Related Experiment Video
Updated: Jan 23, 2026

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for CuII Through Microwave Pre-Pyrolysis
Published on: February 12, 2019
Preparation of aminated chitosan microspheres by one-pot method and their adsorption properties for dye wastewater
Jian Meng1, Jianlan Cui1, Siyuan Yu1
1School of Chemical Engineering and Technology, North University of China, Taiyuan 030051, People's Republic of China.
Abstract:
Polyamine chelating adsorbents have a good removal effect on dye wastewater. In this study, small molecule triethylenetetramine and macromolecular poly(ethylene imine) were selected as aminated reagent, and two kinds of aminated chitosan microspheres, TETA-CTSms and PEI-CTSms, were obtained by emulsion cross-linking method. The microspheres were fully characterized by FTIR, SEM, XRD, EDS and TGA. EDS results showed that the N content of the PEI-CTSms and TETA-CTSms microspheres increased significantly after the cross-linking reaction and can reach 5.7 wt% and 7.3 wt%, respectively. Adsorption experiments confirmed that TETA-CTSms and PEI-CTSms showed greater adsorption characteristics for anionic dye reactive yellow (RY) in aqueous solutions compared with CTSms, and the adsorption capacity per unit area was increased by 39.11% and 88.56%, respectively. The adsorption capacity of aminated microspheres for RY decreased with the increase of pH. The adsorption kinetics conformed to the pseudo-second-order model, and the adsorption process was in accordance with the Langmuir isotherm model. The negative value of ΔG confirmed that the adsorption process was spontaneous, and the dye adsorption was a multiple process dominated by chemical chelating and physical adsorption.
More Related Videos
Related Concept Videos
Physical Properties of Amines
Preparation of Amines: Alkylation of Ammonia and Amines
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Preparation of Amines: Reduction of Amides and Nitriles
Amides can be reduced to primary, secondary, and tertiary amines using catalytic hydrogenation, active metals like Fe,...
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...

