Related Experiment Video
Updated: Jan 25, 2026

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for CuII Through Microwave Pre-Pyrolysis
Published on: February 12, 2019
Mesoporous carbon xerogel material for the adsorption of model naphthenic acids: structure effect and kinetics
Yara Rashed1, Selamawit Ashagre Messele1, Hongbo Zeng2
1Department of Civil & Environmental Engineering, University of Alberta, Edmonton, Canada.
Abstract:
The study examined the preparation, characterization and the use of carbon xerogel (CX) material for the adsorption of three model naphthenic acids (NAs); such as, heptanoic acid (HPA), 5-cyclohexanepentanoic acid (CHPA), and 5-phenylvaleric acid (PVA). CX was synthesized by sol-gel method from resorcinol and formaldehyde. The characterization results showed that CX was a mesoporous material with large surface area (573 m2/g) and high pore volume (1.55 cm3/g), which was mainly composed of carbon (93.20%) and oxygen (6.71%). Adsorption studies revealed that PVA, the NA having an aromatic ring was adsorbed more easily by CX (87 mg/g) due to π-π interactions, followed by HPA (65 mg/g) and CHPA (61 mg/g). In addition, by studying the effect of solution pH, the result confirmed that repulsion greatly hindered the adsorption of HPA onto CX at pHs above that of the pHPZC and at lower pHs attractive electrostatic forces promoted adsorption. Adsorption kinetics fitted the pseudo-first-order model, which suggested that physisorption was most likely the means of adsorption. For the intraparticle diffusion model, the rate of film diffusion was higher than the rate of pore diffusion for each model compound regardless of their structure. Accordingly, this confirmed that pore diffusion was the rate-limiting step, although film diffusion still maintained a significant role in the rate of diffusion. In general, CX exhibited excellent adsorption performance due to its highly mesoporous character so it could be used as a passive treatment method in tailing ponds for removal of organic matters.
More Related Videos
07:13High Temperature Fabrication of Nanostructured Yttria-Stabilized-Zirconia YSZ Scaffolds by In Situ Carbon Templating Xerogels
Published on: April 16, 2017
09:43Study of Short Peptide Adsorption on Solution Dispersed Inorganic Nanoparticles Using Depletion Method
Published on: April 11, 2020
Related Concept Videos
Bicarbonate-Carbonic Acid Buffer
Acid Strength and Molecular Structure
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with increasing...
Molecular Structure and Acidity
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
Nucleic Acid Structure
DNA Structure
DNA...
Structure of Benzene: Kekulé Model
He proposed that benzene has a cyclic structure of six carbon atoms attached to one hydrogen atom each, with three alternating pi bonds.
Structures of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...