首页 所有产品 邻苯二甲酸酐（99.5%） - 中国

邻苯二甲酸酐（99.5%） - 中国

IUPAC Name

:   2-Benzofuran-1,3-dione

Cas Number

:   85-44-9

HS Code

:   2917.35.00

Formula

:  

C8H4O3
Basic Info

Appearance Name

:   Fine White Powder

Common Names

:   Isobenzofuran-1,3-dione

Packaging

:   25 KG PE bag, 1,250 KG Falcon Bag
行业

塑料和聚合物
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Technical Document

Brief Overview

Phthalic anhydride, with the chemical formula C6H4(CO)2O, acts as the anhydride of phthalic acid and represents a significant commercial form of this acid. It stands as a pioneering example of the widespread use of a dicarboxylic acid anhydride, playing a crucial role in industrial chemistry. Particularly, it is instrumental in the extensive production of plasticizers for plastics, contributing to the estimated global production volume of about 3 million tonnes annually in 2000.

Manufacturing Process:

Discovered by Auguste Laurent in 1836, contemporary synthesis of phthalic anhydride employs various methods, including the oxidation of naphthalene or ortho-xylene. These processes involve vanadium pentoxide (V2O5) as the active oxidant, playing a pivotal role in multiple steps and being regenerated by molecular oxygen. Starting from o-xylene, the oxidation reaction is run at about 320–400 °C and has the following stoichiometry:

C6H4(CH3)2 + 3 O2 → C6H4(CO)2O + 3 H2O

The reaction proceeds with about 70% selectivity. About 10% of maleic anhydride is also produced: C6H4(CH3)2 + 7.5 O2 → C4H2O3 +4 H2O + 4 CO2

Phthalic anhydride and maleic anhydride are recovered by distillation by a series of switch condensers.

The naphthalene route (the Gibbs phthalic anhydride process or the Gibbs–Wohg naphthalene oxidation reaction), a process whose use has declined in compared to the o-xylene route, has the following mechanism:

Phthalic anhydride can also be prepared from phthalic acid by simple dehydration.

Brief Overview

Phthalic anhydride, with the chemical formula C6H4(CO)2O, acts as the anhydride of phthalic acid and represents a significant commercial form of this acid. It stands as a pioneering example of the widespread use of a dicarboxylic acid anhydride, playing a crucial role in industrial chemistry. Particularly, it is instrumental in the extensive production of plasticizers for plastics, contributing to the estimated global production volume of about 3 million tonnes annually in 2000.

Manufacturing Process:

Discovered by Auguste Laurent in 1836, contemporary synthesis of phthalic anhydride employs various methods, including the oxidation of naphthalene or ortho-xylene. These processes involve vanadium pentoxide (V2O5) as the active oxidant, playing a pivotal role in multiple steps and being regenerated by molecular oxygen. Starting from o-xylene, the oxidation reaction is run at about 320–400 °C and has the following stoichiometry:

C6H4(CH3)2 + 3 O2 → C6H4(CO)2O + 3 H2O

The reaction proceeds with about 70% selectivity. About 10% of maleic anhydride is also produced: C6H4(CH3)2 + 7.5 O2 → C4H2O3 +4 H2O + 4 CO2

Phthalic anhydride and maleic anhydride are recovered by distillation by a series of switch condensers.

The naphthalene route (the Gibbs phthalic anhydride process or the Gibbs–Wohg naphthalene oxidation reaction), a process whose use has declined in compared to the o-xylene route, has the following mechanism:

Phthalic anhydride can also be prepared from phthalic acid by simple dehydration.

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