School of Applied Chemical Engineering and The Research Institute for Catalysis, Chonnam National University, Yongbong-Dong, Buk-Gu, Gwangju 500-757, Republic of Korea.
J Colloid Interface Sci. 2011 Sep 15;361(2):612-7. doi: 10.1016/j.jcis.2011.05.067. Epub 2011 Jun 12.
The adsorption of pyridine onto the metal organic framework MIL-101 was investigated by experimental and theoretical methods. The amount of pyridine adsorbed on MIL-101 was extraordinarily large at 20 °C, corresponding to about 950 mg/g of dried MIL-101 and approximately half of the voids being filled. Most of the pyridine that had filled the voids was rapidly removed by evacuation at room temperature, but some of the pyridine was so strongly adsorbed that it was retained even under evacuation at 150 °C. Although IR spectra of the adsorbed pyridine indicated the adsorption of pyridine as pyridinium ions and coordinated pyridine at low temperatures, increasing the adsorption temperature induced partial cleavage of the pyridine rings. The high stabilization energy of pyridine on the coordinative unsaturated sites (CUS) of MIL-101, obtained by theoretical calculation, -103 kJ/mol, supported the strong adsorption of pyridine on the CUS.
通过实验和理论方法研究了吡啶在金属有机骨架 MIL-101 上的吸附。在 20°C 时,MIL-101 对吡啶的吸附量非常大,对应于约 950mg/g 的干燥 MIL-101 和大约一半的空隙被填满。大多数填充空隙的吡啶在室温下通过抽空迅速除去,但有些吡啶吸附得非常强,即使在 150°C 下抽空也能保留。尽管吸附吡啶的 IR 光谱表明吡啶在低温下以吡啶离子和配位吡啶的形式被吸附,但提高吸附温度会诱导吡啶环的部分断裂。理论计算得到的吡啶在 MIL-101 的配位不饱和位点(CUS)上的高稳定能,-103kJ/mol,支持了吡啶在 CUS 上的强吸附。