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Molybdenum trioxide

Molybdenum trioxide (MoO₃) is the most and of the , existing as an odorless that ranges in color from to yellow. It features a layered composed of distorted MoO₆ octahedra sharing edges and vertices, forming double layers with van der Waals gaps between them, primarily in its orthorhombic α-phase, though a metastable monoclinic β-phase also exists. With a molecular weight of 143.95 g/mol, a density of 4.69 g/cm³, a melting point of 795 °C, and a sublimation point around 1155 °C, it exhibits slight solubility in water (approximately 1.07 g/L at 18 °C) and behaves as an n-type semiconductor with a band gap of about 3 eV. Commercially, molybdenum trioxide is produced on a large scale by the roasting of molybdenite (MoS₂) ore in air, which oxidizes the sulfide to the trioxide, followed by purification through sublimation or other methods such as ignition of molybdenum metal, sulfides, or lower oxides. This compound serves as a key intermediate in the production of pure molybdenum metal via hydrogen reduction and is essential in various industrial sectors, including as an alloying agent in stainless and high-strength steels to enhance corrosion resistance and strength, and in superalloys for aerospace applications. In , molybdenum trioxide is a vital component in processes like hydrodesulfurization, oxidation to , and epoxidation reactions, owing to its to undergo topotactic chemistry and intercalate . It also finds use in ceramics for pigments and enamels, as a suppressant in (PVC), and in emerging applications such as electrochromic devices and lithium-ion battery electrodes due to its electrochemical properties. Safety considerations include its classification as a possible carcinogen (IARC Group 2B) and its irritant effects on the eyes and respiratory tract, with occupational exposure limits set at 5 mg/m³ (OSHA PEL) and 0.5 mg/m³ (ACGIH TLV).

Properties

Physical properties

Molybdenum trioxide (MoO₃) is typically observed as a white to light yellow crystalline powder or as needle-like crystals, with the color shifting to yellow at elevated temperatures. This appearance corresponds to its orthorhombic , which consists of layered sheets. The compound exhibits a of 4.69 g/cm³ for its orthorhombic form at 25°C. It has a melting point of 795°C, above which it begins to decompose rather than fully liquefy. The boiling point is approximately 1155°C, though MoO₃ primarily sublimes under standard conditions rather than boiling. MoO₃ is slightly soluble in water (solubility ≈ 1 g/L at 20 °C) and most organic solvents, but it shows slight solubility in alkaline solutions such as alkali hydroxides. The material is hygroscopic, readily absorbing atmospheric moisture to form the dihydrate MoO₃·2H₂O, which is bright yellow and loses water upon heating. The specific heat capacity of solid MoO₃ is described by the Shomate equation for temperatures from 298 K to 1700 K, yielding values around 0.51 J/g·K at 298 K. Thermal conductivity for bulk orthorhombic MoO₃ is approximately 5.3 W/m·K at room temperature, though it is anisotropic due to the layered structure. Regarding vapor behavior, MoO₃ has low vapor pressure under ambient conditions but evaporates effectively under vacuum at around 400–500°C, with a vapor pressure reaching 10⁻⁴ Torr near 900°C.
PropertyValueConditions
Density4.69 g/cm³Orthorhombic, 25°C
Melting point795°C (decomposes >800°C)-
Sublimation point~1155°C760 mmHg
Water solubility≈ 1 g/L20°C
Specific heat capacity~0.51 J/g·K298 K
Thermal conductivity~5.3 W/m·KBulk, room temperature

Chemical properties

Molybdenum trioxide (MoO₃) is thermally stable up to its melting point of 795 °C, beyond which it sublimes at 1155 °C and can decompose to molybdenum dioxide (MoO₂) and oxygen (O₂) under certain conditions such as vacuum or high temperatures above 800 °C. As an amphoteric , MoO₃ exhibits reactivity, dissolving in concentrated acids to form molybdic acid and in hydroxides to produce ions, a behavior attributed to the polar Mo-O bonds in its structure. It is a (VI) with Mo in the +6 , enabling it to function as an oxidizing agent in various chemical processes. In reactions, MoO₃ can be reduced to lower-valent molybdenum oxides, such as MoO₂ or Mo₄O₁₁, particularly when exposed to reducing agents or at elevated temperatures. Aqueous suspensions of MoO₃ are weakly acidic with a of approximately 2.5 for saturated solutions at , resulting from partial . MoO₃ demonstrates good compatibility with many acids, remaining largely inert to dilute solutions, but it reacts readily with strong bases to form soluble molybdates and with reducing agents like alkali metals or hydrogen, leading to reduction products.

