Jump to content

Gadolinium

Edit links
From Wikipedia, the free encyclopedia
(Redirected from Gd (element))
For the advanced persistent threat known as GADOLINIUM in cybersecurity, see APT40.

Gadolinium, 64Gd
Gadolinium
Pronunciation/ˌɡædəˈlɪniəm/ ​(GAD-ə-LIN-ee-əm)
Appearancesilvery white
Standard atomic weight Ar°(Gd)
Gadolinium in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
–
↑
Gd
↓
Cm
europium ← gadolinium → terbium
Atomic number (Z)64
Groupf-block groups (no number)
Periodperiod 6
Block  f-block
Electron configuration[Xe] 4f7 5d1 6s2
Electrons per shell2, 8, 18, 25, 9, 2
Physical properties
Phase at STPsolid
Melting point1585 K ​(1312 °C, ​2394 °F)
Boiling point3546 K ​(3273 °C, ​5923 °F)
Density (at 20° C)7.899 g/cm3 [3]
when liquid (at m.p.)7.4 g/cm3
Heat of fusion10.05 kJ/mol
Heat of vaporization301.3 kJ/mol
Molar heat capacity37.03 J/(mol·K)
Vapor pressure (calculated)
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1836 2028 2267 2573 2976 3535
Atomic properties
Oxidation statescommon: +3
0,[4] +1,[5] +2[5]
ElectronegativityPauling scale: 1.20
Ionization energies
  • 1st: 593.4 kJ/mol
  • 2nd: 1170 kJ/mol
  • 3rd: 1990 kJ/mol
Atomic radiusempirical: 180 pm
Covalent radius196±6 pm
Color lines in a spectral range
Spectral lines of gadolinium
Other properties
Natural occurrenceprimordial
Crystal structure ​hexagonal close-packed (hcp) (hP2)
Lattice constants
Hexagonal close packed crystal structure for gadolinium
a = 363.37 pm
c = 578.21 pm (at 20 °C)[3]
Thermal expansion−21.4×10−6/K (at 20 °C)
11.1×10−6/K (at 100 °C)[3][a]
Thermal conductivity10.6 W/(m⋅K)
Electrical resistivityα, poly: 1.310 µΩ⋅m
Magnetic orderingferromagnetic–paramagnetic transition at 293.4 K
Molar magnetic susceptibility+755000.0×10−6 cm3/mol (300.6 K)[6]
Young's modulusα form: 54.8 GPa
Shear modulusα form: 21.8 GPa
Bulk modulusα form: 37.9 GPa
Speed of sound thin rod2680 m/s (at 20 °C)
Poisson ratioα form: 0.259
Vickers hardness510–950 MPa
CAS Number7440-54-2
History
Namingafter the mineral gadolinite (itself named after Johan Gadolin)
DiscoveryJean Charles Galissard de Marignac (1880)
First isolationLecoq de Boisbaudran (1886)
Isotopes of gadolinium
Main isotopes[7] Decay
abun­dance half-life (t1/2) mode pro­duct
148Gd synth 86.9 y[8] α 144Sm
150Gd synth 1.79×106 y α 146Sm
152Gd 0.2% 1.08×1014 y α 148Sm
153Gd synth 240.6 d ε 153Eu
154Gd 2.18% stable
155Gd 14.8% stable
156Gd 20.5% stable
157Gd 15.7% stable
158Gd 24.8% stable
160Gd 21.9% stable
 Category: Gadolinium
| references

Gadolinium is a chemical element; it has symbol Gd and atomic number 64. Gadolinium is a silvery-white metal when oxidation is removed. It is a malleable and ductile rare-earth element. Gadolinium reacts with atmospheric oxygen or moisture slowly to form a black coating. Gadolinium below its Curie point of 20 °C (68 °F) is ferromagnetic, with an attraction to a magnetic field higher than that of nickel. Above this temperature it is the most paramagnetic element. It is found in nature only in an oxidized form. When separated, it usually has impurities of the other rare earths because of their similar chemical properties.

Gadolinium was discovered in 1880 by Jean Charles de Marignac, who detected its oxide by using spectroscopy. It is named after the mineral gadolinite, one of the minerals in which gadolinium is found, itself named for the Finnish chemist Johan Gadolin. Pure gadolinium was first isolated by the chemist Paul-Émile Lecoq de Boisbaudran around 1886.

Gadolinium possesses unusual metallurgical properties, to the extent that as little as 1% of gadolinium can significantly improve the workability and resistance to oxidation at high temperatures of iron, chromium, and related metals. Gadolinium as a metal or a salt absorbs neutrons and is, therefore, used sometimes for shielding in neutron radiography and in nuclear reactors.

Like most of the rare earths, gadolinium forms trivalent ions with fluorescent properties, and salts of gadolinium(III) are used as phosphors in various applications.

Gadolinium(III) ions in water-soluble salts are highly toxic to mammals. However, chelated gadolinium(III) compounds prevent the gadolinium(III) from being exposed to the organism, and the majority is excreted by healthy[9] kidneys before it can deposit in tissues. Because of its paramagnetic properties, solutions of chelated organic gadolinium complexes are used as intravenously administered gadolinium-based MRI contrast agents in medical magnetic resonance imaging.

The main uses of gadolinium, in addition to use as a contrast agent for MRI scans, are in nuclear reactors, in alloys, as a phosphor in medical imaging, as a gamma ray emitter, in electronic devices, in optical devices, and in superconductors.

