molecular formula Ce B080170 Cerium CAS No. 13550-45-3

Cerium

Cat. No.: B080170
CAS No.: 13550-45-3
M. Wt: 140.12 g/mol
InChI Key: GWXLDORMOJMVQZ-UHFFFAOYSA-N
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Description

Cerium (Ce) is a lanthanide element with atomic number 58, noted for its dual oxidation states (Ce³⁺ and Ce⁴⁺). It is the most abundant rare earth metal, constituting ~0.0046% of the Earth’s crust . Its compounds, particularly this compound oxide (CeO₂), exhibit unique redox properties due to rapid cycling between Ce³⁺ and Ce⁴⁺, enabling applications in catalysis, energy storage, and biomedicine . This compound’s versatility stems from its oxygen storage capacity, surface defects (e.g., oxygen vacancies), and catalytic activity, which are tunable via synthesis methods and particle size .

Preparation Methods

Synthetic Routes and Reaction Conditions: Cerium can be prepared by several methods, including:

Industrial Production Methods:

Types of Reactions:

Common Reagents and Conditions:

Major Products:

Scientific Research Applications

Catalytic Applications

Cerium Oxide as a Catalyst
this compound oxide (CeO₂), commonly referred to as ceria, is widely recognized for its catalytic properties. Its unique fluorite structure allows it to participate in redox reactions, making it a valuable catalyst in various chemical processes:

  • Automotive Catalysts : Ceria is used in catalytic converters to reduce harmful emissions from vehicles by facilitating the oxidation of carbon monoxide and hydrocarbons.
  • Industrial Catalysis : It serves as a catalyst in the production of chemicals, including ethanol and biodiesel, enhancing reaction rates and selectivity .

Nanoparticle Formulations
this compound oxide nanoparticles (CeONPs) have emerged as a promising material due to their enhanced surface area and reactivity. These nanoparticles are being explored for applications such as:

  • Environmental Remediation : CeONPs can degrade pollutants in wastewater through catalytic processes.
  • Energy Storage : They are utilized in solid oxide fuel cells (SOFCs) due to their ionic conductivity .

Biomedical Applications

Antioxidant Properties
this compound oxide nanoparticles exhibit significant antioxidant properties that make them suitable for biomedical applications:

  • Cancer Treatment : Studies have shown that CeONPs can induce oxidative stress in cancer cells, leading to decreased viability and potential anti-tumor effects . They have been tested as anti-angiogenic agents in preclinical models of ovarian cancer.
  • Wound Healing : this compound nitrate has been used in treating deep burns and has antimicrobial properties that facilitate wound healing. It mimics calcium's role in biological systems, promoting tissue regeneration .

Therapeutic Agents
Recent research highlights the potential of this compound-based compounds in treating diseases associated with inflammation and oxidative stress:

  • Neurodegenerative Diseases : CeONPs are being investigated for their ability to combat oxidative damage in conditions like Alzheimer's disease .
  • Inflammatory Disorders : The antioxidant activity of ceria has implications for treating chronic inflammatory diseases, including arthritis and cardiovascular diseases .

Environmental Applications

Pollution Control
this compound compounds are being explored for their efficacy in environmental applications:

  • Air Quality Improvement : this compound oxide is used in air purification systems due to its ability to catalyze the oxidation of volatile organic compounds (VOCs).
  • Water Treatment : The photocatalytic properties of ceria enable it to break down organic pollutants in water under UV light .

Case Studies

Application AreaStudy ReferenceKey Findings
Cancer Treatment CeONPs reduced viability of lung and colon cancer cells.
Wound Healing This compound nitrate promotes healing through antimicrobial action.
Neurodegenerative Diseases CeONPs showed potential in reducing oxidative stress.
Environmental Remediation CeONPs effective in degrading wastewater pollutants.