Structure

Crystal structure

Molybdenum trioxide (MoO₃) exists predominantly in the thermodynamically stable orthorhombic α-phase under ambient conditions, crystallizing in the space group Pnma (No. 62) with lattice parameters a = 3.962 Å, b = 13.855 Å, and c = 3.697 Å. This structure features layers of distorted MoO₆ octahedra that share edges to form double sheets, which are stacked along the b-axis and separated by van der Waals gaps, enabling intercalation and anisotropic properties. Within each octahedron, molybdenum is coordinated to two short terminal Mo=O double bonds (≈1.67 Å), two shorter bridging Mo–O bonds (≈1.73–1.96 Å), and two longer bridging Mo–O bonds (≈2.25–2.30 Å), contributing to the overall distortion from ideal octahedral geometry. Metastable polymorphs include the monoclinic β-MoO₃ phase (space group P2₁/c, with lattice parameters a ≈ 7.12 Å, b ≈ 5.37 Å, c ≈ 5.57 Å, β ≈ 91.9°), which consists of corner-sharing MoO₆ octahedra in a distorted ReO₃-like framework, and a metastable hexagonal h-MoO₃ phase (space group P6₃cm) featuring hexagonal tunnels formed by edge- and corner-sharing octahedra. Amorphous MoO₃ can also be prepared via precipitation from aqueous solutions, such as hydrolysis of molybdates, resulting in non-crystalline solids that lack long-range order but retain local octahedral coordination. The polymorphic forms are commonly identified and distinguished using powder (), where the orthorhombic α-phase exhibits characteristic peaks at 2θ ≈ 12.8° (), 23.4° (), 25.7° (), and 39.0° (), while β- and h-phases show distinct patterns with peaks shifted due to their different symmetries.

Bonding and electronic

Molybdenum trioxide (MoO₃) features covalent Mo-O bonds that exhibit significant ionic character due to charge transfer from oxygen 2p orbitals to molybdenum, as revealed by energy decomposition . Each molybdenum atom is in the +6 oxidation , coordinated octahedrally within MoO₆ units, where one terminal Mo=O (bond length ≈1.67 Å) provides substantial π-bonding contributions, while bridging Mo-O-Mo linkages show longer distances ranging from 1.73–2.33 Å. This asymmetry in bond lengths reflects the distorted octahedral geometry, with the terminal double bond dominating the local electronic environment around each Mo(VI) center. The electronic configuration of MoO₃ is characterized by Mo(VI) in a d⁰ state, resulting in a wide-bandgap semiconductor behavior with an indirect bandgap of approximately 3.16 eV in the orthorhombic phase, closely matching experimental values of 3.2 eV. The valence band primarily arises from O 2p states, while the conduction band consists of empty Mo 6d orbitals, leading to an indirect transition where the valence band maximum and conduction band minimum occur at different points in the Brillouin zone. Doping possibilities include n-type conductivity via oxygen vacancies acting as shallow donors, whereas p-type doping is challenging but feasible with certain substitutional acceptors like Mn or Fe on Mo sites under specific conditions. Spectroscopic studies confirm motifs through vibrational modes: Raman and bands for Mo=O stretch appear around 820–1000 ⁻¹, with prominent peaks at 819 ⁻¹ (symmetric) and 995 ⁻¹ (antisymmetric), while Mo-O-Mo bridging modes are observed at lower frequencies, typically 200–400 ⁻¹, reflecting the weaker interactions in the shared edges. In the gas phase, MoO₃ exists as a monomeric species with three oxygen atoms directly bonded to the central Mo atom, forming a compact structure that decomposes from oligomeric precursors under mild conditions.

Occurrence and production

Natural occurrence

Molybdenum trioxide occurs naturally in only trace amounts as the rare mineral molybdite, typically in the form of MoO₃·H₂O, which forms as a secondary mineral through the oxidation of primary molybdenum sulfides such as molybdenite (MoS₂). Molybdite is uncommon and is most often found as yellow to greenish crusts or powders in oxidized zones of molybdenum deposits, with notable occurrences in locations such as Krupka in the Czech Republic, Siberia in Russia, and various sites in Arizona and California in the United States. In nature, molybdenum trioxide is closely associated with molybdenite deposits, which are predominantly hosted in ore systems, where molybdenum serves as a valuable byproduct during . These deposits form in magmatic-hydrothermal environments linked to zones, concentrating molybdenum alongside and other metals. Global distribution of molybdenum trioxide-bearing minerals aligns with major molybdenum-rich regions, including the and Henderson mines in , ; the and Collahuasi deposits in ; and numerous porphyry-style deposits in , which collectively account for a significant portion of the world's molybdenum resources. itself has an average crustal abundance of approximately 1.2 parts per million, making it one of the rarer elements in the , though the pure MoO₃ form remains exceptionally uncommon outside of secondary products. Indirect sources of molybdenum trioxide include hydrated molybdate minerals such as wulfenite (PbMoO₄) and powellite (CaMoO₄), which occur in oxidized lead and calcium-rich environments and can yield molybdenum trioxide upon further weathering or processing, though they are not primary sources of the oxide itself. Due to its rarity in native form, molybdenum trioxide is seldom mined directly and is instead derived as a byproduct from the roasting of molybdenum sulfide ores in industrial settings.

