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Monomers studied

The monomers studied, 2-hydroxyethyl methacrylate (HEMA) and diethylene glycol dimethacrylate (DEGDMA), were obtained from Aldrich (Milwaukee, WI) and Polysciences, Inc. (Warrington, PA), respectively, and were used after dehibition to remove the hydroquinone inhibitor. 2,2-Dimethoxy-2-phenyl acetophenone (DMPA), the conventional initiator used in this study, was obtained from Ciba-Geigy (Hawthorne, NY) and the tetraethylthiuram disufide (TED) was obtained from Aldrich. [Pg.53]

Hermann Staudinger, on developing a new and simple preparation of the monomer, studied the polymerization of isoprene as early as 1910 (42). Stimulated by the differences in physical properties between his synthetic rubber and natural rubber, he turned his full attention to the study of polymers. [Pg.33]

Organometallic compounds containing polymerizable carbon-carbon double bonds have been synthesized and their polymerization studied [Archer, 2001 Pittman et al., 1987]. Among the organometallic monomers studied are vinylferrrocene and trialkyltin methacrylate. Much of the interest in these polymerizations has been to obtain polymers with... [Pg.330]

Among the nucleophilic monomers studied are 5,6-dihydro-4T/-l,3-oxazines, cyclic phosphites and phosphonites, iminodioxolanes, and imines electrophilic monomers include... [Pg.605]

In contrast, Kanca et al. observed that aliphatic AB monomers (Scheme 11) comprising a secondary hydroxyl group and an ester moiety did show high enantioselectivities in a Novozym-435-catalyzed transesterification reaction [104]. The E was high for all monomers studied E > 200). An additional advantage... [Pg.105]

Polyurethane hydrogels derived from UV curable urethane prepolymer and hydrophilic monomers were prepared and their properties were evaluated. The urethane prepolymer used in this study contained well-defined hard segments centered with a polyether-based soft segment and end-capped with methacrylate groups. The hydrophilic monomers studied were 2-hydroxyethyl methacrylate (HEMA), N-vinyl pyrrolidone, and glycerol methacrylate. Methacryloxypropyl tris(trimethysiloxy) silane (TRIS) was also used in some cases to modify properties. All compositions were UV... [Pg.175]

Table II shows the experimental data as well as the maximum overall reaction rates of the monomers studied. All figures are average values of at least two preparations—i.e., four dilatometric measurements. The last column gives the reaction rate relative to that of a comparable styrene emulsion under the same conditions of temperature and dose rate whose reaction rate was accepted as unity. Table II shows the experimental data as well as the maximum overall reaction rates of the monomers studied. All figures are average values of at least two preparations—i.e., four dilatometric measurements. The last column gives the reaction rate relative to that of a comparable styrene emulsion under the same conditions of temperature and dose rate whose reaction rate was accepted as unity.
Methyl acrylate gave by far the highest absolute reaction rates of all monomers studied. [Pg.201]

Vinyl monomers studied were acrylonitrile, methyl methacrylate and methacrylic acid The toxicity or hazardous nature of ferric azide is not given in Sax nor were there found any other expl props repotted in the literature (Refs 7 8)... [Pg.544]

Armstrong, and Rutherford have reported extensive studies on the vapor phase grafting of vinyl monomers to cellulosic fibers both mutual and pre-irradiation methods have been used (97, 120). Again, water or another swelling agent was found to be necessary for effective grafting to rayon and cotton for all the monomers studied. In the case of cellulose acetate water was helpful but not necessary except for styrene. Acetic acid and methanol vapors were also found to be effective promotors of vapor phase grafting to cotton and cellulose acetate fibers. [Pg.138]

Bemocco, S., Ferri, F., Profumo, A., Cuniberti, C., and Rocco, M. (2000). Polymerization of rod-like macromolecular monomers studied by stopped-flow, multiangle light scattering Set-up, data processing, and application to fibrin formation. Biophys.J. 79, 561—583. [Pg.286]

Electrochemical measurements are useful for determining concentrations of electroactive species in solution. Playing the role of solvent, the monomer studied in this chapter is styrene. One of its most remarkable characteristics is the low dielectric constant (e=2.43 at 298.0K) compared with that of water (e=78 at 298.0K). A solvent with a low dielectric constant is a highly resistive medium, in which voltammetric measurements are not evident. Voltammetric measurements in styrene as solvent have not been described before. Papers describing an electrochemical method for the determination of styrene in more polar organic solvents can be found in the literature13-17. [Pg.309]

The first approach has found limited applications. Concerning the direct copolymerization of olefins with functional monomers, studies of copolymerization of olefins by metallocene catalysts have been reported with functional... [Pg.81]

Regeneration of impurity is dictated by the failure to observe any acceleration in the rate of polymerization with conversion, of most monomers studied, because of consumption of inhibitor. Radiolytic formation of inhibitor is suggested by the fact that in most monomers studied,... [Pg.226]

The only other dienic monomer studied in this context is sp/f )[2,4Ihepta-4,6-diene. Its polymerisation by various trityl salts was investi ted by Kunitake et al. in methylene chloride-toluene mixtures at —76°C. This study was entirely devoted to the alternative 1,2 and 1,4 propagation modes and no attention was given to the mechanism of initiation or other fundamental problems. [Pg.196]

