Radium bromide

Radium bromide[1][2]

Radium bromide
Names
IUPAC name
radium bromide
Other names
radium bromide
Identifiers
CAS Number
  • 10031-23-9 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 20138062 checkY
ECHA InfoCard 100.030.066 Edit this at Wikidata
EC Number
  • 233-086-5
UNII
  • R74O7T8569 checkY
CompTox Dashboard (EPA)
  • DTXSID40881395 Edit this at Wikidata
InChI
  • InChI=1S/2BrH.Ra/h2*1H;/q;;+2/p-2 checkY
    Key: GIKWXTHTIQCTIH-UHFFFAOYSA-L checkY
  • InChI=1/2BrH.Ra/h2*1H;/q;;+2/p-2
    Key: GIKWXTHTIQCTIH-NUQVWONBAJ
  • Br[Ra]Br
Properties
Chemical formula
RaBr2
Molar mass 385.782 g/mol
Appearance white orthorhombic crystals
Density 5.79 g/cm3
Melting point 728 °C (1,342 °F; 1,001 K)
Boiling point 900 °C (1,650 °F; 1,170 K) sublimes
Solubility in water
70.6 g/100 g at 20°C
Related compounds
Other anions
Radium chloride
Other cations
Beryllium bromide
Magnesium bromide
Calcium bromide
Strontium bromide
Barium bromide
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Radioactive, highly toxic, explosive, dangerous for the environment
GHS labelling:
GHS01: ExplosiveGHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 0: Will not burn. E.g. waterInstability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxideSpecial hazard RA: Radioactive. E.g. plutonium
4
0
3
Special hazard RA: Radioactive. E.g. plutonium
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references
Chemical compound

Radium bromide is the bromide salt of radium, with the formula RaBr2. It is produced during the process of separating radium from uranium ore. This inorganic compound was discovered by Pierre and Marie Curie in 1898, and the discovery sparked a huge interest in radiochemistry and radiotherapy. Since elemental radium oxidizes readily in air and water, radium salts are the preferred chemical form of radium to work with.[3] Even though it is more stable than elemental radium, radium bromide is still extremely toxic, and can explode under certain conditions.[4]

History

After the Curies discovered radium (in the form of radium chloride) in 1898, scientists began to isolate radium on an industrial scale, with the intent of using it for radiotherapy treatments. Radium salts, including radium bromide, were most often used by placing the chemical in a tube that was then passed over or inserted into diseased tissue in the body. Many of the first scientists to try to determine radium's uses were affected by their exposure to the radioactive material. Pierre Curie went so far as to self-inflict a severe chemical skin reaction by applying a radium source directly to his forearm, which ultimately created a skin lesion.[5] All types of therapeutic tests were performed for different skin diseases including eczema, lichen and psoriasis. Later, it was hypothesized that radium could be used to treat cancerous diseases.

However, during this time frame, radium also gained popularity among pseudoscientific "health remedy" industries, which promoted radium as an essential element that could "heal" and "reinvigorate" cells in the human body and remove poisonous substances. As a result, radium gained popularity as a "health trend" in the 1920s and radium salts were added to food, drinks, clothing, toys, and even toothpaste.[6] Furthermore, many respectable journals and newspapers in the early 1900s published statements claiming that radium posed no health hazard.

The main problem with the growth of interest in radium was the lack of radium on earth itself. In 1913, it was reported that the Radium Institute had four grams of radium total, which at the time was more than half the world supply.[6] Numerous countries and institutions across the world set out to extract as much radium as possible, a time-consuming and expensive task. It was reported in Science magazine in 1919 that the United States had produced approximately 55 grams of radium since 1913, which was also more than half the radium produced in the world at the time.[7] A principal source for radium is pitchblende, which holds a total of 257 mg of radium per ton of U3O8.[3] With so little product recovered from such a large amount of material, it was difficult to extract a large quantity of radium. This was the reason radium bromide became one of the most expensive materials on earth. In 1921, it was stated in Time magazine that one ton of radium cost 17,000,000,000 Euros, whereas one ton of gold cost 208,000 Euros and one ton of diamond cost 400,000,000 Euros.[6]

Radium bromide was also found to induce phosphorescence at normal temperatures.[8] This led to the US army manufacturing and supplying luminous watches and gun sights to soldiers. It also allowed for the invention of the spinthariscope, which soon became a popular household item.[9]

Properties

Radium bromide is a luminous salt that causes the air surrounding it, even when encased in a tube, to glow a brilliant green and demonstrate all bands of the nitrogen spectrum. It is possible that the effect of the alpha radiation on the nitrogen in the air causes this luminescence. Radium bromide is highly reactive and crystals can sometimes explode, especially if heated. Helium gas evolved from alpha particles can accumulate within the crystals, which can cause them to weaken and rupture.