Industrial production

The primary industrial production of molybdenum trioxide (MoO₃) involves the oxidative roasting of molybdenite (MoS₂) concentrate, the main ore feedstock, in multi-stage furnaces at temperatures between 500 and 700 °C. The key reaction is 2 MoS₂ + 7 O₂ → 2 MoO₃ + 4 SO₂, conducted in multiple steps to control sulfur release and minimize the formation of sulfur trioxide (SO₃), which can lead to equipment corrosion; rotary kilns or hearth furnaces are commonly used, with air or oxygen-enriched atmospheres to achieve desulfurization below 0.1% sulfur in the product. Following roasting, the technical-grade MoO₃ (typically 57–85% Mo content) undergoes purification to remove impurities such as , , and other metals. Common methods include under or at 600–800 °C to volatilize pure MoO₃, or chemical with alkaline solutions followed by and to high-purity product (>99.9% MoO₃). The (SO₂) from roasting is captured and converted to in integrated , enhancing and reducing emissions. Global production of molybdenum trioxide, reported as molybdenum content, reached 248,000 metric tons in 2023 and an estimated 260,000 metric tons in 2024; China dominates as the top producer, accounting for 110,000 metric tons in 2024, followed by Peru (41,000 tons), Chile (38,000 tons), the United States (33,000 tons), and Mexico (17,000 tons). Declining ore grades at major porphyry copper mines are anticipated to pose challenges to future supply. Alternative production routes include the oxidation of ferromolybdenum scrap at elevated temperatures to recover MoO₃, though this is less common, and recycling from spent catalysts such as hydrodesulfurization units via roasting or hydrometallurgical leaching to extract and precipitate molybdic acid, which is then calcined to MoO₃. Modern facilities incorporate energy-efficient designs like heat recovery systems and advanced emission controls, including SO₂ scrubbers with lime or double-contact sulfuric acid processes, to comply with environmental regulations and minimize particulate and gaseous releases.

Reactions

Laboratory preparation

Molybdenum trioxide (MoO₃) can be prepared in the laboratory through several small-scale methods suitable for research and educational purposes, often starting from soluble molybdate salts or metal precursors. These approaches emphasize controlled conditions to achieve high purity and defined morphology, contrasting with large-scale industrial processes. A widely used method involves the acidification of sodium molybdate solutions to precipitate hydrated molybdenum trioxide, which is then dehydrated to the anhydrous form. An aqueous solution of sodium molybdate (Na₂MoO₄) is treated with hydrochloric acid (HCl), resulting in the formation of molybdic acid hydrate (MoO₃·H₂O) via the reaction: \text{Na}_2\text{MoO}_4 + 2 \text{HCl} \rightarrow \text{MoO}_3 \cdot \text{H}_2\text{O} + 2 \text{NaCl} The precipitate is filtered, washed to remove sodium chloride, and dried. Subsequent dehydration occurs by heating the hydrate at 300–500 °C in air, yielding anhydrous orthorhombic α-MoO₃. This temperature range ensures complete removal of water while minimizing sublimation losses, as the transformation from β-MoO₃ (formed around 260–320 °C) to stable α-MoO₃ completes above 350 °C. Yields typically reach 80–90% based on molybdenum content, with phase purity confirmed by X-ray diffraction (XRD) showing characteristic peaks for α-MoO₃ and minimal impurities if excess acid is avoided. Another common route is the thermal decomposition of ammonium heptamolybdate tetrahydrate ((NH₄)₆Mo₇O₂₄·4H₂O), a commercially available precursor. The compound undergoes stepwise decomposition upon heating in air, releasing ammonia and water vapor to form MoO₃: (\text{NH}_4)_6\text{Mo}_7\text{O}_{24} \cdot 4\text{H}_2\text{O} \rightarrow 7 \text{MoO}_3 + 6 \text{NH}_3 + 7 \text{H}_2\text{O} Heating is typically conducted at 400–500 °C for 2–4 hours in a muffle furnace, producing fine powders of high purity α-MoO₃. This method is favored for its simplicity and ability to control particle size by varying the heating rate; slower ramps (e.g., 5 °C/min) yield larger crystallites. Reported yields exceed 95%, with purity levels suitable for catalytic studies, as evidenced by thermogravimetric analysis (TGA) showing complete decomposition without residual ammonium species. Oxidation of molybdenum metal powder or lower molybdenum oxides (e.g., MoO₂) provides an alternative direct synthesis. Molybdenum powder is oxidized by heating in air at 500–700 °C, where surface oxidation progresses to form a protective MoO₃ layer, though prolonged exposure (several hours) is needed for complete conversion. Alternatively, treatment with concentrated nitric acid (HNO₃) dissolves the metal, forming soluble molybdic acid, which precipitates as MoO₃·nH₂O upon dilution or neutralization; dehydration follows as described above. These oxidation methods yield purities above 98% when starting from high-grade metal (99.9% Mo), but require careful temperature control to prevent volatilization of MoO₃ above 700 °C. Precipitation from molybdic acid solutions offers versatility for tailored morphologies. Molybdic acid (H₂MoO₄, equivalent to MoO₃·H₂O) is dissolved in dilute acid (e.g., HCl at pH 1–2), and upon heating or aging, it polymerizes and precipitates as hydrated MoO₃. This is often combined with additives like surfactants for nanostructured products, followed by calcination at 350–450 °C. Lab-scale yields are 85–95%, with high purity achievable through repeated washing, as impurities like chloride ions are minimized below 0.1 wt% via ion detection. Overall, these methods produce lab-grade MoO₃ with purities of 99% or higher, suitable for spectroscopic and electrochemical applications, though analytical verification (e.g., inductively coupled plasma mass spectrometry for trace metals) is recommended.

