Acrylic acid depolymerizing

The drive to use starch at higher addition levels requires it to contribute to the expected strength properties. For this to happen, the starch must be disrupted or destructured so that it can form a continuous phase in an extruded matrix. This can be done by extrusion of starch under low moisture conditions, which effects granular fragmentation, melting of hydrogen-bonded crystallites and partial depolymerization. Thermoplastic blends of up to 50% starch and poly(ethylene-co-acrylic acid) (EAA) were produced in the presence of aqueous base, which solubilized EAA and increased its compatibility with starch and urea, which aids in starch gelatinization.147,148... 

Historically, the development of the acrylates proceeded slowly they first received seiious attention from Otto Rohm. Acrylic acid (propenoic acid) was first prepared by the ah oxidation of acrolein in 1843 (1,2). Methyl and ethyl acrylate were prepared in 1873, but were not observed to polymerize at that time (3). In 1880 poly(metliyl acrylate) was reported by G. W. A. Kahlbaum, who noted that on dry distillation up to 320°C the polymer did not depolymerize (4). Rohm observed the remarkable properties of acrylic polymers while preparing for his doctoral dissertation in 1901 however, a quarter of a century elapsed before he was able to translate his observations into commercial reality. He obtained a U.S. patent on the sulfur vulcanization of acrylates in 1912 (5). Based on the continuing work in Robin s laboratory, the first limited production of acrylates began in 1927 by the Rohm and Haas Company in Darmstadt, Germany (6). Use of this class of compounds has grown from that time to a total U.S. consumption in 1989 of approximately 400,000 metric tons. Total worldwide consumption is probably twice that. 

In addition to the depolymerization reaction discussed earlier, other reactions may be favoured. These are elimination from a side chain and cyclization. For example, propylene is eliminated from the side chain of poly (isopropyl acrylate) as shown in Scheme 1.51(a), leaving poly(acrylic acid). This occurs in all polymers having ester side groups with P-hydrogens available to form a six-membered transition state, as shown. Thus both acrylate and methacrylate polymers will undergo this reaction and, since depolymerization is the dominant thermal-degradation reaction in methacrylates, elimination of alkenes is more important in the poly(acrylates). 

Acrylic acid, CH2=CHCOOH, can be produced by a series of processes direct oxidation of acrolein oxidation of ethylene to ethylene oxide, with further reaction with hydrogen cyanide to ethylene cyanhydrin, which is then saponified and dehydrated addition of carbon monoxide and water to acetylene and from acetone by pyrolysis to ketene and addition of formaldehyde to the ketene to produce jS-propiolactone. jS-Propiolactone polymerizes to the corresponding polyester, which depolymerizes at 150 C to acrylic acid ... 

The usage of acrylic esters as building blocks for polymers of industrial importance began in earnest with the experimentation of Otto Rohm (1). The first recorded preparation of the basic building block for acrylic ester polymers, acrylic acid, took place in 1843 this synthesis relied on the air oxidation of acrolein (2,3). The first acrylic acid derivatives to be made were methyl acrylate and ethyl acrylate. Although these two monomers were synthesized in 1873, their utility in the polymer area was not discovered until 1880 when Kahlbaum polymerized methyl acrylate and tested its thermal stability. To his surprise, the polymerized methyl acrylate did not depolymerize at temperatures up to 320°C (4). Despite this finding of incredibly high thermal stability, the industrial production of acrylic ester polymers did not take place for almost another 50 years. 

Poly(acrylic acid) and poly(methacrylic acid) are hygroscopic, brittle, colorless solids with glass transitions of 106 [443] and 130 °C [444], respectively. Above 200 to 250 °C they lose water and become insoluble cross-linked polymer anhydrides. Poly(methacrylic acid) depolymerizes partially at this temperature. The anhydride is not hydrolyzable by water alone but by aqueous alkaline solutions at room temperature [443]. Decomposition takes place at about 350 °C. 

The characteristic features of the degradation of alkyl methacrylate polymers are considered elsewhere (see Section 15.3.2). In contrast to PEMA, PFEMA gives no monomer. In addition to the ester decomposition products vinyl fluoride and CO2, acetaldehyde and fluoroacetaldehyde are produced. Explanations have been proposed for the latter products on the basis of meth-acrylic acid/FEMA and FEMA/radical end FEMA adjacent unit interactions. It is argued that the ester decomposition route is favoured by F atom activation of the hydrogens, so suppressing depolymerization. 

Acrylic adhesives are essentially acrylic monomers which achieve excellent bonding upon polymerization. Typical examples are cyanoacrylates and ethylene glycol dimethacrylates. Cyanoacrylates [28] are obtained by depolymerization of a condensation polymer derived from a malonic acid derivative and formaldehyde. 

There has been a slight increase in activity in this area compared with that in the previous two year period. For the polymeric esters of acrylic, methacrylic acids, and related polymers the simplest reaction, apart from thermal depolymerization, is hydrolysis, and one or two papers on this subject have appeared. One of these concerns a comparison of the kinetics of hydrolysis of a number of methacrylate esters and a further two deal with the formation of copolymers containing carboxylic acid functions. Methyl trifluoroacrylate forms alternating copolymers with cE-olefins (ethylene, propylene, isobutylene) and these are readily hydrolysed in boiling aqueous methanolic sodium hydroxide to yield hydrophilic fluoropolymers. Hydrolysis is reported to be nearly quantitative with no chain scission. An alternating copolymer is also formed by radical polymerization of maleic anhydride with A-vinyl succinimide. On hydrolysis this copolymer is... 

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