Indirect Aqueous Mineral Carbonation of Samples of Linz–Donawitz Slag from the Steel Industry in Eastern IndiaSource: Journal of Hazardous, Toxic, and Radioactive Waste:;2023:;Volume ( 027 ):;issue: 004::page 04023031-1Author:Sasmita Chand
,
Soubhagya Keshari Chand
,
Biswajit Paul
,
Manish Kumar
,
Prangya Ranjan Rout
DOI: 10.1061/JHTRBP.HZENG-1203Publisher: ASCE
Abstract: In this study, aqueous mineral carbonation of Linz–Donawitz (LD) slag waste from Rourkela, Bokaro, and Tata steel industries was undertaken at a room temperature of 30°C and elevated CO2 pressure (9 bar) to assess the feasibility and quantification of carbonation primarily as CaCO3. Also, the effect of physical, i.e., sonication (40 kHz) and chemical activation (1 M NH4Cl, CH3COONH4, and NH4NO3) on calcium dissolution/extraction and its carbonation was compared with control, i.e., without chemical activators. Calcium dissolution from LD slag samples (solid:liquid ratio 1 g/50 mL) showed a significant increase in all samples, i.e., 23.92, 25.60, and 20.90 mg/L for Rourkela, Bokaro, and Tata LD slag samples, respectively. XRD and FTIR analyses of carbonated LD slag residue confirmed calcite formation. Thermal gravimetric analysis/differential scanning calorimetry analysis of carbonated samples showed a relatively high degree of carbonation for the Rourkela, Bokaro, and Tata LD slag samples with chemical activators, CH3COONH4 (56%), NH4NO3 (55%), and control (48%), respectively. The present work estimates CO2 capture in LD slag samples to be 0.126, 0.084, and 0.153 kg/kg, respectively. The research findings highlight the scope of mineral carbonation of LD slag samples at relatively low pressure and temperature using physical and chemical activators.
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contributor author | Sasmita Chand | |
contributor author | Soubhagya Keshari Chand | |
contributor author | Biswajit Paul | |
contributor author | Manish Kumar | |
contributor author | Prangya Ranjan Rout | |
date accessioned | 2023-11-27T23:30:43Z | |
date available | 2023-11-27T23:30:43Z | |
date issued | 10/1/2023 12:00:00 AM | |
date issued | 2023-10-01 | |
identifier other | JHTRBP.HZENG-1203.pdf | |
identifier uri | http://yetl.yabesh.ir/yetl1/handle/yetl/4293617 | |
description abstract | In this study, aqueous mineral carbonation of Linz–Donawitz (LD) slag waste from Rourkela, Bokaro, and Tata steel industries was undertaken at a room temperature of 30°C and elevated CO2 pressure (9 bar) to assess the feasibility and quantification of carbonation primarily as CaCO3. Also, the effect of physical, i.e., sonication (40 kHz) and chemical activation (1 M NH4Cl, CH3COONH4, and NH4NO3) on calcium dissolution/extraction and its carbonation was compared with control, i.e., without chemical activators. Calcium dissolution from LD slag samples (solid:liquid ratio 1 g/50 mL) showed a significant increase in all samples, i.e., 23.92, 25.60, and 20.90 mg/L for Rourkela, Bokaro, and Tata LD slag samples, respectively. XRD and FTIR analyses of carbonated LD slag residue confirmed calcite formation. Thermal gravimetric analysis/differential scanning calorimetry analysis of carbonated samples showed a relatively high degree of carbonation for the Rourkela, Bokaro, and Tata LD slag samples with chemical activators, CH3COONH4 (56%), NH4NO3 (55%), and control (48%), respectively. The present work estimates CO2 capture in LD slag samples to be 0.126, 0.084, and 0.153 kg/kg, respectively. The research findings highlight the scope of mineral carbonation of LD slag samples at relatively low pressure and temperature using physical and chemical activators. | |
publisher | ASCE | |
title | Indirect Aqueous Mineral Carbonation of Samples of Linz–Donawitz Slag from the Steel Industry in Eastern India | |
type | Journal Article | |
journal volume | 27 | |
journal issue | 4 | |
journal title | Journal of Hazardous, Toxic, and Radioactive Waste | |
identifier doi | 10.1061/JHTRBP.HZENG-1203 | |
journal fristpage | 04023031-1 | |
journal lastpage | 04023031-11 | |
page | 11 | |
tree | Journal of Hazardous, Toxic, and Radioactive Waste:;2023:;Volume ( 027 ):;issue: 004 | |
contenttype | Fulltext |