TY - JOUR
T1 - UiO-66-Type Metal-Organic Framework with Free Carboxylic Acid
T2 - Versatile Adsorbents via H-bond for Both Aqueous and Nonaqueous Phases
AU - Song, Ji Yoon
AU - Ahmed, Imteaz
AU - Seo, Pill Won
AU - Jhung, Sung Hwa
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/10/12
Y1 - 2016/10/12
N2 - The metal-organic framework (MOF) UiO-66 was synthesized in one step from zirconium chloride and isophthalic acid (IPA), together with the usual link material, terephthalic acid (TPA). UiO-66 with free -COOH can be obtained in a facile way by replacing up to 30% of the TPA with IPA. However, the chemical and thermal stability of the synthesized MOFs decreased with increasing IPA content used in the syntheses, suggesting an increase in the population of imperfect bonds in the MOFs because of the asymmetrical structure of IPA. The obtained MOFs with free -COOH were applied in liquid-phase adsorptions from both water and model fuel to not only estimate the potential applications but also confirm the presence of -COOH in the MOFs. The adsorbed amounts of several organics (triclosan and oxybenzone from water and indole and pyrrole from fuel) increased monotonously with increasing IPA content applied in MOF synthesis (or -COOH in the MOFs). The favorable contribution of free -COOH to adsorption can be explained by H-bonding, and the direction of H-bonds (adsorbates: H donor; MOFs: H acceptor) was confirmed by the adsorption of oxybenzone in a wide pH range. The versatile applications of the MOFs with -COOH in adsorptions from both polar and nonpolar phases are remarkable considering that hydrophobic and hydrophilic adsorbents are generally required for water and fuel purification, respectively. Finally, the presence of free -COOH in the MOFs was confirmed by liquid-phase adsorptions together with general Fourier transform infrared analyses and decreased chemical and thermal stability.
AB - The metal-organic framework (MOF) UiO-66 was synthesized in one step from zirconium chloride and isophthalic acid (IPA), together with the usual link material, terephthalic acid (TPA). UiO-66 with free -COOH can be obtained in a facile way by replacing up to 30% of the TPA with IPA. However, the chemical and thermal stability of the synthesized MOFs decreased with increasing IPA content used in the syntheses, suggesting an increase in the population of imperfect bonds in the MOFs because of the asymmetrical structure of IPA. The obtained MOFs with free -COOH were applied in liquid-phase adsorptions from both water and model fuel to not only estimate the potential applications but also confirm the presence of -COOH in the MOFs. The adsorbed amounts of several organics (triclosan and oxybenzone from water and indole and pyrrole from fuel) increased monotonously with increasing IPA content applied in MOF synthesis (or -COOH in the MOFs). The favorable contribution of free -COOH to adsorption can be explained by H-bonding, and the direction of H-bonds (adsorbates: H donor; MOFs: H acceptor) was confirmed by the adsorption of oxybenzone in a wide pH range. The versatile applications of the MOFs with -COOH in adsorptions from both polar and nonpolar phases are remarkable considering that hydrophobic and hydrophilic adsorbents are generally required for water and fuel purification, respectively. Finally, the presence of free -COOH in the MOFs was confirmed by liquid-phase adsorptions together with general Fourier transform infrared analyses and decreased chemical and thermal stability.
KW - free carboxylic acid
KW - H-bond
KW - isophthalic acid
KW - liquid-phase adsorption
KW - metal-organic frameworks
UR - http://www.scopus.com/inward/record.url?scp=84991704765&partnerID=8YFLogxK
U2 - 10.1021/acsami.6b10098
DO - 10.1021/acsami.6b10098
M3 - Article
AN - SCOPUS:84991704765
SN - 1944-8244
VL - 8
SP - 27394
EP - 27402
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 40
ER -