Preparation of Calcium Silicate Absorbent from Iron Blast Furnace Slag

2000 ◽  
Vol 50 (9) ◽  
pp. 1655-1662 ◽  
Author(s):  
Lia F. Brodnax ◽  
Gary T. Rochelle
2008 ◽  
Vol 368-372 ◽  
pp. 1548-1551
Author(s):  
Guo Zhuo Gong ◽  
Shu Feng Ye ◽  
Feng Li ◽  
Yan Bin Cui ◽  
Ya Jun Tian ◽  
...  

A series of sorbents for SO2 in flue gas were prepared from hydrated lime and blast furnace slag using a factorial experiment design. It is found that the reaction between hydrated lime and blast furnace slag is fast. The reactivities of the as-prepared sorbents are higher than those of hydrated lime alone due to the formation of calcium silicate hydrates, and hence the utilization of hydrated lime as well as the Ca in the blast furnace slag is improved. Furthermore, the effects of preparation variables on the reactivity of the sorbents are also discussed.


2009 ◽  
Vol 405-406 ◽  
pp. 142-148
Author(s):  
Dong Min Wang ◽  
Yan Feng Zuo ◽  
Wei Feng Xiong

Naphthalene sulfate based superplasticizer and poly carboxylate superplasticizer (characterized by different polymerization of graft chain and backbone chain, different reaction temperature and different carboxyl/graft chain ratio) were applied to investigate their influences on fluidity of mineral admixtures (fly ash, granulated ground iron blast furnace slag, silica fume) -Portland cement-water system.


Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4787
Author(s):  
Junho Kim ◽  
Seunghyun Na ◽  
Yukio Hama

The frost damage resistance of blast-furnace slag (BFS) cement is affected by carbonation. Hence, this study investigates the carbonation properties of pastes incorporating BFS with different replacement ratios, such as 15%, 45%, and 65% by weight, and different curing conditions, including air and carbonation. The BFS replacement ratio properties, determined by the Ca/Si ratio of calcium silicate hydrate in the cement paste sample, were experimentally investigated using mercury intrusion porosimetry, X-ray diffraction, and thermal analysis. The experimental investigation of the pore structure revealed that total porosity decreased after carbonation. In addition, the porosity decreased at a higher rate as the BFS replacement rate increased. Results obtained from this study show that the chemical change led to the higher replacement rate of BFS, which produced a higher amount of vaterite. In addition, the lower the Ca/Si ratio, the higher the amount of calcium carbonate originating from calcium silicate hydrate rather than from calcium hydroxide. As a result of the pore structure change, the number of ink-bottle pores was remarkably reduced by carbonation. Comparing the pore structure change in air-cured and carbonation test specimens, it was found that as the replacement rate of BFS increased, the number of pores with a diameter of 100 nm or more also increased. The higher the replacement rate of BFS, the higher the amount of calcium carbonate produced compared with the amount of calcium hydroxide produced during water curing. Due to the generation of calcium carbonate and the change in pores, the overall number of pores decreased as the amount of calcium carbonate increased.


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