Principal reactions

Molybdenum trioxide undergoes to metallic via gas at elevated temperatures, following the overall : \ce{MoO3 + 3 H2 -> Mo + 3 H2O} This occurs in two stages: initial partial to at 450–650 °C, followed by complete to the metal at 800–1000 °C, where the increases significantly above 800 °C due to and vapor . In aqueous suspensions, molybdenum trioxide reacts with water to form molybdic acid, represented as: \ce{MoO3 + H2O -> H2MoO4} This dissolution equilibrium yields low solubility, with the reaction proceeding via protonation to form H₂MoO₄(aq) species, particularly under mildly acidic conditions, and is characterized by a solubility product log₁₀K = -2.40 ± 0.20. As an amphoteric oxide, molybdenum trioxide reacts with bases such as sodium hydroxide to produce soluble molybdates, exemplified by: \ce{MoO3 + 2 NaOH -> Na2MoO4 + H2O} This metathesis reaction dissolves the oxide in alkaline media, forming the sodium molybdate anion, which is commonly used in molybdenum sourcing and occurs effectively at 50–70 °C. Partial reduction of molybdenum trioxide with hydrogen yields molybdenum dioxide as the primary product, via: \ce{MoO3 + H2 -> MoO2 + H2O} This first-stage reduction, occurring at 450–650 °C, involves intermediate magnéli phases like Mo₄O₁₁ and proceeds through chemical vapor transport, with water vapor facilitating the transformation and controlling particle morphology. In concentrated aqueous solutions, particularly under acidic conditions, dissolved molybdenum trioxide species polymerize to form polymolybdates, such as [Mo₈O₂₆]⁴⁻, through condensation reactions that link molybdate units via oxygen bridges, influencing solubility and speciation at pH below 6.

Applications

Metallurgical applications

Molybdenum trioxide serves as a key precursor in metallurgical processes for producing high-purity molybdenum metal and molybdenum-containing alloys, particularly for enhancing steel properties. It is reduced to metallic molybdenum through hydrogen or carbon-based processes, yielding material suitable for demanding applications such as lamp filaments and electrodes due to its high melting point and thermal stability. In the production of pure molybdenum, technical-grade molybdenum trioxide undergoes stepwise reduction, first to molybdenum dioxide and then to metal powder, often using hydrogen gas at elevated temperatures to achieve high purity levels essential for filament supports in lighting and grids in electron tubes. Alternatively, carbon reduction methods are employed for certain industrial scales, though hydrogen reduction predominates for premium applications requiring minimal impurities. This pure molybdenum is critical in components exposed to extreme heat, such as electrodes in glass-melting furnaces, where its compatibility with glass and resistance to oxidation at high temperatures provide operational advantages. For alloy production, molybdenum trioxide is converted to ferromolybdenum via aluminothermic , involving the of the with aluminum and iron sources in a controlled to form an typically containing 60-70% . This ferromolybdenum is then added to melts as an alloying agent, improving tensile strength, , and resistance—particularly against pitting and in aggressive environments. Approximately 80-90% of molybdenum trioxide is directed toward these metallurgical uses, underscoring its dominance in the sector. Historically, the of into evolved in the 1930s from earlier, less controlled methods—such as incorporation of impure concentrates—toward the use of purified molybdenum trioxide, precise alloying and broader in high-performance steels. This shift facilitated the of specialized grades, including high-strength low-alloy (HSLA) steels, where molybdenum additions of 0.2-0.5% refine microstructure, enhance , and strengths above for applications in pipelines and structural components.

