Fact-checked by Grok 2 weeks ago

Strontium nitrate

Strontium nitrate is an inorganic with the Sr(NO₃)₂, existing as a white crystalline solid that is highly soluble in and acts as a strong . It has a molecular weight of 211.63 g/, a of approximately 2.98–2.99 g/cm³, a of around 570°C, and a of about 645°C, making it stable under normal conditions but reactive with reducing agents. The compound is primarily produced by reacting with , followed by evaporation and crystallization to yield the pure nitrate salt. is widely used in to produce a vivid color in , road flares, and signal lights due to the characteristic of strontium ions when heated. It also finds applications as a precursor in the synthesis of other strontium compounds, in catalysts, nanoscale materials, and occasionally in glass manufacturing and for nutrient provision. As a strong oxidizer, strontium nitrate accelerates combustion and can pose explosion risks when mixed with combustible materials or subjected to heat, shock, or friction; it is noncombustible itself but generates toxic nitrogen oxides upon decomposition. Health hazards include irritation to the skin, eyes, and respiratory system from dust exposure, with low oral toxicity (LD50 2750 mg/kg in rats) and moderate toxicity via intraperitoneal route (LD50 approximately 540 mg/kg in rats). Proper handling requires protective equipment and storage away from flammables to mitigate these risks.

Properties

Physical properties

Strontium nitrate is an with the Sr(NO₃)₂ in its form and Sr(NO₃)₂·4H₂O in its tetrahydrate form. It typically appears as a white, odorless crystalline solid, often in the form of colorless cubic crystals for the variant or monoclinic crystals for the tetrahydrate. The of the anhydrous form is 211.63 g/mol, while the tetrahydrate has a of 283.69 g/mol. The of the anhydrous form is 2.986 g/cm³ at 20 °C, compared to 2.20 g/cm³ for the tetrahydrate.
PropertyAnhydrous FormTetrahydrate Form
570 °C (decomposes)100 °C (loses )
Decomposes before Decomposes before
Cubic (space group Pa3)Monoclinic
The anhydrous form melts at 570 °C but decomposes rather than boiling, with decomposition initiating as low as 545 °C in some conditions. The tetrahydrate loses its four molecules of water upon heating to approximately 100 °C, transitioning to the anhydrous form. The anhydrous strontium nitrate adopts a cubic crystal structure in the Pa3 space group, where strontium ions are coordinated to twelve oxygen atoms in cuboctahedral geometry. Strontium nitrate exhibits high solubility in water, reaching 710 g/L at 18 °C for the anhydrous form and increasing with temperature to over 2000 g/L at 100 °C for the tetrahydrate. It is also soluble in liquid ammonia but only slightly soluble in alcohols such as ethanol. These solubility characteristics stem from the ionic nature of the compound, influenced by the nitrate ions, though detailed ionic interactions are addressed elsewhere.

Chemical properties

Strontium nitrate is an ionic compound with the Sr(NO₃)₂, consisting of one cation (Sr²⁺) and two anions (NO₃⁻) in a 1:2 . The bonding between the Sr²⁺ cation and the NO₃⁻ anions is primarily ionic, while the nitrate groups themselves feature covalent bonds between and oxygen atoms, with stabilization across the three oxygen atoms. Upon heating, strontium nitrate undergoes at approximately 570 °C, producing (SrO), (NO₂), and oxygen (O₂). The balanced equation for this process is: $2 \text{Sr(NO}_3)_2 \rightarrow 2 \text{SrO} + 4 \text{NO}_2 + \text{O}_2 This decomposition is characteristic of alkaline earth metal nitrates and occurs without prior melting. As a strong oxidizing agent, strontium nitrate owes its reactivity to the nitrate group, which readily releases oxygen to support the combustion of organic materials or other combustibles, potentially accelerating fire intensity or causing explosions when mixed with reducing agents like phosphorus or alkyl esters. In aqueous solutions, strontium nitrate is stable and highly soluble, dissociating completely into its ions without significant under neutral conditions; however, the Sr²⁺ ion undergoes minor , contributing to a range of 5.0–7.0 for a 5% at 25 °C, which is neutral to slightly acidic. It remains stable in mildly acidic environments, though reactions with specific anions like can lead to .

