当前位置: 中文主页 >> 研究成果 >> 论文成果
论文成果

In situ synthesis of titanium doped hybrid metal-organic framework UiO-66 with enhanced adsorption capacity for organic dyes

发表时间:2019-03-11
点击次数:
论文类型:
期刊论文
第一作者:
Han, Yitong
通讯作者:
Guo, XW (reprint author), Dalian Univ Technol, Sch Chem Engn, PSU DUT Joint Ctr Energy Res, State Key Lab Fine Chem, Dalian 116024, Peoples R China.; Zhang, ZC (reprint author), Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China.
合写作者:
Liu, Min,Li, Keyan,Sun, Qiao,Zhang, Wensheng,Song, Chunshan,Zhang, Guoliang,Zhang, Z. Conrad,Guo, Xinwen
发表时间:
2017-11-01
发表刊物:
INORGANIC CHEMISTRY FRONTIERS
收录刊物:
SCIE
文献类型:
J
卷号:
4
期号:
11
页面范围:
1870-1880
ISSN号:
2052-1553
摘要:
Titanium in different amounts has been successfully doped into the zirconium-based metal-organic framework UiO-66 via an in situ synthesis method, resulting in a series of hybrid UiO-66-nTi MOFs. These materials maintain a relatively high crystallinity and excellent structural stability. The addition of titanium has a significant effect on the crystal size and morphology of UiO-66. The UiO-66-nTi MOFs exhibit a sphere-like crystal morphology with a smaller crystal size and a rougher surface compared to the octahedral UiO-66 crystals. The framework order and porosity of the UiO-66-nTi MOFs decrease slightly due to titanium doping. The UiO-66-nTi MOFs were studied as adsorbents for the removal of an organic dye from water. The results demonstrate that these hybrid materials have enhanced adsorption capacity for the organic dye Conge red in comparison with the parent UiO-66. UiO-66-2.7Ti with 2.7% titanium doping shows the highest adsorption capacity of 979 mg g(-1), which is three times higher than that of the parent UiO-66. The strong electrostatic attraction between the positively charged surface of UiO-66-2.7Ti and the negatively charged Congo red molecules was identified as the main driving force for the high adsorption capacity.
是否译文:

辽ICP备05001357号  地址:中国·辽宁省大连市甘井子区凌工路2号 邮编:116024 版权所有:大连理工大学


访问量:    最后更新时间:..