Characteristics

[edit]
A sample of gadolinium metal

Physical properties

[edit]

Gadolinium is the eighth member of the lanthanide series. In the periodic table, it appears between the elements europium to its left and terbium to its right, and above the actinide curium. It is a silvery-white, malleable, ductile rare-earth element. Its 64 electrons are arranged in the configuration of [Xe]4f75d16s2, of which the ten 4f, 5d, and 6s electrons are valence.

Like most other metals in the lanthanide series, three electrons are usually available as valence electrons. The remaining 4f electrons are too strongly bound: this is because the 4f orbitals penetrate the most through the inert xenon core of electrons to the nucleus, followed by 5d and 6s, and this increases with higher ionic charge. Gadolinium crystallizes in the hexagonal close-packed α-form at room temperature. At temperatures above 1,235 °C (2,255 °F), it forms or transforms into its β-form, which has a body-centered cubic structure.[10]

The isotope gadolinium-157 has the highest thermal-neutron capture cross-section among any stable nuclide: about 259,000 barns. Only xenon-135 has a higher capture cross-section, about 2.0 million barns, but this isotope is radioactive.[11]

Gadolinium is believed to be ferromagnetic at temperatures below 20 °C (68 °F)[12] and is strongly paramagnetic above this temperature. In fact, at body temperature, gadolinium exhibits the greatest paramagnetic effect of any element.[13] There is evidence that gadolinium is a helical antiferromagnetic, rather than a ferromagnetic, below 20 °C (68 °F).[14] Gadolinium demonstrates a magnetocaloric effect whereby its temperature increases when it enters a magnetic field and decreases when it leaves the magnetic field. A significant magnetocaloric effect is observed at higher temperatures, up to about 300 kelvins, in the compounds Gd5(Si1-xGex)4.[15]

Individual gadolinium atoms can be isolated by encapsulating them into fullerene molecules, where they can be visualized with a transmission electron microscope.[16] Individual Gd atoms and small Gd clusters can be incorporated into carbon nanotubes.[17]

Chemical properties

[edit]
See also: Category:Gadolinium compounds

Gadolinium combines with most elements to form Gd(III) derivatives. It also combines with nitrogen, carbon, sulfur, phosphorus, boron, selenium, silicon, and arsenic at elevated temperatures, forming binary compounds.[18]

Unlike the other rare-earth elements, metallic gadolinium is relatively stable in dry air. However, it tarnishes quickly in moist air, forming a loosely-adhering gadolinium(III) oxide (Gd2O3):

4 Gd + 3 O2 → 2 Gd2O3,

which spalls off, exposing more surface to oxidation.

Gadolinium is a strong reducing agent, which reduces oxides of several metals into their elements. Gadolinium is quite electropositive and reacts slowly with cold water and quite quickly with hot water to form gadolinium(III) hydroxide (Gd(OH)3):

2 Gd + 6 H2O → 2 Gd(OH)3 + 3 H2.

Gadolinium metal is attacked readily by dilute sulfuric acid to form solutions containing the colorless Gd(III) ions, which exist as [Gd(H2O)9]3+ complexes:[19]

2 Gd + 3 H2SO4 + 18 H2O → 2 [Gd(H2O)9]3+ + 3 SO2−
4 + 3 H2.

Chemical compounds

[edit]

In the great majority of its compounds, like many rare-earth metals, gadolinium adopts the oxidation state +3. However, gadolinium can be found on rare occasions in the 0, +1 and +2 oxidation states. All four trihalides are known. All are white, except for the iodide, which is yellow. Most commonly encountered of the halides is gadolinium(III) chloride (GdCl3). The oxide dissolves in acids to give the salts, such as gadolinium(III) nitrate.

Gadolinium(III), like most lanthanide ions, forms complexes with high coordination numbers. This tendency is illustrated by the use of the chelating agent DOTA, an octadentate ligand. Salts of [Gd(DOTA)]− are useful in magnetic resonance imaging. A variety of related chelate complexes have been developed, including gadodiamide.

Reduced gadolinium compounds are known, especially in the solid state. Gadolinium(II) halides are obtained by heating Gd(III) halides in presence of metallic Gd in tantalum containers. Gadolinium also forms the sesquichloride Gd2Cl3, which can be further reduced to GdCl by annealing at 800 °C (1,470 °F). This gadolinium(I) chloride forms platelets with layered graphite-like structure.[20]

Isotopes

[edit]
Main article: Isotopes of gadolinium

Naturally occurring gadolinium is composed of six stable isotopes, 154Gd, 155Gd, 156Gd, 157Gd, 158Gd and 160Gd, and one radioisotope, 152Gd, with the isotope 158Gd being the most abundant (24.8% natural abundance). The predicted double beta decay of 160Gd has never been observed (an experimental lower limit on its half-life of more than 1.3×1021 years has been measured[21]).

Thirty-three radioisotopes of gadolinium have been observed, with the most stable being 152Gd (naturally occurring), with a half-life of about 1.08×1014 years, and 150Gd, with a half-life of 1.79×106 years. All of the remaining radioactive isotopes have half-lives of less than 75 years. The majority of these have half-lives of less than 25 seconds. Gadolinium isotopes have four metastable isomers, with the most stable being 143mGd (t1/2= 110 seconds), 145mGd (t1/2= 85 seconds) and 141mGd (t1/2= 24.5 seconds).

The isotopes with atomic masses lower than the most abundant stable isotope, 158Gd, primarily decay by electron capture to isotopes of europium. At higher atomic masses, the primary decay mode is beta decay, and the primary products are isotopes of terbium.

