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Polyfmethyl methacrylate

As an example of the use of Small s table the solubility parameter of polyfmethyl methacrylate) may be computed as follows ... [Pg.91]

Weak links, particularly terminal weak links, can be the site of initiation of a chain unzipping reaction. A monomer or other simple molecule may be abstracted from the end of the chain in such a way that the new chain end is also unstable. The reaction repeats itself and the polymer depolymerises or otherwise degrades. This phenomenon occurs to a serious extent with polyacetals, polyfmethyl methacrylate) and, it is believed, with PVC. [Pg.97]

Flow properties of polyethylene have been widely studied. Because of the wide range of average molecular weights amongst commercial polymers the viscosities vary widely. The most commonly used materials, however, have viscosities lower than for unplasticised PVC and polyfmethyl methacrylate) and higher than for the nylons. [Pg.222]

VV -values for bromoform and pyrrole, acidic liquids, against poly(vinyl chloride), an acidic polymer, and dimethyl sulfoxide, a predominantly basic liquid, against polyfmethyl methacrylate), a basic polymer, but large values for the acidic liquids against PMMA and the basic liquid against PVC. 2-Iodoethanol, a bifunctional liquid, showed appreciable -values with both polymers. Despite these results in line with expectations, other results based on wettability measurements are not so clear-cut. For example, Vrbanac [94] found significant apparent acid-base interactions of various aromatic liquids against poly(ethylene), presumably a neutral substrate. [Pg.40]

J.P. Berry, Fracture processes in polymeric materials. I. The surface energy of polyfmethyl methacrylate), J. Polymer Sci., 50, 107-115, 1961. [Pg.20]

Whitney, R.S. and Burchard, W. Molecular size and gel formation in branched polyfmethyl methacrylate) copol3miers, Makromol. Chem., 181, 869, 1980. [Pg.219]

Polymer properties, influence of ions, 258 Polymer surface reactions, kinetics, 322-323 Polymer transformation reactions configurational effect, 38 conformational effects, 38 hydrolysis of polyfmethyl methacrylate), 38 neighboring groups, 37-38 quaternization of poly(4-vinyl pyridine), 37-38 Polymerization, siloxanes, 239... [Pg.481]

Figure 6 (A) Non-isothermal chemiluminescence runs for oxidation of polystyrene (PS), polyethylene terephthalate) (PETP) and polyfmethyl methacrylate) (PMMA), in oxygen, heating rate 2.5°C/min. (B) Non-isothermal chemiluminescence runs for oxidation of polypropylene (PP), polyamide 6 (PA 6), poly(vinyl pyrrolidone) (PVP), polyethylene (PE) and polyamide 66 (PA 66), in oxygen, heating rate 2.5°C/min. Figure 6 (A) Non-isothermal chemiluminescence runs for oxidation of polystyrene (PS), polyethylene terephthalate) (PETP) and polyfmethyl methacrylate) (PMMA), in oxygen, heating rate 2.5°C/min. (B) Non-isothermal chemiluminescence runs for oxidation of polypropylene (PP), polyamide 6 (PA 6), poly(vinyl pyrrolidone) (PVP), polyethylene (PE) and polyamide 66 (PA 66), in oxygen, heating rate 2.5°C/min.
Figure 5 Molecular structures of the cis and trans conformations in polyfmethyl-methacrylate). Figure 5 Molecular structures of the cis and trans conformations in polyfmethyl-methacrylate).
X-ray diffraction data are given for 182.221 2,4,6,8-Tetrathiaadamantane-thiol was tested for antibacterial and antiviral activity.222 1,3,5,7-Tetraalkyl-2,4,6,8-tetrathiaadamantane derivatives are used for lubricant additives.223 Polyfmethyl methacrylate) with good resistance to heat and air oxidation is prepared by polymerization of the monomer in the presence of 182.224... [Pg.116]

Poly(styrene)-poly(acrylate) colloidal suspensions, 7 275 Polystyrene/polyfmethyl methacrylate) commercial block copolymers, 7 648t Polystyrenes. See also Polystyrene (PS) commercial, 23 364 general-purpose, 23 364 specialty, 23 364-366 stabilized, 23 366 tactic, 23 365... [Pg.744]