Polymerizing Tendency of Different Monomers. Among the monomers studied by us the acrylates polymerized most rapidly by far. In sequence follow MMA, styrene, and far behind methyl isopropenyl ketone. Some monomers (methacrylonitrile and vinylidene chloride) showed no polymerization, even at rather high doses. As to methacrylonitrile, this may be due to the technical grade monomer. During the irradiation of the vinylidene chloride emulsion, the pH value of the water phase was not controlled this is probably the reason for the complications. [Pg.66]

Scheme 1. Polymerization of a mixed unit monomer studied by MALDI TOP. Scheme 1. Polymerization of a mixed unit monomer studied by MALDI TOP.
All protic solvents undergo multiple relaxation processes due to the presence of hydrogen bonding. In the case of water and formamide (F), the data can be described in terms of two Debye relaxations. For the alcohols and A-methyl-formamide (NMF), three Debye relaxations are required for the description. In all of these solvents, the low-frequency process involves the cooperative motion of hydrogen-bonded clusters. In the case of water and the alcohols the high-frequency process involves the formation and breaking of hydrogen bonds. The intermediate process in the alcohols is ascribed to rotational diffusion of monomers. Studies of dielectric relaxation in these systems have been carried out for the -alkyl alcohols up to dodecanol [8]. Values of the relaxation parameters for water and the lower alcohols are summarized in table 4.5. [Pg.182]

Table I lists the decay constants, X, obtained for the different concentrations of the monomers studied. These Xs are the average of the left and right values obtained for each concentration (11). Though statistical errors range from 5% to 17%, experimental irreproducibilities in target geometry, field homogeneity, detector thresholds, muon beam asymmetry and background result in a more probable error of 25% ( ). This level of reproducibility is quite reasonable when compared to rate constants obtained by competitive rate techniques and direct physical methods. Table I lists the decay constants, X, obtained for the different concentrations of the monomers studied. These Xs are the average of the left and right values obtained for each concentration (11). Though statistical errors range from 5% to 17%, experimental irreproducibilities in target geometry, field homogeneity, detector thresholds, muon beam asymmetry and background result in a more probable error of 25% ( ). This level of reproducibility is quite reasonable when compared to rate constants obtained by competitive rate techniques and direct physical methods.
The Fourier Transform spectra of the monomers studied indicate that Mu reacts to give only one free radical (at the time observed, 10 s) because there is only one pair of radical frequencies in each system. The comparison with substantiates the assumption that Mu is indeed adding across the vinyl bond of these monomers as shown in equation (5) ... [Pg.44]

This technique has been used to study the wettability of different conducting polymer systems (see Table 1.8) and how this is influenced by the counterion incorporated during synthesis and/or functionalization of the monomer.156 The monomers studied are shown in Table 1.8. [Pg.42]

Fig. 6 Structures of the non-mesogenic bis-pyridyl (2) and bis-benzoic acid (3) monomers studied by Griffin et al. [67] and the proposed structure of the main chain liquid crystalline supramolecular polymer (2-3) highlighting the length of supramolecular mesogen... Fig. 6 Structures of the non-mesogenic bis-pyridyl (2) and bis-benzoic acid (3) monomers studied by Griffin et al. [67] and the proposed structure of the main chain liquid crystalline supramolecular polymer (2-3) highlighting the length of supramolecular mesogen...
In a series of papers43 4S), the kinetics of anionic polymerization of ethylene oxide in conjunction with different catalysts were studied. These studies expand our understanding of the mechanism of living polymerization systems and provide new information on the processes of active center association. Herein, primarily, lies the specific nature of the heteroatomic systems, as compared with the vinyl monomers studied earlier 9 ... [Pg.112]

Fig. 7 Schematic of the tyrosine and phenolic monomers studied, DELT and DEDT self-assembly, and the adsorption vs electropolymerization processes occurring at the Pt electrode surface. For simplicity, we have not attempted to indicate the - 0-ether linkage products that may also represent a minor fraction of the linkages foimd in the electropolymerized phenolic film products. This figure was reprinted with permission from [71]... Fig. 7 Schematic of the tyrosine and phenolic monomers studied, DELT and DEDT self-assembly, and the adsorption vs electropolymerization processes occurring at the Pt electrode surface. For simplicity, we have not attempted to indicate the - 0-ether linkage products that may also represent a minor fraction of the linkages foimd in the electropolymerized phenolic film products. This figure was reprinted with permission from [71]...
With residual monomer studies, polymer spheres are mostly involved since the polymers are produced as latices, suspension polymers or powders. The half time... [Pg.109]


See other pages where Monomers studied is mentioned: [Pg.453]    [Pg.77]    [Pg.286]    [Pg.554]    [Pg.13]    [Pg.168]    [Pg.422]    [Pg.118]    [Pg.14]    [Pg.458]    [Pg.2]    [Pg.45]    [Pg.585]    [Pg.6]    [Pg.292]    [Pg.1001]    [Pg.469]    [Pg.968]    [Pg.219]   
See also in sourсe #XX -- [ Pg.305 ]




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