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Synergistic enhancement of CO2 adsorption on Cu2(OH)PO4 via iron doping and polyethylenimine loading
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK). Chongqing Jiaotong University, China; Key Laboratory of Hydraulic and Waterway Engineering of the Ministry of Education, China; National Engineering Research Center for Inland Waterway Regulation, Chongqing, China.ORCID-id: 0000-0003-3091-2994
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Rekke forfattare: 72025 (engelsk)Inngår i: Environmental Research, ISSN 0013-9351, E-ISSN 1096-0953, Vol. 286, part 2, artikkel-id 122873Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A novel polyethyleneimine (PEI)-loaded Fe-doped Cu2(OH)PO4 adsorbent was synthesized via physical impregnation and characterized using XRD, FT-IR, SEM, XPS, and N2 adsorption. Key parameters (Fe doping, PEI loading, temperature, flow rate) affecting CO2 adsorption were optimized using the response surface methodology (RSM, Box–Behnken design), and flow rate was identified as the most influential factor. The optimal adsorbent, 8 %Fe–Cu2(OH)PO4@50 %PEI, achieved a CO2 adsorption capacity of 3.95 mmol/g (60 °C, 30 ml/min). A significant synergistic effect (α = 3.2426) existed between Fe doping and PEI loading. RSM predictions (8.8 mol %Fe, 50.6 wt % PEI, 50.1 °C, 28 ml/min; capacity 3.95 mmol/g) closely matched those obtained in the experiment (3.90 mmol/g). The adsorbent exhibited excellent stability over 20 cycles (capacity loss: 0.35 mmol/g). Kinetic and thermodynamic studies indicated barrier-free (Ea = −41.66 kJ/mol), exothermic, spontaneous, and entropy-driven monolayer adsorption. This demonstrates that 8 %Fe–Cu2(OH)PO4@50 %PEI is a highly efficient and recyclable CO2 adsorbent.

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2025. Vol. 286, part 2, artikkel-id 122873
Emneord [en]
CO2adsorption, Cyclic regeneration, Fe-doped Cu2(OH)PO4@PEI, Response surface methodology, Synergistic effect
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Identifikatorer
URN: urn:nbn:se:su:diva-247846DOI: 10.1016/j.envres.2025.122873PubMedID: 40957472Scopus ID: 2-s2.0-105016310980OAI: oai:DiVA.org:su-247846DiVA, id: diva2:2004846
Tilgjengelig fra: 2025-10-08 Laget: 2025-10-08 Sist oppdatert: 2025-10-08bibliografisk kontrollert

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