
Barium(2+) dichloride
Overview
Description
Barium(2+) dichloride, commonly known as barium chloride (BaCl₂), is an inorganic compound with a molecular formula of BaCl₂ and a molar mass of 208.228 g/mol . It exists in anhydrous (BaCl₂) and dihydrate (BaCl₂·2H₂O) forms, with the latter being more stable under standard conditions . The compound is highly soluble in water and is used extensively in industrial applications, including as a precursor for barium sulfate production, in heat treatment salts, and as an analytical titrant . Barium chloride is classified as toxic, requiring careful handling due to its acute health hazards .
Key identifiers include CAS No. 10361-37-2 (anhydrous) and ChemSpider ID 23540, with synonyms such as barium dichloride, dichlorobarium, and hydrochloric acid barium salt .
Scientific Research Applications
Analytical Chemistry
Gravimetric Determination of Sulfates
Barium dichloride is primarily used in analytical chemistry for the gravimetric determination of sulfate ions. In this process, a solution containing sulfate ions is treated with barium dichloride, resulting in the formation of barium sulfate, which precipitates out of solution. This reaction can be represented as follows:
The precipitate is then filtered, dried, and weighed to determine the sulfate content in the original sample. This method is widely employed due to its accuracy and reliability in quantifying sulfate concentrations in various samples, such as water and soil .
Industrial Applications
Purification of Brine Solutions
In industrial settings, barium dichloride is utilized for the purification of brine solutions in caustic chlorine plants. It helps remove impurities that can affect the quality of chlorine produced . Additionally, it plays a role in the manufacturing of heat treatment salts used in metal processing.
Production of Pigments
Barium dichloride serves as a precursor for producing various pigments, including Lithol red and Red Lake C. These pigments are used in paints and coatings due to their vibrant colors and stability .
Oil and Gas Industry
In the oil and gas sector, barium compounds are essential for creating drilling muds. Barium sulfate, derived from barium dichloride, is commonly used to enhance the density of drilling fluids, aiding in the lubrication and cooling of drill bits during operations .
Environmental Applications
Water Treatment
Barium dichloride is employed in water treatment processes to remove sulfate ions from wastewater. Its ability to precipitate barium sulfate makes it effective in reducing sulfate levels to meet environmental regulations .
Case Study 1: Barium Chloride Toxicity Management
A recent case study highlighted the toxic effects of barium dichloride when ingested. The study documented a fatal case of barium chloride poisoning, emphasizing the importance of handling this compound with care due to its high toxicity levels. The report noted that while barium sulfate is safe for ingestion, other forms such as barium chloride are bioavailable and pose significant health risks .
Case Study 2: Industrial Use in Drilling Fluids
Another study focused on the application of barium sulfate derived from barium dichloride in drilling fluids for oil extraction. The research demonstrated that using barium-based drilling muds improved drilling efficiency and reduced equipment wear by providing better lubrication compared to traditional fluids .
Summary Table of Applications
Application Area | Specific Use | Chemical Reaction/Process |
---|---|---|
Analytical Chemistry | Gravimetric determination of sulfates | |
Industrial Production | Purification of brine solutions | Removal of impurities |
Production of pigments | Synthesis of Lithol red | |
Oil & Gas Industry | Drilling muds | Enhances density and lubricates drill bits |
Environmental Science | Water treatment | Precipitation of barium sulfate |
Chemical Reactions Analysis
Precipitation Reactions
Barium chloride reacts with various anions to form insoluble precipitates, a property widely exploited in analytical chemistry.
1.1 Sulfate Precipitation
BaCl₂ reacts with sulfate ions to form barium sulfate, a key reaction for sulfate detection:
This white precipitate is insoluble in water, acids, and bases, making it ideal for gravimetric analysis .
1.2 Carbonate Precipitation
Ammonium carbonate induces precipitation of barium carbonate:
The precipitate dissolves in dilute acetic acid or strong acids .
1.3 Chromate and Oxalate Reactions
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Chromate : Forms yellow barium chromate, soluble in strong acids to produce orange dichromate:
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Oxalate : Produces white barium oxalate, soluble in hot acetic acid:
Thermal Decomposition
Barium chloride undergoes distinct thermal transitions:
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Dehydration : The dihydrate (BaCl₂·2H₂O) loses water at 55°C (→ BaCl₂·H₂O) and becomes anhydrous above 121°C .
