the present process is amply relevant and justified.
partitioning volatile organic contaminants between a liquid phase and a gas phase. In yet a further embodiment, the above versions of the invention are simultaneously performed in the same reaction vessel.

In the above prior art processes, active carbon from coke breeze was not used. Coke breeze, a waste material, was unused for the purpose of manufacturing active carbon, useful for removal of toxicants from effluent water.
The main object of the invention is to provide a process for the manufacture of active carbon from coke breeze, useful for removal of toxicants from effluent water of coke plants which obviates the drawbacks as detailed above.
Another object of the invention is to prepare a highly porous, relatively dense active carbon from comparatively cheap raw material like coke breeze, abundantly available from coke oven plants, for removal of toxicants from effluent water of coke plants. Still another object of the invention is to provide pollution free process for preparation of active carbon from coke breeze.
This invention describes a process for the manufacture of active carbon from coke breeze in a fluid bed reactor, pre-heated at 600 degree Celsius, allowing the temperature of the reactor, containing crushed and screened coke breeze, to rise steadily to 900 degree Celsius, injecting superheated steam from below the reactor, allowing the carbon materials to remain in a fluidised state for a time period in the range of 1 to 2 hours. After the activation period is over, the reactor is allowed to cool down to 350 degree Celsius. The product is discharged after adjusting the pH between 6.5-7.0 by known methods. The active carbon so obtained is useful for removing toxicants from effluent water from coke plants
Accordingly the present invention provides a process for the manufacture of active carbon, which comprises (a) crushing coke breeze to -6+14 BSS size in a crusher; (b) charging the screened material into a fluid bed reactor, preheated at 600 degree Celsius; (c) allowing the temperature of the reactor to rise steadily till it reaches 900 degree Celsius; (d) injecting superheated steam from below the reactor; (e) allowing the carbon
materials to remain in a fluidised state for a time period in the range of 1 to 2 hours, maintaining the temperature of the reactor at a temperature in the range of 900 to 920 degree Celsius; (f) after the activation period is over, allowing the reactor temperature to cool till the temperature comes down to 350 degree Celsius and discharging the product after adjusting the pH between 6.5-7.0 by known methods.
In an embodiment of the present invention the reactor is cooled by quenching by ice.
The novelty of the present invention resides with obtaining active carbon from coke breeze, under environment friendly conditions in comparison to available prior art, for removing toxicants from effluent water of coke plants, which was other wise was not utilised for economic reasons by this process active carbon is obtained from a waste product such as coke breeze and the active carbon so obtained can be used for converting waste water into potable water.
The following examples are given by way of illustration of the present invention and should not be construed to limit the scope of the present invention.
Example-1
160 grams of coke breeze was crushed and sized to -6+14 BSS. The screened material was then charged into a fluid bed reactor, which was pre-heated to 600 degree Celsius. The temperature of the reactor was allowed to increase steadily to 900 degree Celsius, after which superheated steam was injected from below the reactor and carbon materials were allowed to remain in fluidised state for one hour. After the activation period was over, the reactor temperature was cooled down by steam quenching till the reactor temperature reaches 350 degree Celsius. The product was taken out and pH was adjusted to 6.7. The yield was 78%. The product was used for effluent water purification.

