When were acrylic polymers invented?

Group of polymers prepared from acrylate monomers

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Structure of a polyacrylate polymer

An acrylate polymer (also known as acrylic or polyacrylate) is any of a group of polymers prepared from acrylate monomers. These plastics are noted for their transparency, resistance to breakage, and elasticity.

Acrylate polymer is commonly used in cosmetics, such as nail polish, as an adhesive.[1]

History

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The first synthesis of acrylic polymer was reported by G. W. A. Kahlbaum in .[2]

Acrylic elastomers

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Acrylic elastomer is a general term for a type of synthetic rubber whose primary component is acrylic acid alkylester (ethyl or butyl ester).[3] Acrylic elastomer possesses characteristics of heat and oil resistance, with the ability to withstand temperatures of 170&#;180 °C. It is used primarily for producing oil seals and packaging related to automobiles.

Acrylic elastomer can generally be characterized as one of two types. "Old" types include ACM (copolymer of acrylic acid ester and 2-chloroethyl vinyl ether) containing chlorine and ANM (copolymer of acrylic acid ester and acrylonitrile) without chloride. "New" types do not contain chlorine and are less prone to mold-related staining. Other than the slightly better water resistance of ANM there are no physical differences between the two types.

The material is less resistant in terms of cold weather with a saturation point of &#;15 °C for old types and &#;28 °C to &#;30 °C for new types. In terms of vulcanization, the standard method for the old type is amine vulcanization. To minimize permanent deformation, the old type requires curing for 24 hours at a temperature of 150 °C. On the other hand, for the new type, the press curing time and follow-up vulcanization time are significantly reduced by combining metal soap and sulfur. It has no special characteristics. The rebound resilience and abrasion resistance of the new type are poor, and even its electrical characteristics are considerably poor compared with acrylonitrile-butadiene rubber and butyl rubber.

Uses

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Related polymers

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• PVAc copolymer emulsion glue of vinyl acetate (VAM) and acrylic acid (VAA)
• Polyacrylamide copolymer used as flocculation agent in water treatment

See also

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References

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Acrylic polymers were developed in Germany over the course of around 70 years, despite technical and economic hurdles and battles over intellectual property and professional pride. (Photo: Evonik)

During the era when many of the polymers we have discussed previously (nylon, PET, PBT, PC, acetal) were undergoing development, another member of the family that has become a mainstay in the industry was following its own lengthy path to commercialization. This was the material that has become known generically as acrylic.

The process from the first synthesis of acrylic acid, the base from which the monomer is derived, to introduction of the commercial polymer, was an 85-year journey. Even after commercialization of the first compounds, the process of getting to the acrylic materials that we are familiar with today was fraught with a number of technical and economic hurdles, as well as battles involving intellectual property and professional pride. The process was driven almost exclusively by German chemists; even when contributions were made by scientists from other countries like England, they were working in or had been educated in Germany.

Acrylic acid was first synthesized in the laboratory in . Methacrylic acid was derived from acrylic acid in and shortly thereafter it was reacted with methanol to produce the compound known as methyl methacrylate. This is the monomer that is the primary ingredient in what would eventually become the acrylic polymer. The accompanying figure shows the chemical structure of these three compounds. Both methacrylic acid and methyl methacrylate contain the double bond that is crucial in promoting polymerization. In , the German chemist Wilhelm Rudolph Fittig, Professor of Chemistry at Tübingen University, discovered the process for polymerizing methacrylic acid.

 

Acrylic acid was first synthesized in , methacrylic acid in , and methyl methacrylate monomer soon after. Acrylic polymers as we know them didn&#;t appear until the s. (Image: M. Sepe)

The commercial significance of the material was not immediately recognized. At the time there was not a clear understanding of the composition of materials in this chemical family, and in particular there was poor comprehension of the difference between the organic acids and their esters. Today we know that esters of organic acids are more difficult to polymerize but produce more stable products. But the distinction between acrylic acids and their esters was not well understood at the time.

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In , Georg Kahlbaum, a professor at Basel University, carried out research on methyl acrylate, which he polymerized into polymethyl acrylate, the precursor to our PMMA of today. The initial polymers were not of very high molecular weight, taking the form of high-viscosity, gelatinous materials whose utility was not apparent at first. But it was noted that as the polymer formed, the clear monomers remained clear in polymerized form.

One of the big challenges was developing an efficient method for manufacturing the acrylic acid esters to be used as monomers.

