Phosphorus adsorption efficiency and characteristic analysis of basic oxygen furnace slag

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL International Journal of Chemical Kinetics Pub Date : 2023-06-13 DOI:10.1002/kin.21673
Shu-Lung Kuo, Ching-Lin Ho, I-Chan Kao
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Abstract

A large amount of furnace slag is produced from steelmaking every year. The resultant by-products will severely damage the natural environment and ecosystems if not treated properly. Businesses worldwide have thus been striving for slag recycling and solving various complex problems. In this study, basic oxygen furnace slag (BOFS) was regarded as an adsorbent to adsorb phosphate in water. In addition to a physical–chemical property analysis of the by-products, the present study explored the performance of basic oxygen furnace slag in adsorbing phosphorous (P) with different size settings, and observed the surface structure of fused basic oxygen furnace slag.The results revealed that free-state Ca accounts for the majority in basic oxygen furnace slag content, demonstrating the removal of nearly all phosphorous in water. The results of Fourier-transform infrared spectroscopy (FT-IR) on basic oxygen furnace slag with >200 mesh size revealed complex wave crests at the fingerprint region (570–980 cm−1). The result signifies that the basic oxygen furnace slag samples comprise strong Si─O and O─Si─O bonds within silicate minerals. Moreover, basic oxygen furnace slag samples with a particle size >200 mesh contain very high content of lime (CaO) (reaching 49.5%). This property fully demonstrates that basic oxygen furnace slag samples in a small particle size were more active as an aggregate. This study found that the Langmuir adsorption isotherm model (R2 = 0.997) is slightly better than the Freundlich adsorption isotherm model (R2 = 0.984), which shows that the process in which basic oxygen furnace slag adsorbs P is monolayer adsorption, and the adsorption energy is more uniformly distributed among BOFS samples. This study also found that basic oxygen furnace slag samples melted at 1200°C can effectively encapsulate some heavy metal pollutants and form stable glassy slag. The change proved that a fused basic oxygen furnace slag sample could effectively encapsulate heavy metal pollutants and formed glassy-state slag with high stability. This mechanism would reduce the likelihood of heavy metal leaching when basic oxygen furnace slag serves as a subgrade aggregate, permeable material, or concrete aggregate in the future.

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碱性氧炉渣对磷的吸附效率及特性分析
炼钢每年产生大量的炉渣。由此产生的副产品如果处理不当,将严重破坏自然环境和生态系统。因此,世界各地的企业都在努力实现渣的回收利用,解决各种复杂的问题。本研究以碱性氧炉渣(BOFS)为吸附剂吸附水中的磷酸盐。本研究除了对副产物进行理化性质分析外,还探讨了不同粒度设置下碱性氧炉渣对磷的吸附性能,并观察了熔融碱性氧炉渣的表面结构。结果表明,游离态Ca在碱性氧炉渣中占大部分,表明水中磷几乎全部去除。对200目碱性氧炉渣进行傅里叶变换红外光谱(FT-IR)分析,发现指纹区(570 ~ 980 cm−1)有复杂的波峰。结果表明,碱性氧炉渣样品在硅酸盐矿物中存在很强的Si─O键和O─Si─O键。此外,粒径为200目的碱性氧炉渣样品中石灰(CaO)含量非常高,达到49.5%。这一特性充分说明,小粒度的碱性氧炉渣样品作为集料具有更高的活性。本研究发现Langmuir吸附等温线模型(R2 = 0.997)略优于Freundlich吸附等温线模型(R2 = 0.984),说明碱性氧炉渣吸附P的过程为单层吸附,吸附能在BOFS样品间分布更为均匀。本研究还发现,1200℃熔炼的碱性氧炉渣样品能有效封装部分重金属污染物,形成稳定的玻璃状炉渣。这一变化证明了熔融碱性氧炉渣试样能有效封装重金属污染物,形成稳定性高的玻璃态炉渣。这一机制将减少将来碱性氧炉渣作为路基骨料、透水材料或混凝土骨料时重金属浸出的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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