Thin-film versus slurry-phase carbonation of steel slag: CO2 uptake and effects on mineralogy

被引:105
作者
Baciocchi, R. [1 ]
Costa, G. [1 ]
Di Gianfilippo, M. [1 ]
Polettini, A. [2 ]
Pomi, R. [2 ]
Stramazzo, A. [2 ]
机构
[1] Univ Roma Tor Vergata, Dept Civil Engn & Comp Sci Engn, Lab Environm Engn, I-00133 Rome, Italy
[2] Univ Roma La Sapienza, Dept Civil & Environm Engn, I-00184 Rome, Italy
关键词
Steel slag; Accelerated carbonation; CO2; uptake; Conversion yield; Mineralogical characterization; BASIC OXYGEN FURNACE; METALWORKING WASTE-WATER; GAS-SOLID CARBONATION; ACCELERATED CARBONATION; STEELMAKING SLAGS; SEQUESTRATION; DIOXIDE; STORAGE; CAPTURE;
D O I
10.1016/j.jhazmat.2014.09.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The results of direct aqueous accelerated carbonation of three types of steel manufacturing residues, including an electric arc furnace (EAF) slag and two basic oxygen furnace (BOF) slags, are reported. Batch accelerated carbonation tests were conducted at different temperatures and CO2 pressures applying the thin-film route (liquid to solid, LIS, ratio = 0.3 L/kg) or the slurry-phase route (LIS ratio =5 L/kg). The CO2 uptake strongly depended on both the slag characteristics and the process route; maximum yields of 280 (EAF), 325 (BOF1) and 403 (BOF2) gCO(2)/kg slag were achieved in slurry phase at T= 100 degrees C and PCO2 = 10 bar. Differently from previous studies, additional carbonates (other than Ca-based phases) were retrieved in the carbonated BOF slags, indicating that also Mg-, Fe-and Mn-containing phases partially reacted with CO2 under the tested conditions. The results hence show that the effects of accelerated carbonation in terms of CO2 uptake capacity, yield of mineral conversion into carbonates and mineralogy of the treated product, strongly rely on several factors. These include, above all, the mineralogy of the original material and the operating conditions adopted, which thus need specific case-by-case optimization to maximize the CO2 sequestration yield. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:302 / 313
页数:12
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