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Acrylic acid (IUPAC: prop-2-enoic acid) is an organic compound with the formula CH2=CHCOOH. It is the simplest unsaturated carboxylic acid, consisting of a vinyl group connected directly to a carboxylic acid terminus. This colorless liquid has a characteristic acrid or tart smell. It is miscibility with water, alcohols, , and chloroform. More than a million tons are produced annually.
This method requires nickel carbonyl, high pressures of carbon monoxide, and acetylene, which is relatively expensive compared to propylene.
Acrylic acid was once manufactured by the hydrolysis of acrylonitrile, a material derived from propene by ammoxidation, but this route was abandoned because it cogenerates ammonium side products, which must be disposed of. Other now abandoned precursors to acrylic acid include ethenone and ethylene cyanohydrin.
Acrylic acid and its esters readily combine with themselves (to form polyacrylic acid) or other (e.g. , acrylonitrile, Vinyl group compounds, styrene, and butadiene) by reacting at their double bond, forming or , which are used in the manufacture of various , , , , as well as floor polishes and paints.
Acrylic acid is used in many industries, including the diaper industry, the water treatment industry, and the textile industry. The annual worldwide consumption of acrylic acid is projected to reach more than an estimated 8,000 kilotons by 2020. This increase is expected due to its use in new applications, including personal care products, Detergent, and products for adult incontinence.
More specifically, these are:
Animal studies showed that high doses of acrylic acid decreased weight gain. Acrylic acid can be converted to non-toxic lactic acid.
Acrylic acid is a constituent of tobacco smoke.
Research
carboxylation ethylene to acrylic acid under supercritical carbon dioxide is thermodynamically possible, but efficient catalysts have not been developed. 3-Hydroxypropionic acid (3HP), an acrylic-acid precursor by dehydration, can be produced from sugars, but the process is not competitive. Sweet Deal: Dow and Partner Cook up Sugar-to-Acrylic Plan. Durabilityanddesign.com. Retrieved on 2012-05-24. Better Bugs to Make Plastics, Technology Review, September 20, 2010, retrieved January 9, 2012. Technologyreview.com (2010-09-20). Retrieved on 2012-05-24.
Reactions and uses
Acrylic acid undergoes the typical reactions of a carboxylic acid. When reacted with an alcohol, it forms the corresponding ester. The esters and salts of acrylic acid are collectively known as (or propenoates). The most common alkyl esters of acrylic acid are Methyl acrylate, butyl, ethyl, and 2-ethylhexyl acrylate.
Substituents
As a substituent acrylic acid can be found as an acyl group or a carboxyalkyl group, depending on the removal of the group from the molecule.
Safety
Acrylic acid is severely irritating and corrosive to the skin and the respiratory tract. Eye contact can result in severe and irreversible injury. Low exposure will cause minimal or no health effects, while high exposure could result in pulmonary edema. The is 340 mg/kg (rat, oral) with the lowest recorded being 293 mg/kg (oral, rat), comparable to ethylene glycol, which is indicative of being a potent poison. Ethyl acrylate was once used as a synthetic food flavoring and was withdrawn by the FDA possibly due to carcinogenic effects observed in lab animals.
See also
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