Production

Laboratory preparation

Strontium nitrate is commonly prepared in laboratory settings through the acid-base of with , a method that allows for controlled on a small scale suitable for or educational purposes. The balanced for this primary is: \ce{SrCO3 + 2 HNO3 -> Sr(NO3)2 + [CO2](/page/Carbon_dioxide) + H2O} In the procedure, finely powdered is gradually added to dilute (typically 1-2 M) in a or flask, with stirring to facilitate dissolution and the release of gas. The mixture is heated gently if necessary to complete the , ensuring all carbonate reacts without excessive foaming from CO₂ evolution. Any undissolved impurities are removed by , and the clear filtrate is concentrated by slow at low heat or under reduced pressure to induce of strontium nitrate. The crystals are then collected, washed with cold water or , and dried to yield the product. An alternative laboratory method involves reacting with , following the equation: \ce{Sr(OH)2 + 2 HNO3 -> Sr(NO3)2 + 2 H2O} This approach is analogous, where the hydroxide is dissolved in dilute , producing from the exothermic neutralization; the solution is filtered if needed and evaporated similarly to obtain the crystals. Both methods leverage the high of strontium nitrate in (approximately 71 g/100 mL at 20°C), facilitating easy recovery via cooling or evaporation-based . These preparations can achieve high purity levels up to 99%, particularly when using reagent-grade starting materials. Strontium nitrate has been routinely prepared in laboratories since the , primarily for applications in , such as standard solutions and qualitative tests for strontium ions.

Industrial production

Strontium nitrate is produced on an industrial scale primarily through a double displacement reaction between strontium carbonate and nitric acid, scaled up from laboratory methods. The balanced equation for this process is: \text{SrCO}_3 + 2\text{HNO}_3 \rightarrow \text{Sr(NO}_3)_2 + \text{CO}_2 + \text{H}_2\text{O} This reaction occurs in large continuous reactors where strontium carbonate is gradually added to a solution of concentrated nitric acid, ensuring efficient conversion while controlling exothermic heat release. The key raw material, , is derived from celestite (SrSO₄), the primary mineral source of , which is mined predominantly in , , , and . Celestite is first converted to via the black ash reduction process: the is roasted with at high temperatures to form strontium sulfide (SrS), which is then leached and reacted with to precipitate . , the other reactant, is manufactured separately through the involving the catalytic oxidation of . These supply chains are economically driven by the abundance of celestite deposits in these regions, making production cost-effective where extraction and processing are localized. Following the reaction, the resulting strontium nitrate solution undergoes to separate unreacted s and impurities, followed by to concentrate the liquor and cooling-induced to yield product. The crystals are then centrifuged, dried, and packaged, achieving a typical purity of 98-99% suitable for industrial applications. By-products include gas, which is often captured and reused in the upstream strontium carbonate production to enhance efficiency. The overall is energy-intensive, primarily due to the corrosive nature of requiring specialized corrosion-resistant equipment and precise temperature control. Global production of strontium compounds is based on celestite output of approximately 520,000 metric tons as of 2023, with major contributions from , , , and .

Applications

Pyrotechnics

Strontium nitrate plays a crucial role in as a colorant and oxidizer, particularly for producing vibrant crimson-red in , flares, and signal devices. When heated in a , the Sr²⁺ ions from strontium nitrate are excited and emit primarily in the region of the , with a dominant around 650 , resulting from molecular emissions of like SrCl and SrOH. This coloration is achieved through compositions where strontium nitrate is incorporated at concentrations typically ranging from 30% to 80%, ensuring intense and stable color output without overpowering other components. As an oxidizer, strontium nitrate decomposes during combustion to release oxygen, supporting the rapid burning of fuels and enhancing flame brightness and duration. A simplified representation of its reaction in a flare composition is: \text{Sr(NO}_3)_2 + \text{fuels} \rightarrow \text{SrO} + \text{N}_2 + \text{O}_2 + \text{heat/light} This oxygen supply is essential for efficient combustion in oxygen-limited environments, such as pyrotechnic stars or flares. Common formulations for fireworks include strontium nitrate mixed with potassium perchlorate as a secondary oxidizer, fine magnesium powder as fuel, and binders like dextrin or shellac to form cohesive stars that produce sustained red effects. In road flares, it is often combined with sodium nitrate, sulfur, and lignite to create long-burning, highly visible signals for emergency use. The use of strontium nitrate in dates back to the , when it was adopted for signal flares to provide distinctive lights for communication and distress indications. In modern applications, it features prominently in holiday fireworks displays for aerial shells and ground effects, as well as in emergency road flares for highway safety. Compared to other strontium salts like , strontium nitrate offers advantages in and reduced hygroscopicity, minimizing that could degrade during and handling.

