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Bismuth is a white, crystalline, brittle metal with a pinkish tinge. It is the most diamagnetic of all metals, and the thermal conductivity is lower than any metal. Bismuth occurs naturally in the metallic state and in minerals such as bismite. It is the 70th most abundant element, widely spread over the Earth’s crust, but in very small amounts. Bismuth is mainly produced as a by-product from lead and copper smelting. It is insoluble in hot or cold water and has unusually low toxicity for a heavy metal.

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  • 7440-69-9 Structure
  • Basic information

    1. Product Name: Bismuth
    2. Synonyms: bismuth,elemental;Bismuth-209;BISMUTH METAL;BISMUTH METALLO-ORGANIC STANDARD;BISMUTH ICP STANDARD;BISMUTH ATOMIC ABSORPTION SINGLE ELEMENT STANDARD;BISMUTH ATOMIC ABSORPTION STANDARD;BISMUTH
    3. CAS NO:7440-69-9
    4. Molecular Formula: Bi
    5. Molecular Weight: 208.98
    6. EINECS: 231-177-4
    7. Product Categories: Industrial/Fine Chemicals;Inorganics;FUNGICIDE;Bismuth;Metal and Ceramic Science;Metals;BismuthMetal and Ceramic Science;Catalysis and Inorganic Chemistry;Chemical Synthesis;AAS;AAS CRMsAlphabetic;AASSpectroscopy;Application CRMs;B;BI - BZSpectroscopy;Matrix Selection;Nitrate;Spectroscopy;metal or element;#N/A
    8. Mol File: 7440-69-9.mol
  • Chemical Properties

    1. Melting Point: 271 °C(lit.)
    2. Boiling Point: 1560 °C(lit.)
    3. Flash Point: N/A
    4. Appearance: Silver-white or red/shot
    5. Density: 9.8 g/mL at 25 °C(lit.)
    6. Vapor Pressure: <0.1 mm Hg ( 20 °C)
    7. Refractive Index: N/A
    8. Storage Temp.: Flammables area
    9. Solubility: N/A
    10. Water Solubility: insoluble
    11. Stability: Stable. Incompatible with strong acids, strong oxidizing agents, nitrosyl fluoride, fused ammonium nitrate, interhalogen compoun
    12. Merck: 13,1256
    13. CAS DataBase Reference: Bismuth(CAS DataBase Reference)
    14. NIST Chemistry Reference: Bismuth(7440-69-9)
    15. EPA Substance Registry System: Bismuth(7440-69-9)
  • Safety Data

    1. Hazard Codes: F,C,Xi,O
    2. Statements: 34-11-36/37/38-8
    3. Safety Statements: 16-45-36/37/39-26
    4. RIDADR: UN 3264 8/PG 3
    5. WGK Germany: 1
    6. RTECS: EB2600000
    7. TSCA: Yes
    8. HazardClass: 8
    9. PackingGroup: III
    10. Hazardous Substances Data: 7440-69-9(Hazardous Substances Data)

7440-69-9 Usage

Uses

Used in Pharmaceutical Industry:
Bismuth is used as an active ingredient for gastrointestinal distress in drugs such as Pepto-Bismol, which contains bismuth subsalicylate. It is also used in medicine to treat intestinal infections and has been used in the past to treat syphilis and malaria.
Used in Cosmetics Industry:
Bismuth is used in the cosmetics industry to provide the "shine" for lipsticks, eye shadow, and other products. Bismuth oxychloride and bismuth subnitrate are also used in cosmetics.
Used in Metallurgy:
Bismuth is added to steel and other metals as an alloy to make the metals easier to roll, press, pull into wires, and turn on a lathe. It is also used in the production of low melting solders and fusible alloys.
Used in Semiconductor Industry:
Bismuth is used in the semiconductor industry and to make permanent magnets.
Used in Manufacturing:
Bismuth is used in the manufacturing of acrylonitrile and as the starting material for synthetic fibers and rubbers.
Used in Nuclear Research:
Bismuth has been proposed as a solvent coolant system for nuclear power reactors. It is also used as neutron windows in nuclear reactors due to its high density and low thermal neutron capture cross-section.
Used in Fire-Detection Devices:
Bismuth's property of expanding when it solidifies makes it useful in fire-detection devices, as it can be combined with other metals and minerals to create low melting point alloys.
Used in Safety Devices:
Bismuth is used to make thermally activated safety devices for fire-detection and sprinkler systems, as well as safety plugs in compressed gas cylinders.

Isotopes

There are a total of 59 radioactive isotopes for bismuth, ranging in half-livesfrom a few milliseconds to thousands of years. At one time it was thought that there wasjust one stable isotope (Bi-209), but it was later found that Bi-209 is radioactive witha half-life of 19,000,000,000,000,000,000 years. Such a long half-life means that Bi-209 has not completely disintegrated and is still found in nature, and is thus consideredstable. In this case, Bi-209 makes up 100% of Bismuth’s natural abundance.

Origin of Name

Bismuth was known and used by the ancient alchemists along with other metals both for chemical reactions and for medical purposes. The name comes from the German bismu, which had been changed from wismu, meaning “white.”

Characteristics

Bismuth is more resistant to electrical current in its solid state than it is in its liquid form.Its thermal conductivity is the lowest of all metals, except mercury. Even though it is considereda metal-like element, it is a very poor conductor of heat and electricity.Bismuth has a characteristic similar to water. It expands when changing from the liquidphase to the solid phase. This factor makes it useful as an alloy in metals that are used to fillmolds, given that it will expand to the cast’s dimensions.