Catalytic and industrial applications

Molybdenum trioxide (MoO₃) serves as a key promoter in catalysts for selective oxidation reactions, particularly in the industrial production of acrylonitrile via the ammoxidation of propylene. In these processes, MoO₃ is often supported on alumina and combined with bismuth molybdate phases, such as α-Bi₂Mo₃O₁₂, which exhibit high activity due to the synergistic interaction between bismuth sites for allyl intermediate formation and molybdenum sites for oxygen activation. This configuration enables high selectivity toward acrylonitrile, with yields exceeding 70% under optimized conditions, making it a cornerstone of commercial propylene ammoxidation. MoO₃ is used in pigments for ceramics and enamels. MoO₃ is used as a hole injection layer in light-emitting diodes (OLEDs), facilitating efficient hole injection and charge , owing to its high work function (~3 eV band gap) and deep valence band that enable interfacial dipoles lowering the hole injection barrier and improving device luminance and efficiency. This property stems from its electronic structure, where oxygen vacancies promote doping, enhancing hole mobility at the anode-organic interface. In photovoltaic devices, MoO₃ acts as a layer in both and cells, improving and . As an , it reduces recombination losses and enhances , leading to efficiencies 20% higher than without it, particularly in architectures where it stabilizes the against . In , MoO₃ layers mitigate and extend operational under ambient conditions by passivating surface defects. Beyond , MoO₃ finds use as a in coatings, especially for automotive components. Incorporated into primer formulations, it forms protective layers that inhibit formation in humid environments, offering non-toxic alternatives to chromates with inhibition efficiencies above 90% in spray tests. Additionally, MoO₃ serves as a in lithium-ion batteries, where its layered structure accommodates Li⁺ intercalation, delivering reversible capacities around 200 mAh/g with good cycling stability due to minimal volume expansion during charge-discharge. Recent advancements since 2020 have focused on nanostructured MoO₃ for green chemistry applications, enhancing catalytic performance in environmentally benign processes. For instance, α-MoO₃ nanorods and nanospheres, often synthesized via green methods like plant extract-mediated reduction, exhibit superior photocatalytic activity for pollutant degradation and epoxidation reactions under visible light, achieving turnover numbers over 500 while minimizing energy input and waste. These structures leverage increased surface area and defect sites to promote selective oxidation in solvent-free conditions, aligning with sustainable catalysis goals.

Safety and environmental aspects

Health and safety hazards

Molybdenum trioxide is to the eyes, , and respiratory tract upon or . of its can lead to , a form of lung fibrosis, characterized by respiratory inflammation and scarring. Acute exposure effects include coughing, , and irritation of the mucous membranes, with no observed lethality in rats at concentrations 5,840 mg/m³ for 4 hours. Oral toxicity is low, with an LD50 greater than 2,000 mg/kg in rats, indicating minimal risk from ingestion under normal conditions. Chronic exposure to molybdenum trioxide dust may result in accumulation of molybdenum in the body, potentially leading to gout-like symptoms from elevated serum uric acid levels or anemia due to interference with copper metabolism. Prolonged inhalation at concentrations as low as 6.7 mg/m³ has been associated with respiratory lesions, including squamous metaplasia in animal studies. Safe handling requires personal protective equipment such as gloves, safety goggles, and respiratory masks to prevent dust inhalation; operations should minimize dust generation through wet methods or local exhaust ventilation. The occupational exposure limit is 5 mg/m³ (as Mo) for an 8-hour time-weighted average, per OSHA permissible exposure limits for related molybdenum compounds. As a strong oxidizer, molybdenum trioxide is incompatible with reducing agents and combustibles, potentially accelerating or causing vigorous ; it decomposes at high temperatures, releasing oxygen. It is non-flammable itself but requires measures for surrounding materials, avoiding that may generate . Molybdenum trioxide is classified as hazardous under OSHA regulations, requiring under SARA III 313 for facilities exceeding thresholds. It is not classified as a known but is listed as possibly carcinogenic () based on .

Environmental impact

The of molybdenum trioxide primarily through the of concentrate generates significant emissions, including (SO₂) from the oxidation of and trace amounts of molybdenum . roasting facilities employ desulfurization systems, such as or lime scrubbers, to capture over 99% of SO₂ and convert it into sulfuric acid, thereby minimizing atmospheric releases and acid rain contributions. Trace molybdenum emissions occur during mining and processing stages, with historical data indicating elevated atmospheric concentrations near production sites, though current controls have reduced these levels substantially. Runoff from molybdenum trioxide production sites can introduce soluble molybdate ions into water bodies, posing risks to aquatic ecosystems. These compounds exhibit moderate toxicity to fish and invertebrates, with acute 96-hour LC50 values ranging from approximately 70 to over 2,000 mg/L depending on water hardness and species, such as rainbow trout. Chronic exposure at lower concentrations may affect reproduction and growth in sensitive aquatic organisms. In soils, accumulation of molybdenum from industrial deposition or agricultural applications can lead to molybdenosis in grazing livestock, characterized by copper deficiency symptoms when dietary molybdenum exceeds 5–10 mg/kg dry matter, particularly in sulfur-rich environments. Regulatory guidelines, such as those from the U.S. EPA for ore mining wastewater, aim to limit molybdenum discharges to protect ecosystems, with local effluent limits as low as 0.43 mg/L in some jurisdictions to prevent bioaccumulation. Recycling efforts mitigate environmental burdens by recovering from spent catalysts and alloys, for about % of supply and reducing the need for primary , which lowers and use. initiatives include adopting low-emission technologies and leveraging molybdenum trioxide in green applications, such as , which has cut SO₂ emissions from by hundreds of thousands of tonnes annually in regions like the .