History

[edit]

Gadolinium is named after the mineral gadolinite. Gadolinite was first chemically analyzed by the Finnish chemist Johan Gadolin in 1794.[22][23] In 1802 German chemist Martin Klaproth gave gadolinite its name[24][10] In 1880, the Swiss chemist Jean Charles Galissard de Marignac observed the spectroscopic lines from gadolinium in samples of gadolinite (which actually contains relatively little gadolinium, but enough to show a spectrum) and in the separate mineral cerite. The latter mineral proved to contain far more of the element with the new spectral line. De Marignac eventually separated a mineral oxide from cerite, which he realized was the oxide of this new element. He named the oxide "gadolinia". Because he realized that "gadolinia" was the oxide of a new element, he is credited with the discovery of gadolinium. The French chemist Paul-Émile Lecoq de Boisbaudran carried out the separation of gadolinium metal from gadolinia in 1886.[25][26][27][28]

Occurrence

[edit]
Gadolinite

Gadolinium is a constituent in many minerals, such as monazite and bastnäsite. The metal is too reactive to exist naturally. Paradoxically, as noted above, the mineral gadolinite actually contains only traces of this element. The abundance in the Earth's crust is about 6.2 mg/kg.[10] The main mining areas are in China, the US, Brazil, Sri Lanka, India, and Australia with reserves expected to exceed one million tonnes. World production of pure gadolinium is about 400 tonnes per year. The only known mineral with essential gadolinium, lepersonnite-(Gd), is very rare.[29][30]

Production

[edit]

Gadolinium is produced both from monazite and bastnäsite.

  1. Crushed minerals are extracted with hydrochloric acid or sulfuric acid, which converts the insoluble oxides into soluble chlorides or sulfates.
  2. The acidic filtrates are partially neutralized with caustic soda to pH 3–4. Thorium precipitates as its hydroxide, and is then removed.
  3. The remaining solution is treated with ammonium oxalate to convert rare earths into their insoluble oxalates. The oxalates are converted to oxides by heating.
  4. The oxides are dissolved in nitric acid that excludes one of the main components, cerium, whose oxide is insoluble in HNO3.
  5. The solution is treated with magnesium nitrate to produce a crystallized mixture of double salts of gadolinium, samarium and europium.
  6. The salts are separated by ion exchange chromatography.
  7. The rare-earth ions are then selectively washed out by a suitable complexing agent.[10]

Gadolinium metal is obtained from its oxide or salts by heating it with calcium at 1,450 °C (2,640 °F) in an argon atmosphere. Sponge gadolinium can be produced by reducing molten GdCl3 with an appropriate metal at temperatures below 1,312 °C (2,394 °F) (the melting point of Gd) at reduced pressure.[10]

Applications

[edit]

Gadolinium has no large-scale applications, but it has a variety of specialized uses.

Neutron absorber

[edit]

Because gadolinium has a high neutron cross-section, it is effective for use with neutron radiography and in shielding of nuclear reactors. It is used as a secondary, emergency shut-down measure in some nuclear reactors, particularly of the CANDU reactor type.[10] Gadolinium is used in nuclear marine propulsion systems as a burnable poison. The use of gadolinium in neutron capture therapy to target tumors has been investigated, and gadolinium-containing compounds have proven promising.[31]

Alloys

[edit]

Gadolinium possesses unusual metallurgic properties, with as little as 1% of gadolinium improving the workability of iron, chromium, and related alloys, and their resistance to high temperatures and oxidation.[32]

Magnetic contrast agent

[edit]

Gadolinium is paramagnetic at room temperature, with a ferromagnetic Curie point of 20 °C (68 °F).[12] Paramagnetic ions, such as gadolinium, increase nuclear spin relaxation rates, making gadolinium useful as a contrast agent for magnetic resonance imaging (MRI). Solutions of organic gadolinium complexes and gadolinium compounds are used as intravenous contrast agents to enhance images in medical and magnetic resonance angiography (MRA) procedures. Magnevist is the most widespread example.[33][34] Nanotubes packed with gadolinium, called "gadonanotubes", are 40 times more effective than the usual gadolinium contrast agent.[35] Traditional gadolinium-based contrast agents are un-targeted, generally distributing throughout the body after injection, but will not readily cross the intact blood–brain barrier.[36] Brain tumors, and other disorders that degrade the blood-brain barrier, allow these agents to penetrate into the brain and facilitate their detection by contrast-enhanced MRI. Similarly, delayed gadolinium-enhanced magnetic resonance imaging of cartilage uses an ionic compound agent, originally Magnevist, that is excluded from healthy cartilage based on electrostatic repulsion but will enter proteoglycan-depleted cartilage in diseases such as osteoarthritis.[medical citation needed]

Phosphors

[edit]

Gadolinium is used as a phosphor in medical imaging. It is contained in the phosphor layer of X-ray detectors, suspended in a polymer matrix. Terbium-doped gadolinium oxysulfide (Gd2O2S:Tb) at the phosphor layer converts the X-rays released from the source into light. This material emits green light at 540 nm because of the presence of Tb3+, which is very useful for enhancing the imaging quality. The energy conversion of Gd is up to 20%, which means that one fifth of the X-ray energy striking the phosphor layer can be converted into visible photons.[citation needed] Gadolinium oxyorthosilicate (Gd2SiO5, GSO; usually doped by 0.1–1.0% of Ce) is a single crystal that is used as a scintillator in medical imaging such as positron emission tomography, and for detecting neutrons.[37]