History

In early times bismuth was confused with tin and lead. Claude Geoffroy the Younger showed it to be distinct from lead in 1753. It is a white crystalline, brittle metal with a pinkish tinge. It occurs native. The most important ores are bismuthinite or bismuth glance (Bi2S3) and bismite (Bi2O3). Peru, Japan, Mexico, Bolivia, and Canada are major bismuth producers. Much of the bismuth produced in the U.S. is obtained as a by-product in refining lead, copper, tin, silver, and gold ores. Bismuth is the most diamagnetic of all metals, and the thermal conductivity is lower than any metal, except mercury. It has a high electrical resistance, and has the highest Hall effect of any metal (i.e., greatest increase in electrical resistance when placed in a magnetic field). “Bismanol” is a permanent magnet of high coercive force, made of MnBi, by the U.S. Naval Surface Weapons Center. Bismuth expands 3.32% on solidification. This property makes bismuth alloys particularly suited to the making of sharp castings of objects subject to damage by high temperatures. With other metals such as tin, cadmium, etc., bismuth forms low-melting alloys that are extensively used for safety devices in fire detection and extinguishing systems. Bismuth is used in producing malleable irons and is finding use as a catalyst for making acrylic fibers. When bismuth is heated in air it burns with a blue flame, forming yellow fumes of the oxide. The metal is also used as a thermocouple material, and has found application as a carrier for U235 or U233 fuel in atomic reactors. Its soluble salts are characterized by forming insoluble basic salts on the addition of water, a property sometimes used in detection work. Bismuth oxychloride is used extensively in cosmetics. Bismuth subnitrate and subcarbonate are used in medicine. Natural bismuth contains only one isotope 209Bi. Forty-four isotopes and isomers of bismuth are known. Bismuth metal (99.5%) costs about $250/kg.

Production Methods

Bismuth is obtained as a by-product in smelting and refining of lead, copper or tungsten ores. The metal is partially volatilized when the ore is smelted at the high temperature. Separation from copper is achieved by electrolytic refining, bismuth accumulating in the anode slimes with lead, arsenic, antimony, tellurium, and other metal impurities. All throughout the smelting and refining operations bismuth accompanies lead. It finally is removed from lead by Betterton-Kroll or Betts processes. The Betterton-Kroll process involves the addition of calcium-lead alloy or magnesium metal to lead slime, thus converting bismuth to high-melting bismuthides of calcium or magnesium, Ca3Bi2 or Mg3Bi2, respectively. These bismuthides liquate from the bath and are separated as dross. Bismuth dross is then melted in kettles forming Bi7Mg6K9 which liquates to the top of the bath and is removed from the molten lead. Treatments with caustic soda finally produce the high quality bismuth.In a modified process, potassium substitutes for calcium to form Bi7Mg6Ca9 which liquates to the top of the bath and is removed from the molten lead. The Betts process is based on electrolytic refining using a solution of lead fluorosilicate and fluorosilicic acid. While lead is deposited on the cathode, bismuth goes to the anode where it is collected with other impurity metals. It is then filtered, dried, smelted, and further refined, depending on the purity desired. Impurities are removed by adding molten caustic and zinc, and finally by chlorination.Bismuth may be obtained from other ores, too. The recovery process however, depends primarily on the chemical nature of the ores. For example, the sulfide ore requires smelting, carbon reduction, and the addition of iron (to decompose any bismuth sulfide present). Oxide ores, on the other hand, are treated with hydrochloric acid to leach bismuth from the mineral. The bismuth chloride solution is then diluted with water to precipitate bismuth oxy-chloride. The precipitate is roasted with lime and charcoal. Satisfactory recovery of the metal from its carbonate ore may be achieved by both the above techniques.Bismuth is sold in the form of rod, lump, powder, and wire.

Hazard

Bismuth is flammable as a powder. The halogen compounds of bismuth are toxic wheninhaled or ingested. Some of the salts of bismuth can cause metallic poisoning in a mannersimilar to mercury and lead.At the beginning of the twentieth century, before penicillin, bismuth compounds wereused to treat some venereal diseases. However, the treatment was generally unsuccessful.

Health Hazard

Exposures to bismuth salts are associated primarily by ingestion. Bismuth is known to cause adverse health effects. The symptoms include, but are not limited to, irritation of the eyes, skin, respiratory tract, lungs, foul breath, metallic taste, and gingivitis. On ingestion, bismuth causes nausea, loss of appetite, weight, malaise, albuminuria, diarrhea, skin reactions, stomatitis, headache, fever, sleeplessness, depression, rheumatic pain, and a black line may form on gums in the mouth due to deposition of bismuth sulfi de. Prolonged exposure to bismuth causes mild but deleterious effects on the kidneys and high concentrations of bismuth result in fatalities. Occupational exposures to bismuth occur during the manufacture of cosmetics, industrial chemicals, and pharmaceuticals. Acute exposure with over dosage of bismuth-containing drugs causes anorexia, nausea, vomiting, abdominal pain, and possibly a dry mouth and thirst. Bismuth also causes neurotoxicity. Bismuth pentafl uoride is highly toxic and causes irritation to the skin, eyes, and respiratory tract, while bismuth subnitrate causes blurred vision.

Flammability and Explosibility

Nonflammable

Potential Exposure

Bismuth is used as a constituent of tempering baths for steel alloys; in low Freezing/Melting point alloys which expand on cooling; in aluminum and steel alloys to increase machinability; and in printing type metal. Bismuth compounds are found primarily in pharmaceuticals as antiseptics, antacids, antiluetics, and as a medicament in the treatment of acute angina. They are also used as a contrast medium in roentgenoscopy and in cosmetics. For the general population the total intake from food is 5 20 μg with much smaller amounts contributed by air and water.

Carcinogenicity

An old lifetime study with rats fed 2% bismuth subcarbonate (BSC) in the diet did not show an increase of tumors or a decrease of survival.

Environmental Fate

The mechanism by which bismuth produces toxicity has not been identified. Interaction with thiol compounds has been proposed as a primary mechanism.

Shipping

UN3089 Metal powders, flammable, n.o.s., Hazard Class: 4.1; Labels: 4.1—Flammable solid.

Purification Methods

Melt it in an atmosphere of dry helium, then filter through dry Pyrex wool to remove any bismuth oxide present [Mayer et al. J Phys Chem 64 238 1960].

Toxicity evaluation

In aerated water, bismuth oxidizes; however, in an anaerobic aqueous environment, bismuth is unaffected. Similarly, in the atmosphere, bismuth is unaffected unless condensation or deposition of water occurs. Due to the inability for air and water to affect bismuth under most circumstances, bismuth tends to persist until wet or dry deposition, and therefore long-range transport is possible and likely.

Incompatibilities

Finely divided powder is highly flammable. Reacts with strong acids and strong oxidizers, chlorine, fused ammonium nitrates, iodine pentafluoride, and nitrosyl fluoride.

Waste Disposal

Dissolve in a minimum amount of concentrated HCl. Dilute with water until precipitate is formed. Redissolve in HCl. Then saturate with H2S. Filter, wash, dry and return to supplier.

