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Poly phosphonated methacrylate

Figure 10.1 shows an almost linear trend for the evolution of corrosion as a function of time when the diblock copolymer is used as additive. As expected, virgin poly(VDF) alone is not able to prevent the metal from corrosion as the surface is almost completely corroded after only 48 h. Figure 10.1 also shows a high improvement when poly(VDF) is blended with poly(MMA)-b-poly(phosphonate methacrylate) diblock copolymer additive, although the statistical copolymer seems to afford better adhesion towards the metallic surface and hence better anticorrosion properties. [Pg.230]

A Poly(butadieneacrylonitrile) poly (butadiene) (-OH terminated) octadecylvinyl ether/maleic anhydride copolymer blend poly(vinyl stearate) poly (butadiene methacrylate) poly(l-butadiene) Generally exhibited highest sensitivity to test vapors, especially phosphonates (DMMP, DIMP) and octane... [Pg.324]

Spontaneous polymerization of 4-vinyl pyridine in the presence of polyacids was one of the earliest cases of template polymerization studied. Vinyl pyridine polymerizes without an additional initiator in the presence of both low molecular weight acids and polyacids such as poly(acrylic acid), poly(methacrylic acid), polyCvinyl phosphonic acid), or poly(styrene sulfonic acid). The polyacids, in comparison with low molecular weight acids, support much higher initial rates of polymerization and lead to different kinetic equations. The authors suggested that the reaction was initiated by zwitterions. The chain reaction mechanism includes anion addition to activated double bonds of quaternary salt molecules of 4-vinylpyridine, then propagation in the activated center, and termination of the growing center by protonization. The proposed structure of the product, obtained in the case of poly(acrylic acid), used as a template is ... [Pg.27]

D. Price, L.K. Cunliffe, K.J. Bullett (formerly Pyrah), T.R. Huh, G.J. Milnes, J.R. Ebdon, B.J. Hunl, and P. Joseph, Thermal behavior of covalently bonded phosphonate flame retarded poly(methyl methacrylate) systems. Polym. Adv. Technol., 19 (6), 710-723 (2008) and previous references therein. [Pg.41]

In contrast to stabilizers, fire retardants must be added in much higher concentrations, which affect thermal and mechanical properties as well as cost. Sherr and co-workers report that novel derivatives of phosphine oxides, phosphonic acids, phosphinic acid, and phosphonium halides may be used generally in concentrations as low as 2.5-5 p.p.h. to be effective fire retardants in polyethylene and poly (methyl methacrylate). [Pg.14]

In our studies we found that phosphonic acids (16), phosphinic acids (25), and phosphine oxides (17) are additives capable of imparting fire retardant properties to thermoplastic polymers. Tables I and II present data for some of these compounds when added to polyethylene or to poly (methyl methacrylate). The concentration reported is not necessarily the lowest effective concentration for the additive in the polymer. These additives also were effective in other thermoplastic polymers such as polystyrene, impact polystyrene, polypropylene and ABS. The compounds were completely compatible with the polymers. [Pg.325]

Some other interesting copolymers having properties of PVC thermal stabUizers, like poly[Af-(a-benzothiazolonylmethyl)methacrylate-co-methyl methacrylate] [45], of flame retardants like a terpolymer of styrene, acrylonitrile and a polymerizable perbrominated phenol [76] or poly[4-methacryloyloxy-2,3,5,6-tetrabromobenzyldi-phenyl phosphonate-co-methyl methacrylate] [104] (93), bioddes, mostly copolymers of monomers containing tris(n-butyl tin) or triphenyl tin moieties and alkyl acrylates, methacrylates, vinyl acetate, acrylonitrile, styrene or A-vinylpyrrolidone [105], e.g. a terpolymer of styrene, MMA and tri(n-butyl tin) itaconate [106] (94),... [Pg.93]

Dausend J, Musyanovych A, Dass M, et al. (2008) Uptake mechanism of oppositely charged fluorescent nanoparticles in HeLa cells. Macromol Biosci 8 1135-1143 Ziegler A, Landfester K, Musyanovych A (2009) Synthesis of phosphonate-functionalized polystyrene and poly(methyl methacrylate) particles and their kinetic behavior in miniemulsion polymerization. Colloid Polym Sci. http //dx.doi.Org/10.1007/s00396-009-2087-z Lorenz MR, Kohnle MV, Dass M, et al. (2008) Synthesis of fluorescent polyisoprene nanoparticles and their uptake into various cells. Macromol Biosci 8 711-727... [Pg.41]

Ziegler A, Landfester K, Musyanovych A (2009) Synthesis of phosphonate-functionalized polystyrene and poly(methyl methacrylate) particles and their kinetic behavior in miniemulsion polymerization. Colloid Polym Sci 287 1261-1271... [Pg.229]

Dimethyl [2-(methactyloylo qr)ethyl]phosphonate (MAPC2) (Scheme lO.l) has been successfully copolymerized with methyl methacrylate (MMA) and used as an additive with poly(vinylidene fluoride) [poly(VDF)]. The incorporation of a phosphonic component results in a copolymer with highly... [Pg.227]

Poly(methyl methacrylate) 1.6 Phosphonate (pendant) with sUieon atoms Decreased (nitrogen) Slightly 13 ... [Pg.270]

Poly(methyl methacrylate) 10 Phosphonate (MAPCl) Slightiy enhanced (nitrogen) Yes 14 ... [Pg.270]


See other pages where Poly phosphonated methacrylate is mentioned: [Pg.284]    [Pg.208]    [Pg.234]    [Pg.19]    [Pg.21]    [Pg.30]    [Pg.2]    [Pg.52]    [Pg.33]    [Pg.116]    [Pg.388]    [Pg.50]    [Pg.530]    [Pg.395]    [Pg.296]    [Pg.1621]    [Pg.20]    [Pg.231]    [Pg.236]    [Pg.271]    [Pg.271]    [Pg.584]    [Pg.274]    [Pg.38]    [Pg.315]    [Pg.416]   


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