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Methyl methacrylate mechanical properties

Mechanical properties of a hydrogel lens also are affected by the use of a hydrophobic monomer, such as a low alkyl methacrylate. This is particularly important when the water content of the hydrogel lens is very high. The use of these methacrylates helps preserve the required mechanical strength. Methyl methacrylate [80-62-6] (MMA) (I2I), isobutyl methacrylate [97-86-9] (122), and / -pentyl methacrylate [2849-98-1] (123) all have been used for this purpose. [Pg.104]

Most of the polymer s characteristics stem from its molecular stmcture, which like POE, promotes solubiUty in a variety of solvents in addition to water. It exhibits Newtonian rheology and is mechanically stable relative to other thermoplastics. It also forms miscible blends with a variety of other polymers. The water solubiUty and hot meltable characteristics promote adhesion in a number of appHcations. PEOX has been observed to promote adhesion comparable with PVP and PVA on aluminum foil, cellophane, nylon, poly(methyl methacrylate), and poly(ethylene terephthalate), and in composite systems improved tensile strength and Izod impact properties have been noted. [Pg.320]

Mechanical Properties Related to Polymer Structure. Methacrylates are harder polymers of higher tensile strength and lower elongation than thek acrylate counterparts because substitution of the methyl group for the a-hydrogen on the main chain restricts the freedom of rotation and motion of the polymer backbone. This is demonstrated in Table 3. [Pg.261]

Table 3. Comparison of Mechanical Properties of Polyacrylate and Methyl Methacrylate ... Table 3. Comparison of Mechanical Properties of Polyacrylate and Methyl Methacrylate ...
The dynamic mechanical properties of VDC—VC copolymers have been studied in detail. The incorporation of VC units in the polymer results in a drop in dynamic modulus because of the reduction in crystallinity. However, the glass-transition temperature is raised therefore, the softening effect observed at room temperature is accompanied by increased brittleness at lower temperatures. These copolymers are normally plasticized in order to avoid this. Small amounts of plasticizer (2—10 wt %) depress T significantly without loss of strength at room temperature. At higher levels of VC, the T of the copolymer is above room temperature and the modulus rises again. A minimum in modulus or maximum in softness is usually observed in copolymers in which T is above room temperature. A thermomechanical analysis of VDC—AN (acrylonitrile) and VDC—MMA (methyl methacrylate) copolymer systems shows a minimum in softening point at 79.4 and 68.1 mol % VDC, respectively (86). [Pg.434]

Hard lenses can be defined as plastic lenses that contain no water, have moduli in excess of 5 MPa (500 g/mm ), and have T well above the temperature of the ocular environment. Poly(methyl methacrylate) (PMMA) has excellent optical and mechanical properties and scratch resistance and was the first and only plastic used as a hard lens material before higher oxygen-permeable materials were developed. PMMA lenses also show excellent wetting in the ocular environment even though they are hydrophobic, eg, the contact angle is 66°. [Pg.101]

Pure polymeric acrylonitrile is not an interesting fiber and it is virtually undyeable. In order to make fibers of commercial iaterest acrylonitrile is copolymerized with other monomers such as methacrylic acid, methyl methacrylate, vinyl compounds, etc, to improve mechanical, stmctural, and dyeing properties. Eibers based on at least 85% of acrylonitrile monomer are termed acryHc fibers those containing between 35—85% acrylonitrile monomer, modacryhc fibers. The two types are in general dyed the same, although the type and number of dye sites generated by the fiber manufacturing process have an influence (see Eibers, acrylic). [Pg.362]

Mechanical properties are typical of a rigid plastics material and numerical values (Table 30.2) are similar to those for poly(methyl methacrylate). Although thermosetting, it has a low heat distortion temperature ( 80°C) and is not particularly useful at elevated temperatures. [Pg.859]

Siloxane containing interpenetrating networks (IPN) have also been synthesized and some properties were reported 59,354 356>. However, they have not received much attention. Preparation and characterization of IPNs based on PDMS-polystyrene 354), PDMS-poly(methyl methacrylate) 354), polysiloxane-epoxy systems 355) and PDMS-polyurethane 356) were described. These materials all displayed two-phase morphologies, but only minor improvements were obtained over the physical and mechanical properties of the parent materials. This may be due to the difficulties encountered in controlling the structure and morphology of these IPN systems. Siloxane modified polyamide, polyester, polyolefin and various polyurethane based IPN materials are commercially available 59). Incorporation of siloxanes into these systems was reported to increase the hydrolytic stability, surface release, electrical properties of the base polymers and also to reduce the surface wear and friction due to the lubricating action of PDMS chains 59). [Pg.62]

Trialkyl (triaryl)stannyl methacrylates were copolymerized with ethylene and methyl methacrylate and it was shown that the resulting copolymer offers improved mechanical properties as compared to ethylene, and high fungicidal activity. It was suggested that homopolymers and copolymers of triethylstannyl methacrylate contain a covalent and an ionic bond between the carboxy group and the tin atom 63). [Pg.119]

A study of the polymerization kinetics of methyl methacrylate, in the presence of PBN, and of molecular-mass properties of the obtained polymers shows that the systems react by the pseudoliving mechanism (699). In the first stages of the polymerization process, PBN reacts with oligomeric radicals, forming stable nitroxyl radical-spin adducts A-, see Scheme 2.207. [Pg.295]

FIGURE 14.9 Influence of temperature on the stress-strain behavior of a sample of poly(methyl methacrylate). (Modeled after Carswell, T.S. and Nason, H.K. Effects of Environmental Conditions on the Mechanical Properties of Organic Plastics, 1944. Copyright, ASTM, Philadelphia, PA. With permission.)... [Pg.468]


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