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Poly , dimethacrylate

Procedure proposed by Papirer et al. [28,37-39,53] was used in characterization of silicas, modified silicas, oxides and minerals. Authors of refs. [23-28,30,54] used this method for characterization of carbon fibers, solid polymers, i.e. conducting polypyrroles, polycarbonates and poly (dimethacrylates), respectively. Voelkel and Krysztafkiewicz [55] characterized silicas modified by organic compounds. [Pg.472]

Reactive (unsaturated) epoxy resins (qv) are reaction products of multiple glycidyl ethers of phenoHc base polymer substrates with methacrylic, acryhc, or fumaric acids. Reactive (unsaturated) polyester resins are reaction products of glycols and diacids (aromatic, aUphatic, unsaturated) esterified with acryhc or methacrylic acids (see POLYESTERS,unsaturated). Reactive polyether resins are typically poly(ethylene glycol (600) dimethacrylate) or poly(ethylene glycol (400) diacrylate) (see PoLYETPiERs). [Pg.428]

Polymeric Calcium Phosphate Cements. Aqueous solutions of polymers such as poly(acryHc acid), poly(vinyl alcohol), gelatin, etc, and/or autopolymerizable monomer systems, eg, 2-hydroxyethyl methacrylate, glycerol dimethacrylate, calcium dimethacrylate, etc, have been used as Hquid vehicles (41,42,76) for the self-setting calcium phosphate cement derived from tetracalcium phosphate and dicalcium phosphate [7757-93-9J. [Pg.474]

Mention may also be made here of a number of polyfunctional compounds such as allyl methacrylate and glycol dimethacrylates which have been used to produce a cross-linked sheet of enhanced heat resistance compared with conventional poly(methyl methacrylate). Some manufacturers supply the sheet in an incompletely cross-linked state which allows a limited amount of forming after which the sheet may be further heated to complete the cure. [Pg.423]

Beaded methacrylate polymers, poly(hydroxyethylmethacrylate), Spheron, Separon (29), and poly(glycidylmethacrylate), Eupergin (30,31), are studied extensively at the Czechoslovak Academy of Macromolecular Sciences. An addition to this type of support is poly(oxyethylene-dimethacrylate) (32). Heitz et al. (33) described the preparation of beaded poly(methylacrylates) cross-linked with ethanedimethacrylates. [Pg.9]

Monodispersed poly (methyl methacrylate-ethyleneglycol dimethacrylate) is prepared by a multistep swelling and polymerization method. When a good solvent such as toluene is applied as a porogen, the seed polymer severely affects the pore structure, whereas no effects are observed with poor solvents, such as cyclohexanol, as a porogen, in comparison with the conventional suspension polymerization (68,69). [Pg.18]

The mixture of deprotected amino acid derivatives in solution was then immobilized onto a polymeric solid support, typically activated 5-)xm macroporous poly(hydroxyethyl methacrylate-co-ethylene dimethacrylate) beads, to afford the chiral stationary phases with a multiplicity of selectors. Although the use of columns... [Pg.86]

Various dimethacrylates have been polymerized in an effort to synthesize a poly(melhacrylale) with head-to-bead linkages.114 115 Various 1,6- e.g. dimcthacrylamidcs - see Tabic 4.4), 1,7- (e.g, dimcthacrylhydrazincs) and 1,8-dienes (e.g. dimethacryloylureas) are reported to give head-to-head addition (five-,... [Pg.193]

Another development has been the advent of the dual-cure resin cements. These are hybrids of glass polyalkenoate cements and methacrylates that set both by an add-base cementation reaction and by vinyl polymerization (which may be initiated by light-curing). In these materials, the solvent is not water but a mixture of water and hydroxyethylmethacrylate which is capable of taking dimethacrylates and poly(acrylic add)-containing vinyl groups into solution. In the absence of light these materials set slowly and... [Pg.3]

Figure 3. Time dependence of the fraction R of unreacted aminostyrene residues during acetylation by 0.14 M acetic anhydride at 30°C. Methyl methacrylate copolymer in acetonitrile solution (0) linear poly-(methyl methacrylate-co-butyl methacrylate) swollen with acetonitrile Cd) methyl methacrylate copolymer crosslinked with 1 mole% ( ) and with 15 mole% ( ) ethylene dimethacrylate poly(methacrylate crosslinked with 3 mole% ethylene dimethacrylate containing entrapped poly(methyl acrylate-co-aminostyrene) ( ). Figure 3. Time dependence of the fraction R of unreacted aminostyrene residues during acetylation by 0.14 M acetic anhydride at 30°C. Methyl methacrylate copolymer in acetonitrile solution (0) linear poly-(methyl methacrylate-co-butyl methacrylate) swollen with acetonitrile Cd) methyl methacrylate copolymer crosslinked with 1 mole% ( ) and with 15 mole% ( ) ethylene dimethacrylate poly(methacrylate crosslinked with 3 mole% ethylene dimethacrylate containing entrapped poly(methyl acrylate-co-aminostyrene) ( ).
The synthesis of organotin oligosteracrylate i.e. dimethylstannyl dimethacrylate, and the production of the cross-linked homopolymers on its basis have been reported. Morphology, mechanical and relaxation properties of poly(dimethyl-stannyl dimethacrylate) have been investigated 67). [Pg.120]

