ISSN: 0256-1115 (print version) ISSN: 1975-7220 (electronic version)
Copyright © 2024 KICHE. All rights reserved

Articles & Issues

Language
English
Conflict of Interest
In relation to this article, we declare that there is no conflict of interest.
Publication history
Received February 8, 2017
Accepted August 15, 2017
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright © KIChE. All rights reserved.

All issues

Preparation and characterization of a porous silicate material from silica fume

College of Chemical Engineering, Inner Mongolia University of Technology, Hohhot, 010051 China
pzqm163@163.com
Korean Journal of Chemical Engineering, December 2017, 34(12), 3185-3194(10), 10.1007/s11814-017-0228-5
downloadDownload PDF

Abstract

A porous silicate material derived from silica fume was successfully prepared and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FT-IR) spectroscopy, Thermogravimetry and Differential thermal gravity (TG-DTG), N2 adsorption and desorption isotherms, and scanning electron microscopy (SEM). Raw silica fume was analyzed by XRD, FT-IR and SEM. The analysis results of silica fume indicated that SiO2 in silica fume is mainly determined as amorphous state, and that the particles of raw silica fume exhibited characteristic spherical structure with a diameter of from 50 nm to 200 nm. The preparation of the porous silicate material involved two steps. The first step was the extraction of the SiO3 2- leachate from raw silica fume. The maximum value of SiO3 2- extraction yield was obtained under the following conditions: reaction temperature of 120 °C, reaction time of 120 min, NaOH concentration of 15%, and alkali to SiO2 molar ratio of 2. The second step was the preparation of the porous silicate material though the reaction of SiO3 2- leachate and Ca(OH)2 suspension liquid. The optimum preparation conditions were as follows: preparation temperature of 90 °C, preparation time of 1.5 h, Si/Ca molar ratio of 1 : 1, and stirring rate of 100 r/min. The BET surface area and pore size of the porous silicate material were 220.7m2·g-1 and 8.55 cm3/g, respectively. The porous silicate material presented an amorphous and unordered structure. The spectroscopic results indicated that the porous silicate material was mainly composed of Si, Ca, O, C, and Na, in the form of Ca2+, SiO3 2-, CO3 2- and Na+ ions, respectively, which agreed with the XRD, TG-DSC, and FT-IR data. The N2 adsorption-desorption isotherm mode indicates that the porous silicate material belonged to a typical mesoporous material. The porous silicate material presented efficiency for the removal of formaldehyde: it showed a formaldehyde adsorption capacity of 8.01mg/g for 140 min at 25 °C.

References

Li X, Korayem AH, Li C, Liu Y, He H, Sanjayan JG, Duan WH, Constr Build Mater., 123 (2016).
Jinliang Z, Zhancheng G, Xin Z, Huiqing T, Chin. J. Pro. Eng., 12 (2012).
Zhou C, Yan C, Zhao J, Wang H, Zhou Q, Luo W, J. Taiwan. Inst. Chem. E, 62 (2016).
Ji H, Huang Z, Chen K, Li W, Gao Y, Fang M, Liu Y, Wu X, Powder. Technol., 252 (2014).
Mastali M, Dalvand A, Constr. Build. Mater., 125 (2016).
Fakhri M, Saberi F. K, J. Clean. Prod., 129 (2016).
Ramezanianpour AA, Springer Berlin Heidelberg, 193 (2014).
Lijuan L, Tielong L, Zhaohui J, Chin. J. Enviro. Eng., 4 (2010).
Lilkov V, Petrov O, Kovacheva D, Rostovsky I, Tzvetanova Y, Petkova V, Petrova N, Constr. Build. Mater., 124 (2016).
Okoye FN, Durgaprasad J, Singh NB, Ceram. Int., 42 (2016).
Gaoping H, Weidong X, Henan. Chem. Ind., 07 (2006).
Deyi Z, Huixia F, Heming L, Yi W, Xuefu C, Yanjun W, Chin. Non-Metallic. Miner. Ind., 5 (2009).
Li W, Ping X, Xu Y, Li H, Yi Z, Tang Y, Concrete., 6 (2011).
Zhu H, Shandong University of Science and Technology Doctor Degree (2009).
Hai H, Zhang Y, Zhang Y, Sun J, Hao Z, Chin. J. Enviro. Eng., 11 (2017).
Zhang J, Guo Z, XZ, HT, Chinese J. Environ. Eng., 12, 2 (2012)
Azouaoua N, Sadaou Z, Djaafri A, et al., J. Hazar. Mater., 184 (2010).
Anirudhan T S, RadhakrishLnan P G, Thermodynamics., 40 (2008).
Langmuir I, J. Am. Chem. Soc., 40, 1361 (1918)
Onisei S, Pontikes Y, Gerven TV, Angelopoulos GN, Velea T, Predica V, Moldovan P, J. Hazard. Mater., 101 (2012).
Gao Y, Huang H, Tang W, Liu X, Yang X, Zhang J, Micropor, Mesopor. Mater., 217 (2015).
Maximo GJ, Meirelles AJA, Batista EAC, Fluid Phase Equilibr., 299 (2010).
Wang R, Zhai Y, Ning Z, Ma P, T Nonferr Metal Soc., 24 (2014).
Yadav RR, Mudliar SN, Shekh AY, Fulke AB, Devi SS, Krishnamurthi K, Juwarkar A, Chakrabarti T, Process Biochem., 47 (2012).
Sun J, Wu Z, Cheng H, Zhang Z, Frost RL, Spectro. Act. Part A: Mole. and Biomo. Spec., 117 (2014).
Yang X, Liu X, Tang W, Gao Y, Ni H, Zhang J, Korean J. Chem. Eng., 34, 3 (2017)
Li L, Zhang Y, Zhang Y, Sun J, Hao Z, J. Therm. Anal. Calorim. (2016), DOI:10.1007/s10973-016-5711-4.
Zaitan H, Bianchi D, Achak O, Chafik T, J. Hazard. Mater., 153 (2008).
Meiszterics A, Rosta L, Peterlik H, Rohonczy J, Kubuki S, Henits P, Sinko K, J. Phys. Chem. A, 114 (2010).
Zhang Y, Liu Q, Wu Z, Zheng Q, Cheng H, J. Therm. Anal. Calorim. (2012), DOI:10.1007/s10973-011-2038-z.
Zhang Y, Liu Q, Wu Z, Zhang Y, J. Therm. Anal. Calorim. (2015), DOI:10.1007/s10973-015-4652-7.
Xiaoqin P, Huixing Z, Xiaohua J, Guowei X, J. Chin. Cer. Soc., 36 (2008).
Xiaoqin P, Fang H, Le Z, Xuejun Q, Yuanyan T, J. Southwest Jiaotong Univ., 44 (2009).
Jilin H, Xin L, Hanning X, Zhishu Y, Yangxi P, Inorgan Chem. Ind., 41 (2009).
Jingnan H, Junmin S, Xuebin X, Huibin Y, Yungai L, Bulle. Chin. Cer. Soc., 35 (2016).
Tang W, Huang H, Gao Y, Liu X, Yang X, Ni H, Zhang J, Mater. Des., 88 (2015).
Ozkaya B, J. Hazard. Mater., B129, 158 (2006)

The Korean Institute of Chemical Engineers. F5, 119, Anam-ro, Seongbuk-gu, 233 Spring Street Seoul 02856, South Korea.
TEL. No. +82-2-458-3078FAX No. +82-507-804-0669E-mail : kiche@kiche.or.kr

Copyright (C) KICHE.all rights reserved.

- Korean Journal of Chemical Engineering 상단으로