Origin of the Springback Effect in Ambient-Pressure-Dried Silica Aerogels: The Effect of Surface Silylation
Fabian Zemke,
Julien Gonthier,
Ernesto Scoppola,
Ulla Simon,
Maged F. Bekheet,
Wolfgang Wagermaier,
Aleksander Gurlo
Affiliations
Fabian Zemke
Chair of Advanced Ceramic Materials, Institute of Materials Science and Technology, Faculty III Process Sciences, Technische Universität Berlin, Straße des 17. Juni 135, 10623 Berlin, Germany
Julien Gonthier
Department of Biomaterials, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Potsdam, Germany
Ernesto Scoppola
Department of Biomaterials, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Potsdam, Germany
Ulla Simon
Chair of Advanced Ceramic Materials, Institute of Materials Science and Technology, Faculty III Process Sciences, Technische Universität Berlin, Straße des 17. Juni 135, 10623 Berlin, Germany
Maged F. Bekheet
Chair of Advanced Ceramic Materials, Institute of Materials Science and Technology, Faculty III Process Sciences, Technische Universität Berlin, Straße des 17. Juni 135, 10623 Berlin, Germany
Wolfgang Wagermaier
Department of Biomaterials, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Potsdam, Germany
Aleksander Gurlo
Chair of Advanced Ceramic Materials, Institute of Materials Science and Technology, Faculty III Process Sciences, Technische Universität Berlin, Straße des 17. Juni 135, 10623 Berlin, Germany
Ambient pressure drying (APD) can prospectively reduce the costs of aerogel fabrication and processing. APD relies solely on preventing shrinkage or making it reversible. The latter, i.e., the aerogel re-expansion after drying (so-called springback effect—SBE), needs to be controlled for reproducible aerogel fabrication by APD. This can be achieved by an appropriate surface functionalization of aerogel materials (e.g., SiO2). This work addresses the fabrication of monolithic SiO2 aerogels and xerogels by APD. The effect of several silylation agents, i.e., trimethylchlorosilane, triethylchlorosilane, and hexamethyldisilazane on the SBE is studied in detail, applying several complementary experimental techniques, allowing the evaluation of the macroscopic and microscopic morphology as well as the composition of SiO2 aerogels. Here, we show that some physical properties, e.g., the bulk density, the macroscopic structure, and pore sizes/volumes, were significantly affected by the re-expansion. However, silylation did not necessarily lead to full re-expansion. Therefore, similarities in the molecular composition could not be equated to similarities in the SBE. The influences of steric hindrance and reactivity are discussed. The impact of silylation is crucial in tailoring the SBE and, as a result, the APD of monolithic aerogels.