Figure 5 The mutual diffusion coefficient, D, of sodium chloride as a function of reciprocal matrix hydration, H, in various methacrylate gels. HPMA-GMA polyfhydroxypro-pyl methacrylate-co-glyceryl methacrylate) HEMA polyfhydroxyethyl methacrylate) MMA-GMA poly(methyl methacrylate-co-glyceryl methacrylate) HEMA-MMA poly-(hydroxyethyl methacrylate-co-methyl methacrylate) HPMA-MMA polyfhydroxypropyl methacrylate-co-methyl methacrylate) HPMA-GDMA polyfhydroxypropyl methacry-late-co-glyceryl dimethacrylate). (From Ref. 64.)... Figure 5 The mutual diffusion coefficient, D, of sodium chloride as a function of reciprocal matrix hydration, H, in various methacrylate gels. HPMA-GMA polyfhydroxypro-pyl methacrylate-co-glyceryl methacrylate) HEMA polyfhydroxyethyl methacrylate) MMA-GMA poly(methyl methacrylate-co-glyceryl methacrylate) HEMA-MMA poly-(hydroxyethyl methacrylate-co-methyl methacrylate) HPMA-MMA polyfhydroxypropyl methacrylate-co-methyl methacrylate) HPMA-GDMA polyfhydroxypropyl methacry-late-co-glyceryl dimethacrylate). (From Ref. 64.)...
TP Davis, MB Hughn, DCF Yip. Properties of poly(N-vinyl-2-pyrrolidone) hydrogels crosshnked with ethylene glycol dimethacrylate. Polymer 29 701-706, 1988. [Pg.551]

S Wisniewski, SW Kim. Permeation of water-soluble solutes through poly(2-hydroxyethyl methacrylate) and poly(2-hydroxyethyl methacrylate) crosslinked with ethylene glycol dimethacrylate. J Membrane Sci 6 299-308, 1980. [Pg.584]

A rather limited range of mesopores in terms of size and volume were observed in the skeletons of polymer monoliths. The porosity of the polymer monolith seems to be lower than that of silica monolith. The total porosity of these monoliths is in the range of 0.61-0.73, whereas interstitial (through-pore) porosity and mesopore porosity are 0.28-0.70 and 0.03-0.24, respectively. In the case of poly(butyl methacrylate-co-ethylene dimethacrylate), the observed porosity is around 0.61-0.71, resulting in permeability 0.15-8.43 x 10 14 m2, whereas the observed porosity of silica monoliths prepared in a capillary is 0.86-0.96 and the permeability is 7-120 x 10 14 m2. Higher permeability will be advantageous for 2D applications, as mentioned later. [Pg.149]

Ayhan, F., Yousefi Rad, A., and Ayhan, H. (2002) Biocompatibility investigation and urea removal from blood by urease-immobilized HEMA incorporated poly(ethyleneglycol dimethacrylate) microbeads. J. Biomed. Mater. Res. B Appl. Biomat. 64B(1), 13-18. [Pg.1044]

Fig. 3. Effect of dodecanol in the porogenic solvent on the differential pore size distribution of molded poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoliths (Reprinted with permission from [62]. Copyright 1996 American Chemical Society). Conditions polymerization time 24 h, temperature 70 °C, polymerization mixture glycidyl methacrylate 24%, ethylene dimethacrylate 16%, cyclohexanol and dodecanol contents in mixtures 60/0 (curve 1), 57/3 (curve 2), 54/6 (curve 3), and 45/15 vol.% (4)... Fig. 3. Effect of dodecanol in the porogenic solvent on the differential pore size distribution of molded poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoliths (Reprinted with permission from [62]. Copyright 1996 American Chemical Society). Conditions polymerization time 24 h, temperature 70 °C, polymerization mixture glycidyl methacrylate 24%, ethylene dimethacrylate 16%, cyclohexanol and dodecanol contents in mixtures 60/0 (curve 1), 57/3 (curve 2), 54/6 (curve 3), and 45/15 vol.% (4)...
Fig. 6. Reaction of poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith with diethylamine... Fig. 6. Reaction of poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith with diethylamine...
Fig. 8. Effect of linear flow velocity of an L-benzoyl arginine ethylester solution (0.2 mol/1) on the enzymatic activity of trypsin immobilized on poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads (curve 1) and monolith (curve 2) (Reprinted with permission from [90]. Copyright 1996 Wiley-VCH). Reactor 50 mm x 8 mm i.d., temperature 25 °C... Fig. 8. Effect of linear flow velocity of an L-benzoyl arginine ethylester solution (0.2 mol/1) on the enzymatic activity of trypsin immobilized on poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads (curve 1) and monolith (curve 2) (Reprinted with permission from [90]. Copyright 1996 Wiley-VCH). Reactor 50 mm x 8 mm i.d., temperature 25 °C...
Table 1. Porous properties and enzymatic activities of monolithic poly(2-vinyl-4,4-dimethyl-azlactone-co-acrylamide-co-ethylene dimethacrylate) reactors3... [Pg.102]


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See also in sourсe #XX -- [ Pg.150 ]

See also in sourсe #XX -- [ Pg.96 ]

See also in sourсe #XX -- [ Pg.96 ]




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