Gadolinium compounds were also used for making green phosphors for color TV tubes.[38]

Gamma ray emitter

[edit]

Gadolinium-153 is produced in a nuclear reactor from elemental europium or enriched gadolinium targets. It has a half-life of 240±10 days and emits gamma radiation with strong peaks at 41 keV and 102 keV. It is used in many quality-assurance applications, such as line sources and calibration phantoms, to ensure that nuclear-medicine imaging systems operate correctly and produce useful images of radioisotope distribution inside the patient.[39] It is also used as a gamma-ray source in X-ray absorption measurements and in bone density gauges for osteoporosis screening.[citation needed]

Electronic and optical devices

[edit]

Gadolinium is used for making gadolinium yttrium garnet (Gd:Y3Al5O12), which has microwave applications and is used in fabrication of various optical components and as substrate material for magneto-optical films.[40]

Electrolyte in fuel cells

[edit]

Gadolinium can also serve as an electrolyte in solid oxide fuel cells (SOFCs). Using gadolinium as a dopant for materials like cerium oxide (in the form of gadolinium-doped ceria) gives an electrolyte having both high ionic conductivity and low operating temperatures.

Magnetic refrigeration

[edit]

Research is being conducted on magnetic refrigeration near room temperature, which could provide significant efficiency and environmental advantages over conventional refrigeration methods. Gadolinium-based materials, such as Gd5(SixGe1−x)4, are currently the most promising materials, owing to their high Curie temperature and giant magnetocaloric effect. Pure Gd itself exhibits a large magnetocaloric effect near its Curie temperature of 20 °C (68 °F), and this has sparked interest into producing Gd alloys having a larger effect and tunable Curie temperature. In Gd5(SixGe1−x)4, Si and Ge compositions can be varied to adjust the Curie temperature.[15]

Superconductors

[edit]

Gadolinium barium copper oxide (GdBCO) is a superconductor[41][42][43] with applications in superconducting motors or generators such as in wind turbines.[44] It can be manufactured in the same way as the most widely researched cuprate high temperature superconductor, yttrium barium copper oxide (YBCO) and uses an analogous chemical composition (GdBa2Cu3O7−δ ).[45] It was used in 2014 to set a new world record for the highest trapped magnetic field in a bulk high temperature superconductor, with a field of 17.6T being trapped within two GdBCO bulks.[46][47]

Asthma treatment

[edit]

Gadolinium is being investigated as a possible treatment for preventing lung tissue scarring in asthma. A positive effect has been observed in mice.[48]

Niche and former applications

[edit]

Gadolinium is used for antineutrino detection in the Japanese Super-Kamiokande detector in order to sense supernova explosions. Low-energy neutrons that arise from antineutrino absorption by protons in the detector's ultrapure water are captured by gadolinium nuclei, which subsequently emit gamma rays that are detected as part of the antineutrino signature.[49]

Gadolinium gallium garnet (GGG, Gd3Ga5O12) was used for imitation diamonds and for computer bubble memory.[50]

Safety

[edit]
Main articles: MRI contrast agent and Nephrogenic systemic fibrosis
Gadolinium
Hazards
GHS labelling:
GHS02: Flammable
Danger
H261
P231+P232, P422[51]
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 0: Will not burn. E.g. waterInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid
0
0
1
W

As a free ion, gadolinium is reported often to be highly toxic, but MRI contrast agents are chelated compounds and are considered safe enough to be used in most persons. The toxicity of free gadolinium ions in animals is due to interference with a number of calcium-ion channel dependent processes. The 50% lethal dose is about 0.34 mmol/kg (IV, mouse)[52] or 100–200 mg/kg. Toxicity studies in rodents show that chelation of gadolinium (which also improves its solubility) decreases its toxicity with regard to the free ion by a factor of 31 (i.e., the lethal dose for the Gd-chelate increases by 31 times).[53][54][55] It is believed therefore that clinical toxicity of gadolinium-based contrast agents (GBCAs[56]) in humans will depend on the strength of the chelating agent; however this research is still not complete.[when?] About a dozen different Gd-chelated agents have been approved as MRI contrast agents around the world.[57][58][59]

Use of gadolinium-based contrast agents results in deposition of gadolinium in tissues of the brain, bone, skin, and other tissues in amounts that depend on kidney function, structure of the chelates (linear or macrocyclic) and the dose administered.[60] In patients with kidney failure, there is a risk of a rare but serious illness called nephrogenic systemic fibrosis (NSF)[61] that is caused by the use of gadolinium-based contrast agents. The disease resembles scleromyxedema and to some extent scleroderma. It may occur months after a contrast agent has been injected. Its association with gadolinium and not the carrier molecule is confirmed by its occurrence with various contrast materials in which gadolinium is carried by very different carrier molecules. Because of the risk of NSF, use of these agents is not recommended for any individual with end-stage kidney failure as they may require emergent dialysis.

