Cross-Linked Chitosan Terephthaldehyde for Removal of Congo red: Synthesis, Characterization, and Adsorption Studies

Document Type : Original Article

Authors

1 Ministry of Education, Educational Directorate of Karbala, Iraq

2 College of Pharmacy, University of Babylon, Babylon, Iraq

3 Chemistry Department, College of Education for Pure Sciences, University of Kerbala, Kerbala/ Iraq

Abstract

A cross-linked chitosan (denoted as TCCS) was synthesized by dissolving chitosan in acidic aqueous solution and addition of minimum amount of terephthaldehyde as cross-linker, the synthesized polymer was characterized by Fourier-transform infrared spectroscopy (FT IR) and scanning electron microscopy (SEM). TCCS was used as an adsorbent to remove the organic dye congo red (CR) from aqueous solutions. The effects of contact time, pH, adsorbent weight, and initial dye concentration were studied. The results indicated the 0.02 g of TCCS can remove more than 98% of CR form 25 ml aqueous solution with 40 ppm solution after 60 min with no significant effect observed with changing the pH. Langmuir, Freundlich, and Temkin isotherm models were implemented to on the experimental data, the best fit was with Langmuir isotherm model, the correlation coefficient (R2) value for this isotherm was (0.998), while for Freundlich, and Temkin isotherms the R2 values were 0.8824 and 0.933 respectively. The results of the kinetic studies revealed that the adsorption of CR on TCCS is a pseudo second order process, with R2 value of 0.9982, and the calculated adsorption capacity (qe) values for this model 49.26 mg/g, which is very close to the experimental result (49.04 mg/g). The thermodynamic parameters indicated that the adsorption of CR on TCCS is spontaneous with negative ΔG values, endothermic with positive ΔH and positive ΔS which indicates that the disorder of the CR molecules increases at the adsorbent-solution interface.

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Egyptian Journal of Chemistry
Volume 65, Issue 132 - Serial Number 13
Special Issue: Chemistry and Global Challenges (Part B)
December 2022
Pages 895-901

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History

  • Receive Date: 05 August 2022
  • Revise Date: 01 September 2022
  • Accept Date: 03 September 2022

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