Fig. 17. Experimentally measured values of the exit concentration as a function of pressure for a polymeric solution consisting of methyl methacrylate-polyfmethyl methacrylate). Data were obtained by Werner using a twin-screw extruder. (Reproduced with permission from Werner, 1980.)... Fig. 17. Experimentally measured values of the exit concentration as a function of pressure for a polymeric solution consisting of methyl methacrylate-polyfmethyl methacrylate). Data were obtained by Werner using a twin-screw extruder. (Reproduced with permission from Werner, 1980.)...
Amorphous polymers are characterized by the following properties They are transparent and very often soluble in common organic solvents at room temperature. The following amorphous polymers have gained industrial importance as thermoplastic materials polyfvinyl chloride), polystyrene, polyfmethyl methacrylate), ABS-polymers, polycarbonate, cycloolefine copolymers, polysulfone, poly( ether sulfone), polyfether imide). [Pg.24]

Galloway M, Stryjewski W, Henry A et al. Contact conductivity detection in polyfmethyl methacrylate)-based microfluidic devices for analysis of mono- and polyanionic molecules. Analytical Chemistry 74, 2407-2415, 2002. [Pg.230]

A similar method of hydrolysis was described for poly( vinyl alcohol) used as a template. In this case, T was -CH2-CH- and, after hydrolysis, poly(vinyl alcohol) and polyacrylic or polymethacrylic acid were obtained. The hydrolyzed product gives the color reaction with I2 in the presence of H3BO3 - specific to poly(vinyl alcohol). The second product of hydrolysis, after esterification by diazomethane, was identified as polyfmethyl methacrylate) by NMR and IR spectrometry. Hydrolysis was also applied in the case of ladder-type polymers obtained by polymerization of mutliallyl monomers. The polymerization should result in polymer consisting, at least partly, ladder-type blocks ... [Pg.144]

After hydrolysis by 2N methanol solution of H2SO4, the product was neutralized with KOH to pH=5 and methanol evaporated. The dry residue was expected to be poly(allilamine), polymethacrylic acid, and K2SO4. Indeed, after extraction with anhydrous methanol and acetone, poly(allilamine) was identified by NMR and IR spectrometries. After evaporation, solvent from the methanol part of the extract insoluble in chloroform part was obtained. After esterification by diazomethane the product was identified as polyfmethyl methacrylate) on the basis of IR and H-NMR spectroscopy. IR spectroscopy was applied in order to examine the copolymerization of multimethacrylate (p-cresyl-formaldehyde oligomers with methacrylic groups) with st3rrene. It was found that double bond peak at 1650 cm disappeared during the process and it was absent in the product of polymerization. Polymerization and... [Pg.144]

Oommen, Z., S. Thomas, C. K. Premalatha, and B. Kuriakose, Melt rheological behavior of natural rubber/polyfmethyl methacrylate)/natural rubber-g-poly(methy methacrylate) blends. Polymer, 38(22), 5611-5621 (1997). [Pg.374]

Benzoquinone amount, mg Benzoquinone % of polyfmethyl methacrylate) Q content %... [Pg.10]

Polyfmethyl methacrylate), initiated and polymerized at 250 by t-butylmagnesium bromide in toluene-THF solution (—). Mole fraction of monomer, X.VJM = 0.1 OM. XTHF is indicated in each case. A mixture of standard polystyrene samples of indicated molar mass (------). All traces are aligned so that the elution volumes correspond. [Pg.192]

Figure 3. Meso (isotactic) dyad frequency (m) of polyfmethyl methacrylate), prepared at 250 initiated by t-butylmagnesium bromide, as a function of solvent composition. The meso-frequency m is indicated for each point. The solvent composition, given in terms of mole fractions of THF, XThf, of toluene, Xtoiimie and of monomer, , ore indicated by the scale on each median, with each apex corresponding to the pure component indicated. Figure 3. Meso (isotactic) dyad frequency (m) of polyfmethyl methacrylate), prepared at 250 initiated by t-butylmagnesium bromide, as a function of solvent composition. The meso-frequency m is indicated for each point. The solvent composition, given in terms of mole fractions of THF, XThf, of toluene, Xtoiimie and of monomer, , ore indicated by the scale on each median, with each apex corresponding to the pure component indicated.

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Acrylic polymers Polyfmethyl methacrylate)

Polyfmethyl methacrylate) additives

Polyfmethyl methacrylate) applications

Polyfmethyl methacrylate) diblock copolymers

Polyfmethyl methacrylate) graft

Polyfmethyl methacrylate) radical

Polyfmethyl methacrylate) solubility parameter

Polyfmethyl methacrylate) stability

Polyfmethyl methacrylate) viscosity

Polyfmethyl methacrylate), PMMA

Polyfmethyl methacrylate-methyl

Polymer blends with polyfmethyl methacrylate)

Polymer polyfmethyl methacrylate)

Polystyrene, Styrene-Copolymers, PolyfMethyl Methacrylate)

Processing polyfmethyl methacrylate)

Resist polyfmethyl methacrylate)

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