Check Digit Verification of cas no

The CAS Registry Mumber 7440-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7440-69:
(6*7)+(5*4)+(4*4)+(3*0)+(2*6)+(1*9)=99
99 % 10 = 9
So 7440-69-9 is a valid CAS Registry Number.
InChI:InChI=1/Bi

7440-69-9 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (452386)  Bismuth  beads, 1-5 mm, 99.999% trace metals basis

  • 7440-69-9

  • 452386-50G

  • 5,133.96CNY

  • Detail
  • Aldrich

  • (556130)  Bismuth  pieces, 1-12 mm, 99.999% trace metals basis

  • 7440-69-9

  • 556130-250G

  • 1,396.98CNY

  • Detail
  • Aldrich

  • (264008)  Bismuth  powder, −100 mesh, ≥99.99% trace metals basis

  • 7440-69-9

  • 264008-25G

  • 1,180.53CNY

  • Detail
  • Aldrich

  • (265462)  Bismuth  powder, −100 mesh, 99% trace metals basis

  • 7440-69-9

  • 265462-100G

  • 576.81CNY

  • Detail
  • Aldrich

  • (265462)  Bismuth  powder, −100 mesh, 99% trace metals basis

  • 7440-69-9

  • 265462-500G

  • 1,852.11CNY

  • Detail
  • Aldrich

  • (265470)  Bismuth  shot, 4-30 mesh, 99.9% trace metals basis

  • 7440-69-9

  • 265470-500G

  • 1,932.84CNY

  • Detail

7440-69-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name bismuth atom

1.2 Other means of identification

Product number -
Other names UNII-U015TT5I8H

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,Intermediates,Pigments
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7440-69-9 SDS

7440-69-9Synthetic route

bismuth(III) oxide
1304-76-3

bismuth(III) oxide

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With zinc In neat (no solvent) byproducts: ZnO; complete reduction at 500°C;;100%
With Zn In neat (no solvent) byproducts: ZnO; complete reduction at 500°C;;100%
With urea byproducts: H2O, CO2, N2; react. in a crucible over a low Meker flame, heating gently for 10 min; metal was extd. manually with a spatula;71%
bismuth(III) sulfide

bismuth(III) sulfide

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
In neat (no solvent) decomposition on heating above boiling temperature;; re-sulphuration on cooling down under exclusion of air; formation of Bi oxide in presence of air;;100%
With sodium hydroxide In neat (no solvent) heating of Bi2S3 with NaOH at 400-500°C; thermodynamic calculations;;
With iron In neat (no solvent) byproducts: FeS; heating of the sulfide with Fe; formation of Bi and Bi containing dross;; addition of alkaline or earth alkaline sulfides to the reaction mixture; separation from As and Sb containing speiss;;
bismuth(III) bromide
7787-58-8

bismuth(III) bromide

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With calcium reduction with Ca at 220°C;;100%
With magnesium In diethyl ether reduction in presence of ether at 25°C;;100%
With Mg In diethyl ether reduction in presence of ether at 25°C;;100%
bismuth(III) acetate oxide

bismuth(III) acetate oxide

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With hydrogen In acetic acid reduction at 150°C, 100 atm., 24 hours, 1,25n solution (acetic acid), 0.1n acetate;;100%
vanadocene

vanadocene

(C6F5)3GeBi(C2H5)2
69162-04-5

(C6F5)3GeBi(C2H5)2

A

bismuth
7440-69-9

bismuth

B

(C5H5)2VC2H5

(C5H5)2VC2H5

C

(C5H5)2VGe(C6F5)3

(C5H5)2VGe(C6F5)3

Conditions
ConditionsYield
In toluene mixt. held for 5 h at 20°C; org. layer decanted; solvent evapd. (vac.); extd. (hexane); recrystd. (toluene/hexane=8/1); ESR;A 100%
B 86%
C 90%
triphenylbismuthane
603-33-8

triphenylbismuthane

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With hydrogen In xylene byproducts: C6H6; 60 atm, 124 h, 225°C;99.4%
With hydrogen In xylene reduction of triphenyl Bi with H2 under a pressure of 60 at on heating at 250°C;;99.4%
With hydrogen In xylene byproducts: C6H6; 60 atm, 124 h, 150°C;6.9%
sodium octahydrotriborate tridioxanate

sodium octahydrotriborate tridioxanate

bismuth(III)

bismuth(III)

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
In water room temp.; X-ray diffraction, gravimetric anal.;99%
vanadocene

vanadocene

{(C6F5)3Ge}2BiC2H5
69202-61-5

{(C6F5)3Ge}2BiC2H5

A

bismuth
7440-69-9

bismuth

B

(C5H5)2VC2H5

(C5H5)2VC2H5

C

(C5H5)2VGe(C6F5)3

(C5H5)2VGe(C6F5)3

Conditions
ConditionsYield
In toluene mixt. held for 5 h at 20°C; org. layer decanted; solvent evapd. (vac.); extd. (hexane); recrystd. (toluene/hexane=8/1); ESR;A 90%
B 97%
C 74%
benzene-d6
1076-43-3

benzene-d6

triphenylbismuthane
603-33-8

triphenylbismuthane

A

bismuth
7440-69-9

bismuth

B

biphenyl
92-52-4

biphenyl

C

biphenyl-d10
1486-01-7

biphenyl-d10

D

2,3,4,5,6-pentadeuterio-biphenyl
20637-23-4

2,3,4,5,6-pentadeuterio-biphenyl

Conditions
ConditionsYield
In benzene-d6 Irradiation (UV/VIS); 40-50°C, 150 h;A n/a
B 2.5%
C 2.3%
D 95.2%
(4-bromobenzoylseleno)bis(4-methylphenyl)bismuth

(4-bromobenzoylseleno)bis(4-methylphenyl)bismuth

A

bismuth
7440-69-9

bismuth

B

tri(p-tolyl)bismuth
5142-75-6

tri(p-tolyl)bismuth

Conditions
ConditionsYield
In neat (no solvent) byproducts: Se-(4-CH3C6H4) 4-bromobenzenecarboselenoate; Bi-compound under N2 in an ampoule was heated at 150°C for 2 h; ppt. was filtered (Bi), washed with diethyl ether and CH2Cl2, evapd., column chromy. on silica gel (hexane-diethyl ether);A 1%
B 95%
bismuth(III) chloride
7787-60-2

bismuth(III) chloride

triethylstannane
997-50-2

triethylstannane

A

bismuth
7440-69-9

bismuth

B

chlorotriethylstannane
994-31-0

chlorotriethylstannane

Conditions
ConditionsYield
byproducts: H2; heating dry powdered BiCl3 with (C2H5)3SnH under reflux;;A n/a
B 93%
byproducts: H2; heating dry powdered BiCl3 with (C2H5)3SnH under reflux;;A n/a
B 93%
(4-methylbenzoylseleno)bis(4-methylphenyl)bismuth