Mechanism of Action

Cerium exerts its effects through various mechanisms:

Comparison with Similar Compounds

Structural and Chemical Properties

  • CeO₂ vs. Other Rare Earth Oxides (REOs):
    CeO₂ adopts a fluorite structure with high oxygen mobility, unlike La₂O₃ (hexagonal) or Pr₆O₁₁ (mixed-phase). CeO₂’s reducibility (Ce⁴⁺ → Ce³⁺) surpasses that of ZrO₂ or TiO₂, enhancing its catalytic efficiency in redox reactions . For instance, CeO₂ shows 2–3× higher oxygen storage capacity than ZrO₂-CeO₂ composites .
  • Ce³⁺ vs. Ce⁴⁺ Compounds:
    XANES spectra distinguish Ce³⁺ (e.g., Ce₂(CO₃)₃) from Ce⁴⁺ (e.g., CeO₂, Ce(OH)₄). Ce³⁺ compounds exhibit single-peak XANES profiles, while Ce⁴⁺ displays a doublet peak due to 4f⁰ electronic configurations . Magnetic susceptibility studies confirm intermediate valency (Ce³.⁰⁵–³.¹³) in intermetallic compounds like CeRh₁₋ₓPdₓSn, aligning with XANES data .

Catalytic and Redox Activities

  • Enzymatic Mimetic Behavior: CeO₂ nanoparticles (NPs) mimic catalase, superoxide dismutase (SOD), and oxidase activities, outperforming Fe₃O₄ or MnO₂ NPs in scavenging reactive oxygen species (ROS). For example, CeO₂ NPs exhibit 85% ROS inhibition in diabetic models, compared to 40–60% for MnO₂ .
  • Anticorrosion Mechanisms:
    Ce-based layered double hydroxides (LDHs) release Ce³⁺ ions in NaCl solutions, forming CeO₂/Ce(OH)₃ precipitates that inhibit cathodic reactions. This mechanism is absent in Zn-Al LDHs, which rely on anion exchange .

Stability and Toxicity

  • Toxicity Profile:
    CeO₂ NPs exhibit low acute toxicity (LD₅₀ > 2,000 mg/kg in rats) but induce pulmonary inflammation at 50 mg/m³ doses, unlike inert TiO₂ NPs . Chronic exposure risks remain understudied .
  • Environmental Persistence: CeO₂ NPs persist in soils for >6 months, whereas ionic Ce³⁺ forms (e.g., CeCl₃) rapidly oxidize or precipitate, reducing bioavailability .

Biological Activity

Cerium, a rare earth element, has garnered significant attention in recent years due to its unique biological activities, particularly in the form of this compound oxide nanoparticles (CeO₂ NPs). These nanoparticles exhibit a range of properties that contribute to their potential applications in medicine, particularly as antimicrobial and antioxidant agents.

Overview of this compound Compounds

This compound primarily exists in two oxidation states: Ce(III) and Ce(IV). The ability of this compound to switch between these states is crucial for its biological activity, particularly in redox reactions that can influence oxidative stress and cellular responses. This duality allows this compound compounds to function both as antioxidants and pro-oxidants under different conditions.

Antimicrobial Activity

Mechanisms of Action

This compound oxide nanoparticles have demonstrated significant antimicrobial properties against various pathogens, including bacteria and fungi. The mechanisms through which they exert their antimicrobial effects include:

  • Production of Reactive Oxygen Species (ROS): The conversion between Ce(III) and Ce(IV) states generates ROS, which can damage microbial cell components such as DNA, proteins, and lipids .
  • Interaction with Cell Membranes: CeO₂ NPs can disrupt bacterial cell membranes, leading to nutrient loss and cell death. This interaction is facilitated by the high surface area of the nanoparticles, enhancing their reactivity .
  • Electrostatic Interactions: The charged nature of this compound nanoparticles allows them to interact with negatively charged microbial cell walls, facilitating their uptake and subsequent antimicrobial action .

Antioxidant Activity

Redox Properties

The antioxidant capabilities of this compound compounds are attributed to their ability to scavenge free radicals and reduce oxidative stress. This property is particularly beneficial in biomedical applications where oxidative damage is a concern:

  • Scavenging Free Radicals: this compound oxide nanoparticles can neutralize free radicals produced during metabolic processes, thereby protecting cells from oxidative damage .
  • Cellular Protection: Studies have shown that this compound compounds can enhance the survival of cells exposed to oxidative stress by modulating cellular signaling pathways .

