Related Experiment Video
Updated: Jan 8, 2026

Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
Basic Aluminum Benzoate is Low-Cost, Porous, and Superhydrophobic
Zhi-Shuo Wang1, Mu-Yang Zhou1, Ding-Yi Hu1
1MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, GBRCE for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou 510275, China.
None:
Superhydrophobic materials are of tremendous application prospects, but they typically need to be prepared by relatively expensive reagents or complex treatments. Here, we report a simple aluminum-based coordination polymer [Al(OH)(ba)2] (MCF-66, Hba = benzoic acid), which can be facilely synthesized by various low-cost raw materials. For example, based on the simple acid-base reaction between Hba and Al(OH)3 (raw material costs ∼ 1 USD kg-1), MCF-66 can be synthesized in ca. 100% yield without using any solvent or additive, with water as the sole byproduct. MCF-66 consists of insufficiently packed butterfly-like chains, with hydrophobic phenyl rings exposed on the crystal surfaces, enabling superhydrophobicity. The compressed pellet showed a high water contact angle of 152°, which identified MCF-66 as a rare superhydrophobic material. Although the small discrete pores formed between the chains are just slightly larger than H2, it can deform to adsorb various small molecules and show special separation behavior for the n-C4H10/i-C4H10 mixture. MCF-66 can also be directly grown on aluminum meshes for highly efficient oil-water separation (8.8 × 103 L m-2 h-1 bar-1).
More Related Videos
Related Concept Videos
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Hydroboration-Oxidation of Alkenes