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High-Temperature Breakdown : Above 963°C, anhydrous BaCl₂ decomposes:
Acid-Base and Redox Reactions
3.1 Reaction with Hydroxides
Barium hydroxide forms upon reaction with NaOH:
3.2 Redox Processes
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Heating BaCl₂ with sulfur yields sulfur dioxide and barium sulfate:
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In aqueous solution, Ba²⁺ imparts a yellow-green flame color due to electron transitions .
Key Reaction Data
Reaction Type | Reagents | Products | Conditions |
---|---|---|---|
Sulfate Precipitation | Na₂SO₄ | BaSO₄ ↓ + 2NaCl | Aqueous, RT |
Chromate Precipitation | K₂CrO₄ | BaCrO₄ ↓ + 2KCl | Aqueous, RT |
Thermal Decomposition | Heat (>963°C) | BaO + Cl₂ ↑ | High temperature |
Hydroxide Formation | NaOH | Ba(OH)₂ + 2NaCl | Aqueous, RT |
Barium chloride’s reactivity and stability under varied conditions make it indispensable in chemical synthesis, environmental monitoring, and industrial processes. Its toxicity necessitates careful handling, particularly in applications involving aqueous solutions or high-temperature reactions .
Q & A
Basic Research Questions
Q. What are the standard methods for synthesizing anhydrous barium(2+) dichloride, and how can purity be validated?
Anhydrous BaCl₂ is typically synthesized via dehydration of barium chloride dihydrate (BaCl₂·2H₂O) under controlled heating (120–150°C in vacuum) or by direct chlorination of barium carbonate (BaCO₃) with HCl gas. Purity validation requires thermogravimetric analysis (TGA) to confirm complete dehydration and atomic absorption spectroscopy (AAS) to quantify residual impurities (e.g., Sr²⁺ or Ca²⁺) . X-ray diffraction (XRD) should confirm crystallographic phase purity .
Q. How does this compound solubility vary in polar vs. non-polar solvents, and what factors influence this behavior?
BaCl₂ is highly soluble in water (≈35.8 g/100 mL at 20°C) due to its ionic nature but insoluble in non-polar solvents like toluene. Solubility decreases in mixed solvents (e.g., ethanol-water systems) due to reduced dielectric constants. Researchers should use conductivity measurements to assess ion dissociation and UV-Vis spectroscopy to monitor solubility limits in novel solvent systems .
Q. What are the critical safety protocols for handling this compound in laboratory settings?
BaCl₂ is toxic upon ingestion or inhalation. Researchers must use fume hoods for powder handling, wear nitrile gloves, and employ secondary containment for solutions. Waste disposal should follow EPA guidelines for heavy metals, including precipitation as BaSO₄ using sodium sulfate .
Advanced Research Questions
Q. How can discrepancies in spectroscopic data (e.g., Raman shifts) for this compound solutions be resolved?
Observed variations in Raman spectra (e.g., shifts in Ba–Cl stretching modes) may arise from hydration state differences or counterion interactions. To resolve discrepancies:
- Compare spectra of anhydrous vs. hydrated forms.
- Use density functional theory (DFT) simulations to model vibrational modes under varying hydration conditions.
- Cross-validate with X-ray absorption spectroscopy (XAS) to probe local coordination environments .
Q. What experimental strategies optimize this compound’s role in synthesizing coordination complexes (e.g., crown ether adducts)?
BaCl₂ forms stable complexes with crown ethers (e.g., 15-crown-5) via ion-dipole interactions. Key steps include:
- Adjusting stoichiometric ratios to prevent ligand overcrowding.
- Using slow crystallization in aqueous/organic solvent mixtures to enhance crystal quality.
- Employing single-crystal XRD to resolve disorder in crown ether conformations, as seen in Ba²⁺–15-crown-5 systems .
Q. How can researchers address contradictory reports on this compound’s thermodynamic properties (e.g., enthalpy of solution)?