(4-methylbenzoylseleno)bis(4-methylphenyl)bismuth

A

bismuth
7440-69-9

bismuth

B

tri(p-tolyl)bismuth
5142-75-6

tri(p-tolyl)bismuth

Conditions
ConditionsYield
In neat (no solvent) byproducts: Se-(4-CH3C6H4) 4-methylbenzenecarboselenoate; Bi-compound under N2 in an ampoule was heated at 150°C for 2 h; ppt. was filtered (Bi), washed with diethyl ether and CH2Cl2, evapd., column chromy. on silica gel (hexane-diethyl ether);A 1%
B 93%
(4-methoxybenzoylseleno)bis(4-methylphenyl)bismuth

(4-methoxybenzoylseleno)bis(4-methylphenyl)bismuth

A

bismuth
7440-69-9

bismuth

B

tris(4-methoxyphenyl)bismuth
33397-21-6

tris(4-methoxyphenyl)bismuth

Conditions
ConditionsYield
In neat (no solvent) byproducts: Se-(4-CH3C6H4)-4-methoxybenzenecarboselenoate; Bi-compound under N2 in an ampoule was heated at 150°C for 2 h; ppt. was filtered (Bi), washed with diethyl ether and CH2Cl2, evapd., column chromy. on silica gel (hexane-diethyl ether);A 1%
B 92%
(3-chloro-2,6-dimethoxybenzoylseleno)bis(4-methylphenyl)bismuth

(3-chloro-2,6-dimethoxybenzoylseleno)bis(4-methylphenyl)bismuth

A

bismuth
7440-69-9

bismuth

B

tri(p-tolyl)bismuth
5142-75-6

tri(p-tolyl)bismuth

Conditions
ConditionsYield
In neat (no solvent) byproducts: Se-(4-CH3C6H4) 3-Cl-2,6-CH3Obenzenecarboselenoate; Bi-compound under N2 in an ampoule was heated at 150°C for 2 h; ppt. was filtered (Bi), washed with diethyl ether and CH2Cl2, evapd., column chromy. on silica gel (hexane-diethyl ether);A 1%
B 92%
bismuth(III) sulfide

bismuth(III) sulfide

bismuth(III) oxide
1304-76-3

bismuth(III) oxide

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With carbon dioxide In neat (no solvent) byproducts: SO2, (BiO)2SO4; reaction in stream of CO2 under layer of salt;;90%
With iron; pyrographite In melt melting with C in a flame- or crucible furnace; addition of Na2CO3 with formation of dross; complete reduction by addition of Fe;; removal of As and Sb as speiss;;
With pyrographite In melt melting an ore containing 25-30 % Bi with Fe oxide and C in a cupola furnace;; Bi with impurities of Sb, Pb, As and a small amount of Cu; Bi containing speiss, dross (0.2-0.6 % Bi) and further products;;
triphenylbismuthane
603-33-8

triphenylbismuthane

A

bismuth
7440-69-9

bismuth

B

benzene
71-43-2

benzene

Conditions
ConditionsYield
With sodium In ammoniaA n/a
B 90%
bismuth(III) chloride
7787-60-2

bismuth(III) chloride

5-aza-2,2,8,8-tetramethylnonane-3,7-dione
88686-46-8

5-aza-2,2,8,8-tetramethylnonane-3,7-dione

A

bismuth
7440-69-9

bismuth

tris(4-aza-1,7-dioxa-2,6-ditert-butylhepta-2,5-dien-1,4,7-triyl)bismuth

tris(4-aza-1,7-dioxa-2,6-ditert-butylhepta-2,5-dien-1,4,7-triyl)bismuth

Conditions
ConditionsYield
With (C2H5)3N In tetrahydrofuran byproducts: (C2H5)3NHCl; at -78 °C; extd. (pentane), crystd. from pentane at -28 °C;A n/a
B 90%
Yb(C4H8O)6(2+)*2(C6H5)3C(1-)=[Yb(C4H8O)6][(C6H5)3C]2

Yb(C4H8O)6(2+)*2(C6H5)3C(1-)=[Yb(C4H8O)6][(C6H5)3C]2

triphenylbismuthane
603-33-8

triphenylbismuthane

A

bismuth
7440-69-9

bismuth

B

2C(C6H5)3(1-)*YbC6H5(C4H8O)3(2+)=(C(C6H5)3)2YbC6H5(C4H8O)3

2C(C6H5)3(1-)*YbC6H5(C4H8O)3(2+)=(C(C6H5)3)2YbC6H5(C4H8O)3

Conditions
ConditionsYield
In tetrahydrofuran Ph3Bi in THF was added to soln. of Yb-complex in THF, heated at 40-50°C for 24 h in evacuated sealed ampules; sepd. by centrifugation; elem. anal.;A 90%
B 68%
(benzoylseleno)bis(4-methylphenyl)bismuth

(benzoylseleno)bis(4-methylphenyl)bismuth

A

bismuth
7440-69-9

bismuth

B

tri(p-tolyl)bismuth
5142-75-6

tri(p-tolyl)bismuth

Conditions
ConditionsYield
In neat (no solvent) byproducts: Se-(4-CH3C6H4) benzenecarboselenoate; Bi-compound under N2 in an ampoule was heated at 150°C for 2 h; ppt. was filtered (Bi), washed with diethyl ether and CH2Cl2, evapd., column chromy. on silica gel (hexane-diethyl ether);A 1%
B 90%
α-naphthol
90-15-3