References

  1. [1]
    Molybdenum trioxide | MoO3 | CID 14802 - PubChem
    Pure molybdenum trioxide is used in chemical and catalyst manufacture and the technical product is added to steel as an alloying agent. International Labour ...
  2. [2]
    Molybdenum Trioxide - an overview | ScienceDirect Topics
    Molybdenum trioxide (MoO3) has two crystal forms, a distorted MoO6 octahedron structure, and is formed from molybdenite (MoS2) and used in alloys, chemicals, ...
  3. [3]
    molybdenum trioxide moo3: Topics by Science.gov
    The mechanisms of molecular doping in organic electronic materials are explored through investigation of pentacene p -doped with molybdenum trioxide (MoO3) .
  4. [4]
    molybdenum trioxide - the NIST WebBook
    Solid Phase Heat Capacity (Shomate Equation)​​ t = temperature (K) / 1000. View table.
  5. [5]
    Thermal conductivity across the van der Waals layers of α-MoO3 thin ...
    Aug 23, 2021 · The mean thermal conductivity across the van der Waals layers of the three α-MoO 3 thin films was evaluated to be 1.2 ± 0.3 W m −1 K −1.
  6. [6]
    Molybdenum Oxide MoO 3 Evaporation Process Notes
    Molybdenum oxide has a vapor pressure of 10 -4 Torr at ~900°C. It will have a slight O 2 loss during evaporation so supplemental oxygen may be necessary.
  7. [7]
    [PDF] MOLYBDENUM TRIOXIDE - IARC Publications
    Molybdenum trioxide is a high production volume chemical. High production volume chemicals “are produced or imported at levels greater than 1,000 tonnes per ...
  8. [8]
    Thermal Reduction of MoO3 Particles and Formation of MoO2 ...
    At ∼350°C, a dominant α-MoO3 cryst. phase started to emerge, and XAS spectra ruled out the formation of a molybdenum dioxide phase. A further increase of the ...Introduction · Methods · Results and Discussion · Conclusions
  9. [9]
    mp-20589: MoO3 (Orthorhombic, Pnma, 62) - Materials Project
    The crystal structure of molybdenum trioxide mo o3. Zeitschrift fuer ... heat capacity (specific heat) · magnetic susceptibility · permittivity ...<|separator|>
  10. [10]
    Growth modes in vapour-phase prepared orthorhombic ...
    Aug 18, 2025 · Within a MoO6 octahedron, Mo–O bonding situations differ. There are five different types of Mo–O bond lengths: 1.67, 1.73, 1.95 (twice), 2.25 ...
  11. [11]
    Crystallization, Phase Stability, and Electrochemical Performance of ...
    Apr 28, 2020 · In this paper, we investigate the conversion of X-ray amorphous molybdenum trioxide (MoO3) into the α- and β-MoO3 polymorphs with the aim of ...
  12. [12]
    mp-18856: MoO3 (Monoclinic, P2_1/c, 14) - Materials Project
    MoO3 crystallizes in monoclinic P21/c space group, with two Mo⁶⁺ sites and six O²⁻ sites. Lattice parameters are a=7.18 Å, b=7.61 Å, c=10.50 Å.
  13. [13]
    Amorphous–crystalline transition studied in hydrated MoO 3
    Results show that the hydrated MoO3·1.4H2O glass transforms in an amorphous MoO3·0.7H2O phase prior to its crystallization, while the sample heated at 500 °C ...
  14. [14]
    The Synergic Effect of h-MoO3, α-MoO3, and β-MoO3 Phase Mixture ...
    Molybdenum oxide naturally exhibits three defined stoichiometric structures, commonly known as alpha, beta, and monoclinic phases. The alpha phase (α-MoO3) is ...
  15. [15]
    [PDF] Molybdenum - Mineral Commodity Summaries 2024 - USGS.gov
    Molybdenum is a refractory metallic element used principally as an alloying agent in cast iron, steel, and superalloys and is also used in numerous chemical ...
  16. [16]
    Molybdite: Mineral information, data and localities.
    Čech, F., Povondra, P. (1963) Natural occurrence of molybdenum trioxide, MoO3, in Krupka (Molybdite, a new mineral). Acta Universitatis Carolinae - Geologica: 1 ...
  17. [17]
    By-Products of Porphyry Copper and Molybdenum Deposits
    Jan 1, 2016 · Porphyry Cu and porphyry Mo deposits are large to giant deposits ranging up to >20 and 1.6 Gt of ore, respectively, that supply about 60 and 95% ...Abstract · Introduction · Porphyry Copper and... · Summary and Conclusions
  18. [18]
    Molybdenum - USGS Publications Warehouse
    May 7, 2024 · Molybdenum is somewhat enriched in felsic rocks, such as granite or rhyolite, with an average concentration of about 1.5 mg/kg. Sedimentary ...
  19. [19]
    Production process and Application of Molybdenum trioxide
    Oct 14, 2019 · Molybdenum trioxide occurs naturally as the rare mineral molybdite, but is obtained commercially almost exclusively from molybdenite (molybdenum ...
  20. [20]
    Molybdenum Processing