Contradictions often stem from variations in experimental conditions (e.g., temperature, solvent purity). To mitigate:
- Replicate measurements using calorimetry under inert atmospheres to exclude CO₂ absorption.
- Validate data against the NIST Chemistry WebBook or peer-reviewed compilations.
- Publish raw datasets and uncertainty analyses to support reproducibility .
Q. What methodologies are recommended for studying this compound’s environmental impact in aqueous ecosystems?
- Use ion-selective electrodes to monitor Ba²⁺ concentrations in simulated natural waters.
- Conduct toxicity assays with model organisms (e.g., Daphnia magna) under controlled pH and ionic strength.
- Pair with geochemical modeling (e.g., PHREEQC) to predict BaCl₂ interactions with common anions (SO₄²⁻, CO₃²⁻) .
Q. Key Considerations for Researchers
- Reproducibility : Document experimental parameters (e.g., heating rates, solvent grades) meticulously to enable replication .
- Data Contradictions : Use multi-technique validation (e.g., XRD + spectroscopy) to resolve inconsistencies .
- Ethical Reporting : Disclose all synthetic byproducts and unanticipated results to avoid publication bias .
Comparison with Similar Compounds
Alkaline Earth Metal Chlorides
Barium chloride shares structural similarities with other alkaline earth metal chlorides, such as magnesium chloride (MgCl₂), calcium chloride (CaCl₂), and strontium chloride (SrCl₂). However, differences arise in solubility, toxicity, and applications:
- Solubility : BaCl₂ (31.2 g/100 mL at 20°C) is less soluble than CaCl₂ (74.5 g/100 mL) but more soluble than SrCl₂ (53.8 g/100 mL) .
- Toxicity : BaCl₂ is significantly more toxic than CaCl₂ or MgCl₂, with ingestion causing severe neuromuscular and cardiovascular effects .
- Applications : While CaCl₂ is widely used for de-icing and desiccation, BaCl₂ is restricted to niche industrial processes due to its toxicity .
Transition Metal Dichlorides
Transition metal dichlorides, such as mercury(II) chloride (HgCl₂) and nickel(II) chloride (NiCl₂), exhibit distinct chemical behaviors:
- Toxicity : HgCl₂ (LD₅₀: 1–5 mg/kg in rats) is far more toxic than BaCl₂ (LD₅₀: 11–23 mg/kg in rats) and is a potent neurotoxin . NiCl₂, while toxic, is less hazardous than both .
- Reactivity : BaCl₂ is relatively inert under standard conditions, whereas HgCl₂ reacts violently with reducing agents and organic materials .
Other Barium Salts
- Barium sulfate (BaSO₄): Unlike BaCl₂, BaSO₄ is insoluble in water and non-toxic, making it ideal for medical imaging (e.g., X-ray contrast agent) .
- Barium nitrate (Ba(NO₃)₂): Highly soluble and oxidizing, it is used in pyrotechnics for green flame production, contrasting with BaCl₂’s industrial applications .
Data Table: Comparative Properties of Selected Compounds
Research Findings and Stability
- Stability: Barium chloride dihydrate (BaCl₂·2H₂O) is thermally stable up to 120°C, decomposing to the anhydrous form at higher temperatures .
- Comparative Reactivity: Unlike HgCl₂, which forms toxic vapors upon heating, BaCl₂ releases non-hazardous decomposition products (e.g., chlorine gas only under extreme conditions) .
- Handling : BaCl₂ requires stringent safety protocols, including PPE and proper ventilation, due to its acute toxicity, whereas BaSO₄ and CaCl₂ pose minimal risks .
Properties
Molecular Formula |
BaCl2 |
---|---|
Molecular Weight |
208.23 g/mol |
IUPAC Name |
barium(2+);dichloride |
InChI |
InChI=1S/Ba.2ClH/h;2*1H/q+2;;/p-2 |
InChI Key |
WDIHJSXYQDMJHN-UHFFFAOYSA-L |
SMILES |
[Cl-].[Cl-].[Ba+2] |
Canonical SMILES |
[Cl-].[Cl-].[Ba+2] |
Origin of Product |
United States |
Synthesis routes and methods I
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Synthesis routes and methods II
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