Case Studies

  • Antimicrobial Efficacy Against Pathogens:
    A study demonstrated that CeO₂ NPs exhibited strong antibacterial activity against Staphylococcus aureus and Escherichia coli, with inhibition zones measuring 15 mm and 14 mm, respectively. This was attributed to the nanoparticles' ability to produce ROS upon contact with bacterial membranes .
  • Wound Healing Applications:
    Research indicated that nanocrystalline this compound oxide enhanced the metabolic activity of human fibroblast cell cultures at specific concentrations (10^-4M), promoting wound healing processes. However, higher concentrations exhibited cytotoxic effects, underscoring the importance of dosage in therapeutic applications .
  • Cytotoxicity Studies:
    Investigations into the cytotoxic effects of this compound nanoparticles revealed that concentrations above 10^-2M significantly reduced cell viability in human keratinocytes. In contrast, lower concentrations (10^-4M and 10^-6M) stimulated cell proliferation, highlighting a concentration-dependent response .

Data Table: Biological Activity of this compound Compounds

Study FocusKey FindingsConcentration Range
Antimicrobial ActivityInhibition zones against S. aureus and E. coli15 mm (S. aureus), 14 mm (E. coli)
Wound HealingEnhanced fibroblast activity10^-4M (optimal)
CytotoxicityReduced viability at high concentrations10^-2M (cytotoxic), 10^-4M (stimulative)

Q & A

Basic Research Questions

Q. What key physicochemical properties of cerium make it suitable for catalytic applications?

this compound's redox activity (Ce³⁺ ↔ Ce⁴⁺) and oxygen storage capacity (OSC) are critical in catalysis. These properties enable dynamic oxygen vacancy formation in this compound oxide (CeO₂), enhancing catalytic cycles in reactions like VOC oxidation. Methodologically, OSC is measured via temperature-programmed reduction (TPR) or pulsed chemisorption, while redox behavior is analyzed using X-ray absorption spectroscopy (XAS) .

Q. How is this compound characterized in alloy systems to confirm its structural role?

Energy-dispersive X-ray spectroscopy (EDX) quantifies this compound distribution in alloys, while X-ray diffraction (XRD) identifies phase changes. For example, in Cu-30%Zn alloys doped with 3 wt% Ce, EDX maps elemental segregation, and XRD detects intermetallic phases like CeZn₅. Mechanical properties (e.g., hardness) are tested via Vickers microhardness indentation .

Q. What standard protocols ensure reproducibility in synthesizing this compound oxide nanoparticles?

Sol-gel synthesis with controlled hydrolysis rates (e.g., using this compound nitrate precursors and ammonia) yields uniform CeO₂ nanoparticles. Particle size distribution is validated via dynamic light scattering (DLS) and transmission electron microscopy (TEM). Surface area is quantified using Brunauer-Emmett-Teller (BET) analysis, with protocols emphasizing precursor purity and calcination temperature .

Advanced Research Questions

Q. How can experimental design optimize this compound doping in metallurgical systems?

Factorial designs (e.g., varying Ce wt% and cooling rates) coupled with response surface methodology (RSM) identify optimal doping parameters. For Cu-Zn alloys, a 3 wt% Ce addition maximizes grain refinement, as shown in hardness tests and microstructure analysis. Sensitivity analyses (e.g., ANOVA) validate statistical significance of variables .

Q. What methodologies resolve contradictions in reported catalytic efficiencies of CeO₂ nanoparticles?

Contradictions arise from synthesis-dependent surface defects (e.g., oxygen vacancies) and testing conditions (temperature, gas composition). Comparative studies using in situ diffuse reflectance infrared Fourier-transform spectroscopy (DRIFTS) under controlled atmospheres isolate defect-driven mechanisms. Meta-analyses of published data (e.g., Arrhenius plots) reconcile activation energy discrepancies .

