But-1-en Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
GERUCHLOSES, FARBLOSES, KOMPRIMIERTES FLüSSIGGAS.
PHYSIKALISCHE GEFAHREN
Das Gas ist schwerer als Luft. und kann sich am Boden ausbreiten. Fernzündung möglich.
CHEMISCHE GEFAHREN
Kann polymerisieren. Reagiert sehr heftig mit Sauerstoff und Oxidationsmitteln unter Feuer- und Explosionsgefahr.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation.
INHALATIONSGEFAHREN
Beim Entweichen aus dem Behälter kann das Gas die Luft verdrängen. Erstickungsgefahr in geschlossenen Räumen.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Schnelle Verdampfung kann zu Erfrierungen führen.
LECKAGE
Gefahrenbereich verlassen! Belüftung. Zündquellen entfernen. Persönliche Schutzausrüstung: Vollschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.
R-Sätze Betriebsanweisung:
R12:Hochentzündlich.
S-Sätze Betriebsanweisung:
S9:Behälter an einem gut gelüfteten Ort aufbewahren.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S33:Maßnahmen gegen elektrostatische Aufladungen treffen.
Beschreibung
1-Butene is a colourless, stable but polymerises exothermically, extremely flammable liquefied
gas with an aromatic odour. It is insoluble in water and is one of the isomers of butane. 1-Butene readily forms explosive mixtures with air. It is incompatible with strong oxidising
agents, halogens, halogen acids, metal salts, boron trifluoride, fluorine, and nitrogen oxides.
1-Butene of high purity is made by cracking naphtha and separating it from other products
by an extra-high-purity distillation column. It is an important organic compound in the production
of several industrial materials – for instance, linear low-density polyethylene (LLDPE),
a more flexible and resilient polyethylene, and a range of polypropylene resins – and in the
production of polybutene, butylene oxide, and the C4 solvents secondary butyl alcohol (SBA)
and MEK. The vapour of 1-butene is heavier than air and may travel long distances to an ignition
source and flash back.
Chemische Eigenschaften
1-Butene is a colorless, extremely flammable liquefi ed gas with an aromatic odor. It is insol uble in water and is an isomer of butane. It is highly flammable and readily forms explo sive mixtures with air. 1-Butene of high purity is made by cracking naphtha and separating
it from other products by an extra-high purity distillation column. However, 1-butene is
incompatible with metal salts, fl uorine, nitrogen oxides, boron trifl uoride, halogen acids,
halogens, and strong oxidizing agents. It is an important organic compound in the produc tion of several industrial materials, i.e., linear low density polyethylene (LLDPE), a more
fl exible and resilient polyethylene, a range of polypropylene resins, and in the production
of polybutene, butylene oxide and in the C4 solvents, secondary butyl alcohol (SBA) and
methyl ethyl ketone (MEK). The vapor of 1-butene is heavier than air and may travel long
distances to an ignition source and fl ash back.
Physikalische Eigenschaften
Butenes or butylenes are hydrocarbon alkenes that exist as four different isomers. Each isomer is a flammable gas at normal room temperature and one atmosphere pressure, but their boiling points indicate that butenes can be condensed at low ambient temperatures and/or increase pressure similar to propane and butane. The “2” designation in the names indicates the position of the double bond. The cis and trans labels indicate geometric isomerism. Geometric isomers are molecules that have similar atoms and bonds but different spatial arrangement of atoms. The structures indicate that three of the butenes are normal butenes, n-butenes, but that methylpropene is branched. Methylpropene is also called isobutene or isobutylene. Isobutenes are more reactive than n-butenes, and reaction mechanisms involving isobutenes differ from those of normal butenes.
Verwenden
Butenes are used extensively in gasoline production to produce high-octane gasoline compounds.Another large use of normal butenes in the petrochemical industry is in the production of 1,3-butadiene. Butene is used in the plastics industry to make both homopolymers and copolymers. Another use of 1-butene is in the production of solvents containing four carbons such as secondary butyl alcohol and methyl ethyl ketone (MEK).
Vorbereitung Methode
Most butenes are produced in the cracking process in refineries along with other C-4 fractions such as the butanes. Butenes are separated from other compounds and each other by several methods. Isobutene is separated from normal butanes by absorption in a sulfuric acid solution. Normal butenes can be separated from butanes by fractionation. The close boiling points of butanes and butenes make straight fractional distillation an inadequate separation method, but extractive distillation can be used. Butenes can also be prepared from the dehydrogenation (elimination of hydrogen) of butane.
Definition
ChEBI: A butene with unsaturation at position 1.
Allgemeine Beschreibung
Colorless gas.
Air & Water Reaktionen
Highly flammable. Insoluble in water.
Reaktivität anzeigen
The unsaturated aliphatic hydrocarbons, such as 1-BUTENE, are generally much more reactive than the alkanes. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. In the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions. May react with oxidizing materials. Aluminum borohydride reacts with alkenes and in the presence of oxygen, combustion is initiated even in the absence of moisture.
Health Hazard
Exposures to 1-butene cause the effects of an asphyxiant and/or an anesthetic (at high
concentrations). Workers exposed to 1-butene develop eye irritation.
Brandgefahr
1-BUTENE is flammable. Vapor is heavier than air and may travel long distances to an ignition source and flash back.
Environmental Fate
Biological. Biooxidation of 1-butene may occur yielding 3-buten-1-ol, which may oxidize to
give 3-butenoic acid (Dugan, 1972). Washed cell suspensions of bacteria belonging to the genera
Mycobacterium, Nocardia, Xanthobacter, and Pseudomonas and growing on selected alkenes
metabolized 1-butene to 1,2-epoxybutane (Van Ginkel et al., 1987).
Photolytic. Products identified from the photoirradiation of 1-butene with nitrogen dioxide in air
are epoxybutane, 2-butanone, propanal, ethanol, ethyl nitrate, carbon monoxide, carbon dioxide,
methanol, and nitric acid (Takeuchi et al., 1983).
The following rate constants were reported for the reaction of 1-butene and OH radicals in the
atmosphere: 1.0 x 10
-17 cm
3/molecule?sec (Bufalini and Altshuller, 1965); 2.70 x 10
-11
cm
3/molecule?sec (Atkinson et al., 1979); 3.14 x 10
-11 cm
3/molecule?sec (Atkinson, 1990; Sablji?
and Güsten, 1990). Reported photooxidation reaction rate constants for the reaction of 1-butene
and ozone are 1.23 x 10
-17, 1.0 x 10
-17, 1.03 x 10
-17 cm
3/molecule?sec (Adeniji et al., 1981). Based
on the reaction of 1-butene and OH radicals gas phase, the atmospheric lifetime was estimated to
be 5.5 h in summer sunlight.
Chemical/Physical. Complete combustion in air yields carbon dioxide and water. Incomplete
combustion will generate carbon monoxide.
Hydrolysis in water is not expected to be signicant because 1-butene is very volatile.
Vorsichtsmaßnahmen
When working with 1-butene, occupational workers should wear proper protectives,
preferably a NIOSH-approved full-face positive pressure supplied-air respirator or a self contained breathing apparatus (SCBA). Workers should not wear contact lenses.
But-1-en Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
