A Co-Precursor Approach Coupled with a Supercritical Modification Method for Constructing Highly Transparent and Superhydrophobic Polymethylsilsesquioxane Aerogels

Polymethylsilsesquioxane (PMSQ) aerogels obtained from methyltrimethoxysilane (MTMS) are well-known high-performance porous materials. Highly transparent and hydrophobic PMSQ aerogel would play an important role in transparent vacuum insulation panels. Herein, the co-precursor approach and supercritical modification method were developed to prepare the PMSQ aerogels with high transparency and superhydrophobicity. Firstly, benefiting from the introduction of tetramethoxysilane (TMOS) in the precursor, the pore structure became more uniform and the particle size was decreased. As the TMOS content increased, the light transmittance increased gradually from 54.0% to 81.2%, whereas the contact angle of water droplet decreased from 141° to 99.9°, ascribed to the increase of hydroxyl groups on the skeleton surface. Hence, the supercritical modification method utilizing hexamethyldisilazane was also introduced to enhance the hydrophobic methyl groups on the aerogel’s surface. As a result, the obtained aerogels revealed superhydrophobicity with a contact angle of 155°. Meanwhile, the developed surface modification method did not lead to any significant changes in the pore structure resulting in the superhydrophobic aerogel with a high transparency of 77.2%. The proposed co-precursor approach and supercritical modification method provide a new horizon in the fabrication of highly transparent and superhydrophobic PMSQ aerogels

High Nanopore Volume Tetrethoxysilane Based Aerogels Prepared with Addition of N, N-Dimethylformamide at Different Stage of the Sol-Gel Process

Using tetraethoxysilane (TEOS) as a precursor, silica aerogels were synthesized via the sol-gel polymerization followed by supercritical drying process. During the polymerization period, N, N-dimethylformamide (DMF), acting as a chemical additive for the structure control, was introduced in the hydrolysis step and condensation step, respectively. As a result, the nanopore volumes for the pores smaller than 100 nm were up to 6.0 cm3/g and 5.7 cm3/g for the samples that produced with DMF addition in the hydrolysis step and condensation step, while the value for the sample without DMF was only 4.6 cm3/g. Besides, the sample with DMF addition in the condensation step possessed more uniform pore size distribution while compared with that with DMF addition in the hydrolysis step. DMF can provide a shielding layer around the colloid particles through hydrogen bonds, inhibiting the aggregation of colloid particles and the enlarging of pore sizes