Ethylene-methyl acrylate Subject

IR spectroscopy was used for quantitative analysis of the composition of three ethylene-acrylate copolymers, i.e. ethylene-methyl acrylate, ethylene-butyl acrylate and ethylene-2-ethylhexyl acrylate copolymers. Based on a simple model which explicitly considered vibrational band intensities characteristic for CH and for C 0, copolymer composition could be derived from the ratio of C 0 and CH integrated absorbances with a precision of + or -3 mol %. It was not necessary to know the optical path length of the copolymer samples which were subjected to IR analysis as pressed films. 15 refs. 

Poly (methyl methacrylate) was also subjected to mechanical reaction in a vibrating mill in common solvent for several monomers (ethylene, acrylic acid and its esters, acrylonitrile and styrene) at temperatures from —196 to 20° C (22). The formation of macroradicals and their reactions were followed by EPR (electron paramagnetic resonance). The macroradicals reacted with vinyl monomers at temperatures less than —100° C, while quinones underwent reaction as low as —196° C. The same experiments were performed also with polystyrene and polybutylenedimethacrylate. The radicals from polystyrene were more reactive than those from poly(methyl methacrylate). 

An MIP adsorbent is prepared for the extraction of 7-diethylamino-4-methyl-coumarin (Fig. 3). The print molecule, 7-diethylamino-4-methylcoumarin (4 mmol, 0.925 g), a functional monomer, 2-(trifluoromethyl) acrylic acid (12 mmol, 1.681 g), a cross-linking monomer, ethylene glycol dimethacrylate (60 mmol, 11.893 g) and a polymerization initiator, 2,2 -azobis(2,4-dimethylvaleronitrile) (0.140 g) are dissolved in anhydrous toluene (18 mL) in a 50-mL borosilicate PYREX tube.The solution is briefly purged with dry nitrogen for 5 min and sealed with a screw cap. The PYREX tube is transferred to a water bath preset at 45°C and maintained for 16 h. After polymerization, the polymer monolith is taken from the PYREX tube and fractured. This is further ground with a mechanical mortar (Retsch, Haan, ERG) and wet-sieved with 5% ethanol (v/v), and subjected to repetitive sedimentation in... 

Wang et al. (2002) demonstrated a composite membrane (subjected to PV) of an asymmetric poly(4-methyl-l-pentene) (TPX) membrane dip-coated with poly(acrylic acid) (PAA). To improve the interface peeling of the PA A/TPX composite membranes, the surfaces of TPX membranes were modified by residual air plasma in a tubular-type reactor. The plasma treatments were effective in rendering the asymmetric TPX membrane hydrophilic. Optimal results were obtained with PAA/TPX composite membrane prepared from the PAA/ethylene glycol (EG)/aluminum nitrate = 1/2/0.05 coating solution at 5 W/30 s plasma treatment condition. Concentration of the water in the permeate was nearly 100%, and a permeate flux of 960 g/m h was obtained with a 3 wt% feed acetic acid concentration. 

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... 

Poly(methyl methacrylate) was also subjected to mechanical reaction in a vibrating mill in a common solvent for several monomers (ethylene, acrylic acid and its esters, acrylonitrile, and styrene) at temperatures from —196... 

Although not strictly the subject matter of this book, work is briefly reviewed next on the application of non mass spectrometric Py-GC methods in the determination of polymer structure. This information is inclnded in the hope, when necessary, that chemists will be able to adapt these methods by including a mass spectrometric detailed information on polymer structure acrylates [63, 105-107], rubbers [63, 108-110], PVC [63,111-115], aliphatic polyhydrazides [116], polyoxamides [116], polyamides [117], polyether imides [118], methacrylamide [119], aromatic aliphatic polyamides [117], polyurethanes [120], chitin graft poly(2-methyl 2-oxazolone) [121, 122], polyxylyl sulfide [123-126], epoxy resins [127], polyethylene oxalate [128], polytetrafluoroethylene [129], polyvinylidene chloride [129], polyepichlorohydrin, fluorinated ethylene-propylene copolymer [129], polyvinyl fluoride [129], polyvinylidene [129], fluoride [129], SBR copolymer [129] and styrene-isoprene copolymer [130]. 

There is a large amount of literature and many patents in this area, as well as many good reviews and books [8,9,10,11,12,13,14,15,16,17,18,19]. The recent review by Coates [10] describing stereoselective polymerization overlaps considerably with this chapter, and is recommended for consultation. In this chapter, metallocene-catalyzed olefin polymerization is discussed, focusing on the synthesis of stereoregulated polymers. The aim of this review is not to be a complete survey the outline and some recent topics in polymerization of propylene, higher a-olefins, styrene, acrylate esters such as methyl methacrylate (MMA), 1,3-butadienes, and cycloolefins will be described. Polyethylene is one of the most important commercially manufactured polymers. The homopolymer, as well as the copolymer with ethylene and other olefins, is an important subject in the polyolefin industry. However, it will be only briefly mentioned because the stereochemistry is less involved. 

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