Abstract

Mesoporous aluminas (MAs) with tunable structural properties including BET surface area, pore volume and pore size were successfully synthesized. The synthesis method was based on a sol–gel process via hydrolysis of aluminium isopropoxide associated with non-ionic block copolymer P123 as the structure-directing template in an acidic aqueous system. The MAs were characterized using thermogravimetry – differential thermal analysis (TG-DTA) for decomposition and mass loss characteristics during calcination, X-ray diffraction (XRD) for bulk crystallinity, transmission electron microscopy (TEM) for nano-scale morphology, selected area electron diffraction (SAED) for local crystallinity and N2 adsorption–desorption techniques for porous structural properties. By tailoring the amount of P123 and HNO3 addition, inorganic aluminium precursor Al(NO3)3 doping ratio and calcination temperature, MAs with controllable structural properties were obtained, leading to regular variations in the surface area (up to 409 m2g−1), pore volume (0.4 cm3g−1 ∼ 2.8 cm3g−1) and pore size (5.0 nm ∼ 33.1 nm). Bovine serum albumin (BSA) was employed to evaluate the adsorption capability of the synthesized MAs. It was found that the structural properties of MA had a crucial effect on the BSA adsorption capability, increasing dramatically with increasing surface area, pore volume and pore size. For the sample MA4P15AlN (surface area 287 m2g−1, pore volume 2.8 cm3g−1 and pore size around 33.1 nm), the BSA adsorption amount reached 182.7 mgg−1 in 2 h, higher than other MA samples as well as a silicon based reference sorbent material, SBA-15 (133.3 mgg−1).

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.