α-naphthol

tri(naphthalen-1-yl)bismuth
33397-22-7

tri(naphthalen-1-yl)bismuth

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
130°C, 3 h;89.1%
bismuth(III) sulfide

bismuth(III) sulfide

A

bismuth
7440-69-9

bismuth

B

bismuth(III) sulfate

bismuth(III) sulfate

Conditions
ConditionsYield
reaction at 800 °C;;A 87.41%
B 4.83%
reaction at 800 °C;;A 87.41%
B 4.83%
reaction at 700 °C;;A 74.63%
B 7.61%
tris(pentafluorophenyl)bismuth
34422-57-6

tris(pentafluorophenyl)bismuth

A

bismuth
7440-69-9

bismuth

B

bismuth hydroxide

bismuth hydroxide

C

Pentafluorobenzene
363-72-4

Pentafluorobenzene

D

decafluorobiphenyl
434-90-2

decafluorobiphenyl

Conditions
ConditionsYield
With waterA 0%
B n/a
C 87%
D 0%
With H2OA 0%
B n/a
C 87%
D 0%
With waterA 0%
B n/a
C n/a
D 0%
water
7732-18-5

water

bismuth(III) chloride
7787-60-2

bismuth(III) chloride

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With Zn; HCl In water BiCl3 added to water with stirring, Zn powder added, stirred at room temp. for 2-4 h, mixture added to diluted aq. HCl for several min; ppt. filtered, washed (water), dried (vac., 60°C, 4 h); elem. anal.;80%
triethylsilane
617-86-7

triethylsilane

bismuth(III) chloride
7787-60-2

bismuth(III) chloride

A

bismuth
7440-69-9

bismuth

B

triethylsilyl chloride
994-30-9

triethylsilyl chloride

Conditions
ConditionsYield
byproducts: H2; heating dry powdered BiCl3 with triethyl silane under reflux;;A n/a
B 79%
byproducts: H2; heating dry powdered BiCl3 with triethyl silane under reflux;;A n/a
B 79%
bismuth(III) 2-ethylhexanoate

bismuth(III) 2-ethylhexanoate

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
With 1-dodecylthiol In tetrahydrofuran-d8 byproducts: 2-ethylhexanoic acid, CH3(CH2)11SS(CH2)11CH3; Irradiation (UV/VIS); (N2); addn. of thiol deriv. to soln. of bismuth compd. in THF-d8, exposure to 365 nm light for 4 d at power of 7mW/cm**2; NMR monitoring;75%
With 1-dodecylthiol In tetrahydrofuran byproducts: 2-ethylhexanoic acid, CH3(CH2)11SS(CH2)11CH3; Irradiation (UV/VIS); (N2); addn. of 3 equiv. of thiol deriv. to soln. of bismuth compd. in dry THF, exposure to ambient light at room temp. for 24 h or 2 wks; exposure to air, cenrifugation for 2 min at 9000 rpm, removing supernatant, suspending in THF, centrifugation, drying at room temp. in vac.;
tri(naphthalen-1-yl)bismuth
33397-22-7

tri(naphthalen-1-yl)bismuth

2-hydroxyresorcinol
87-66-1

2-hydroxyresorcinol

bismuth
7440-69-9

bismuth

Conditions
ConditionsYield
130°C, 4 h;70.5%
130°C, 3 h;64.9%
130°C, 2 h;49.9%
130°C, 1 h;17.5%
praseodymium

praseodymium

bis[tris(pentafluorophenyl)germyl]mercury

bis[tris(pentafluorophenyl)germyl]mercury

{(C6F5)3Ge}2BiC2H5
69202-61-5

{(C6F5)3Ge}2BiC2H5

A

bismuth
7440-69-9

bismuth

B

praseodymium heptakis[tris(pentafluorophenyl)germanyl]dimercurate*3(dimethoxyethane)

praseodymium heptakis[tris(pentafluorophenyl)germanyl]dimercurate*3(dimethoxyethane)

C

mercury

mercury

Conditions
ConditionsYield
In 1,2-dimethoxyethane fivefold excess of compound I in evacuated ampul shaken for 5 h at 20°C; centrifugated, decanted, solvent removed (vac.), ppt. washed (toluene);dried (vac.);A 70%
B 263.6 %
C 22.5%
diphenylbismuth(III) chloride
5153-28-6

diphenylbismuth(III) chloride

A

bismuth
7440-69-9

bismuth

B

Bi(3+)*C6H5(1-)

Bi(3+)*C6H5(1-)

C

Bi(3+)*2C6H5(1-)

Bi(3+)*2C6H5(1-)

Conditions
ConditionsYield
other Radiation; on neutron radiation;A 56.5%
B 16.4%
C 2.4%
other Radiation; on neutron radiation;A 56.5%
B 16.4%
C 2.4%
Et2BiTeEt

Et2BiTeEt

A

bismuth
7440-69-9

bismuth

Bi2Te

Bi2Te

Conditions
ConditionsYield
With (Z)-9-octadecen-1-amine at 100℃; for 14h; Inert atmosphere; Schlenk technique;A n/a
B 55.4%
Li[Al(perfluoro-tertbutoxide)4]

Li[Al(perfluoro-tertbutoxide)4]

Bi5(3+)*3AsF6(1-)*SO2=[Bi5](AsF6)3*SO2

Bi5(3+)*3AsF6(1-)*SO2=[Bi5](AsF6)3*SO2

Hexamethylbenzene
87-85-4

Hexamethylbenzene

A

bismuth
7440-69-9

bismuth

B

[(C6Me6)H][Al(OC(CF3)3)4]
874445-84-8

[(C6Me6)H][Al(OC(CF3)3)4]

C

[Bi5(hexamethylbenzene)4][Al(OC(CF3)3)4]3

[Bi5(hexamethylbenzene)4][Al(OC(CF3)3)4]3

D

[Bi4OF2Cl6(hexamethylbenzene)4][Al(OC(CF3)3)4]2*hexamethylbenzene

[Bi4OF2Cl6(hexamethylbenzene)4][Al(OC(CF3)3)4]2*hexamethylbenzene

Conditions
ConditionsYield
In dichloromethane byproducts: LiAsF6; under N2, 1 equiv. of Li-compd., 1 equiv. of Bi-compd. and 2 equiv. of C6Me6 were stirred in CH2Cl2 for 4 h, 5 °C; soln. was concd., held at -24 °C for 2 d, crystals were sepd., another crop was given after 2 d at this temp., elem. anal.; keeping the mother liq. for 2 weeks, Bi, the Bi4OF2Cl6(2+) and C6Me6H(1+)-cation con tg. compds. were formed.;A n/a
B n/a
C 55%
D n/a
bismuth
7440-69-9

