Efficacy of zirconium hydroxide and cerium hydroxide for carbon dioxide adsorption and subsequent ethylene urea synthesis

The elevating levels of atmospheric CO 2 present a dual challenge of environmental degradation and the underutilization of potential carbon resources. Addressing these issues, our study explores innovative adsorbent materials, Zirconium Hydroxide (Zr(OH)₄) and Cerium Hydroxide (Ce(OH)₄), synthesized via both co-precipitation and sol-gel methods, for their efficacy in CO 2 adsorption and conversion into ethylene urea (EU), a valuable chemical intermediate. Through meticulous characterization and comparative analysis, we discovered that sol-gel synthesized Zr(OH)₄ outperformed other synthesized adsorbents, displaying the highest pore volume (0.65 cm³/g) and average pore diameter (66.7 nm), indicative of internal hollow spaces and inter-particle pores, thereby enhancing porosity and CO₂ trapping efficiency. This material demonstrated a notable CO 2 adsorption capacity of 1.18 mmol/g, exceeding that of co-precipitated Zr(OH)₄ (0.92 mmol/g), co-precipitated Ce(OH)₄ (0.25 mmol/g), and sol-gel synthesized Ce(OH)₄ (0.45 mmol/g). Following CO₂ adsorption, Zr(OH)₄ and Ce(OH)₄ were utilized in a reaction with ethylene diamine (EDA) in a 2-propanol solvent, achieving successful synthesis of EU. Remarkably, at 160 °C, sol-gel derived Zr(OH)₄ produced the maximum yield of EU (0.23 mmol), surpassing co-precipitated Zr(OH)₄ (0.16 mmol), co-precipitated Ce(OH)₄ (0.12 mmol), and sol-gel Ce(OH)₄ (0.12 mmol). Our findings underscore the potential of employing Zr(OH)₄, particularly synthesized via the sol-gel method, as an efficient CO 2 adsorbent and accelerator in EU production. This research contributes to the field of CO 2 capture and utilization and opens avenues for developing cost-effective and environmentally friendly processes for synthesizing industrially relevant compounds. • Zr(OH)₄ and Ce(OH)₄, noble materials, synthesized via co-precipitation and sol-gel methods. • CO₂-adsorbing materials act as CO₂ reservoirs and accelerators for ethylene urea production. • Sol-gel Zr(OH)₄ with hollow spaces displayed superior CO₂ adsorption and ethylene urea production. • Transition metal hydroxides recommended for capturing, utilizing, and converting CO 2 into valuable compounds.

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Publication Details

Journal
Journal of Cleaner Production
Published
2025-02-01
DOI
https://doi.org/10.1016/j.jclepro.2025.144956
Citations
6
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
4.28

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article

Efficacy of zirconium hydroxide and cerium hydroxide for carbon dioxide adsorption and subsequent ethylene urea synthesis

Mir Tamzid Rahman, Tomohito Kameda, Toshiaki Yoshioka, Farzana Rahman et al.
6 citations
Journal of Cleaner Production
Carbon Dioxide Capture Technologies
4.28
article

Efficacy of zirconium hydroxide and cerium hydroxide for carbon dioxide adsorption and subsequent ethylene urea synthesis

Mir Tamzid Rahman, Tomohito Kameda, Toshiaki Yoshioka, Farzana Rahman, Yota kunii, Shogo Kumagai, Yuko Saito
article en
6 citations

Abstract

The elevating levels of atmospheric CO 2 present a dual challenge of environmental degradation and the underutilization of potential carbon resources. Addressing these issues, our study explores innovative adsorbent materials, Zirconium Hydroxide (Zr(OH)₄) and Cerium Hydroxide (Ce(OH)₄), synthesized via both co-precipitation and sol-gel methods, for their efficacy in CO 2 adsorption and conversion into ethylene urea (EU), a valuable chemical intermediate. Through meticulous characterization and comparative analysis, we discovered that sol-gel synthesized Zr(OH)₄ outperformed other synthesized adsorbents, displaying the highest pore volume (0.65 cm³/g) and average pore diameter (66.7 nm), indicative of internal hollow spaces and inter-particle pores, thereby enhancing porosity and CO₂ trapping efficiency. This material demonstrated a notable CO 2 adsorption capacity of 1.18 mmol/g, exceeding that of co-precipitated Zr(OH)₄ (0.92 mmol/g), co-precipitated Ce(OH)₄ (0.25 mmol/g), and sol-gel synthesized Ce(OH)₄ (0.45 mmol/g). Following CO₂ adsorption, Zr(OH)₄ and Ce(OH)₄ were utilized in a reaction with ethylene diamine (EDA) in a 2-propanol solvent, achieving successful synthesis of EU. Remarkably, at 160 °C, sol-gel derived Zr(OH)₄ produced the maximum yield of EU (0.23 mmol), surpassing co-precipitated Zr(OH)₄ (0.16 mmol), co-precipitated Ce(OH)₄ (0.12 mmol), and sol-gel Ce(OH)₄ (0.12 mmol). Our findings underscore the potential of employing Zr(OH)₄, particularly synthesized via the sol-gel method, as an efficient CO 2 adsorbent and accelerator in EU production. This research contributes to the field of CO 2 capture and utilization and opens avenues for developing cost-effective and environmentally friendly processes for synthesizing industrially relevant compounds. • Zr(OH)₄ and Ce(OH)₄, noble materials, synthesized via co-precipitation and sol-gel methods. • CO₂-adsorbing materials act as CO₂ reservoirs and accelerators for ethylene urea production. • Sol-gel Zr(OH)₄ with hollow spaces displayed superior CO₂ adsorption and ethylene urea production. • Transition metal hydroxides recommended for capturing, utilizing, and converting CO 2 into valuable compounds.

Journal of Cleaner ProductionVol. 493
Daffodil International University (BD), Tohoku University (JP), Jahangirnagar University (BD)
New Energy and Industrial Technology Development Organization
Clean water and sanitation
Openalex Percentile: Top 6%
Carbon Dioxide Capture Technologies
4.28
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