Q. How do high-throughput screening (HTS) methods accelerate this compound-based catalyst discovery?

HTS workflows employ combinatorial libraries (e.g., CeO₂-supported Pt, Pd, Cu) and automated testing rigs. For VOC oxidation, design-of-experiments (DoE) models (e.g., full factorial designs) screen variables like metal loading and calcination time. Data-driven algorithms (e.g., machine learning) prioritize candidates with >85% conversion efficiency, validated via gas chromatography (GC) .

Q. What statistical models best describe this compound oxide carbochlorination kinetics?

Stat-Ease Design-Expert software models % conversion as a function of temperature (600–900°C), Cl₂ flow rate, and carbon ratio. For CeO₂, quadratic regression equations (R² > 0.95) predict optimal conversion at 900°C, 4 h reaction time, and 1:2 C/CeO₂ molar ratio. Sensitivity analyses confirm Cl₂ flow as the most influential parameter .

Q. How can bibliometric analysis track emerging trends in this compound oxide nanoparticle research?

Tools like Publish or Perish aggregate publication data (2012–2022) to map growth areas (e.g., biomedical applications vs. environmental catalysis). Co-citation networks in VOSviewer identify clusters (e.g., "CeO₂ in photocatalysis") and gaps (e.g., long-term toxicity studies). Annual publication counts and h-index trends highlight leading institutions .

Q. What in situ techniques elucidate this compound’s redox mechanisms during catalytic cycles?

Operando XAS tracks Ce³⁺/Ce⁴⁺ ratios under reaction conditions, while Raman spectroscopy detects oxygen vacancy dynamics. For CO oxidation, time-resolved mass spectrometry correlates vacancy density with turnover frequency (TOF). These methods require synchrotron facilities and controlled reactor environments .

Q. How do hybrid DFT-MD simulations enhance understanding of this compound’s electronic structure?

Density functional theory (DFT) combined with molecular dynamics (MD) predicts CeO₂ surface interactions (e.g., H₂O adsorption). Charge density difference maps and projected density of states (PDOS) reveal hybridization between Ce-4f and O-2p orbitals. Validation involves comparing computed oxygen vacancy formation energies with experimental values (~2.5 eV) .

Methodological Notes

  • Data Validation : Cross-reference experimental results with theoretical models (e.g., DFT for redox properties) to address contradictions .
  • Ethical Reproducibility : Publish raw datasets (e.g., XRD/EDX files) and synthesis protocols in supplementary materials to enable replication .
  • Interdisciplinary Integration : Combine materials science (alloy design) and computational chemistry (HTS workflows) for holistic this compound studies .

Properties

IUPAC Name

cerium
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Description Data deposited in or computed by PubChem

InChI

InChI=1S/Ce
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InChI Key

GWXLDORMOJMVQZ-UHFFFAOYSA-N
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Canonical SMILES

[Ce]
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Molecular Formula

Ce
Record name CERIUM, TURNINGS OR GRITTY POWDER
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DSSTOX Substance ID

DTXSID0058641
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Molecular Weight

140.116 g/mol
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Physical Description

Cerium, turnings or gritty powder appears as a gray metallic solid. Specific gravity 6.78. Turnings or gritty powder. Contact may burn skin, eyes or mucous membranes. May be toxic by ingestion, inhalation or skin absorption. Used to make other chemicals., Other Solid; Pellets or Large Crystals, Gray solid; [CAMEO] Ceric salts: yellow or red-orange; Cerous salts: usually white; [Reference #1] Ductile and highly reactive; Readily oxidizes; [Hawley], Solid
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CAS No.

7440-45-1, 13864-02-3
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Melting Point

795 °C
Record name Cerium
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Synthesis routes and methods

Procedure details

Example 73 was repeated except that before aging a solution of cerium nitrate and a solution of ammonium vanadate were added sufficient to obtain about 8% by weight of cerium as cerium oxide and 4% by weight of vanadium as vanadium oxide on the final product based on the Al2O3 content. The rest of the processing was the same. XRD analysis indicated the products were Alumina doped with anionic clay.
Name
cerium nitrate
Quantity
0 (± 1) mol
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Reaction Step One
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