Included in the current guidelines from the Canadian Association of Radiologists[62] are that dialysis patients should receive gadolinium agents only where essential and that they should receive dialysis after the exam. If a contrast-enhanced MRI must be performed on a dialysis patient, it is recommended that certain high-risk contrast agents be avoided but not that a lower dose be considered.[62] The American College of Radiology recommends that contrast-enhanced MRI examinations be performed as closely before dialysis as possible as a precautionary measure, although this has not been proven to reduce the likelihood of developing NSF.[63] The FDA recommends that potential for gadolinium retention be considered when choosing the type of GBCA used in patients requiring multiple lifetime doses, pregnant women, children, and patients with inflammatory conditions.[64]

Anaphylactoid reactions are rare, occurring in approximately 0.03–0.1%.[65]

Long-term environmental impacts of gadolinium contamination due to human usage are a topic of ongoing research.[66][67]

Biological use

[edit]

Gadolinium has no known native biological role, but its compounds are used as research tools in biomedicine. Gd3+ compounds are components of MRI contrast agents.[68] It is used in various ion channel electrophysiology experiments to block sodium leak channels and stretch activated ion channels.[69] Gadolinium has recently been used to measure the distance between two points in a protein via electron paramagnetic resonance, something that gadolinium is especially amenable to thanks to EPR sensitivity at w-band (95 GHz) frequencies.[70]

Notes

[edit]
  1. ^ The thermal expansion of a Gd crystal is highly anisotropic and temperature-dependent: the parameters for each crystal axis at 20 °C are: αa = 9.37×10−6/K, αc = −83.0×10−6/K, and αaverage = αV/3 = −21.4×10−6/K. At at 100 °C: αa = 6.6×10−6/K, αc = 20.1×10−6/K, and αaverage = 11.1×10−6/K.

