Maleic anhydride is primarily used to manufacture polyester and alkyd resins for fiberglass reinforced plastics. It is also used to make lacquers, lube oil additives, and agricultural products. Traditionally, maleic anhydride was produced through the catalytic oxidation of benzene, but this process utilized the hazardous chemical benzene. More recently, n-butane has replaced benzene as the feedstock due to its safety advantages and the ability to achieve higher yields. The n-butane oxidation process employs a fixed-bed reactor to pass a low concentration of butane over a catalyst at temperatures of 400-480°C to produce maleic anhydride and water.
Maleic anhydride is primarily used to manufacture polyester and alkyd resins for fiberglass reinforced plastics. It is also used to make lacquers, lube oil additives, and agricultural products. Traditionally, maleic anhydride was produced through the catalytic oxidation of benzene, but this process utilized the hazardous chemical benzene. More recently, n-butane has replaced benzene as the feedstock due to its safety advantages and the ability to achieve higher yields. The n-butane oxidation process employs a fixed-bed reactor to pass a low concentration of butane over a catalyst at temperatures of 400-480°C to produce maleic anhydride and water.
Maleic anhydride is primarily used to manufacture polyester and alkyd resins for fiberglass reinforced plastics. It is also used to make lacquers, lube oil additives, and agricultural products. Traditionally, maleic anhydride was produced through the catalytic oxidation of benzene, but this process utilized the hazardous chemical benzene. More recently, n-butane has replaced benzene as the feedstock due to its safety advantages and the ability to achieve higher yields. The n-butane oxidation process employs a fixed-bed reactor to pass a low concentration of butane over a catalyst at temperatures of 400-480°C to produce maleic anhydride and water.
Maleic anhydride is primarily used to manufacture polyester and alkyd resins for fiberglass reinforced plastics. It is also used to make lacquers, lube oil additives, and agricultural products. Traditionally, maleic anhydride was produced through the catalytic oxidation of benzene, but this process utilized the hazardous chemical benzene. More recently, n-butane has replaced benzene as the feedstock due to its safety advantages and the ability to achieve higher yields. The n-butane oxidation process employs a fixed-bed reactor to pass a low concentration of butane over a catalyst at temperatures of 400-480°C to produce maleic anhydride and water.
Download as PPT, PDF, TXT or read online from Scribd
Download as ppt, pdf, or txt
You are on page 1of 9
MALEIC ANHYDRIDE
Introduction
Maleic anhydride (MA) has numerous
industrial uses and is of significant commercial interest worldwide. Primary use - is in the manufacture of polyester and alkyd resins. These resins are added to fiberglass reinforced plastics to make a strong, lightweight, and corrosion resistant material.
MA is also employed in the manufacture of
- lacquers, the addition of MA to drying oils decreases the required drying time and improves the coating quality of lacquers - lube-oil additives, dispersants derived from MA prolong oil change intervals and improve the efficiency of automotive engines - agricultural products, include herbicides, pesticides, and plant growth regulators.
First synthesized in the 1830s,
manufactured commercially about 1930. Catalytic oxidation of benzene over vanadium oxide catalysts was integral to the creation of a commercially viable process for MA. Today, nearly three billion pounds of MA are made, using variations of this process.
Drawbacks of Benzene
Benzene is a hazardous chemical.
Efforts to find a suitable replacement have been pursued. Over the years, both n-butane and butylene have been utilized with increasingly successful results and are gradually overtaking benzene as the reactant of choice.
Benzene Oxidation Process
Traditional process, begins by mixing
benzene with an excess of air to give concentrations from 1-1.4 mole %. A low benzene concentration must be utilized in order not to exceed the flammability limit of the mixture. The reaction gas mixture then passes over the catalyst in a multitubular fixed-bed reactor atO an optimum pressure of 0.15-0.25 O + 9/2range O + 2 CO +MPa. 2
2 H2O
Butane Oxidation Process
Recent processes for the manufacture of MA.
Employ C4 hydrocarbons, such as n-butane and n-butylene, as feedstocks. A major advantage of C4 HC over benzene is that no carbon is lost in the reaction to form MA. Theoretically achievable conversion of 100%, the yield from butane is a third greater than that from benzene. The relatively low purchase price of C4 is much more attractive than the expense of benzene.
Other factors that favor C4s are safety,
health, and the environment. Benzene is a known carcinogen and one of the chemicals most stringently regulated by the government. The flammability limits for C4 HC are also lower than those for benzene, which is an additional safety advantage of the process. For all of these reasons, the fixed-bed process with n-butane has been the only MA route used commercially since 1985 in the United States.
Reaction Details
The process employs a fixed-bed which
allows a low concentration of butane passed over the catalyst in tubular reactors similar to the benzeneO process. n-C4H8 + 3 O2
+ 3 H 2O
The reactor is operated at temperatures from 400-480 C,
and the pressure is held at 0.3-0.4 MPa in order to force the exit gases downstream for scrubbing and purification. Unlike the benzene process, only a small amount of the MA can be condensed from the reactor effluent due to the increased formation of water.