bismuth

aqueous H2 O2

aqueous H2 O2

sulfuric acid
7664-93-9

sulfuric acid

pyrographite
7440-44-0

pyrographite

2-butyl-5-hydroxymethyl-1H-imidazole
68283-19-2

2-butyl-5-hydroxymethyl-1H-imidazole

platinum
7440-06-4

platinum

2-butyl-1H-imidazole-5-carboxaldehyde
68282-49-5

2-butyl-1H-imidazole-5-carboxaldehyde

Conditions
ConditionsYield
With sodium hydroxide In water100%
With sodium hydroxide In water98.2%
With sodium hydroxide In methanol; water94.5%
bismuth
7440-69-9

bismuth

iodine
7553-56-2

iodine

bismuth(III) iodide
7787-64-6

bismuth(III) iodide

Conditions
ConditionsYield
In melt passing a stream of I2/inert gas into molten Bi with formation of volatile BiI3; description of the aparatus given;;100%
In melt passing a stream of I2/inert gas into molten Bi with formation of volatile BiI3; description of the aparatus given;;100%
In melt passing a stream of I2/inert gas into molten Bi with formation of volatile BiI3; description of the aparatus given;;100%
bismuth
7440-69-9

bismuth

bromine
7726-95-6

bromine

bismuth(III) bromide
7787-58-8

bismuth(III) bromide

Conditions
ConditionsYield
In melt passing a stream of Br2/inert gas into molten Bi with formation of volatile BiBr3; description of the aparatus given;;100%
In melt passing a stream of Br2/inert gas into molten Bi with formation of volatile BiBr3; description of the aparatus given;;100%
In melt passing a stream of Br2/inert gas into molten Bi with formation of volatile BiBr3; description of the aparatus given;;100%
bismuth
7440-69-9

bismuth

nitrogen
7727-37-9

nitrogen

bismuth nitride

bismuth nitride

Conditions
ConditionsYield
In neat (no solvent) Electrochem. Process; cothodic pulverization within 10 hours of Bi under pure N2 (0.1 - 0.3 Torr), glow-discharge at 1000-1500 V; anode Fe; description of the aparatus given;; 359.8 mg BiN; deposition of 12.1 weight % on cathode, of 45.4 weight % on anode, 25.2 weight % on glass parts of the aparatus, 17.3 weight % on Fe- (or Al-) protecting ring of the aparatus;;100%
In further solvent(s) Electric Arc; between Bi-cathode and Cu-anode in a liquid mixture of argon and nitrogen;;
In further solvent(s) Electric Arc; between Bi-cathode and Cu-anode in a liquid mixture of argon and nitrogen;;
In neat (no solvent) cathodic pulverization of Bi during glow discharge under N2 (0.1 - 0.3 torr);;
bismuth
7440-69-9

bismuth

sodium
7440-23-5

sodium

sodium bismuthide

sodium bismuthide

Conditions
ConditionsYield
In neat (no solvent) heating a mixture of Na and Bi (molar ratio 3 : 1) at 775°C under Ar;;100%
determined by thermal analysis;;
determined by chemical methods;;
bismuth
7440-69-9

bismuth

sulfur
7704-34-9

sulfur

bismuth(III) sulfide

bismuth(III) sulfide

Conditions
ConditionsYield
In neat (no solvent) under dry N2 atm. in vac. glovebox; mixt. of Bi and S was transferred inquartz tube, with was flame sealed under vac.; tube was heated to 650.d egree.C for 48 h; stayed at 650°C for 2 ds; cooled to 50°Cin 10 h; ground into powder;100%
In melt by melting at possible min. temp.;
In melt addition of S to molten Bi at 600-700°C;; Bi content 1 - 2 %;;
disulfur dichloride
10025-67-9

disulfur dichloride

bismuth
7440-69-9

bismuth

bismuth(III) chloride
7787-60-2

bismuth(III) chloride

Conditions
ConditionsYield
heating Bi with S2Cl2 at 138.6°C, 10 hours;;100%
addition of S2Cl2 to Bi;;
addition of S2Cl2 to Bi;;
bismuth
7440-69-9

bismuth

chlorine
7782-50-5

chlorine

bismuth(III) chloride
7787-60-2

bismuth(III) chloride

Conditions
ConditionsYield
In melt passing a stream of Cl2/inert gas into molten Bi with formation of volatile BiCl3; description of the aparatus given;;100%
In melt passing a stream of Cl2/inert gas into molten Bi with formation of volatile BiCl3; description of the aparatus given;;100%
In melt passing a stream of Cl2/inert gas into molten Bi with formation of volatile BiCl3; description of the aparatus given;;100%
bismuth
7440-69-9

bismuth

selenium
7782-49-2

selenium

bismuth(III) selenide

bismuth(III) selenide

Conditions
ConditionsYield
In neat (no solvent) under dry N2 atm. in vac. glovebox; mixt. of Bi and Se was transferred in quartz tube, with was flame sealed under vac.; tube was heated to 600°C for 48 h; stayed at 600°C for 2 ds; cooled to 50°C in 10 h; ground into powder;100%
high pressure at 420°C;
on Al plate at 47-180°C; tempering under m.p. of Se; no reaction at 130°C without tempering;
bismuth
7440-69-9

bismuth

iodine(I) bromide
7789-33-5

iodine(I) bromide

bismuth(III) bromide
7787-58-8

bismuth(III) bromide

Conditions
ConditionsYield
In melt100%
In melt100%
In melt addition of Bi powder to molten IBr;; extraction with CCl4;;
In melt addition of Bi powder to molten IBr;; extraction with CCl4;;
bismuth
7440-69-9

bismuth

tellurium

tellurium

bismuth telluride

bismuth telluride

Conditions
ConditionsYield
In neat (no solvent) Bi and Te ground, pressed at 650 K, homogenizing calcination (570 K, 400h) in evacuated quartz ampoules; single phase (X-ray- and electron-microprobe analyses);100%
bismuth
7440-69-9

bismuth

selenium
7782-49-2

selenium

tellurium

tellurium

Bi(x)(Te0.9Se0.1)3 x:1.96-2.04;

Bi(x)(Te0.9Se0.1)3 x:1.96-2.04;

Conditions
ConditionsYield
In neat (no solvent) Bi, Se and Te ground, pressed at 650 K, homogenizing calcination (570 K, 400h) in evacuated quartz ampoules; single phase (X-ray- and electron-microprobe analyses);100%
bismuth
7440-69-9

bismuth

selenium
7782-49-2

selenium

tellurium

tellurium

Bi(x)(Te0.8Se0.2)3 x:1.8-2.2;

Bi(x)(Te0.8Se0.2)3 x:1.8-2.2;