    Molybdenum metal is produced by hydrogen reduction of pure molybdic oxide or ammonium molybdate. The chemical reduction of pure molybdenum trioxide or ammonium ...
  21. [21]
    Roasting Kinetics of Molybdenite Concentrates
    Jul 18, 2013 · Roasting of MoS2 concentrate is an important step in the production of commercial molybdenum trioxide. The oxidation kinetics of two different ...
  22. [22]
    Industrial-Scale Technology for Molybdic Acid Production from ...
    Aug 23, 2023 · The article describes the technology of molybdic acid recovery from spent petrochemical catalysts (HDS) developed and implemented in industrial activity.
  23. [23]
    [PDF] Large-Batch Reduction of Molybdenum Trioxide - INFO
    Above 750°C, the MoO2 begins to be reduced to Mo metal with reduction completed by 1100°C. Additional reductions runs were conducted in the ceramic tube ...
  24. [24]
    [PDF] Mechanisms of the Hydrogen Reduction of Molybdenum Oxides
    Starting from molybdenum-containing ores, the hydrogen reduction of molybdenum trioxide to molybdenum is the last step in producing molybdenum powders.
  25. [25]
    Solubility of MoO3 in acid solutions and vapor-liquid distribution of ...
    May 25, 2017 · This study reports the measurements of the solubility of crystalline molybdenum trioxide, MoO 3 , in acid (HClO 4 , HCl) aqueous solutions at 563, 573, 593, ...
  26. [26]
    SODIUM MOLYBDATE - Ataman Kimya
    Sodium molybdate reacts with the acids of dithiophosphates: Na2MoO4 + (R = Me, Et)(RO)2PS2H → [MoO2(S2P(OR)2)2] which further reacts to form [MoO3(S2P(OR)2)4].Missing: NaOH | Show results with:NaOH
  27. [27]
    Species in aqueous solutions - International Molybdenum Association
    At pH 0.9 MoO3 precipitates and in more acidic solutions the [MoO2]2+ ion is formed. The usual source of molybdenum in the physiological work described later is ...
  28. [28]
    Thermal Atomic Layer Etching of MoS2 Using MoF6 and H2O
    Jan 12, 2023 · We show that MoF6 can be used as a fluorination source, which, when combined with alternating exposures of H2O, etches both amorphous and ...
  29. [29]
    Entering molybdenum chemistry - making molybdenum compounds
    Molybdenum chemistry starts with molybdenum trioxide, made by roasting molybdenum disulfide, and uses molybdenum trioxide, ammonium and sodium molybdates as ...
  30. [30]
    Molybdenum Touches Our Lives Every Day - Rembar Co.
    Oct 16, 2019 · Molybdenum's high-temperature strength and stability and compatibility with many glass compositions make it a perfect electrode material in ...
  31. [31]
    [PDF] Applications of Molybdenum Metal and Its Alloys
    Uncoated molybdenum loses weight catastrophically at low temperatures due to evaporation of MoO3. Coated molybdenum shows no change in weight until above ...Missing: recycling | Show results with:recycling
  32. [32]
    Mechanism and Kinetic Study of Reducing MoO3 to MoO2 with CO ...
    Nov 15, 2019 · Molybdenum trioxide (MoO3) is produced from the sulfide conc. and used by the steel industry to produce steel alloys. An alternative and ...
  33. [33]
    [PDF] Ferro Molybdenum - Cometal S.A.
    Ferro Molybdenum is a Ferro Alloy that is generally obtained by the aluminothermic reduction of Ferro. Silicon and technical grade molybdic oxide. After the ...
  34. [34]
    Metallurgy of Mo in Stainless Steel
    Molybdenum adds corrosion resistance and high temperature strength. Molybdenum primarily increases the corrosion resistance of stainless steels (see Grades and ...
  35. [35]
    Exposure Data - Welding, molybdenum trioxide, and indium tin oxide
    Molybdenum trioxide occurs naturally as the rare mineral molybdite. However, environmental levels of molybdenum trioxide have not been reported in the ...
  36. [36]
    Molybdenum history
    Around 90 chemical elements are found in nature, including molybdenum, which occurs in compound minerals called molybdenite, wulfenite, and powellite.
  37. [37]
    High Strength Low Alloy (HSLA) Steel
    ... Mo (0.2-0.3%) steel. Even with this small alloy content, the finished pipeline contains approximately 10,000 tons of molybdenum. The widespread but ...
  38. [38]
    Molybdenum in carbon steels
    Molybdenum alloying typically becomes relevant when yield strength of above 500 MPa is to be achieved and sometimes also for lower strength levels when heavy ...Missing: corrosion | Show results with:corrosion
  39. [39]
    Propene ammoxidation over an industrial bismuth molybdate-based ...
    Feb 25, 2024 · Propene ammoxidation to acrylonitrile (ACN) over bismuth molybdate-based catalysts has been commercialized for more than 60 years.
  40. [40]
