Methyl methacrylate

Not to be confused with methyl acrylate

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Chemical compound

Methyl methacrylate (MMA) is an organic compound with the formula CH2=C(CH3)COOCH3. This colorless liquid, the methyl ester of methacrylic acid (MAA), is a monomer produced on a large scale for the production of poly(methyl methacrylate) (PMMA).[4]

History

MMA was discovered by Bernhard Tollens and his student W. A. Caspary in ,[5] who noticed and described its tendency to change into a clear, hard, transparent substance especially in sunlight.[6] Studies on acrylic esters slowly developed until the Staudinger's theory of macromolecules and his research into the nature of polyacrylates allowed to control the polymerization. Company Rohm and Haas founded by German chemist Otto Röhm, who investigated the topic for three decades, was finally able to start its industrial production in .[7]

Production and properties

Given the scale of production, many methods have been developed starting from diverse two- to four-carbon precursors.[4][8] Two principal routes appear to be commonly practiced.

Cyanohydrin route

The principal route begins with the condensation of acetone and hydrogen cyanide:

(CH3)2CO + HCN &#; (CH3)2C(OH)CN

Sulfuric acid then hydrolyzes acetone cyanohydrin (ACH) to a sulfate ester-adduct, which is cracked to the ester:[9]

(CH3)2C(OH)CN + 2H2SO4 &#; ((CH3)2C(OSO3H)C(O)NH2·H2SO4 &#; (CH3)2C(OSO3H)C(O)NH2 + H2SO4.

Methanolysis gives ammonium bisulfate and MMA:

(CH3)2C(OSO3H)C(O)NH2 + CH3OH &#; CH2 =C(CH3)C(O)OCH3 + NH4HSO4

This technology affords more than 3 billion kilograms per year, and the economics have been heavily optimized.[10][11] Nevertheless, the ACH route coproduces substantial amounts of ammonium sulfate: roughly 1.1 kg/(kg MMA). Disposal of the salt is very energy intensive.

Methyl propionate routes

The first stage involves carboalkoxylation of ethylene to produce methyl propionate (MeP):[12]

C2H4 + CO + CH3OH &#; CH3CH2CO2CH3

The MeP synthesis is conducted in a continuous-stirred tank reactor at moderate temperature and pressure using proprietary agitation and gas-liquid mixing arrangement.

In a second set of reactions, MeP is condensed with formaldehyde in a single heterogeneous reaction step to form MMA:[13]

CH3CH2CO2CH3 + CH2O &#; CH3(CH2)CCO2CH3 + H2O

The reaction of MeP and formaldehyde takes place over a fixed bed of catalyst. This catalyst, caesium oxide on silica, achieves good selectivity to MMA from MeP. The formation of a small amount of heavy, relatively involatile compounds poisons the catalyst. The coke is easily removed and catalyst activity and selectivity restored by controlled, in-situ regeneration. The reactor product stream is separated in a primary distillation so that a crude MMA product stream, free from water, MeP and formaldehyde, is produced. Unreacted MeP and water are recycled via the formaldehyde dehydration process. MMA (>99.9%) is purified by vacuum distillations. The separated streams are returned to the process; there being only a small heavy ester purge stream, which is disposed of in a thermal oxidizer with heat recovered for use in the process.

In , Lucite International commissioned an Alpha MMA plant on Jurong Island in Singapore. This process plant was cheaper to build and run than conventional systems, produces virtually no waste and the feedstocks can even be made from biomass.

Other routes to MMA

Via propionaldehyde

Ethylene is first hydroformylated to give propanal, which is then condensed with formaldehyde to produce methacrolein, The condensation is catalyzed by a secondary amine. Air oxidation of methacrolein to methacrylic acid completes the synthesis of the acid:[10]

CH3CH2CHO + HCHO &#; CH2=C(CH3)CHO + H2O

CH2=C(CH3)CHO +

1

&#;

2

 O2 &#; CH2=C(CH3)CO2H

From isobutyric acid

As developed by Atochem and Röhm, isobutyric acid is produced by hydrocarboxylation of propene, using HF as a catalyst:

CH2=CHCH3 + CO + H2O &#; (CH3)2CHCO2H

Oxidative dehydrogenation of the isobutyric acid yields methacrylic acid. Metal oxides catalyse this process:[10]

(CH3)2CHCO2H + O &#; CH2=C(CH3)CO2H + H2O

Methyl acetylene (propyne) process

Using Reppe chemistry, methyl acetylene is converted to MMA. As developed by Shell, this process produces MMA in one step reaction with 99% yield with a catalyst derived from palladium acetate, phosphine ligands, and Bronsted acids as catalyst:[10]

CH&#;CCH3 + CO + CH3OH &#; CH2=C(CH3)CO2CH3

Isobutylene routes

The reactions by the direct oxidation method consist of two-step oxidation of isobutylene or TBA with air to produce methacrylic acid and esterification by methanol to produce MMA.[10]

CH2=C(CH3)2 (or (CH3)3C&#;OH) + O2 &#; CH2=C(CH3)&#;CHO + H2O

CH2=C(CH3)CHO +

1

&#;

2

 O2 &#; CH2=C(CH3)CO2H

CH2=C(CH3)CO2H + CH3OH &#; CH2=C(CH3)CO2CH3 + H2O

A process using isobutylene as a raw material has been commercialized by Escambia Co. Isobutylene is oxidized to provide α-hydroxy isobutyric acid. The conversion uses N2O4 and nitric acid at 5&#;10 °C in the liquid phase. After esterification and dehydration MMA is obtained. Challenges with this route, aside from yield, involve the handling of large amounts of nitric acid and NOx. This method was discontinued in after an explosion at an operation plant.[10]