References

[edit]
  1. ^ "Standard Atomic Weights: Gadolinium". CIAAW. 2024.
  2. ^ Prohaska, Thomas; Irrgeher, Johanna; Benefield, Jacqueline; Böhlke, John K.; Chesson, Lesley A.; Coplen, Tyler B.; Ding, Tiping; Dunn, Philip J. H.; Gröning, Manfred; Holden, Norman E.; Meijer, Harro A. J. (4 May 2022). "Standard atomic weights of the elements 2021 (IUPAC Technical Report)". Pure and Applied Chemistry. doi:10.1515/pac-2019-0603. ISSN 1365-3075.
  3. ^ a b c Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
  4. ^ Yttrium and all lanthanides except Ce and Pm have been observed in the oxidation state 0 in bis(1,3,5-tri-t-butylbenzene) complexes, see Cloke, F. Geoffrey N. (1993). "Zero Oxidation State Compounds of Scandium, Yttrium, and the Lanthanides". Chem. Soc. Rev. 22: 17–24. doi:10.1039/CS9932200017. and Arnold, Polly L.; Petrukhina, Marina A.; Bochenkov, Vladimir E.; Shabatina, Tatyana I.; Zagorskii, Vyacheslav V.; Cloke (15 December 2003). "Arene complexation of Sm, Eu, Tm and Yb atoms: a variable temperature spectroscopic investigation". Journal of Organometallic Chemistry. 688 (1–2): 49–55. doi:10.1016/j.jorganchem.2003.08.028.
  5. ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 28. ISBN 978-0-08-037941-8.
  6. ^ Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN 0-8493-0464-4.
  7. ^ Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3): 030001. doi:10.1088/1674-1137/abddae.
  8. ^ Chiera, Nadine M.; Dressler, Rugard; Sprung, Peter; Talip, Zeynep; Schumann, Dorothea (2023). "Determination of the half-life of gadolinium-148". Applied Radiation and Isotopes. 194. Elsevier BV: 110708. doi:10.1016/j.apradiso.2023.110708. ISSN 0969-8043.
  9. ^ Donnelly, L., Nelson, R. "Renal excretion of gadolinium mimicking calculi on non-contrast CT". Pediatric Radiology 28, 417 (1998). doi:10.1007/s002470050374.
  10. ^ a b c d e f Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  11. ^ "Gadolinium". Neutron News. 3 (3): 29. 1992. Retrieved 6 June 2009.
  12. ^ a b Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. p. 4.122. ISBN 0-8493-0486-5.
  13. ^ Wininger, Kevin (January–February 2022). "Contrast Media's Molecular Architecture" (PDF). Radiologic Technology. 93 (3): 341. PMID 35017275. Retrieved 27 November 2023.
  14. ^ Coey JM, Skumryev V, Gallagher K (1999). "Rare-earth metals: Is gadolinium really ferromagnetic?". Nature. 401 (6748): 35–36. Bibcode:1999Natur.401...35C. doi:10.1038/43363. ISSN 0028-0836. S2CID 4383791.
  15. ^ a b Gschneidner, K.; Pecharsky, V.; Tsokol, A. (2005). "Recent Developments in Magnetocaloric Materials" (PDF). Reports on Progress in Physics. 68 (6): 1479. Bibcode:2005RPPh...68.1479G. doi:10.1088/0034-4885/68/6/R04. S2CID 56381721. Archived from the original (PDF) on 9 November 2014.
  16. ^ Suenaga, Kazu; Taniguchi, Risa; Shimada, Takashi; Okazaki, Toshiya; Shinohara, Hisanori; Iijima, Sumio (2003). "Evidence for the Intramolecular Motion of Gd Atoms in a Gd2@C92 Nanopeapod". Nano Letters. 3 (10): 1395. Bibcode:2003NanoL...3.1395S. doi:10.1021/nl034621c.
  17. ^ Hashimoto A, Yorimitsu H, Ajima K, Suenaga K, Isobe H, Miyawaki J, Yudasaka M, Iijima S, Nakamura E (June 2004). "Selective deposition of a gadolinium(III) cluster in a hole opening of single-wall carbon nanohorn". Proceedings of the National Academy of Sciences, USA. 101 (23): 8527–30. Bibcode:2004PNAS..101.8527H. doi:10.1073/pnas.0400596101. PMC 423227. PMID 15163794.
  18. ^ Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.), Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, ISBN 0-12-352651-5
  19. ^ Mark Winter (1993–2018). "Chemical reactions of Gadolinium". The University of Sheffield and WebElements. Retrieved 6 June 2009.
  20. ^ Cotton (2007). Advanced inorganic chemistry (6th ed.). Wiley-India. p. 1128. ISBN 978-81-265-1338-3.
  21. ^ Danevich, F. A.; Kobychev, V. V.; Ponkratenko, O. A.; Tretyak, V. I.; Zdesenko, Yu. G. (5 November 2001). "Quest for double beta decay of 160Gd and Ce isotopes". Nuclear Physics A. 694 (1): 375–391. arXiv:nucl-ex/0011020. doi:10.1016/S0375-9474(01)00983-6. ISSN 0375-9474.
  22. ^ Gadolin, Johan (1794). "Undersokning af en svart tung Stenart ifrån Ytterby Stenbrott i Roslagen" [Examination of a black heavy type of stone from Ytterby Quarry in Roslagen]. Kongliga Vetenskaps Academiens Nya Handlingar [Royal Academy of Science's New Proceedings] (in Swedish). 15: 137–155.
  23. ^ Gadolin, J. (1796). "Von einer schwarazen, schweren Steinart aus Ytterby Steinbruch in Roslagen in Schweden" [Of a black, heavy type of stone from the Ytterby quarry in Roslagen in Sweden]. Chemische Annalen für die Freunde der Naturlehre, Arzneygelahrtheit, Haushaltungskunst und Manufakturen [Chemical Annals for the Friends of Science, Medicine, Domestic Economy and Manufacture] (in German). 1: 313–329.