Other uses

In skincare products, strontium nitrate is combined with to mitigate irritation from chemical exfoliants, with formulations typically containing up to 4% strontium nitrate to significantly reduce the duration and intensity of stinging sensations. This anti-irritation effect stems from the strontium cation's ability to suppress sensory responses in , as demonstrated in studies where mixtures shortened irritation periods compared to alone (p<0.01). The approach was ed in the late 1990s for topical anti-sting compositions, enabling safer use of alpha-hydroxy acids in cosmetic and medicinal products at concentrations of 0.5-10% by weight. Strontium nitrate functions as a key additive in the glass and ceramics industry, where it introduces strontium ions during manufacturing to create specialized strontium-containing glasses with enhanced optical properties. These glasses exhibit improved refractive indices, making them suitable for specialty optics and high-performance applications requiring precise light transmission. By increasing hardness, strength, and refractive index, the compound contributes to higher-quality optical materials, often used as a precursor in formulations for lenses and ceramic components. For , strontium nitrate aids in precipitating certain , such as actinides like , as strontium salts in specialized industrial and radioactive effluents, forming insoluble complexes for removal. This method, often combined with , targets chelate-bearing wastes and has been applied in remediation processes to enhance separation efficiency. Strontium nitrate acts as an oxidizer in safety matches, providing a stable combustion source without the risks associated with more volatile alternatives. It is also utilized in marine signals and red tracers, where its oxidation properties produce vivid red emissions for emergency and navigation applications. Strontium nitrate serves as a precursor in the synthesis of other strontium compounds and is used in catalysts and the production of nanoscale materials.

Safety and environmental considerations

Toxicity and health effects

Strontium nitrate acts as a strong irritant to the eyes, , and upon contact or , leading to symptoms such as redness, pain, coughing, wheezing, and . of the compound may result in gastrointestinal distress, including , , and . The oral LD50 for strontium nitrate in rats is approximately 2,750 mg/kg, indicating moderate . Chronic exposure to strontium nitrate can lead to accumulation of strontium in the body, particularly in bones, where it mimics calcium and may disrupt normal bone development, potentially causing conditions like rickets or osteomalacia, especially in cases of prolonged inhalation of dust. This accumulation raises the risk of organ damage, affecting the lungs, heart, liver, kidneys, and nervous system. Strontium nitrate is not classified as a carcinogen by the International Agency for Research on Cancer (IARC Group 3, not classifiable as to its carcinogenicity to humans). However, at high doses, the nitrate moiety can be reduced to , potentially inducing . No specific OSHA (PEL) exists for strontium nitrate, though it is regulated as a dust with limits of 15 mg/m³ (total dust) and 5 mg/m³ (respirable fraction); protective measures are recommended to stay below these thresholds to prevent health effects from dust inhalation.

Environmental impact

Strontium nitrate, upon release into the , dissociates into strontium ions (Sr²⁺) and nitrate ions (NO₃⁻), contributing to across multiple media. In systems, the high of strontium nitrate—approximately 66 g/100 mL at 20°C—facilitates its entry into surface and , where nitrates leach readily and promote by stimulating excessive algal growth and depleting oxygen levels in water bodies. Strontium ions bioaccumulate in organisms, with bioconcentration factors in fish bone tissue exceeding 50,000 due to its to calcium; lower in soft tissues and like mussels (BCF 500–1,000), potentially disrupting calcium-dependent physiological processes in these ecosystems. In soils, strontium nitrate elevates both and concentrations, as the strontium component can accumulate in sandy, low-organic-matter soils with limited capacity, leading to increased that stresses plant roots and reduces crop yields in sensitive species such as . Elevated nitrates further exacerbate by enhancing during wet periods, while the persistence of strontium in —often lasting years due to into less mobile forms like —limits natural attenuation and prolongs to terrestrial plants. Atmospheric emissions from strontium nitrate primarily arise from thermal decomposition during industrial processes or pyrotechnic use, yielding (NO₂) as a key product alongside and oxygen, with NO₂ contributing to photochemical formation through reactions forming and . These emissions are regulated under the U.S. Clean Air Act, which sets for NO₂ at an annual average of 53 ppb to mitigate and respiratory impacts on ecosystems. Regulatory frameworks address strontium nitrate's hazards due to its oxidizing properties. Under the REACH regulation, it is classified as an oxidizing solid (category 2), causing serious eye damage (category 1), requiring risk assessments for environmental releases. In the United States, the EPA enforces effluent limits for nitrates at less than 10 mg/L (as ) in wastewater discharges to prevent contamination, while recommending a strontium concentration of 4 mg/L in sources, though stable strontium lacks a formal maximum contaminant level. Mitigation strategies for strontium nitrate in include resins, which selectively remove Sr²⁺ with efficiencies up to 99% in low-calcium environments, and chemical using sulfates or carbonates to form insoluble strontium compounds for solid-waste disposal. Its low volatility as a non-volatile solid further minimizes direct atmospheric dispersal, concentrating remediation efforts on aqueous pathways.

