Preparation of Fe3O4-octadecyltrichlorosilane for removal of methyl orange and methylene blue: Influence of pH and ionic strength on competitive adsorption

被引:0
作者
Yaoqiang Hu
Chaoming Quan
Min Guo
Xiushen Ye
Zhijian Wu
机构
[1] Chinese Academy of Sciences,Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources, Qinghai Institute of Salt Lakes
[2] Guangdong Ocean University,College of Ocean and Meteorology
[3] Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province,undefined
来源
Journal of Wuhan University of Technology-Mater. Sci. Ed. | 2017年 / 32卷
关键词
Fe; O; -octadecyltrichlorosilane; competitive adsorption mechanism; pH; ionic strength; dye;
D O I
暂无
中图分类号
学科分类号
摘要
Fe3O4-octadecyltrichlorosilane (Fe3O4-OTS) was synthesized and used to remove dyes in a competitive system. Fe3O4-OTS was prepared by slow hydrolysis of OTS in cyclohexane on the surface of Fe3O4 obtained through coprecipitation method. Scanning electron microscope (SEM), energy dispersive spectrometer (EDS), and contact angle analyzer (CA) were used to analyze the properties of Fe3O4-OTS. Methyl orange (MO) and methylene blue (MB) were selected as model molecules to study the influence mechanism of pH and ionic strength on competitive adsorption. The results of EDS and CA indicated that Fe3O4 was modified successfully with OTS on the surface. Silicon appeared and carbon content increased obviously on the surface of adsorbent. Contact angle of adsorbent increased from 0° to 107° after being modified by OTS. Fe3O4-OTS showed good separation for MO and MB in competitive system, which has potential to separate dyes in sewage. Separation factor (βBO) changed from 18.724 to 0.017, when pH changed from 7 to 12, revealing that MO and MB could be separated almost thoroughly by Fe3O4-OTS. pH could change the surface charge of Fe3O4-OTS and structure of dyes, and thus change the interactions of competitive system indirectly. Even though hydrophobic interaction was enhanced, ionic strength reduced the difference of electrostatic interaction between dyes and Fe3O4-OTS. So it is unfavorable to separate dyes with opposite charges when ionic strength increases. These findings may provide theoretical guidances to separate two-component dye pollutants.
引用
收藏
页码:1413 / 1419
页数:6
相关论文
共 53 条
  • [1] Chevremont AC(2013)Fate of Carbamazepine and Anthracene in Soils Watered with UV-LED Treated Wastewaters [J] Water Res. 47 6 574-6 584
  • [2] Boudenne JL(2013)Heavy Metal Removal from Water by Magnetite Nanorods [J] Chem. Eng. J. 219 209-216
  • [3] Coulomb B(2013)TiO Water Res. 47 6 052-6 063
  • [4] Karami H(2013) Nanoparticles Aggregation and Disaggregation in Presence of Alginate and Suwannee River Humic Acids. pH and Concentration Effects on Nanoparticle Stability[J] Bioresource Technol. 144 485-491
  • [5] Loosli F(2013)Effective Removal of Congo Red Dye from Aqueous Solution Using Modified Xanthan Gum/Silica Hybrid Nanocomposite as Adsorbent[J] Dyes Pigments 99 496-501
  • [6] Le Coustumer P(2013)Characterization of Metabolites of Genotoxic 4,4 '-aminoalkoxyazobenzene Dyes[J] Clean-Soil, Air, Water 41 992-1
  • [7] Stoll S(2010)Removal of Organic Dyes in Environmental Water on to Magnetic-Sulfonic Graphene Nanocomposite [J] J. Hazard. Mate. 178 349-355
  • [8] Ghorai S(2011)Application of AlMCM-41 for Competitive Adsorption of Methylene Blue and Rhodamine B: Thermodynamic and Kinetic Studies[J] Desalination 280 1-13
  • [9] Sarkar AK(2013)Cationic and Anionic Dye Adsorption by Agricultural Solid Wastes: A Comprehensive Review[J] Chem. Eng. J. 215–216 122-127
  • [10] Panda AB(2013)Effect of pH on the Adsorption of Sunset Yellow FCF Food Dye into a Layered Double Hydroxide (CaAl-LDH-NO Chem. Eng. J. 228 392-397