Methacrylonitrile (MAN) process

MAN can be produced by ammoxidation from isobutylene:

(CH3)2C=CH2 + NH3 +

3

&#;

2

 O2 &#; CH2=C(CH3)CN + 3 H2O

This step is analogous to the industrial route to acrylonitrile, a related commodity chemical. MAN can be hydrated by sulfuric acid to methacrylamide:

CH2=C(CH3)CN + H2SO4 + H2O &#; CH2=C(CH3)&#;CONH2·H2SO4

CH2=C(CH3)&#;CONH2·H2SO4 + CH3OH &#; CH2=C(CH3)COOCH3 + NH4HSO4

Mitsubishi Gas Chemicals proposed that MAN can be hydrated to methacrylamide without using sulfuric acid and is then esterified to obtain MMA by methylformate.[10]

CH2=C(CH3)CN + H2O &#; CH2=C(CH3)&#;CONH2

CH2=C(CH3)&#;CONH2 + HCOOCH3 &#; CH2=C(CH3)COOCH3 + HCONH2

HCONH2 &#; NH3 + CO

Esterification of methacrolein

Asahi Chemical developed a process based on direct oxidative esterification of methacrolein, which does not produce by-products such as ammonium bisulfate. The raw material is tert-butanol, as in the direct oxidation method. In the first step, methacrolein is produced in the same way as in the direct oxidation process by gas phase catalytic oxidation, is simultaneously oxidized and is esterified in liquid methanol to get MMA directly.[10]

CH2=C(CH3)&#;CHO + CH3OH +

1

&#;

2

For more MMA Plantinformation, please contact us. We will provide professional answers.

 O2 &#; CH2=C(CH3)&#;COOCH3 + H2O

Uses

The principal application, consuming approximately 75% of the MMA, is the manufacture of polymethyl methacrylate acrylic plastics (PMMA). Methyl methacrylate is also used for the production of the co-polymer methyl methacrylate-butadiene-styrene (MBS), used as a modifier for PVC. Another application is as cement used in total hip replacements as well as total knee replacements. Used as the "grout" by orthopedic surgeons to make the bone inserts fix into bone, it greatly reduces post-operative pain from the insertions but has a finite lifespan. Typically the lifespan of methylmethacrylate as bone cement is 20 years before revision surgery is required. Cemented implants are usually only done in elderly populations that require more immediate short term replacements. In younger populations, cementless implants are used because their lifespan is considerably longer.[14] Also used in fracture repair in small exotic animal species using internal fixation.

MMA is a raw material for the manufacture of other methacrylates. These derivatives include ethyl methacrylate (EMA), butyl methacrylate (BMA) and 2-ethyl hexyl methacrylate (2-EHMA). Methacrylic acid (MAA) is used as a chemical intermediate as well as in the manufacture of coating polymers, construction chemicals and textile applications.[15]

Wood can be impregnated with MMA and polymerized in situ to produce stabilized wood.

Environmental issues and health hazards

In terms of the acute toxicity of methyl methacrylate, the LD50 is 7&#;10 g/kg (oral, rat). It is an irritant to the eyes and can cause redness and pain.[16][17] Irritation of the skin, eye, and nasal cavity has been observed in rodents and rabbits exposed to relatively high concentrations of methyl methacrylate. Methyl methacrylate is a mild skin irritant in humans and has the potential to induce skin sensitization in susceptible individuals.[18][19]

See also

References

Methyl methacrylate, otherwise known as MMA, is a bonding agent used in some artificial nail products making it set much faster and adhere stronger to the nail than other products.  

MMA exposure has been linked to adverse health effects including dermal toxicity and respiratory tract effects. 

History of MMA

Methyl methacrylate is used as cement in dentistry, orthopedic surgery and ophthalmology.

After receiving complaints of injury associated with the use of artificial nails containing MMA in the s, the U.S. Food & Drug Administration (FDA) removed products containing 100% MMA from the market.

MMA is cheaper in comparison to other agents which is why it is still used. However, Ethyl Methacrylate or EMA, is the alternative monomer used in most acrylic nail liquids. 

Arizona Administrative Code R4-10-112(M) prohibits the use of products containing hazardous substances banned by the FDA from being used in a salon or school.

What to Look Out For

Nail liquid containing MMA has been known to cause allergic reactions, permanent loss of the nail plate and in some cases, permanent loss of sensation in the fingertips. It has a strong irritating chemical odor that does not smell like other acrylic liquids.
 

How do you know if a product contains MMA?

• MMA is listed as an active ingredient on the product label.

• It has a strong irritating chemical odor that does not smell like other acrylic liquids.

• The product sets much harder, feels less flexible and is very difficult to file using a nail file.

• Acrylic nails that contain MMA are extremely hard or virtually impossible to remove using normal solvents.

• It is a much cheaper product (approximately one third of the price) in comparison to other acrylic nail products.

Consumers have the right to ask, and be informed of, whether a product contains MMA.

Substitutes for MMA

There are a number of alternatives to MMA including ethyl methacrylate (EMA), light cure gels, wraps and natural nail manicures.

If you believe a salon is using MMA, please file a complaint with the Arizona Barbering & Cosmetology Board. 

For more information, please visit MEG Plant.