Biological aspects

Biochemical interactions

Strontium ions (Sr²⁺) exhibit in biological systems by substituting for calcium ions (Ca²⁺) in proteins and enzymes, owing to their comparable ionic radii of 1.18 for Sr²⁺ and 1.00 for Ca²⁺ in six-coordinate environments. This substitution occurs preferentially at solvent-exposed, flexible Ca²⁺-binding sites with fewer strong ligands, such as those involving backbone carbonyls or weakly coordinating side chains, while rigid, buried sites with bidentate aspartate or glutamate residues resist replacement due to Sr²⁺'s larger size and weaker acidity. In signaling pathways, Sr²⁺ activates the calcium-sensing receptor (CaSR) with lower potency than Ca²⁺ but sufficient to modulate differentiation and , thereby influencing processes. In vivo, Sr²⁺ from strontium nitrate accumulates primarily in the , comprising up to 99% of the body burden, where it incorporates into crystals of newly formed , replacing 5-10% of Ca²⁺ and altering mineralization dynamics. This heteroionic disrupts and maturation, potentially leading to reduced density at high concentrations, while lower doses stimulate proliferation via Wnt and Ras/MAPK pathways and inhibit resorption. Such effects position Sr²⁺ as a tool in studies of calcium , where it competes with Ca²⁺ for intestinal absorption and renal reabsorption, mediated by shared transporters like TRPV6 and CaSR, thereby providing insights into mineral ion balance regulation. The component of strontium nitrate undergoes metabolism distinct from the cation, with reduction to primarily by oral and gut possessing s, such as those in and Lactobacillus plantarum, yielding concentrations that support production but also risk formation upon reaction with secondary amines under acidic conditions. Mammals lack dedicated enzymes, relying instead on microbial symbionts for this initial step, with no direct enzymatic role for in mammalian biochemistry beyond passive and bacterial conversion. Pharmacokinetically, strontium nitrate is absorbed in the with 20-30% in adults, influenced by dietary calcium levels and meal composition, achieving peak plasma concentrations within hours before rapid distribution to . occurs mainly via in a 3:1 ratio relative to feces, with multiphasic elimination kinetics featuring short-term half-lives of approximately 2-50 days in soft tissues and longer retention (up to years) in due to slow release from . In comparative biochemistry among alkaline earth metals, Sr²⁺ demonstrates intermediate toxicity, less severe than (Ba²⁺), which potently blocks channels leading to and cardiac effects, but more disruptive than calcium analogs due to its higher affinity for bone incorporation and interference with Ca²⁺-dependent processes like activation and signaling.

Research applications

Strontium ions (Sr²⁺) derived from strontium nitrate are employed in research, particularly in patch-clamp experiments to investigate voltage-gated calcium . Due to their ability to permeate calcium while being less avidly buffered by intracellular calcium-binding proteins compared to Ca²⁺, Sr²⁺ serves as a useful substitute, allowing researchers to study permeation and gating without buffering effects. Typical extracellular concentrations range from 1 to 10 mM, enabling selective examination of properties in various cell types, such as hair cells, where Sr²⁺ alters single- conductance and open probability. In bone research, strontium nitrate provides a soluble source of Sr²⁺, which acts as a tracer analogous to calcium for studying incorporation into matrix in models. This application mimics the effects of therapeutic agents like , allowing evaluation of bone formation and resorption dynamics in animal models of postmenopausal . Incorporation of the tracer can be monitored non-invasively using (SPECT) imaging with radioactive isotopes such as Sr-85, revealing preferential uptake in osteoporotic sites and aiding assessment of treatment efficacy on bone mineral density. Strontium nitrate serves as a key precursor in for synthesizing strontium-doped nanoparticles targeted at systems, especially for bone-related therapies. Through sol-gel methods, Sr(NO₃)₂ is incorporated into mesoporous nanoparticles, enhancing their osteogenic properties and enabling controlled release of therapeutic agents like antibiotics or growth factors at defect sites. These doped nanoparticles promote formation and , offering potential for localized treatment in osteoporotic conditions by improving and release . In environmental studies, strontium nitrate is utilized as a marker to track nitrate pollution and ion transport in ecosystems, leveraging the conservative behavior of Sr²⁺ relative to reactive nitrate species. By adding isotopically labeled strontium nitrate to soil or water systems, researchers can trace fertilizer-derived nitrate movement and assess contamination sources through isotopic analysis of Sr ratios (e.g., ⁸⁷Sr/⁸⁶Sr), distinguishing anthropogenic inputs from natural weathering. This approach has been applied in agricultural ecosystems to quantify nitrate leaching and its impact on groundwater quality.