Document Type
Article
Source of Publication
Energy Reports
Publication Date
9-1-2021
Abstract
In this work, carbon dioxide uptake value by acetylene by-products was evaluated through two types of carbonation reactions. In the first reaction, solid acetylene by-products were reacted with a simulated effluent CO2 gas (10% CO2 and 90% air) and the maximum uptake value of carbon dioxide per unit mass of reacted solids was calculated. In the second reaction, the mixed solid acetylene by-product with distilled water at a specific mass to volume ratio was reacted with the same effluent CO2 gas to compare the maximum CO2 uptake value with the first reaction. It was found that a superior CO2 uptake in the case of G-S-L reaction with a value of 0.34 g CO2/g ABP over that found in the case of G-S system of 0.14 g CO2/g ABP. The fresh (unreacted) and treated acetylene by-products from both reactions were analyzed to study the effect of carbonation process on solids morphology, average particle size and carbon content. The structural and chemical characteristics of the fresh and carbonated acetylene by-products were investigated using X-ray diffraction, scanning electron microscopy and thermogravimetric analysis. The fresh acetylene by-products showed a major structure of portlandite crystals. All carbonated products exhibited a calcite crystal structure but with different morphology and particle size for each specific chemical reaction.
DOI Link
ISSN
Publisher
Elsevier
Volume
7
First Page
193
Last Page
198
Disciplines
Engineering
Keywords
Acetylene by-products, Carbonation, CO2uptake value, Solid waste, Waste utilization
Scopus ID
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
Recommended Citation
El Gamal, Maisa; Mohammad, Ameera; Hameedi, Suhaib; and AlZawahreh, Hadeel, "Carbon dioxide uptakes by acetylene by-products through gas–solid and gas–solid–liquid reactions" (2021). All Works. 4576.
https://zuscholars.zu.ac.ae/works/4576
Indexed in Scopus
yes
Open Access
yes
Open Access Type
Gold: This publication is openly available in an open access journal/series