  24. ^ Klaproth, Martin Heinrich (1802). "Ch. LXXVI: Chemische Untersuchung des Gadolinits [Ch. 76: Chemical investigation of gadolinite". Beiträge zur chemischen Kenntniss der Mineralkörper [Contribution to Our Knowledge of Mineral Substances] (in German). Berlin, (Germany): Heinrich August Rottmann. pp. 52–79. Because Gadolin had found a new ore ("einer unbekannten Erdart" (an unknown type of ore)) in a mineral which had previously been called "Ytterbite" (because it had been found near the town of Ytterby in Sweden), Klaproth proposed to rename the mineral "Gadolinite". From p. 54: "Herr Gadolin hat also das Verdienst, diese neue Erde im gegenwärtigen Fossil zuerst entdeckt zu haben; weshalb ich auch, mit mehrern Naturforschern, dessen Namen Gadolinit der erstern Benennung Ytterbit vorziehe." (Mr. Gadolin thus has the merit of having first discovered this new ore in the present rock; for which reason I, with several [other] scientists, prefer the name "gadolinite" to the first name "ytterbite".) Klaproth used the name "gadolinite" as early as 1801: Klaproth (1801). "Einige Bemerkungen über den Gadolinit, den Chryolith und die Honigsteinsäure" [Some observations on gadolinite, cryolite and mellitic acid]. Chemische Annalen für die Freunde der Naturlehre, Arzneygelahrtheit, Haushaltungskunst und Manufakturen [Chemical Annals for the Friends of Science, Medicine, Domestic Economy and Manufacture] (in German): 307–308.
  25. ^ Marshall, James L.; Marshall, Virginia R. (2008). "Rediscovery of the Elements: Yttrium and Johan Gadolin" (PDF). The Hexagon (Spring): 8–11.
  26. ^ Marshall, James L. Marshall; Marshall, Virginia R. Marshall (2015). "Rediscovery of the elements: The Rare Earths–The Confusing Years" (PDF). The Hexagon: 72–77. Retrieved 30 December 2019.
  27. ^ Weeks, Mary Elvira (1956). The discovery of the elements (6th ed.). Easton, PA: Journal of Chemical Education.
  28. ^ Weeks, Mary Elvira (1932). "The discovery of the elements: XVI. The rare earth elements". Journal of Chemical Education. 9 (10): 1751–1773. Bibcode:1932JChEd...9.1751W. doi:10.1021/ed009p1751.
  29. ^ Deliens, M. and Piret, P. (1982). "Bijvoetite et lepersonnite, carbonates hydrates d'uranyle et des terres rares de Shinkolobwe, Zaïre". Canadian Mineralogist 20, 231–38
  30. ^ "Lepersonnite-(Gd): Lepersonnite-(Gd) mineral information and data". Mindat.org. Retrieved 4 March 2016.
  31. ^ Kouri, Maria Anthi; Polychronidou, Konstantina; Loukas, Grigorios; Megapanou, Aikaterini; Vagena, Ioanna-Aglaia; Gerardos, Angelica M.; Spyratou, Ellas; Eftsathopoulos, Eftstathios P. (26 April 2023). "Consolidation of Gold and Gadolinium Nanoparticles: An Extra Step towards Improving Cancer Imaging and Therapy". Journal of Nanotheranostics. 4 (2). MDPI AG: 127–149. doi:10.3390/jnt4020007. ISSN 2624-845X.
  32. ^ National Center for Biotechnology Information. "Element Summary for AtomicNumber 64, Gadolinium". PubChem. Retrieved 25 October 2021.
  33. ^ Liney, Gary (2006). MRI in clinical practice. Springer. pp. 13, 30. ISBN 978-1-84628-161-7.
  34. ^ Raymond KN, Pierre VC (2005). "Next generation, high relaxivity gadolinium MRI agents". Bioconjugate Chemistry. 16 (1): 3–8. doi:10.1021/bc049817y. PMID 15656568.
  35. ^ Wendler, Ronda (1 December 2009) Magnets Guide Stem Cells to Damaged Hearts. Texas Medical Center.
  36. ^ Bagnato F, Gauthier SA, Laule C, Moore G, Bove R, Cai Z, et al. (May 2020). "Imaging mechanisms of disease progression in multiple sclerosis: Beyond brain atrophy". Journal of Neuroimaging. 30 (3): 251–266. doi:10.1111/jon.12700. PMID 32418324. S2CID 218677556.
  37. ^ Ryzhikov VD, Grinev BV, Pirogov EN, Onyshchenko GM, Bondar VG, Katrunov KA, Kostyukevich SA (2005). "Use of gadolinium oxyorthosilicate scintillators in x-ray radiometers". Optical Engineering. 44: 016403. Bibcode:2005OptEn..44a6403R. doi:10.1117/1.1829713.
  38. ^ Sajwan, Reena K.; Tiwari, Samit; Harshit, Tulika; Singh, Ajaya Kumar (10 October 2017). "Recent progress in multicolor tuning of rare earth-doped gadolinium aluminate phosphors GdAlO3". Optical and Quantum Electronics. 49 (11): 344. doi:10.1007/s11082-017-1158-5. ISSN 1572-817X. S2CID 254897308.
  39. ^ "Gadolinium-153". Pacific Northwest National Laboratory. Archived from the original on 27 May 2009. Retrieved 6 June 2009.
  40. ^ Cuomo, J. J.; Chaudhari, P.; Gambino, R. J. (1 May 1974). "Amorphous magnetic materials for bubble domain and magneto-optics application". Journal of Electronic Materials. 3 (2): 517–529. Bibcode:1974JEMat...3..517C. doi:10.1007/BF02652955. ISSN 1543-186X. S2CID 97662638.
  41. ^ Shi, Y; Babu, N Hari; Iida, K; Cardwell, D A (1 February 2008). "Superconducting properties of Gd-Ba-Cu-O single grains processed from a new, Ba-rich precursor compound". Journal of Physics: Conference Series. 97 (1): 012250. Bibcode:2008JPhCS..97a2250S. doi:10.1088/1742-6596/97/1/012250. ISSN 1742-6596.
  42. ^ Cardwell, D A; Shi, Y-H; Hari Babu, N; Pathak, S K; Dennis, A R; Iida, K (1 March 2010). "Top seeded melt growth of Gd–Ba–Cu–O single grain superconductors". Superconductor Science and Technology. 23 (3): 034008. Bibcode:2010SuScT..23c4008C. doi:10.1088/0953-2048/23/3/034008. ISSN 0953-2048. S2CID 121381965.
  43. ^ Zhang, Y F; Wang, J J; Zhang, X J; Pan, C Y; Zhou, W L; Xu, Y; Liu, Y S; Izumi, M (2017). "Flux pinning properties of GdBCO bulk through the infiltration and growth process". IOP Conference Series: Materials Science and Engineering. 213 (1): 012049. Bibcode:2017MS&E..213a2049Z. doi:10.1088/1757-899X/213/1/012049. ISSN 1757-8981.
  44. ^ Wang, Brian (22 November 2018). "European EcoSwing Builds First Full Scale Superconductor Wind Turbine".
  45. ^ Zhang, Yufeng; Zhou, Difan; Ida, Tetsuya; Miki, Motohiro; Izumi, Mitsuru (1 April 2016). "Melt-growth bulk superconductors and application to an axial-gap-type rotating machine". Superconductor Science and Technology. 29 (4): 044005. Bibcode:2016SuScT..29d4005Z. doi:10.1088/0953-2048/29/4/044005. ISSN 0953-2048. S2CID 124770013.
