Tellur Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
DUNKELGRAUES BIS BRAUNES, AMORPHES PULVER MIT METALLEIGENSCHAFTEN ODER SILBRIGWEISSER, GLäNZENDER, KRISTALLINER FESTSTOFF.
CHEMISCHE GEFAHREN
Beim Erhitzen bilden sich giftige Rauche. Reagiert heftig mit Halogenen oder Interhalogenenunter Feuergefahr. Reagiert mit Zink unter Weißglut. Lithiumsilicid greift Tellur unter Weißglut an.
ARBEITSPLATZGRENZWERTE
TLV: 0,1 mg/m?(als TWA); (ACGIH 2005).
MAK: IIb (nicht festgelegt, aber Informationen vorhanden) (DFG 2006.
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation des Aerosols
INHALATIONSGEFAHREN
Verdampfung bei 20°C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch beim Dispergieren schnell erreicht werden.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Das Aerosol reizt die Augen und die Atemwege. Möglich sind Auswirkungen auf Leberund Zentralnervensystem. Exposition kann zu knoblauchartigem Atem führen. ärztliche Beobachtung notwendig.
LECKAGE
Verschüttetes Material in abgedichteten Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgfältig sammeln. An sicheren Ort bringen. Persönliche Schutzausrüstung: Atemschutzgerät, P3-Filter für giftige Partikel.
R-Sätze Betriebsanweisung:
R25:Giftig beim Verschlucken.
S-Sätze Betriebsanweisung:
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
Aussehen Eigenschaften
Te. Silberweiße bis dunkelgraue, spröde, leicht pulverisierbare kristalline Stücke, Barren, Granulate oder amorphes, braunes, geruchloses Pulver. Aufnahme geringster Mengen durch Einatmen oder Verschlucken erzeugt starken, teilweise über Monate anhaltenden Knoblauchgeruch.
Gefahren für Mensch und Umwelt
Gesundheitsschädlich beim Einatmen, Verschlucken und Berührung mit der Haut. Hautresorption löslicher Salze möglich. Größere Mengen verursachen gastrointestinale Störungen sowie Leber- und Nierenschäden.
Möglicherweise fortpflanzungsschädigend. Mutagene Wirkung im Tierversuch.
Hefitge Reaktionen mitstarke Oxidationsmitteln und Säuren möglich.
LD
50 (oral, Ratte): 83 mg/kg.
Schutzmaßnahmen und Verhaltensregeln
Schutzhandschuhe als kurzzeitiger Staubschutz.
Verhalten im Gefahrfall
Trocken aufnehmen. Der Entsorgung zuführen. Staubentwicklung vermeiden.
Wasser, Kohlendioxid, Sand, Pulver, Schaum.
Brennbar. Im Brandfall kann Telluroxid entstehen. Brandgase nicht einatmen.
Erste Hilfe
Nach Hautkontakt: Mit reichlich Wasser abwaschen.
Nach Augenkontakt: Mit reichlich Wasser bei geöffnetem Lidspalt mindestens 10 Minuten ausspülen. Sofort Augenarzt hinzuziehen.
Nach Einatmen: Frischluft, Arzt hinzuziehen.
Nach Verschlucken: Viel Wasser trinken lassen. Erbrechen vermeiden. Sofort Arzt hinzuziehen.
Nach Kleidungskontakt: Kontaminierte Kleidung sofort entfernen.
Ersthelfer: siehe gesonderten Anschlag
Sachgerechte Entsorgung
Getrennt als tellurhaltige Abfälle sammeln und der Entsorgung zuführen.
Beschreibung
Tellurium is one of the rarest elements on earth similar to
selenium, and was discovered in Transylvania in 1782 by
Franz-Joseph Muller von Reichenstein. The name derived from
the Latin word for earth. Tellurium is occasionally found
naturally, more often as telluride of gold, calaverite.
Chemische Eigenschaften
Tellurium is a grayish or silvery white, lustrous, crystalline, semimetallic element. It may exist in a hexagonal crystalline form or an amorphous powder.Soluble in sulfuric acid, nitric acid, potassium hydroxide, and potassium cyanide solutions; insoluble in water. Imparts garlic-like odor to breath, can be depilatory. It is a ptype semiconductor and its conductivity is sensitive to light exposure. It is found in sulfide ores and is produced as a by-product of copper or bismuth refining.
Physikalische Eigenschaften
Tellurium is a silver-white, brittle crystal with a metallic luster and has semiconductorcharacteristics. It is a metalloid that shares properties with both metals and nonmetals, andit has some properties similar to selenium and sulfur, located just above it in group 16 of theperiodic table.
There are two allotropic forms of tellurium: (1) the crystalline form that has a silvery metallicappearance and a density of 6.24 g/cm
3, a melting point of 499.51°C, and a boiling point of988°C; and (2) the amorphous allotrope that is brown in color and has a density of 6.015g/cm
3and ranges for the melting and boiling point temperatures similar to the crystalline form.
Isotopes
There are a total of 48 isotopes of tellurium. Eight of these are consideredstable. Three of the stable ones are actually radioactive but have such long half-livesthat they still contribute to the natural abundance of tellurium in the crust of the Earth.The isotope Te-123 (half-life of 6×10
+14 years) contributes 0.89% of the total telluriumfound on Earth, Te-128 (half-life of 7.7×10
+24 years) contributes 31.74% to the naturalabundance, and Te-130 (half-life of 0.79×10
+21 years) contributes 34.08% to the telluriumin the Earth’s crust. The other five stable isotopes and the percentage of theirnatural abundance are as follows: Te-120 = 0.09%, Te-122 = 2.55%, Te-124 = 4.74%,Te-125 = 7.07%, and Te-126 = 18.84%. The other 40 isotopes are all radioactive withshort half-lives.
Origin of Name
The name “tellurium” is derived from the Latin word for Earth, tellus.
Occurrence
Tellurium is the 71st most abundant element on Earth. It makes up a small portion ofigneous rocks and is sometimes found as a free element, but is more often recovered fromseveral ores. Its major ores are sylvanite (AgAuTe
4), also known as graphic tellurium, calaverite,sylvanite, and krennerite, all with the same general formula (AuTe
2). Other minor ores arenagyagite, black tellurium, hessite, altaite, and coloradoite. In addition, it is recovered fromgold telluride (AuTe
2). Significant quantities are also recovered from the anode “slime” of theelectrolytic refining process of copper production.
Charakteristisch
The pure form of tellurium burns with a blue flame and forms tellurium dioxide (TeO
2).It is brittle and is a poor conductor of electricity. It reacts with the halogens of group 17, butnot with many metals. When it reacts with gold, it forms gold telluride. Tellurium is insolublein water but readily reacts with nitric acid to produce tellurous acid. If inhaled, it produces agarlic-like odor on one’s breath.
Verwenden
Tellurium is a common constituent of ores that contain silver, gold, lead, antimony, and bismuth, and it is often present in small amounts in coal. Tellurium is widely used in metallurgy because it improves the properties of copper, tin, lead-based alloys, steel, and cast iron. It is used in rubber manufacturing to increase heat resistance and to retard the aging of rubber hoses and cable coatings. Small amounts are used in the electronics industry for lasers and photoreceptors. Tellurium is not an essential micronutrient; therefore, it is not found in nutritional supplements.
As coloring agent in chinaware, porcelains, enamels, glass; reagent in producing black finish on silverware; in manufacture of special alloys of marked electrical resistance; in semiconductor research.
Vorbereitung Methode
Elemental tellurium (Te) has some metallic properties,
although it is classed as a nonmetal or metalloid. The
name is derived from the Latin word for earth, tellus.
Tellurium is occasionally found naturally, more often as
telluride of gold, calaverite. The elemental form has a bright
luster, is brittle, readily powders, and burns slowly in air.
Tellurium exists in two allotropic forms, in the form of
powder and hexagonal crystalline (isomorphous) with gray
selenium. The concentration in the earth’s crust is about
0.002 ppm. It is recovered from anode muds during the
refining of blister copper. It is also found in various sulfide
ores along with selenium and is produced as a by-product of
metal refineries. The United States, Canada, Peru, and Japan
are the largest producers.
Tellurium’s industrial applications include its use as a
metallurgical additive to improve the characteristics of alloys
of copper, steel, lead, and bronze. Increased ductility results
from its use in steel and copper alloys. Addition of tellurium
to cast iron is used for chill control, and it is a basic part of
blasting caps. It is used in some chemical processes as a
catalyst for synthetic fiber production, and as a vulcanizing
agent and accelerator in the processing of rubber.
Definition
tellurium: Symbol Te. A silvery metalloidelement belonging to group16 (formerly VIB) of the periodictable; a.n. 52; r.a.m. 127.60; r.d. 6.24(crystalline); m.p. 449.5°C; b.p.989.8°C. It occurs mainly as telluridesin ores of gold, silver, copper,and nickel and it is obtained as a byproductin copper refining. There areeight natural isotopes and nine radioactiveisotopes. The element is usedin semiconductors and smallamounts are added to certain steels.Tellurium is also added in smallquantities to lead. Its chemistry issimilar to that of sulphur. It was discoveredby Franz Müller (1740–1825)in 1782.
Allgemeine Beschreibung
Grayish-white, lustrous, brittle, crystalline solid; dark-gray to brown, amorphous powder with metallic characteristics. Used as a coloring agent in chinaware, porcelains, enamels, glass; producing black finish on silverware; semiconductor devices and research; manufacturing special alloys of marked electrical resistance. Improves mechanical properties of lead; powerful carbide stabilizer in cast iron, Tellurium vapor in "daylight" lamps, vulcanization of rubber. Blasting caps. Semiconductor research.
Reaktivität anzeigen
Tellurium is attacked by chlorine fluoride with incandescence. When Tellurium and potassium are warmed in an atmosphere of hydrogen, combination occurs with incandescence [Mellor 11:40. 1946-47]. Burning Tellurium produces toxic Tellurium oxide gas. Avoid solid sodium, halogens, interhalogens, metals, hexalithium disilicide. Reacts with nitric acid; reacts with concentrated sulfuric acid forming a red solution. Dissolves in potassium hydroxide in the presence of air with formation of deep red solution; combines with halogens. Avoid antimony and chlorine trifluoride; chlorine trifluoride reacts vigorously with Tellurium producing flame. Fluorine and Tellurium react with incandescence. Lithium silicide attacks Tellurium with incandescence. Reaction with zinc is accompanied by incandescence (same potential with cadmium, only hazard is less). A vigorous reaction results when liquid Tellurium is poured over solid sodium [EPA, 1998].
Hazard
All forms of tellurium are toxic in gas form. The vapors of all the compounds of the dustand powder forms of the element should not be inhaled or ingested. When a person is poisonedwith tellurium, even in small amounts, the breath will smell like garlic.
Health Hazard
Although tellurium in elemental form haslow toxicity, ingestion can produce nausea,vomiting, tremors, convulsions, and centralnervous system depression. In addition,exposure to the metal or to its compoundscan generate garlic-like odor in breath, sweat,and urine. Such odor is imparted by dimethyltelluride that is formed in the body. Oralintake of large doses of the metal or itscompounds can be lethal. Clinical symptomsare similar for most tellurium salts,which include headache, drowsiness, lossof appetite, nausea, tremors, and convulsions.High exposure can produce metallictaste, dry throat, chill and other symptoms.Inhalation of dust or fume of the metalcan cause irritation of the respiratory tract.Chronic exposure can produce bronchitis andpneumonia.
Brandgefahr
A finely divided suspension of elemental Tellurium in air will explode. Insoluble in water. Burning Tellurium produces toxic Tellurium oxide gas. Avoid solid sodium, halogens, interhalogens, metals, hexalithium disilicide. Reacts with nitric acid; reacts with concentrated sulfuric acid forming a red solution. Dissolves in potassium hydroxide in the presence of air with formation of deep red solution; combines with halogens. Avoid antimony and chlorine trifluoride; chlorine trifluoride reacts vigorously with Tellurium producing flame. Fluorine and Tellurium react with incandescence. Lithium silicide attacks Tellurium with incandescence. Reaction with zinc is accompanied by incandescence (same potential with cadmium, only hazard is less). A vigorous reaction results when liquid Tellurium is poured over solid sodium.
Sicherheitsprofil
Poison by ingestion and intratracheal routes. An experimental teratogen. Exposure causes nausea, vomiting, tremors, convulsions, respiratory arrest, central nervous system depression, and garlic odor to breath. Aerosols of tellurium, tellurium dioxide, and hydrogen telluride cause irritation of the respiratory system and may lead to the development of bronchitis and pneumonia. Experimental reproductive effects. Under the proper conditions it undergoes hazardous reactions with halogens (e.g., chlorine, fluorine), interhalogens (e.g., bromine pentafluoride, chlorine fluoride, chlorine trifluoride), metals (e.g., cadmium, potassium, sodium, platinum, tin, zinc), hexalithium disilicide, silver bromate, silver iodate. When heated to decomposition it emits toxic fumes of Te. See also TELLURIUM COMPOUNDS.
mögliche Exposition
The primary use of tellurium is in the vulcanization of rubber and as an additive in ferritic steel production. It is also used as a carbide stabilizer in cast iron, a chemical catalyst; a coloring agent in glazes and glass; a thermocoupling material in refrigerating equipment; as an additive to selenium rectifiers; in alloys of lead, copper, steel, and tin for increased resistance to corrosion and stress, workability, machinability, and creep strength; and in certain culture media in bacteriology. Since tellurium is present in silver, copper, lead, and bismuth ores, exposure may occur during purification of these ores.
Environmental Fate
Metals are recalcitrant to degradation; therefore, no biodegradation studies have been performed on tellurium. No aquatic bioaccumulation data exist for tellurium; however, based on its density and low water solubility, it is unlikely to present a concern for bioaccumulation in the water column. No environmental monitoring data are available on the levels of tellurium in sediment or sediment-dwelling organisms. Therefore, it is unclear whether tellurium has the potential to bioaccumulate in this compartment. In humans, tellurium accumulates in the bones. Based on this, it may be assumed that tellurium has the potential to bioaccumulate in vertebrates.
Versand/Shipping
UN3288 Toxic solids, inorganic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.
läuterung methode
Purify it by zone refining and repeated sublimation to an impurity of less than 1 part in 108 (except for surface contamination by TeO2). [Machol & Westrum J Am Chem Soc 80 2950 1958.] Tellurium is volatile at 500o/0.2mm. It has also been purified by electrode deposition [Mathers & Turner Trans Amer Electrochem Soc 54 293 1928].
Inkompatibilitäten
Finely divided powder or dust may be flammable and explosive. Violent reaction with halogens, interhalogens, zinc and lithium silicide; with incandescence. Incompatible with oxidizers, cadmium; strong bases; chemically active metals; silver bromate; nitric acid.
Tellur Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
