Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Collins Onyango
  • Wilfrida Nyairo
  • Bowa Kwach
  • Victor Shikuku
  • Tome Sylvain
  • Hermann Dzoujo Tamaguelon
  • Claus Ruscher

Organisationseinheiten

Externe Organisationen

  • Maseno University
  • Kaimosi Friends University College
  • University of Douala
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)8546-8563
Seitenumfang18
FachzeitschriftMaterials Advances
Jahrgang5
Ausgabenummer21
Frühes Online-Datum8 Okt. 2024
PublikationsstatusVeröffentlicht - 2024

Abstract

In this study, four geopolymer composites, GP-0, GP-10, GP-20 and GP-30, were synthesized from pumice, an abundant and inexpensive volcanic rock precursor, substituted with fractions of 0, 10, 20 and 30% by weight of medical waste incinerator fly ash (MWI-FA), respectively. The materials were characterized by standard methods (FTIR, XRF, BET surface area measurement, XRD, SEM-EDX and TGA). The materials were morphologically distinct and the specific surface areas (SSA) decreased with an increase in MWI-FA fraction. The adsorption performances of the geocomposites were evaluated in batch mode for the removal of methylene blue (MB), a toxic dye, from water. The study determined that the dye was optimally removed at circumneutral pH, 303 K temperature, 0.6 g/40 mL adsorbent dosage and 30 min contact time. The equilibrium data were best described using the Sips isotherm model. The geopolymers had ∼30 times higher adsorption capacities than pristine pumice. The maximum adsorption capacities of the geopolymers, ∼31 mg g−1, were indistinguishable despite an increase in MWI-FA indicating that MWI-FA provided new energetically favorable adsorption sites compensating diminished SSA. The adsorption kinetics was best described using the pseudo-second order kinetic model wherein the rate constant (K2) increased with the MWI-FA fraction suggesting porosity structures with reduced tortuosity. Thermodynamically, the adsorption process was exothermic (ΔH < 0), physical (ΔH and Ea < 40 kJ mol−1) spontaneous (ΔG < 0) and enthalpy-driven. Adsorption diminished in a saline environment. The exhausted adsorbent was recoverable and recycled twice using hot water before significant loss of adsorption potential. The composite geopolymers present a plausible strategy for stabilization of up to 30% MWI-FA without compromising the adsorptive properties for dye removal from water.

ASJC Scopus Sachgebiete

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Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism. / Onyango, Collins; Nyairo, Wilfrida; Kwach, Bowa et al.
in: Materials Advances, Jahrgang 5, Nr. 21, 2024, S. 8546-8563.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Onyango, C, Nyairo, W, Kwach, B, Shikuku, V, Sylvain, T, Dzoujo Tamaguelon, H & Ruscher, C 2024, 'Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism', Materials Advances, Jg. 5, Nr. 21, S. 8546-8563. https://doi.org/10.1039/d4ma00779d
Onyango, C., Nyairo, W., Kwach, B., Shikuku, V., Sylvain, T., Dzoujo Tamaguelon, H., & Ruscher, C. (2024). Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism. Materials Advances, 5(21), 8546-8563. https://doi.org/10.1039/d4ma00779d
Onyango C, Nyairo W, Kwach B, Shikuku V, Sylvain T, Dzoujo Tamaguelon H et al. Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism. Materials Advances. 2024;5(21):8546-8563. Epub 2024 Okt 8. doi: 10.1039/d4ma00779d
Onyango, Collins ; Nyairo, Wilfrida ; Kwach, Bowa et al. / Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption : co-valorization, parameters and mechanism. in: Materials Advances. 2024 ; Jahrgang 5, Nr. 21. S. 8546-8563.
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title = "Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption: co-valorization, parameters and mechanism",
abstract = "In this study, four geopolymer composites, GP-0, GP-10, GP-20 and GP-30, were synthesized from pumice, an abundant and inexpensive volcanic rock precursor, substituted with fractions of 0, 10, 20 and 30% by weight of medical waste incinerator fly ash (MWI-FA), respectively. The materials were characterized by standard methods (FTIR, XRF, BET surface area measurement, XRD, SEM-EDX and TGA). The materials were morphologically distinct and the specific surface areas (SSA) decreased with an increase in MWI-FA fraction. The adsorption performances of the geocomposites were evaluated in batch mode for the removal of methylene blue (MB), a toxic dye, from water. The study determined that the dye was optimally removed at circumneutral pH, 303 K temperature, 0.6 g/40 mL adsorbent dosage and 30 min contact time. The equilibrium data were best described using the Sips isotherm model. The geopolymers had ∼30 times higher adsorption capacities than pristine pumice. The maximum adsorption capacities of the geopolymers, ∼31 mg g−1, were indistinguishable despite an increase in MWI-FA indicating that MWI-FA provided new energetically favorable adsorption sites compensating diminished SSA. The adsorption kinetics was best described using the pseudo-second order kinetic model wherein the rate constant (K2) increased with the MWI-FA fraction suggesting porosity structures with reduced tortuosity. Thermodynamically, the adsorption process was exothermic (ΔH < 0), physical (ΔH and Ea < 40 kJ mol−1) spontaneous (ΔG < 0) and enthalpy-driven. Adsorption diminished in a saline environment. The exhausted adsorbent was recoverable and recycled twice using hot water before significant loss of adsorption potential. The composite geopolymers present a plausible strategy for stabilization of up to 30% MWI-FA without compromising the adsorptive properties for dye removal from water.",
author = "Collins Onyango and Wilfrida Nyairo and Bowa Kwach and Victor Shikuku and Tome Sylvain and {Dzoujo Tamaguelon}, Hermann and Claus Ruscher",
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TY - JOUR