  46. ^ Durrell, J H; Dennis, A R; Jaroszynski, J; Ainslie, M D; Palmer, K G B; Shi, Y-H; Campbell, A M; Hull, J; Strasik, M (1 August 2014). "A trapped field of 17.6 T in melt-processed, bulk Gd-Ba-Cu-O reinforced with shrink-fit steel". Superconductor Science and Technology. 27 (8): 082001. arXiv:1406.0686. Bibcode:2014SuScT..27h2001D. doi:10.1088/0953-2048/27/8/082001. ISSN 0953-2048. S2CID 4890081.
  47. ^ "Strongest magnetic field trapped in a superconductor". 25 June 2014. Retrieved 15 August 2019.
  48. ^ Asthma: Scientists find new cause of lung damage – BBC News
  49. ^ Abe, K.; Bronner, C.; Hayato; et al. (2022). "First gadolinium loading to Super-Kamiokande". Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. 1027: 166248. arXiv:2109.00360. Bibcode:2022NIMPA102766248A. doi:10.1016/j.nima.2021.166248. ISSN 0168-9002. S2CID 237372721.
  50. ^ Hammond, C. R. The Elements, in Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  51. ^ "Gadolinium 691771". Sigma-Aldrich.
  52. ^ Bousquet et coll., 1988
  53. ^ "Profil toxicologique des chélates de gadolinium pour l'IRM : où en est-on ?" (PDF).
  54. ^ Ersoy, Hale; Rybicki, Frank J. (November 2007). "Biochemical Safety Profiles of Gadolinium-Based Extracellular Contrast Agents and Nephrogenic Systemic Fibrosis". Journal of Magnetic Resonance Imaging. 26 (5): 1190–1197. doi:10.1002/jmri.21135. ISSN 1053-1807. PMC 2709982. PMID 17969161.
  55. ^ Penfield JG, Reilly RF (December 2007). "What nephrologists need to know about gadolinium". Nature Clinical Practice. Nephrology. 3 (12): 654–68. doi:10.1038/ncpneph0660. PMID 18033225. S2CID 22435496.
  56. ^ "Gadolinium Deposition Disease (GDD) in Patients with Normal Renal Function". Gadolinium Toxicity. 1 November 2015. Retrieved 3 February 2016.
  57. ^ "Questions and Answers on Magnetic resonance imaging" (PDF). International Society for Magnetic Resonance in Medicine. Archived (PDF) from the original on 29 November 2007. Retrieved 6 June 2009.
  58. ^ "Information on Gadolinium-Containing Contrast Agents". US Food and Drug Administration. Archived from the original on 6 September 2008.
  59. ^ Gray, Theodore (2009). The Elements, Black Dog & Leventhal Publishers, ISBN 1-57912-814-9.
  60. ^ Tweedle, Michael F. (2021). "Gadolinium Retention in Human Brain, Bone, and Skin". Radiology. 300 (3): 570–571. doi:10.1148/radiol.2021210957. ISSN 0033-8419. PMID 34128728.
  61. ^ Thomsen HS, Morcos SK, Dawson P (November 2006). "Is there a causal relation between the administration of gadolinium based contrast media and the development of nephrogenic systemic fibrosis (NSF)?". Clinical Radiology. 61 (11): 905–06. doi:10.1016/j.crad.2006.09.003. PMID 17018301.
  62. ^ a b Schieda N, Blaichman JI, Costa AF, Glikstein R, Hurrell C, James M, Jabehdar Maralani P, Shabana W, Tang A, Tsampalieros A, van der Pol CB, Hiremath S (2018). "Gadolinium-Based Contrast Agents in Kidney Disease: A Comprehensive Review and Clinical Practice Guideline Issued by the Canadian Association of Radiologists". Canadian Journal of Kidney Health and Disease. 5: 2054358118778573. doi:10.1177/2054358118778573. PMC 6024496. PMID 29977584.
  63. ^ ACR Committee on Drugs; Contrast Media (2010). ACR Manual on Contrast Media Version 7. American College of Radiology. ISBN 978-1-55903-050-2.
  64. ^ Center for Drug Evaluation and Research. "FDA warns that gadolinium-based contrast agents (GBCAs) are retained in the body; requires new class warnings". www.fda.gov. Drug Safety and Availability – FDA Drug Safety Communication. Retrieved 20 September 2018.
  65. ^ Murphy KJ, Brunberg JA, Cohan RH (October 1996). "Adverse reactions to gadolinium contrast media: a review of 36 cases". AJR. American Journal of Roentgenology. 167 (4): 847–49. doi:10.2214/ajr.167.4.8819369. PMID 8819369.
  66. ^ Gwenzi, Willis; Mangori, Lynda; Danha, Concilia; Chaukura, Nhamo; Dunjana, Nothando; Sanganyado, Edmond (15 September 2018). "Sources, behaviour, and environmental and human health risks of high-technology rare-earth elements as emerging contaminants". The Science of the Total Environment. 636: 299–313. Bibcode:2018ScTEn.636..299G. doi:10.1016/j.scitotenv.2018.04.235. ISSN 1879-1026. PMID 29709849. S2CID 19076605.
  67. ^ Rogowska J, Olkowska E, Ratajczyk W, Wolska L (June 2018). "Gadolinium as a new emerging contaminant of aquatic environments". Environmental Toxicology and Chemistry. 37 (6): 1523–34. Bibcode:2018EnvTC..37.1523R. doi:10.1002/etc.4116. PMID 29473658.
  68. ^ Tircsó, Gyulia; Molńar, Enricő; Csupász, Tibor; Garda, Zoltan; Botár, Richárd; Kálmán, Ferenc K.; Kovács, Zoltan; Brücher, Ernő; Tóth, Imre (2021). "Chapter 2. Gadolinium(III)-Based Contrast Agents for Magnetic Resonance Imaging. A Re-Appraisal". Metal Ions in Bio-Imaging Techniques. Springer. pp. 39–70. doi:10.1515/9783110685701-008. S2CID 233702931.
  69. ^ Yeung EW, Allen DG (August 2004). "Stretch-activated channels in stretch-induced muscle damage: role in muscular dystrophy". Clinical and Experimental Pharmacology & Physiology. 31 (8): 551–56. doi:10.1111/j.1440-1681.2004.04027.x. hdl:10397/30099. PMID 15298550. S2CID 9550616.
  70. ^ Yang Y, Yang F, Gong Y, Bahrenberg T, Feintuch A, Su X, Goldfarb, D (October 2018). "High Sensitivity In-Cell EPR Distance Measurements on Proteins using and Optimized Gd(III) Spin Label". The Journal of Physical Chemistry Letters. 9 (20): 6119–23. doi:10.1021/acs.jpclett.8b02663. PMID 30277780. S2CID 52909932.
[edit]
Wikimedia Commons has media related to Gadolinium.
Look up gadolinium in Wiktionary, the free dictionary.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Gadolinium&oldid=1256451188"