Related Experiment Video
Updated: Jul 19, 2025

Surface Functionalization of Metal-Organic Frameworks for Improved Moisture Resistance
Published on: September 5, 2018
Hydrophobic Modification of Sulfonated Carbon Aerogels from Coir Fibers To Enhance Their Catalytic Performance for
Ade Sonya Suryandari1,2, Tantular Nurtono1, Widiyastuti Widiyastuti1
1Department of Chemical Engineering, Faculty of Industrial Technology and System Engineering, Sepuluh Nopember Institute of Technology, Kampus ITS Sukolilo, Surabaya 60111, Indonesia.
Abstract:
The hydrophilicity of sulfonic acid-functionalized solid catalysts tends to accelerate the deactivation of the catalyst for chemical reactions where water is produced during the process. In this work, we proposed a hydrophobic carbon aerogel acid catalyst derived from coir fibers by a sulfonation-hydrophobization route via the diazo reduction method. Sulfonation using the diazo reduction method offers some advantages such as the process takes only a few minutes and the modified surface can be easily modified further to be hydrophobic. The carbon aerogel was produced by direct pyrolysis of cellulose aerogels derived from coir fibers using an NH4OH-urea method and then sulfonated and hydrophobized using sulfanilic acid and 4-tert-butylaniline (TBA), respectively. The carbon aerogel exhibited a very high surface area (2624.93-3911.05 m2 g-1), which provides a lot of number of sites for sulfonate groups (2.30-2.70 mmol g-1). The water contact angle of the sulfonated catalyst after hydrophobization ranged from 70 to 115°, depending on the mass ratio of the TBA-to-solid catalyst. The hydrophobic catalyst exhibited better catalytic performance toward esterification of acetic acid with ethanol. A conversion of 65-74% could be achieved in a brief time using the hydrophobic catalyst. The conversions were much higher than that obtained by the unmodified hydrophilic catalyst. Our study offers a strategy to tune the surface hydrophobicity of the sulfonated solid acid catalyst to match for specific chemical reactions.
Related Concept Videos
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...