T1 - Synthesis of pumice and medical waste incinerator fly ash based phosphate geopolymers for methylene blue dye adsorption

T2 - co-valorization, parameters and mechanism

AU - Onyango, Collins

AU - Nyairo, Wilfrida

AU - Kwach, Bowa

AU - Shikuku, Victor

AU - Sylvain, Tome

AU - Dzoujo Tamaguelon, Hermann

AU - Ruscher, Claus

N1 - Publisher Copyright: © 2024 RSC.

PY - 2024

Y1 - 2024

N2 - In this study, four geopolymer composites, GP-0, GP-10, GP-20 and GP-30, were synthesized from pumice, an abundant and inexpensive volcanic rock precursor, substituted with fractions of 0, 10, 20 and 30% by weight of medical waste incinerator fly ash (MWI-FA), respectively. The materials were characterized by standard methods (FTIR, XRF, BET surface area measurement, XRD, SEM-EDX and TGA). The materials were morphologically distinct and the specific surface areas (SSA) decreased with an increase in MWI-FA fraction. The adsorption performances of the geocomposites were evaluated in batch mode for the removal of methylene blue (MB), a toxic dye, from water. The study determined that the dye was optimally removed at circumneutral pH, 303 K temperature, 0.6 g/40 mL adsorbent dosage and 30 min contact time. The equilibrium data were best described using the Sips isotherm model. The geopolymers had ∼30 times higher adsorption capacities than pristine pumice. The maximum adsorption capacities of the geopolymers, ∼31 mg g−1, were indistinguishable despite an increase in MWI-FA indicating that MWI-FA provided new energetically favorable adsorption sites compensating diminished SSA. The adsorption kinetics was best described using the pseudo-second order kinetic model wherein the rate constant (K2) increased with the MWI-FA fraction suggesting porosity structures with reduced tortuosity. Thermodynamically, the adsorption process was exothermic (ΔH < 0), physical (ΔH and Ea < 40 kJ mol−1) spontaneous (ΔG < 0) and enthalpy-driven. Adsorption diminished in a saline environment. The exhausted adsorbent was recoverable and recycled twice using hot water before significant loss of adsorption potential. The composite geopolymers present a plausible strategy for stabilization of up to 30% MWI-FA without compromising the adsorptive properties for dye removal from water.

AB - In this study, four geopolymer composites, GP-0, GP-10, GP-20 and GP-30, were synthesized from pumice, an abundant and inexpensive volcanic rock precursor, substituted with fractions of 0, 10, 20 and 30% by weight of medical waste incinerator fly ash (MWI-FA), respectively. The materials were characterized by standard methods (FTIR, XRF, BET surface area measurement, XRD, SEM-EDX and TGA). The materials were morphologically distinct and the specific surface areas (SSA) decreased with an increase in MWI-FA fraction. The adsorption performances of the geocomposites were evaluated in batch mode for the removal of methylene blue (MB), a toxic dye, from water. The study determined that the dye was optimally removed at circumneutral pH, 303 K temperature, 0.6 g/40 mL adsorbent dosage and 30 min contact time. The equilibrium data were best described using the Sips isotherm model. The geopolymers had ∼30 times higher adsorption capacities than pristine pumice. The maximum adsorption capacities of the geopolymers, ∼31 mg g−1, were indistinguishable despite an increase in MWI-FA indicating that MWI-FA provided new energetically favorable adsorption sites compensating diminished SSA. The adsorption kinetics was best described using the pseudo-second order kinetic model wherein the rate constant (K2) increased with the MWI-FA fraction suggesting porosity structures with reduced tortuosity. Thermodynamically, the adsorption process was exothermic (ΔH < 0), physical (ΔH and Ea < 40 kJ mol−1) spontaneous (ΔG < 0) and enthalpy-driven. Adsorption diminished in a saline environment. The exhausted adsorbent was recoverable and recycled twice using hot water before significant loss of adsorption potential. The composite geopolymers present a plausible strategy for stabilization of up to 30% MWI-FA without compromising the adsorptive properties for dye removal from water.

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U2 - 10.1039/d4ma00779d

DO - 10.1039/d4ma00779d

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SP - 8546

EP - 8563

JO - Materials Advances

JF - Materials Advances

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