Conditions
ConditionsYield
In neat (no solvent) Bi, Se and Te ground, pressed at 650 K, homogenizing calcination (730 K, 400h) in evacuated quartz ampoules; single phase (X-ray- and electron-microprobe analyses);100%
bismuth
7440-69-9

bismuth

potassium sulfide

potassium sulfide

bismuth(III) sulfide

bismuth(III) sulfide

Bi2K8S7

Bi2K8S7

Conditions
ConditionsYield
differential thermal anal.;100%
bismuth
7440-69-9

bismuth

potassium
7440-09-7

potassium

sulfur
7704-34-9

sulfur

potassium metathiobismuthite

potassium metathiobismuthite

Conditions
ConditionsYield
In neat (no solvent)100%
differential thermal anal.;100%
bismuth
7440-69-9

bismuth

silver perchlorate

silver perchlorate

bismuth(III) perchlorate

bismuth(III) perchlorate

Conditions
ConditionsYield
In acetonitrile Electrolysis; electrolysis of AgClO4 in acetonitrile, Bi anode;; not isolated;;100%
bismuth
7440-69-9

bismuth

potassium sulfide

potassium sulfide

bismuth(III) sulfide

bismuth(III) sulfide

K2Bi4S7

K2Bi4S7

Conditions
ConditionsYield
differential thermal anal.;100%
bismuth
7440-69-9

bismuth

bismuth(III) sulfide

bismuth(III) sulfide

potassium metathiobismuthite

potassium metathiobismuthite

Bi3KS5, low temperature

Bi3KS5, low temperature

Conditions
ConditionsYield
annealing at 650°C; differential thermal anal.;100%
bismuth
7440-69-9

bismuth

bismuth(III) sulfide

bismuth(III) sulfide

potassium metathiobismuthite

potassium metathiobismuthite

Bi3KS5, high temperature

Bi3KS5, high temperature

Conditions
ConditionsYield
quenching from 830°C; differential thermal anal.;100%
bismuth
7440-69-9

bismuth

europium

europium

Eu4Bi3

Eu4Bi3

Conditions
ConditionsYield
In neat (no solvent) Ar atm.; stoichiometric ratio, heating (1100°C, 24-48 h);100%
In neat (no solvent) induction heating at 1400°C of stoich. amounts of elements in a sealed tungsten crucible; XRD;
In neat (no solvent, solid phase) Electric Arc; Bi and Eu were arc-melted under Ar in silica ampules, heated to 700°C for 6 h, at 1050°C for 6 h, quenched to room temp., reheatedat 1100°C for 36 h, cooled to room temp. at 3°C/h;
bismuth
7440-69-9

bismuth

manganese
7439-96-5

manganese

Yb

Yb

Yb14MnBi11

Yb14MnBi11

Conditions
ConditionsYield
Stage #1: bismuth; manganese; Yb for 1h; Milling; Inert atmosphere;
Stage #2: at 1125 - 1225℃; for 96h; Inert atmosphere; Sealed tube;
100%
bismuth
7440-69-9

bismuth

selenium
7782-49-2

selenium

caesium selenide

caesium selenide

cadmium
7440-43-9

cadmium

Cs1.13Cd1.13Bi2.87Se6

Cs1.13Cd1.13Bi2.87Se6

Conditions
ConditionsYield
In neat (no solvent) at 750℃; for 48h; Inert atmosphere;100%
bismuth
7440-69-9

bismuth

lithium sulfide

lithium sulfide

sulfur
7704-34-9

sulfur

Li0.97Sn2.06Bi4.97S10

Li0.97Sn2.06Bi4.97S10

Conditions
ConditionsYield
Stage #1: bismuth; tin; lithium sulfide; sulfur at 800℃; under 0.00150015 Torr; for 10h; Inert atmosphere; Glovebox; Sealed tube;
Stage #2: at 800℃; for 26h;
100%
bismuth
7440-69-9

bismuth

sulfuric acid
7664-93-9

sulfuric acid

bismuth(III) sulfate

bismuth(III) sulfate

Conditions
ConditionsYield
In further solvent(s) H2SO4 was added to Bi in HNO3 with stirring and heating; more H2SO4 wasadded and suspn. was heated for 40 h; heated in a muffle furnace at 648K; elem. anal.;99.8%
In sulfuric acid byproducts: SO2; by dissolving in boiling concd. H2SO4;;
In sulfuric acid byproducts: SO2; very weak reaction with diluted H2SO4.;;
In nitric acid Bi dissolved in HNO3 and treated with H2SO4, heated for several hours at 380 °C;;

7440-69-9Relevant articles and documents

Interfacial reactions in Sn/Bi2Te3, Sn/Bi 2Se3 and Sn/Bi2(Te1-xSe x)3 couples

Chen, Sinn-Wen,Wu, Chih-Yu,Wu, Hsin-Jay,Chiu, Wan-Ting

, p. 313 - 318 (2014)

Bi2(Te1-xSex)3 is an important kind of n-type thermoelectric material. In this study, interfacial reactions at 250 °C in the Sn/Bi2Te3, Sn/Bi2Se 3 and Sn/Bi2/sub

Syntheses and characterizations of bismuth nanofilms and nanorhombuses by the structure-controlling solventless method

Chen, Jing,Wu, Li-Ming,Chen, Ling

, p. 586 - 591 (2007)

Substrate-free bismuth nanofilms with an average thickness of 0.6 nm (σ = ±14.1%) and monodisperse layered Bi nanorhombuses with an average edge length of 21.5 nm (σ = ±14.7%) and thickness of 0.9 nm (σ = ±25.8%) have been successively synthesized by structure-controlling solventless thermolysis from a new layered bismuth thiolate precursor with a 31.49 A spacing. The morphologies result from self-control at an atomic level by the layered Bi(SC12H 25)3 crystal structure. The formation of the Bi nanofilm intermediate provides significant substantiation for this synthesis method, and detailed evidence on the conversion progress has been obtained. Both the films and the rhombuses have been characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectrometry (EDX), high-resolution TEM (HRTEM), and atomic force microscopy (AFM) measurements. Special UV-vis electronic absorption spectra of the nanoproducts have been studied.