    Identifying the Unique Properties of α-Bi2Mo3O12 for the Activation ...
    Bi3+ cations in Bi2Mo3O12 thus promote catalytic activity by providing both strong adsorption sites for propene and forcing molybdate into 5-coordinate ...
  41. [41]
    Oxidation and Ammoxidation of Propylene over Bismuth Molybdate ...
    A critical perspective on the design and development of metal oxide catalysts for selective propylene ammoxidation and oxidation. Applied Catalysis A: General ...
  42. [42]
    Spectroscopic Study of V2O5 Supported on Zirconia and Modified ...
    Raman Spectrum of Vanadium-Zirconia Yellow Pigment. Spectroscopy Letters ... Spectroscopic study of V2O5 supported on zirconia and modified with MoO3.
  43. [43]
    Synthesis and properties of MoO3–V2O5–PbO glasses
    Aug 9, 2025 · It is assumed that MoO3 plays the role of a glass former by increasing the activation energy for the glass transition and the activation energy ...
  44. [44]
    [PDF] Electronic structure of molybdenum-oxide films and associated ...
    MoO3-mediated hole injection would proceed by hole transfer through the oxide valence-band maximum, and the large gap and high conduction-band minimum would ...
  45. [45]
    Preparation and characterization of MoO 3 hole-injection layer for ...
    Aug 5, 2025 · ... Mo(VI) to Mo(V) to form HMoOx. Such a process could proceed under the illumination of different light sources, even sunlight. In addition ...
  46. [46]
    Solution-Processed MoO3 Thin Films As a Hole-Injection Layer for ...
    Aug 10, 2011 · We report on a sol–gel-based technique to fabricate MoO 3 thin films as a hole-injection layer for solution-processed or thermally evaporated organic solar ...
  47. [47]
    The effect of MoO3 interlayer on electro-physical characteristics of ...
    This report shows that sequentially deposited CuPc and MoO x films are an effective hole-transport layer (HTL) for perovskite solar cells (PSCs).
  48. [48]
    Studying the Effect of MoO3 in Hole-Conductor-Free Perovskite ...
    Finally, it was observed that the MoO3 forms a noncontinuous layer on the perovskite surface, which on the one hand improves its PV performance but on the other ...
  49. [49]
    Molybdenum-Oxide-Modified PEDOT:PSS as Efficient Hole ...
    Oct 26, 2024 · This study emphasizes the potential of MoO3 in contributing to the development of more efficient and stable PSCs. Keywords: perovskite solar ...
  50. [50]
    USE OF MoO3 AS CORROSION INHIBITOR, AND COATING ...
    Advantageously, the molybdenum oxide M0O 3 will be used in the anti-corrosion compositions in the form of particles having dimensions of between 1 and 200 μm.
  51. [51]
    Molybdenum oxide corrosion inhibitor, for motor vehicle metal parts ...
    Until now, MoO3 molybdenum oxide was not known as a corrosion inhibitor. Some molybdates, i.e. MoO4 ~~ ions, have already been shown as corrosion inhibitors.
  52. [52]
    Intercalation Reaction of Molybdenum Trioxide Cathode for ...
    Mar 5, 2023 · In this review, we comprehensively summarize the application of MoO3 as the cathode in rechargeable ion batteries based on intercalation ...
  53. [53]
    Shape-controlled nanostructured MoO3/CeO2 catalysts for selective ...
    Apr 11, 2022 · This study reported a vital role of CeO 2 shape on the structure-activity properties of MoO x /CeO 2 catalysts for cyclohexene epoxidation.
  54. [54]
    Synergistic Photocatalysis by α-MoO 3 Nanostructures and SWCNT ...
    Jul 24, 2024 · Synergistic Photocatalysis by α-MoO3 Nanostructures and SWCNT Nanocomposites for Efficient Cross-Linking and Oxidative Degradation of Polystyrene Nanoplastics.
  55. [55]
    Green synthesized, photocatalytic Co-doped MoO3 nanospheres for ...
    Mar 15, 2024 · This work created pure MoO3 and 1–5%Co:MoO3 nanostructures using an easy green synthesis method. Advanced characterizations using XRD, SEM, EDX, Raman, FTIR ...
  56. [56]
    [PDF] ATSDR Molybdenum Tox Profile
    Each profile will be revised and republished as necessary. The ATSDR toxicological profile succinctly characterizes the toxicologic and adverse health effects.
  57. [57]
    Mechanisms of cell injury induced by inhaled molybdenum trioxide ...
    The purpose of this study is to evaluate a possible molecular mechanism leading to cell damage and death following pulmonary exposure to inhaled MoO 3 NPs.
  58. [58]
    [PDF] SAFETY DATA SHEET - Fisher Scientific
    Nov 8, 2010 · Precautionary Statements. Prevention. Obtain special instructions before use. Do not handle until all safety precautions have been read and ...
  59. [59]