Rapid microwave synthesis of sustainable magnetic framework composites of UTSA-16(Zn) with Fe 3 O 4 nanoparticles for efficient CO 2 capture
Rapid microwave synthesis of sustainable magnetic framework composites of UTSA-16(Zn) with Fe 3 O 4 nanoparticles for efficient CO 2 capture
复制标题
快速微波合成 UTSA-16(Zn) 与 Fe 3 O 4 纳米颗粒的可持续磁性框架复合材料,用于高效捕获 CO 2
DOI:
10.1039/d3ma00351e
复制
发表时间:
2023
影响因子:
5
通讯作者:
Woodliffe J
中科院分区:
文献类型:
--
作者:
Woodliffe J
Metal–organic frameworks (MOFs) have shown excellent potential for carbon dioxide capture applications due to their high sorption capacities and selectivities. However, MOFs are typically thermally insulating, and so thermal CO2 regeneration is challenging, especially on the large scales required in industry. This limitation can be overcome by inclusion of magnetic nanoparticles within the MOF structure, enabling rapid and energy efficient CO2 regeneration using induction heating. To this end we have developed novel magnetic framework composites (MFCs) comprised of MOF UTSA-16(Zn) (UTSA: University of Texas at San Antonio, a Zn-based MOF with citrate linkers) and Fe3O4 nanoparticles. Our work also addresses the sustainability and scalability challenges faced by MFCs required for industrial application, considering the use of inexpensive and widely-available materials. Herein we report a two-step procedure for preparing the MFCs. Firstly, a scalable single-step continuous hydrothermal synthesis method is used to produce highly pure, stable, and crystalline citrate-coated Fe3O4 nanoparticles (62% yield). The nanoparticles exhibit a uniform particle size (19 ± 11 nm) and a very high saturation magnetisation (78 emu g−1) compared with previously published citrate-coated Fe3O4 nanoparticles. Next, various concentrations (2.6–18.7 wt%) of these nanoparticles were incorporated into UTSA-16(Zn) via a rapid microwave-assisted direct-growth strategy (10 min) to form the MFCs (81–83% yield). The MFCs demonstrate high CO2 adsorption capacities (2.8–3.3 mmol g−1) and recyclability. In addition, the MFCs heat rapidly in an applied magnetic field for CO2 release, reaching regeneration temperatures in remarkably short times (e.g. 60 °C in 8 seconds). The MFCs developed in this work combine strong CO2 adsorption profiles and substantial regeneration heating capabilities, whilst being produced in a scalable and sustainable manner. The methods developed to prepare MFCs herein are also applicable to other MOFs, opening routes for a variety of sustainable MFCs to deliver impact for a range of applications across carbon capture and triggered release of other guest molecules.