Analysis of coke plant effluent before and after treatment with active carbon obtained
from coke breeze:
Parameters
Analysed
Phenol
Oil & Grease
Iron
Concentration
in the effluent
before
treatment (ppm)
1037.5
326.0
5.0
Concentration
in the effluent
after treatment
(ppm)
37.0
22.8
Below
detectable limit
% Removal
96.43
93.0
100.0
Example-2
160 grams of coke breeze was crushed and sized to -6 to +14 BSS. The screened material
was then charged into a fluid bed reactor, which was pre-heated to 600 degree Celsius.
The temperature of the reactor was allowed to increase steadily to 900 degree Celsius,
after which superheated steam was injected from below the reactor and carbon materials
were allowed to remain in fluidised state for one and half hours. After the activation
period was over, the reactor temperature was cooled down by steam quenching till the
reactor temperature reaches 350 degree Celsius. The product was taken out and pH was
adjusted to 6.8. The yield was 63%. The product was used for effluent water purification.
Analysis of coke plant effluent before and after treatment with active carbon obtained
from coke breeze:
Parameters anlysed
Phenol
Oil & Grease
Iron
Concentration in the
effluent before
treatment (ppm)
1013.12
359.0
5.8
Concentration in the
effluent after
treatment (ppm)
30.19
10.0
0.1
% Removal
97.02
97.21
98.28
Example-3
160 grams of coke breeze was crushed and sized to -6 to +14 BSS. The screened
material was then charged into a fluid bed reactor, which was pre-heated to 600 degree
Celsius. The temperature of the reactor was allowed to increase steadily to 900 degree
Celsius, after which superheated steam was injected from below the reactor and carbon
materials were allowed to remain in fluidised state for two hours. After the activation
period was over, the reactor temperature was cooled down by steam quenching till the
reactor temperature reaches 350 degree Celsius. The product was taken out and pH was
adjusted to 6.8. The yield was 59%. The product was used for effluent water purification.
Parameters analysed
Phenol
Oil & Grease
Iron
Concentration in the
effluent before
treatment ( ppm)
897.91
413.0
4.6
Concentration in the
effluent after
treatment ( ppm)
13.33
8.20
0.1
% Removal
98.52
98.01
97.83
Typical Results and evaluation characteristics of the products of the different examples
cited
Table-1
Adsorption
Qualities
Methylene Blue
Adsorption
(mg/g)
Iodine
Adsorption
(mg/g)
Phenol
Adsorption(%)
Example- 1
(one hour)
38.4
226.96
99.9
Example-2
(one & half
hours)
37.0
220.83
99.8
Example-3
(two hours)
38.4
220.82
99.34
Table-2
Other characteristics
pH value
Bulk density(kg/ltr)
Moisture(%)
Ash(%)
Volatile Matter (%)
Fixed Carbon(%)
Example- 1
6.7
0.64
1.7
15.2
1.3
81.8
Example-2
6.8
0.49
1.5
16.8
1.0
80.7
Example-3
6.8
0.48
-
--
-
10
The main advantages of the present invention are:
1. The adsorbate can be removed from liquid streams without significant expenditure.
2. The raw material is easily available from coke oven industries and at comparatively
cheaper price.
3. The yield of product is much higher than any other raw materials.
4. Conventional chemical impregnation step can be avoided, there by pollution is
controlled.
5. Since active carbon obtained from the process is highly porous, degradation of
particles during handling is much less.




We claim:
1. A process for the manufacture of active carbon from coke breeze, which comprises the steps of:
a. crushing coke breeze to -6 to +14 British Standard Sieve (BSS) in a
crusher to screen the material;
b. charging the screened material as obtained in step (a) into a fluid bed
reactor which has been preheated to 600 degree Celsius;
c. allowing the temperature to rise steadily till it reaches 900 degree Celsius;
d. injecting superheated steam from below the reactor;
e. allowing the carbon materials to remain in a fluidized state for a time
period in the range of 1 to 2 hours, maintaining the temperature in the
range of 900 to 920 degree Celsius;
f. allowing the reactor temperature to cool till the temperature comes down
to 350 degree Celsius and discharging the product after adjusting the pH
between 6.5 to 7.
2. A process as claimed in claim 1, wherein the reactor is cooled by quenching with ice.

Documents:

334-DEL-2002-Abstract-(17-10-2008).pdf

334-del-2002-abstract.pdf

334-DEL-2002-Claims-(17-10-2008).pdf

334-del-2002-claims.pdf

334-DEL-2002-Correspondence-Others-(17-10-2008).pdf

334-del-2002-correspondence-others.pdf

334-del-2002-correspondence-po.pdf

334-DEL-2002-Description (Complete)-(17-10-2008).pdf

334-del-2002-description (complete).pdf

334-DEL-2002-Form-1-(17-10-2008).pdf

334-del-2002-form-1.pdf

334-DEL-2002-Form-18-(17-10-2008).pdf

334-del-2002-form-18.pdf

334-DEL-2002-Form-2-(17-10-2008).pdf

334-del-2002-form-2.pdf

334-del-2002-form-3.pdf


Patent Number 225782
Indian Patent Application Number 334/DEL/2002
PG Journal Number 01/2009
Publication Date 02-Jan-2009
Grant Date 28-Nov-2008
Date of Filing 27-Mar-2002
Name of Patentee COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH
Applicant Address RAFI MARG, NEW DELHI-110 001, INDIA.
Inventors:
# Inventor's Name Inventor's Address
1 SATINATH MAZUMDAR CENTRAL FUEL RESEARCH INSTITUTE, P.O. F.R.I.-828108, DHANBAD, JHARKHAND, INDIA.
2 JANARDAN SINGH CENTRAL FUEL RESEARCH INSTITUTE, P.O. F.R.I.-828108, DHANBAD, JHARKHAND, INDIA.
3 SIBENDRA KUMAR BASU CENTRAL FUEL RESEARCH INSTITUTE, P.O. F.R.I.-828108, DHANBAD, JHARKHAND, INDIA.
4 PRADIP BHATTACHARYA CENTRAL FUEL RESEARCH INSTITUTE, P.O. F.R.I.-828108, DHANBAD, JHARKHAND, INDIA.
5 KALYAN SEN CENTRAL FUEL RESEARCH INSTITUTE, P.O. F.R.I.-828108, DHANBAD, JHARKHAND, INDIA.
PCT International Classification Number C01B 31/08
PCT International Application Number N/A
PCT International Filing date
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 NA