TY - JOUR
T1 - A salt-assisted approach for the pore-size-tailoring of the ionic-liquid-templated TiO2 photocatalysts exhibiting high activity
AU - Chang, Su-Min
AU - Lee, Chung Yu
PY - 2013/3/7
Y1 - 2013/3/7
N2 - In this study, we develop a novel salt-assisted approach to adjusting the pore size of ionic-liquid-templated TiO2 photocatalysts by simply changing the concentrations and types of the inorganic salts. Four types of salts, including NaCl, CaCl2, NH4Cl, and NH4NO3, are selected in order to investigate the effects of the ionic radii and the charges of the constituent ions on the resulting textures. In addition, a mechanism that the salts assist the self-assembly of hydrophilic 1-butyl-3-methylimidazolium chloride (C4mimCl) molecules in hydrophobic benzyl alcohol is proposed. The templated TiO2 powder, which incorporates phosphate species to enhance its structural stability, exhibits a small pore size of 4.2nm and a high surface area of 164m2g-1. Small amounts of the salts increase the ionic strength, slightly shrinking the template and the pore size, and pore expansion results when the salt/Ti ratio is above 0.2. The salts at a salt/Ti ratio of 1.0 remarkably extend the pore size to 8.7-16.8nm in the order of NH4NO3 (16.8nm)>NH4Cl (13.7nm)>CaCl2 (12.4nm)>NaCl (8.7nm). Moreover, high surface areas of 154-199m2g-1 are still achieved. The ions that have large radii and high valence numbers are more capable of expanding the pores because of strong volume exclusion and Coulomb repulsion. The critical pore size for the adsorption of hydrated bisphenol A molecules within the pores is ca. 4.2nm. Pore expansion facilitates mass diffusion in the channels and turns internal surface areas available for reactions, thus greatly enhancing the activity of the mesoporous photocatalyst by 2.7-5.5 times.
AB - In this study, we develop a novel salt-assisted approach to adjusting the pore size of ionic-liquid-templated TiO2 photocatalysts by simply changing the concentrations and types of the inorganic salts. Four types of salts, including NaCl, CaCl2, NH4Cl, and NH4NO3, are selected in order to investigate the effects of the ionic radii and the charges of the constituent ions on the resulting textures. In addition, a mechanism that the salts assist the self-assembly of hydrophilic 1-butyl-3-methylimidazolium chloride (C4mimCl) molecules in hydrophobic benzyl alcohol is proposed. The templated TiO2 powder, which incorporates phosphate species to enhance its structural stability, exhibits a small pore size of 4.2nm and a high surface area of 164m2g-1. Small amounts of the salts increase the ionic strength, slightly shrinking the template and the pore size, and pore expansion results when the salt/Ti ratio is above 0.2. The salts at a salt/Ti ratio of 1.0 remarkably extend the pore size to 8.7-16.8nm in the order of NH4NO3 (16.8nm)>NH4Cl (13.7nm)>CaCl2 (12.4nm)>NaCl (8.7nm). Moreover, high surface areas of 154-199m2g-1 are still achieved. The ions that have large radii and high valence numbers are more capable of expanding the pores because of strong volume exclusion and Coulomb repulsion. The critical pore size for the adsorption of hydrated bisphenol A molecules within the pores is ca. 4.2nm. Pore expansion facilitates mass diffusion in the channels and turns internal surface areas available for reactions, thus greatly enhancing the activity of the mesoporous photocatalyst by 2.7-5.5 times.
KW - Ionic liquids
KW - Mesoporous materials
KW - Photocatalysis
KW - Pore expansion
KW - Salt-assisting
UR - http://www.scopus.com/inward/record.url?scp=84871655174&partnerID=8YFLogxK
U2 - 10.1016/j.apcatb.2012.11.026
DO - 10.1016/j.apcatb.2012.11.026
M3 - Article
AN - SCOPUS:84871655174
SN - 0926-3373
VL - 132-133
SP - 219
EP - 228
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -