Arsentrichlorid Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
FARBLOSE, ?LIGE, RAUCHENDE FLüSSIGKEIT MIT STECHENDEM GERUCH.
CHEMISCHE GEFAHREN
Zersetzung beim Erhitzen unter Bildung giftiger Rauche mit Chlorwasserstoff (s. ICSC 0163) und Arsenoxiden. Reagiert sehr heftig mit feuchter Luftoder Wasser unter Bildung von Chlorwasserstoff (s. ICSC-Nr. 0163) Greift viele Metalle unter Bildung brennbarer/explosionsf?higer Gase an (z.B. Wasserstoff, ICSC-Nr. 0001).
ARBEITSPLATZGRENZWERTE
TLV: 0.01 mg/m?(als TWA); Krebskategorie A1(best?tigte krebserzeugende Wirkung beim Menschen); BEI vorhanden; (ACGIH 2005).
MAK: Krebserzeugend Kategorie 1; Keimzellmutagen Kategorie 3A; (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den K?rper durch Inhalation der D?mpfe und durch Verschlucken.
INHALATIONSGEFAHREN
Beim Verdampfen bei 20°C kann sehr schnell eine gesundheitssch?dliche Kontamination der Luft eintreten.
LECKAGE
Gefahrenbereich verlassen! Fachmann zu Rate ziehen! Pers?nliche Schutzausrüstung: Vollschutzanzug mit umgebungsluftunabh?ngigem Atemschutzger?t. NICHT in die Umwelt gelangen lassen. Ausgelaufene Flüssigkeit m?glichst in abdichtbaren Kunststoffbeh?ltern sammeln. Reste mit trockenem Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen.
R-S?tze Betriebsanweisung:
R23/25:Giftig beim Einatmen und Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.
S-S?tze Betriebsanweisung:
S20/21:Bei der Arbeit nicht essen, trinken,rauchen.
S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S60:Dieses Produkt und sein Beh?lter sind als gef?hrlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
Chemische Eigenschaften
colourless oily liquid
Physikalische Eigenschaften
Colorless oily liquid; fumes in air; density 2.163 g/ml at 20°C; refractive index 1.621 at 14°C; melts at 0.16°C; boils at 130.2°C; vapor pressure 9.75 torr at 25°C; decomposes in water; soluble in alcohol, ether, HCl and HBr.
Verwenden
Arsenic Trichloride is an highly toxic inorganic compounds and is an intermediate in the manufacture of organoarsenic compounds.
synthetische
The compound is generally made from arsenic trioxide by (i) passing chlorine over it or (ii) treating the trioxide with sulfur monochloride, S2Cl2. Alternatively it is prepared from arsenic trioxide by distillation with either concentrated hydrochloric acid or a mixture of sulfuric acid and a metal chloride. Arsenic trichloride may also be prepared by combination of arsenic and chlorine.
Definition
A poisonous oily liquid. It fumesin moist air due to hydrolysis with water
vapor:AsCl
3 + 3H
2O = As
2O
3 + 6HCl
Arsenic(III) chloride is covalent and exhibits nonmetallic properties.
Allgemeine Beschreibung
A colorless to yellow oily fuming liquid. ARSENIC(III) CHLORIDE is irritating to the skin, eyes, and mucous membranes. Very toxic by inhalation and ingestion.
Air & Water Reaktionen
Fumes in air. Reacts with water to form hydrochloric acid and As(OH)3.
Reaktivit?t anzeigen
When ARSENIC CHLORIDE is heated to decomposition or on contact with mineral acids, ARSENIC(III) CHLORIDE emits highly toxic fumes of hydrogen chloride and of metallic arsenic. Explodes with Na, K, and Al on impact [Sax, 9th ed., 1996, p. 275]. The interaction of hexafluoroisopropylideneaminolithium with a range of chlorinated and /or fluorinated derivatives of arsenic, boron, phosphorus, silicon, and sulfur yielded a violently exothermic reaction.
Hazard
Strong irritant to eyes and skin.
Health Hazard
ARSENIC(III) CHLORIDE can cause death. In acute exposures, it is extremely toxic and caustic, owing not only to the poisonous nature of arsenic, but also to the release of hydrochloric acid in the presence of water. Exposure to the skin causes local irritation and blisters. Inhalation or ingestion causes hemorrhagic gastroenteritis resulting in loss of fluids and electrolytes, collapse, shock and death. Chronic poisoning can lead to peripheral nerve damage, skin conditions, liver damage and it has been implicated in the induction of skin and lung cancer. The fatal human dose is 70-180 mg depending on the weight of the victim.
Brandgefahr
When in contact with active metals such as arsenic, iron, aluminum, zinc, or when heated to decomposition, ARSENIC(III) CHLORIDE emits highly toxic fumes of arsenic. Upon contact with water hydrogen chloride is produced. Water causes ARSENIC(III) CHLORIDE to decompose to yield arsenic acid and hydrochloric acid. Avoid active metals such as arsenic, iron, aluminum, zinc, decomposed by water to form arsenic hydroxide and hydrogen chloride. Avoid air, ultraviolet light. Hazardous polymerization may not occur.
Sicherheitsprofil
Confirmed human
carcinogen. A poison via inhalation. See also
ARSENIC COMPOUNDS and
CHLORIDES. Very poisonous; fumes in
air. Mutation data reported. When heated to
decomposition it emits very toxic fumes of
As and Cl-. Highly reactive. Explodes with
Na, K, and Al on impact.
Synthese
The direct synthesis of AsCl3 is uneconom ical. An old commercial production method is the Glauber process using arsenic trioxide:
As2O3 +6NaCl+3H2SO4?→ 2AsCl3+3Na2SO4+3H2O
However, AsCl3 is easier to produce by react ing As2O3 with gaseous hydrogen chloride at 180–200℃.
m?gliche Exposition
Arsenic chloride is used in the ceramics
industry; in the synthesis of chlorine-containing
arsenicals; as a chemical intermediate for arsenic insecticides,
pharmaceuticals; and has been used in chemical warfare
agents.
Versand/Shipping
UN1560 Arsenic trichloride, Hazard class 6.1;
Labels: 6.1-Poison Inhalation Hazard, Inhalation Hazard
Zone B.
l?uterung methode
Reflux the trichloride with arsenic for 4hours, then fractionally distil it. The middle fraction is stored with sodium wire for two days, then again distilled [Lewis & Sowerby J Chem Soc 336 1957]. It fumes in moist air forming the solid hydroxy-chloride [AsCl(OH)2] and is readily hydrolysed by H2O to form arsenious acid. POISONOUS. [Schenk in Handbook of Preparative Inorganic Chemistry (Ed. Brauer) Academic Press Vol I p 596 1963.]
Inkompatibilit?ten
Contact with sodium, potassium, or powdered
aluminum may cause a violent reaction. It is decomposed
in water, forming arsenic hydroxide and hydrogen
chloride. Exposure to light forms toxic gas. Violent reaction
with anhydrous ammonia, strong acids; strong oxidizers
and halogens. Incompatible with alkali metals; active
metals, such as arsenic, iron, aluminum, zinc. Corrodes
metals in the presence of moisture and forms flammable
and explosive hydrogen gas.
Waste disposal
Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Generators of waste containing this contaminant
(≥100 kg/mo) must conform with EPA regulations governing
storage, transportation, treatment, and waste disposal.
Dissolve in a minimum of concentrated hydrochloric acid.
Dilute with water until white precipitate forms. Add HCl to
dissolve. Saturate with H2S; filter and wash precipitate and
return to supplier. Alternatively, precipitate with heavy
metals, such as lime or ferric hydroxide in lieu of H2S.If needed, seek professional environmental engineering
assistance from the United States Environmental Protection
Agency Environmental Response Team at (908) 548-8730
(24-hour response line). In accordance with 40CFR165, follow
recommendations for the disposal of pesticides and
pesticide containers. Must be disposed properly by following
package label directions or by contacting your local or
federal environmental control agency, or by contacting
your regional EPA office.
Arsentrichlorid Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