In Otto Röhm published his doctoral dissertation on polymerization products of acrylic acid. Röhm&#;s thesis advisor at the beginning of his doctoral studies was Hans von Pechmann, also a Professor of Chemistry at Tübingen University and the person who had first created polyethylene in while studying diazomethane. Von Pechmann was persuaded that acrylic-based materials had the same potential as other notable successes of the time such as rubber, celluloid, and casein. He asked Röhm to conduct his doctorate research on esters of acrylic acid. Röhm quickly figured out that methyl acrylate polymerized more easily than ethyl acrylate and focused on creating a solid material using a combination of light, heat, and a chemical initiator. He produced a colorless, transparent material that had characteristics &#;between tough, flexible glass and stiff rubber.&#;

If von Pechmann had remained as Röhm&#;s advisor, Röhm would likely have transitioned smoothly into an academic position at Tübingen. But by the fall of , when Röhm was concluding his work, von Pechmann left the university, having been diagnosed with &#;severe melancholy,&#; what today would be called depression, and took his own life in April of . Röhm set aside his doctorate, but appeared to have an instinctive appreciation of the potential for these materials, and in he teamed up with banker Otto Haas to form the Rohm & Haas chemical company, a name which became synonymous with acrylic polymers.

The initial focus for the use of these materials was in textiles and leather goods. Röhm used the proceeds from the sales of these products to resume his acrylic chemistry research. But the history of the development of modern acrylic polymers was characterized by Röhm&#;s approach as a businessman rather than a chemist. This led to long periods of attempts to develop products that reflected a poor understanding of the acrylic chemistry because the focus was on developing a product that was marketable. Röhm observed that the acrylic polymers he was creating had a rubber-like set of properties.

Aware of the success of natural and synthetic rubber, Rohm sought to produce an ester-based rubber using the mechanism of vulcanization. In Röhm received a German patent for the &#;process for manufacturing a product with the properties of vulcanized rubber.&#; A special rolling mill was installed at Rohm & Haas to carry out the vulcanization process. But the patent was not technically viable because vulcanization relies on unsaturated sites where the sulfur can attach chemically to create the crosslinked structure. Röhm did not realize that the ester-based polymers were saturated structures that could not be vulcanized.

Rohm observed that the acrylic polymers he was creating had a rubber-like set of properties.

Nevertheless, in , Röhm secured a German patent for the use of polymerized acrylic acid esters as paint binders and for use in drying oils in industrial paints and lacquers. During this time period, Röhm came up with about 20 different proposed routes for creating useful products based on acrylic acid chemistry. By he had brought on six chemists to work through these ideas. One of these chemists was Dr. Walter Bauer, who became Röhm&#;s point man for all things acrylic. Bauer dutifully worked through Röhm&#;s proposals, but had a much better fundamental understanding of organic chemistry. After going through Röhm&#;s laundry list without success, he began to work on his own ideas for synthesizing acrylic esters.

One of the big challenges was developing an efficient method for manufacturing the acrylic acid esters to be used as monomers. Many experimenters had started with organic acids, aldehydes or ketones that had chemical structures similar to acrylic acid. These various approaches were plagued by poor yields. Bauer developed a complex multi-step process dubbed the ethylene approach. Because ethylene was difficult to obtain at the time, Bauer started with acetylene, reacting it with hydrogen bromide to form ethylene bromide. This was a route that most chemists felt was fruitless, but Bauer showed that in the presence of the appropriate catalysts, it worked.

This reaction, which was only the beginning of the process, became the subject of two patents issued to Rohm & Haas in and . The process concluded with an innovative approach to the chemistry that was called the &#;one-pot process.&#; In doing so, Bauer exploited a chemistry that had been developed in but had problems with yield that he was able to solve, making the route to commercial application viable.

Bauer, in commenting on his experiences in investigating new approaches to chemistries that were thought to be useless, delivered a quote that should resonate with all innovators: &#;Doubts about the accuracy of existing thinking prove to be justified again and again. Research scientists frequently need to act in a way that appears irrational.&#;

The monomer that Bauer succeeded in synthesizing was ethyl acrylate. While the breakthrough was made in the very early s, a combination of technical challenges related to polymerization, economic difficulties in Germany during the s, and a healthy dose of paranoia regarding the intellectual property associated with the one-pot process, delayed the development of useful commercial products for about a decade. And that part of the story will be told in our next installment.

ABOUT THE AUTHOR: Michael Sepe is an independent materials and processing consultant based in Sedona, Ariz., with clients throughout North America, Europe, and Asia. He has more than 45 years of experience in the plastics industry and assists clients with material selection, designing for manufacturability, process optimization, troubleshooting, and failure analysis. Contact: (928) 203- &#; 

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