Radium bromide will crystallize when separated from aqueous solution. It forms a dihydrate, very similar to barium bromide.[4]

Production

Radium is obtained from uranium or pitchblende ores by the "Curie method", which involves two major stages. In the first stage the ore is treated with sulfuric acid dissolves many components. The residue contains, barium, radium, and lead sulfates. The mixture will then be treated with sodium chloride and sodium carbonate to remove the lead. The second stage involves separation of the barium from the radium.[3][4]

Radium bromide can be obtained from radium chloride by reaction with a stream of hydrogen bromide.[4]

Hazards

Radium bromide, like all radium compounds, is highly radioactive and very toxic. Due to its chemical similarity to calcium, radium tends to accumulate in the bones, where it irradiates the bone marrow and can cause anemia, leukemia, sarcoma, bone cancer, genetic defects, infertility, ulcers, and necrosis. Symptoms of poisoning can take years to develop, by which time it is usually too late for any effective medical treatment. Radium bromide also poses a severe environmental hazard, amplified due to its high solubility in water, and it can bioaccumulate and cause long-lasting damage to organisms.[citation needed]

Radium bromide is highly reactive, and crystals can explode if violently shocked or heated. This is, in part, due to self-damage of the crystals by alpha radiation, which weakens the lattice structure.[dubious – discuss]

Uses

Radium and radium salts were commonly used for treating cancer; however, these treatments have been mostly phased out in favor of less toxic chemicals such as technetium or strontium-89.[6] Radium bromide was also used in luminous paint on watches, but its use was ultimately phased out in the 1960-1970s in favor of less dangerous chemicals like promethium and tritium.

See also

References

  1. ^ Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, FL: CRC Press. pp. 4–78. ISBN 0-8493-0594-2.
  2. ^ Chemical Compounds (Inorganic); B-Table, Record No. 2630. International Critical Tables of Numerical Data, Physics, Chemistry and Technology (1st Electronic Edition). 2000
  3. ^ a b c Babcock, A.B., Jr. Survey of Processes for Radium Recovery from Pitchblende Ores. AEC Research and Development Report. 23 Feb 1950. No. NYO—112
  4. ^ a b c d Kirby, H.W; Salutsky, Murrell L. The Radiochemistry of Radium. Energy Citations Database Dec 1964.[1]
  5. ^ Dutreix, Jean; Pierquin, Bernard; Tubiana, Maurice. The Hazy Dawn of Brachytherapy. Radiotherapy and Oncology (49) 1998 223-232
  6. ^ a b c d Harvie, David I. The Radium Century. Endeavor 1999 Vol. 23, Issue 3: 100-105
  7. ^ Voil, Charles H. Radium Production. Science 17 March 1919 Vol. 49, No 1262: 227-228
  8. ^ 100 and 50 years ago. Nature 24 July 2003 Vol. 424, Issue 6927: 381
  9. ^ Schwarcz, Joe. A Dazzling display in a little jar. The Gazette: Saturday Extra; The Right Chemistry pg B5
  • v
  • t
  • e
  • Ra(N3)2
  • RaCO3
  • RaF2
  • RaCl2
  • RaBr2
  • RaSO4
  • Ra(NO3)2
  • RaI2
  • Ra(OH)2
  • RaO
  • Ra3N2
  • RaWO4
  • Ra(ClO3)2
  • Ra(IO3)2
  • v
  • t
  • e
Salts and covalent derivatives of the bromide ion
HBr He
LiBr BeBr2 BBr3
+BO3
CBr4
+C
NBr3
BrN3
NH4Br
NOBr
+N
Br2O
BrO2
Br2O3
Br2O5
BrF
BrF3
BrF5
Ne
NaBr MgBr2 AlBr
AlBr3
SiBr4 PBr3
PBr5
PBr7
+P
S2Br2
SBr2
BrCl Ar
KBr CaBr2
ScBr3 TiBr2
TiBr3
TiBr4
VBr2
VBr3
CrBr2
CrBr3
MnBr2 FeBr2
FeBr3
CoBr2 NiBr2
NiBr42−
CuBr
CuBr2
ZnBr2 GaBr3 GeBr2
GeBr4
AsBr3
+As
+AsO3
SeBr2
SeBr4
Br2 Kr
RbBr SrBr2 YBr3 ZrBr3
ZrBr4
NbBr5 MoBr2
MoBr3
MoBr4
TcBr4 RuBr3 RhBr3 PdBr2 AgBr CdBr2 InBr
InBr3
SnBr2
SnBr4
SbBr3
+Sb
-Sb
Te2Br
TeBr4
+Te
IBr
IBr3
XeBr2
CsBr BaBr2 * LuBr3 HfBr4 TaBr5 WBr5
WBr6
ReBr3 OsBr3
OsBr4
IrBr3
IrBr
4
PtBr2
PtBr4
AuBr
AuBr3
Hg2Br2
HgBr2
TlBr PbBr2 BiBr3 PoBr2
PoBr4
AtBr Rn
FrBr RaBr2 ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* LaBr3 CeBr3 PrBr3 NdBr2
NdBr3
PmBr3 SmBr2
SmBr3
EuBr2
EuBr3
GdBr3 TbBr3 DyBr3 HoBr3 ErBr3 TmBr2
TmBr3
YbBr2
YbBr3
** AcBr3 ThBr4 PaBr4
PaBr5
UBr4
UBr5
NpBr3
NpBr4
PuBr3 AmBr2
AmBr3
CmBr3 BkBr3 CfBr3 EsBr2
EsBr3
Fm Md No