Facile synthesis of Bi/BiOCl composite with selective photocatalytic properties

Chen, Dongling,Zhang, Min,Lu, Qiuju,Chen, Junfang,Liu, Bitao,Wang, Zhaofeng

, p. 647 - 654 (2015)

This paper presents a novel and facile method to fabricate Bi/BiOCl composites with dominant (001) facets in situ via a microwave reduction route. Different characterization techniques, including X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission scanning electron microscopy (TEM), UV-vis diffuse reflectance spectrometry (DRS), X-ray photoelectron spectroscopy (XPS), electron spin resonance spectroscopy (ESR), cathodoluminescence spectrum (CL), and lifetime, have been employed to investigate the structure, optical and electrical properties of the Bi/BiOCl composites. The experimental results show that the introduction of Bi particles can efficiently enhance the photocatalytic performance of BiOCl for the degradation of several dyes under ultraviolet (UV) light irradiation, especially for negative charged methyl orange (MO). Unlike the UV photocatalytic performance, such Bi/BiOCl composite shows higher degradation efficiency towards rhodamine B (RhB) than MO and methylene blue (MB) under visible light irradiation. This special photocatalytic performance can be ascribed to the synergistic effect between oxygen vacancies and Bi particles. This work provides new insights about the photodegradation mechanisms of MO, MB and RhB under UV and visible light irradiation, which would be helpful to guide the selection of an appropriate catalyst for other pollutants.

Effect of the surface configuration on the oxidation of bismuth nanowire

Huang,Fung

, p. 1604 - 1611 (2006)

Incorporating nanoprocessing into the metal oxidation, it was a facile way to synthesize functional oxide with desired nanostructure. In this work, δ-Bi2O3 nanowires were successfully fabricated by the oxidation of electroplated Bi nanowires at 350 °C. δ-Bi2O3 is the high-temperature phase of Bi2O3 and only stable at 723-823 °C. Partially oxidized nanowires showed core-shell structure composed of metallic Bi and δ-Bi2O3. To investigate the mechanism of oxidation reaction, the Bi/Bi2O3 interface was characterized by high resolution transmission electron microscopy (HRTEM). HRTEM images showed rapid growth of oxide layer on (2 over(1, ?) 0) plane of rhombohedral Bi metal. The coherency between (10 over(2, ?)) of metallic Bi and (1 0 0) of cubic Bi2O3 was observed. A schematic model was also used to describe the oxidation process. The coherency Bi and Bi2O3 and the stabilization of high-temperature (fluorite structure) Bi2O3 were also discussed based on this model.

Structure and resistivity of bismuth nanobelts in situ synthesized on silicon wafer through an ethanol-thermal method

Gao, Zheng,Qin, Haiming,Yan, Tao,Liu, Hong,Wang, Jiyang

, p. 3257 - 3261 (2011)

Bismuth nanobelts in situ grown on a silicon wafer were synthesized through an ethanol-thermal method without any capping agent. The structure of the bismuth beltsilicon composite nanostructure was characterized by scanning electron microscope, energy-dis

Synthesis and single crystal X-ray structure analysis of bromodi(isopropenyl)bismuthane

Schumann, Herbert,Muehle, Stefan H.

, p. 629 - 632 (1999)

Tri(isopropenyl)bismuthane (1) reacts with bromine to form bromodi(isopropenyl)bismuthane (2) and dibromo(isopropenyl)bismuthane (3). The single crystal X-ray structure determination of 2 (monoclinic, P21/c; a = 1058.6(3), b = 1127.0(3), c = 1561.3(4) pm, and β = 109.26(2)°; Z = 8 molecules; dc = 2.803 g/cm3; R = 0.059) shows two crystallographically independent molecules which are connected by Bi-Br...Bi bridges (Bi-Br 282.3(2) and 284.7(2); Br...Bi 302.9(2) and 303.6(2) pm) forming helical chains directed along the b-axis of the unit cell. Every turn of the helix (360°) consists of four molecules and corresponds to the length of the b-axis (1127.0(3) pm).

Structural and magneto-transport properties of electrodeposited bismuth nanowires

Liu, Kai,Chien,Searson,Yu-Zhang, Kui

, p. 1436 - 1438 (1998)

Arrays of semimetallic Bi nanowires have been successfully fabricated by electrodeposition. Each nanowire consists of elongated Bi grains along the wire direction. Very large positive magnetoresistance of 300% at low temperatures and 70% at room temperatu

Bismuth oxychloride nanoflake assemblies as a new anode for potassium ion batteries

Li, Wei,Xu, Yang,Dong, Yulian,Wu, Yuhan,Zhang, Chenglin,Zhou, Min,Fu, Qun,Wu, Minghong,Lei, Yong

, p. 6507 - 6510 (2019)

This work reports the first demonstration of bismuth oxyhalides as anode materials in potassium-ion batteries. BiOCl nanoflake assemblies deliver high capacities of 367 mA h g-1 at 50 mA g-1 and 175 mA h g-1 at 1 A g-1. The formation of K-Bi alloys at an early stage of potassiation is observed.

Orientation-controlled phase transformation of Bi2O3 during oxidation of electrodeposited Bi film

Huang, Chaur-Chi,Wen, Teng-Yi,Fung, Kuan-Zong

, p. 110 - 118 (2006)

High-temperature fluorite structure Bi2O3 is a well-known solid electrolyte owing to its high oxygen ion conductivity. In this study, Bi2O3 thin film was prepared by the oxidation process of the electrodeposited metallic Bi film. The crystal structures of the oxidized Bi films varied with the applied voltages during the electroplating process. Pure α-Bi2O3 was obtained when the oxidation was conducted for the metallic Bi film electrodeposited at -0.1 V. Only β-Bi2O3 was observed as a -0.5 V electrodeposited Bi film was oxidized. The crystal structure of Bi 2O3 obtained by oxidation of metallic Bi film may dominantly be affected by the orientation of as-electrodeposited Bi film. Such kind of process is favorable to the preparation of functional ceramic with specific crystal structure.

The kinetics of thermal decomposition of bismuth oxohydroxolaurate

Logvinenko,Mikhailov,Yukhin

, p. 47 - 49 (2007)

The bismuth salt of lauric (dodecanic) acid Bi6O 4(OH)4(C11H23COO)6 was studied earlier. This salt has layer structure (the interlaminar distance=37.50 A), under heating this liquid-crystalline state has the mesomorphic transformation, turns to the amorphous state, decomposes stepwise with the formation of well-ordered layers of bismuth nanoparticles. DSC-curves were used for the study of the decomposition kinetics in the area of decomposition with small mass loss and exothermic effect (423-483 K). Springer-Verlag 2007.

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